# terms

id: PBO:0086124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for flavinylation of Sdh1p; binds to Sdh1p and promotes FAD cofactor attachment, which is necessary for succinate dehydrogenase (SDH) complex assembly and activity; mutations in human ortholog PGL2 are associated with neuroendocrine tumors (paraganglioma)","termid":"PBO:0086124"}


id: SO:0001554
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant which changes polypeptide functioning with respect to a reference sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translational_product_function_variant","termid":"SO:0001539"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polypeptide_function_variant","synonyms":[{"name":"polypeptide function variant","type":"exact"}],"termid":"SO:0001554"}


id: PBO:0044302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome b5 type A pseudogene 5","termid":"PBO:0044302"}


id: PBO:0066804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 103","termid":"PBO:0066804"}


id: GO:0030279
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of ossification, the formation of bone or of a bony substance or the conversion of fibrous tissue or of cartilage into bone or a bony substance.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ossification","termid":"GO:0030278"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"ossification","termid":"GO:0001503"}],"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 ossification","synonyms":[{"name":"down regulation of ossification","type":"exact"},{"name":"down-regulation of ossification","type":"exact"},{"name":"downregulation of ossification","type":"exact"},{"name":"inhibition of ossification","type":"narrow"},{"name":"negative regulation of bone biosynthesis","type":"exact"},{"name":"negative regulation of bone formation","type":"exact"}],"termid":"GO:0030279"}


id: MONDO:0003243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A morphologic variant of hepatocellular carcinoma characterized by the presence of clear cells.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clear cell adenocarcinoma","termid":"MONDO:0005004"},{"relation_name":"is_a","term_name":"hepatocellular carcinoma","termid":"MONDO:0007256"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515","MONDO:0004992"],"is_obsolete":false,"name":"hepatocellular clear cell carcinoma","secondary_identifiers":["MEDGEN:690059","ICDO:8174/3","NCIT:C5754","DOID:5016","UMLS:C1266020"],"synonyms":[{"name":"clear cell carcinoma of liver cells","type":"exact"},{"name":"clear cell carcinoma of the liver cells","type":"exact"},{"name":"clear cell hepatocellular cancer","type":"exact"},{"name":"clear cell hepatocellular carcinoma","type":"exact"},{"name":"hepatocellular clear cell carcinoma","type":"exact"},{"name":"liver cell clear cell carcinoma","type":"exact"}],"termid":"MONDO:0003243","xrefs":{"Monarch":{"xref_id":"0003243"}}}


id: PBO:0062147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily F member 17","termid":"PBO:0062147"}


id: PBO:0083617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"E1 alpha subunit of the pyruvate dehydrogenase (PDH) complex; catalyzes the direct oxidative decarboxylation of pyruvate to acetyl-CoA; phosphorylated; regulated by glucose; PDH complex is concentrated in spots within the mitochondrial matrix, often near the ERMES complex and near peroxisomes","termid":"PBO:0083617"}


id: PBO:0018230
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae BTS1","termid":"PBO:0018230"}


id: GO:0018924
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving mandelate, the anion of mandelic acid. Mandelic acid (alpha-hydroxybenzeneacetic acid) is an 8-carbon alpha-hydroxy acid (AHA) that is used in organic chemistry and as a urinary antiseptic.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"mandelate metabolic process","secondary_identifiers":["UM-BBD_pathwayID:mca"],"synonyms":[{"name":"mandelate metabolism","type":"exact"},{"name":"mandelic acid metabolic process","type":"exact"},{"name":"mandelic acid metabolism","type":"exact"}],"termid":"GO:0018924"}


id: GO:0048712
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of astrocyte differentiation.","definition_xrefs":["GOC:vp","PMID:15139015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of glial cell differentiation","termid":"GO:0045686"},{"relation_name":"is_a","term_name":"regulation of astrocyte differentiation","termid":"GO:0048710"},{"relation_name":"negatively_regulates","term_name":"astrocyte differentiation","termid":"GO:0048708"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of astrocyte differentiation","synonyms":[{"name":"down regulation of astrocyte differentiation","type":"exact"},{"name":"down-regulation of astrocyte differentiation","type":"exact"},{"name":"downregulation of astrocyte differentiation","type":"exact"},{"name":"inhibition of astrocyte differentiation","type":"narrow"}],"termid":"GO:0048712"}


id: FYPO:0006099
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 cytoplasm is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to cytoplasm","termid":"FYPO:0006098"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0000138"],"is_obsolete":false,"name":"decreased protein localization to cytoplasm","synonyms":[{"name":"decreased protein localisation to cytoplasm","type":"exact"},{"name":"decreased protein localization to cytoplasm during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to cytoplasm during vegetative growth","type":"exact"},{"name":"reduced protein localization to cytoplasm","type":"exact"}],"termid":"FYPO:0006099"}


id: GO:0030224
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized myeloid precursor cell acquires the specialized features of a monocyte.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid leukocyte differentiation","termid":"GO:0002573"},{"relation_name":"is_a","term_name":"mononuclear cell differentiation","termid":"GO:1903131"}],"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":"monocyte differentiation","synonyms":[{"name":"monocyte cell differentiation","type":"exact"}],"termid":"GO:0030224"}


id: GO:0046505
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving sulfolipids, any compound containing a sulfonic acid residue joined by a carbon-sulfur bond to a lipid.","definition_xrefs":["PMID:9751667"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid metabolic process","termid":"GO:0006629"},{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0006790"],"is_obsolete":false,"name":"sulfolipid metabolic process","synonyms":[{"name":"sulfolipid metabolism","type":"exact"},{"name":"sulpholipid metabolic process","type":"exact"},{"name":"sulpholipid metabolism","type":"exact"}],"termid":"GO:0046505"}


id: GO:0018058
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The oxidative deamination of the alpha carbon of an encoded N-terminal amino acid, to form pyruvic acid retaining an amide bond between its 1-carboxyl group and the adjacent residue. The pyruvate 2-oxo group may become an enzyme active site, or it may be reduced to an alcohol.","definition_xrefs":["RESID:AA0129","RESID:AA0127","RESID:AA0128"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-cysteine modification","termid":"GO:0018198"},{"relation_name":"is_a","term_name":"protein deamination","termid":"GO:0018277"},{"relation_name":"is_a","term_name":"N-terminal protein amino acid deamination","termid":"GO:0031363"}],"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":"N-terminal protein amino acid deamination, from amino carbon","termid":"GO:0018058"}


id: GO:0010158
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell becomes capable of differentiating autonomously into an abaxial cell in an environment that is neutral with respect to the developmental pathway; upon specification, the cell fate can be reversed.","definition_xrefs":["GOC:mg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate specification","termid":"GO:0001708"}],"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":"abaxial cell fate specification","termid":"GO:0010158"}


id: MONDO:0044872
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute or chronic disorder, affecting the sympathetic or parasympathetic nervous system. It can be primary, the result of central nervous system degeneration, or secondary due to diabetes or alcoholism. Patients with the chronic form of this disorder usually have a progressive clinical course and a poor prognosis.","definition_xrefs":["NCIT:C53439"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autonomic nervous system disorder","termid":"MONDO:0001292"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dysautonomia","secondary_identifiers":["MEDGEN:8511","UMLS:C0013363"],"synonyms":[{"name":"dysautonomia","type":"exact"}],"termid":"MONDO:0044872","xrefs":{"Monarch":{"xref_id":"0044872"}}}


id: PBO:0088652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"choline transporter-like, implicated in autophagy Ctl1","termid":"PBO:0088652"}


id: GO:0035296
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the diameter of a tube.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of tube size","termid":"GO:0035150"}],"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 tube diameter","termid":"GO:0035296"}


id: PBO:0080371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VOPP1 divergent transcript","termid":"PBO:0080371"}


id: PBO:0077317
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 52B","termid":"PBO:0077317"}


id: MONDO:0957786
data:
  {"annotated_genes":["SJAG_01433"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85980],"is_not":false,"summary":null,"term":"MONDO:0957786"}]},"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":1,"genes_by_uniquename":{"SJAG_01433":null},"genotype_count":0,"is_obsolete":false,"name":"xerosis and growth failure with immune and pulmonary dysfunction syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620510","UMLS:C5882692","MEDGEN:1848919"],"termid":"MONDO:0957786","terms_by_termid":{"MONDO:0957786":null},"xrefs":{"Monarch":{"xref_id":"0957786"}}}


id: MONDO:0017416
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Postpoliomyelitis syndrome (PPS) is a neurologic disorder characterized by the development of new neuromuscular symptoms such as progressive muscular weakness or abnormal muscle fatigability occurring in survivors of the acute paralytic form of poliomyelitis, 15-40 years after recovery from the disease, and that is unexplained by other medical causes. Other manifestations that can occur gradually include generalized fatigue, muscle atrophy, muscle and joint pain, intolerance to cold, and difficulties sleeping, swallowing or breathing.","definition_xrefs":["Orphanet:2942"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poliomyelitis","termid":"MONDO:0017373"}],"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":"postpoliomyelitis syndrome","secondary_identifiers":["MESH:D016262","SCTID:31097004","GARD:4454","NORD:1600","DOID:4952","UMLS:C0080040","icd11.foundation:2018885243","EFO:0007454","MEDGEN:36363"],"synonyms":[{"name":"Post Polio Syndrome","type":"exact"},{"name":"polio late effects","type":"related"},{"name":"post polio syndrome","type":"related"},{"name":"post-polio muscular atrophy","type":"related"},{"name":"post-polio sequelae","type":"related"},{"name":"post-poliomyelitic syndrome","type":"related"},{"name":"postpolio sequelae","type":"exact"},{"name":"postpolio syndrome","type":"exact"},{"name":"postpoliomyelitic syndrome","type":"exact"},{"name":"postpoliomyelitis sequelae","type":"exact"},{"name":"postpoliomyelitis syndrome","type":"exact"}],"termid":"MONDO:0017416","xrefs":{"Monarch":{"xref_id":"0017416"}}}


id: GO:0007553
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving ecdysteroids, a group of polyhydroxylated ketosteroids which initiate post-embryonic development, including the metamorphosis of immature forms and the development of the reproductive system and the maturation of oocytes in adult females.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ketone metabolic process","termid":"GO:0010565"},{"relation_name":"is_a","term_name":"regulation of steroid metabolic process","termid":"GO:0019218"},{"relation_name":"is_a","term_name":"regulation of hormone metabolic process","termid":"GO:0032350"},{"relation_name":"regulates","term_name":"ecdysteroid metabolic process","termid":"GO:0045455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"regulation of ecdysteroid metabolic process","synonyms":[{"name":"regulation of ecdysteroid metabolism","type":"exact"}],"termid":"GO:0007553"}


id: PBO:0041908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cobalamin binding intrinsic factor","termid":"PBO:0041908"}


id: PBO:0087337
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Specificity factor required for Rsp5p-dependent ubiquitination; also required for sorting of cargo proteins at the multivesicular body; identified as a high-copy suppressor of a SHR3 deletion, increasing steady-state levels of amino acid permeases","termid":"PBO:0087337"}


id: GO:0140315
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an iron ion to prevent it from interacting with other partners or to inhibit its localization to the area of the cell or complex where it is active.","definition_xrefs":["PMID:27780864"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metal ion sequestering activity","termid":"GO:0140487"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140313"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140313","GO:0003674"],"is_obsolete":false,"name":"iron ion sequestering activity","termid":"GO:0140315"}


id: GO:1904117
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 vasopressin stimulus.","definition_xrefs":["GO_REF:0000071","GOC:TermGenie","PMID:22811487"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to peptide hormone stimulus","termid":"GO:0071375"},{"relation_name":"is_a","term_name":"response to vasopressin","termid":"GO:1904116"}],"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 vasopressin","termid":"GO:1904117"}


id: PR:O94448
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A CAAX prenyl protease 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR13046:SF0","OMA:SCHPO00351"],"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":"CAAX prenyl protease 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1687.02","secondary_identifiers":["UniProtKB:O94448"],"synonyms":[{"name":"PPSEP 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-RCE1","type":"exact"},{"name":"prenyl protein-specific endoprotease 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94448"}


id: PBO:0066038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAN pseudogene 7","termid":"PBO:0066038"}


id: FYPO:0007579
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A localization phenotype observed in the vegetative growth phase of the life cycle in which the distribution of sterols in the medial membrane band is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","PMID:15517003","GO:0032178"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal plasma membrane sterol distribution","termid":"FYPO:0004963"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000257","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"normal medial membrane band sterol distribution","synonyms":[{"name":"normal medial membrane band sterol distribution during mitotic cell cycle","type":"related"},{"name":"normal medial membrane band sterol distribution during vegetative growth","type":"exact"},{"name":"normal medial membrane domain sterol distribution","type":"exact"}],"termid":"FYPO:0007579"}


id: MONDO:0859278
data:
  {"annotated_genes":["SJAG_05194"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85620],"is_not":false,"summary":null,"term":"MONDO:0859278"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05194":null},"genotype_count":0,"is_obsolete":false,"name":"keratoderma-ichthyosis-deafness syndrome, autosomal recessive","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620009","UMLS:C5774200","MEDGEN:1823973"],"termid":"MONDO:0859278","terms_by_termid":{"MONDO:0859278":null},"xrefs":{"Monarch":{"xref_id":"0859278"}}}


id: PBO:0039443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat and KH domain containing 1","termid":"PBO:0039443"}


id: GO:0045110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of the bundles of intermediate filaments. Intermediate filament-associated proteins (IFAPs) cross-link intermediate filaments with one another, forming a bundle or a network, and with other cell structures, including the plasma membrane. The organization of intermediate filaments and their supportive function in various cells types depends in large part on their linkage to other cell structures via IFAPs.","definition_xrefs":["ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"is_a","term_name":"intermediate filament organization","termid":"GO:0045109"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007010","GO:0044085"],"is_obsolete":false,"name":"intermediate filament bundle assembly","synonyms":[{"name":"tonofilament assembly","type":"narrow"}],"termid":"GO:0045110"}


id: RO:0002331
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"c involved_in p if and only if c enables some process p', and p' is part of p","direct_ancestors":[{"relation_name":"is_a","term_name":"involved_in_or_involved_in_regulation_of","termid":"RO:0002431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"involved_in","termid":"RO:0002331"}


id: FYPO:0006687
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which DNA double-strand break resection that occurs as part of double-strand break repair via homologous recombination is decreased. DNA double-strand break resection is the process by which long-tract single-stranded 3'-end DNA is generated by removal of bases from a 5' end from which SPO11/Rec12-oligonucleotide complexes have been removed.","definition_xrefs":["PMID:21931565","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased DNA double-strand break processing","termid":"FYPO:0006686"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000293","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased DNA double-strand break processing during double-strand break repair via homologous recombination","synonyms":[{"name":"decreased DNA double-strand break resection during double-strand break repair via homologous recombination","type":"exact"},{"name":"decreased DNA double-strand break resectioning during double-strand break repair via homologous recombination","type":"exact"},{"name":"decreased DSB processing during double-strand break repair via homologous recombination","type":"exact"},{"name":"reduced DNA double-strand break processing during double-strand break repair via homologous recombination","type":"exact"}],"termid":"FYPO:0006687"}


id: MONDO:0006600
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pigmentation disease (obsolete MONDO:0006600)","secondary_identifiers":["SCTID:414032001"],"synonyms":[{"name":"disorder of pigmentation","type":"exact"}],"termid":"MONDO:0006600","xrefs":{"Monarch":{"xref_id":"0006600"}}}


id: PBO:0065188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PROX1 antisense RNA 1","termid":"PBO:0065188"}


id: PBO:0004896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJ/TPR domain protein DNAJC7 family","termid":"PBO:0004896"}


id: MONDO:0005716
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pleuropneumonia of cattle and goats caused by species of mycoplasma.","definition_xrefs":["MESH:D011002"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pneumonia","termid":"MONDO:0005249"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"contagious pleuropneumonia","secondary_identifiers":["UMLS:C0032243","EFO:0007221","MEDGEN:19357"],"termid":"MONDO:0005716","xrefs":{"Monarch":{"xref_id":"0005716"}}}


id: GO:0007605
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events required for an organism to receive an auditory stimulus, convert it to a molecular signal, and recognize and characterize the signal. Sonic stimuli are detected in the form of vibrations and are processed to form a sound.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensory perception of mechanical stimulus","termid":"GO:0050954"}],"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":"sensory perception of sound","secondary_identifiers":["Wikipedia:Hearing_(sense)","Reactome:R-HSA-9659379"],"synonyms":[{"name":"hearing","type":"exact"},{"name":"perception of sound","type":"exact"}],"termid":"GO:0007605"}


id: MONDO:0024973
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cattle disease of uncertain cause, probably an allergic reaction.","definition_xrefs":["MESH:D011016"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bovine respiratory disease complex","termid":"MONDO:0005678"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pneumonia, atypical interstitial, of cattle","synonyms":[{"name":"Adenomatoses, bovine pulmonary","type":"related"},{"name":"Fog fever","type":"related"},{"name":"adenomatosis, bovine pulmonary","type":"related"},{"name":"adenomatosis, pulmonary, bovine","type":"related"},{"name":"atypical interstitial pneumonia of cattle","type":"related"},{"name":"bovine pulmonary Adenomatoses","type":"related"},{"name":"bovine pulmonary adenomatosis","type":"related"},{"name":"emphysema, acute bovine pulmonary","type":"related"},{"name":"fever, Fog","type":"related"},{"name":"pulmonary Adenomatoses, bovine","type":"related"},{"name":"pulmonary adenomatosis, bovine","type":"related"}],"termid":"MONDO:0024973","xrefs":{"Monarch":{"xref_id":"0024973"}}}


id: PBO:0074543
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SND1 divergent transcript","termid":"PBO:0074543"}


id: GO:0004323
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4 Fe2+ + 4 H+ + O2 = 4 Fe3+ + 2 H2O.","definition_xrefs":["EC:1.16.3.1"],"gene_count":0,"genotype_count":0,"name":"obsolete multicopper ferroxidase iron transport mediator activity (obsolete GO:0004323)","synonyms":[{"name":"multicopper ferroxidase iron transport mediator activity","type":"exact"}],"termid":"GO:0004323"}


id: PBO:0084540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of the p24 family involved in ER to Golgi transport; similar to Emp24p and Erv25p; ERP4 has a paralog, ERP2, that arose from the whole genome duplication","termid":"PBO:0084540"}


id: PBO:0064651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTPRF interacting protein alpha 2","termid":"PBO:0064651"}


id: FYPO:0001147
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A biological process phenotype in which the observed mating efficiency, as determined by counting zygotes, asci, and sometimes spores, is normal (i.e. the same as in wild-type cells).","definition_xrefs":["PomBase:mah","PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population phenotype","termid":"FYPO:0000003"},{"relation_name":"is_a","term_name":"normal phenotype","termid":"FYPO:0000257"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0000257"],"is_obsolete":false,"name":"normal mating efficiency","termid":"FYPO:0001147"}


id: GO:0046434
data:
  {"annotated_genes":["SJAG_01519","SJAG_01310","SJAG_03903","SJAG_04048","SJAG_02785","SJAG_03977","SJAG_03828","SJAG_01974","SJAG_02369","SJAG_02247","SJAG_03091","SJAG_04334","SJAG_02945","SJAG_01595","SJAG_03852","SJAG_05314","SJAG_01012","SJAG_00622","SJAG_00839","SJAG_04169","SJAG_00409","SJAG_04110","SJAG_02100","SJAG_02796","SJAG_02481","SJAG_03797","SJAG_01970","SJAG_00027","SJAG_03204","SJAG_04067","SJAG_06622","SJAG_06621","SJAG_04495","SJAG_02093","SJAG_02161","SJAG_02009","SJAG_02135","SJAG_00605","SJAG_04870","SJAG_04939","SJAG_04487","SJAG_01055","SJAG_03660","SJAG_03373","SJAG_02091","SJAG_00685","SJAG_03676","SJAG_00461","SJAG_00244","SJAG_00633","SJAG_02107","SJAG_04192","SJAG_04311"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[113144,113145],"is_not":false,"summary":null,"term":"GO:0046434"},{"annotations":[78948],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901911"},{"annotations":[116187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006198"},{"annotations":[109194,97772,109196,105626,105255,103173,109193,109198,116159,98051,77597,94773,103427,94284,105625,109195,105257,109197,109192,105256],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061621"},{"annotations":[77786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015938"},{"annotations":[75359,116987],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009159"},{"annotations":[61718],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009204"},{"annotations":[78947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901909"},{"annotations":[78946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901907"},{"annotations":[116897,111247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015964"},{"annotations":[98774],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035863"},{"annotations":[79216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046081"},{"annotations":[68686,62548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046168"},{"annotations":[71230,77033,97543,76232,78294],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046475"},{"annotations":[88353],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061613"},{"annotations":[97969,111374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061688"},{"annotations":[114853,88460],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071545"},{"annotations":[72060],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019677"},{"annotations":[72063],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006742"},{"annotations":[75754,72758],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0045820"},{"annotations":[70177],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009134"},{"annotations":[116785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034638"},{"annotations":[74102],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006660"},{"annotations":[74029,101647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009395"},{"annotations":[69732],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0006110"},{"annotations":[113118],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009191"},{"annotations":[75997],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006256"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of organophosphates, any phosphate-containing organic compound.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"organophosphate metabolic 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catabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"organophosphate breakdown","type":"exact"},{"name":"organophosphate catabolism","type":"exact"},{"name":"organophosphate degradation","type":"exact"}],"termid":"GO:0046434","terms_by_termid":{"GO:0006110":null,"GO:0006198":null,"GO:0006256":null,"GO:0006660":null,"GO:0006742":null,"GO:0009134":null,"GO:0009159":null,"GO:0009191":null,"GO:0009204":null,"GO:0009395":null,"GO:0015938":null,"GO:0015964":null,"GO:0019677":null,"GO:0034638":null,"GO:0035863":null,"GO:0045820":null,"GO:0046081":null,"GO:0046168":null,"GO:0046434":null,"GO:0046475":null,"GO:0061613":null,"GO:0061621":null,"GO:0061688":null,"GO:0071545":null,"GO:1901907":null,"GO:1901909":null,"GO:1901911":null}}


id: GO:0019860
data:
  {"annotated_genes":["SJAG_04354"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91729],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006223"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving uracil, 2,4-dioxopyrimidine, one of the pyrimidine bases occurring in RNA, but not in DNA.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleobase metabolic process","termid":"GO:0006206"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04354":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"uracil metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"uracil metabolism","type":"exact"}],"termid":"GO:0019860","terms_by_termid":{"GO:0006223":null}}


id: PBO:0052505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch like family member 18","termid":"PBO:0052505"}


id: PR:P87179
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- wsc1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P87179"],"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":"cell wall integrity and stress response component 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC30B4.01c","synonyms":[{"name":"Spom972h-wsc1","type":"exact"}],"termid":"PR:P87179"}


id: PBO:0069279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 535, pseudogene","termid":"PBO:0069279"}


id: PBO:0074486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMYD3 intronic transcript 1","termid":"PBO:0074486"}


id: GO:0010719
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of epithelial to mesenchymal transition. Epithelial to mesenchymal transition where an epithelial cell loses apical/basolateral polarity, severs intercellular adhesive junctions, degrades basement membrane components and becomes a migratory mesenchymal cell.","definition_xrefs":["GOC:dph","GOC:tb","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial to mesenchymal transition","termid":"GO:0010717"},{"relation_name":"is_a","term_name":"negative regulation of cell differentiation","termid":"GO:0045596"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"epithelial to mesenchymal transition","termid":"GO:0001837"}],"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 epithelial to mesenchymal transition","termid":"GO:0010719"}


id: PBO:0072461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S29 pseudogene 25","termid":"PBO:0072461"}


id: MONDO:0850129
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A gastrointestinal system cancer that is located in the proximal esophagus and the distal stomach.","definition_xrefs":["DOID:0080374"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system cancer","termid":"MONDO:0002516"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"gastroesophageal cancer","secondary_identifiers":["UMLS:C0346619","MEDGEN:577508"],"termid":"MONDO:0850129","xrefs":{"Monarch":{"xref_id":"0850129"}}}


id: PBO:0088614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamine aminotransferase subunit Sno1","termid":"PBO:0088614"}


id: GO:0102768
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: flavan-3,3',4,4',5,5',7-heptol + O2 + 2-oxoglutarate = H+ + delphinidin + 2 H2O + carbon dioxide + succinate.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete anthocyanidin synthase activity (obsolete GO:0102768)","termid":"GO:0102768"}


id: GO:1902392
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of exodeoxyribonuclease activity.","definition_xrefs":["GOC:jl","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of exodeoxyribonuclease activity (obsolete GO:1902392)","termid":"GO:1902392"}


id: PBO:0025537
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by N. crassa TNC","termid":"PBO:0025537"}


id: GO:0090401
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A cellular senescence process associated with the dismantling of a cell as a response to viral infection.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete viral-induced premature senescence (obsolete GO:0090401)","termid":"GO:0090401"}


id: FYPO:0001046
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cells enter mitosis earlier, relative to cell size or DNA integrity checkpoint status, than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mistimed mitosis","termid":"FYPO:0001204"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000337","FYPO:0000631","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"premature mitosis","synonyms":[{"name":"advanced mitosis","type":"exact"},{"name":"early mitosis","type":"exact"},{"name":"premature mitosis during mitotic cell cycle","type":"related"},{"name":"premature mitosis during vegetative growth","type":"exact"}],"termid":"FYPO:0001046"}


id: MONDO:0012635
data:
  {"annotated_genes":["SJAG_03054"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86691],"is_not":false,"summary":null,"term":"MONDO:0012635"}]},"cv_name":"mondo","definition":"The CDG (Congenital Disorders of Glycosylation) syndromes are a group of autosomal recessive disorders affecting glycoprotein synthesis. CDG syndrome type IIh is characterized by severe psychomotor retardation, failure to thrive and intolerance to wheat and dairy products.","definition_xrefs":["Orphanet:95428"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type II","termid":"MONDO:0005501"},{"relation_name":"is_a","term_name":"defect in conserved oligomeric Golgi complex","termid":"MONDO:0017750"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03054":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322"],"is_obsolete":false,"name":"COG8-congenital disorder of glycosylation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070260","GARD:12411","OMIM:611182","SCTID:717774004","UMLS:C1970021","MEDGEN:409971","MESH:C566987"],"synonyms":[{"name":"CDG IIh","type":"related"},{"name":"CDG syndrome type IIh","type":"exact"},{"name":"CDG-IIh","type":"exact"},{"name":"CDG2H","type":"exact"},{"name":"COG8-CDG","type":"exact"},{"name":"COG8-CDG (CDG-IIh)","type":"related"},{"name":"COG8-congenital disorder of glycosylation","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type IIh","type":"exact"},{"name":"congenital disorder of glycosylation type 2h","type":"exact"},{"name":"congenital disorder of glycosylation type IIh","type":"exact"},{"name":"congenital disorder of glycosylation, type IIh","type":"related"}],"termid":"MONDO:0012635","terms_by_termid":{"MONDO:0012635":null},"xrefs":{"Monarch":{"xref_id":"0012635"}}}


id: PBO:0075639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small proline rich protein 4","termid":"PBO:0075639"}


id: PBO:0050373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 76","termid":"PBO:0050373"}


id: MONDO:0007515
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":"ectopia pupillae","secondary_identifiers":["MEDGEN:224790","MESH:C536185","icd11.foundation:70138444","OMIM:129750","HP:0009918","SCTID:193523008","UMLS:C1271219"],"synonyms":[{"name":"congenital eye malformation in which the pupils are displaced from their normal central position","type":"related"},{"name":"ectopia pupillae","type":"exact"},{"name":"ectopia pupillae (disease)","type":"exact"},{"name":"familial ectopic pupil","type":"related"}],"termid":"MONDO:0007515","xrefs":{"Monarch":{"xref_id":"0007515"}}}


id: MONDO:0015237
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Arrhinia is an extremely rare, major congenital malformation consisting of an absence of the nose ranging from hyporrhinia (absence of external nasal structures) to total arrhinia (absence of external nose, nasal airways, olfactory bulbs, or olfactory nerve) often causing respiratory distress and requiring surgical correction. Arrhinia can be bilateral or unilateral (hemiarrhinia). Associated anomalies include ocular features (hypertelorism, microphthalmia, eyelid coloboma), facial clefts, midline defects and microtia.","definition_xrefs":["Orphanet:1134"],"direct_ancestors":[{"relation_name":"is_a","term_name":"otorhinolaryngologic disease","termid":"MONDO:0024623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrhinia","secondary_identifiers":["SCTID:111317000","UMLS:C0265740","GARD:364","icd11.foundation:409489963","MEDGEN:120555","ICD9:748.1","MESH:C537438"],"synonyms":[{"name":"Nose agenesia","type":"related"},{"name":"Nose agenesis","type":"exact"},{"name":"congenital absence of the nose","type":"related"},{"name":"isolated arrhinia","type":"related"},{"name":"isolated nose agenesis","type":"exact"}],"termid":"MONDO:0015237","xrefs":{"Monarch":{"xref_id":"0015237"}}}


id: MONDO:0004549
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extrinsic allergic alveolitis caused by inhalation of cork dust containing the antigens produced by the fungus Penicillium glabrum. The symptoms include dyspnea, wheezing cough, fever and asthenia.","definition_xrefs":["DOID:840"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fungal lung infectious disease","termid":"MONDO:0005766"},{"relation_name":"is_a","term_name":"hypersensitivity pneumonitis","termid":"MONDO:0017853"}],"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":"cork-handlers' disease","secondary_identifiers":["UMLS:C0152108","ICD9:495.3","MEDGEN:508891","SCTID:13394002"],"synonyms":[{"name":"Suberosis","type":"exact"},{"name":"cork worker's lung","type":"exact"},{"name":"cork workers lung","type":"exact"},{"name":"cork-handlers' disease or lung","type":"exact"},{"name":"cork-handlers' lung","type":"exact"}],"termid":"MONDO:0004549","xrefs":{"Monarch":{"xref_id":"0004549"}}}


id: FYPO:0005961
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which a meiotic spindle forms with microtubules emanating from three or more poles.","definition_xrefs":["PomBase:mah","PMID:15992541"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic spindle","termid":"FYPO:0000734"},{"relation_name":"is_a","term_name":"multipolar spindle","termid":"FYPO:0005959"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"output_of","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0000120","FYPO:0000054","FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0002399"],"is_obsolete":false,"name":"multipolar meiotic spindle","synonyms":[{"name":"multipolar meiotic spindles","type":"exact"},{"name":"multipolar spindle during meiosis","type":"exact"}],"termid":"FYPO:0005961"}


id: PBO:0055201
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 2626","termid":"PBO:0055201"}


id: PBO:0064606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POU class 3 homeobox 4","termid":"PBO:0064606"}


id: PBO:0044024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"casein kinase 2 alpha 3","termid":"PBO:0044024"}


id: PBO:0071288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L26 pseudogene 11","termid":"PBO:0071288"}


id: PBO:0046720
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EVA1C pseudogene 6","termid":"PBO:0046720"}


id: GO:0015947
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving methane, a colorless, odorless, flammable gas with the formula CH4. It is the simplest of the alkanes.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkane metabolic process","termid":"GO:0043446"}],"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":"methane metabolic process","synonyms":[{"name":"methane metabolism","type":"exact"}],"termid":"GO:0015947"}


id: FYPO:0001700
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to the receptor agonist GW 7647. Cells stop growing (and may die) at a concentration of GW 7647 that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0001985","FYPO:0002683","FYPO:0005447","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to GW 7647","synonyms":[{"name":"hypersensitive to GW 7647","type":"exact"},{"name":"sensitive to GW 7647 during mitotic cell cycle","type":"related"},{"name":"sensitive to GW 7647 during vegetative growth","type":"exact"}],"termid":"FYPO:0001700"}


id: GO:0030304
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Stops, prevents or reduces the activity of the serine endopeptidase trypsin.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete trypsin inhibitor activity (obsolete GO:0030304)","synonyms":[{"name":"trypsin inhibitor activity","type":"exact"}],"termid":"GO:0030304"}


id: PBO:0066209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 22 pseudogene 2","termid":"PBO:0066209"}


id: PBO:0073542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3RF3 antisense RNA 1","termid":"PBO:0073542"}


id: PBO:0067681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 868, pseudogene","termid":"PBO:0067681"}


id: GO:0072095
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of branch elongation involved in ureteric bud branching, the growth of a branch of the ureteric bud along its axis.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental growth","termid":"GO:0048638"},{"relation_name":"regulates","term_name":"branch elongation involved in ureteric bud branching","termid":"GO:0060681"}],"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 branch elongation involved in ureteric bud branching","termid":"GO:0072095"}


id: GO:1990460
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a leptin receptor.","definition_xrefs":["PMID:22405007","GOC:pm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"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":"leptin receptor binding","termid":"GO:1990460"}


id: MOD:01530
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 iTRAQ8plex-113 reporter+balance group.","definition_xrefs":["Unimod:730#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iTRAQ8plex-113 reporter+balance reagent acylated residue","termid":"MOD:01528"},{"relation_name":"is_a","term_name":"iTRAQ8plex reporter+balance reagent N-acylated residue","termid":"MOD:01710"},{"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":"iTRAQ8plex-113 reporter+balance reagent N6-acylated lysine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry","type":"related"},{"name":"Representative mass and accurate mass for 113, 114, 116 & 117","type":"related"},{"name":"iTRAQ8plex","type":"related"},{"name":"iTRAQ8plex:13C(7)15N(1)","type":"related"}],"termid":"MOD:01530"}


id: GO:0043135
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-phospho-alpha-D-ribose 1-diphosphate + H2O = ribose 1,5 bisphosphate + phosphate + H+.","definition_xrefs":["MetaCyc:RXN-10969","PMID:12370170"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"5-phosphoribosyl 1-pyrophosphate pyrophosphatase activity","synonyms":[{"name":"PRPP pyrophosphatase activity","type":"exact"}],"termid":"GO:0043135"}


id: FYPO:0005558
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the amount, distribution, or morphology of microtubule bundles is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule cytoskeleton","termid":"FYPO:0002399"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000054","FYPO:0005447","FYPO:0001985","FYPO:0002399"],"is_obsolete":false,"name":"abnormal microtubule bundle","secondary_identifiers":["FYPO:0005795"],"synonyms":[{"name":"abnormal MT bundle","type":"exact"},{"name":"abnormal microtubule array","type":"related"},{"name":"abnormal microtubule bundle physical object quality","type":"exact"},{"name":"abnormal microtubule bundle structure","type":"narrow"}],"termid":"FYPO:0005558"}


id: PBO:0108603
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-indirectly_regulates","termid":"PBO:0108603"}


id: PBO:0047505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fer-1 like family member 6","termid":"PBO:0047505"}


id: PBO:0028415
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_frequency_of_meiosis_I","termid":"PBO:0028415"}


id: PBO:0079888
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uridine phosphorylase 1","termid":"PBO:0079888"}


id: MONDO:0011013
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant hypocalcemia in which the cause of the disease is a mutation in the CASR gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant hypocalcemia","termid":"MONDO:0018543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005066"],"is_obsolete":false,"name":"autosomal dominant hypocalcemia 1","secondary_identifiers":["UMLS:C0342345","DOID:0090107","MEDGEN:87438","OMIM:601198"],"synonyms":[{"name":"CASR autosomal dominant hypocalcemia","type":"exact"},{"name":"HYPOC1","type":"exact"},{"name":"autosomal dominant hypocalcemia caused by mutation in CASR","type":"exact"},{"name":"autosomal dominant hypocalcemia type 1","type":"exact"},{"name":"hypercalciuric hypocalcemia","type":"related"},{"name":"hypocalcemia, autosomal dominant","type":"broad"},{"name":"hypocalcemia, autosomal dominant 1","type":"related"},{"name":"hypocalcemia, autosomal dominant 1, with Bartter syndrome","type":"related"},{"name":"hypocalcemia, autosomal dominant type 1","type":"exact"},{"name":"hypocalcemia, autosomal dominant, with Bartter syndrome","type":"exact"},{"name":"hypocalcemia, familial","type":"related"}],"termid":"MONDO:0011013","xrefs":{"Monarch":{"xref_id":"0011013"}}}


id: GO:1901734
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of quercetin.","definition_xrefs":["GOC:TermGenie","UniPathway:UPA00724","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flavone biosynthetic process","termid":"GO:0051553"},{"relation_name":"is_a","term_name":"quercetin metabolic process","termid":"GO:1901732"}],"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":"quercetin biosynthetic process","synonyms":[{"name":"quercetin anabolism","type":"exact"},{"name":"quercetin biosynthesis","type":"exact"},{"name":"quercetin formation","type":"exact"},{"name":"quercetin synthesis","type":"exact"}],"termid":"GO:1901734"}


id: PBO:0054869
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 2283","termid":"PBO:0054869"}


id: PATO:0000700
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A texture quality inhering in a bearer by virtue of the bearer's irregular surface.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"texture","termid":"PATO:0000150"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rough","secondary_identifiers":["PATO:0001616"],"synonyms":[{"name":"coarse","type":"exact"}],"termid":"PATO:0000700"}


id: GO:0031461
data:
  {"annotated_genes":["SJAG_05329","SJAG_03350","SJAG_02591","SJAG_03575","SJAG_03809","SJAG_03680","SJAG_02651","SJAG_04087","SJAG_01801","SJAG_04540","SJAG_03728","SJAG_02186","SJAG_05236","SJAG_02162","SJAG_03561","SJAG_03130","SJAG_02044","SJAG_00615","SJAG_03454","SJAG_02119","SJAG_03219","SJAG_04520","SJAG_01540","SJAG_01022","SJAG_02837","SJAG_01573","SJAG_02822","SJAG_04853","SJAG_03651","SJAG_00071","SJAG_05297","SJAG_00756","SJAG_04335","SJAG_04971","SJAG_03858","SJAG_03417","SJAG_04142","SJAG_01956","SJAG_00146","SJAG_03037","SJAG_00192","SJAG_00666","SJAG_00439","SJAG_04661","SJAG_01480","SJAG_03351","SJAG_04574","SJAG_00341"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[88992],"is_not":false,"summary":null,"term":"GO:0031461"},{"annotations":[76266,77526,72686,77997,93506,73592,94922,79741,78829,70391,72822,69828,57790,78669,78854,70356,79932,112012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005680"},{"annotations":[94104,96492,118617,113784,110277,117502],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043494"},{"annotations":[74519],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031463"},{"annotations":[70411,90663,75861,96449,105138,90615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0080008"},{"annotations":[69696],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031464"},{"annotations":[79134,75661,79160,97268],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035361"},{"annotations":[108877,90355,104659,110117,97545,94107],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043224"},{"annotations":[88307,102656,73694,95300,98237,79918],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019005"}]},"cv_name":"cellular_component","definition":"Any ubiquitin ligase complex in which the catalytic core consists of a member of the cullin family and a RING domain protein; the core is associated with one or more additional proteins that confer substrate specificity.","definition_xrefs":["PMID:15571813","PMID:15688063"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin ligase complex","termid":"GO:0000151"}],"gene_count":48,"genes_by_uniquename":{"SJAG_00071":null,"SJAG_00146":null,"SJAG_00192":null,"SJAG_00341":null,"SJAG_00439":null,"SJAG_00615":null,"SJAG_00666":null,"SJAG_00756":null,"SJAG_01022":null,"SJAG_01480":null,"SJAG_01540":null,"SJAG_01573":null,"SJAG_01801":null,"SJAG_01956":null,"SJAG_02044":null,"SJAG_02119":null,"SJAG_02162":null,"SJAG_02186":null,"SJAG_02591":null,"SJAG_02651":null,"SJAG_02822":null,"SJAG_02837":null,"SJAG_03037":null,"SJAG_03130":null,"SJAG_03219":null,"SJAG_03350":null,"SJAG_03351":null,"SJAG_03417":null,"SJAG_03454":null,"SJAG_03561":null,"SJAG_03575":null,"SJAG_03651":null,"SJAG_03680":null,"SJAG_03728":null,"SJAG_03809":null,"SJAG_03858":null,"SJAG_04087":null,"SJAG_04142":null,"SJAG_04335":null,"SJAG_04520":null,"SJAG_04540":null,"SJAG_04574":null,"SJAG_04661":null,"SJAG_04853":null,"SJAG_04971":null,"SJAG_05236":null,"SJAG_05297":null,"SJAG_05329":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"cullin-RING ubiquitin ligase complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"CRL complex","type":"exact"},{"name":"cullin complex","type":"exact"},{"name":"cullin-RING ligase","type":"related"}],"termid":"GO:0031461","terms_by_termid":{"GO:0005680":null,"GO:0019005":null,"GO:0031461":null,"GO:0031463":null,"GO:0031464":null,"GO:0035361":null,"GO:0043224":null,"GO:0043494":null,"GO:0080008":null}}


id: PBO:0079446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TUB like protein 3 pseudogene 1","termid":"PBO:0079446"}


id: MONDO:0008814
data:
  {"annotated_genes":["SJAG_03398"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85463],"is_not":false,"summary":null,"term":"MONDO:0008814"}]},"cv_name":"mondo","definition":"Arginase deficiency is a rare autosomal recessive amino acid metabolism disorder characterized clinically by variable degrees of hyperammonemia, developing from about 3 years of age, and leading to progressive loss of developmental milestones and spasticity in the absence of treatment.","definition_xrefs":["Orphanet:90"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urea cycle disorder or inherited hyperammonemia","termid":"MONDO:0800153"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03398":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"hyperargininemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:2200482","UMLS:C0268548","OMIM:207800","NCIT:C84568","NANDO:1200807","DOID:9278","icd11.foundation:1619102598","MedDRA:10062695","GARD:5840","MESH:D020162","MEDGEN:78688","SCTID:23501004"],"synonyms":[{"name":"Arg1 deficiency","type":"related"},{"name":"arginase deficiency","type":"exact"},{"name":"argininemia","type":"exact"},{"name":"deficiency of canavanase","type":"exact"},{"name":"hyperargininemia","type":"exact"}],"termid":"MONDO:0008814","terms_by_termid":{"MONDO:0008814":null},"xrefs":{"Monarch":{"xref_id":"0008814"}}}


id: GO:0005074
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete inhibitory SMAD protein (obsolete GO:0005074)","synonyms":[{"name":"inhibitory SMAD protein","type":"exact"}],"termid":"GO:0005074"}


id: MONDO:0005452
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by recurrent episodes of binge-eating over which the individual feels a lack of control; these episodes of binge-eating are followed by recurrent compensatory behavior to prevent weight gain, usually self-induced vomiting. In addition, self-evaluation is unduly influenced by body image.","definition_xrefs":["NCIT:C34440"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eating disorder","termid":"MONDO:0005451"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bulimia nervosa","secondary_identifiers":["MEDGEN:389218","SCTID:78004001","UMLS:C2267227","icd11.foundation:509381842","NCIT:C97162","DOID:12129","ICD9:307.51","MESH:D002032","ICD10CM:F50.2","MESH:D052018","EFO:0005204"],"synonyms":[{"name":"bulimia","type":"exact"},{"name":"hyperorexia nervosa","type":"exact"}],"termid":"MONDO:0005452","xrefs":{"Monarch":{"xref_id":"0005452"}}}


id: MONDO:0018548
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute poisoning with a membrane-stabilizing effect is potentially life-threatening. The principle drugs involved are tricyclic antidepressants, chloroquine, some types of beta blockers, class IA antiarrhythmics, carbamazepin and cocaine.","definition_xrefs":["Orphanet:43119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute poisoning by drugs with membrane-stabilizing effect","termid":"MONDO:0018548","xrefs":{"Monarch":{"xref_id":"0018548"}}}


id: PBO:0011183
data:
  {"annotation_feature_type":"gene","cv_name":"feature_cvtermprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"approver_email","termid":"PBO:0011183"}


id: GO:0044534
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with the resultant modulation of apoptosis in the bitten organism.","definition_xrefs":["GOC:jl","PMID:17983639","GOC:fj"],"gene_count":0,"genotype_count":0,"name":"obsolete envenomation resulting in modulation of apoptotic process in another organism (obsolete GO:0044534)","synonyms":[{"name":"envenomation resulting in modulation of apoptotic process in other organism","type":"exact"}],"termid":"GO:0044534"}


id: MONDO:0017832
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease caused by infection with Mycobacterium xenopi.","definition_xrefs":["MONDO:patterns/infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mycobacterial infectious disease","termid":"MONDO:0020590"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mycobacterium xenopi infection","secondary_identifiers":["UMLS:C0275715","MEDGEN:546776","Orphanet:314946"],"synonyms":[{"name":"M. xenopi","type":"related"},{"name":"Mycobacterium xenopi","type":"related"},{"name":"Mycobacterium xenopi caused disease or disorder","type":"exact"},{"name":"Mycobacterium xenopi disease or disorder","type":"exact"},{"name":"Mycobacterium xenopi infectious disease","type":"exact"}],"termid":"MONDO:0017832","xrefs":{"Monarch":{"xref_id":"0017832"}}}


id: PR:Q9Y7P9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC191.05c gene.","definition_xrefs":["UniProtKB:Q9Y7P9","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C191.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC191.05c","synonyms":[{"name":"Spom972h-SPCC191.05c","type":"exact"}],"termid":"PR:Q9Y7P9"}


id: MONDO:0014243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Prader-Willi syndrome","termid":"MONDO:0008300"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0700092"],"is_obsolete":false,"name":"Schaaf-Yang syndrome","secondary_identifiers":["MEDGEN:1807366","DOID:0111715","Orphanet:398069","UMLS:C5575066","OMIM:208080","GARD:13316","MESH:C535385","OMIM:615547"],"synonyms":[{"name":"Chitayat-Hall syndrome","type":"related"},{"name":"MAGEL2-related PWLS","type":"exact"},{"name":"MAGEL2-related Prader-Willi-like syndrome","type":"exact"},{"name":"PWS due to a point mutation","type":"related"},{"name":"Prader-Willi syndrome due to point mutation","type":"related"},{"name":"Prader-Willi-like syndrome","type":"related"},{"name":"SHFYNG","type":"exact"},{"name":"Schaaf-Yang syndrome","type":"exact"},{"name":"arthrogryposis, distal, with hypopituitarism, intellectual disability, and facial anomalies","type":"exact"},{"name":"arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies","type":"exact"},{"name":"distal arthrogryposis with hypopituitarism, intellectual disability and facial anomalies","type":"related"}],"termid":"MONDO:0014243","xrefs":{"Monarch":{"xref_id":"0014243"}}}


id: FYPO:0006204
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 dCTP 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 cellular phosphorus level","termid":"FYPO:0001543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001320","FYPO:0001312"],"is_obsolete":false,"name":"normal cellular dCTP level","synonyms":[{"name":"normal cellular dCTP level during mitotic cell cycle","type":"related"},{"name":"normal cellular dCTP level during vegetative growth","type":"exact"},{"name":"normal dCTP accumulation","type":"related"}],"termid":"FYPO:0006204"}


id: PBO:0041877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"castor zinc finger 1","termid":"PBO:0041877"}


id: GO:0035725
data:
  {"annotated_genes":["SJAG_04616","SJAG_04028","SJAG_04167","SJAG_01541"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[60991,67058,89063],"is_not":false,"summary":null,"term":"GO:0035725"},{"annotations":[66634],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036376"}]},"cv_name":"biological_process","definition":"A process in which a sodium ion is transported from one side of a membrane to the other by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sodium ion transport","termid":"GO:0006814"},{"relation_name":"is_a","term_name":"monoatomic cation transmembrane transport","termid":"GO:0098655"},{"relation_name":"is_a","term_name":"inorganic cation transmembrane transport","termid":"GO:0098662"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01541":null,"SJAG_04028":null,"SJAG_04167":null,"SJAG_04616":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"sodium ion transmembrane transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"sodium ion membrane transport","type":"exact"}],"termid":"GO:0035725","terms_by_termid":{"GO:0035725":null,"GO:0036376":null}}


id: PBO:0070763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L10 pseudogene 19","termid":"PBO:0070763"}


id: PBO:0081974
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and SCAN domain containing 1","termid":"PBO:0081974"}


id: PBO:0088061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-protein ligase (E3); interacts with Rpt4p and Rpt6p, two subunits of the 19S particle of the 26S proteasome; involved in K29-linked ubiquitin-dependent protein catabolism, including ubiquitin fusion proteins; relative distribution to the nucleus increases upon DNA replication stress","termid":"PBO:0088061"}


id: PR:000027570
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A fungal histone H3.1 that is encoded in the genome of Schizosaccharomyces pombe.","definition_xrefs":["PomBase:MAH","PMID:11242054","PMID:20929775"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fungal histone H3.1","termid":"PR:000027569"},{"relation_name":"is_a","term_name":"core histone (Schizosaccharomyces pombe)","termid":"PR:000041293"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3.1 (Schizosaccharomyces pombe)","pombase_gene_id":"SPAC1834.04","synonyms":[{"name":"SPAC1834.04","type":"related"},{"name":"Spom-hht1","type":"exact"}],"termid":"PR:000027570"}


id: PR:Q10951
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- byr4 gene.","definition_xrefs":["UniProtKB:Q10951","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein byr4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC222.10c","synonyms":[{"name":"Spom972h-byr4","type":"exact"}],"termid":"PR:Q10951"}


id: PATO:0002453
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer bring gradually worn away.","definition_xrefs":["PATOC:JL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eroding","termid":"PATO:0002453"}


id: FYPO:0007684
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA transcribed from early meiotic genes measured in a cell is higher than normal (i.e. higher than observed in wild-type cells during vegetative growth). Early meiotic genes are normally transcribed during pre-meiotic S phase and recombination.","definition_xrefs":["PomBase:mah","PMID:33574613"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of meiotic gene mRNA during vegetative growth","termid":"FYPO:0002173"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"increased level of early meiotic gene mRNA during vegetative growth","synonyms":[{"name":"increased level of early meiosis gene mRNA during vegetative growth","type":"exact"},{"name":"increased level of early meiotic gene RNA during vegetative growth","type":"exact"},{"name":"increased level of early meiotic gene mRNA during vegetative growth during mitotic cell cycle","type":"related"},{"name":"increased level of early meiotic gene transcripts during vegetative growth","type":"exact"}],"termid":"FYPO:0007684"}


id: FYPO:0005704
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a smaller than normal proportion of cells in the population remains viable after exposure to hydroxyurea.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"},{"relation_name":"is_a","term_name":"cell population viability","termid":"FYPO:0002057"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002057","FYPO:0001985"],"is_obsolete":false,"name":"loss of viability following cellular response to hydroxyurea","synonyms":[{"name":"decreased viability following cellular response to hydroxyurea","type":"exact"},{"name":"loss of cell population viability following cellular response to hydroxyurea","type":"exact"},{"name":"loss of viability following HU exposure","type":"exact"},{"name":"loss of viability following cellular response to HU","type":"exact"},{"name":"reduced viability following cellular response to hydroxyurea","type":"related"}],"termid":"FYPO:0005704"}


id: FYPO:0007208
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 microtubule bundle length is normal (i.e. indistinguishable from wild type) during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component during vegetative growth","termid":"FYPO:0001313"},{"relation_name":"is_a","term_name":"normal microtubule bundle","termid":"FYPO:0007114"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal microtubule bundle length during mitotic interphase","synonyms":[{"name":"normal interphase microtubule bundle length","type":"exact"},{"name":"normal microtubule bundle length during interphase of mitotic cell cycle","type":"exact"}],"termid":"FYPO:0007208"}


id: GO:1900113
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of histone H3-K9 trimethylation.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of histone H3-K9 trimethylation (obsolete GO:1900113)","synonyms":[{"name":"down regulation of histone H3-K9 trimethylation","type":"exact"},{"name":"down-regulation of histone H3-K9 trimethylation","type":"exact"},{"name":"downregulation of histone H3-K9 trimethylation","type":"exact"},{"name":"inhibition of histone H3-K9 trimethylation","type":"narrow"}],"termid":"GO:1900113"}


id: PBO:0002008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L11 (predicted)","termid":"PBO:0002008"}


id: MOD:00158
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively cross-links two L-tryptophan residues by a carbon-carbon bond to form 4'-(L-tryptophan)-L-tryptophyl quinone.","definition_xrefs":["PubMed:2028257","RESID:AA0149","ChEBI:20251","DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uncategorized crosslinked residues","termid":"MOD:00692"},{"relation_name":"is_a","term_name":"crosslinked L-tryptophan residue","termid":"MOD:02057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4'-(L-tryptophan)-L-tryptophyl quinone","synonyms":[{"name":"2,4-BisTrp-6,7-dione (from Tryptophan)","type":"exact"},{"name":"2-amino-3-[2-[2-amino-3-(2-carboxyethyl)-6,7-dioxo-1H-indol-4-yl]-1H-indol-3-yl]propanoic acid","type":"exact"},{"name":"3-[(2S)-2-amino-2-carboxyethyl]-4-(3-[(2S)-2-amino-2-carboxyethyl]-1H-indol-2-yl)-6,7-indolinedione","type":"exact"},{"name":"4'-tryptophan-tryptophylquinone","type":"exact"},{"name":"4-(2'-tryptophyl)tryptophan-6,7-dione","type":"exact"},{"name":"4-(L-tryptophan-2-yl)-L-tryptophyl quinone","type":"exact"},{"name":"CROSSLNK Tryptophan tryptophylquinone (Trp-Trp)","type":"exact"},{"name":"TTQ","type":"exact"},{"name":"XLNK-4'Trp-TrpQ","type":"exact"},{"name":"alpha,alpha'-diamino-6',7'-dihydro-6',7'-dioxo-(2,4'-bi-1H-indole)-3,3'-dipropanoic acid","type":"exact"}],"termid":"MOD:00158"}


id: GO:0007096
data:
  {"annotated_genes":["SJAG_01050","SJAG_04943","SJAG_00082","SJAG_04464","SJAG_03126","SJAG_03048","SJAG_01801"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[69821,110809],"is_not":false,"summary":null,"term":"GO:0007096"},{"annotations":[102154,67516],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001100"},{"annotations":[111759,93509,102161,89745],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031536"}]},"cv_name":"biological_process","definition":"Any process involved in the progression from anaphase/telophase to G1 that is associated with a conversion from high to low mitotic CDK activity.","definition_xrefs":["GOC:rn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic cell cycle phase transition","termid":"GO:1901990"},{"relation_name":"regulates","term_name":"exit from mitosis","termid":"GO:0010458"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_01050":null,"SJAG_01801":null,"SJAG_03048":null,"SJAG_03126":null,"SJAG_04464":null,"SJAG_04943":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044772"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0044772"],"is_obsolete":false,"name":"regulation of exit from mitosis","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-176409"],"termid":"GO:0007096","terms_by_termid":{"GO:0001100":null,"GO:0007096":null,"GO:0031536":null}}


id: PBO:0057400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548h-2","termid":"PBO:0057400"}


id: PBO:0071811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S2 pseudogene 6","termid":"PBO:0071811"}


id: PBO:0082718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the Paf1 complex; which associates with RNA polymerase II and is involved in histone methylation; plays a role in regulating Ty1 transposition; involved in transcription elongation as demonstrated by the G-less-based run-on (GLRO) assay","termid":"PBO:0082718"}


id: PBO:0033752
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_sister_chromatid_meiotic_recombination","termid":"PBO:0033752"}


id: PR:Q9UTM3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 26S proteasome non-ATPase regulatory subunit 12 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10855:SF1","PRO:DNx","OMA:SCHPO02037"],"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":"26S proteasome regulatory subunit rpn5 (Schizosaccharomyces pombe 972h-)","secondary_identifiers":["UniProtKB:Q9UTM3"],"synonyms":[{"name":"Spom972h-PSMD12","type":"exact"}],"termid":"PR:Q9UTM3"}


id: PBO:0043608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper metabolism domain containing 1","termid":"PBO:0043608"}


id: PBO:0071803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reprimo, TP53 dependent G2 arrest mediator homolog","termid":"PBO:0071803"}


id: MONDO:0030378
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive disorder characterized by hypomyelination, microcephaly, liver dysfunction, and recurrent hypomyelination.","definition_xrefs":["OMIM:619423"],"direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"combined oxidative phosphorylation deficiency 53","secondary_identifiers":["MEDGEN:1779083","UMLS:C5543631","DOID:0070426"],"synonyms":[{"name":"COXPD53","type":"exact"},{"name":"combined oxidative phosphorylation deficiency due to C2orf69 deficiency","type":"exact"}],"termid":"MONDO:0030378","xrefs":{"Monarch":{"xref_id":"0030378"}}}


id: PR:P87310
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mediator of RNA polymerase II transcription subunit 10 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR13345:SF2","OMA:SCHPO03848"],"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":"mediator of RNA polymerase II transcription subunit 10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC31F10.09c","secondary_identifiers":["UniProtKB:P87310"],"synonyms":[{"name":"Spom972h-MED10","type":"exact"},{"name":"mediator complex subunit 10 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P87310"}


id: PBO:0031077
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cellular_response_phenotype","termid":"PBO:0031077"}


id: GO:1990117
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An extrinsic apoptotic signaling pathway initiated by the cross-linking of an antigen receptor on a B cell.","definition_xrefs":["GOC:BHF","GOC:mtg_apoptosis","GOC:rl","PMID:15214043"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B cell receptor signaling pathway","termid":"GO:0050853"},{"relation_name":"is_a","term_name":"extrinsic apoptotic signaling pathway","termid":"GO:0097191"},{"relation_name":"part_of","term_name":"B cell apoptotic process","termid":"GO:0001783"}],"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":"B cell receptor apoptotic signaling pathway","synonyms":[{"name":"B cell receptor extrinsic apoptotic signaling pathway","type":"exact"},{"name":"extrinsic apoptotic signaling pathway via B cell antigen receptor","type":"related"},{"name":"extrinsic apoptotic signaling pathway via BCR","type":"related"}],"termid":"GO:1990117"}


id: PBO:0059942
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND2 pseudogene 28","termid":"PBO:0059942"}


id: PBO:0059780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 6","termid":"PBO:0059780"}


id: PBO:0062591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 10 subfamily J member 1","termid":"PBO:0062591"}


id: MONDO:0024530
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Bethlem myopathy","termid":"MONDO:0008029"},{"relation_name":"is_a","term_name":"collagen 6-related myopathy","termid":"MONDO:0100225"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320"],"is_obsolete":false,"name":"Bethlem myopathy 1A","secondary_identifiers":["OMIM:158810"],"synonyms":[{"name":"BTHLM1","type":"related"},{"name":"Bethlem myopathy","type":"related"},{"name":"Bethlem myopathy 1","type":"broad"},{"name":"muscular dystrophy, benign congenital","type":"related"},{"name":"myopathy, benign congenital, with contractures","type":"related"}],"termid":"MONDO:0024530","xrefs":{"Monarch":{"xref_id":"0024530"}}}


id: PBO:0066468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"replication factor C subunit 5","termid":"PBO:0066468"}


id: PBO:0045362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double PHD fingers 2","termid":"PBO:0045362"}


id: PBO:0045272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynamin 1 pseudogene 19","termid":"PBO:0045272"}


id: GO:0015954
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways by which a pyrimidine ribonucleotide is synthesized from another pyrimidine ribonucleotide.","definition_xrefs":["ISBN:0306444747","GOC:mah","ISBN:0471394831"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine ribonucleotide metabolic process","termid":"GO:0009218"},{"relation_name":"is_a","term_name":"pyrimidine nucleotide interconversion","termid":"GO:0015953"}],"gene_count":0,"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":"pyrimidine ribonucleotide interconversion","termid":"GO:0015954"}


id: GO:0003138
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that results in the delineation of a specific region of the lateral mesoderm into the area which will form the primary beating heart tube. In mammals the primary heart field gives rise to the left ventricle.","definition_xrefs":["GOC:mtg_heart","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart field specification","termid":"GO:0003128"}],"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":"primary heart field specification","synonyms":[{"name":"FHS specification","type":"exact"},{"name":"first heart field specification","type":"exact"}],"termid":"GO:0003138"}


id: GO:0033748
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2 + A = AH2.","definition_xrefs":["EC:1.12.99.6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on hydrogen as donor","termid":"GO:0016695"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"hydrogenase (acceptor) activity","secondary_identifiers":["MetaCyc:RXN0-4141","RHEA:12116"],"synonyms":[{"name":"H2 producing hydrogenase activity","type":"broad"},{"name":"hydrogen-lyase activity","type":"broad"},{"name":"hydrogen:(acceptor) oxidoreductase activity","type":"related"},{"name":"hydrogen:acceptor oxidoreductase activity","type":"related"},{"name":"hydrogenlyase activity","type":"broad"},{"name":"uptake hydrogenase activity","type":"broad"}],"termid":"GO:0033748"}


id: PR:O13894
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug103 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13894"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 103 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22A12.02c","synonyms":[{"name":"Spom972h-mug103","type":"exact"}],"termid":"PR:O13894"}


id: PBO:0110402
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol glycan anchor biosynthesis class G (EMM blood group)","termid":"PBO:0110402"}


id: PBO:0047894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, folic acid type, rare, fra(7)(p11.2)","termid":"PBO:0047894"}


id: GO:1901697
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of olivetolic acid.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyketide biosynthetic process","termid":"GO:0030639"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"},{"relation_name":"is_a","term_name":"phenol-containing compound biosynthetic process","termid":"GO:0046189"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"olivetolic acid biosynthetic process","synonyms":[{"name":"olivetolic acid anabolism","type":"exact"},{"name":"olivetolic acid biosynthesis","type":"exact"},{"name":"olivetolic acid formation","type":"exact"},{"name":"olivetolic acid synthesis","type":"exact"}],"termid":"GO:1901697"}


id: GO:0034072
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: squalene = triterpene.","definition_xrefs":["GOC:cb","PMID:18033581"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclase activity","termid":"GO:0009975"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0009975"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0009975","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"squalene cyclase activity","termid":"GO:0034072"}


id: PBO:0077880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripeptidyl peptidase 2","termid":"PBO:0077880"}


id: PBO:0024840
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"not functionally complemented by S. cerevisiae DSS1","termid":"PBO:0024840"}


id: MONDO:0044227
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete dimples, facial (obsolete MONDO:0044227)","secondary_identifiers":["OMIM:126100"],"synonyms":[{"name":"cheek dimples","type":"related"},{"name":"dimples, FACIAL","type":"related"},{"name":"smiling dimples","type":"related"}],"termid":"MONDO:0044227","xrefs":{"Monarch":{"xref_id":"0044227"}}}


id: MONDO:0020136
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete neurodegenerative disease with dementia (obsolete MONDO:0020136)","secondary_identifiers":["Orphanet:98534"],"termid":"MONDO:0020136","xrefs":{"Monarch":{"xref_id":"0020136"}}}


id: GO:0010049
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a plant acquires the ability to respond to a floral inductive signal.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic development","termid":"GO:0009791"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"acquisition of plant reproductive competence","synonyms":[{"name":"acquisition of reproductive competence","type":"broad"}],"termid":"GO:0010049"}


id: PBO:0053562
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 572","termid":"PBO:0053562"}


id: GO:0120206
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The distal region of the photoreceptor connecting cilium is structurally unique to the photoreceptor and is maintained by retina-specific protein, SPATA7, and its interacting partners RPGR and RPGRIP1. It is essential for photoreceptor sensory cilium stability.","definition_xrefs":["PMID:29899041","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"photoreceptor connecting cilium","termid":"GO:0032391"}],"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":"photoreceptor distal connecting cilium","synonyms":[{"name":"DCC","type":"related"},{"name":"photoreceptor DCC","type":"related"}],"termid":"GO:0120206"}


id: PBO:0045550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 5","termid":"PBO:0045550"}


id: PBO:0001679
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit Med11 (predicted)","termid":"PBO:0001679"}


id: GO:0019453
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-cysteine, via the intermediate cystine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-cysteine catabolic process","termid":"GO:0019448"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044248","GO:0008150","GO:0006520","GO:0006790","GO:0044281"],"is_obsolete":false,"name":"L-cysteine catabolic process via cystine","synonyms":[{"name":"L-cysteine breakdown via cystine","type":"exact"},{"name":"L-cysteine degradation via cystine","type":"exact"}],"termid":"GO:0019453"}


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: PBO:0061130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NMD3 ribosome export adaptor","termid":"PBO:0061130"}


id: PBO:0005017
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.1.1.56","termid":"PBO:0005017"}


id: MONDO:0009381
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hyperbilirubinemia","termid":"MONDO:0002408"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"hyperbilirubinemia, conjugated, type 3","secondary_identifiers":["MESH:C562885","OMIM:237550","MEDGEN:98323","SCTID:235906009","UMLS:C0400964"],"synonyms":[{"name":"hyperbilirubinemia, conjugated, type III","type":"related"}],"termid":"MONDO:0009381","xrefs":{"Monarch":{"xref_id":"0009381"}}}


id: GO:0010499
data:
  {"annotated_genes":["SJAG_02625","SJAG_00591","SJAG_05252","SJAG_00837"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70287,75019,76837,78762],"is_not":false,"summary":null,"term":"GO:0010499"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a protein or peptide by hydrolysis of its peptide bonds that is mediated by the proteasome but do not involve ubiquitin.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteasomal protein catabolic process","termid":"GO:0010498"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00591":null,"SJAG_00837":null,"SJAG_02625":null,"SJAG_05252":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0030163"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0030163"}],"interesting_parent_ids":["GO:0008150","GO:0030163"],"is_obsolete":false,"name":"proteasomal ubiquitin-independent protein catabolic process","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0010499","terms_by_termid":{"GO:0010499":null}}


id: MONDO:0010709
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A basal ganglia disorder characterized by Parkinsonian-type symptoms (postural changes, tremor, rigidity), megalencephaly and variable intellectual deficit. Other signs are frontal bossing, persistent frontal lobe reflexes, strabismus and seizures. It has been described in three generations of one family. Transmission is X-linked, and the gene is located on chromosomal region Xq27.3-qter.","definition_xrefs":["Orphanet:2379"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"parkinsonian disorder","termid":"MONDO:0021095"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"early-onset parkinsonism-intellectual disability syndrome","secondary_identifiers":["MESH:C537179","DOID:0111781","GARD:3203","MEDGEN:208674","OMIM:311510","UMLS:C0796195","SCTID:716107009","icd11.foundation:937544163"],"synonyms":[{"name":"BGMR","type":"related"},{"name":"Laxova Brown hogan syndrome","type":"related"},{"name":"Laxova-Opitz syndrome","type":"exact"},{"name":"Parkinsonism, early onset with intellectual disability","type":"related"},{"name":"Parkinsonism, early onset with mental retardation","type":"related"},{"name":"Parkinsonism, early-onset, with intellectual disability","type":"related"},{"name":"Parkinsonism, early-onset, with mental retardation","type":"related"},{"name":"WAISMAN syndrome","type":"related"},{"name":"WSMN","type":"related"},{"name":"Waisman syndrome","type":"exact"},{"name":"Waisman syndrome, X-linked recessive","type":"exact"},{"name":"Wsn","type":"related"},{"name":"X-linked recessive basal ganglia disorder with intellectual disability","type":"related"},{"name":"X-linked recessive basal ganglia disorder with mental retardation","type":"related"},{"name":"basal ganglia disorder with intellectual disability","type":"related"},{"name":"basal ganglia disorder with mental retardation","type":"related"},{"name":"basal ganglion disorder with intellectual disability","type":"related"},{"name":"basal ganglion disorder with mental retardation","type":"related"},{"name":"early-onset parkinsonism-intellectual disability syndrome","type":"exact"}],"termid":"MONDO:0010709","xrefs":{"Monarch":{"xref_id":"0010709"}}}


id: PBO:0061142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NME/NM23 family member 5","termid":"PBO:0061142"}


id: MONDO:0000600
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A specific phobia that involves an irrational fear of contracting a disease.","definition_xrefs":["DOID:0060048"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specific phobia","termid":"MONDO:0012000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nosophobia","secondary_identifiers":["UMLS:C0522182","MEDGEN:637105"],"termid":"MONDO:0000600","xrefs":{"Monarch":{"xref_id":"0000600"}}}


id: PBO:0058188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4481","termid":"PBO:0058188"}


id: GO:0021762
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the substantia nigra over time from its initial formation until its mature state. The substantia nigra is the layer of gray substance that separates the posterior parts of the cerebral peduncles (tegmentum mesencephali) from the anterior parts; it normally includes a posterior compact part with many pigmented cells (pars compacta) and an anterior reticular part whose cells contain little pigment (pars reticularis).","definition_xrefs":["ISBN:0878937420","GOC:dph","GOC:cls","GOC:jid","ISBN:0838580343","GO_REF:0000021","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural nucleus development","termid":"GO:0048857"},{"relation_name":"part_of","term_name":"midbrain development","termid":"GO:0030901"}],"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":"substantia nigra development","termid":"GO:0021762"}


id: GO:0050161
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: oxalate + succinyl-CoA = oxalyl-CoA + succinate.","definition_xrefs":["RHEA:23588","EC:2.8.3.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CoA-transferase activity","termid":"GO:0008410"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016782","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"succinyl-CoA:oxalate CoA-transferase","secondary_identifiers":["MetaCyc:OXALATE-COA-TRANSFERASE-RXN","KEGG_REACTION:R01559"],"synonyms":[{"name":"oxalate CoA-transferase activity","type":"related"},{"name":"oxalate coenzyme A-transferase activity","type":"related"},{"name":"succinyl-CoA:oxalate CoA-transferase activity","type":"related"},{"name":"succinyl-beta-ketoacyl-CoA transferase activity","type":"related"}],"termid":"GO:0050161"}


id: SO:0001842
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A promoter element with consensus sequence TGACTCA, bound by AP-1 and related transcription factors.","definition_xrefs":["PMID:1899230","PMID:3034432","PMID:3125983"],"direct_ancestors":[{"relation_name":"is_a","term_name":"promoter_element","termid":"SO:0001659"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP_1_binding_site","synonyms":[{"name":"AP-1 binding site","type":"exact"}],"termid":"SO:0001842"}


id: MONDO:0009615
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency is a rare inborn error of metabolism disease characterized by mild to moderate, persistent elevation of methylmalonic acid in plasma, urine and cerebrospinal fluid. Clinical presentation may include acute metabolic decompensation with metabolic acidosis (presenting with vomiting, dehydration, confusion, hallucinations), nonspecific neurological symptoms, or may also be asymptomatic.","definition_xrefs":["Orphanet:308425"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylmalonic acidemia","termid":"MONDO:0002012"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency","secondary_identifiers":["UMLS:C1855100","SCTID:765137006","GARD:17390","OMIM:251120","MEDGEN:344419","MESH:C565386"],"synonyms":[{"name":"MCEE deficiency","type":"exact"},{"name":"methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency","type":"exact"},{"name":"methylmalonic acidemia due to methylmalonyl-CoA racemase deficiency","type":"exact"},{"name":"methylmalonic aciduria III","type":"related"},{"name":"methylmalonic aciduria III, formerly","type":"related"},{"name":"methylmalonic aciduria due to methylmalonyl-CoA epimerase deficiency","type":"exact"},{"name":"methylmalonic aciduria due to methylmalonyl-CoA racemase deficiency","type":"exact"},{"name":"methylmalonyl-CoA epimerase deficiency","type":"related"},{"name":"methylmalonyl-Coa epimerase deficiency with sepiapterin reductase deficiency","type":"related"},{"name":"methylmalonyl-Coa racemase deficiency","type":"related"}],"termid":"MONDO:0009615","xrefs":{"Monarch":{"xref_id":"0009615"}}}


id: GO:1903256
data:
  {"annotated_genes":["SJAG_00832","SJAG_03856"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111335,103413],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903257"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving selenoneine.","definition_xrefs":["GOC:TermGenie","GO_REF:0000068","PMID:24828577"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino-acid betaine metabolic process","termid":"GO:0006577"},{"relation_name":"is_a","term_name":"modified histidine metabolic process","termid":"GO:0052701"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00832":null,"SJAG_03856":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"selenoneine metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"L-selenoneine metabolic process","type":"narrow"},{"name":"selenoneine metabolism","type":"exact"}],"termid":"GO:1903256","terms_by_termid":{"GO:1903257":null}}


id: PBO:0073974
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 25","termid":"PBO:0073974"}


id: GO:0047943
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-glutamate + ATP + methylammonium = N(5)-methyl-L-glutamine + ADP + 2 H+ + phosphate.","definition_xrefs":["RHEA:17117","EC:6.3.4.12"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-nitrogen bonds","termid":"GO:0016879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016874"],"is_obsolete":false,"name":"glutamate-methylamine ligase activity","secondary_identifiers":["KEGG_REACTION:R01585","MetaCyc:GLUTAMATE--METHYLAMINE-LIGASE-RXN"],"synonyms":[{"name":"L-glutamate:methylamine ligase (ADP-forming)","type":"related"},{"name":"gamma-glutamylmethylamide synthetase activity","type":"related"}],"termid":"GO:0047943"}


id: PBO:0057492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 610","termid":"PBO:0057492"}


id: PBO:0057814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3135a","termid":"PBO:0057814"}


id: GO:0000189
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a MAP kinase to the nucleus upon activation.","definition_xrefs":["PMID:9561267"],"gene_count":0,"genotype_count":0,"name":"obsolete MAPK import into nucleus (obsolete GO:0000189)","synonyms":[{"name":"nuclear translocation of MAPK","type":"narrow"}],"termid":"GO:0000189"}


id: FYPO:0006477
data:
  {"alleles_by_uniquename":{"SJAG_01330:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01330","name":"mad2delta","uniquename":"SJAG_01330:allele-1"},"SJAG_01956:allele-1":{"allele_type":"amino_acid_mutation","description":"E405K ts","gene_uniquename":"SJAG_01956","name":"nuc2-1051","uniquename":"SJAG_01956:allele-1"},"SJAG_03351:allele-1":{"allele_type":"amino_acid_mutation","description":"A186T ts","gene_uniquename":"SJAG_03351","name":"cut23-415","uniquename":"SJAG_03351:allele-1"},"SJAG_03575:allele-1":{"allele_type":"amino_acid_mutation","description":"E548K ts","gene_uniquename":"SJAG_03575","name":"apc2-361","uniquename":"SJAG_03575:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119335,118925],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004318"},{"annotations":[118983,118984,118985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000324"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the metaphase/anaphase transition of the mitotic cell cycle is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"},{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle phase transition","termid":"FYPO:0005275"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01330":null,"SJAG_01956":null,"SJAG_03351":null,"SJAG_03575":null},"genotype_count":4,"genotypes_by_uniquename":{"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"apc2-361(E548K ts)","display_uniquename":"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03575:allele-1","expression":"Not assayed or wild type"}]}]},"cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cut23-415(A186T ts)","display_uniquename":"cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03351:allele-1","expression":"Not assayed or wild type"}]}]},"mad2delta":{"display_name":"mad2delta","display_uniquename":"mad2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01330:allele-1","expression":"Null"}]}]},"nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"nuc2-1051(E405K ts)","display_uniquename":"nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01956:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"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:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000631","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"abnormal mitotic metaphase/anaphase transition","references_by_uniquename":{"PMID:21802294":null,"PMID:23786411":null,"PMID:32109380":null},"single_locus_annotated_genes":["SJAG_01956","SJAG_01330","SJAG_03351","SJAG_03575"],"single_locus_genotype_uniquenames":["cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","mad2delta","nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"abnormal cell cycle passage through mitotic metaphase-anaphase transition","type":"exact"},{"name":"abnormal cell cycle progression through the metaphase/anaphase transition","type":"exact"},{"name":"abnormal metaphase/anaphase transition during mitotic cell cycle","type":"exact"},{"name":"abnormal mitotic cell cycle metaphase/anaphase transition","type":"exact"},{"name":"abnormal mitotic metaphase/anaphase cell cycle phase transition","type":"exact"},{"name":"abnormal mitotic metaphase/anaphase transition during vegetative growth","type":"exact"},{"name":"abnormal onset of mitotic anaphase","type":"related"}],"termid":"FYPO:0006477","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYPO:0000324":null,"FYPO:0004318":null}}


id: PBO:0114287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces pombe specific cell surface glycoprotein","termid":"PBO:0114287"}


id: MONDO:0013010
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 8p22-p21.3.","definition_xrefs":["DOID:0110522","PMID:19229252"],"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:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 71","secondary_identifiers":["OMIM:612789","MESH:C567562","UMLS:C2748554","GARD:22630","MEDGEN:411609"],"synonyms":[{"name":"DFNB71","type":"narrow"},{"name":"autosomal recessive deafness 71","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 71","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 71","type":"narrow"},{"name":"deafness, autosomal recessive 71","type":"narrow"}],"termid":"MONDO:0013010","xrefs":{"Monarch":{"xref_id":"0013010"}}}


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


id: GO:0043738
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: methanophenazine + reduced coenzyme F420 = dihydromethanophenazine + coenzyme F420.","definition_xrefs":["RHEA:54752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors","termid":"GO:0016645"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"reduced coenzyme F420 dehydrogenase activity","secondary_identifiers":["MetaCyc:RXN-8106","EC:1.5.98.3"],"synonyms":[{"name":"1,5-dihydrocoenzyme F420 dehydrogenase activity","type":"exact"},{"name":"F420H2 dehydrogenase activity","type":"exact"}],"termid":"GO:0043738"}


id: MONDO:0010199
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"White forelock with malformations is a multiple congenital anomalies syndrome characterized by poliosis, distinct facial features (epicanthal folds, hypertelorism, posterior rotation of ears, prominent philtrum, high-arched palate) and congenital anomalies/malformations of the eye (blue sclera), cardiopulmonary (atrial septal defect, prominent thoracic and abdominal veins), and skeletal (clinodactyly, syndactyly of the fingers and 2nd and 3rd toes) systems. There have been no further descriptions in the literature since 1980.","definition_xrefs":["Orphanet:2475"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart disorder","termid":"MONDO:0005267"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"white forelock with malformations","secondary_identifiers":["MEDGEN:376362","MESH:C536700","UMLS:C1848463","SCTID:763619009","GARD:10081","OMIM:277740"],"synonyms":[{"name":"white forelock with malformations","type":"exact"}],"termid":"MONDO:0010199","xrefs":{"Monarch":{"xref_id":"0010199"}}}


id: GO:0005593
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen trimer that associates with collagen fibrils and consists of collagen monomers that contain two or more relatively short triple-helical domains connected by non-triple-helical sequences.","definition_xrefs":["ISBN:0198599587","PMID:21421911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"collagen trimer","termid":"GO:0005581"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"FACIT collagen trimer","secondary_identifiers":["Wikipedia:FACIT_collagen"],"termid":"GO:0005593"}


id: MONDO:0005175
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Insulitis is an inflammatory infiltration of the islets of Langerhans found especially in young patients with recent onset type 1 diabetes.","definition_xrefs":["EFO:0002498"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine pancreas disorder","termid":"MONDO:0001933"},{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"aggressive insulitis","termid":"MONDO:0005175","xrefs":{"Monarch":{"xref_id":"0005175"}}}


id: MOD:00880
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification produced by formation of an adduct with 6x(13)C labeled 4-sulfophenyl isothiocyanate.","definition_xrefs":["Unimod:464","PubMed:15536630","PubMed:16526082"],"direct_ancestors":[{"relation_name":"is_a","term_name":"4-sulfophenyl isothiocyanate derivatized residue","termid":"MOD:00584"},{"relation_name":"is_a","term_name":"(13)C isotope tagged reagent","termid":"MOD:01428"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6x(13)C labeled 4-sulfophenyl isothiocyanate derivatized residue","synonyms":[{"name":"4-sulfophenyl isothiocyanate (Heavy C13)","type":"related"},{"name":"SPITC:13C(6)","type":"related"}],"termid":"MOD:00880"}


id: MONDO:0011338
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID).","definition_xrefs":["Orphanet:39041"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"non-SCID combined immunodeficiency","termid":"MONDO:0018814"},{"relation_name":"is_a","term_name":"T-B- severe combined immunodeficiency","termid":"MONDO:0017855"},{"relation_name":"is_a","term_name":"familial severe combined immunodeficiency","termid":"MONDO:0031520"}],"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":"Omenn syndrome","secondary_identifiers":["GARD:8198","OMIM:603554","UMLS:C2700553","NANDO:2200697","SCTID:722067005","NCIT:C61240","MedDRA:10069097","DOID:0060010","NANDO:1200324","MEDGEN:398130"],"synonyms":[{"name":"Omenn syndrome","type":"exact"},{"name":"combined immunodeficiency with hypereosinophilia","type":"exact"},{"name":"reticuloendotheliosis familial with eosinophilia","type":"related"},{"name":"reticuloendotheliosis, familial, with eosinophilia","type":"related"},{"name":"severe combined immunodeficiency with hypereosinophilia","type":"related"}],"termid":"MONDO:0011338","xrefs":{"Monarch":{"xref_id":"0011338"}}}


id: FYPO:0006219
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell growth phenotype in which vegetative cell population growth is cell population growth is normal (i.e. indistinguishable from wild type) under conditions of potassium ion starvation.","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:0000003"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0002060","FYPO:0000139","FYPO:0000003","FYPO:0002058","FYPO:0002057"],"is_obsolete":false,"name":"normal cell population growth during potassium ion starvation","synonyms":[{"name":"normal cell population growth during potassium ion depletion","type":"exact"},{"name":"normal cell population growth during potassium ion deprivation","type":"exact"},{"name":"normal cell population growth during potassium starvation","type":"exact"},{"name":"normal cell population growth in response to potassium ion starvation","type":"exact"},{"name":"normal vegetative cell population growth during potassium ion starvation","type":"exact"}],"termid":"FYPO:0006219"}


id: GO:0140052
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an oxidized lipoprotein particle stimulus.","definition_xrefs":["GOC:aruk","PMID:27607416","GOC:BHF","PMID:20037584"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to low-density lipoprotein particle stimulus","termid":"GO:0071404"}],"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 oxidised low-density lipoprotein particle stimulus","synonyms":[{"name":"cellular response to ox-LDL particle stimulus","type":"exact"},{"name":"cellular response to oxLDL particle stimulus","type":"exact"},{"name":"cellular response to oxidised LDL particle stimulus","type":"exact"},{"name":"cellular response to oxidized LDL particle stimulus","type":"exact"},{"name":"cellular response to oxidized low-density lipoprotein particle stimulus","type":"exact"}],"termid":"GO:0140052"}


id: GO:0021804
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that results in the loss of attachments of a cell in the ventricular zone.","definition_xrefs":["GOC:dgh","GOC:cls","GO_REF:0000021","GOC:dph","GOC:jid","PMID:12626695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell adhesion","termid":"GO:0007162"},{"relation_name":"part_of","term_name":"somal translocation","termid":"GO:0021802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of cell adhesion in ventricular zone","synonyms":[{"name":"down regulation of cell adhesion in ventricular zone","type":"exact"},{"name":"down-regulation of cell adhesion in ventricular zone","type":"exact"},{"name":"downregulation of cell adhesion in ventricular zone","type":"exact"},{"name":"inhibition of cell adhesion in ventricular zone","type":"narrow"}],"termid":"GO:0021804"}


id: FYPO:0007190
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cohesion between sister chromatids is increased along the length of the chromosome arms during interphase of the mitotic cell cycle.","definition_xrefs":["PMID:31483748","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid cohesion","termid":"FYPO:0006521"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000641","FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased sister chromatid cohesion along chromosome arms during mitotic interphase","synonyms":[{"name":"increased mitotic sister chromatid cohesion along chromosome arms during interphase","type":"exact"},{"name":"increased sister chromatid cohesion along chromosome arms during interphase of mitotic cell cycle","type":"exact"},{"name":"increased sister chromatid cohesion along chromosome arms during mitotic interphase during vegetative growth","type":"exact"}],"termid":"FYPO:0007190"}


id: PR:O13984
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A replication-associated recombination protein A that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01708"],"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":"ATPase WRNIP1 homolog C26H5.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC26H5.02c","secondary_identifiers":["UniProtKB:O13984"],"synonyms":[{"name":"Spom972h-rarA","type":"exact"}],"termid":"PR:O13984"}


id: PBO:0055616
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 3055","termid":"PBO:0055616"}


id: GO:0032103
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the rate of a response to an external stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to external stimulus","termid":"GO:0032101"},{"relation_name":"is_a","term_name":"positive regulation of response to stimulus","termid":"GO:0048584"},{"relation_name":"positively_regulates","term_name":"response to external stimulus","termid":"GO:0009605"}],"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 response to external stimulus","synonyms":[{"name":"activation of response to external stimulus","type":"narrow"},{"name":"stimulation of response to external stimulus","type":"narrow"},{"name":"up regulation of response to external stimulus","type":"exact"},{"name":"up-regulation of response to external stimulus","type":"exact"},{"name":"upregulation of response to external stimulus","type":"exact"}],"termid":"GO:0032103"}


id: PBO:0074643
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 35B","termid":"PBO:0074643"}


id: PBO:0058419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4788","termid":"PBO:0058419"}


id: PBO:0030141
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_GTP_binding","termid":"PBO:0030141"}


id: MONDO:0010604
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hemophilia B is a form of hemophilia characterized by spontaneous or prolonged hemorrhages due to factor IX deficiency.","definition_xrefs":["Orphanet:98879"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemorrhagic disease","termid":"MONDO:0002243"},{"relation_name":"is_a","term_name":"hemophilia","termid":"MONDO:0018660"},{"relation_name":"is_a","term_name":"inherited blood coagulation disorder","termid":"MONDO:0021181"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"hemophilia B","secondary_identifiers":["NCIT:C26721","ICD9:286.1","MedDRA:10016077","MESH:D002836","MEDGEN:945","icd11.foundation:1901375668","DOID:12259","OMIM:306900","GARD:8732","NANDO:2200677","NORD:1222","SCTID:41788008","UMLS:C0008533"],"synonyms":[{"name":"Christmas disease","type":"exact"},{"name":"F9 deficiency","type":"related"},{"name":"HEMB","type":"related"},{"name":"congenital factor IX deficiency","type":"exact"},{"name":"congenital factor IX disorder","type":"exact"},{"name":"deficiency, functional factor IX","type":"exact"},{"name":"factor 9 deficiency","type":"related"},{"name":"factor IX deficiency","type":"exact"},{"name":"haemophilia B Leyden","type":"related"},{"name":"haemophilia B(M)","type":"related"},{"name":"haemophilia b, X-linked recessive","type":"exact"},{"name":"haemophilia type B","type":"exact"},{"name":"hem B","type":"related"},{"name":"hemophilia B","type":"exact"},{"name":"hemophilia B Leyden","type":"related"},{"name":"hemophilia B(M)","type":"related"},{"name":"hemophilia b, X-linked recessive","type":"exact"},{"name":"hemophilia type B","type":"exact"},{"name":"hereditary Factor IX deficiency","type":"exact"},{"name":"hereditary Factor IX deficiency disease","type":"exact"},{"name":"plasma thromboplastin component deficiency","type":"related"}],"termid":"MONDO:0010604","xrefs":{"Monarch":{"xref_id":"0010604"}}}


id: SO:0001650
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant which does not cause a disruption of the translational reading frame.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein_altering_variant","termid":"SO:0001818"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inframe_variant","synonyms":[{"name":"ANNOVAR:nonframeshift block substitution","type":"related"},{"name":"ANNOVAR:nonframeshift substitution","type":"related"},{"name":"VAAST:inframe_variant","type":"exact"},{"name":"cds-indel","type":"exact"},{"name":"inframe variant","type":"exact"}],"termid":"SO:0001650"}


id: MOD:00777
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"Natural or modified residues with a mass of 182.96-182.98 Da.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"residues isobaric at a resolution below 0.01 Da","termid":"MOD:00770"},{"relation_name":"is_a","term_name":"residues isobaric at 182.9-183.0 Da","termid":"MOD:00778"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"residues isobaric at 182.96-182.98 Da","termid":"MOD:00777"}


id: PBO:0048683
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GLI family zinc finger 2","termid":"PBO:0048683"}


id: MONDO:0019509
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cutaneous leukocytoclastic angiitis is a small-vessel vasculitis presenting with palpable purpura and urticarial lesions which predate the purpuric lesions most frequently observed on the legs. Systemic symptoms including fever, cough, hemoptysis, sinusitis, arthralgia, arthritis, myalgia, abdominal pain, diarrhea, hematochezia, paresthesia, weakness, and hematuria may be observed. Skin biopsy reveals exudates rich in neutrophils, endothelial damage, fibrin deposition, and leukocytoclasis in postcapillary venules of small vessels. Cutaneous leukocytoclastic angiitis can be idiopathic (in up to 50% of cases) or secondary to infections, medications (such as antituberculosis medication), collagen vascular diseases, or neoplasms.","definition_xrefs":["Orphanet:889"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune complex mediated vasculitis","termid":"MONDO:0015491"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cutaneous leukocytoclastic angiitis","secondary_identifiers":["SCTID:718217000","GARD:7851","icd11.foundation:71458216","NCIT:C122919","UMLS:C4049638","MEDGEN:881641"],"synonyms":[{"name":"cutaneous hypersensitivity vasculitis","type":"exact"},{"name":"cutaneous leukocytoclastic vasculitis","type":"exact"},{"name":"cutaneous small vessel vasculitis","type":"exact"},{"name":"cutaneous small-vessel vasculitis","type":"exact"},{"name":"hypersensitivity angiitis","type":"exact"},{"name":"leukocytoclastic angiitis","type":"related"}],"termid":"MONDO:0019509","xrefs":{"Monarch":{"xref_id":"0019509"}}}


id: GO:0070203
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 protein to a specific location in the telomeric region of a chromosome.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of establishment of protein localization to chromosome","termid":"GO:0070202"},{"relation_name":"is_a","term_name":"regulation of protein localization to chromosome, telomeric region","termid":"GO:1904814"},{"relation_name":"regulates","term_name":"establishment of protein localization to telomere","termid":"GO:0070200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of establishment of protein localization to telomere","synonyms":[{"name":"regulation of establishment of protein localisation to telomere","type":"exact"}],"termid":"GO:0070203"}


id: PBO:0091673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane glycerophosphodiester transmembrane transporter","termid":"PBO:0091673"}


id: GO:0120198
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the size of an imaginal disc-derived wing.","definition_xrefs":["PIMD:23485686","GOC:ha"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of imaginal disc-derived wing size","termid":"GO:0044719"}],"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 imaginal disc-derived wing size","termid":"GO:0120198"}


id: PBO:0041399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C6orf47 antisense RNA 1","termid":"PBO:0041399"}


id: PBO:0054301
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 1692","termid":"PBO:0054301"}


id: PBO:0065092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase AMP-activated non-catalytic subunit gamma 1","termid":"PBO:0065092"}


id: PBO:0110413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSBP3 pseudogene 3","termid":"PBO:0110413"}


id: PBO:0005465
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.1.20","termid":"PBO:0005465"}


id: GO:0000154
data:
  {"annotated_genes":["SJAG_02024","SJAG_03572","SJAG_00566","SJAG_03016","SJAG_00943","SJAG_03289","SJAG_04754","SJAG_03008","SJAG_03332","SJAG_00722","SJAG_00744","SJAG_02350","SJAG_02417","SJAG_01234","SJAG_01877","SJAG_03410","SJAG_03877","SJAG_02821","SJAG_02281","SJAG_00083","SJAG_01172","SJAG_01958","SJAG_03755","SJAG_03773","SJAG_03713","SJAG_02377"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[57145,106027,75095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000455"},{"annotations":[79754],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070476"},{"annotations":[71888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904812"},{"annotations":[77888,78424,75454,79253,78717],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070475"},{"annotations":[63999,59356,63641,65452,79062,74763,78380],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031167"},{"annotations":[89760,77536,79951],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031118"},{"annotations":[98577,111145,109998,93887,107891],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000452"},{"annotations":[74169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000454"}]},"cv_name":"biological_process","definition":"The covalent alteration of one or more nucleotides within an rRNA molecule to produce an rRNA molecule with a sequence that differs from that coded genetically.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA processing","termid":"GO:0006364"},{"relation_name":"is_a","term_name":"RNA modification","termid":"GO:0009451"}],"gene_count":26,"genes_by_uniquename":{"SJAG_00083":null,"SJAG_00566":null,"SJAG_00722":null,"SJAG_00744":null,"SJAG_00943":null,"SJAG_01172":null,"SJAG_01234":null,"SJAG_01877":null,"SJAG_01958":null,"SJAG_02024":null,"SJAG_02281":null,"SJAG_02350":null,"SJAG_02377":null,"SJAG_02417":null,"SJAG_02821":null,"SJAG_03008":null,"SJAG_03016":null,"SJAG_03289":null,"SJAG_03332":null,"SJAG_03410":null,"SJAG_03572":null,"SJAG_03713":null,"SJAG_03755":null,"SJAG_03773":null,"SJAG_03877":null,"SJAG_04754":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0042254"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0044085","GO:0042254"],"is_obsolete":false,"name":"rRNA modification","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["Reactome:R-HSA-6793080","GO:0016548","Reactome:R-HSA-6790901"],"synonyms":[{"name":"rRNA editing","type":"narrow"}],"termid":"GO:0000154","terms_by_termid":{"GO:0000452":null,"GO:0000454":null,"GO:0000455":null,"GO:0031118":null,"GO:0031167":null,"GO:0070475":null,"GO:0070476":null,"GO:1904812":null}}


id: PBO:0078157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha variable 35","termid":"PBO:0078157"}


id: PATO:0000555
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000555 heat sensitive (obsolete PATO:0000555)","termid":"PATO:0000555"}


id: GO:0140042
data:
  {"annotated_genes":["SJAG_01537","SJAG_02980","SJAG_04059","SJAG_03162","SJAG_03609","SJAG_01180","SJAG_04049"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[62077,88515,94409,110783,111859,113989,118689],"is_not":false,"summary":null,"term":"GO:0140042"}]},"cv_name":"biological_process","definition":"A process that results in the assembly, arrangement of constituent parts of a lipid droplet.","definition_xrefs":["PMID:28011631"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid droplet organization","termid":"GO:0034389"},{"relation_name":"is_a","term_name":"membraneless organelle assembly","termid":"GO:0140694"},{"relation_name":"part_of","term_name":"lipid storage","termid":"GO:0019915"}],"gene_count":7,"genes_by_uniquename":{"SJAG_01180":null,"SJAG_01537":null,"SJAG_02980":null,"SJAG_03162":null,"SJAG_03609":null,"SJAG_04049":null,"SJAG_04059":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"lipid droplet formation","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"adiposome formation","type":"exact"},{"name":"lipid body formation","type":"exact"},{"name":"lipid particle formation","type":"exact"}],"termid":"GO:0140042","terms_by_termid":{"GO:0140042":null}}


id: GO:0071488
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 very low light intensity stimulus. A very low light intensity stimulus is defined as a level of electromagnetic radiation below 0.001 mmol/m2/sec.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to very low light intensity stimulus","termid":"GO:0055122"},{"relation_name":"is_a","term_name":"cellular response to light intensity","termid":"GO:0071484"}],"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 very low light intensity stimulus","termid":"GO:0071488"}


id: PBO:0031209
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-premature_activation_of_bipolar_cell_growth","termid":"PBO:0031209"}


id: GO:0050100
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-methylene-3-methylsuccinate = dimethylmaleate.","definition_xrefs":["RHEA:23480"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, transposing C=C bonds","termid":"GO:0016863"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016853","GO:0003674"],"is_obsolete":false,"name":"methylitaconate delta-isomerase activity","secondary_identifiers":["MetaCyc:METHYLITACONATE-DELTA-ISOMERASE-RXN","EC:5.3.3.6","KEGG_REACTION:R03070"],"synonyms":[{"name":"methylitaconate D-isomerase activity","type":"exact"},{"name":"methylitaconate delta2-delta3-isomerase activity","type":"related"},{"name":"methylitaconate isomerase activity","type":"related"}],"termid":"GO:0050100"}


id: MONDO:0002043
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The turning outward (eversion) of the edge of the eyelid, resulting in the exposure of the palpebral conjunctiva. (Dorland, 27th ed)","definition_xrefs":["MESH:D004483"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eyelid disorder","termid":"MONDO:0003382"}],"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":"ectropion","secondary_identifiers":["MEDGEN:4448","DOID:1570","ICD9:374.10","UMLS:C0013592","SCTID:62909004","HP:0000656","ICD9:374.1"],"synonyms":[{"name":"ectropion","type":"exact"},{"name":"ectropion (disease)","type":"exact"},{"name":"ectropion of eyelid","type":"exact"},{"name":"everted margin","type":"exact"}],"termid":"MONDO:0002043","xrefs":{"Monarch":{"xref_id":"0002043"}}}


id: GO:0045647
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of erythrocyte differentiation.","definition_xrefs":["GOC:go_curators"],"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 erythrocyte differentiation","termid":"GO:0045646"},{"relation_name":"negatively_regulates","term_name":"erythrocyte differentiation","termid":"GO:0030218"}],"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 erythrocyte differentiation","synonyms":[{"name":"down regulation of erythrocyte differentiation","type":"exact"},{"name":"down-regulation of erythrocyte differentiation","type":"exact"},{"name":"downregulation of erythrocyte differentiation","type":"exact"},{"name":"inhibition of erythrocyte differentiation","type":"narrow"},{"name":"negative regulation of RBC differentiation","type":"exact"},{"name":"negative regulation of red blood cell differentiation","type":"exact"}],"termid":"GO:0045647"}


id: GO:1902513
data:
  {"annotated_genes":["SJAG_04597"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902854"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of organelle transport along microtubule.","definition_xrefs":["PMID:21147087","GOC:TermGenie","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular transport","termid":"GO:0032386"},{"relation_name":"is_a","term_name":"regulation of microtubule-based movement","termid":"GO:0060632"},{"relation_name":"regulates","term_name":"organelle transport along microtubule","termid":"GO:0072384"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04597":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of organelle transport along microtubule","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of microtubule-based organelle localization","type":"exact"}],"termid":"GO:1902513","terms_by_termid":{"GO:1902854":null}}


id: MONDO:0022802
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":"Collins-Sakati syndrome","synonyms":[{"name":"Collins Sakati syndrome","type":"related"}],"termid":"MONDO:0022802","xrefs":{"Monarch":{"xref_id":"0022802"}}}


id: PBO:0067008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 15, pseudogene","termid":"PBO:0067008"}


id: PBO:0067029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 42, pseudogene","termid":"PBO:0067029"}


id: MONDO:0850301
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoimmune disease of skin and connective tissue that is characterized by subepidermal blistering especially in the lower abdomen, groin, and flexor surfaces of the extremities, creating tense blisters that do not break easily.","definition_xrefs":["DOID:0080841"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune bullous skin disease","termid":"MONDO:0019337"}],"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":"pemphigoid","secondary_identifiers":["icd11.foundation:445309625","SCTID:86142006"],"termid":"MONDO:0850301","xrefs":{"Monarch":{"xref_id":"0850301"}}}


id: GO:0050171
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-glucose + a phenol = UDP + an aryl beta-D-glucoside.","definition_xrefs":["MetaCyc:PHENOL-BETA-GLUCOSYLTRANSFERASE-RXN","EC:2.4.1.35"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016757","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"phenol beta-glucosyltransferase activity","synonyms":[{"name":"UDP glucosyltransferase activity","type":"related"},{"name":"UDP-glucose glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:phenol beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:phenol beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucosyltransferase activity","type":"related"},{"name":"phenol b-glucosyltransferase activity","type":"exact"},{"name":"phenol-beta-D-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucosyltransferase activity","type":"related"}],"termid":"GO:0050171"}


id: MONDO:0005475
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A migraine disorder characterized by episodes that are preceded by focal neurological symptoms.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"migraine disorder","termid":"MONDO:0005277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"migraine with aura","secondary_identifiers":["MESH:D020325","DOID:10024","icd11.foundation:525744634","ICD9:346.0","MEDGEN:57822","HP:0002077","NCIT:C117005","SCTID:4473006","UMLS:C0154723","ICD9:346.00"],"synonyms":[{"name":"classic migraine","type":"exact"}],"termid":"MONDO:0005475","xrefs":{"Monarch":{"xref_id":"0005475"}}}


id: PBO:0032758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDP-diacylglycerol-glycerol-3-phosphate3-phosphatidyltransferase Pgs1 (predicted)","termid":"PBO:0032758"}


id: PBO:0082516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Catalytic subunit of the NatC type N-terminal acetyltransferase (NAT); involved in subcellular targeting of select N-terminally acetylated substrates to the Golgi apparatus (Arl3p and Grh1p) and the inner nuclear membrane (Trm1p); required for replication of dsRNA virus; human NatC ortholog, NAA30, functionally complements the null, requiring either auxiliary subunit Mak10p or co-expression of human ortholog, NAA35; NAA60, the human NatF gene, also complements the null allele","termid":"PBO:0082516"}


id: GO:0099030
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the postsynaptic specialization membrane consisting of the gene products that are tethered to the membrane only by a covalently attached anchor, such as a lipid group that is embedded in the membrane. Gene products with peptide sequences that are embedded in the membrane are excluded from this grouping.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete anchored component of postsynaptic specialization membrane (obsolete GO:0099030)","termid":"GO:0099030"}


id: GO:0030294
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Stops, prevents or reduces the activity of a receptor signaling protein tyrosine kinase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein tyrosine kinase inhibitor activity","termid":"GO:0030292"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0004857","GO:0140678","GO:0003674","GO:0098772","GO:0030234"],"is_obsolete":false,"name":"receptor signaling protein tyrosine kinase inhibitor activity","synonyms":[{"name":"receptor signalling protein tyrosine kinase inhibitor activity","type":"exact"}],"termid":"GO:0030294"}


id: FYPO:0004718
data:
  {"alleles_by_uniquename":{"SJAG_01050:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01050","name":"nur1delta","uniquename":"SJAG_01050:allele-1"},"SJAG_03892:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03892","name":"vps4delta","uniquename":"SJAG_03892:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[118948],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001132"}],"single_locus_phenotype":[{"annotations":[118947],"is_not":false,"summary":null,"term":"FYPO:0004718"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to heterochromatin is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to chromatin","termid":"FYPO:0001679"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01050":null,"SJAG_01745":null,"SJAG_03892":null},"genotype_count":2,"genotypes_by_uniquename":{"nur1delta__vps4delta":{"display_name":"nur1delta vps4delta","display_uniquename":"nur1delta__vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01050:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]},"vps4delta":{"display_name":"vps4delta","display_uniquename":"vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_03892","SJAG_01050"],"name":"abnormal protein localization to heterochromatin","references_by_uniquename":{"PMID:32109380":null},"single_locus_annotated_genes":["SJAG_03892"],"single_locus_genotype_uniquenames":["vps4delta"],"synonyms":[{"name":"abnormal protein localisation to heterochromatin","type":"exact"}],"termid":"FYPO:0004718","terms_by_termid":{"FYPO:0001132":null,"FYPO:0004718":null,"FYPO_EXT:0000001":null}}


id: PBO:0044955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dehydrogenase/reductase 2","termid":"PBO:0044955"}


id: GO:0030046
data:
  {"annotated_genes":["SJAG_00938","SJAG_03011"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107934,115988],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070649"}]},"cv_name":"biological_process","definition":"Assembly of actin filament bundles in which the filaments are tightly packed (approximately 10-20 nm apart) and oriented with the same polarity.","definition_xrefs":["ISBN:0815316194","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament bundle assembly","termid":"GO:0051017"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00938":null,"SJAG_03011":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0030036"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007010","GO:0030036","GO:0044085"],"is_obsolete":false,"name":"parallel actin filament bundle assembly","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0030046","terms_by_termid":{"GO:0070649":null}}


id: FYPO:0001628
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 L-valine measured in the vacuole is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in vacuole","termid":"FYPO:0001603"},{"relation_name":"is_a","term_name":"normal cellular valine level","termid":"FYPO:0002746"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001320","FYPO:0001312"],"is_obsolete":false,"name":"normal vacuolar valine level","synonyms":[{"name":"normal level of valine in vacuole","type":"exact"},{"name":"normal vacuolar L-valine level","type":"exact"},{"name":"normal vacuolar valine level during mitotic cell cycle","type":"related"},{"name":"normal vacuolar valine level during vegetative growth","type":"exact"}],"termid":"FYPO:0001628"}


id: PBO:0081190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zic family member 3","termid":"PBO:0081190"}


id: MONDO:0000298
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease caused by infection with Dioctophyme renale.","definition_xrefs":["MONDO:patterns/infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Enoplea infectious disease","termid":"MONDO:0005745"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dioctophymiasis","secondary_identifiers":["DOID:0050260","MEDGEN:4326","SCTID:40410004","UMLS:C0012482"],"synonyms":[{"name":"Dioctophyme renale caused disease or disorder","type":"exact"},{"name":"Dioctophyme renale disease or disorder","type":"exact"},{"name":"Dioctophyme renale infection","type":"exact"},{"name":"Dioctophyme renale infectious disease","type":"exact"},{"name":"dioctophyma renale infection","type":"related"},{"name":"dioctophymosis","type":"related"},{"name":"giant kidney worm disease","type":"related"}],"termid":"MONDO:0000298","xrefs":{"Monarch":{"xref_id":"0000298"}}}


id: SO:0001974
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcription factor binding site with consensus sequence CCGCGNGGNGGCAG, bound by CCCTF-binding factor.","definition_xrefs":["EBI:nj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"promoter_element","termid":"SO:0001659"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTCF_binding_site","synonyms":[{"name":"CCCTF binding site","type":"exact"},{"name":"CTCF binding site","type":"exact"}],"termid":"SO:0001974"}


id: FYPO:0003622
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 posttranscriptional addition of a methyl group to the 2'-oxygen atom of the adenine residue at position 41 in an U6 snRNA molecule is abolished.","definition_xrefs":["GO:1990438","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished U6 2'-O-snRNA methylation","termid":"FYPO:0003621"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abolished U6 2'-O-snRNA methylation at residue A41","synonyms":[{"name":"U6 2'-O-snRNA methylation abolished at residue A41 during vegetative growth","type":"exact"},{"name":"U6 2'-O-snRNA methylation at residue A41 abolished","type":"exact"},{"name":"abolished U6 2'-O-snRNA methylation at residue A41 during mitotic cell cycle","type":"related"},{"name":"abolished U6 A41 2'-O-snRNA methylation","type":"exact"}],"termid":"FYPO:0003622"}


id: PBO:0070311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, Ro60-associated Y3","termid":"PBO:0070311"}


id: MONDO:0001076
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The inability to regulate blood glucose levels resulting in hyperglycemia.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucose metabolism disease","termid":"MONDO:0002908"},{"relation_name":"is_a","term_name":"glucose-galactose malabsorption","termid":"MONDO:0011731"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066","MONDO:0004335"],"is_obsolete":false,"name":"glucose intolerance","secondary_identifiers":["NCIT:C34646","MESH:D018149","DOID:10603","SCTID:267426009","UMLS:C0271650","ICD9:271.3","icd11.foundation:1392580302","MEDGEN:75760"],"synonyms":[{"name":"glucose: [intolerance] or [malabsorption]","type":"exact"},{"name":"glucose: intolerance","type":"exact"},{"name":"glucose: malabsorption","type":"exact"},{"name":"malabsorption of glucose","type":"exact"}],"termid":"MONDO:0001076","xrefs":{"Monarch":{"xref_id":"0001076"}}}


id: PBO:0074518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small NF90 (ILF3) associated RNA A10","termid":"PBO:0074518"}


id: MONDO:0001727
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Meniere disease","termid":"MONDO:0007972"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"active cochleovestibular Meniere disease","secondary_identifiers":["ICD9:386.01","MEDGEN:509989","SCTID:194348002","DOID:13490","UMLS:C0155496"],"synonyms":[{"name":"active Meniere's disease, cochleovestibular","type":"exact"},{"name":"active cochleovestibular Meniere disease","type":"exact"},{"name":"active cochleovestibular Meniere's disease","type":"exact"},{"name":"cochleovestibular active Mnire's disease","type":"exact"}],"termid":"MONDO:0001727","xrefs":{"Monarch":{"xref_id":"0001727"}}}


id: MONDO:0020920
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection with the organism Escherichia Coli.","definition_xrefs":["NCIT:C34594"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial infectious disease","termid":"MONDO:0005113"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"escherichia coli infection","secondary_identifiers":["MESH:D004927","HP:0002740","SCTID:71057007","MEDGEN:4543","EFO:1001318","GTR:AN0485755","GTR:AN0485754","UMLS:C0014836","GTR:AN0474198"],"synonyms":[{"name":"Bacterial infection caused by E. coli","type":"related"},{"name":"Bacterial infection due to E. coli","type":"related"},{"name":"Colibacillosis","type":"related"},{"name":"E COLI INFECT","type":"related"},{"name":"E Coli Infection","type":"related"},{"name":"E coli Infection","type":"related"},{"name":"E coli Infections","type":"related"},{"name":"E coli infections","type":"related"},{"name":"E coli infections, recurrent","type":"related"},{"name":"E. coli Infection","type":"related"},{"name":"E. coli Infections","type":"related"},{"name":"E. coli infection","type":"related"},{"name":"ESCHERICHIA COLI INFECT","type":"related"},{"name":"Escherichia Coli Infection","type":"related"},{"name":"Escherichia coli Infection","type":"related"},{"name":"Escherichia coli Infections","type":"related"},{"name":"Escherichia coli infection","type":"related"},{"name":"INFECT E COLI","type":"related"},{"name":"INFECT ESCHERICHIA COLI","type":"related"},{"name":"Infection caused by Escherichia coli","type":"related"},{"name":"Infection due to Escherichia coli","type":"related"},{"name":"Infection, E coli","type":"related"},{"name":"Infection, E. coli","type":"related"},{"name":"Infection, Escherichia coli","type":"related"},{"name":"Infections, E coli","type":"related"},{"name":"Infections, Escherichia coli","type":"related"},{"name":"Recurrent E. coli infections","type":"related"},{"name":"e coli infection","type":"exact"},{"name":"escherichia coli infection","type":"exact"}],"termid":"MONDO:0020920","xrefs":{"Monarch":{"xref_id":"0020920"}}}


id: GO:0075329
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of symbiont arbuscule formation for nutrient acquisition from host. 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":"regulation of anatomical structure morphogenesis","termid":"GO:0022603"},{"relation_name":"is_a","term_name":"modulation of formation of structure involved in a symbiotic process","termid":"GO:0044145"},{"relation_name":"is_a","term_name":"regulation of feeding behavior","termid":"GO:0060259"},{"relation_name":"regulates","term_name":"formation of arbuscule for nutrient acquisition","termid":"GO:0075328"}],"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 arbuscule formation for nutrient acquisition from host","termid":"GO:0075329"}


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


id: PBO:0078207
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 6-9","termid":"PBO:0078207"}


id: MONDO:0003492
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma that involves the lacrimal gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lacrimal gland carcinoma","termid":"MONDO:0002463"},{"relation_name":"is_a","term_name":"head and neck squamous cell carcinoma","termid":"MONDO:0010150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005328"],"is_obsolete":false,"name":"lacrimal gland squamous cell carcinoma","secondary_identifiers":["NCIT:C6092","MEDGEN:233607","DOID:5529","UMLS:C1334360"],"synonyms":[{"name":"epidermoid carcinoma of lacrimal gland","type":"exact"},{"name":"epidermoid carcinoma of the lacrimal gland","type":"exact"},{"name":"lacrimal gland epidermoid carcinoma","type":"exact"},{"name":"lacrimal gland squamous cell carcinoma","type":"exact"},{"name":"squamous cell carcinoma of lacrimal gland","type":"exact"},{"name":"squamous cell carcinoma of the lacrimal gland","type":"exact"}],"termid":"MONDO:0003492","xrefs":{"Monarch":{"xref_id":"0003492"}}}


id: SO:0001726
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 27th residue (a lysine), from the start of the H3 histone protein is di-methylated.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"H3K27_methylation_site","termid":"SO:0001732"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"H3K27_dimethylation_site","synonyms":[{"name":"H3K27 di-methylation site","type":"exact"},{"name":"H3K27Me2","type":"related"}],"termid":"SO:0001726"}


id: GO:0018977
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane (DDT), a chlorinated broad spectrum contact insecticide.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"insecticide metabolic process","termid":"GO:0017143"},{"relation_name":"is_a","term_name":"chlorinated hydrocarbon metabolic process","termid":"GO:0042196"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane metabolic process","secondary_identifiers":["UM-BBD_pathwayID:ddt"],"synonyms":[{"name":"1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane metabolism","type":"exact"},{"name":"DDT metabolic process","type":"exact"},{"name":"DDT metabolism","type":"exact"}],"termid":"GO:0018977"}


id: PBO:0064358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pro-melanin concentrating hormone like 1 (pseudogene)","termid":"PBO:0064358"}


id: GO:0050210
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dimethylallyl diphosphate + H2O = diphosphate + prenol.","definition_xrefs":["RHEA:21496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diphosphoric monoester hydrolase activity","termid":"GO:0016794"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0016788","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"prenyl-diphosphatase activity","secondary_identifiers":["MetaCyc:PRENYL-PYROPHOSPHATASE-RXN","EC:3.1.7.1"],"synonyms":[{"name":"prenol pyrophosphatase activity","type":"related"},{"name":"prenyl-diphosphate diphosphohydrolase activity","type":"related"},{"name":"prenyl-pyrophosphatase activity","type":"exact"},{"name":"prenylphosphatase activity","type":"related"}],"termid":"GO:0050210"}


id: PBO:0042916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CF transmembrane conductance regulator","termid":"PBO:0042916"}


id: MONDO:0005814
data:
  {"annotated_genes":["SJAG_04206","SJAG_03453","SJAG_04699","SJAG_02426","SJAG_02226","SJAG_02748","SJAG_04394","SJAG_01837","SJAG_01620","SJAG_01082","SJAG_00980","SJAG_02187","SJAG_02231"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86237,86239,86240,87085,86233,86235,86236,86238,86234],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0005575"},{"annotations":[86125],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007356"},{"annotations":[84946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012249"},{"annotations":[85396],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013699"},{"annotations":[85398],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013710"},{"annotations":[85408,85409],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008018"}]},"cv_name":"mondo","definition":"A malignant neoplasm involving the intestine","direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system cancer","termid":"MONDO:0002516"},{"relation_name":"is_a","term_name":"intestinal neoplasm","termid":"MONDO:0021118"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00980":null,"SJAG_01082":null,"SJAG_01620":null,"SJAG_01837":null,"SJAG_02187":null,"SJAG_02226":null,"SJAG_02231":null,"SJAG_02426":null,"SJAG_02748":null,"SJAG_03453":null,"SJAG_04206":null,"SJAG_04394":null,"SJAG_04699":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"intestinal cancer","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C4572","SCTID:363508008","EFO:0007330","ICD9:159.0","UMLS:C0346627","MEDGEN:87562","MESH:D007414","DOID:10155"],"synonyms":[{"name":"bowel cancer","type":"exact"},{"name":"cancer of intestine","type":"exact"},{"name":"cancer of the intestine","type":"exact"},{"name":"intestinal cancer","type":"exact"},{"name":"intestinal neoplasms, malignant","type":"exact"},{"name":"intestinal tumors, malignant","type":"exact"},{"name":"intestine cancer","type":"exact"},{"name":"malignant intestinal neoplasm","type":"exact"},{"name":"malignant intestinal neoplasms","type":"exact"},{"name":"malignant intestinal tumor","type":"exact"},{"name":"malignant intestinal tumors","type":"exact"},{"name":"malignant intestinal tumour","type":"exact"},{"name":"malignant intestinal tumours","type":"exact"},{"name":"malignant intestine neoplasm","type":"exact"},{"name":"malignant intestine tumor","type":"exact"},{"name":"malignant intestine tumour","type":"exact"},{"name":"malignant neoplasm of intestine","type":"exact"},{"name":"malignant neoplasm of the intestine","type":"exact"},{"name":"malignant tumor of intestine","type":"exact"},{"name":"malignant tumor of the intestine","type":"exact"},{"name":"malignant tumour of intestine","type":"exact"},{"name":"malignant tumour of the intestine","type":"exact"}],"termid":"MONDO:0005814","terms_by_termid":{"MONDO:0005575":null,"MONDO:0007356":null,"MONDO:0008018":null,"MONDO:0012249":null,"MONDO:0013699":null,"MONDO:0013710":null},"xrefs":{"Monarch":{"xref_id":"0005814"}}}


id: GO:0015090
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: Fe2+(out) = Fe2+(in). In low-affinity transport the transporter is able to bind the solute only if it is present at very high concentrations.","definition_xrefs":["TC:9.A.9.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ferric iron transmembrane transporter activity","termid":"GO:0015091"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"low-affinity ferric iron ion transmembrane transporter activity","synonyms":[{"name":"low affinity iron ion transmembrane transporter activity","type":"exact"},{"name":"low affinity iron transporter activity","type":"exact"}],"termid":"GO:0015090"}


id: MONDO:0006005
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition caused by infection by the Venezuelan equine encephalitis virus, which is characterized by headache, fever, myalgia, nausea, and vomiting.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"encephalomyelitis","termid":"MONDO:0005156"},{"relation_name":"is_a","term_name":"Alphavirus infectious disease","termid":"MONDO:0005643"},{"relation_name":"is_a","term_name":"viral hemorrhagic fever","termid":"MONDO:0018087"},{"relation_name":"is_a","term_name":"viral infection of central nervous system","termid":"MONDO:0024318"},{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Venezuelan equine encephalitis","secondary_identifiers":["EFO:0007534","ICD10CM:A92.2","DOID:9584","ICD9:066.2","NCIT:C35121","GARD:6355","MESH:D004685","SCTID:417067005","icd11.foundation:608978790","UMLS:C0014078","MEDGEN:4036"],"synonyms":[{"name":"Venezuelan equine encephalitis virus caused disease or disorder","type":"exact"},{"name":"Venezuelan equine encephalitis virus disease or disorder","type":"exact"},{"name":"Venezuelan equine encephalitis virus infectious disease","type":"exact"},{"name":"Venezuelan equine fever","type":"related"}],"termid":"MONDO:0006005","xrefs":{"Monarch":{"xref_id":"0006005"}}}


id: PBO:0063657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoglycerate mutase 2","termid":"PBO:0063657"}


id: GO:0180002
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The elimination of zinc ions from peritubular capillaries (or surrounding hemolymph in invertebrates) into the renal tubules to be incorporated subsequently into the urine.","definition_xrefs":["PMID:28196538"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal tubular secretion","termid":"GO:0097254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"renal zinc excretion","synonyms":[{"name":"renal zinc ion excretion","type":"exact"},{"name":"renal zinc secretion","type":"exact"}],"termid":"GO:0180002"}


id: PBO:0042165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-C motif chemokine ligand 26","termid":"PBO:0042165"}


id: PBO:0063154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pro-apoptotic WT1 regulator pseudogene 2","termid":"PBO:0063154"}


id: MONDO:0044629
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"arthrogryposis syndrome","termid":"MONDO:0015225"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital amyoplasia","secondary_identifiers":["Orphanet:488586","GARD:22002","MEDGEN:678346","UMLS:C0812412"],"synonyms":[{"name":"amyoplasia congenita","type":"exact"}],"termid":"MONDO:0044629","xrefs":{"Monarch":{"xref_id":"0044629"}}}


id: GO:0018045
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The formation of a C-terminal peptidyl-lysine amide by hydrolysis and oxidation of an interior Lys-Gly peptide in a secreted protein.","definition_xrefs":["RESID:AA0092"],"gene_count":0,"genotype_count":0,"name":"obsolete C-terminal peptidyl-lysine amidation (obsolete GO:0018045)","termid":"GO:0018045"}


id: PBO:0087764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of TORC2 membrane-associated complex; involved in regulation of cell cycle-dependent actin cytoskeletal dynamics during polarized growth and cell wall integrity; BIT61 has a paralog, BIT2, that arose from the whole genome duplication","termid":"PBO:0087764"}


id: GO:0002845
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of tolerance induction to tumor cell.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of peripheral tolerance induction","termid":"GO:0002660"},{"relation_name":"is_a","term_name":"positive regulation of immune response to tumor cell","termid":"GO:0002839"},{"relation_name":"is_a","term_name":"regulation of tolerance induction to tumor cell","termid":"GO:0002843"},{"relation_name":"positively_regulates","term_name":"tolerance induction to tumor cell","termid":"GO:0002413"}],"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 tolerance induction to tumor cell","synonyms":[{"name":"activation of tolerance induction to tumor cell","type":"narrow"},{"name":"positive regulation of tolerance induction to tumour cell","type":"exact"},{"name":"stimulation of tolerance induction to tumor cell","type":"narrow"},{"name":"up regulation of tolerance induction to tumor cell","type":"exact"},{"name":"up-regulation of tolerance induction to tumor cell","type":"exact"},{"name":"upregulation of tolerance induction to tumor cell","type":"exact"}],"termid":"GO:0002845"}


id: PBO:0052760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 18 pseudogene 52","termid":"PBO:0052760"}


id: MONDO:0859516
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum","secondary_identifiers":["OMIM:620250","UMLS:C5830296","MEDGEN:1840932"],"termid":"MONDO:0859516","xrefs":{"Monarch":{"xref_id":"0859516"}}}


id: GO:0050843
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of S-adenosylmethionine, S-(5'-adenosyl)-L-methionine, an important intermediate in one-carbon metabolism.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound catabolic process","termid":"GO:0044273"},{"relation_name":"is_a","term_name":"S-adenosylmethionine metabolic process","termid":"GO:0046500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006790","GO:0008150","GO:0044248"],"is_obsolete":false,"name":"S-adenosylmethionine catabolic process","synonyms":[{"name":"S-adenosyl methionine catabolic process","type":"exact"},{"name":"S-adenosyl methionine catabolism","type":"exact"},{"name":"S-adenosylmethionine breakdown","type":"exact"},{"name":"S-adenosylmethionine catabolism","type":"exact"},{"name":"S-adenosylmethionine degradation","type":"exact"},{"name":"SAM catabolic process","type":"exact"}],"termid":"GO:0050843"}


id: FYPO:0000673
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 septum assembly is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"},{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"},{"relation_name":"is_a","term_name":"normal cell cycle process","termid":"FYPO:0006915"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001320","FYPO:0001312"],"is_obsolete":false,"name":"normal septum assembly","synonyms":[{"name":"normal division septum assembly","type":"exact"},{"name":"normal septation","type":"broad"},{"name":"normal septum assembly during mitotic cell cycle","type":"related"},{"name":"normal septum assembly during vegetative growth","type":"exact"}],"termid":"FYPO:0000673"}


id: PBO:0062940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prolyl 4-hydroxylase subunit beta","termid":"PBO:0062940"}


id: PBO:0056168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucosal vascular addressin cell adhesion molecule 1","termid":"PBO:0056168"}


id: PBO:0002298
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease kappa ortholog (predicted)","termid":"PBO:0002298"}


id: MONDO:0004050
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An osteosarcoma usually arising from the metaphysis of long bones. It is characterized by the presence of a cystic architecture with blood-filled spaces. The prognosis is similar to that of conventional osteosarcoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"conventional osteosarcoma","termid":"MONDO:0002631"},{"relation_name":"is_a","term_name":"bone osteosarcoma","termid":"MONDO:0002629"}],"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":"telangiectatic osteogenic sarcoma","secondary_identifiers":["MEDGEN:78059","ICDO:9183/3","NCIT:C3902","ONCOTREE:TEOS","DOID:6951","UMLS:C0259782"],"synonyms":[{"name":"TEOS","type":"related"},{"name":"malignant bone aneurysm","type":"exact"},{"name":"telangiectatic osteosarcoma","type":"exact"},{"name":"telangiectatic osteosarcoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0004050","xrefs":{"Monarch":{"xref_id":"0004050"}}}


id: PBO:0029253
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_negative_regulation_of_DNA_replication_during_cellular_response_to_methyl_methanesulfonate","termid":"PBO:0029253"}


id: PR:O13911
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A bifunctional polynucleotide phosphatase/kinase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00882","PANTHER:PTHR12083:SF5","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":"bifunctional polynucleotide phosphatase/kinase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23C11.04c","secondary_identifiers":["UniProtKB:O13911"],"synonyms":[{"name":"DNA 5'-kinase/3'-phosphatase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PNKP","type":"exact"},{"name":"polynucleotide kinase-3'-phosphatase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13911"}


id: MONDO:0007721
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Herniation of the upper part of the stomach through the diaphragm.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"stomach disorder","termid":"MONDO:0004298"}],"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":"hiatus hernia","secondary_identifiers":["MEDGEN:483347","UMLS:C3489393","SCTID:84089009","NCIT:C98945","MESH:D006551","DOID:12642","HP:0002036","OMIM:142400"],"synonyms":[{"name":"diaphragmatic - hiatus -hernia","type":"exact"},{"name":"hernia, hiatus","type":"related"},{"name":"hiatal hernia","type":"exact"},{"name":"hiatus hernia","type":"exact"},{"name":"hiatus hernia (disease)","type":"exact"}],"termid":"MONDO:0007721","xrefs":{"Monarch":{"xref_id":"0007721"}}}


id: MONDO:0054764
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurodegeneration with brain iron accumulation","termid":"MONDO:0018307"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005066","MONDO:0002039"],"is_obsolete":false,"name":"neurodegeneration with brain iron accumulation 8","secondary_identifiers":["MEDGEN:1645224","OMIM:617917","UMLS:C4693587"],"synonyms":[{"name":"NBIA8","type":"related"},{"name":"neurodegeneration with brain iron accumulation 8","type":"exact"}],"termid":"MONDO:0054764","xrefs":{"Monarch":{"xref_id":"0054764"}}}


id: PBO:0082153
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Adapter that links synaptojanins to the cortical actin cytoskeleton; the synaptojanins are Inp52p and Inp53p","termid":"PBO:0082153"}


id: PBO:0002420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial conserved protein","termid":"PBO:0002420"}


id: PBO:0066712
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 9","termid":"PBO:0066712"}


id: GO:0035990
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a tendon cell. Tendon cell are elongated fibrocytes in which the cytoplasm is stretched between the collagen fibres of the tendon. Tendon cells have a central cell nucleus with a prominent nucleolus, a well-developed rough endoplasmic reticulum, and are responsible for synthesis and turnover of tendon fibres and ground substance.","definition_xrefs":["GOC:yaf","CL:0000388","PMID:21412429"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"tendon formation","termid":"GO:0035992"}],"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":"tendon cell differentiation","synonyms":[{"name":"muscle attachment cell differentiation","type":"exact"},{"name":"tenocyte differentiation","type":"related"}],"termid":"GO:0035990"}


id: PBO:0084553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of the seripauperin multigene family; encoded mainly in subtelomeric regions; SWAT-GFP and mCherry fusion proteins localize to the vacuole; active during alcoholic fermentation; regulated by anaerobiosis, negatively regulated by oxygen; repressed by heme; identical to Pau14p","termid":"PBO:0084553"}


id: PBO:0064207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasminogen activator, tissue type","termid":"PBO:0064207"}


id: GO:0007034
data:
  {"annotated_genes":["SJAG_03783","SJAG_01445","SJAG_01809","SJAG_01913","SJAG_00380","SJAG_00416","SJAG_02587","SJAG_01598","SJAG_03848","SJAG_01876","SJAG_07012","SJAG_05245","SJAG_00821","SJAG_04489","SJAG_01981","SJAG_03726","SJAG_00299","SJAG_00301","SJAG_01586","SJAG_03892","SJAG_03511","SJAG_05210","SJAG_02117","SJAG_03756","SJAG_02240","SJAG_01281","SJAG_04931","SJAG_04552","SJAG_01324","SJAG_01488","SJAG_03072","SJAG_04643","SJAG_01360","SJAG_04822","SJAG_04902","SJAG_03970","SJAG_03403","SJAG_02584","SJAG_16459","SJAG_01242","SJAG_00204","SJAG_03347","SJAG_03137","SJAG_03250","SJAG_04349","SJAG_02453","SJAG_02912","SJAG_00108","SJAG_01080","SJAG_02315","SJAG_01367","SJAG_03005","SJAG_04912","SJAG_03442","SJAG_01088","SJAG_01527","SJAG_02811","SJAG_04936","SJAG_03385","SJAG_00181","SJAG_04023","SJAG_00916","SJAG_00900","SJAG_01645","SJAG_03962","SJAG_00208","SJAG_02349","SJAG_03976","SJAG_02049","SJAG_04070","SJAG_03963","SJAG_05303","SJAG_04024","SJAG_05207","SJAG_04966","SJAG_01229","SJAG_04047","SJAG_00777","SJAG_02234"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70526,71660,77229,88852,95594,114321],"is_not":false,"summary":null,"term":"GO:0007034"},{"annotations":[87834,87869,113113,90823,91393,91258,87756,105557,114254],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120113"},{"annotations":[75890,99701,77363,69487,77804,75726,95894,96918,99300,79226,93947,73025,77405,96648,111297,117363,101237,90330,77524,108600,110063],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006896"},{"annotations":[89929,109608,108793,116707,105514,110686,100099,73743,75338,100907,107427,101771,118242,76965,76381,100041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045324"},{"annotations":[106928,103911,70450,98651,75704,98472,110007,79056,102933,74950],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032511"},{"annotations":[90759],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044395"},{"annotations":[76967,96316,70886,76923,77361,72485,77803,73744,75339,80027],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006623"},{"annotations":[71780,78185,97737,70609,87872,70626,114515,106360,95726,87703,71774,77402,100678,109177,91396,77969,91261,73048,73022],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043328"}]},"cv_name":"biological_process","definition":"The directed movement of substances into, out of or within a vacuole.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular transport","termid":"GO:0046907"}],"gene_count":79,"genes_by_uniquename":{"SJAG_00108":null,"SJAG_00181":null,"SJAG_00204":null,"SJAG_00208":null,"SJAG_00299":null,"SJAG_00301":null,"SJAG_00380":null,"SJAG_00416":null,"SJAG_00777":null,"SJAG_00821":null,"SJAG_00900":null,"SJAG_00916":null,"SJAG_01080":null,"SJAG_01088":null,"SJAG_01229":null,"SJAG_01242":null,"SJAG_01281":null,"SJAG_01324":null,"SJAG_01360":null,"SJAG_01367":null,"SJAG_01445":null,"SJAG_01488":null,"SJAG_01527":null,"SJAG_01586":null,"SJAG_01598":null,"SJAG_01645":null,"SJAG_01809":null,"SJAG_01876":null,"SJAG_01913":null,"SJAG_01981":null,"SJAG_02049":null,"SJAG_02117":null,"SJAG_02234":null,"SJAG_02240":null,"SJAG_02315":null,"SJAG_02349":null,"SJAG_02453":null,"SJAG_02584":null,"SJAG_02587":null,"SJAG_02811":null,"SJAG_02912":null,"SJAG_03005":null,"SJAG_03072":null,"SJAG_03137":null,"SJAG_03250":null,"SJAG_03347":null,"SJAG_03385":null,"SJAG_03403":null,"SJAG_03442":null,"SJAG_03511":null,"SJAG_03726":null,"SJAG_03756":null,"SJAG_03783":null,"SJAG_03848":null,"SJAG_03892":null,"SJAG_03962":null,"SJAG_03963":null,"SJAG_03970":null,"SJAG_03976":null,"SJAG_04023":null,"SJAG_04024":null,"SJAG_04047":null,"SJAG_04070":null,"SJAG_04349":null,"SJAG_04489":null,"SJAG_04552":null,"SJAG_04643":null,"SJAG_04822":null,"SJAG_04902":null,"SJAG_04912":null,"SJAG_04931":null,"SJAG_04936":null,"SJAG_04966":null,"SJAG_05207":null,"SJAG_05210":null,"SJAG_05245":null,"SJAG_05303":null,"SJAG_07012":null,"SJAG_16459":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"vacuolar transport","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0007034","terms_by_termid":{"GO:0006623":null,"GO:0006896":null,"GO:0007034":null,"GO:0032511":null,"GO:0043328":null,"GO:0044395":null,"GO:0045324":null,"GO:0120113":null}}


id: PBO:0057510
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 628","termid":"PBO:0057510"}


id: GO:0046647
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of gamma-delta T cell proliferation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of T cell proliferation","termid":"GO:0042130"},{"relation_name":"is_a","term_name":"negative regulation of gamma-delta T cell activation","termid":"GO:0046644"},{"relation_name":"is_a","term_name":"regulation of gamma-delta T cell proliferation","termid":"GO:0046646"},{"relation_name":"negatively_regulates","term_name":"gamma-delta T cell proliferation","termid":"GO:0046630"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"negatively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"negative regulation of gamma-delta T cell proliferation","synonyms":[{"name":"down regulation of gamma-delta T cell proliferation","type":"exact"},{"name":"down-regulation of gamma-delta T cell proliferation","type":"exact"},{"name":"downregulation of gamma-delta T cell proliferation","type":"exact"},{"name":"inhibition of gamma-delta T cell proliferation","type":"narrow"},{"name":"negative regulation of gamma-delta T lymphocyte proliferation","type":"exact"},{"name":"negative regulation of gamma-delta T-cell proliferation","type":"exact"},{"name":"negative regulation of gamma-delta T-lymphocyte proliferation","type":"exact"}],"termid":"GO:0046647"}


id: GO:0034043
data:
  {"annotated_genes":["SJAG_03724"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[95909],"is_not":false,"summary":null,"term":"GO:0034043"}]},"cv_name":"molecular_function","definition":"Catalysis of the removal of 5-hydroxymethyluracil bases by cleaving the N-C1' glycosidic bond between the oxidized pyrimidine and the deoxyribose sugar.","definition_xrefs":["PMID:17641464","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidized pyrimidine nucleobase lesion DNA N-glycosylase activity","termid":"GO:0000703"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03724":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140097","GO:0003824","GO:0003674","GO:0016787","GO:0016798"],"is_obsolete":false,"name":"5-hydroxymethyluracil DNA N-glycosylase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"5-hmU DNA N-glycosylase activity","type":"exact"}],"termid":"GO:0034043","terms_by_termid":{"GO:0034043":null}}


id: PBO:0054015
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 1345","termid":"PBO:0054015"}


id: GO:0008192
data:
  {"annotated_genes":["SJAG_01724","SJAG_04233"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75287],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004484"},{"annotations":[73083],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008193"}]},"cv_name":"molecular_function","definition":"Catalysis of the posttranscriptional addition of a guanyl residue to the 5' end of an RNA molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"guanylyltransferase activity","termid":"GO:0070568"},{"relation_name":"is_a","term_name":"catalytic activity, acting on RNA","termid":"GO:0140098"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01724":null,"SJAG_04233":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0140098","GO:0016779"],"is_obsolete":false,"name":"RNA guanylyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0008192","terms_by_termid":{"GO:0004484":null,"GO:0008193":null}}


id: FYPO:0003617
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to cytochalasin D. Cells stop growing (and may die) at a concentration of cytochalasin D that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0002683","FYPO:0001985","FYPO:0000139","FYPO:0000003","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to cytochalasin D","synonyms":[{"name":"hypersensitive to cytochalasin D","type":"exact"},{"name":"sensitive to cytochalasin D during mitotic cell cycle","type":"related"},{"name":"sensitive to cytochalasin D during vegetative growth","type":"exact"}],"termid":"FYPO:0003617"}


id: PBO:0075879
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ST3GAL5 antisense RNA 1 (head to head)","termid":"PBO:0075879"}


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


id: GO:0047855
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dihydrobunolol + NADP+ = bunolol + H+ + NADPH.","definition_xrefs":["EC:1.1.1.160","RHEA:15925"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"dihydrobunolol dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R04623","MetaCyc:DIHYDROBUNOLOL-DEHYDROGENASE-RXN"],"synonyms":[{"name":"(+-)-5-[(tert-butylamino)-2'-hydroxypropoxy]-1,2,3,4-tetrahydro-1-naphthol:NADP+ oxidoreductase activity","type":"related"},{"name":"bunolol reductase activity","type":"related"}],"termid":"GO:0047855"}


id: PBO:0044017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"casein kinase 1 gamma 1","termid":"PBO:0044017"}


id: PR:O74788
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- iml1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74788"],"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":"vacuolar membrane-associated protein iml1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC26H8.04c","synonyms":[{"name":"Spom972h-iml1","type":"exact"}],"termid":"PR:O74788"}


id: GO:0042711
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Female behaviors associated with the care and rearing of offspring.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parental behavior","termid":"GO:0060746"}],"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":"maternal behavior","synonyms":[{"name":"maternal behaviour","type":"exact"}],"termid":"GO:0042711"}


id: PR:Q10483
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A UBX domain-containing protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C17C9.11c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17C9.11c","secondary_identifiers":["UniProtKB:Q10483"],"synonyms":[{"name":"Spom972h-UBXN1","type":"exact"}],"termid":"PR:Q10483"}


id: GO:1904880
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 hydrogen sulfide stimulus.","definition_xrefs":["GO_REF:0000071","GOC:TermGenie","PMID:24012591"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to hydrogen sulfide","synonyms":[{"name":"response to dihydridosulfur","type":"exact"},{"name":"response to sulfane","type":"exact"}],"termid":"GO:1904880"}


id: PBO:0063079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PAPPA antisense RNA 1","termid":"PBO:0063079"}


id: MONDO:1011401
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Type 1 diabetes mellitus that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder, non-human animal","termid":"MONDO:0700106"},{"relation_name":"is_a","term_name":"diabetes mellitus, non-human animal","termid":"MONDO:1010052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"type 1 diabetes mellitus, non-human animal","secondary_identifiers":["OMIA:000283"],"termid":"MONDO:1011401","xrefs":{"Monarch":{"xref_id":"1011401"}}}


id: PR:O74308
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gsf1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74308"],"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 transcriptional regulatory protein C15D4.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC15D4.02","synonyms":[{"name":"Spom972h-gsf1","type":"exact"}],"termid":"PR:O74308"}


id: PBO:0068698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 79, pseudogene","termid":"PBO:0068698"}


id: PBO:0038822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 28","termid":"PBO:0038822"}


id: FYPO:0001212
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 Glc1Man9GlcNAc2 measured in a cell is lower than normal. Glc1Man9GlcNAc2 is an N-glycan that is involved in post-translational modification of proteins, and consists of a branched ten-membered mannooligosaccharide containing one D-glucose residue, nine D-mannosyl residues and two N-acetylglucosamine residues.","definition_xrefs":["PMID:9813085","CHEBI:59080","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased polysaccharide level during vegetative growth","termid":"FYPO:0001080"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased Glc1Man9GlcNAc level","synonyms":[{"name":"decreased Glc1Man9GlcNAc accumulation","type":"related"},{"name":"decreased Glc1Man9GlcNAc level during mitotic cell cycle","type":"related"},{"name":"decreased Glc1Man9GlcNAc level during vegetative growth","type":"exact"},{"name":"decreased Glc1Man9GlcNAc2 level","type":"exact"},{"name":"decreased cellular Glc1Man9GlcNAc level","type":"exact"},{"name":"reduced Glc1Man9GlcNAc level","type":"exact"}],"termid":"FYPO:0001212"}


id: GO:0072148
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into an epithelial cell.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate commitment","termid":"GO:0045165"},{"relation_name":"part_of","term_name":"epithelial cell differentiation","termid":"GO:0030855"}],"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":"epithelial cell fate commitment","termid":"GO:0072148"}


id: GO:1904081
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any positive regulation of transcription from RNA polymerase II promoter that is involved in neuron differentiation.","definition_xrefs":["PMID:24353061","GO_REF:0000060","GOC:TermGenie","GOC:kmv"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter involved in neuron differentiation (obsolete GO:1904081)","synonyms":[{"name":"activation of global transcription from RNA polymerase II promoter involved in neuron differentiation","type":"related"},{"name":"activation of transcription from RNA polymerase II promoter involved in neuron differentiation","type":"exact"},{"name":"positive regulation of gene-specific transcription from RNA polymerase II promoter involved in neuron differentiation","type":"related"},{"name":"positive regulation of global transcription from Pol II promoter involved in neuron differentiation","type":"related"},{"name":"positive regulation of transcription from Pol II promoter involved in neuron differentiation","type":"exact"},{"name":"positive regulation of transcription from RNA polymerase II promoter, global involved in neuron differentiation","type":"related"},{"name":"stimulation of global transcription from RNA polymerase II promoter involved in neuron differentiation","type":"narrow"},{"name":"stimulation of transcription from RNA polymerase II promoter involved in neuron differentiation","type":"exact"},{"name":"up regulation of global transcription from RNA polymerase II promoter involved in neuron differentiation","type":"related"},{"name":"up regulation of transcription from RNA polymerase II promoter involved in neuron differentiation","type":"exact"},{"name":"up-regulation of global transcription from RNA polymerase II promoter involved in neuron differentiation","type":"related"},{"name":"up-regulation of transcription from RNA polymerase II promoter involved in neuron differentiation","type":"exact"},{"name":"upregulation of global transcription from RNA polymerase II promoter involved in neuron differentiation","type":"related"},{"name":"upregulation of transcription from RNA polymerase II promoter involved in neuron differentiation","type":"exact"}],"termid":"GO:1904081"}


id: GO:2000102
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of mammary stem cell proliferation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell population proliferation","termid":"GO:0008285"},{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of mammary stem cell proliferation","termid":"GO:2000101"},{"relation_name":"negatively_regulates","term_name":"mammary stem cell proliferation","termid":"GO:0002174"}],"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 mammary stem cell proliferation","termid":"GO:2000102"}


id: MONDO:0958122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral neuropathy","termid":"MONDO:0005244"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"idiopathic small fibers neuropathy","secondary_identifiers":["Orphanet:658549"],"termid":"MONDO:0958122","xrefs":{"Monarch":{"xref_id":"0958122"}}}


id: PR:Q9P7Q2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pfl9 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7Q2"],"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":"cell agglutination protein C186.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC186.01","synonyms":[{"name":"Spom972h-pfl9","type":"exact"}],"termid":"PR:Q9P7Q2"}


id: GO:1905332
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of morphogenesis of an epithelium.","definition_xrefs":["PMID:25745997","GO_REF:0000058","GOC:bhm","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"regulation of morphogenesis of an epithelium","termid":"GO:1905330"},{"relation_name":"positively_regulates","term_name":"morphogenesis of an epithelium","termid":"GO:0002009"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of morphogenesis of an epithelium","synonyms":[{"name":"activation of epithelium morphogenesis","type":"narrow"},{"name":"activation of morphogenesis of an epithelium","type":"narrow"},{"name":"positive regulation of epithelium morphogenesis","type":"exact"},{"name":"up regulation of epithelium morphogenesis","type":"exact"},{"name":"up regulation of morphogenesis of an epithelium","type":"exact"},{"name":"up-regulation of epithelium morphogenesis","type":"exact"},{"name":"up-regulation of morphogenesis of an epithelium","type":"exact"},{"name":"upregulation of epithelium morphogenesis","type":"exact"},{"name":"upregulation of morphogenesis of an epithelium","type":"exact"}],"termid":"GO:1905332"}


id: MONDO:0003059
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the bile duct","direct_ancestors":[{"relation_name":"is_a","term_name":"biliary tract cancer","termid":"MONDO:0003060"},{"relation_name":"is_a","term_name":"bile duct neoplasm","termid":"MONDO:0021662"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"bile duct cancer","secondary_identifiers":["NCIT:C7483","ICD9:156.1","DOID:4606","SCTID:363416002","NCIT:C2898"],"synonyms":[{"name":"Ca extrahepatic bile ducts","type":"exact"},{"name":"bile duct cancer","type":"exact"},{"name":"bile duct tumor","type":"broad"},{"name":"bile duct tumour","type":"broad"},{"name":"cancer of bile duct","type":"exact"},{"name":"malignant bile duct neoplasm","type":"exact"},{"name":"malignant neoplasm of bile duct","type":"exact"},{"name":"malignant neoplasm of the extrahepatic bile duct","type":"narrow"}],"termid":"MONDO:0003059","xrefs":{"Monarch":{"xref_id":"0003059"}}}


id: MONDO:1011338
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nutritional disorder that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nutritional disorder, non-human animal","termid":"MONDO:1011338","xrefs":{"Monarch":{"xref_id":"1011338"}}}


id: MONDO:0001472
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lymphoma that arises from the testis and is not associated with lymphoma in another anatomic site.","definition_xrefs":["NCIT:C6810"],"direct_ancestors":[{"relation_name":"is_a","term_name":"testicular sex cord-stromal neoplasm","termid":"MONDO:0003125"},{"relation_name":"is_a","term_name":"testicular cancer","termid":"MONDO:0005447"}],"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":"testicular lymphoma","secondary_identifiers":["ICD9:186.9","DOID:12253","MEDGEN:138110","ONCOTREE:TLYM","SCTID:277664004","UMLS:C0349644"],"synonyms":[{"name":"TLYM","type":"related"},{"name":"lymphoma of testis","type":"exact"},{"name":"lymphoma of the testis","type":"exact"},{"name":"malignant lymphoma of testis","type":"exact"},{"name":"primary testicular lymphoma","type":"exact"},{"name":"testicular lymphoma","type":"exact"}],"termid":"MONDO:0001472","xrefs":{"Monarch":{"xref_id":"0001472"}}}


id: PBO:0068498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 83, pseudogene","termid":"PBO:0068498"}


id: MONDO:0958117
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"combined immunodeficiency","termid":"MONDO:0015131"},{"relation_name":"is_a","term_name":"hyper-IgE syndrome","termid":"MONDO:0018037"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"autosomal dominant combined immunodeficiency due to partial IL6ST deficiency","secondary_identifiers":["Orphanet:656313"],"termid":"MONDO:0958117","xrefs":{"Monarch":{"xref_id":"0958117"}}}


id: PBO:0089227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane phospholipid-translocating ATPase complex, ATPase subunit","termid":"PBO:0089227"}


id: PATO:0000532
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000532 micronutrient sensitivity value (obsolete PATO:0000532)","termid":"PATO:0000532"}


id: PBO:0063467
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate dehydrogenase E1 subunit alpha 1","termid":"PBO:0063467"}


id: GO:0102713
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: gibberellin A25 + 2-oxoglutarate(2-) + O2 = gibberellin A46 + succinate(2-) + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete gibberellin A25 hydroxylase activity (obsolete GO:0102713)","termid":"GO:0102713"}


id: MONDO:0100002
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign inflammatory colitis caused by a non-IgE-mediated immune reaction to ingested food proteins.","definition_xrefs":["PMID:17584315"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastrointestinal allergy","termid":"MONDO:0000777"},{"relation_name":"is_a","term_name":"proctocolitis","termid":"MONDO:0024278"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"food protein-induced allergic proctocolitis","secondary_identifiers":["MEDGEN:1663071","UMLS:C4750318"],"synonyms":[{"name":"FPIPC","type":"exact"},{"name":"allergic proctocolitis","type":"broad"},{"name":"milk protein proctocololitis","type":"narrow"}],"termid":"MONDO:0100002","xrefs":{"Monarch":{"xref_id":"0100002"}}}


id: MONDO:0004612
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distinctive neoplastic disorders of histiocytes. Included are malignant neoplasms of macrophages and dendritic cells.","definition_xrefs":["MESH:D015620"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histiocytosis","termid":"MONDO:0002637"}],"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":"malignant histiocytosis","secondary_identifiers":["MEDGEN:5569","MESH:D054747","NCIT:C7202","ICDO:9750/3","DOID:8580","UMLS:C0019623","DOID:2570","SCTID:118612006","ICD10CM:C96.A","ICD9:202.3"],"synonyms":[{"name":"Stewart's granuloma","type":"exact"},{"name":"disorders, malignant histiocytic","type":"related"},{"name":"histiocytic disorder, malignant","type":"related"},{"name":"histiocytic medullary reticulosis","type":"exact"},{"name":"malignant histiocytic disease","type":"exact"},{"name":"malignant histiocytic disorders","type":"related"},{"name":"malignant midline reticulosis","type":"exact"},{"name":"malignant reticulosis","type":"exact"}],"termid":"MONDO:0004612","xrefs":{"Monarch":{"xref_id":"0004612"}}}


id: PBO:0030503
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_nocodazole","termid":"PBO:0030503"}


id: FYPO:0000039
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"Auxotrophy in which a cell is unable to synthesize lysine, and therefore requires lysine in the medium for vegetative cell growth.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auxotrophy","termid":"FYPO:0000128"},{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype","termid":"FYPO:0004638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"growth auxotrophic for lysine","synonyms":[{"name":"growth auxotrophic for lysine during mitotic cell cycle","type":"related"},{"name":"growth auxotrophic for lysine during vegetative growth","type":"exact"},{"name":"lysine auxotrophy","type":"exact"}],"termid":"FYPO:0000039"}


id: PBO:0064391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PMS1 homolog 2, mismatch repair system component pseudogene 13","termid":"PBO:0064391"}


id: MONDO:0002585
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Breast fibrocystic change characterized by the presence of epithelial cell hyperplasia. Epithelial atypia may be present or absent.","definition_xrefs":["NCIT:C6940"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast fibrocystic disease","termid":"MONDO:0005219"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast fibrocystic change, proliferative type","secondary_identifiers":["UMLS:C1332629","DOID:3274","MEDGEN:231967"],"synonyms":[{"name":"benign proliferative breast disease","type":"exact"},{"name":"breast fibrocystic change, proliferative type","type":"exact"},{"name":"fibrocystic change, proliferative type with atypia","type":"exact"},{"name":"fibrocystic disease, proliferative type with atypia","type":"exact"},{"name":"proliferating lesion of breast without atypia","type":"exact"},{"name":"proliferating lesion of the breast without atypia","type":"exact"},{"name":"proliferative breast disease","type":"exact"},{"name":"proliferative breast lesion","type":"exact"},{"name":"proliferative fibrocystic change","type":"broad"},{"name":"proliferative type fibrocystic change of breast","type":"exact"},{"name":"proliferative type fibrocystic change of the breast","type":"exact"}],"termid":"MONDO:0002585","xrefs":{"Monarch":{"xref_id":"0002585"}}}


id: PBO:0068946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 190, pseudogene","termid":"PBO:0068946"}


id: GO:0061250
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a mesonephric glomerular epithelial cell. Mesonephric glomerular epithelial cells are specialized epithelial cells that form part of the mesonephric glomerulus; there are two types, mesonephric glomerular parietal epithelial cells and mesonephric glomerular visceral epithelial cells.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation involved in mesonephros development","termid":"GO:0061208"},{"relation_name":"is_a","term_name":"glomerular epithelial cell differentiation","termid":"GO:0072311"},{"relation_name":"part_of","term_name":"mesonephric glomerular epithelium development","termid":"GO:0061232"}],"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":"mesonephric glomerular epithelial cell differentiation","termid":"GO:0061250"}


id: PBO:0042812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ceramide synthase 2","termid":"PBO:0042812"}


id: PBO:0030293
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-glossy_colony_morphology","termid":"PBO:0030293"}


id: GO:0046793
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus activates the frequency, rate or extent of phosphorylation of host RNA polymerase II.","definition_xrefs":["PMID:7637000"],"gene_count":0,"genotype_count":0,"name":"obsolete induction by virus of phosphorylation of host RNA polymerase II (obsolete GO:0046793)","synonyms":[{"name":"induction by virus of modification of host RNA polymerase II","type":"broad"},{"name":"virus-induced modification of host RNA polymerase II","type":"exact"}],"termid":"GO:0046793"}


id: PBO:0048507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growth differentiation factor 7","termid":"PBO:0048507"}


id: FYPO:0004868
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to ionizing radiation during G1 phase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensitive to ionizing radiation during vegetative growth","termid":"FYPO:0000267"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0005447","FYPO:0000139","FYPO:0001985"],"is_obsolete":false,"name":"sensitive to ionizing radiation during mitotic G1 phase","synonyms":[{"name":"decreased growth during cellular response to ionizing radiation during mitotic G1 phase","type":"exact"},{"name":"decreased vegetative cell population growth during cellular response to ionizing radiation during mitotic G1 phase","type":"exact"},{"name":"hypersensitive to ionizing radiation during mitotic G1 phase","type":"exact"},{"name":"sensitive to IR during mitotic G1 phase","type":"exact"},{"name":"sensitive to gamma irradiation during mitotic G1 phase","type":"narrow"},{"name":"sensitive to gamma radiation during mitotic G1 phase","type":"narrow"},{"name":"sensitive to ionizing radiation during G1 phase of mitotic cell cycle","type":"exact"},{"name":"sensitive to ionizing radiation during mitotic G1 phase during mitotic cell cycle","type":"related"},{"name":"sensitive to ionizing radiation during mitotic G1 phase during vegetative growth","type":"exact"}],"termid":"FYPO:0004868"}


id: PBO:0073882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 11 member 2","termid":"PBO:0073882"}


id: PBO:0113182
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lipid-binding ER protein, enriched at nucleus-vacuolar junctions (NVJ); involved in nonvesicular transfer of ceramides from ER to Golgi during ER stress; may be involved in sterol metabolism or signaling at the NVJ; contains a synaptotagmin-like-mitochondrial-lipid binding protein (SMP) domain; binds phosphatidylinositols and other lipids in a large-scale study; may interact with ribosomes, based on co-purification experiments","termid":"PBO:0113182"}


id: SO:0002062
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A contiguous cluster of translocations, usually the result of a single catastrophic event such as chromothripsis or chromoanasynthesis.","definition_xrefs":["NCBI:th"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex_structural_alteration","termid":"SO:0001784"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complex_chromosomal_rearrangement","synonyms":[{"name":"complex chromosomal rearrangement","type":"exact"}],"termid":"SO:0002062"}


id: CHEBI:17568
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":"uracil","termid":"CHEBI:17568"}


id: PBO:0058026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3976","termid":"PBO:0058026"}


id: GO:0097007
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (EE)-geranyllinalool + NADPH + O2 = 4,8,12-trimethyl-1,3,7,11-tridecatetraene + NADP+ + 2 H2O. It is unknown whether this reaction proceeds by the direct release of the 4-carbon compound but-1-en-3-one, or whether the substrate is first degraded to C18-farnesylacetone and then cleaved to produce 4,8,12-trimethyl-1,3,7,11-tridecatetraene (TMTT) and acetone.","definition_xrefs":["MetaCyc:RXN-8620","GOC:kad","PMID:21088219"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"4,8,12-trimethyltrideca-1,3,7,11-tetraene synthase activity","secondary_identifiers":["RHEA:13545"],"synonyms":[{"name":"4,8,12-trimethyl-1,3,7,11-tridecatetraene synthase activity","type":"exact"},{"name":"TMTT synthase activity","type":"exact"}],"termid":"GO:0097007"}


id: GO:2000193
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of fatty acid transport.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of lipid transport","termid":"GO:0032370"},{"relation_name":"is_a","term_name":"positive regulation of organic acid transport","termid":"GO:0032892"},{"relation_name":"is_a","term_name":"regulation of fatty acid transport","termid":"GO:2000191"},{"relation_name":"positively_regulates","term_name":"fatty acid transport","termid":"GO:0015908"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of fatty acid transport","termid":"GO:2000193"}


id: PBO:0061563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5'-nucleotidase ecto","termid":"PBO:0061563"}


id: PBO:0113029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Catalytic subunit of DNA polymerase zeta (pol zeta); involved in translesion synthesis during post-replication repair; required for mutagenesis induced by DNA damage; involved in double-strand break repair; may be involved in meiosis; forms a complex with Rev7p, Pol31p and Pol32p","termid":"PBO:0113029"}


id: PBO:0028414
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_glycerol_level","termid":"PBO:0028414"}


id: MONDO:0015255
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete blepharophimosis-radioulnar synostosis syndrome (obsolete MONDO:0015255)","secondary_identifiers":["Orphanet:1256","MESH:C536292"],"synonyms":[{"name":"Jorgenson Lenz syndrome","type":"related"},{"name":"Jorgenson-Lenz syndrome","type":"exact"},{"name":"blepharophimosis radioulnar synostosis","type":"related"},{"name":"mild short stature, microcephaly, ptosis-blepharophimosis, facial asymmetry, and radioulnar synostosis","type":"related"},{"name":"ptosis, prognathism, microcephaly, radio-ulnar synostosis, short stature/dwarfism","type":"related"}],"termid":"MONDO:0015255","xrefs":{"Monarch":{"xref_id":"0015255"}}}


id: PBO:0041162
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BTG anti-proliferation factor 1","termid":"PBO:0041162"}


id: PBO:0065111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRKCE antisense RNA 1","termid":"PBO:0065111"}


id: GO:1900732
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of polyketide biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ketone biosynthetic process","termid":"GO:0010566"},{"relation_name":"is_a","term_name":"regulation of secondary metabolite biosynthetic process","termid":"GO:1900376"},{"relation_name":"regulates","term_name":"polyketide biosynthetic process","termid":"GO:0030639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"regulation of polyketide biosynthetic process","synonyms":[{"name":"regulation of polyketide anabolism","type":"exact"},{"name":"regulation of polyketide biosynthesis","type":"exact"},{"name":"regulation of polyketide formation","type":"exact"},{"name":"regulation of polyketide synthesis","type":"exact"}],"termid":"GO:1900732"}


id: FYPO:0001454
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population growth phenotype in which vegetative cells grow normally (i.e. indistinguishably from wild type) during a cellular response to freezing conditions.","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:0000257"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002058"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0000003","FYPO:0002058","FYPO:0000257","FYPO:0002060","FYPO:0002057"],"is_obsolete":false,"name":"normal growth during cellular response to freezing","synonyms":[{"name":"normal cell population growth during cellular response to freezing","type":"exact"},{"name":"normal cellular response to freeze-thawing","type":"related"},{"name":"normal cellular response to freezing","type":"related"},{"name":"normal vegetative cell population growth during cellular response to freezing","type":"exact"}],"termid":"FYPO:0001454"}


id: PBO:0050682
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family A (Hsp70) member 8 pseudogene 9","termid":"PBO:0050682"}


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


id: MOD:01209
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-aspartic acid residue to the copper(1+) aspartate salt.","definition_xrefs":["Unimod:531#D"],"direct_ancestors":[{"relation_name":"is_a","term_name":"copper containing modified residue","termid":"MOD:00742"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-aspartic acid residue","termid":"MOD:02066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper(1+) L-aspartate","synonyms":[{"name":"Cation:Cu[I]","type":"related"},{"name":"Replacement of proton by copper","type":"related"},{"name":"cuprous salt","type":"exact"}],"termid":"MOD:01209"}


id: GO:0033080
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The expansion of an immature T cell population by cell division in the thymus.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immature T cell proliferation","termid":"GO:0033079"},{"relation_name":"part_of","term_name":"T cell differentiation in thymus","termid":"GO:0033077"}],"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":"immature T cell proliferation in thymus","synonyms":[{"name":"thymic T cell proliferation","type":"exact"},{"name":"thymocyte cell proliferation","type":"exact"},{"name":"thymocyte proliferation","type":"exact"}],"termid":"GO:0033080"}


id: PBO:0041411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement C7","termid":"PBO:0041411"}


id: PBO:0068304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 8","termid":"PBO:0068304"}


id: PBO:0035862
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K9_methylation_at_protein_coding_gene_during_vegetative_growth","termid":"PBO:0035862"}


id: PBO:0000269
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rad6 homolog, ubiquitin conjugating enzyme E2 Rhp6","termid":"PBO:0000269"}


id: PATO:0001367
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A surface feature shape quality inhering in a bearer by virtue of the bearer's having deeply undulating edges forming lobes.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"surface feature shape","termid":"PATO:0001925"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lobate","termid":"PATO:0001367"}


id: GO:0019216
data:
  {"annotated_genes":["SJAG_02380","SJAG_02044","SJAG_02196","SJAG_02104","SJAG_02613","SJAG_00053","SJAG_03130","SJAG_03940","SJAG_01906","SJAG_04018","SJAG_01307","SJAG_01402","SJAG_04092","SJAG_02641","SJAG_01187","SJAG_03170"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75917,117877],"is_not":false,"summary":null,"term":"GO:0019216"},{"annotations":[90163,104165],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902647"},{"annotations":[93640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010895"},{"annotations":[70409],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045717"},{"annotations":[115287,111170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001211"},{"annotations":[112545,109530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071072"},{"annotations":[117345],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902648"},{"annotations":[109652],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070452"},{"annotations":[94840],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045834"},{"annotations":[74830],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010510"},{"annotations":[75289],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045540"},{"annotations":[105641,88310],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032443"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving lipids.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of primary metabolic process","termid":"GO:0080090"},{"relation_name":"regulates","term_name":"lipid metabolic process","termid":"GO:0006629"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_01187":null,"SJAG_01307":null,"SJAG_01402":null,"SJAG_01906":null,"SJAG_02044":null,"SJAG_02104":null,"SJAG_02196":null,"SJAG_02380":null,"SJAG_02613":null,"SJAG_02641":null,"SJAG_03130":null,"SJAG_03170":null,"SJAG_03940":null,"SJAG_04018":null,"SJAG_04092":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"regulation of lipid metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-400206","Reactome:R-HSA-2426168"],"synonyms":[{"name":"regulation of lipid metabolism","type":"exact"}],"termid":"GO:0019216","terms_by_termid":{"GO:0010510":null,"GO:0010895":null,"GO:0019216":null,"GO:0032443":null,"GO:0045540":null,"GO:0045717":null,"GO:0045834":null,"GO:0070452":null,"GO:0071072":null,"GO:1902647":null,"GO:1902648":null,"GO:2001211":null}}


id: GO:0070202
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 protein to a specific location on a chromosome.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of establishment of protein localization","termid":"GO:0070201"},{"relation_name":"regulates","term_name":"establishment of protein localization to chromosome","termid":"GO:0070199"}],"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 establishment of protein localization to chromosome","synonyms":[{"name":"regulation of establishment of protein localisation to chromosome","type":"exact"}],"termid":"GO:0070202"}


id: PBO:0060474
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nanog homeobox","termid":"PBO:0060474"}


id: PBO:0000758
data:
  {"annotation_feature_type":"gene","cv_name":"genome_org","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tandem duplication","termid":"PBO:0000758"}


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:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant severe congenital neutropenia","secondary_identifiers":["DOID:0112130","NCIT:C166155","MEDGEN:1665322","UMLS:C4749612","Orphanet:486","GARD:9558"],"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: MONDO:0004574
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Deficiency of vitamin B6. It is usually caused by alcoholism, malabsorption, or as a side effect of medications. Signs and symptoms include stomatitis, glossitis, dermatitis, peripheral neuropathy, irritability, seizures, and anemia.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin B deficiency","termid":"MONDO:0042976"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyridoxine deficiency anemia","secondary_identifiers":["MEDGEN:543733","SCTID:86448001","NCIT:C85221","MESH:D026681","DOID:8455","UMLS:C0272013","ICD9:266.1","ICD9:281.8"],"synonyms":[{"name":"B6 deficiencies, vitamin","type":"related"},{"name":"B6 deficiency, vitamin","type":"related"},{"name":"B6 vitamin deficiencies","type":"related"},{"name":"B6 vitamin deficiency","type":"related"},{"name":"deficiencies, B6 vitamin","type":"related"},{"name":"deficiencies, vitamin B6","type":"related"},{"name":"deficiency, B6 vitamin","type":"related"},{"name":"deficiency, pyridoxine","type":"related"},{"name":"deficiency, vitamin B 6","type":"related"},{"name":"deficiency, vitamin B6","type":"related"},{"name":"pyridoxine Deficincy","type":"exact"},{"name":"pyridoxine deficiency","type":"related"},{"name":"vitamin B6 deficiencies","type":"related"},{"name":"vitamin B6 deficiency","type":"related"},{"name":"vitamin B6 deficiency syndrome","type":"exact"},{"name":"vitamin deficiencies, B6","type":"related"},{"name":"vitamin deficiency, B6","type":"related"}],"termid":"MONDO:0004574","xrefs":{"Monarch":{"xref_id":"0004574"}}}


id: PBO:0000899
data:
  {"annotation_feature_type":"gene","cv_name":"DNA_binding_specificity","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"binds STREP motif","termid":"PBO:0000899"}


id: PBO:0005148
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.6.1.17","termid":"PBO:0005148"}


id: PBO:0062397
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 19 pseudogene","termid":"PBO:0062397"}


id: GO:0009020
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: S-adenosyl-L-methionine + tRNA = S-adenosyl-L-homocysteine + tRNA containing 2'-O-methylguanosine.","definition_xrefs":["RHEA:20077","EC:2.1.1.34"],"gene_count":0,"genotype_count":0,"name":"obsolete tRNA (guanosine-2'-O-)-methyltransferase activity (obsolete GO:0009020)","termid":"GO:0009020"}


id: FYPO:0002809
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of 6,7-dimethyl-8-ribityllumazine synthase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal 6,7-dimethyl-8-ribityllumazine synthase activity","termid":"FYPO:0002808"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0001985","FYPO:0000654","FYPO:0000661","FYPO:0000652"],"is_obsolete":false,"name":"decreased 6,7-dimethyl-8-ribityllumazine synthase activity","synonyms":[{"name":"reduced 6,7-dimethyl-8-ribityllumazine synthase activity","type":"exact"}],"termid":"FYPO:0002809"}


id: PBO:0005094
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human hAGO2","termid":"PBO:0005094"}


id: PBO:0053161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"low density lipoprotein receptor class A domain containing 3","termid":"PBO:0053161"}


id: PBO:0087642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the GINS complex (Sld5p, Psf1p, Psf2p, Psf3p); complex is localized to DNA replication origins and implicated in assembly of the DNA replication machinery","termid":"PBO:0087642"}


id: PBO:0054291
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 1682","termid":"PBO:0054291"}


id: GO:0016915
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. A nonsteroidal regulator, composed of two covalently linked beta subunits, that is synthesized in the pituitary gland and gonads and stimulates the secretion of follicle-stimulating hormone.","definition_xrefs":["ISBN:0721662544","ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete activin (obsolete GO:0016915)","synonyms":[{"name":"activin","type":"exact"}],"termid":"GO:0016915"}


id: PBO:0001865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome small subunit biogenesis protein (predicted)","termid":"PBO:0001865"}


id: GO:0034029
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-oxoglutarate + ATP + bicarbonate = ADP + 2 H+ + oxalosuccinate + phosphate.","definition_xrefs":["EC:6.4.1.7","RHEA:20425"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-carbon bonds","termid":"GO:0016885"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016874"],"is_obsolete":false,"name":"2-oxoglutarate carboxylase activity","secondary_identifiers":["KEGG_REACTION:R08201","MetaCyc:RXN-8457"],"synonyms":[{"name":"CFI","type":"related"},{"name":"OGC","type":"related"},{"name":"carboxylating factor for ICDH","type":"related"},{"name":"oxalosuccinate synthetase activity","type":"related"}],"termid":"GO:0034029"}


id: GO:0072683
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The migration of a T cell from the blood vessels into the surrounding tissue.","definition_xrefs":["GOC:mah","GOC:BHF","CL:0000084"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular extravasation","termid":"GO:0045123"},{"relation_name":"is_a","term_name":"T cell migration","termid":"GO:0072678"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"T cell extravasation","synonyms":[{"name":"T lymphocyte extravasation","type":"exact"},{"name":"T-cell extravasation","type":"exact"},{"name":"T-lymphocyte extravasation","type":"exact"}],"termid":"GO:0072683"}


id: GO:0046604
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of centrosome separation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic centrosome separation","termid":"GO:0046602"},{"relation_name":"is_a","term_name":"positive regulation of cell cycle process","termid":"GO:0090068"},{"relation_name":"positively_regulates","term_name":"mitotic centrosome separation","termid":"GO:0007100"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"positively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"positive regulation of mitotic centrosome separation","synonyms":[{"name":"activation of mitotic centrosome separation","type":"narrow"},{"name":"stimulation of mitotic centrosome separation","type":"narrow"},{"name":"up regulation of mitotic centrosome separation","type":"exact"},{"name":"up-regulation of mitotic centrosome separation","type":"exact"},{"name":"upregulation of mitotic centrosome separation","type":"exact"}],"termid":"GO:0046604"}


id: PBO:0072962
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secretogranin III","termid":"PBO:0072962"}


id: PBO:0030680
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-elongated_spore","termid":"PBO:0030680"}


id: MONDO:0000503
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A localized non-invasive adenocarcinoma of the lung measuring 3 cm or less. It is characterized by a pure lepidic growth pattern and the lack of stromal, vascular, or pleural invasion.","definition_xrefs":["NCIT:C136486"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma in situ","termid":"MONDO:0003218"},{"relation_name":"is_a","term_name":"lung carcinoma in situ","termid":"MONDO:0004660"},{"relation_name":"is_a","term_name":"lung adenocarcinoma","termid":"MONDO:0005061"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"lung adenocarcinoma in situ","secondary_identifiers":["MEDGEN:1620128","DOID:0050870","NCIT:C8748","ONCOTREE:LAIS","UMLS:C4521520"],"synonyms":[{"name":"adenosquamous cell carcinoma in situ of lung","type":"related"},{"name":"adenosquamous cell carcinoma in situ of the lung","type":"related"},{"name":"bronchioalveolar carcinoma","type":"related"},{"name":"bronchioloalveolar carcinoma","type":"narrow"},{"name":"in situ pulmonary adenocarcinoma","type":"related"},{"name":"lung adenocarcinoma In situ","type":"exact"},{"name":"lung adenosquamous cell carcinoma in situ","type":"related"},{"name":"stage 0 adenosquamous cell carcinoma of lung","type":"related"},{"name":"stage 0 adenosquamous cell carcinoma of the lung","type":"related"},{"name":"stage 0 adenosquamous cell lung carcinoma","type":"related"},{"name":"stage 0 adenosquamous lung cancer","type":"related"},{"name":"stage 0 adenosquamous lung carcinoma aJCC v6","type":"related"},{"name":"stage 0 adenosquamous lung carcinoma aJCC v6 and v7","type":"related"},{"name":"stage 0 adenosquamous lung carcinoma aJCC v7","type":"related"}],"termid":"MONDO:0000503","xrefs":{"Monarch":{"xref_id":"0000503"}}}


id: PBO:0047845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"formyl peptide receptor 1","termid":"PBO:0047845"}


id: FYECO:0000358
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed in rich medium containing yeast extract, galactose, glucose, and other components. The concentrations of galactose and glucose are typically around 2-3% each.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping rich medium","termid":"FYECO:0000080"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YES + galactose","synonyms":[{"name":"rich medium with glucose and galactose","type":"related"}],"termid":"FYECO:0000358"}


id: GO:0006282
data:
  {"annotated_genes":["SJAG_00823","SJAG_02104","SJAG_03160","SJAG_00369","SJAG_01205","SJAG_03417","SJAG_03048","SJAG_00573","SJAG_03695","SJAG_04457"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001033"},{"annotations":[111557],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904332"},{"annotations":[111834,117086],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045739"},{"annotations":[109981,93642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000781"},{"annotations":[107206],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001034"},{"annotations":[90666,72369],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000779"},{"annotations":[109120],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010569"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of DNA repair.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA metabolic process","termid":"GO:0051052"},{"relation_name":"is_a","term_name":"regulation of cellular response to stress","termid":"GO:0080135"},{"relation_name":"regulates","term_name":"DNA repair","termid":"GO:0006281"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00369":null,"SJAG_00573":null,"SJAG_00823":null,"SJAG_01205":null,"SJAG_02104":null,"SJAG_03048":null,"SJAG_03160":null,"SJAG_03417":null,"SJAG_03695":null,"SJAG_04457":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006281"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006281","GO:0006259"],"is_obsolete":false,"name":"regulation of DNA repair","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0006282","terms_by_termid":{"GO:0010569":null,"GO:0045739":null,"GO:1904332":null,"GO:2000779":null,"GO:2000781":null,"GO:2001033":null,"GO:2001034":null}}


id: GO:1904534
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of telomeric loop disassembly.","definition_xrefs":["GO_REF:0000058","GOC:nc","GOC:TermGenie","GOC:BHF","PMID:22579284","GOC:BHF_telomere"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of telomere maintenance","termid":"GO:0032205"},{"relation_name":"is_a","term_name":"regulation of telomeric loop disassembly","termid":"GO:1904533"},{"relation_name":"negatively_regulates","term_name":"telomeric loop disassembly","termid":"GO:0090657"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0032200"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0032200"}],"interesting_parent_ids":["GO:0032200","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"negative regulation of telomeric loop disassembly","synonyms":[{"name":"down regulation of T loop disassembly","type":"exact"},{"name":"down regulation of telomeric loop disassembly","type":"exact"},{"name":"down-regulation of T loop disassembly","type":"exact"},{"name":"down-regulation of telomeric loop disassembly","type":"exact"},{"name":"downregulation of T loop disassembly","type":"exact"},{"name":"downregulation of telomeric loop disassembly","type":"exact"},{"name":"inhibition of T loop disassembly","type":"narrow"},{"name":"inhibition of telomeric loop disassembly","type":"narrow"},{"name":"negative regulation of T loop disassembly","type":"exact"}],"termid":"GO:1904534"}


id: GO:0060459
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The biological process whose specific outcome is the progression of a left lung from an initial condition to its mature state. This process begins with the formation of the left lung and ends with the mature structure. The left lung is the lung which is on the left side of the anterior posterior axis looking from a dorsal to ventral aspect.","definition_xrefs":["GOC:dph","GOC:mtg_lung"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung development","termid":"GO:0030324"}],"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":"left lung development","synonyms":[{"name":"left pulmonary development","type":"exact"}],"termid":"GO:0060459"}


id: GO:0002467
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which germinal centers form. A germinal center is a specialized microenvironment formed when activated B cells enter lymphoid follicles. Germinal centers are the foci for B cell proliferation and somatic hypermutation.","definition_xrefs":["GOC:jal","ISBN:081533642X","GO_REF:0000022"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains","termid":"GO:0002460"},{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"}],"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":"germinal center formation","termid":"GO:0002467"}


id: PR:O14087
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rim1 gene.","definition_xrefs":["UniProtKB:O14087","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":"single-stranded DNA-binding protein rim1, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2F3.04c","synonyms":[{"name":"Spom972h-rim1","type":"exact"},{"name":"mitochondrial ssDNA-binding protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14087"}


id: PBO:0091125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial methyltransferase Oms1","termid":"PBO:0091125"}


id: MONDO:0043895
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Harm or hurt to the ankle or ankle joint usually inflicted by an external source.","definition_xrefs":["MESH:D016512"],"direct_ancestors":[{"relation_name":"is_a","term_name":"injury","termid":"MONDO:0021178"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankle injury","secondary_identifiers":["SCTID:125603006"],"synonyms":[{"name":"Injuries, ankle","type":"related"},{"name":"Injuries, syndesmotic","type":"related"},{"name":"Sprains, ankle","type":"related"},{"name":"ankle Sprains","type":"related"},{"name":"ankle injury","type":"exact"},{"name":"ankle sprain","type":"related"},{"name":"injury of ankle","type":"exact"},{"name":"injury of tarsal region","type":"exact"},{"name":"injury, ankle","type":"related"},{"name":"injury, syndesmotic","type":"related"},{"name":"sprain, ankle","type":"related"},{"name":"syndesmotic Injuries","type":"related"},{"name":"syndesmotic injury","type":"related"},{"name":"tarsal region injury","type":"exact"}],"termid":"MONDO:0043895","xrefs":{"Monarch":{"xref_id":"0043895"}}}


id: PBO:0018152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA endoribonuclease involved in mRNP quality control Swt1 (predicted)","termid":"PBO:0018152"}


id: FYPO:0002565
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 histone methylation does not occur. All histone methylation may be affected, or methylation of specific sites on specific histones may be abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone methylation during vegetative growth","termid":"FYPO:0000457"},{"relation_name":"is_a","term_name":"abolished protein modification during vegetative growth","termid":"FYPO:0000544"},{"relation_name":"is_a","term_name":"abolished biological process","termid":"FYPO:0005448"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0005447","FYPO:0002494","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abolished histone methylation during vegetative growth","synonyms":[{"name":"abolished histone methylation during mitotic cell cycle","type":"related"},{"name":"histone methylation abolished during vegetative growth","type":"exact"},{"name":"histone methylation absent during vegetative growth","type":"exact"}],"termid":"FYPO:0002565"}


id: MONDO:1012063
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ocular-skeletal dysplasia, non-human animal","termid":"MONDO:1011940"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ocular-skeletal dysplasia, dog","secondary_identifiers":["OMIA:000301-9615"],"termid":"MONDO:1012063","xrefs":{"Monarch":{"xref_id":"1012063"}}}


id: GO:0009101
data:
  {"annotated_genes":["SJAG_03764","SJAG_03333","SJAG_05219","SJAG_02163","SJAG_03555","SJAG_04954","SJAG_04316","SJAG_00816","SJAG_04090","SJAG_03150","SJAG_01972","SJAG_01069","SJAG_04127","SJAG_00924","SJAG_03188","SJAG_01491","SJAG_02102","SJAG_03311","SJAG_04363","SJAG_00747","SJAG_03790","SJAG_00598","SJAG_04231","SJAG_04821","SJAG_04095","SJAG_00437","SJAG_01595","SJAG_04053","SJAG_03056","SJAG_03149","SJAG_01950","SJAG_01276","SJAG_04906","SJAG_00334","SJAG_03774","SJAG_02648","SJAG_03330","SJAG_02996","SJAG_04571","SJAG_02056","SJAG_04401","SJAG_00183","SJAG_00554","SJAG_03032","SJAG_01389","SJAG_04770","SJAG_01021","SJAG_04952","SJAG_05348","SJAG_00831","SJAG_04728","SJAG_03871","SJAG_01006","SJAG_00394","SJAG_03656","SJAG_03082","SJAG_02903","SJAG_01264","SJAG_02519","SJAG_03676","SJAG_02783"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87249,77884,71574,77337,76573,74278,74503,79167,80153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000032"},{"annotations":[110881,90883,61237,72785,99780,76868,79873,93657,68705,63119,104801,64096,74718,76459,99572,65197],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006488"},{"annotations":[63235,58443,95468,66423,75205,99816,74154,108192,68098,113760,117637,71647],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006486"},{"annotations":[62746,79165,78887,74501,75441,77335,76571,75092,77883,78072,69593,74277,110502,110508,73275,79573],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006487"},{"annotations":[100117,98562,98560,78938,78529,76038,104747,117860,79276,74058,87252,98563,97663,98561],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0018279"},{"annotations":[77336,110509,79166,74502,117861,62649,110503],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006493"},{"annotations":[101330,105763,92793],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035269"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of glycoproteins, a protein that contains covalently bound glycose (i.e. monosaccharide) residues; the glycose occurs most commonly as oligosaccharide or fairly small polysaccharide but occasionally as monosaccharide.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule biosynthetic process","termid":"GO:0009059"},{"relation_name":"is_a","term_name":"glycoprotein metabolic process","termid":"GO:0009100"},{"relation_name":"is_a","term_name":"carbohydrate derivative biosynthetic process","termid":"GO:1901137"}],"gene_count":61,"genes_by_uniquename":{"SJAG_00183":null,"SJAG_00334":null,"SJAG_00394":null,"SJAG_00437":null,"SJAG_00554":null,"SJAG_00598":null,"SJAG_00747":null,"SJAG_00816":null,"SJAG_00831":null,"SJAG_00924":null,"SJAG_01006":null,"SJAG_01021":null,"SJAG_01069":null,"SJAG_01264":null,"SJAG_01276":null,"SJAG_01389":null,"SJAG_01491":null,"SJAG_01595":null,"SJAG_01950":null,"SJAG_01972":null,"SJAG_02056":null,"SJAG_02102":null,"SJAG_02163":null,"SJAG_02519":null,"SJAG_02648":null,"SJAG_02783":null,"SJAG_02903":null,"SJAG_02996":null,"SJAG_03032":null,"SJAG_03056":null,"SJAG_03082":null,"SJAG_03149":null,"SJAG_03150":null,"SJAG_03188":null,"SJAG_03311":null,"SJAG_03330":null,"SJAG_03333":null,"SJAG_03555":null,"SJAG_03656":null,"SJAG_03676":null,"SJAG_03764":null,"SJAG_03774":null,"SJAG_03790":null,"SJAG_03871":null,"SJAG_04053":null,"SJAG_04090":null,"SJAG_04095":null,"SJAG_04127":null,"SJAG_04231":null,"SJAG_04316":null,"SJAG_04363":null,"SJAG_04401":null,"SJAG_04571":null,"SJAG_04728":null,"SJAG_04770":null,"SJAG_04821":null,"SJAG_04906":null,"SJAG_04952":null,"SJAG_04954":null,"SJAG_05219":null,"SJAG_05348":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"glycoprotein biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"glycoprotein anabolism","type":"exact"},{"name":"glycoprotein biosynthesis","type":"exact"},{"name":"glycoprotein formation","type":"exact"},{"name":"glycoprotein synthesis","type":"exact"}],"termid":"GO:0009101","terms_by_termid":{"GO:0000032":null,"GO:0006486":null,"GO:0006487":null,"GO:0006488":null,"GO:0006493":null,"GO:0018279":null,"GO:0035269":null}}


id: MONDO:0004569
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"brachial plexus neuropathy","termid":"MONDO:0006683"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"brachial plexus neuropathy from injury","secondary_identifiers":["DOID:8443","ICD9:353.0","MEDGEN:507501","UMLS:C0006091"],"synonyms":[{"name":"brachial plexus lesion","type":"exact"},{"name":"brachial plexus lesions","type":"exact"}],"termid":"MONDO:0004569","xrefs":{"Monarch":{"xref_id":"0004569"}}}


id: PR:Q9UT92
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC323.07c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UT92"],"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 transporter C323.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC323.07c","synonyms":[{"name":"Spom972h-SPAC323.07c","type":"exact"}],"termid":"PR:Q9UT92"}


id: GO:0010453
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell fate commitment. Cell fate commitment is the commitment of cells to specific cell fates and their capacity to differentiate into particular kinds of cells. Positional information is established through protein signals that emanate from a localized source within a cell (the initial one-cell zygote) or within a developmental field.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"is_a","term_name":"regulation of cellular process","termid":"GO:0050794"},{"relation_name":"regulates","term_name":"cell fate commitment","termid":"GO:0045165"}],"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 cell fate commitment","termid":"GO:0010453"}


id: FYPO:0007220
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which acetylation of lysine at position 9 of histone H3 in regions containing protein-coding genes is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","PMID:31260531"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone H3-K9 acetylation during vegetative growth","termid":"FYPO:0003223"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal histone H3-K9 acetylation at protein coding gene during vegetative growth","synonyms":[{"name":"normal histone H3-K9 acetylation at protein coding gene during mitotic cell cycle","type":"related"},{"name":"normal histone H3-K9 acetylation at protein-coding gene during vegetative growth","type":"exact"},{"name":"normal histone H3K9 acetylation at protein coding gene during vegetative growth","type":"exact"}],"termid":"FYPO:0007220"}


id: FYPO:0003536
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which the septation index is higher than normal in a population in stationary phase. The septation index is the proportion of the population undergoing septation at any given time.","definition_xrefs":["PomBase:vw","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased septation index","termid":"FYPO:0000650"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"increased septation index in stationary phase","synonyms":[{"name":"increased septation in stationary phase","type":"related"},{"name":"increased septation index during stationary phase","type":"exact"},{"name":"septated in stationary phase","type":"related"}],"termid":"FYPO:0003536"}


id: MONDO:0016780
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"motor developmental delay due to 14q32.2 paternally expressed gene defect","termid":"MONDO:0014541"},{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 14","termid":"MONDO:0016912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paternal 14q32.2 microdeletion syndrome","secondary_identifiers":["UMLS:C5679639","GARD:17220","Orphanet:254525","MEDGEN:1842589"],"synonyms":[{"name":"paternal del(14)(q32.2)","type":"exact"},{"name":"paternal monosomy 14q32.2","type":"exact"}],"termid":"MONDO:0016780","xrefs":{"Monarch":{"xref_id":"0016780"}}}


id: GO:0033238
data:
  {"annotated_genes":["SJAG_04546"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110971],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010967"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways by which individual cells transform amines.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of metabolic process","termid":"GO:0019222"},{"relation_name":"regulates","term_name":"amine metabolic process","termid":"GO:0009308"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04546":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of amine metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of amine metabolism","type":"exact"},{"name":"regulation of cellular amine metabolic process","type":"exact"}],"termid":"GO:0033238","terms_by_termid":{"GO:0010967":null}}


id: PBO:0027626
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_transcriptional_response_to_pheromone","termid":"PBO:0027626"}


id: PATO:0001469
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A curvature quality inhering in a bearer by virtue of the bearer's being curved towards the abdomen of an organism.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"curved","termid":"PATO:0000406"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"curved ventral","synonyms":[{"name":"curved anterior (human torso)","type":"exact"},{"name":"curved inferior (human head)","type":"exact"}],"termid":"PATO:0001469"}


id: MONDO:0017091
data:
  {"annotated_genes":["SJAG_04537","SJAG_04003","SJAG_02289"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85237],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012986"},{"annotations":[85238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012399"},{"annotations":[87011],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030669"},{"annotations":[84853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014679"},{"annotations":[85797],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030482"}]},"cv_name":"mondo","definition":"Bilateral polymicrogyria is a rare cerebral malformation due to abnormal neuronal migration defined as a cerebral cortex with many excessively small convolutions. It presents with developmental delay, intellectual disability, seizures and various neurological impairments and may be isolated or comprise a clinical feature of many genetic syndromes. It may also be associated with perinatal cytomegalovirus infection.","definition_xrefs":["Orphanet:268940"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polymicrogyria","termid":"MONDO:0000087"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02289":null,"SJAG_04003":null,"SJAG_04537":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"bilateral polymicrogyria","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1647593","SCTID:765757003","GARD:17269","icd11.foundation:422828750","UMLS:C4707565"],"termid":"MONDO:0017091","terms_by_termid":{"MONDO:0012399":null,"MONDO:0012986":null,"MONDO:0014679":null,"MONDO:0030482":null,"MONDO:0030669":null},"xrefs":{"Monarch":{"xref_id":"0017091"}}}


id: PBO:0061996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily F member 1","termid":"PBO:0061996"}


id: GO:0030998
data:
  {"annotated_genes":["SJAG_05333","SJAG_02652","SJAG_03843","SJAG_03438","SJAG_02490","SJAG_04303","SJAG_07002","SJAG_00172","SJAG_04748"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[88804,90085,91225,94505,104671,109353,109446,110919,115342],"is_not":false,"summary":null,"term":"GO:0030998"}]},"cv_name":"cellular_component","definition":"A proteinaceous scaffold associated with fission yeast chromosomes during meiotic prophase. Linear elements consist of a protein complex, LinE, with four main structural components (Rec10, Rec25, Rec27, and Mug20 in S. pombe) associated with chromatin. The resulting structure is related to but not equivalent to the synaptonemal complex.","definition_xrefs":["DOI:10.2323/jgam.28.263","PMID:30640914","PMID:12665553","GOC:jb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synaptonemal structure","termid":"GO:0099086"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00172":null,"SJAG_02490":null,"SJAG_02652":null,"SJAG_03438":null,"SJAG_03843":null,"SJAG_04303":null,"SJAG_04748":null,"SJAG_05333":null,"SJAG_07002":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005694","GO:0005634"],"is_obsolete":false,"name":"linear element","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0030998","terms_by_termid":{"GO:0030998":null}}


id: MONDO:0032908
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":"CEBALID syndrome","secondary_identifiers":["MEDGEN:1710973","OMIM:618774","UMLS:C5394044"],"synonyms":[{"name":"CEBALID","type":"related"},{"name":"CEBALID SYNDROME","type":"related"},{"name":"Craniofacial Defects, Dysmorphic Ears, Structural Brain Abnormalities, Expressive Language Delay, and Impaired Intellectual Development","type":"related"},{"name":"MCTT","type":"exact"},{"name":"MN1 C-Terminal Truncation Syndrome","type":"exact"},{"name":"MN1 C-terminal truncation syndrome","type":"exact"}],"termid":"MONDO:0032908","xrefs":{"Monarch":{"xref_id":"0032908"}}}


id: MONDO:0800149
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any commonn variable immunodeficiency in which the cause of the disease is an autosomal recessive variation in the TNFS13 gene.","definition_xrefs":["PMID:32298700"],"direct_ancestors":[{"relation_name":"is_a","term_name":"common variable immunodeficiency","termid":"MONDO:0015517"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"immunodeficiency, common variable, due to APRIL deficiency","termid":"MONDO:0800149","xrefs":{"Monarch":{"xref_id":"0800149"}}}


id: PBO:0071969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S6 kinase B2","termid":"PBO:0071969"}


id: GO:0031746
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 1 cysteinyl leukotriene receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysteinyl leukotriene receptor binding","termid":"GO:0031745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"type 1 cysteinyl leukotriene receptor binding","synonyms":[{"name":"type 1 cysteinyl leukotriene receptor ligand","type":"narrow"}],"termid":"GO:0031746"}


id: PBO:0079385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin beta 2A class IIa","termid":"PBO:0079385"}


id: PATO:0000882
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000882 litter size value (obsolete PATO:0000882)","termid":"PATO:0000882"}


id: FYPO:0004205
data:
  {"alleles_by_uniquename":{"SJAG_03689:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03689","name":"dcr1delta","uniquename":"SJAG_03689:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119386],"is_not":false,"summary":null,"term":"FYPO:0004205"}]},"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 siRNA measured in a cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased mature ncRNA level","termid":"FYPO:0006466"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03689":null},"genotype_count":1,"genotypes_by_uniquename":{"dcr1delta":{"display_name":"dcr1delta","display_uniquename":"dcr1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03689:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0006551","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased siRNA level","references_by_uniquename":{"PMID:35226668":null},"single_locus_annotated_genes":["SJAG_03689"],"single_locus_genotype_uniquenames":["dcr1delta"],"synonyms":[{"name":"decreased mature siRNA level","type":"exact"},{"name":"decreased siRNA accumulation","type":"related"},{"name":"decreased siRNA level during mitotic cell cycle","type":"related"},{"name":"decreased siRNA level during vegetative growth","type":"exact"},{"name":"decreased siRNA transcript level","type":"exact"},{"name":"decreased small interfering RNA level","type":"exact"},{"name":"reduced siRNA level","type":"exact"}],"termid":"FYPO:0004205","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000162":null,"FYPO:0004205":null,"FYPO_EXT:0000001":null}}


id: PBO:0062684
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 A member 5 pseudogene","termid":"PBO:0062684"}


id: GO:0010349
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-galactose + NAD+ = L-galactono-1,4-lactone + NADH + H+.","definition_xrefs":["RHEA:31559","PMID:12047629"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"L-galactose dehydrogenase activity","secondary_identifiers":["MetaCyc:RXN-1884","EC:1.1.1.316"],"synonyms":[{"name":"L-galactose 1-dehydrogenase activity","type":"related"}],"termid":"GO:0010349"}


id: PBO:0087825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TFIIE large subunit; involved in recruitment of RNA polymerase II to the promoter, activation of TFIIH, and promoter opening","termid":"PBO:0087825"}


id: PBO:0046710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ETV7 and PTX1 antisense RNA 1","termid":"PBO:0046710"}


id: GO:0036265
data:
  {"annotated_genes":["SJAG_04680","SJAG_04848","SJAG_02281","SJAG_04034"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59723],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106005"},{"annotations":[79754],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070476"},{"annotations":[67260,58824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106004"}]},"cv_name":"biological_process","definition":"The addition of a methyl group to the N7 atom in the base portion of a guanine nucleotide residue in an RNA molecule.","definition_xrefs":["GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA methylation","termid":"GO:0001510"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02281":null,"SJAG_04034":null,"SJAG_04680":null,"SJAG_04848":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"RNA (guanine-N7)-methylation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000108":null},"termid":"GO:0036265","terms_by_termid":{"GO:0070476":null,"GO:0106004":null,"GO:0106005":null}}


id: PBO:0052940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 24-1","termid":"PBO:0052940"}


id: GO:0034005
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,6-trans-farnesyl diphosphate = (+)-(R)-germacrene A + diphosphate.","definition_xrefs":["RHEA:12516","EC:4.2.3.23"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sesquiterpene synthase activity","termid":"GO:0010334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"germacrene-A synthase activity","secondary_identifiers":["KEGG_REACTION:R07649","MetaCyc:RXN-11527"],"synonyms":[{"name":"(+)-(10R)-germacrene A synthase activity","type":"related"},{"name":"(+)-germacrene A synthase activity","type":"related"},{"name":"2-trans,6-trans-farnesyl-diphosphate diphosphate-lyase (germacrene-A-forming) activity","type":"related"},{"name":"2-trans,6-trans-farnesyl-diphosphate diphosphate-lyase [(+)-germacrene-A-forming] activity","type":"related"},{"name":"GAS","type":"related"},{"name":"germacrene A synthase activity","type":"related"}],"termid":"GO:0034005"}


id: PBO:0084871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial ribosomal protein of the small subunit; has similarity to mammalian apoptosis mediator proteins; null mutation prevents induction of apoptosis by overproduction of metacaspase Mca1p","termid":"PBO:0084871"}


id: PBO:0047063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 120C","termid":"PBO:0047063"}


id: PBO:0029645
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_vegetative_cell_population_at_high_temperature_(obsolete_FYPO:0002075)","termid":"PBO:0029645"}


id: PBO:0041833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer susceptibility 9","termid":"PBO:0041833"}


id: PBO:0062763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 52 subfamily Q member 1 pseudogene","termid":"PBO:0062763"}


id: GO:1990976
data:
  {"annotated_genes":["SJAG_03437","SJAG_01546","SJAG_01775","SJAG_01371","SJAG_00918","SJAG_01224","SJAG_05266","SJAG_01211","SJAG_05319","SJAG_05220","SJAG_02731"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88889,89494,90737,96546,98411,100308,107305,108688,109694,113901,116725],"is_not":false,"summary":null,"term":"GO:1990976"}]},"cv_name":"biological_process","definition":"The directed movement of a protein along a microtubule to the mitotic spindle pole body, mediated by motor proteins.","definition_xrefs":["PMID:25987607"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to mitotic spindle pole body","termid":"GO:1902440"},{"relation_name":"is_a","term_name":"protein transport along microtubule to spindle pole body","termid":"GO:1990852"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00918":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01371":null,"SJAG_01546":null,"SJAG_01775":null,"SJAG_02731":null,"SJAG_03437":null,"SJAG_05220":null,"SJAG_05266":null,"SJAG_05319":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"protein transport along microtubule to mitotic spindle pole body","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990976","terms_by_termid":{"GO:1990976":null}}


id: GO:0010091
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the formation of branches in plant hair cells. An example of this process is found in Arabidopsis thaliana.","definition_xrefs":["GOC:mtg_sensu","GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell morphogenesis","termid":"GO:0000902"},{"relation_name":"part_of","term_name":"trichome morphogenesis","termid":"GO:0010090"}],"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":"trichome branching","secondary_identifiers":["GO:0048274"],"termid":"GO:0010091"}


id: PBO:0054444
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 1841","termid":"PBO:0054444"}


id: MONDO:1012069
data:
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id: GO:0048014
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id: GO:2000555
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id: GO:0045458
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id: MONDO:0004415
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id: MONDO:0019637
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id: PR:Q10056
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id: GO:1902197
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id: GO:0016747
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id: MONDO:0024487
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id: PBO:0072960
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id: FYPO:0004730
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  {"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 a protein that is not normally found at the lateral cell cortex is observed there. The lateral cell cortex is the region directly beneath the plasma membrane of the lateral portion of the cell.","definition_xrefs":["PomBase:mah","GO:0097575"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein mislocalized to cytoplasm during vegetative growth","termid":"FYPO:0000783"},{"relation_name":"output_of","term_name":"abnormal protein localization to lateral cell cortex","termid":"FYPO:0007869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"protein mislocalized to lateral cell cortex","synonyms":[{"name":"ectopic protein localization to lateral cell cortex","type":"exact"},{"name":"protein mislocalised to lateral cell cortex","type":"exact"},{"name":"protein mislocalised to lateral cell cortex during vegetative growth","type":"exact"},{"name":"protein mislocalized to cell side during vegetative growth","type":"related"},{"name":"protein mislocalized to lateral cell cortex during mitotic cell cycle","type":"related"},{"name":"protein mislocalized to lateral cell cortex during vegetative growth","type":"exact"},{"name":"protein mislocalized to lateral cortex","type":"exact"}],"termid":"FYPO:0004730"}


id: PBO:0050557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HRas proto-oncogene, GTPase","termid":"PBO:0050557"}


id: MONDO:0011616
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A holoprosencephaly that has material basis in variation in the chromosome region 2q37.1-q37.3.","definition_xrefs":["PMID:11343300","DOID:0110874"],"direct_ancestors":[{"relation_name":"is_a","term_name":"holoprosencephaly","termid":"MONDO:0016296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"holoprosencephaly 6","secondary_identifiers":["UMLS:C1853830","MESH:C565274","MEDGEN:342979","OMIM:605934"],"synonyms":[{"name":"HPE6","type":"exact"},{"name":"holoprosencephaly 6","type":"exact"},{"name":"holoprosencephaly type 6","type":"exact"}],"termid":"MONDO:0011616","xrefs":{"Monarch":{"xref_id":"0011616"}}}


id: PBO:0017906
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sSuppressor for K-252a Sensitivity","termid":"PBO:0017906"}


id: PBO:0029331
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H2A_phosphorylation","termid":"PBO:0029331"}


id: PBO:0074042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 25","termid":"PBO:0074042"}


id: FYPO:0005408
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of progression through S phase of the mitotic cell cycle is shorter than normal during a cellular response to methyl methanesulfonate.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased duration of mitotic S phase","termid":"FYPO:0000615"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0000631"],"is_obsolete":false,"name":"decreased duration of mitotic S phase during cellular response to methyl methanesulfonate","synonyms":[{"name":"decreased duration of S phase during cellular response to methyl methanesulfonate during mitotic cell cycle","type":"exact"},{"name":"decreased duration of mitotic S phase during cellular response to MMS","type":"exact"},{"name":"decreased duration of mitotic S phase during cellular response to methyl methanesulfonate during vegetative growth","type":"exact"},{"name":"decreased duration of mitotic S phase during cellular response to methyl methanesulphonate","type":"exact"},{"name":"reduced duration of mitotic S phase during cellular response to methyl methanesulfonate","type":"exact"}],"termid":"FYPO:0005408"}


id: PBO:0055795
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysyl oxidase like 4","termid":"PBO:0055795"}


id: GO:0006152
data:
  {"annotated_genes":["SJAG_02580","SJAG_01359","SJAG_02959","SJAG_04927","SJAG_00957"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74962,90829,111970],"is_not":false,"summary":null,"term":"GO:0006152"},{"annotations":[87329,87330],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006154"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of purine nucleoside, one of a family of organic molecules consisting of a purine base covalently bonded to a sugar ribose (a ribonucleoside) or deoxyribose (a deoxyribonucleoside).","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside catabolic process","termid":"GO:0009164"},{"relation_name":"is_a","term_name":"purine nucleoside metabolic process","termid":"GO:0042278"},{"relation_name":"is_a","term_name":"purine-containing compound catabolic process","termid":"GO:0072523"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00957":null,"SJAG_01359":null,"SJAG_02580":null,"SJAG_02959":null,"SJAG_04927":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"purine nucleoside catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"purine nucleoside breakdown","type":"exact"},{"name":"purine nucleoside catabolism","type":"exact"},{"name":"purine nucleoside degradation","type":"exact"}],"termid":"GO:0006152","terms_by_termid":{"GO:0006152":null,"GO:0006154":null}}


id: GO:0034821
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: citronellol + NAD+ = citronellal + NADH + H+.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete citronellol dehydrogenase activity (obsolete GO:0034821)","termid":"GO:0034821"}


id: PBO:0079623
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 M pseudogene 1","termid":"PBO:0079623"}


id: PBO:0047079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 135 member A","termid":"PBO:0047079"}


id: GO:0032459
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein oligomerization.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein-containing complex assembly","termid":"GO:0043254"},{"relation_name":"regulates","term_name":"protein complex oligomerization","termid":"GO:0051259"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"regulation of protein oligomerization","termid":"GO:0032459"}


id: MOD:01475
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O-[S-(carboxamidomethyl)phosphopantetheine]-L-serine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"O-phosphopantetheine-L-serine","termid":"MOD:00159"},{"relation_name":"is_a","term_name":"iodoacetamide derivatized residue","termid":"MOD:00397"},{"relation_name":"is_a","term_name":"phosphorus containing modified residue","termid":"MOD:00861"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-[S-(carboxamidomethyl)phosphopantetheine]-L-serine","termid":"MOD:01475"}


id: GO:0016175
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NAD(P)H + O2 = NAD(P)H + O2-.","definition_xrefs":["GOC:ai","PMID:10806195"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on NAD(P)H, oxygen as acceptor","termid":"GO:0050664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"superoxide-generating NAD(P)H oxidase activity","secondary_identifiers":["Reactome:R-HSA-5668629","Reactome:R-HSA-5218841","Reactome:R-HSA-6807557","Reactome:R-HSA-1236967","Reactome:R-HSA-5668718","Reactome:R-HSA-9673797","Reactome:R-HSA-1222376","Reactome:R-HSA-1497810","Reactome:R-HSA-5668731","Reactome:R-HSA-6789092"],"synonyms":[{"name":"cytochrome B-245","type":"related"}],"termid":"GO:0016175"}


id: FYPO:0000287
data:
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id: GO:0070055
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The endonucleolytic cleavage of a mRNA containing an HAC1-type intron at the 5' and 3' splice sites. The cleavage step is part of unconventional mRNA splicing, and contributes to the endoplasmic reticulum unfolded protein response.","definition_xrefs":["GOC:bf","GOC:mah","GOC:krc","PMID:10357823"],"gene_count":0,"genotype_count":0,"name":"obsolete mRNA endonucleolytic cleavage involved in unfolded protein response (obsolete GO:0070055)","synonyms":[{"name":"ERN1-mediated XBP-1 mRNA cleavage","type":"related"},{"name":"HAC1 mRNA cleavage","type":"narrow"},{"name":"HAC1-type intron splice site recognition and cleavage","type":"narrow"},{"name":"IRE1-mediated XBP-1 mRNA cleavage","type":"narrow"},{"name":"XBP1 mRNA cleavage","type":"narrow"}],"termid":"GO:0070055"}


id: MONDO:0032938
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  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bilateral striopallidodentate calcinosis","termid":"MONDO:0008947"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0002039"],"is_obsolete":false,"name":"basal ganglia calcification, idiopathic, 8, autosomal recessive","secondary_identifiers":["MEDGEN:1713414","OMIM:618824","UMLS:C5394199","GARD:16384"],"synonyms":[{"name":"BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 8, AUTOSOMAL RECESSIVE","type":"related"},{"name":"IBGC8","type":"related"}],"termid":"MONDO:0032938","xrefs":{"Monarch":{"xref_id":"0032938"}}}


id: RO:0002461
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  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"participates_in","termid":"RO:0000056"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partner_in","termid":"RO:0002461"}


id: GO:1900125
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id: GO:0001067
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id: MONDO:0009777
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oliver syndrome is a very rare syndrome characterized by intellectual deficit, postaxial polydactyly, and epilepsy.","definition_xrefs":["Orphanet:2920"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Oliver syndrome","secondary_identifiers":["OMIM:258200","GARD:4069","MESH:C564931","SCTID:721017000","UMLS:C1850320","icd11.foundation:2072460929","MEDGEN:342472"],"synonyms":[{"name":"Oliver syndrome","type":"exact"},{"name":"postaxial polydactyly and intellectual disability","type":"related"},{"name":"postaxial polydactyly and mental retardation","type":"related"},{"name":"postaxial polydactyly-intellectual disability syndrome","type":"exact"}],"termid":"MONDO:0009777","xrefs":{"Monarch":{"xref_id":"0009777"}}}


id: GO:1905420
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any vascular smooth muscle cell differentiation that is involved in phenotypic switching.","definition_xrefs":["GO_REF:0000060","GOC:BHF_miRNA","GOC:rph","PMID:25089138","GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular associated smooth muscle cell differentiation","termid":"GO:0035886"},{"relation_name":"is_a","term_name":"cell differentiation involved in phenotypic switching","termid":"GO:0090679"}],"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":"vascular associated smooth muscle cell differentiation involved in phenotypic switching","synonyms":[{"name":"VSMC differentiation involved in phenotypic dimorphism","type":"related"},{"name":"VSMC differentiation involved in phenotypic switching","type":"exact"},{"name":"vascular associated smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"vascular smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"vascular smooth muscle cell differentiation involved in phenotypic switching","type":"exact"}],"termid":"GO:1905420"}


id: GO:0061786
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  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A peptidoglycan endopeptidase activity that acts on a stem peptide of peptidoglycan.","definition_xrefs":["GOC:jh","PMID:22748813","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidoglycan endopeptidase activity","termid":"GO:0061785"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0008233"}],"interesting_parent_ids":["GO:0008233","GO:0003824","GO:0003674","GO:0140096","GO:0016787"],"is_obsolete":false,"name":"peptidoglycan stem peptide endopeptidase activity","termid":"GO:0061786"}


id: GO:0048710
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of astrocyte differentiation.","definition_xrefs":["GOC:vp","PMID:15139015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glial cell differentiation","termid":"GO:0045685"},{"relation_name":"regulates","term_name":"astrocyte differentiation","termid":"GO:0048708"}],"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 astrocyte differentiation","termid":"GO:0048710"}


id: GO:0046049
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id: GO:0060529
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id: FYPO:0007598
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A transcription regulation phenotype observed in the vegetative growth phase of the life cycle in which chromatin silencing does not occur at a site where silencing can normally be triggered by the ectopic tethering of a protein.","definition_xrefs":["PomBase:mah","PMID:23613586"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin silencing","termid":"FYPO:0000144"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0006551","FYPO:0005447","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abolished chromatin silencing at ectopic tethering site","synonyms":[{"name":"abolished chromatin silencing at ectopic tethering site during mitotic cell cycle","type":"related"},{"name":"abolished chromatin silencing at ectopic tethering site during vegetative growth","type":"exact"}],"termid":"FYPO:0007598"}


id: PBO:0091765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mating type M-specific polypeptide Mi at silenced MAT3 locus","termid":"PBO:0091765"}


id: MONDO:0013165
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive spastic paraplegia type 45 is a rare, pure or complex form of hereditary spastic paraplegia characterized by onset in infancy of progressive lower limb spasticity, abnormal gait, increased deep tendon reflexes and extensor plantar responses, that may be associated with intellectual disability. Additional signs, such as contractures in the lower limbs, amyotrophy, clubfoot and optic atrophy, have also been reported.","definition_xrefs":["Orphanet:320396"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"}],"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 45","secondary_identifiers":["DOID:0110797","GARD:17477","OMIM:613162","UMLS:C3888209","MEDGEN:854816","SCTID:765753004"],"synonyms":[{"name":"NT5C2 autosomal recessive complex spastic paraplegia","type":"exact"},{"name":"SPG45","type":"exact"},{"name":"SPG65","type":"exact"},{"name":"autosomal recessive complex spastic paraplegia caused by mutation in NT5C2","type":"exact"},{"name":"autosomal recessive spastic paraplegia 45","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 45","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 65","type":"exact"},{"name":"hereditary spastic paraplegia type 45","type":"exact"},{"name":"spastic paraplegia 45, autosomal recessive","type":"related"}],"termid":"MONDO:0013165","xrefs":{"Monarch":{"xref_id":"0013165"}}}


id: PBO:0076452
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TAGAP antisense RNA 1","termid":"PBO:0076452"}


id: PBO:0003154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein Pof13","termid":"PBO:0003154"}


id: PBO:0078203
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 6-5","termid":"PBO:0078203"}


id: GO:1900798
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of cordyol C.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catechol-containing compound catabolic process","termid":"GO:0019614"},{"relation_name":"is_a","term_name":"secondary metabolite catabolic process","termid":"GO:0090487"},{"relation_name":"is_a","term_name":"cordyol C metabolic process","termid":"GO:1900797"},{"relation_name":"is_a","term_name":"ether catabolic process","termid":"GO:1901502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0019748"],"is_obsolete":false,"name":"cordyol C catabolic process","synonyms":[{"name":"cordyol C breakdown","type":"exact"},{"name":"cordyol C catabolism","type":"exact"},{"name":"cordyol C degradation","type":"exact"}],"termid":"GO:1900798"}


id: PBO:0042795
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CEP192 divergent transcript","termid":"PBO:0042795"}


id: PBO:0017524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"folylpolyglutamate synthase Fol3 (predicted)","termid":"PBO:0017524"}


id: PBO:0072671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"receptor transporter protein 4","termid":"PBO:0072671"}


id: PBO:0029770
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_microcolony,_elongated_tapered_cells_(obsolete_FYPO:0002469)","termid":"PBO:0029770"}


id: GO:0043968
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H2A by the addition of an acetyl group.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H2A acetylation (obsolete GO:0043968)","termid":"GO:0043968"}


id: MONDO:0015537
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cutaneous necrobiotic disorder characterized by firm, yellow plaques or nodules, often in a periorbital distribution. It is often accompanied by an elevated erythrocyte sedimentation rate; leukopenia; and monoclonal gammopathy (IgG-kappa type) and systemic involvement.","definition_xrefs":["MESH:D058252"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-Langerhans cell histiocytosis","termid":"MONDO:0015531"}],"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":"necrobiotic xanthogranuloma","secondary_identifiers":["GARD:10951","EFO:1001376","icd11.foundation:2138563851","ICD9:709.8","MEDGEN:266158","Orphanet:158011","SCTID:404164003","UMLS:C1275339"],"synonyms":[{"name":"NXG","type":"related"}],"termid":"MONDO:0015537","xrefs":{"Monarch":{"xref_id":"0015537"}}}


id: PBO:0048369
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GRB2 binding adaptor protein, transmembrane","termid":"PBO:0048369"}


id: PBO:0075059
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 116-22","termid":"PBO:0075059"}


id: PBO:0087817
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TFIID subunit (150 kDa); involved in RNA polymerase II transcription initiation","termid":"PBO:0087817"}


id: PBO:0031274
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_chromatin_silencing_at_silent_mating-type_cassette","termid":"PBO:0031274"}


id: MONDO:0958001
data:
  {"annotated_genes":["SJAG_04653"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85826],"is_not":false,"summary":null,"term":"MONDO:0958001"}]},"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":1,"genes_by_uniquename":{"SJAG_04653":null},"genotype_count":0,"is_obsolete":false,"name":"Alfadhel syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620655","UMLS:C5882735","MEDGEN:1845825"],"termid":"MONDO:0958001","terms_by_termid":{"MONDO:0958001":null},"xrefs":{"Monarch":{"xref_id":"0958001"}}}


id: GO:0016038
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The reception of a (visible light) photon by a cell, visible light being defined as having a wavelength within the range 380-780 nm.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"light absorption","termid":"GO:0016037"}],"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":"absorption of visible light","termid":"GO:0016038"}


id: MONDO:0011535
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any split hand-foot malformation in which the cause of the disease is a mutation in the TP63 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"split hand-foot malformation","termid":"MONDO:0016576"},{"relation_name":"is_a","term_name":"TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations","termid":"MONDO:1040001"}],"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":"split hand-foot malformation 4","secondary_identifiers":["GARD:15378","DOID:0090023","OMIM:605289","MEDGEN:343120","MESH:C565344","UMLS:C1854442"],"synonyms":[{"name":"SHFM4","type":"exact"},{"name":"TP63 split hand-foot malformation","type":"exact"},{"name":"split hand-foot malformation caused by mutation in TP63","type":"exact"},{"name":"split hand-foot malformation type 4","type":"exact"},{"name":"split-hand/foot malformation 4","type":"related"},{"name":"split-hand/foot malformation type 4","type":"exact"}],"termid":"MONDO:0011535","xrefs":{"Monarch":{"xref_id":"0011535"}}}


id: PBO:0087075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L37A; required for processing of 27SB pre-rRNA and formation of stable 66S assembly intermediates; homologous to mammalian ribosomal protein L37, no bacterial homolog; RPL37A has a paralog, RPL37B, that arose from the whole genome duplication","termid":"PBO:0087075"}


id: PBO:0080112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urotensin 2 receptor","termid":"PBO:0080112"}


id: GO:0007381
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specification of the characteristic structures of the labial segment following establishment of segment boundaries. Identity is considered to be the aggregate of characteristics by which a structure is recognized.","definition_xrefs":["ISBN:0878932437"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specification of segmental identity, head","termid":"GO:0007380"},{"relation_name":"part_of","term_name":"posterior head segmentation","termid":"GO:0035289"}],"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":"specification of segmental identity, labial segment","termid":"GO:0007381"}


id: PBO:0043061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chordin like 2","termid":"PBO:0043061"}


id: MONDO:0019193
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acquired generalized lipodystrophy belongs to a group of lipodystrophic syndromes characterized by loss of adipose tissue, and is a syndrome of insulin resistance that leads to increased cardiovascular risk. Acquired generalized lipodystrophy is related to a selective loss of subcutaneous adipose tissue occurring exclusively at the extremities (face, legs, arms, palms and sometimes soles).","definition_xrefs":["Orphanet:79086"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"diabetes mellitus","termid":"MONDO:0005015"},{"relation_name":"is_a","term_name":"acquired lipodystrophy","termid":"MONDO:0020089"},{"relation_name":"is_a","term_name":"generalized lipodystrophy","termid":"MONDO:0027766"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005066"],"is_obsolete":false,"name":"acquired generalized lipodystrophy","secondary_identifiers":["MEDGEN:543499","UMLS:C0271693","NCIT:C131089","NANDO:1200860","DOID:0080300","GARD:12603","SCTID:86907008"],"synonyms":[{"name":"Lawrence syndrome","type":"exact"},{"name":"Lawrence-Seip syndrome","type":"exact"},{"name":"acquired generalized lipodystrophy","type":"exact"},{"name":"acquired lipoatrophic diabetes","type":"exact"}],"termid":"MONDO:0019193","xrefs":{"Monarch":{"xref_id":"0019193"}}}


id: MONDO:0010112
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":"thalamic degeneration, symmetric infantile","secondary_identifiers":["OMIM:273490","Orphanet:3311","UMLS:C2931220","MEDGEN:419748","MESH:C536504","GARD:5160"],"synonyms":[{"name":"symmetric infantile thalamic degeneration","type":"related"},{"name":"symmetrical thalamic degeneration in infants","type":"related"},{"name":"thalamic degeneration, symmetric infantile","type":"exact"}],"termid":"MONDO:0010112","xrefs":{"Monarch":{"xref_id":"0010112"}}}


id: PBO:0044550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DAPK1 intronic transcript 1","termid":"PBO:0044550"}


id: GO:0061884
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mini excitatory postsynaptic potential. Mini excitatory postsynaptic potential is a process that leads to a temporary increase in postsynaptic potential due to the flow of positively charged ions into the postsynaptic cell, induced by the spontaneous release of a single vesicle of an excitatory neurotransmitter into the synapse.","definition_xrefs":["PMID:20395454","GOC:aruk","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation of excitatory postsynaptic potential","termid":"GO:0098815"},{"relation_name":"regulates","term_name":"mini excitatory postsynaptic potential","termid":"GO:0098816"}],"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 mini excitatory postsynaptic potential","termid":"GO:0061884"}


id: FYPO:0003036
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which transcription occurs to a normal (i.e. indistinguishable from wild type) extent during a cellular response to ultraviolet light. All genes, or a specific subset of genes, may be measured.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal transcription during vegetative growth","termid":"FYPO:0001855"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0000257","FYPO:0001320","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal transcription during cellular response to UV","synonyms":[{"name":"normal transcription during cellular response to UV during mitotic cell cycle","type":"related"},{"name":"normal transcription during cellular response to UV during vegetative growth","type":"exact"},{"name":"normal transcription during cellular response to ultraviolet light","type":"exact"}],"termid":"FYPO:0003036"}


id: MONDO:0004436
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A liposarcoma that arises from the ovary and is composed of round to oval mesenchymal cells, small signet ring lipoblasts, and a rich network of capillaries in a myxoid stroma.","definition_xrefs":["NCIT:C5235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liposarcoma of the ovary","termid":"MONDO:0003589"},{"relation_name":"is_a","term_name":"myxoid liposarcoma","termid":"MONDO:0013280"},{"relation_name":"is_a","term_name":"familial ovarian cancer","termid":"MONDO:0016248"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"ovarian myxoid liposarcoma","secondary_identifiers":["MEDGEN:235420","UMLS:C1335170","DOID:8023"],"synonyms":[{"name":"myxoid liposarcoma of ovary","type":"exact"},{"name":"myxoid liposarcoma of the ovary","type":"exact"},{"name":"ovarian myxoid liposarcoma","type":"exact"},{"name":"ovary myxoid liposarcoma","type":"exact"}],"termid":"MONDO:0004436","xrefs":{"Monarch":{"xref_id":"0004436"}}}


id: MONDO:0044319
data:
  {"annotated_genes":["SJAG_02774"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86462],"is_not":false,"summary":null,"term":"MONDO:0044319"}]},"cv_name":"mondo","definition":"IDDFSDA is an autosomal recessive severe multisystem disorder characterized by poor overall growth, developmental delay, early-onset seizures, intellectual disability, and dysmorphic features. There is phenotypic variability. The most severely affected patients have a neurodevelopmental disorder with microcephaly, absent speech, and inability to walk, and they require feeding tubes. Some patients have congenital heart defects or nonspecific abnormalities on brain imaging. Less severely affected individuals have mild to moderate intellectual disability with normal speech and motor development (summary by {1:Santiago-Sim et al., 2017}).","definition_xrefs":["OMIM:617452"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"monogenic epilepsy","termid":"MONDO:0015653"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02774":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0002320"],"is_obsolete":false,"name":"intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4479520","MEDGEN:1375601","GARD:17942","Orphanet:505237"],"synonyms":[{"name":"IDDFSDA","type":"related"},{"name":"intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies","type":"exact"}],"termid":"MONDO:0044319","terms_by_termid":{"MONDO:0044319":null},"xrefs":{"Monarch":{"xref_id":"0044319"}}}


