# terms

id: PBO:0018282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ESCRT III complex subunit Cmp7 (predicted)","termid":"PBO:0018282"}


id: PBO:0040424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase H+ transporting V0 subunit e1 pseudogene 1","termid":"PBO:0040424"}


id: PBO:0001038
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"promoter contains RLM1 element","termid":"PBO:0001038"}


id: MONDO:0007228
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":"brachymesomelia-renal syndrome","secondary_identifiers":["UMLS:C1862084","MESH:C537096","OMIM:113470","MEDGEN:350586"],"synonyms":[{"name":"brachymesomelia renal syndrome","type":"related"},{"name":"brachymesomelia-renal syndrome","type":"exact"},{"name":"severe upper limb brachymesomelia, glomerulocystic renal dysplasia, cranial and facial abnormalities, corneal opacities","type":"related"}],"termid":"MONDO:0007228","xrefs":{"Monarch":{"xref_id":"0007228"}}}


id: MONDO:0044765
data:
  {"annotated_genes":["SJAG_04000","SJAG_04621","SJAG_00933","SJAG_04148","SJAG_03361","SJAG_00093","SJAG_03182","SJAG_01185"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86068],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013836"},{"annotations":[84869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011303"},{"annotations":[85675],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014752"},{"annotations":[85599,85600],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014817"},{"annotations":[85598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014818"},{"annotations":[84786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014099"},{"annotations":[85604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014257"}]},"cv_name":"mondo","definition":"Nephrotic syndrome, occurring in the pediatric population, in which proteinuria does not normalize with administration of steroids; this condition is unresponsive to a minimum of four weeks administration of oral corticosteroids.","definition_xrefs":["NCIT:C122798"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephrotic syndrome","termid":"MONDO:0005377"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00093":null,"SJAG_00933":null,"SJAG_01185":null,"SJAG_03182":null,"SJAG_03361":null,"SJAG_04000":null,"SJAG_04148":null,"SJAG_04621":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"steroid-resistant nephrotic syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0403397","GTR:AN0096395","GTR:AN0200342","MEDGEN:588369","SCTID:236381000","GTR:AN0096391","GTR:AN0255485"],"synonyms":[{"name":"NPHS2","type":"related"},{"name":"SRNS - steroid-resistant nephrotic syndrome","type":"related"},{"name":"nephrotic syndrome of childhood - steroid resistant","type":"exact"},{"name":"nephrotic syndrome, idiopathic, steroid-resistant","type":"narrow"},{"name":"nephrotic syndrome, steroid-resistant, autosomal recessive","type":"narrow"},{"name":"nephrotic syndrome-steroid-resistant","type":"exact"},{"name":"steroid-resistant nephrotic syndrome","type":"exact"},{"name":"steroid-unresponsive nephrotic syndrome","type":"related"}],"termid":"MONDO:0044765","terms_by_termid":{"MONDO:0011303":null,"MONDO:0013836":null,"MONDO:0014099":null,"MONDO:0014257":null,"MONDO:0014752":null,"MONDO:0014817":null,"MONDO:0014818":null},"xrefs":{"Monarch":{"xref_id":"0044765"}}}


id: PBO:0079126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"teashirt zinc finger homeobox 2","termid":"PBO:0079126"}


id: PBO:0031333
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_caffeine_during_vegetative_growth","termid":"PBO:0031333"}


id: PBO:0053797
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 1052","termid":"PBO:0053797"}


id: FYPO:0003169
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the import of one or more amino acids into the cell occurs to a greater extent than normal in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal amino acid import during vegetative growth","termid":"FYPO:0001361"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"increased amino acid import during vegetative growth","synonyms":[{"name":"increased amino acid import across plasma membrane during vegetative growth","type":"exact"},{"name":"increased amino acid import during mitotic cell cycle","type":"related"},{"name":"increased amino acid import into cell during vegetative growth","type":"exact"},{"name":"increased amino acid uptake during vegetative growth","type":"exact"}],"termid":"FYPO:0003169"}


id: PBO:0075719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRI antisense RNA 1","termid":"PBO:0075719"}


id: SO:0000524
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Genomic DNA of immunoglobulin/T-cell receptor gene in rearranged configuration including at least one V-gene and one VJ-gene.","direct_ancestors":[{"relation_name":"has_part","term_name":"V_gene_segment","termid":"SO:0000466"},{"relation_name":"has_part","term_name":"VJ_gene_segment","termid":"SO:0000576"},{"relation_name":"is_a","term_name":"vertebrate_immunoglobulin_T_cell_receptor_rearranged_gene_cluster","termid":"SO:0000938"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V_VJ_cluster","synonyms":[{"name":"V VJ cluster","type":"exact"},{"name":"V-(VJ)-CLUSTER","type":"exact"}],"termid":"SO:0000524"}


id: PBO:0004389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L29","termid":"PBO:0004389"}


id: PBO:0014601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aconitate hydratase/mitochondrial ribosomal protein subunit L21, fusion protein (predicted)","termid":"PBO:0014601"}


id: PBO:0088171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Xanthine-guanine phosphoribosyl transferase; required for xanthine utilization and for optimal utilization of guanine","termid":"PBO:0088171"}


id: PR:O94480
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC1919.13c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94480"],"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":"25S rRNA (uridine-N(3))-methyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1919.13c","synonyms":[{"name":"Spom972h-SPCC1919.13c","type":"exact"}],"termid":"PR:O94480"}


id: PBO:0072158
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 35","termid":"PBO:0072158"}


id: PBO:0088803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteasome complex subunit beta 2 Pup1","termid":"PBO:0088803"}


id: PBO:0109399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed transcript, Y-linked 26, pseudogene","termid":"PBO:0109399"}


id: PBO:0063113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(ADP-ribose) polymerase 1","termid":"PBO:0063113"}


id: GO:0046141
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of corrin, C19H22N4, the fundamental heterocyclic skeleton of the corrinoids. It consists of four reduced pyrrole rings joined into a macrocyclic ring. Corrin is the core of the vitamin B12 molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"corrin metabolic process","termid":"GO:0015009"},{"relation_name":"is_a","term_name":"tetrapyrrole catabolic process","termid":"GO:0033015"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0033013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0033013"],"is_obsolete":false,"name":"corrin catabolic process","synonyms":[{"name":"corrin breakdown","type":"exact"},{"name":"corrin catabolism","type":"exact"},{"name":"corrin degradation","type":"exact"}],"termid":"GO:0046141"}


id: PBO:0055844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LRIG3 divergent transcript","termid":"PBO:0055844"}


id: MONDO:0000104
data:
  {"annotated_genes":["SJAG_01007"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84866],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008787"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypochromic microcytic anemia","termid":"MONDO:0000387"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01007":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"anemia, hypochromic microcytic with iron overload","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C567144","MEDGEN:388759","OMIMPS:206100","UMLS:C2673913"],"synonyms":[{"name":"anemia, hypochromic microcytic, with iron overload","type":"exact"}],"termid":"MONDO:0000104","terms_by_termid":{"MONDO:0008787":null},"xrefs":{"Monarch":{"xref_id":"0000104"}}}


id: MONDO:0044998
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A disease or disorder that involves the carpal region.","definition_xrefs":["MONDO:patterns/location"],"gene_count":0,"genotype_count":0,"name":"obsolete carpal region disorder (obsolete MONDO:0044998)","secondary_identifiers":["SCTID:128130001"],"synonyms":[{"name":"carpal region disease or disorder","type":"exact"},{"name":"disease of carpal region","type":"exact"},{"name":"disease or disorder of carpal region","type":"exact"},{"name":"disorder of carpal region","type":"exact"},{"name":"disorder of wrist region","type":"exact"},{"name":"wrist region disease","type":"exact"}],"termid":"MONDO:0044998","xrefs":{"Monarch":{"xref_id":"0044998"}}}


id: PBO:0089967
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial Mam33 family protein","termid":"PBO:0089967"}


id: PBO:0075625
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPRING1 pseudogene 2","termid":"PBO:0075625"}


id: MOD:01017
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because redundant and identical to MOD:00403. Remap to MOD:00403.","definition_xrefs":["DeltaMass:113"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:01017 homoseryl (-Hse-) (obsolete MOD:01017)","termid":"MOD:01017"}


id: MONDO:1012791
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any osteogenesis imperfecta that occurs in dogs due to a mutation in the COL1A2 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteogenesis imperfecta, dog","termid":"MONDO:1011581"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteogenesis imperfecta, COL1A2-related, dog","secondary_identifiers":["OMIA:002112-9615"],"termid":"MONDO:1012791","xrefs":{"Monarch":{"xref_id":"1012791"}}}


id: GO:0006075
data:
  {"annotated_genes":["SJAG_03705","SJAG_00876","SJAG_04668","SJAG_00610","SJAG_05285","SJAG_02222","SJAG_01835","SJAG_04666","SJAG_00218","SJAG_03587","SJAG_04483","SJAG_04771","SJAG_01787","SJAG_04462","SJAG_01288","SJAG_01290","SJAG_01255","SJAG_04659"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034413"},{"annotations":[75565,70582,115562,72797,74275,91359,112908,105864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071970"},{"annotations":[87281,92184],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0140748"},{"annotations":[102597,92168,90533,117651,105106,105677,117776],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090334"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (1->3)-beta-D-glucans, compounds composed of glucose residues linked by (1->3)-beta-D-glucosidic bonds.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(1->3)-beta-D-glucan metabolic process","termid":"GO:0006074"},{"relation_name":"is_a","term_name":"beta-glucan biosynthetic process","termid":"GO:0051274"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00218":null,"SJAG_00610":null,"SJAG_00876":null,"SJAG_01255":null,"SJAG_01288":null,"SJAG_01290":null,"SJAG_01787":null,"SJAG_01835":null,"SJAG_02222":null,"SJAG_03587":null,"SJAG_03705":null,"SJAG_04462":null,"SJAG_04483":null,"SJAG_04659":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04771":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"(1->3)-beta-D-glucan biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"1,3-beta-D-glucan biosynthetic process","type":"exact"},{"name":"1,3-beta-glucan anabolism","type":"exact"},{"name":"1,3-beta-glucan biosynthesis","type":"exact"},{"name":"1,3-beta-glucan formation","type":"exact"},{"name":"1,3-beta-glucan synthesis","type":"exact"},{"name":"beta-1,3 glucan anabolism","type":"exact"},{"name":"beta-1,3 glucan biosynthesis","type":"exact"},{"name":"beta-1,3 glucan biosynthetic process","type":"exact"},{"name":"beta-1,3 glucan formation","type":"exact"},{"name":"beta-1,3 glucan synthesis","type":"exact"}],"termid":"GO:0006075","terms_by_termid":{"GO:0034413":null,"GO:0071970":null,"GO:0090334":null,"GO:0140748":null}}


id: GO:0005014
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jid"],"gene_count":0,"genotype_count":0,"name":"obsolete neurotrophin TRKA receptor activity (obsolete GO:0005014)","synonyms":[{"name":"neurotrophin TRKA receptor activity","type":"exact"}],"termid":"GO:0005014"}


id: PBO:0030484
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_sodium_export","termid":"PBO:0030484"}


id: PBO:0044521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DAB1 antisense RNA 1","termid":"PBO:0044521"}


id: GO:0102810
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-oxopentanoate + NADP + H2O = glutarate + NADPH + 2 H+.","definition_xrefs":["RHEA:57832","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor","termid":"GO:0016620"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO: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":"glutarate-semialdehyde dehydrogenase (NADP+) activity","secondary_identifiers":["EC:1.2.1.20","MetaCyc:RXN-8182"],"termid":"GO:0102810"}


id: GO:1905928
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of invadopodium disassembly.","definition_xrefs":["PMID:15684033","GO_REF:0000058","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of invadopodium disassembly (obsolete GO:1905928)","synonyms":[{"name":"down regulation of invadopodium disassembly","type":"exact"},{"name":"down-regulation of invadopodium disassembly","type":"exact"},{"name":"downregulation of invadopodium disassembly","type":"exact"},{"name":"inhibition of invadopodium disassembly","type":"narrow"}],"termid":"GO:1905928"}


id: PBO:0061681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin 107","termid":"PBO:0061681"}


id: MONDO:0007207
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Book syndrome is a rare autosomal dominant ectodermal dysplasia syndrome reported in a Swedish family (25 cases from 4 generations), and one isolated case, and is characterized by premolar aplasia, hyperhidrosis, and premature graying of the hair. Additional features reported in the isolated case include a narrow palate, hypoplastic nails, eyebrow anomalies, a unilateral simian crease, and poorly formed dermatoglyphics.","definition_xrefs":["Orphanet:1262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"Böök syndrome","secondary_identifiers":["MESH:C562993","UMLS:C0457014","MEDGEN:99140","OMIM:112300","GARD:932","SCTID:722296002"],"synonyms":[{"name":"Böök syndrome","type":"exact"},{"name":"PHC syndrome","type":"related"},{"name":"book syndrome","type":"exact"},{"name":"premolar aplasia, hyperhidrosis, and canities prematura","type":"related"}],"termid":"MONDO:0007207","xrefs":{"Monarch":{"xref_id":"0007207"}}}


id: GO:0160176
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of magnesium ion from cytosol to endoplasmic reticulum.","definition_xrefs":["PMID:38513662"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytosol to endoplasmic reticulum transport","termid":"GO:0046967"},{"relation_name":"is_a","term_name":"magnesium ion transmembrane transport","termid":"GO:1903830"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"magnesium ion transport from cytosol to endoplasmic reticulum","termid":"GO:0160176"}


id: FYPO:0005512
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the meiosis I spindle assembly checkpoint is activated more frequently than normal, typically under conditions that do not cause checkpoint activation in wild-type cells. The meiosis I spindle assembly checkpoint normally delays the metaphase/anaphase transition of the first meiotic nuclear division until the spindle is correctly assembled and chromosomes are attached to the spindle.","definition_xrefs":["PomBase:mah","PomBase:vw","PMID:26483559"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic cell cycle checkpoint phenotype","termid":"FYPO:0005511"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000002","FYPO:0000298"],"is_obsolete":false,"name":"increased activation of meiosis I spindle assembly checkpoint","synonyms":[{"name":"increased activation of first meiotic nuclear division spindle assembly checkpoint","type":"exact"},{"name":"increased activation of meiosis I cell cycle spindle assembly checkpoint","type":"exact"},{"name":"increased activation of spindle assembly checkpoint during meiosis I","type":"exact"},{"name":"increased meiosis I spindle assembly checkpoint activation","type":"exact"}],"termid":"FYPO:0005512"}


id: MONDO:0019298
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare urticaria.","gene_count":0,"genotype_count":0,"name":"obsolete rare urticaria (obsolete MONDO:0019298)","secondary_identifiers":["Orphanet:79384"],"synonyms":[{"name":"rare hives","type":"exact"},{"name":"rare urticaria","type":"exact"},{"name":"rare urticaria (disease)","type":"exact"}],"termid":"MONDO:0019298","xrefs":{"Monarch":{"xref_id":"0019298"}}}


id: GO:0036023
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring in the embryo, in which the anatomical structures of a skeletal limb joint are generated and organized. A skeletal limb joint is the connecting structure between the bones of a limb.","definition_xrefs":["Wikipedia:Joint","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"limb joint morphogenesis","termid":"GO:0036022"},{"relation_name":"is_a","term_name":"embryonic skeletal joint morphogenesis","termid":"GO:0060272"},{"relation_name":"part_of","term_name":"embryonic limb morphogenesis","termid":"GO:0030326"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"embryonic skeletal limb joint morphogenesis","termid":"GO:0036023"}


id: MONDO:0957953
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"progeria","termid":"MONDO:0020732"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019303"}],"interesting_parent_ids":["MONDO:0019303"],"is_obsolete":false,"name":"Garg-Mishra progeroid syndrome","secondary_identifiers":["UMLS:C5882717","MEDGEN:1847272","OMIM:620601"],"termid":"MONDO:0957953","xrefs":{"Monarch":{"xref_id":"0957953"}}}


id: GO:0021715
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to the inferior olivary nucleus. This process pertains to the initial formation of a structure from unspecified parts. The inferior olivary nucleus is a capsule-shaped structure in the ventral medulla located just lateral and dorsal to the medullary pyramids. Neurons in the inferior olivary nucleus are the source of climbing fiber input to the cerebellar cortex; these neurons have been implicated in various functions, such as learning and timing of movements.","definition_xrefs":["GOC:cls","GOC:jid","GOC:dph","GO_REF:0000021","GOC:dgh","ISBN:0838580343"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"medulla oblongata formation","termid":"GO:0021580"},{"relation_name":"part_of","term_name":"inferior olivary nucleus morphogenesis","termid":"GO:0021714"}],"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":"inferior olivary nucleus formation","synonyms":[{"name":"inferior olive biosynthesis","type":"related"},{"name":"inferior olive formation","type":"related"}],"termid":"GO:0021715"}


id: GO:0004381
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-galactose + glycoprotein-alpha-L-fucosyl-(1,2)-D-galactose = UDP + glycoprotein-alpha-D-galactosyl-(1,3)-(alpha-L-fucosyl-(1,2))-D-galactose.","definition_xrefs":["EC:2.4.1.37"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-galactosyltransferase activity","termid":"GO:0035250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016757","GO:0016740"],"is_obsolete":false,"name":"fucosylgalactoside 3-alpha-galactosyltransferase activity","secondary_identifiers":["MetaCyc:2.4.1.37-RXN","Reactome:R-HSA-9034053","Reactome:R-HSA-9033961","RHEA:14349"],"synonyms":[{"name":"B transferase activity","type":"related"},{"name":"UDP-galactose:alpha-L-fucosyl-(1,2)-D-galactoside 3-alpha-D-galactosyltransferase activity","type":"related"},{"name":"UDP-galactose:alpha-L-fucosyl-(1->2)-D-galactoside 3-alpha-D-galactosyltransferase activity","type":"related"},{"name":"UDPgalactose:O-alpha-L-fucosyl(1,2)D-galactose alpha-D-galactosyltransferase activity","type":"related"},{"name":"UDPgalactose:O-alpha-L-fucosyl(1->2)D-galactose alpha-D-galactosyltransferase activity","type":"related"},{"name":"UDPgalactose:alpha-L-fucosyl-(1,2)-D-galactoside 3-alpha-D-galactosyltransferase activity","type":"related"},{"name":"UDPgalactose:alpha-L-fucosyl-(1->2)-D-galactoside 3-alpha-D-galactosyltransferase activity","type":"related"},{"name":"UDPgalactose:glycoprotein-alpha-L-fucosyl-(1,2)-D-galactose 3-alpha-D-galactosyltransferase activity","type":"related"},{"name":"[blood group substance] alpha-galactosyltransferase activity","type":"narrow"},{"name":"blood-group substance B-dependent galactosyltransferase activity","type":"narrow"},{"name":"blood-group substance beta-dependent galactosyltransferase activity","type":"narrow"},{"name":"fucosylglycoprotein 3-alpha-galactosyltransferase activity","type":"related"},{"name":"glycoprotein-fucosylgalactoside alpha-galactosyltransferase activity","type":"exact"},{"name":"histo-blood group B transferase activity","type":"narrow"},{"name":"histo-blood substance B-dependent galactosyltransferase activity","type":"related"},{"name":"histo-blood substance beta-dependent galactosyltransferase activity","type":"narrow"}],"termid":"GO:0004381"}


id: GO:0070393
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of teichoic acid, which is a major component of the cell wall of Gram-positive bacteria and typically consists of a polymer of glycerol-phosphate or ribitol-phosphate to which are attached glycosyl and D-alanyl ester residues.","definition_xrefs":["GOC:add","PMID:14665680"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule catabolic process","termid":"GO:0009057"},{"relation_name":"is_a","term_name":"teichoic acid metabolic process","termid":"GO:0046374"},{"relation_name":"is_a","term_name":"carbohydrate derivative catabolic process","termid":"GO:1901136"}],"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":"teichoic acid catabolic process","synonyms":[{"name":"teichoic acid breakdown","type":"exact"},{"name":"teichoic acid catabolism","type":"exact"},{"name":"teichoic acid degradation","type":"exact"}],"termid":"GO:0070393"}


id: FYPO:0007518
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the amount of DNA damage occurring as a side effect of transcription in a cell is greater than normal. The number, extent, or both of damage sites may be increased.","definition_xrefs":["PomBase:mah","PMID:33153481"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased DNA damage during vegetative growth","termid":"FYPO:0003547"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"name":"increased transcription-induced DNA damage","synonyms":[{"name":"increased DNA damage by transcription","type":"exact"},{"name":"increased transcription-induced DNA damage during mitotic cell cycle","type":"related"},{"name":"increased transcription-induced DNA damage during vegetative growth","type":"exact"}],"termid":"FYPO:0007518"}


id: MONDO:0042912
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":"Schlegelberger-Grote syndrome","secondary_identifiers":["MESH:C536635","MEDGEN:419761","UMLS:C2931273"],"synonyms":[{"name":"Schlegelberger Grote syndrome","type":"related"},{"name":"syndrome with triphalangia of thumbs, thrombasthenia Glanzmann and deafness of internal ear","type":"related"},{"name":"triphalangeal thumbs thrombocytopathy deafness","type":"related"}],"termid":"MONDO:0042912","xrefs":{"Monarch":{"xref_id":"0042912"}}}


id: MONDO:0030523
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited oocyte maturation defect","termid":"MONDO:0014769"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"oocyte maturation defect 12","secondary_identifiers":["MEDGEN:1794273","OMIM:619697","UMLS:C5562063"],"synonyms":[{"name":"OOMD12","type":"exact"}],"termid":"MONDO:0030523","xrefs":{"Monarch":{"xref_id":"0030523"}}}


id: MONDO:0006340
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm of the ovary characterized by the presence of glands with serous epithelial cells in a fibrotic stroma.","definition_xrefs":["NCIT:C40031"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian benign neoplasm","termid":"MONDO:0000646"},{"relation_name":"is_a","term_name":"serous adenofibroma","termid":"MONDO:0024886"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian serous adenofibroma","secondary_identifiers":["MEDGEN:309514","EFO:1000428","UMLS:C1518729","DOID:5474"],"synonyms":[{"name":"ovarian serous adenofibroma","type":"exact"},{"name":"ovary serous adenofibroma","type":"exact"},{"name":"serous adenofibroma of ovary","type":"exact"}],"termid":"MONDO:0006340","xrefs":{"Monarch":{"xref_id":"0006340"}}}


id: PBO:0086094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein possibly involved in assembly of actin patches; interacts with an actin assembly factor Las17p and with the SH3 domains of Type I myosins Myo3p and Myo5p; localized predominantly to cortical actin patches","termid":"PBO:0086094"}


id: PBO:0060642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear receptor coactivator 4 pseudogene 1","termid":"PBO:0060642"}


id: SO:1001288
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A recoding stimulatory signal that is a stop codon and has effect on efficiency of recoding.","definition_xrefs":["PMID:12519954","SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"recoding_stimulatory_region","termid":"SO:1001268"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stop_codon_signal","synonyms":[{"name":"stop codon signal","type":"exact"}],"termid":"SO:1001288"}


id: GO:1904740
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A transcription from RNA polymerase II promoter that results in positive regulation of filamentous growth of a population of unicellular organisms in response to starvation.","definition_xrefs":["GOC:rn","GOC:TermGenie","GO_REF:0000063","PMID:26448198"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by transcription from RNA polymerase II promoter (obsolete GO:1904740)","synonyms":[{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by RNA polymerase II transcription factor activity","type":"related"},{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by gene-specific transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by general transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by specific transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by transcription from Pol II promoter","type":"exact"}],"termid":"GO:1904740"}


id: GO:0097056
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of selenocysteinyl-tRNA(Sec). This process occurs through the following steps: a unique serine-tRNA with a UGA recognizing anticodon is first aminoacylated with serine; this is then phosphorylated by phosphoseryl-tRNA[Ser]Sec kinase; lastly, selenium is swapped for the phosphate on the serine.","definition_xrefs":["GOC:yaf","PMID:15317934"],"gene_count":0,"genotype_count":0,"name":"obsolete selenocysteinyl-tRNA(Sec) biosynthetic process (obsolete GO:0097056)","synonyms":[{"name":"selenocysteinyl-tRNA(Sec) anabolism","type":"exact"},{"name":"selenocysteinyl-tRNA(Sec) biosynthesis","type":"exact"},{"name":"selenocysteinyl-tRNA(Sec) formation","type":"exact"},{"name":"selenocysteinyl-tRNA(Sec) synthesis","type":"exact"}],"termid":"GO:0097056"}


id: FYPO:0003399
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 27S ribosomal RNA precursor measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal rRNA or precursor level","termid":"FYPO:0006000"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0001320","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal 27S rRNA precursor level","synonyms":[{"name":"normal 27S rRNA precursor accumulation","type":"related"},{"name":"normal 27S rRNA precursor level during mitotic cell cycle","type":"related"},{"name":"normal 27S rRNA precursor level during vegetative growth","type":"exact"},{"name":"normal 27S rRNA precursor transcript level","type":"exact"}],"termid":"FYPO:0003399"}


id: GO:0048802
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the dorsal part of the body are generated and organized.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"wing disc morphogenesis","termid":"GO:0007472"},{"relation_name":"part_of","term_name":"notum development","termid":"GO:0007477"}],"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":"notum morphogenesis","termid":"GO:0048802"}


id: PBO:0088485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribonuclease III, endonuclease domain superfamily","termid":"PBO:0088485"}


id: GO:0005569
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 small nucleolar RNA (obsolete GO:0005569)","synonyms":[{"name":"small nucleolar RNA","type":"exact"}],"termid":"GO:0005569"}


id: GO:0046021
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A cell cycle process that modulates the frequency, rate or extent of transcription from an RNA polymerase II promoter that occurs during the mitotic cell cycle.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter during mitotic cell cycle (obsolete GO:0046021)","synonyms":[{"name":"mitotic regulation of transcription from Pol II promoter","type":"exact"},{"name":"regulation of transcription from Pol II promoter, mitotic","type":"exact"},{"name":"regulation of transcription from RNA polymerase II promoter during mitosis","type":"exact"}],"termid":"GO:0046021"}


id: PBO:0062247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily BN member 1 pseudogene","termid":"PBO:0062247"}


id: PBO:0064812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 2","termid":"PBO:0064812"}


id: PBO:0045679
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein cytoplasmic 2 light intermediate chain 1","termid":"PBO:0045679"}


id: MONDO:1011206
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Periodontitis that occurs in Rhesus monkey.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"periodontitis, non-human animal","termid":"MONDO:1010315"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"periodontitis, Rhesus monkey","secondary_identifiers":["OMIA:002056-9544"],"termid":"MONDO:1011206","xrefs":{"Monarch":{"xref_id":"1011206"}}}


id: GO:0032478
data:
  {"annotated_genes":["SJAG_04568","SJAG_01865"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[91590,113487],"is_not":false,"summary":null,"term":"GO:0032478"}]},"cv_name":"cellular_component","definition":"A heterotetrameric complex located in the mitochondrial inner membrane that possesses polyprenyl diphosphate synthase activity involved in the synthesis of the isoprenoid chain of ubiquinone whose length varies between organisms. In S. pombe it is a heterotetramer of Dlp1 and Dps1.","definition_xrefs":["PMID:16262699","PMID:14519123"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyprenyl diphosphate synthase complex","termid":"GO:0032476"},{"relation_name":"is_a","term_name":"inner mitochondrial membrane protein complex","termid":"GO:0098800"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01865":null,"SJAG_04568":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005739"}],"interesting_parent_ids":["GO:0032991","GO:0005739","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"heterotetrameric polyprenyl diphosphate synthase complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"heterotetrameric decaprenyl diphosphate synthase complex","type":"narrow"}],"termid":"GO:0032478","terms_by_termid":{"GO:0032478":null}}


id: PBO:0079966
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP9Y pseudogene 4","termid":"PBO:0079966"}


id: PBO:0110163
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved in eukarytoes only","termid":"PBO:0110163"}


id: GO:1901558
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 metformin stimulus.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to metformin","termid":"GO:1901558"}


id: MONDO:0005552
data:
  {"annotated_genes":["SJAG_00495","SJAG_02286","SJAG_02063"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013644"},{"annotations":[86696],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010557"},{"annotations":[86224],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013805"},{"annotations":[86832],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009796"}]},"cv_name":"mondo","definition":"A disorder that is caused by pathologic changes in the ocular vasculature.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00495":null,"SJAG_02063":null,"SJAG_02286":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"ocular vascular disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0948522","NCIT:C35664","EFO:0005753","MEDGEN:182689"],"synonyms":[{"name":"disease of vasculature of eye","type":"exact"},{"name":"disease or disorder of vasculature of eye","type":"exact"},{"name":"disorder of vasculature of eye","type":"exact"},{"name":"ocular vascular disorder","type":"exact"},{"name":"vasculature of eye disease","type":"exact"},{"name":"vasculature of eye disease or disorder","type":"exact"}],"termid":"MONDO:0005552","terms_by_termid":{"MONDO:0009796":null,"MONDO:0010557":null,"MONDO:0013644":null,"MONDO:0013805":null},"xrefs":{"Monarch":{"xref_id":"0005552"}}}


id: PBO:0044031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondroitin sulfate proteoglycan family member 4B, pseudogene","termid":"PBO:0044031"}


id: GO:0030839
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the assembly of intermediate filaments by the addition of monomers to a filament.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein polymerization","termid":"GO:0032271"},{"relation_name":"is_a","term_name":"regulation of intermediate filament polymerization or depolymerization","termid":"GO:0045108"},{"relation_name":"regulates","term_name":"intermediate filament polymerization","termid":"GO:0045107"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0065003"],"is_obsolete":false,"name":"regulation of intermediate filament polymerization","termid":"GO:0030839"}


id: MONDO:1010782
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Alopecia areata that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alopecia areata, non-human animal","termid":"MONDO:1010140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alopecia areata, cattle","secondary_identifiers":["OMIA:001702-9913"],"termid":"MONDO:1010782","xrefs":{"Monarch":{"xref_id":"1010782"}}}


id: GO:0006370
data:
  {"annotated_genes":["SJAG_04034","SJAG_04488","SJAG_01713","SJAG_01724"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[68457,72149,75358,107446],"is_not":false,"summary":null,"term":"GO:0006370"}]},"cv_name":"biological_process","definition":"The sequence of enzymatic reactions by which the mRNA 5' cap structure, an inverted 7-methylguanosine linked via a 5'-5' triphosphate bridge (m7G(5')ppp(5')X) to the first transcribed residue, is added to a nascent transcript. Additional methylation can occur on the ribose sugars of the first and second nucleotides adjacent to the m7G nRNA cap. These methylations are often referred to as N6,2'-O-dimethyladenosine (m6,2A) and N6,2'-O-dimethylguanosine (m6,2G), respectively.","definition_xrefs":["GOC:mah","PMID:9266685"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA processing","termid":"GO:0006397"},{"relation_name":"is_a","term_name":"7-methylguanosine RNA capping","termid":"GO:0009452"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01713":null,"SJAG_01724":null,"SJAG_04034":null,"SJAG_04488":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0016071"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0016071"],"is_obsolete":false,"name":"7-methylguanosine mRNA capping","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-72086"],"synonyms":[{"name":"5' end capping","type":"broad"},{"name":"5' mRNA capping","type":"exact"},{"name":"5'-end mRNA processing","type":"exact"},{"name":"5'-end processing","type":"broad"},{"name":"mRNA capping","type":"exact"}],"termid":"GO:0006370","terms_by_termid":{"GO:0006370":null}}


id: PBO:0060286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin light chain 3","termid":"PBO:0060286"}


id: PBO:0065763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PIGY upstream open reading frame","termid":"PBO:0065763"}


id: GO:0046465
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving dolichyl diphosphate, a diphosphorylated dolichol derivative. In eukaryotes, these function as carriers of mono- and oligosaccharide residues in the glycosylation of lipids and proteins within intracellular membranes.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid metabolic process","termid":"GO:0006644"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"dolichyl diphosphate metabolic process","synonyms":[{"name":"dolichyl diphosphate metabolism","type":"exact"}],"termid":"GO:0046465"}


id: PBO:0063355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostate and testis expressed opposite C1QTNF9B and MIPEP","termid":"PBO:0063355"}


id: PBO:0090299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERMES complex subunit, membrane tether and lipid transfer protein Mdm12","termid":"PBO:0090299"}


id: PBO:0060184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucin 4, cell surface associated","termid":"PBO:0060184"}


id: PBO:0076210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO2 pseudogene 20","termid":"PBO:0076210"}


id: SO:1000185
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant effect, causing an intron to be gained by the processed transcript; usually a result of a donor acceptor mutation (SO:1000072).","definition_xrefs":["EBI:www.ebi.ac.uk/mutations/recommendations/mutevent.html"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000185 sequence_variant_causes_intron_gain (obsolete SO:1000185)","synonyms":[{"name":"mutation causes intron gain","type":"related"},{"name":"sequence variant causes intron gain","type":"exact"}],"termid":"SO:1000185"}


id: PBO:0067252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 326, pseudogene","termid":"PBO:0067252"}


id: MONDO:0006500
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85471],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007154"}]},"cv_name":"mondo","definition":"A benign vascular lesion characterized by the formation of capillary-sized or cavernous vascular channels.","definition_xrefs":["NCIT:C3085"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign blood vessel neoplasm","termid":"MONDO:0024286"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03453":null},"genotype_count":0,"is_obsolete":false,"name":"hemangioma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:228.09","ICDO:9120/0","ONCOTREE:HEMA","DOID:255","SCTID:400210000","MEDGEN:5477","ICD9:228.00","EFO:1000635","UMLS:C0018916","MESH:D006391","HP:0001028","ICD9:228.0"],"synonyms":[{"name":"angioma","type":"related"},{"name":"benign angioma","type":"related"},{"name":"benign hemangioma","type":"exact"},{"name":"hemangioma","type":"exact"},{"name":"hemangioma, benign","type":"exact"}],"termid":"MONDO:0006500","terms_by_termid":{"MONDO:0007154":null},"xrefs":{"Monarch":{"xref_id":"0006500"}}}


id: PBO:0057020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 107","termid":"PBO:0057020"}


id: PBO:0057181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 335","termid":"PBO:0057181"}


id: MONDO:0005356
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sudden coronary artery smooth muscle contraction leading to lumen constriction and decreased blood flow.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coronary artery disorder","termid":"MONDO:0005010"}],"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":"coronary vasospasm","secondary_identifiers":["MESH:D003329","SCTID:23687008","UMLS:C0010073","EFO:0004225","ICD9:413.9","MEDGEN:3626","DOID:11840"],"synonyms":[{"name":"coronary artery spasm","type":"exact"},{"name":"coronary artery vasospasm","type":"related"},{"name":"coronary vasospasm","type":"exact"}],"termid":"MONDO:0005356","xrefs":{"Monarch":{"xref_id":"0005356"}}}


id: GO:1904100
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein O-linked glycosylation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:24509081"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein glycosylation","termid":"GO:0060050"},{"relation_name":"is_a","term_name":"regulation of protein O-linked glycosylation","termid":"GO:1904098"},{"relation_name":"positively_regulates","term_name":"protein O-linked glycosylation","termid":"GO:0006493"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006486"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006486"}],"interesting_parent_ids":["GO:0008150","GO:0006486"],"is_obsolete":false,"name":"positive regulation of protein O-linked glycosylation","synonyms":[{"name":"activation of protein O-linked glycosylation","type":"narrow"},{"name":"activation of protein amino acid O-linked glycosylation","type":"narrow"},{"name":"positive regulation of protein amino acid O-linked glycosylation","type":"exact"},{"name":"up regulation of protein O-linked glycosylation","type":"exact"},{"name":"up regulation of protein amino acid O-linked glycosylation","type":"exact"},{"name":"up-regulation of protein O-linked glycosylation","type":"exact"},{"name":"up-regulation of protein amino acid O-linked glycosylation","type":"exact"},{"name":"upregulation of protein O-linked glycosylation","type":"exact"},{"name":"upregulation of protein amino acid O-linked glycosylation","type":"exact"}],"termid":"GO:1904100"}


id: RO:0002519
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of has end sequence","direct_ancestors":[{"relation_name":"is_a","term_name":"is_subsequence_of","termid":"RO:0002525"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is_end_sequence_of","termid":"RO:0002519"}


id: PBO:0054564
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 1966","termid":"PBO:0054564"}


id: PBO:0057091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 187","termid":"PBO:0057091"}


id: PBO:0060344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin IXB","termid":"PBO:0060344"}


id: PBO:0087920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcription factor TFIIB; a general transcription factor required for transcription initiation and start site selection by RNA polymerase II","termid":"PBO:0087920"}


id: SO:0001737
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A histone modification, whereby the histone protein is acylated at multiple sites in a region.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_modification","termid":"SO:0001700"}],"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":"histone_acylation_region","synonyms":[{"name":"histone acylation region","type":"related"}],"termid":"SO:0001737"}


id: MONDO:1010491
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ventricular septal defect that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ventricular septal defect, non-human animal","termid":"MONDO:1010022"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ventricular septal defect, horse","secondary_identifiers":["OMIA:001041-9796"],"termid":"MONDO:1010491","xrefs":{"Monarch":{"xref_id":"1010491"}}}


id: RO:0001019
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"contains","termid":"RO:0001019"}


id: PBO:0043647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COP9 signalosome subunit 7A","termid":"PBO:0043647"}


id: MONDO:0015263
data:
  {"annotated_genes":["SJAG_00409","SJAG_01012"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84828,84829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012728"}]},"cv_name":"mondo","definition":"A genetically heterogeneous condition characterized by complete or incomplete right bundle branch block accompanied by ST elevation in leads V1-V3. There is a high incidence of ventricular arrhythmia that may result in sudden death.","definition_xrefs":["NCIT:C142891"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart conduction disease","termid":"MONDO:0000992"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"cardiogenetic disease","termid":"MONDO:0100547"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00409":null,"SJAG_01012":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"Brugada syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:1030","ICD9:746.89","Orphanet:130","MEDGEN:222975","UMLS:C1142166","MedDRA:10059027","NORD:878","icd11.foundation:1250136584","MESH:D053840","SCTID:418818005","DOID:0050451","OMIMPS:601144"],"synonyms":[{"name":"Bangungut","type":"exact"},{"name":"Brugada syndrome","type":"exact"},{"name":"Brugada type idiopathic ventricular fibrillation","type":"exact"},{"name":"Pokkuri death syndrome","type":"exact"},{"name":"SUNDS","type":"exact"},{"name":"dream disease","type":"exact"},{"name":"idiopathic ventricular fibrillation, Brugada type","type":"exact"},{"name":"right bundle branch block, ST segment elevation, and sudden death syndrome","type":"exact"},{"name":"sudden unexpected nocturnal death syndrome","type":"related"},{"name":"sudden unexplained nocturnal death syndrome","type":"exact"}],"termid":"MONDO:0015263","terms_by_termid":{"MONDO:0012728":null},"xrefs":{"Monarch":{"xref_id":"0015263"}}}


id: GO:2000232
data:
  {"annotated_genes":["SJAG_01764","SJAG_04890"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77728,75232],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000234"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of rRNA processing.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of gene expression","termid":"GO:0010468"},{"relation_name":"is_a","term_name":"regulation of RNA metabolic process","termid":"GO:0051252"},{"relation_name":"regulates","term_name":"rRNA processing","termid":"GO:0006364"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01764":null,"SJAG_04890":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of rRNA processing","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"regulation of 35S primary transcript processing","type":"related"}],"termid":"GO:2000232","terms_by_termid":{"GO:2000234":null}}


id: RO:HOM0000065
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Similarity that is characterized by interchangeability in function.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_similarity_relationship_with","termid":"RO:HOM0000000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_functional_equivalence_relationship_with","synonyms":[{"name":"functional similarity","type":"related"}],"termid":"RO:HOM0000065"}


id: GO:0044592
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A 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 pullulan stimulus.","definition_xrefs":["GOC:tt","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to carbohydrate","termid":"GO:0009743"}],"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 pullulan","termid":"GO:0044592"}


id: PBO:0045869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 beta 2 pseudogene 2","termid":"PBO:0045869"}


id: GO:0048792
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The release of a neurotransmitter into the synaptic cleft, where the release step is independent of the presence of calcium ions (Ca2+). The neurotransmitter is contained within a membrane-bounded vesicle, and is released by fusion of the vesicle with the presynaptic plasma membrane of a nerve cell.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurotransmitter secretion","termid":"GO:0007269"},{"relation_name":"is_a","term_name":"synaptic vesicle exocytosis","termid":"GO:0016079"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0016192","GO:0006810","GO:0051179","GO:0008150","GO:0023052"],"is_obsolete":false,"name":"spontaneous exocytosis of neurotransmitter","synonyms":[{"name":"spontaneous synaptic vesicle exocytosis","type":"exact"}],"termid":"GO:0048792"}


id: GO:1905273
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of proton-transporting ATP synthase activity, rotational mechanism.","definition_xrefs":["GOC:als","PMID:21106936","GO_REF:0000059","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of ligase activity","termid":"GO:0051351"},{"relation_name":"is_a","term_name":"positive regulation of cation channel activity","termid":"GO:2001259"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"positive regulation of proton-transporting ATP synthase activity, rotational mechanism","synonyms":[{"name":"activation of H+-transporting ATP synthase activity","type":"narrow"},{"name":"activation of hydrogen ion translocating F-type ATPase activity","type":"narrow"},{"name":"activation of hydrogen ion transporting ATP synthase activity, rotational mechanism","type":"narrow"},{"name":"activation of hydrogen ion transporting two-sector ATPase activity","type":"narrow"},{"name":"activation of proton-transporting ATP synthase activity, rotational mechanism","type":"narrow"},{"name":"positive regulation of H+-transporting ATP synthase activity","type":"exact"},{"name":"positive regulation of hydrogen ion translocating F-type ATPase activity","type":"exact"},{"name":"positive regulation of hydrogen ion transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"positive regulation of hydrogen ion transporting two-sector ATPase activity","type":"exact"},{"name":"up regulation of H+-transporting ATP synthase activity","type":"exact"},{"name":"up regulation of hydrogen ion translocating F-type ATPase activity","type":"exact"},{"name":"up regulation of hydrogen ion transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"up regulation of hydrogen ion transporting two-sector ATPase activity","type":"exact"},{"name":"up regulation of proton-transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"up-regulation of H+-transporting ATP synthase activity","type":"exact"},{"name":"up-regulation of hydrogen ion translocating F-type ATPase activity","type":"exact"},{"name":"up-regulation of hydrogen ion transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"up-regulation of hydrogen ion transporting two-sector ATPase activity","type":"exact"},{"name":"up-regulation of proton-transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"upregulation of H+-transporting ATP synthase activity","type":"exact"},{"name":"upregulation of hydrogen ion translocating F-type ATPase activity","type":"exact"},{"name":"upregulation of hydrogen ion transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"upregulation of hydrogen ion transporting two-sector ATPase activity","type":"exact"},{"name":"upregulation of proton-transporting ATP synthase activity, rotational mechanism","type":"exact"}],"termid":"GO:1905273"}


id: PBO:0078278
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 11-1","termid":"PBO:0078278"}


id: PBO:0063647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoglycerate mutase 1 pseudogene 4","termid":"PBO:0063647"}


id: PBO:0017965
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine-type peptidase activity","termid":"PBO:0017965"}


id: MONDO:0000585
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Good syndrome (obsolete MONDO:0000585)","termid":"MONDO:0000585","xrefs":{"Monarch":{"xref_id":"0000585"}}}


id: GO:1901753
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of leukotriene A4.","definition_xrefs":["PMID:23242647","GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukotriene biosynthetic process","termid":"GO:0019370"},{"relation_name":"is_a","term_name":"long-chain fatty acid biosynthetic process","termid":"GO:0042759"},{"relation_name":"is_a","term_name":"ether biosynthetic process","termid":"GO:1901503"},{"relation_name":"is_a","term_name":"fatty acid derivative biosynthetic process","termid":"GO:1901570"},{"relation_name":"is_a","term_name":"leukotriene A4 metabolic process","termid":"GO:1901751"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"leukotriene A4 biosynthetic process","synonyms":[{"name":"LTA4 biosynthesis","type":"exact"},{"name":"eoxin A4 biosynthesis","type":"exact"},{"name":"leukotriene A4 anabolism","type":"exact"},{"name":"leukotriene A4 biosynthesis","type":"exact"},{"name":"leukotriene A4 formation","type":"exact"},{"name":"leukotriene A4 synthesis","type":"exact"}],"termid":"GO:1901753"}


id: MOD:01252
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because redundant and identical to MOD:00933. Remap to MOD:00933.","definition_xrefs":["PubMed:9448752","Unimod:319#R"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:01252 5-hydro-5-methylimidazol-4-one, methylglyoxal arginine adduct (+54 amu) (obsolete MOD:01252)","synonyms":[{"name":"Delta:H(2)C(3)O(1)","type":"related"},{"name":"MDA adduct +54","type":"related"}],"termid":"MOD:01252"}


id: PBO:0070470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L5 pseudogene 5","termid":"PBO:0070470"}


id: PBO:0085407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane protein with a role in cell wall integrity; co-localizes with Sur7p in punctate membrane patches; null mutant displays decreased thermotolerance; transcription induced upon cell wall damage and metal ion stress","termid":"PBO:0085407"}


id: PBO:0001490
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.1.32","termid":"PBO:0001490"}


id: PBO:0003421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit Med15 (predicted)","termid":"PBO:0003421"}


id: MONDO:0032922
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":"Beck-Fahrner syndrome","secondary_identifiers":["OMIM:618798","UMLS:C5394097","MEDGEN:1711894"],"synonyms":[{"name":"BECK-FAHRNER SYNDROME","type":"related"},{"name":"BEFAHRS","type":"related"}],"termid":"MONDO:0032922","xrefs":{"Monarch":{"xref_id":"0032922"}}}


id: PBO:0039342
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALX homeobox 1","termid":"PBO:0039342"}


id: GO:1902112
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 diethyl maleate stimulus.","definition_xrefs":["PMID:12100563","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"},{"relation_name":"is_a","term_name":"response to diethyl maleate","termid":"GO:1902111"}],"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 diethyl maleate","termid":"GO:1902112"}


id: MONDO:0014386
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bleeding disorder due to CalDAG-GEFI deficiency is a rare hematologic disease due to defective platelet function and characterized by mucocutaneous bleeding starting in infancy (around 18 months of age), presenting with prolonged and severe epistaxis, hematomas and bleeding after tooth extraction. Massive menorrhagia and chronic anemia have also been reported.","definition_xrefs":["Orphanet:420566"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited bleeding disorder, platelet-type","termid":"MONDO:0000009"},{"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":"platelet-type bleeding disorder 18","secondary_identifiers":["OMIM:615888","MEDGEN:863021","UMLS:C4014584","DOID:0111051","GARD:17695"],"synonyms":[{"name":"BDPLT18","type":"exact"},{"name":"RASGRP2 inherited bleeding disorder, platelet-type","type":"exact"},{"name":"bleeding disorder due to CalDAG-GEFI deficiency","type":"exact"},{"name":"bleeding disorder due to calcium- and DAG-regulated guanine exchange factor-1 deficiency","type":"exact"},{"name":"bleeding disorder, platelet-type, 18","type":"related"},{"name":"inherited bleeding disorder, platelet-type caused by mutation in RASGRP2","type":"exact"},{"name":"platelet-type bleeding disorder 18","type":"exact"}],"termid":"MONDO:0014386","xrefs":{"Monarch":{"xref_id":"0014386"}}}


id: GO:0140691
data:
  {"annotated_genes":["SJAG_01819","SJAG_03460","SJAG_04266","SJAG_00195","SJAG_00886","SJAG_03070","SJAG_02469"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[98240,107024,108298,112635,113568,114684,115616],"is_not":false,"summary":null,"term":"GO:0140691"}]},"cv_name":"molecular_function","definition":"Binding to an RNA or an RNA-containing complex to assist the folding process.","definition_xrefs":["PMID:31165735"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_function","termid":"GO:0003674"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00195":null,"SJAG_00886":null,"SJAG_01819":null,"SJAG_02469":null,"SJAG_03070":null,"SJAG_03460":null,"SJAG_04266":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"RNA folding chaperone","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140691","terms_by_termid":{"GO:0140691":null}}


id: PATO:0002037
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer exhibiting deterioration of its structure.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"degeneration","termid":"PATO:0002037"}


id: PBO:0079183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis specific protein Y-linked 12, pseudogene","termid":"PBO:0079183"}


id: MONDO:0020857
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"46 XX gonadal dysgenesis","termid":"MONDO:0009299"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"ovarian dysgenesis 7","secondary_identifiers":["DOID:0080499","GARD:18043","MEDGEN:1648458","OMIM:618117","UMLS:C4748263"],"synonyms":[{"name":"ODG7","type":"exact"},{"name":"OVARIAN DYSGENESIS 7","type":"exact"}],"termid":"MONDO:0020857","xrefs":{"Monarch":{"xref_id":"0020857"}}}


id: PBO:0049886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HERC2 pseudogene 5","termid":"PBO:0049886"}


id: GO:0043758
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + acetate + CoA = ADP + phosphate + acetyl-CoA.","definition_xrefs":["RHEA:15081"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-thiol ligase activity","termid":"GO:0016878"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016874","GO:0003674"],"is_obsolete":false,"name":"acetate-CoA ligase (ADP-forming) activity","secondary_identifiers":["MetaCyc:ACETATE--COA-LIGASE-ADP-FORMING-RXN","GO:0043762","EC:6.2.1.13"],"synonyms":[{"name":"acetate thiokinase activity","type":"broad"},{"name":"acetate--CoA ligase (ADP-forming) activity","type":"exact"},{"name":"acetate:CoA ligase (ADP-forming)","type":"related"},{"name":"acetyl coenzyme A synthetase (adenosine diphosphate-forming)","type":"exact"},{"name":"acetyl-CoA synthetase (ADP-forming) activity","type":"related"},{"name":"aryl-CoA synthetase (ADP-forming) activity","type":"related"}],"termid":"GO:0043758"}


id: MONDO:0004218
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A germ cell tumor arising from brain during childhood.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood central nervous system germ cell tumor","termid":"MONDO:0003750"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"childhood germ cell brain tumor","secondary_identifiers":["UMLS:C1377598","DOID:7430","NANDO:2200108","MEDGEN:277987","NCIT:C5795"],"synonyms":[{"name":"Brain germ cell tumor","type":"exact"},{"name":"Brain germ cell tumour","type":"exact"},{"name":"childhood brain germ cell neoplasm","type":"exact"},{"name":"childhood brain germ cell tumor","type":"exact"},{"name":"childhood brain germ cell tumour","type":"exact"},{"name":"childhood germ cell brain neoplasm","type":"exact"},{"name":"germ cell neoplasm of childhood brain","type":"exact"},{"name":"germ cell neoplasm of paediatric brain","type":"exact"},{"name":"germ cell neoplasm of pediatric brain","type":"exact"},{"name":"germ cell neoplasm of the childhood brain","type":"exact"},{"name":"germ cell neoplasm of the paediatric brain","type":"exact"},{"name":"germ cell neoplasm of the pediatric brain","type":"exact"},{"name":"germ cell tumor of childhood brain","type":"exact"},{"name":"germ cell tumor of pediatric brain","type":"exact"},{"name":"germ cell tumor of the childhood brain","type":"exact"},{"name":"germ cell tumor of the pediatric brain","type":"exact"},{"name":"germ cell tumour of childhood brain","type":"exact"},{"name":"germ cell tumour of paediatric brain","type":"exact"},{"name":"germ cell tumour of the childhood brain","type":"exact"},{"name":"germ cell tumour of the paediatric brain","type":"exact"},{"name":"paediatric brain germ cell neoplasm","type":"exact"},{"name":"paediatric brain germ cell tumour","type":"exact"},{"name":"pediatric brain germ cell neoplasm","type":"exact"},{"name":"pediatric brain germ cell tumor","type":"exact"}],"termid":"MONDO:0004218","xrefs":{"Monarch":{"xref_id":"0004218"}}}


id: GO:0043602
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of nitrates, inorganic or organic salts and esters of nitric acid.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"nitrate metabolic process","termid":"GO:0042126"}],"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":"nitrate catabolic process","synonyms":[{"name":"nitrate disassimilation","type":"exact"},{"name":"nitrate dissimilation","type":"exact"}],"termid":"GO:0043602"}


id: GO:1905518
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of presynaptic active zone assembly.","definition_xrefs":["GO_REF:0000058","GOC:rl","GOC:TermGenie","PMID:15797875","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"regulates","term_name":"presynaptic active zone assembly","termid":"GO:1904071"}],"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 presynaptic active zone assembly","synonyms":[{"name":"regulation of pre-synaptic active zone assembly","type":"exact"},{"name":"regulation of pre-synaptic active zone component assembly","type":"narrow"},{"name":"regulation of pre-synaptic active zone component formation","type":"narrow"},{"name":"regulation of pre-synaptic active zone formation","type":"exact"},{"name":"regulation of presynaptic active zone formation","type":"exact"}],"termid":"GO:1905518"}


id: GO:0098617
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + adenylylselenate => ADP + 3'-phosphoadenylylselenate.","definition_xrefs":["PMID:2537056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"adenylylselenate kinase activity","secondary_identifiers":["Reactome:R-HSA-2408540"],"termid":"GO:0098617"}


id: GO:0045679
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of R8 differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of compound eye photoreceptor cell differentiation","termid":"GO:0110116"},{"relation_name":"regulates","term_name":"R8 cell differentiation","termid":"GO:0045465"}],"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 R8 cell differentiation","termid":"GO:0045679"}


id: PBO:0002916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VanZ-like family protein","termid":"PBO:0002916"}


id: MONDO:0015348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Leukoencephalopathy with bilateral anterior temporal lobe cysts is a nonprogressive neurological disorder marked by intellectual deficit, spasticity and motor retardation associated with characteristic MRI findings of anterior bilateral temporal lobe cysts and multilobar leukoencephalopathy. So far, around 30 cases have been reported in the literature. Onset occurs in the first few months of life. Sensorineural deafness and microcephaly have also been reported. The etiology is unknown but an autosomal recessive mode of inheritance has been suggested.","definition_xrefs":["Orphanet:139444"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"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":"leukoencephalopathy with bilateral anterior temporal lobe cysts","secondary_identifiers":["GARD:19917","icd11.foundation:138159250","UMLS:C4304744","MEDGEN:930413"],"termid":"MONDO:0015348","xrefs":{"Monarch":{"xref_id":"0015348"}}}


id: GO:0032589
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the plasma membrane surrounding a neuron projection.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell projection membrane","termid":"GO:0031253"},{"relation_name":"is_a","term_name":"leading edge membrane","termid":"GO:0031256"},{"relation_name":"part_of","term_name":"neuron projection","termid":"GO:0043005"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886"],"is_obsolete":false,"name":"neuron projection membrane","termid":"GO:0032589"}


id: PR:Q09797
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC22G7.03 gene.","definition_xrefs":["UniProtKB:Q09797","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 C22G7.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22G7.03","synonyms":[{"name":"Spom972h-SPAC22G7.03","type":"exact"}],"termid":"PR:Q09797"}


id: GO:0180024
data:
  {"annotated_genes":["SJAG_05207"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[103487],"is_not":false,"summary":null,"term":"GO:0180024"}]},"cv_name":"molecular_function","definition":"An activity in which a protein, or group of proteins, acts to restrict the size of a fenestration in a membrane or membrane system (i.e. restrict the diameter of a hole in a membrane). An example of this is the molecular function is performed by ESCRT-III proteins at the nuclear envelope of fission yeast during anaphase B.","definition_xrefs":["PMID:37783794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_function","termid":"GO:0003674"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05207":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"membrane grommet activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0180024","terms_by_termid":{"GO:0180024":null}}


id: PBO:0079904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquinol-cytochrome c reductase binding protein pseudogene 2","termid":"PBO:0079904"}


id: MONDO:0023054
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Klumpke paralysis is a type of brachial palsy in newborns. Signs and symptoms include weakness and loss of movement of the arm and hand. Some babies experience drooping of the eyelid on the opposite side of the face as well. This symptom may also be referred to as Horner syndrome. Klumpke paralysis is caused by an injury to the nerves of the brachial plexus which may result from a difficult delivery. This injury can cause a stretching (neuropraxia), tearing (called avulsion when the tear is at the spine, and rupture when it is not), or scarring (neuroma) of the brachial plexus nerves. Most infants with Klumpke paralysis have the more mild form of injury (neuropraxia) and often recover within 6 months.","definition_xrefs":["GARD:0003123"],"direct_ancestors":[{"relation_name":"is_a","term_name":"palsy","termid":"MONDO:0006496"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"klumpke's paralysis","secondary_identifiers":["SCTID:83886009","UMLS:C0270898","MEDGEN:124376","GARD:3123","NCIT:C116724"],"synonyms":[{"name":"Dejerine Klumpke Palsy","type":"related"},{"name":"Dejerine-Klumpke Palsy","type":"related"},{"name":"Dejerine-Klumpke palsy","type":"related"},{"name":"Klumpke Palsy","type":"related"},{"name":"Klumpke Paralysis","type":"related"},{"name":"Klumpke paralysis","type":"related"},{"name":"Klumpke's Palsy","type":"related"},{"name":"Klumpke's palsy","type":"related"},{"name":"Klumpke's paralysis","type":"related"},{"name":"Klumpke-DC)jerine brachial plexus injury","type":"related"},{"name":"Klumpke-DC)jerine paralysis","type":"related"},{"name":"Klumpke-Dejerine paralysis","type":"related"},{"name":"Klumpkes Palsy","type":"related"},{"name":"Lower Brachial Plexus Palsy","type":"related"},{"name":"Lower brachial plexus palsy","type":"related"},{"name":"Palsy, Dejerine-Klumpke","type":"related"},{"name":"Palsy, Klumpke's","type":"related"},{"name":"Paralysis of the Lower Brachial Plexus","type":"related"},{"name":"Paralysis, Klumpke","type":"related"},{"name":"klumpke paralysis","type":"related"},{"name":"klumpke's palsy","type":"related"},{"name":"klumpke's paralysis","type":"exact"},{"name":"klumpke-dC)jerine brachial plexus injury","type":"related"},{"name":"klumpke-dC)jerine paralysis","type":"exact"},{"name":"klumpke-dejerine paralysis","type":"related"}],"termid":"MONDO:0023054","xrefs":{"Monarch":{"xref_id":"0023054"}}}


id: FYPO:0008073
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the assembly of a RITS complex in the vegetative growth phase of the life cycle is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:19394293"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein complex assembly during vegetative growth","termid":"FYPO:0001215"}],"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 RITS complex assembly","termid":"FYPO:0008073"}


id: PBO:0066394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"receptor accessory protein 4","termid":"PBO:0066394"}


id: GO:0090226
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals in which a Ran GTPase relays a signal resulting in the modulation of the rate, frequency or extent of microtubule nucleation.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of microtubule nucleation by Ran protein signal transduction (obsolete GO:0090226)","termid":"GO:0090226"}


id: GO:1900870
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of tatiopterin.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pteridine-containing compound biosynthetic process","termid":"GO:0042559"},{"relation_name":"is_a","term_name":"carboxylic acid biosynthetic process","termid":"GO:0046394"},{"relation_name":"is_a","term_name":"tatiopterin metabolic process","termid":"GO:1900869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0042559"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0042559","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"tatiopterin biosynthetic process","synonyms":[{"name":"tatiopterin anabolism","type":"exact"},{"name":"tatiopterin biosynthesis","type":"exact"},{"name":"tatiopterin formation","type":"exact"},{"name":"tatiopterin synthesis","type":"exact"}],"termid":"GO:1900870"}


id: PATO:0000038
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000038 gel consistency (obsolete PATO:0000038)","termid":"PATO:0000038"}


id: PBO:0064886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 2 regulatory subunit Balpha","termid":"PBO:0064886"}


id: PR:O94393
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 26S proteasome non-ATPase regulatory subunit 9 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02190","PANTHER:PTHR12651:SF0"],"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 p27 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2H10.02c","secondary_identifiers":["UniProtKB:O94393"],"synonyms":[{"name":"Spom972h-PSMD9","type":"exact"}],"termid":"PR:O94393"}


id: FYPO:0005103
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetatively growing cell is elongated, and is curved along the long axis. In a curved cell, the long axis follows a smooth bend rather than a straight line.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"curved vegetative cell","termid":"FYPO:0000016"},{"relation_name":"has_part","term_name":"elongated vegetative cell","termid":"FYPO:0001122"},{"relation_name":"is_a","term_name":"curved vegetative cell","termid":"FYPO:0000016"},{"relation_name":"is_a","term_name":"elongated vegetative cell","termid":"FYPO:0001122"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"curved elongated vegetative cell","synonyms":[{"name":"curved elongated cell","type":"exact"},{"name":"curved elongated cell during vegetative growth","type":"exact"},{"name":"curved elongated vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0005103"}


id: PBO:0074286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLIT and NTRK like family member 1","termid":"PBO:0074286"}


id: GO:0008202
data:
  {"annotated_genes":["SJAG_04810","SJAG_02719","SJAG_03235","SJAG_03018","SJAG_02068","SJAG_03024","SJAG_00453","SJAG_04018","SJAG_03715","SJAG_00717","SJAG_04270","SJAG_03598","SJAG_00413","SJAG_01307","SJAG_02044","SJAG_04499","SJAG_01474","SJAG_03249","SJAG_03750","SJAG_02291","SJAG_03531","SJAG_00370","SJAG_04059","SJAG_04217","SJAG_04049","SJAG_02104","SJAG_04124","SJAG_02855","SJAG_00158","SJAG_00770","SJAG_00624","SJAG_01326","SJAG_04790","SJAG_00261","SJAG_03929","SJAG_03509","SJAG_02982"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[62344,101563,117282],"is_not":false,"summary":null,"term":"GO:0008202"},{"annotations":[74031,75930,69634,89418,108997,109835,79932,107283,73753,88234,107596,71344,80016,71520,94394,114975,116285,72917,70596,65653,76006,80151,76913,76103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006696"},{"annotations":[103107,79980,76023,114816,103751],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008204"},{"annotations":[93645],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0010895"},{"annotations":[109600],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0070452"},{"annotations":[75359],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0045540"},{"annotations":[105603,88324],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032443"},{"annotations":[71775],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016125"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving steroids, compounds with a 1,2,cyclopentanoperhydrophenanthrene nucleus.","definition_xrefs":["ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid metabolic process","termid":"GO:0006629"}],"gene_count":37,"genes_by_uniquename":{"SJAG_00158":null,"SJAG_00261":null,"SJAG_00370":null,"SJAG_00413":null,"SJAG_00453":null,"SJAG_00624":null,"SJAG_00717":null,"SJAG_00770":null,"SJAG_01307":null,"SJAG_01326":null,"SJAG_01474":null,"SJAG_02044":null,"SJAG_02068":null,"SJAG_02104":null,"SJAG_02291":null,"SJAG_02719":null,"SJAG_02855":null,"SJAG_02982":null,"SJAG_03018":null,"SJAG_03024":null,"SJAG_03235":null,"SJAG_03249":null,"SJAG_03509":null,"SJAG_03531":null,"SJAG_03598":null,"SJAG_03715":null,"SJAG_03750":null,"SJAG_03929":null,"SJAG_04018":null,"SJAG_04049":null,"SJAG_04059":null,"SJAG_04124":null,"SJAG_04217":null,"SJAG_04270":null,"SJAG_04499":null,"SJAG_04790":null,"SJAG_04810":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"steroid metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Steroid_metabolism","Reactome:R-HSA-8957322"],"synonyms":[{"name":"steroid metabolism","type":"exact"}],"termid":"GO:0008202","terms_by_termid":{"GO:0006696":null,"GO:0008202":null,"GO:0008204":null,"GO:0010895":null,"GO:0016125":null,"GO:0032443":null,"GO:0045540":null,"GO:0070452":null}}


id: PR:P78847
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A nuclear pore complex protein Nup205 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04901","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":"nucleoporin nup186 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC290.03c","secondary_identifiers":["UniProtKB:P78847"],"synonyms":[{"name":"Spom972h-NUP205","type":"exact"},{"name":"nuclear pore protein nup186 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P78847"}


id: PBO:0059072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"molybdenum cofactor synthesis 2","termid":"PBO:0059072"}


id: GO:0102187
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4alpha-carboxy,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-cholest-24-en-3beta-ol + NAD(1-) = 4alpha,14alpha-dimethyl-9beta,19-cyclo-5alpha-cholest-24-en-3-one + NADH(2-) + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 4alpha-carboxy,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-cholest-24-en-3beta-ol dehydrogenase/C4-decarboxylase activity (obsolete GO:0102187)","termid":"GO:0102187"}


id: PBO:0026883
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_chromatin_binding_during_cellular_response_to_nitrogen_starvation","termid":"PBO:0026883"}


id: GO:0048198
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which cytosolic coat proteins fit together in a basketlike convex framework to form a coated deformed region on the cytoplasmic surface of the membrane. The deformed region forms into a complete vesicle and is released.","definition_xrefs":["PMID:10219233","GOC:jid","ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane organization","termid":"GO:0061024"},{"relation_name":"part_of","term_name":"Golgi vesicle budding","termid":"GO:0048194"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0016192","GO:0061024"],"is_obsolete":false,"name":"Golgi vesicle bud deformation and release","synonyms":[{"name":"Golgi-derived vesicle bud deformation and release","type":"exact"},{"name":"dictyosome vesicle bud deformation","type":"narrow"}],"termid":"GO:0048198"}


id: MONDO:0012753
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the ANG gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"amyotrophic lateral sclerosis type 9","secondary_identifiers":["OMIM:611895","MEDGEN:395629","DOID:0060200","UMLS:C2678468","MESH:C567499","GARD:10498"],"synonyms":[{"name":"ALS9","type":"exact"},{"name":"ANG amyotrophic lateral sclerosis","type":"exact"},{"name":"amyotrophic lateral sclerosis 9","type":"exact"},{"name":"amyotrophic lateral sclerosis caused by mutation in ANG","type":"exact"},{"name":"amyotrophic lateral sclerosis type 9","type":"exact"}],"termid":"MONDO:0012753","xrefs":{"Monarch":{"xref_id":"0012753"}}}


id: GO:0015624
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + ferric-enterobactin(out) = ADP + phosphate + ferric-enterobactin(in).","definition_xrefs":["RHEA:58492"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"},{"relation_name":"is_a","term_name":"iron chelate transmembrane transporter activity","termid":"GO:0015603"},{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"ABC-type ferric-enterobactin transporter activity","secondary_identifiers":["EC:7.2.2.17","MetaCyc:ABC-10-RXN"],"synonyms":[{"name":"ATP-dependent ferric-enterobactin transmembrane transporter activity","type":"exact"},{"name":"ATPase-coupled ferric-enterobactin transmembrane transporter activity","type":"related"},{"name":"ferric-enterobactin ABC transporter","type":"exact"},{"name":"ferric-enterobactin porter activity","type":"broad"},{"name":"ferric-enterobactin-transporting ATPase activity","type":"related"}],"termid":"GO:0015624"}


id: PBO:0038446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AAR2 splicing factor","termid":"PBO:0038446"}


id: PR:P87154
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA polymerase epsilon catalytic subunit A that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03630","PANTHER:PTHR10670:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase epsilon catalytic subunit A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC25H2.13c","secondary_identifiers":["UniProtKB:P87154"],"synonyms":[{"name":"DNA polymerase II subunit A (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-POLE","type":"exact"}],"termid":"PR:P87154"}


id: FYPO:0003448
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is viable, is shaped in the form of a spheroid, has a larger volume than normal, and in which vacuoles are more visible (usually by microscopy) than normal. In a swollen cell, both length and diameter may be greater than normal, although the cell is only considered elongated if the length:diameter ratio is also greater than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"vacuolated","termid":"FYPO:0001581"},{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"},{"relation_name":"is_a","term_name":"viable swollen spheroid vegetative cell","termid":"FYPO:0004559"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0000004","FYPO:0000005"],"is_obsolete":false,"name":"viable swollen vacuolated spheroid vegetative cell","synonyms":[{"name":"viable enlarged vacuolated spheroid vegetative cell","type":"related"},{"name":"viable enlarged volume vacuolated spheroid vegetative cell","type":"exact"},{"name":"viable large vacuolated spheroid vegetative cell","type":"related"},{"name":"viable swollen rounded vacuolated vegetative cell","type":"exact"},{"name":"viable swollen vacuolated spheroid cell during vegetative growth","type":"exact"},{"name":"viable swollen vacuolated spheroid vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0003448"}


id: PBO:0039286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALG1 like 15, pseudogene","termid":"PBO:0039286"}


id: PBO:0112850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"asynchronous replication autosomal RNA 9-3","termid":"PBO:0112850"}


id: PBO:0028627
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_microtubule_cytoskeleton_morphology_during_mitotic_interphase","termid":"PBO:0028627"}


id: MONDO:0019980
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bilateral renal hypoplasia is a form of renal hypoplasia, a renal developmental anomaly in which both kidneys are small and have a deficit in the number of nephrons present.","definition_xrefs":["Orphanet:97362"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal hypoplasia","termid":"MONDO:0019637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"renal hypoplasia, bilateral","secondary_identifiers":["ICD10CM:Q60.4","GARD:19374","MEDGEN:609099","SCTID:268232000","UMLS:C0431692"],"termid":"MONDO:0019980","xrefs":{"Monarch":{"xref_id":"0019980"}}}


id: PBO:0111922
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vezatin family","termid":"PBO:0111922"}


id: FYPO:0000126
data:
  {"alleles_by_uniquename":{"SJAG_00610:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00610","name":"pck2delta","uniquename":"SJAG_00610:allele-1"},"SJAG_01787:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01787","name":"pck1delta","uniquename":"SJAG_01787:allele-1"},"SJAG_04551:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04551","name":"pmk1delta","uniquename":"SJAG_04551:allele-1"},"SJAG_04551:allele-2":{"allele_type":"amino_acid_insertion","description":"82-NITCIYDLDIIINPYNFNEVYIYEE-105","gene_uniquename":"SJAG_04551","name":"Pmk1Sj(ins82-105)","uniquename":"SJAG_04551:allele-2"},"SJAG_04551:allele-3":{"allele_type":"other","description":"Pmk1 from S. pombe","gene_uniquename":"SJAG_04551","name":"Pmk1Sp","uniquename":"SJAG_04551:allele-3"},"SJAG_04551:allele-4":{"allele_type":"partial_amino_acid_deletion","description":"Pmk1 from S. pombe with deleted residues 82-105","gene_uniquename":"SJAG_04551","name":"Pmk1Sp(delta82-105)","uniquename":"SJAG_04551:allele-4"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118900],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0005152"},{"annotations":[118918,118921,118913,118892,118907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007521"}]},"cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased resistance to a chemical stimulus. Resistance to a chemical is usually measured by determining the maximum concentration of the chemical at which a population of cells grow and divide, and cells are deemed resistant to a chemical if they survive at a concentration of the chemical that does not allow wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vegetative cell population growth","termid":"FYPO:0001356"},{"relation_name":"is_a","term_name":"increased resistance to chemical","termid":"FYPO:0002682"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00610":null,"SJAG_01787":null,"SJAG_04551":null},"genotype_count":6,"genotypes_by_uniquename":{"Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sj(ins82-105)(82-NITCIYDLDIIINPYNFNEVYIYEE-105)","display_uniquename":"Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-2","expression":"Not assayed or wild type"}]}]},"Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sp(delta82-105)(Pmk1 from S. pombe with deleted residues 82-105 Δaa)","display_uniquename":"Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-4","expression":"Not assayed or wild type"}]}]},"Pmk1Sp-Pmk1_from_S._pombe-other-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sp(Pmk1 from S. pombe)","display_uniquename":"Pmk1Sp-Pmk1_from_S._pombe-other-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-3","expression":"Not assayed or wild type"}]}]},"pck1delta":{"display_name":"pck1delta","display_uniquename":"pck1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01787:allele-1","expression":"Null"}]}]},"pck2delta":{"display_name":"pck2delta","display_uniquename":"pck2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00610:allele-1","expression":"Null"}]}]},"pmk1delta":{"display_name":"pmk1delta","display_uniquename":"pmk1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002682"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002682","FYPO:0001985","FYPO:0000139","FYPO:0005447"],"is_obsolete":false,"name":"increased resistance to chemical during vegetative growth","references_by_uniquename":{"PMID:34198697":null},"single_locus_annotated_genes":["SJAG_04551","SJAG_00610","SJAG_01787"],"single_locus_genotype_uniquenames":["Pmk1Sp-Pmk1_from_S._pombe-other-expression-not_assayed_or_wild_type","pmk1delta","pck2delta","Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type","Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","pck1delta"],"synonyms":[{"name":"increased resistance to chemical during mitotic cell cycle","type":"related"},{"name":"resistance to chemicals: increased during vegetative growth","type":"exact"},{"name":"resistant to chemical during vegetative growth","type":"exact"}],"termid":"FYPO:0000126","terms_by_termid":{"FYPO:0005152":null,"FYPO:0007521":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: FYPO:0007662
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the kinetochore of a chromosome does not occur during anaphase of the first meiotic nuclear division.","definition_xrefs":["PMID:11331883","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to kinetochore during meiosis I","termid":"FYPO:0004763"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"abolished protein localization to kinetochore during meiotic anaphase I","synonyms":[{"name":"abolished protein localisation to kinetochore during meiotic anaphase I","type":"exact"},{"name":"abolished protein localization to kinetochore during meiosis I anaphase","type":"exact"}],"termid":"FYPO:0007662"}


id: GO:1904679
data:
  {"annotated_genes":["SJAG_04506","SJAG_03595"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71898,72719],"is_not":false,"summary":null,"term":"GO:1904679"}]},"cv_name":"biological_process","definition":"The directed movement of myo-inositol from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["PMID:9560432","GO_REF:0000075","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyol transmembrane transport","termid":"GO:0015791"},{"relation_name":"is_a","term_name":"myo-inositol transport","termid":"GO:0015798"},{"relation_name":"is_a","term_name":"import across plasma membrane","termid":"GO:0098739"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03595":null,"SJAG_04506":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"myo-inositol import across plasma membrane","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["GO:0097357"],"synonyms":[{"name":"myo-inositol import into cell","type":"exact"}],"termid":"GO:1904679","terms_by_termid":{"GO:1904679":null}}


id: MONDO:0850095
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"aortic disorder","termid":"MONDO:0005561"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked severe syndromic thoracic aortic aneurysm and dissection","secondary_identifiers":["Orphanet:622925","GARD:22490"],"termid":"MONDO:0850095","xrefs":{"Monarch":{"xref_id":"0850095"}}}


id: MONDO:0011134
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Curry-Jones syndrome is a form of syndromic craniosynostosis, characterized by unilateral coronal craniosynostosis or multiple suture synostosis associated with complete or partial agenesis of the corpus callosum, preaxial polysyndactyly and syndactyly of hands and/or feet, along with anomalies of the skin (characteristic pearly white areas that become scarred and atrophic, abnormal hair growth around the eyes and/or cheeks, and on the limbs), eyes (iris colobomas, microphthalmia,) and intestine (congenital short gut, malrotation, dysmotility, chronic constipation, bleeding and myofibromas). Developmental delay and variable degrees of intellectual disability may also be observed. Multiple intra-abdominal smooth muscle hamartomas, trichoblastoma of the skin, occipital meningoceles and development of desmoplastic medulloblastoma have been reported.","definition_xrefs":["Orphanet:1553"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"},{"relation_name":"is_a","term_name":"mosaic SMO syndrome","termid":"MONDO:1030005"}],"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":"Curry-Jones syndrome","secondary_identifiers":["GARD:5584","MESH:C536735","SCTID:720819006","UMLS:C0795915","OMIM:601707","MEDGEN:167083"],"synonyms":[{"name":"CRJS","type":"related"},{"name":"Curry-Jones syndrome, somatic mosaic","type":"exact"},{"name":"corpus callosum agenesis polysyndactyly","type":"related"},{"name":"corpus callosum agenesis-polysyndactyly syndrome","type":"exact"},{"name":"craniofacial malformations, asymmetric, with polysyndactyly and abnormal skin and gut development","type":"related"},{"name":"curry Jones syndrome","type":"related"},{"name":"curry-JONES syndrome","type":"related"},{"name":"curry-Jones syndrome","type":"exact"}],"termid":"MONDO:0011134","xrefs":{"Monarch":{"xref_id":"0011134"}}}


id: PBO:0084733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial inorganic pyrophosphatase; required for mitochondrial function and possibly involved in energy generation from inorganic pyrophosphate; human ortholog, PPA2, functionally complements the null mutant; mutations in human PPA2 cause a mitochondrial disease resulting in sudden unexpected cardiac arrest in infants","termid":"PBO:0084733"}


id: PBO:0090799
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAGA complex/ASTRA complex, phosphatidylinositol pseudokinase Tra1","termid":"PBO:0090799"}


id: MONDO:0060549
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":"congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay","secondary_identifiers":["DOID:0112359","MEDGEN:1612119","OMIM:617641","Orphanet:656130","UMLS:C4539968"],"synonyms":[{"name":"CAKUTHED","type":"related"},{"name":"congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay","type":"exact"}],"termid":"MONDO:0060549","xrefs":{"Monarch":{"xref_id":"0060549"}}}


id: PBO:0111464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA N1-methyladenine (m1A58) demethylase","termid":"PBO:0111464"}


id: MONDO:1011657
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease, non-human animal","termid":"MONDO:1011360"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"goldenhar syndrome, non-human animal","secondary_identifiers":["OMIA:002136"],"termid":"MONDO:1011657","xrefs":{"Monarch":{"xref_id":"1011657"}}}


id: PBO:0065849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB11 family interacting protein 1","termid":"PBO:0065849"}


id: MONDO:0005316
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection caused by bacterial overgrowth in the vagina. Most affected women are asymptomatic. When symptoms occur, they include foul-smelling vaginal discharge, vaginal itching, and burning. Risk factors include sexual activity with multiple partners and the use of vaginal douches and intrauterine devices. Up to a third of cases resolve without treatment. Antibiotic treatment is recommended when symptoms are present and for women that are pregnant at the time of infection.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Bifidobacteriales infectious disease","termid":"MONDO:0006706"},{"relation_name":"is_a","term_name":"infective vaginitis","termid":"MONDO:0023557"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bacterial vaginosis","secondary_identifiers":["NCIT:C116973","icd11.foundation:63323819","UMLS:C0085166","DOID:3385","MESH:D016585","SCTID:419760006","EFO:0003932","MEDGEN:43118"],"synonyms":[{"name":"BV","type":"broad"}],"termid":"MONDO:0005316","xrefs":{"Monarch":{"xref_id":"0005316"}}}


id: PBO:0076812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TEN1-CDK3 readthrough (NMD candidate)","termid":"PBO:0076812"}


id: PBO:0057027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 124-3","termid":"PBO:0057027"}


id: MONDO:8000000
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infection of the intervertebral disk space.","definition_xrefs":["PMID:27070599"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vertebral joint disorder","termid":"MONDO:0037847"},{"relation_name":"is_a","term_name":"infective arthritis","termid":"MONDO:0042485"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infectious discitis","secondary_identifiers":["EFO:1000900"],"termid":"MONDO:8000000","xrefs":{"Monarch":{"xref_id":"8000000"}}}


id: GO:0071408
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 cycloalkane stimulus. A cycloalkane is a cyclic saturated hydrocarbon having the general formula CnH2n.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cycloalkane","termid":"GO:0014071"},{"relation_name":"is_a","term_name":"cellular response to chemical stimulus","termid":"GO:0070887"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to cycloalkane","termid":"GO:0071408"}


id: GO:0090667
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a motile cell in response to the presence of vascular endothelial growth factor (VEGF).","definition_xrefs":["GOC:BHF","GOC:BHF_miRNA","GOC:rph","PMID:21885851"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell chemotaxis","termid":"GO:0060326"},{"relation_name":"part_of","term_name":"cellular response to vascular endothelial growth factor stimulus","termid":"GO:0035924"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell chemotaxis to vascular endothelial growth factor","termid":"GO:0090667"}


id: GO:1905282
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of epidermal growth factor receptor signaling pathway involved in heart process.","definition_xrefs":["GOC:TermGenie","PMID:23069713","GOC:BHF_miRNA","GOC:BHF","GOC:bc","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epidermal growth factor receptor signaling pathway","termid":"GO:0042058"},{"relation_name":"regulates","term_name":"epidermal growth factor receptor signaling pathway involved in heart process","termid":"GO:1905251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of epidermal growth factor receptor signaling pathway involved in heart process","synonyms":[{"name":"regulation of EGF receptor signaling pathway involved in cardiac process","type":"related"},{"name":"regulation of EGF receptor signaling pathway involved in heart process","type":"exact"},{"name":"regulation of EGF receptor signalling pathway involved in cardiac process","type":"related"},{"name":"regulation of EGF receptor signalling pathway involved in heart process","type":"exact"},{"name":"regulation of EGFR signaling pathway involved in cardiac process","type":"related"},{"name":"regulation of EGFR signaling pathway involved in heart process","type":"exact"},{"name":"regulation of ERBB1 signaling pathway involved in cardiac process","type":"related"},{"name":"regulation of ERBB1 signaling pathway involved in heart process","type":"exact"},{"name":"regulation of epidermal growth factor receptor signaling pathway involved in cardiac process","type":"related"},{"name":"regulation of epidermal growth factor receptor signalling pathway involved in cardiac process","type":"related"},{"name":"regulation of epidermal growth factor receptor signalling pathway involved in heart process","type":"exact"},{"name":"regulation of receptor tyrosine-protein kinase erbB-1 signaling pathway involved in cardiac process","type":"related"},{"name":"regulation of receptor tyrosine-protein kinase erbB-1 signaling pathway involved in heart process","type":"exact"}],"termid":"GO:1905282"}


id: PBO:0048299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growth associated protein 43","termid":"PBO:0048299"}


id: GO:0048883
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The migration of a cluster of a relatively undifferentiated cell originating at specific cephalic placodes and depositing proneuromasts along a developing lateral line, from which the neuromasts will develop.","definition_xrefs":["PMID:15018940","PMID:15832385"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell migration","termid":"GO:0016477"},{"relation_name":"part_of","term_name":"lateral line development","termid":"GO:0048882"}],"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":"neuromast primordium migration","synonyms":[{"name":"lateral line primordium migration","type":"exact"}],"termid":"GO:0048883"}


id: PBO:0072117
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S14 pseudogene 6","termid":"PBO:0072117"}


id: MONDO:0004157
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pancreatic mucinous cystadenoma (obsolete MONDO:0004157)","termid":"MONDO:0004157","xrefs":{"Monarch":{"xref_id":"0004157"}}}


id: PBO:0005565
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetylornithine aminotransferase","termid":"PBO:0005565"}


id: PBO:0071758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein lateral stalk subunit P1 pseudogene 5","termid":"PBO:0071758"}


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: SO:0001643
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A telomerase RNA gene is a non coding RNA gene the RNA product of which is a component of telomerase.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ncRNA_gene","termid":"SO:0001263"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"telomerase_RNA_gene","secondary_identifiers":["http:http\\://en.wikipedia.org/wiki/Telomerase_RNA_component"],"synonyms":[{"name":"TERC","type":"exact"},{"name":"Telomerase RNA component","type":"exact"},{"name":"telomerase RNA gene","type":"exact"}],"termid":"SO:0001643"}


id: PBO:0079672
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 V2 pseudogene 2","termid":"PBO:0079672"}


id: MOD:01160
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively results in the loss of an ammonia, usually by a process of vicinal dehydration, rearrangement, and rehydration with release of ammonia, resulting in a loss of nitrogen with no gain of oxygen.","definition_xrefs":["Unimod:385"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by chemical process","termid":"MOD:01156"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deaminated residue","synonyms":[{"name":"Ammonia-loss","type":"related"},{"name":"Loss of ammonia","type":"related"}],"termid":"MOD:01160"}


id: FYPO:0002654
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 exocytic vesicles are larger than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"enlarged exocytic vesicles","synonyms":[{"name":"enlarged exocytic vesicles during mitotic cell cycle","type":"related"},{"name":"enlarged exocytic vesicles during vegetative growth","type":"exact"}],"termid":"FYPO:0002654"}


id: PBO:0002765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ESCRT I complex subunit Vps28","termid":"PBO:0002765"}


id: GO:0052570
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. 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 reactive oxygen species produced as part of the defense response of the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete response to defense-related symbiont reactive oxygen species production (obsolete GO:0052570)","synonyms":[{"name":"response to defense-related symbiont reactive oxygen species production","type":"exact"}],"termid":"GO:0052570"}


id: GO:1901026
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of ripoptosome components leading to a necroptotic process.","definition_xrefs":["GOC:mtg_apoptosis","GOC:TermGenie","PMID:22274400"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ripoptosome assembly","termid":"GO:0097343"},{"relation_name":"part_of","term_name":"necroptotic process","termid":"GO:0070266"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"ripoptosome assembly involved in necroptotic process","synonyms":[{"name":"ripoptosome assembly involved in necroptosis","type":"narrow"}],"termid":"GO:1901026"}


id: PBO:0090110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA(Ser) Um(44) 2'-O-methyltransferasetRNA Trm44","termid":"PBO:0090110"}


id: PBO:0034757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP-2 adaptor complex alpha subunit Alp3","termid":"PBO:0034757"}


id: FYPO:0006275
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which pyknosis, the form of chromatin condensation typical of cell death by apoptosis, occurs at a greater frequency than normal when the population in which the cell is found is in stationary phase.","definition_xrefs":["PomBase:mah","GO:0030263","PMID:18653539"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal apoptotic process","termid":"FYPO:0000629"}],"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"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased pyknosis during stationary phase","synonyms":[{"name":"increased apoptotic chromosome condensation during stationary phase","type":"exact"}],"termid":"FYPO:0006275"}


id: PATO:0000547
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A photosensitivity quality inhering in a bearer by virtue of the bearer's exhibiting photosensitivity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"photosensitivity","termid":"PATO:0000927"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"photosensitive","termid":"PATO:0000547"}


id: GO:0000702
data:
  {"annotated_genes":["SJAG_01119","SJAG_02261","SJAG_03724"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[95902],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034042"},{"annotations":[95903],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034043"},{"annotations":[73465,95904,73911],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034039"}]},"cv_name":"molecular_function","definition":"Catalysis of the removal of oxidized bases by cleaving the N-C1' glycosidic bond between the target damaged DNA base and the deoxyribose sugar. The reaction releases a free base and leaves an apurinic/apyrimidinic (AP) site.","definition_xrefs":["PMID:11554296","GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA N-glycosylase activity","termid":"GO:0019104"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01119":null,"SJAG_02261":null,"SJAG_03724":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016798","GO:0003824","GO:0140097","GO:0016787"],"is_obsolete":false,"name":"oxidized base lesion DNA N-glycosylase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0000702","terms_by_termid":{"GO:0034039":null,"GO:0034042":null,"GO:0034043":null}}


id: PBO:0049569
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2B histone pseudogene 6","termid":"PBO:0049569"}


id: PBO:0060136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND6 pseudogene 37","termid":"PBO:0060136"}


id: MONDO:1012556
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitral valve dysplasia, non-human animal","termid":"MONDO:1011652"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitral valve dysplasia, ass","secondary_identifiers":["OMIA:002521-9793"],"termid":"MONDO:1012556","xrefs":{"Monarch":{"xref_id":"1012556"}}}


id: PBO:0004531
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.3.1.15","termid":"PBO:0004531"}


id: FYECO:0000099
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Recovery from nitrogen starvation: cells are first grown in minimal medium containing no nitrogen for 72h-7days. This medium is then replaced with nitrogen containing rich medium and cells are allowed to grow for 4-7 days.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrogen starvation and recovery","termid":"FYECO:0000110"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"72h-7days nitrogen starvation followed by 4-7 days recovery in rich medium","termid":"FYECO:0000099"}


id: MONDO:0002627
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An osteosarcoma characterized by the presence of atypical cartilage of variable cellularity. It may or may not be associated with the presence of myxoid areas or focal bone formation.","definition_xrefs":["NCIT:C4021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"conventional osteosarcoma","termid":"MONDO:0002631"}],"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":"chondroblastic osteosarcoma","secondary_identifiers":["UMLS:C0279603","ONCOTREE:CHOS","ICDO:9181/3","DOID:3372","MEDGEN:79013"],"synonyms":[{"name":"CHOS","type":"related"},{"name":"chondroblastic osteogenic sarcoma","type":"exact"},{"name":"chondroblastic osteosarcoma","type":"exact"},{"name":"chondroblastic osteosarcoma (morphologic abnormality)","type":"exact"},{"name":"chondrosarcomatous osteogenic sarcoma","type":"exact"}],"termid":"MONDO:0002627","xrefs":{"Monarch":{"xref_id":"0002627"}}}


id: GO:0032356
data:
  {"annotated_genes":["SJAG_02261"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73464],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032357"}]},"cv_name":"molecular_function","definition":"Binding to a DNA region containing an oxidized residue.","definition_xrefs":["GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"damaged DNA binding","termid":"GO:0003684"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02261":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003677","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"oxidized DNA binding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"oxidised DNA binding","type":"exact"}],"termid":"GO:0032356","terms_by_termid":{"GO:0032357":null}}


id: PBO:0017710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase involved in depalmitoylation (predicted)","termid":"PBO:0017710"}


id: PBO:0089051
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methyltransferase with rhodanese domain, unknown specificity","termid":"PBO:0089051"}


id: MONDO:0003711
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete malignant peripheral nerve sheath tumor (obsolete MONDO:0003711)","termid":"MONDO:0003711","xrefs":{"Monarch":{"xref_id":"0003711"}}}


id: PBO:0091554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4-alpha-hydroxytetrahydrobiopterin dehydratase","termid":"PBO:0091554"}


id: PBO:0059932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND2 pseudogene 18","termid":"PBO:0059932"}


id: PBO:0065391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostate enriched lncRNA","termid":"PBO:0065391"}


id: SO:0000685
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"DNA region representing open chromatin structure that is hypersensitive to digestion by DNase I.","direct_ancestors":[{"relation_name":"is_a","term_name":"nuclease_hypersensitive_site","termid":"SO:0000322"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNaseI_hypersensitive_site","synonyms":[{"name":"DHS","type":"exact"},{"name":"DNaseI hypersensitive site","type":"exact"},{"name":"INSDC_feature:regulatory","type":"broad"},{"name":"INSDC_qualifier:DNase_I_hypersensitive_site","type":"exact"}],"termid":"SO:0000685"}


id: GO:0042596
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The response of an organism to a perceived external threat.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal response to stress","termid":"GO:0033555"}],"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":"fear response","secondary_identifiers":["GO:0001663"],"synonyms":[{"name":"physiological fear response","type":"exact"}],"termid":"GO:0042596"}


id: GO:0030398
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The controlled breakdown of the membranes of cargo-carrying vesicles formed during peroxisome degradation.","definition_xrefs":["GOC:mah","PMID:11382760"],"gene_count":0,"genotype_count":0,"name":"obsolete peroxisomal membrane disassembly (obsolete GO:0030398)","synonyms":[{"name":"peroxisomal membrane breakdown","type":"exact"},{"name":"peroxisomal membrane catabolism","type":"exact"},{"name":"peroxisomal membrane degradation","type":"exact"}],"termid":"GO:0030398"}


id: PBO:0054818
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 2231","termid":"PBO:0054818"}


id: PBO:0066166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding fox-1 homolog 3","termid":"PBO:0066166"}


id: GO:0018010
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: palmitoyl-CoA + glycoprotein = CoA + N-palmitoylglycoprotein.","definition_xrefs":["EC:2.3.1.96"],"gene_count":0,"genotype_count":0,"name":"obsolete glycoprotein N-palmitoyltransferase activity (obsolete GO:0018010)","synonyms":[{"name":"mucus glycoprotein fatty acyltransferase","type":"narrow"},{"name":"palmitoyl-CoA:glycoprotein N-palmitoyltransferase activity","type":"related"}],"termid":"GO:0018010"}


id: PBO:0031457
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_N-ethylmaleimide","termid":"PBO:0031457"}


id: GO:0006490
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of an oligosaccharide-lipid intermediate, such as a molecule of dolichol-P-man or dolicol-P-Glc used in N-linked glycosylation.","definition_xrefs":["GOC:isa_complete","GOC:pr","GOC:hjd","GOC:rb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete oligosaccharide-lipid intermediate biosynthetic process (obsolete GO:0006490)","synonyms":[{"name":"oligosaccharide-lipid intermediate assembly","type":"narrow"}],"termid":"GO:0006490"}


id: MONDO:0032793
data:
  {"annotated_genes":["SJAG_04396"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86731],"is_not":false,"summary":null,"term":"MONDO:0032793"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04396":null},"genotype_count":0,"is_obsolete":false,"name":"O'Donnell-Luria-Rodan syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1677602","UMLS:C5193138","OMIM:618512"],"synonyms":[{"name":"O'Donnell-Luria-Rodan syndrome","type":"exact"},{"name":"ODLURO","type":"related"}],"termid":"MONDO:0032793","terms_by_termid":{"MONDO:0032793":null},"xrefs":{"Monarch":{"xref_id":"0032793"}}}


id: GO:0002891
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of an immunoglobulin mediated immune response.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of B cell mediated immunity","termid":"GO:0002714"},{"relation_name":"is_a","term_name":"regulation of immunoglobulin mediated immune response","termid":"GO:0002889"},{"relation_name":"positively_regulates","term_name":"immunoglobulin mediated immune response","termid":"GO:0016064"}],"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 immunoglobulin mediated immune response","synonyms":[{"name":"activation of immunoglobulin mediated immune response","type":"narrow"},{"name":"stimulation of immunoglobulin mediated immune response","type":"narrow"},{"name":"up regulation of immunoglobulin mediated immune response","type":"exact"},{"name":"up-regulation of immunoglobulin mediated immune response","type":"exact"},{"name":"upregulation of immunoglobulin mediated immune response","type":"exact"}],"termid":"GO:0002891"}


id: FYPO:0003029
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of mRNA splicing via the spliceosome is decreased.","definition_xrefs":["PMID:24298023","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mRNA splicing, via spliceosome","termid":"FYPO:0000189"},{"relation_name":"is_a","term_name":"decreased RNA splicing","termid":"FYPO:0003040"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0006551","FYPO:0000294","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased mRNA splicing, via spliceosome","synonyms":[{"name":"decreased mRNA splicing, via spliceosome during mitotic cell cycle","type":"related"},{"name":"decreased mRNA splicing, via spliceosome during vegetative growth","type":"exact"},{"name":"decreased nuclear mRNA splicing, via spliceosome","type":"exact"},{"name":"decreased splicing","type":"broad"},{"name":"reduced mRNA splicing, via spliceosome","type":"exact"}],"termid":"FYPO:0003029"}


id: MONDO:0020165
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete syndromic epicanthus (obsolete MONDO:0020165)","secondary_identifiers":["Orphanet:98574"],"termid":"MONDO:0020165","xrefs":{"Monarch":{"xref_id":"0020165"}}}


id: GO:0086027
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that mediates the transfer of information from an AV node cardiac muscle cell to a bundle of His cardiomyocyte.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell signaling involved in cardiac conduction","termid":"GO:0086019"},{"relation_name":"is_a","term_name":"AV node cell to bundle of His cell communication","termid":"GO:0086067"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"AV node cell to bundle of His cell signaling","synonyms":[{"name":"AV node cell to bundle of His cell signalling","type":"exact"},{"name":"atrioventricular node to bundle of His cell signaling","type":"exact"}],"termid":"GO:0086027"}


id: GO:0008742
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-ribulose 5-phosphate = D-xylulose 5-phosphate.","definition_xrefs":["RHEA:22368","EC:5.1.3.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"racemase and epimerase activity, acting on carbohydrates and derivatives","termid":"GO:0016857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016853"],"is_obsolete":false,"name":"L-ribulose-phosphate 4-epimerase activity","secondary_identifiers":["KEGG_REACTION:R05850","MetaCyc:RIBULPEPIM-RXN"],"synonyms":[{"name":"AraD","type":"related"},{"name":"L-Ru5P","type":"related"},{"name":"L-ribulose 5-phosphate 4-epimerase activity","type":"related"},{"name":"L-ribulose-5-phosphate 4-epimerase","type":"broad"},{"name":"L-ru5P activity","type":"related"},{"name":"phosphoribulose isomerase activity","type":"related"},{"name":"ribulose phosphate 4-epimerase activity","type":"related"}],"termid":"GO:0008742"}


id: PBO:0032708
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_error-prone_translesion_synthesis_of_pyrimidine-pyrimidone_6-4_photoproducts","termid":"PBO:0032708"}


id: PBO:0061011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicolin 1, tubulin polyglutamylase complex subunit","termid":"PBO:0061011"}


id: MONDO:0018956
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic bronchiectasis (IB) is a progressive lung disease characterized by chronic dilation of the bronchi and destruction of the bronchial walls in the absence of any underlying cause (such as post infectious disease, aspiration, immunodeficiency, congenital abnormalities and ciliary anomalies).","definition_xrefs":["Orphanet:60033"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bronchiectasis","termid":"MONDO:0004822"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"idiopathic bronchiectasis","secondary_identifiers":["GARD:16664","SCTID:233629001","MEDGEN:573462","UMLS:C0339985"],"termid":"MONDO:0018956","xrefs":{"Monarch":{"xref_id":"0018956"}}}


id: PBO:0031815
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_autophagy","termid":"PBO:0031815"}


id: GO:2000675
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of type B pancreatic cell apoptotic process.","definition_xrefs":["GOC:obol","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of epithelial cell apoptotic process","termid":"GO:1904036"},{"relation_name":"is_a","term_name":"regulation of type B pancreatic cell apoptotic process","termid":"GO:2000674"},{"relation_name":"negatively_regulates","term_name":"type B pancreatic cell apoptotic process","termid":"GO:0097050"}],"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 type B pancreatic cell apoptotic process","synonyms":[{"name":"negative regulation of pancreatic B cell apoptosis","type":"exact"},{"name":"negative regulation of pancreatic beta cell apoptosis","type":"exact"},{"name":"negative regulation of type B pancreatic cell apoptosis","type":"narrow"}],"termid":"GO:2000675"}


id: MONDO:0022975
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":"diaphragmatic agenesis radial aplasia omphalocele","termid":"MONDO:0022975","xrefs":{"Monarch":{"xref_id":"0022975"}}}


id: PBO:0059797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 23","termid":"PBO:0059797"}


id: GO:0007393
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell fate determination process in which a cell within the dorsal ectoderm becomes capable of differentiating autonomously into a leading edge cell regardless of its environment; upon determination, the cell fate cannot be reversed.","definition_xrefs":["PMID:12147138","GOC:go_curators","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leading edge cell fate determination","termid":"GO:0035028"},{"relation_name":"part_of","term_name":"dorsal closure, leading edge cell fate commitment","termid":"GO:0035029"}],"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":"dorsal closure, leading edge cell fate determination","termid":"GO:0007393"}


id: MONDO:0009931
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pulmonary atresia with intact ventricular septum (PA-IVS) is a rare form of cyanotic congenital heart malformation characterized by severe cyanosis and tachypnea. PA-IVS presents significant morphologic diversity: at the end of the spectrum are patients with a mildly hypoplastic and tripartite right ventricle (RV) and mild tricuspid valve (TV) hypoplasia, and at the other end are patients with severe RV and TV hypoplasia, often with RV-dependent coronary circulation.","definition_xrefs":["Orphanet:1208"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"hypoplastic right heart syndrome","termid":"MONDO:0020291"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary atresia-intact ventricular septum syndrome","secondary_identifiers":["MEDGEN:87491","NCIT:C99032","icd11.foundation:131289265","SCTID:253590009","NANDO:1200707","GARD:4600","MESH:C562832","OMIM:265150","NANDO:2200253","UMLS:C0344975"],"synonyms":[{"name":"pulmonary atresia with intact ventricular septum","type":"related"},{"name":"pulmonary valve atresia with intact ventricular septum","type":"exact"}],"termid":"MONDO:0009931","xrefs":{"Monarch":{"xref_id":"0009931"}}}


id: GO:0015423
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + maltose(out) = ADP + phosphate + maltose(in).","definition_xrefs":["RHEA:22132"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maltose transmembrane transporter activity","termid":"GO:0005363"},{"relation_name":"is_a","term_name":"ABC-type oligosaccharide transporter activity","termid":"GO:0015422"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"ABC-type maltose transporter activity","secondary_identifiers":["MetaCyc:ABC-16-RXN","EC:7.5.2.1"],"synonyms":[{"name":"ABC-type maltose transporter","type":"exact"},{"name":"ATP-dependent maltose transmembrane transporter activity","type":"related"},{"name":"ATPase-coupled maltose transmembrane transporter activity","type":"related"},{"name":"maltooligosaccharide-importing ATPase activity","type":"related"},{"name":"maltose ABC transporter","type":"exact"},{"name":"maltose-transporting ATPase activity","type":"related"}],"termid":"GO:0015423"}


id: PBO:0017992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongation factor 1 alpha related protein Hbs1 (predicted)","termid":"PBO:0017992"}


id: PBO:0029753
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_modification","termid":"PBO:0029753"}


id: PBO:0069695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 974, pseudogene","termid":"PBO:0069695"}


id: MONDO:0016482
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Silver-Russell syndrome","termid":"MONDO:0008394"},{"relation_name":"is_a","term_name":"chromosome 11 disorder","termid":"MONDO:0700018"},{"relation_name":"is_a","term_name":"uniparental disomy","termid":"MONDO:0700086"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"silver-Russell syndrome due to maternal uniparental disomy of chromosome 11","secondary_identifiers":["MEDGEN:1843295","Orphanet:231147","UMLS:C5679841","GARD:20606"],"synonyms":[{"name":"Silver-Russell syndrome due to maternal uniparental disomy of chromosome type 11","type":"exact"},{"name":"UPD(11)mat","type":"exact"}],"termid":"MONDO:0016482","xrefs":{"Monarch":{"xref_id":"0016482"}}}


id: MONDO:0017640
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cyanide-induced parkinsonism is a rare parkinsonian syndrome due to intoxication which develops in individuals surviving an acute cyanide intoxication episode or due to chronic exposure to small cyanide doses. It presents several weeks after acute exposure with progressive typical clinical features of parkinsonism including bradykinesia, rigidity, dystonia, hypomimia, hypokinetic dysarthria, postural instability and retropulsion but no resting or postural tremor. Brain MRI reveals bilateral lesions in the pallidum, posterior putamen, substantia nigra, subthalamic nucleus, temporal and occipital cortex, and cerebellum.","definition_xrefs":["Orphanet:306692"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parkinsonian disorder","termid":"MONDO:0021095"},{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyanide-induced parkinsonism","secondary_identifiers":["icd11.foundation:1717111858","MEDGEN:1639789","UMLS:C4707859","GARD:21266","SCTID:766872002"],"termid":"MONDO:0017640","xrefs":{"Monarch":{"xref_id":"0017640"}}}


id: FYPO:0008169
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 the size, shape, and structure of actin cables are normal during mitotic interphase (i.e. indistinguishable from wild type).","direct_ancestors":[{"relation_name":"is_a","term_name":"normal actin cable morphology","termid":"FYPO:0002487"}],"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:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal actin cable morphology during mitotic interphase","termid":"FYPO:0008169"}


id: FYPO:0002685
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of trehalose measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell","termid":"FYPO:0000990"},{"relation_name":"is_a","term_name":"altered cellular trehalose level","termid":"FYPO:0001446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased cellular trehalose level","synonyms":[{"name":"increased trehalose accumulation","type":"related"}],"termid":"FYPO:0002685"}


id: MONDO:1011951
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteodystrophy, non-human animal","secondary_identifiers":["OMIA:000753"],"termid":"MONDO:1011951","xrefs":{"Monarch":{"xref_id":"1011951"}}}


id: PBO:0027161
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_meiotic_spindle_pole_body_during_meiosis_I","termid":"PBO:0027161"}


id: MONDO:0005512
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant mesothelioma that arises from the peritoneum. Patients usually present with abdominal pain and ascites.","definition_xrefs":["EFO:0005567"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peritoneum cancer","termid":"MONDO:0002087"},{"relation_name":"is_a","term_name":"malignant mesothelioma","termid":"MONDO:0006292"},{"relation_name":"is_a","term_name":"peritoneal mesothelioma","termid":"MONDO:0006362"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant peritoneal mesothelioma","secondary_identifiers":["UMLS:C0346109","GARD:20102","MEDGEN:83406","NCIT:C8704","MedDRA:10056558","Orphanet:168811","DOID:1788"],"synonyms":[{"name":"advanced malignant mesothelioma of peritoneum","type":"exact"},{"name":"advanced malignant mesothelioma of the peritoneum","type":"exact"},{"name":"advanced malignant peritoneal mesothelioma","type":"exact"},{"name":"advanced peritoneal malignant mesothelioma","type":"exact"},{"name":"diffuse malignant peritoneal mesothelioma","type":"exact"},{"name":"malignant mesothelioma (disease) of peritoneum","type":"exact"},{"name":"malignant mesothelioma of peritoneum","type":"exact"},{"name":"malignant peritoneal mesothelioma, advanced","type":"exact"},{"name":"peritoneal mesothelioma","type":"related"},{"name":"peritoneal mesothelioma (disease), malignant","type":"exact"},{"name":"peritoneum malignant mesothelioma (disease)","type":"exact"},{"name":"primary malignant peritoneal mesothelioma","type":"exact"}],"termid":"MONDO:0005512","xrefs":{"Monarch":{"xref_id":"0005512"}}}


id: PBO:0065324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine protease 47, pseudogene","termid":"PBO:0065324"}


id: GO:0005773
data:
  {"annotated_genes":["SJAG_02943","SJAG_02656","SJAG_03363","SJAG_02132","SJAG_01571","SJAG_04655","SJAG_01183","SJAG_02117","SJAG_03450","SJAG_01320","SJAG_02023","SJAG_02581","SJAG_01324","SJAG_03656","SJAG_02424","SJAG_01382","SJAG_02716","SJAG_03976","SJAG_01219","SJAG_02114","SJAG_04502","SJAG_01072","SJAG_04963","SJAG_02330","SJAG_04426","SJAG_03608","SJAG_04910","SJAG_01135","SJAG_00589","SJAG_04725","SJAG_00212","SJAG_02723","SJAG_00115","SJAG_00638","SJAG_02699","SJAG_00132","SJAG_04023","SJAG_01868","SJAG_02665","SJAG_00688","SJAG_03089","SJAG_01772","SJAG_04616","SJAG_02495","SJAG_01112","SJAG_03667","SJAG_03401","SJAG_04819","SJAG_04312","SJAG_02957","SJAG_02433","SJAG_03442","SJAG_01598","SJAG_02440","SJAG_02694","SJAG_05342","SJAG_06309","SJAG_04015","SJAG_01493","SJAG_01471","SJAG_00402","SJAG_02103","SJAG_03895","SJAG_00004","SJAG_02414","SJAG_04867","SJAG_02076","SJAG_01527","SJAG_03405","SJAG_01095","SJAG_01913","SJAG_01274","SJAG_05194","SJAG_00771","SJAG_03586","SJAG_04785","SJAG_03447","SJAG_03899","SJAG_00051","SJAG_03909","SJAG_04698","SJAG_03371","SJAG_04506","SJAG_01299","SJAG_03511","SJAG_01319","SJAG_02060","SJAG_05210","SJAG_02782","SJAG_07012","SJAG_03355","SJAG_03022","SJAG_03406","SJAG_02603","SJAG_03928","SJAG_03951","SJAG_03652","SJAG_01803","SJAG_02902","SJAG_04221","SJAG_01407","SJAG_04471","SJAG_02962","SJAG_01344","SJAG_03497","SJAG_00824","SJAG_01080","SJAG_00570","SJAG_00534","SJAG_03072","SJAG_03386","SJAG_01088","SJAG_03508","SJAG_03100","SJAG_04975","SJAG_01991","SJAG_03009","SJAG_03403","SJAG_03848","SJAG_04790","SJAG_03987","SJAG_05213","SJAG_01033","SJAG_00209","SJAG_00299","SJAG_04028","SJAG_02289","SJAG_05245","SJAG_00457","SJAG_03962","SJAG_03385","SJAG_04637","SJAG_03138","SJAG_04955","SJAG_04717","SJAG_01619","SJAG_02565","SJAG_05184","SJAG_01817","SJAG_00877","SJAG_01397","SJAG_01078","SJAG_00029","SJAG_00380","SJAG_01447","SJAG_02344","SJAG_01032","SJAG_01612","SJAG_04232","SJAG_01507","SJAG_04966","SJAG_01509","SJAG_01400","SJAG_00136","SJAG_02578","SJAG_01983","SJAG_03960","SJAG_00587","SJAG_02029","SJAG_02356","SJAG_00821","SJAG_02231","SJAG_01027","SJAG_00516","SJAG_04496","SJAG_02765","SJAG_04167","SJAG_03725","SJAG_02196","SJAG_01978","SJAG_04643","SJAG_01505","SJAG_03315","SJAG_03400","SJAG_00620","SJAG_02432","SJAG_01783","SJAG_03316","SJAG_03005","SJAG_04714","SJAG_01145","SJAG_00181","SJAG_02853","SJAG_05294","SJAG_01941","SJAG_03250","SJAG_01795","SJAG_01036","SJAG_03137","SJAG_01236","SJAG_00204","SJAG_01184","SJAG_03606","SJAG_00018","SJAG_01990","SJAG_03313","SJAG_00561","SJAG_02100","SJAG_00732","SJAG_03256"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[60038,65061,69369,96302,114945],"is_not":false,"summary":null,"term":"GO:0005773"},{"annotations":[76665,79352,104578,72401,79497,99453,94377,72325],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005776"},{"annotations":[71867,70211],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000421"},{"annotations":[102683,94837,112087,98290,76469,94575,95825,109085,101597,69930,87896,107289,78339,112604,113910,70259,87699,74997,89898,103750,104147,109547,96718,80133,97356,70404,71972,71622,75873,73737,79200,96246,74769,109185,98285,103517,117693,72803,116566,109202,101266,75411,79744,89897,107378,88201,112472,108570,73451],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000324"},{"annotations":[70456,97597,113914,101416,97387,105515,87237,113049,93678,114189,115593],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000328"},{"annotations":[78177,93655,72348,95521,70013,96168,110007,93297,87491,113299,98452,114616,95779,69213,92657,108030,116289,76292,78886,70645,88846,108434,117122,109618,72279,110144,88894,90156,91261,70210,116762,116996,117291,112978,74257,97111,117350,88825,98306,79568,103337,95737,93790,102760,107148,101380,109125,62887,104890,71884,103661,109041,99734,116360,114073,113162,87795,72705,76207,97796,98110,117550,98581,73252,80155,95406,93528,72587,87777,93814,95891,99331,99986,70558,70163,93476,88907,103546,106437,75023,98621,117942,106430,79504,72508,101721,72787,73790,94382,91813,78380,79870,99701,104732,94350,106903,106947,107599,114080,115936,95654,93529,111532,92741,71738,104661,105474,97376,74516,79446,79962,95853],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000329"},{"annotations":[109739,113301,87492,79965],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070772"},{"annotations":[92658,104892,107600,93815],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071986"},{"annotations":[76974,79886,79582,104395,74747,94075,70926,71000],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902500"},{"annotations":[110706,88070,73269,67210,106405,89178,109552,112605,75086,73391],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005774"},{"annotations":[103662,99702,89922,91814,61800,95407,95588],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000220"},{"annotations":[70904,118466,102422,60514,109620,87796,98672,96367],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000221"}]},"cv_name":"cellular_component","definition":"A closed structure, found only in eukaryotic cells, that is completely surrounded by unit membrane and contains liquid material. Cells contain one or several vacuoles, that may have different functions from each other. Vacuoles have a diverse array of functions. They can act as a storage organelle for nutrients or waste products, as a degradative compartment, as a cost-effective way of increasing cell size, and as a homeostatic regulator controlling both turgor pressure and pH of the cytosol.","definition_xrefs":["GOC:mtg_sensu","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membrane-bounded organelle","termid":"GO:0043231"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":200,"genes_by_uniquename":{"SJAG_00004":null,"SJAG_00018":null,"SJAG_00029":null,"SJAG_00051":null,"SJAG_00115":null,"SJAG_00132":null,"SJAG_00136":null,"SJAG_00181":null,"SJAG_00204":null,"SJAG_00209":null,"SJAG_00212":null,"SJAG_00299":null,"SJAG_00380":null,"SJAG_00402":null,"SJAG_00457":null,"SJAG_00516":null,"SJAG_00534":null,"SJAG_00561":null,"SJAG_00570":null,"SJAG_00587":null,"SJAG_00589":null,"SJAG_00620":null,"SJAG_00638":null,"SJAG_00688":null,"SJAG_00732":null,"SJAG_00771":null,"SJAG_00821":null,"SJAG_00824":null,"SJAG_00877":null,"SJAG_01027":null,"SJAG_01032":null,"SJAG_01033":null,"SJAG_01036":null,"SJAG_01072":null,"SJAG_01078":null,"SJAG_01080":null,"SJAG_01088":null,"SJAG_01095":null,"SJAG_01112":null,"SJAG_01135":null,"SJAG_01145":null,"SJAG_01183":null,"SJAG_01184":null,"SJAG_01219":null,"SJAG_01236":null,"SJAG_01274":null,"SJAG_01299":null,"SJAG_01319":null,"SJAG_01320":null,"SJAG_01324":null,"SJAG_01344":null,"SJAG_01382":null,"SJAG_01397":null,"SJAG_01400":null,"SJAG_01407":null,"SJAG_01447":null,"SJAG_01471":null,"SJAG_01493":null,"SJAG_01505":null,"SJAG_01507":null,"SJAG_01509":null,"SJAG_01527":null,"SJAG_01571":null,"SJAG_01598":null,"SJAG_01612":null,"SJAG_01619":null,"SJAG_01772":null,"SJAG_01783":null,"SJAG_01795":null,"SJAG_01803":null,"SJAG_01817":null,"SJAG_01868":null,"SJAG_01913":null,"SJAG_01941":null,"SJAG_01978":null,"SJAG_01983":null,"SJAG_01990":null,"SJAG_01991":null,"SJAG_02023":null,"SJAG_02029":null,"SJAG_02060":null,"SJAG_02076":null,"SJAG_02100":null,"SJAG_02103":null,"SJAG_02114":null,"SJAG_02117":null,"SJAG_02132":null,"SJAG_02196":null,"SJAG_02231":null,"SJAG_02289":null,"SJAG_02330":null,"SJAG_02344":null,"SJAG_02356":null,"SJAG_02414":null,"SJAG_02424":null,"SJAG_02432":null,"SJAG_02433":null,"SJAG_02440":null,"SJAG_02495":null,"SJAG_02565":null,"SJAG_02578":null,"SJAG_02581":null,"SJAG_02603":null,"SJAG_02656":null,"SJAG_02665":null,"SJAG_02694":null,"SJAG_02699":null,"SJAG_02716":null,"SJAG_02723":null,"SJAG_02765":null,"SJAG_02782":null,"SJAG_02853":null,"SJAG_02902":null,"SJAG_02943":null,"SJAG_02957":null,"SJAG_02962":null,"SJAG_03005":null,"SJAG_03009":null,"SJAG_03022":null,"SJAG_03072":null,"SJAG_03089":null,"SJAG_03100":null,"SJAG_03137":null,"SJAG_03138":null,"SJAG_03250":null,"SJAG_03256":null,"SJAG_03313":null,"SJAG_03315":null,"SJAG_03316":null,"SJAG_03355":null,"SJAG_03363":null,"SJAG_03371":null,"SJAG_03385":null,"SJAG_03386":null,"SJAG_03400":null,"SJAG_03401":null,"SJAG_03403":null,"SJAG_03405":null,"SJAG_03406":null,"SJAG_03442":null,"SJAG_03447":null,"SJAG_03450":null,"SJAG_03497":null,"SJAG_03508":null,"SJAG_03511":null,"SJAG_03586":null,"SJAG_03606":null,"SJAG_03608":null,"SJAG_03652":null,"SJAG_03656":null,"SJAG_03667":null,"SJAG_03725":null,"SJAG_03848":null,"SJAG_03895":null,"SJAG_03899":null,"SJAG_03909":null,"SJAG_03928":null,"SJAG_03951":null,"SJAG_03960":null,"SJAG_03962":null,"SJAG_03976":null,"SJAG_03987":null,"SJAG_04015":null,"SJAG_04023":null,"SJAG_04028":null,"SJAG_04167":null,"SJAG_04221":null,"SJAG_04232":null,"SJAG_04312":null,"SJAG_04426":null,"SJAG_04471":null,"SJAG_04496":null,"SJAG_04502":null,"SJAG_04506":null,"SJAG_04616":null,"SJAG_04637":null,"SJAG_04643":null,"SJAG_04655":null,"SJAG_04698":null,"SJAG_04714":null,"SJAG_04717":null,"SJAG_04725":null,"SJAG_04785":null,"SJAG_04790":null,"SJAG_04819":null,"SJAG_04867":null,"SJAG_04910":null,"SJAG_04955":null,"SJAG_04963":null,"SJAG_04966":null,"SJAG_04975":null,"SJAG_05184":null,"SJAG_05194":null,"SJAG_05210":null,"SJAG_05213":null,"SJAG_05245":null,"SJAG_05294":null,"SJAG_05342":null,"SJAG_06309":null,"SJAG_07012":null},"genotype_count":0,"in_subsets":["cc_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"vacuole","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"secondary_identifiers":["Wikipedia:Vacuole"],"synonyms":[{"name":"vacuolar carboxypeptidase Y","type":"related"}],"termid":"GO:0005773","terms_by_termid":{"GO:0000220":null,"GO:0000221":null,"GO:0000324":null,"GO:0000328":null,"GO:0000329":null,"GO:0000421":null,"GO:0005773":null,"GO:0005774":null,"GO:0005776":null,"GO:0070772":null,"GO:0071986":null,"GO:1902500":null}}


id: GO:0007224
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of activation of the transmembrane protein Smoothened.","definition_xrefs":["PMID:15205520","GOC:mah","PMID:15057936"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell surface receptor signaling pathway","termid":"GO:0007166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"smoothened signaling pathway","secondary_identifiers":["Wikipedia:Hedgehog_signaling_pathway"],"synonyms":[{"name":"Shh signaling pathway","type":"related"},{"name":"Sonic hedgehog signaling pathway","type":"narrow"},{"name":"hedgehog signaling pathway","type":"exact"},{"name":"hh signaling pathway","type":"narrow"},{"name":"hh signalling pathway","type":"narrow"},{"name":"smoothened signalling pathway","type":"exact"}],"termid":"GO:0007224"}


id: PBO:0070693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L8 pseudogene 2","termid":"PBO:0070693"}


id: PBO:0042745
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENPS-CORT readthrough","termid":"PBO:0042745"}


id: PBO:0002783
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"negatively regulates sexual differentiation in nutrient rich conditions by repression of Ste11","termid":"PBO:0002783"}


id: PATO:0001816
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A fatigability which is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"increased strength","termid":"PATO:0001778"},{"relation_name":"is_a","term_name":"fatigability","termid":"PATO:0001815"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased fatigability","synonyms":[{"name":"high fatigability","type":"exact"}],"termid":"PATO:0001816"}


id: MONDO:0011325
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fanconi anemia caused by mutations of the FANCF gene. This gene encodes a polypeptide with homology to the prokaryotic RNA-binding protein ROM.","definition_xrefs":["NCIT:C125707"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Fanconi anemia","termid":"MONDO:0019391"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0021190","MONDO:0005570","MONDO:0005066","MONDO:0002280"],"is_obsolete":false,"name":"Fanconi anemia complementation group F","secondary_identifiers":["MEDGEN:854016","OMIM:603467","GARD:15355","UMLS:C3469526","DOID:0111088"],"synonyms":[{"name":"FANCF","type":"exact"},{"name":"Fanconi Anemia, complementation group type F","type":"exact"},{"name":"Fanconi anaemia complementation group type F","type":"exact"},{"name":"Fanconi anemia complementation group F","type":"exact"},{"name":"Fanconi anemia complementation group type F","type":"exact"},{"name":"Fanconi anemia, complementation group F","type":"related"}],"termid":"MONDO:0011325","xrefs":{"Monarch":{"xref_id":"0011325"}}}


id: PBO:0088685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein phosphatase PP4 catalytic subunit Pph3","termid":"PBO:0088685"}


id: FYPO:0008306
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the frequency of DNA replication initiation is higher than normal at layte origins.","direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic DNA replication initiation","termid":"FYPO:0001344"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000293","FYPO:0000631","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased mitotic DNA replication initiation from late origin","termid":"FYPO:0008306"}


id: PBO:0017073
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"does not functionally complement S. cerevisiae RPR1","termid":"PBO:0017073"}


id: PBO:0005879
data:
  {"annotation_feature_type":"gene","cv_name":"genome_org","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein in cox1 intron-1","termid":"PBO:0005879"}


id: FYPO:0002425
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 actin cable organization is abnormal during mitosis. The process normally results in the assembly, arrangement of constituent parts, or disassembly of an actin cable. Actin cables are parallel actin filament bundles nucleated by formin, and are the most common form of actin filament bundles found in yeasts.","definition_xrefs":["PomBase:mah","GO:0070648"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actin cable organization","termid":"FYPO:0002030"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0004803","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal actin cable organization during mitosis","synonyms":[{"name":"abnormal actin cable organisation during mitotic interphase","type":"exact"},{"name":"abnormal actin cable organization during mitotic M phase","type":"related"},{"name":"abnormal actin cable organization during mitotic interphase during vegetative growth","type":"exact"},{"name":"abnormal actin cable organization during mitotic nuclear division","type":"exact"},{"name":"abnormal formin-nucleated actin cable organization during mitotic interphase","type":"exact"}],"termid":"FYPO:0002425"}


id: PBO:0041050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bromodomain containing 7 pseudogene 1","termid":"PBO:0041050"}


id: MONDO:0005607
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A type of chronic obstructive pulmonary disease characterized by chronic inflammation in the bronchial tree that results in edema, mucus production, obstruction, and reduced airflow to and from the lung alveoli. The most common cause is tobacco smoking. Signs and symptoms include coughing with excessive mucus production, and shortness of breath.","definition_xrefs":["NCIT:C26722"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bronchitis","termid":"MONDO:0003781"},{"relation_name":"is_a","term_name":"chronic obstructive pulmonary disease","termid":"MONDO:0005002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chronic bronchitis","secondary_identifiers":["MESH:D029481","UMLS:C0008677","EFO:0006505","ICD9:491.9","icd11.foundation:290835130","ICD9:491.8","ICD9:491","MEDGEN:3084","SCTID:63480004"],"synonyms":[{"name":"bronchitis, chronic","type":"exact"}],"termid":"MONDO:0005607","xrefs":{"Monarch":{"xref_id":"0005607"}}}


id: GO:1903504
data:
  {"annotated_genes":["SJAG_01679","SJAG_00883","SJAG_01297","SJAG_02336","SJAG_02169","SJAG_02451","SJAG_03353","SJAG_03126","SJAG_03681","SJAG_04259","SJAG_01837"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[108006,111706,113524,114011,115643,106987,99350,90486,103647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902426"},{"annotations":[93960],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140499"},{"annotations":[116417],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090267"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mitotic spindle checkpoint.","definition_xrefs":["PMID:23442800","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic cell cycle","termid":"GO:0007346"},{"relation_name":"is_a","term_name":"regulation of spindle checkpoint","termid":"GO:0090231"},{"relation_name":"regulates","term_name":"mitotic spindle checkpoint signaling","termid":"GO:0071174"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00883":null,"SJAG_01297":null,"SJAG_01679":null,"SJAG_01837":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02451":null,"SJAG_03126":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04259":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of mitotic spindle checkpoint","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of mitotic cell cycle spindle checkpoint","type":"exact"}],"termid":"GO:1903504","terms_by_termid":{"GO:0090267":null,"GO:0140499":null,"GO:1902426":null}}


id: GO:0001692
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving histamine, a physiologically active amine, found in plant and animal tissue and released from mast cells as part of an allergic reaction in humans.","definition_xrefs":["ISBN:0395825172","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biogenic amine metabolic process","termid":"GO:0006576"},{"relation_name":"is_a","term_name":"imidazole-containing compound metabolic process","termid":"GO:0052803"},{"relation_name":"is_a","term_name":"ammonium ion metabolic process","termid":"GO:0097164"}],"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":"histamine metabolic process","synonyms":[{"name":"histamine metabolism","type":"exact"}],"termid":"GO:0001692"}


id: MONDO:0054782
data:
  {"annotated_genes":["SJAG_03277","SJAG_01259"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85774,85775],"is_not":false,"summary":null,"term":"MONDO:0054782"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01259":null,"SJAG_03277":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"leukodystrophy, hypomyelinating, 15","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1633653","UMLS:C4693733","DOID:0070398","OMIM:617951"],"synonyms":[{"name":"HLD15","type":"related"},{"name":"leukodystrophy, hypomyelinating, 15","type":"exact"}],"termid":"MONDO:0054782","terms_by_termid":{"MONDO:0054782":null},"xrefs":{"Monarch":{"xref_id":"0054782"}}}


id: PBO:0030668
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_35S_rRNA_precursor_level","termid":"PBO:0030668"}


id: MONDO:0005380
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A none disease characterized by death of bone tissue due to a lack of blood supply.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare rheumatologic disease (obsolete MONDO:0015940)","termid":"MONDO:0015940"},{"relation_name":"is_a","term_name":"bone disorder","termid":"MONDO:0005381"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteonecrosis","secondary_identifiers":["SCTID:240196003","NCIT:C35476","DOID:0080008","NORD:1537","ICD9:733.4","ICD9:733.41","DOID:10159","EFO:0004259","ICD9:733.44","icd11.foundation:536467755","ICD9:733.43","ICD9:733.49","MEDGEN:45249","MESH:D010020","NCIT:C34880","UMLS:C0029445","GARD:21657","ICD9:733.42","ICD9:732.3","ICD10CM:M87","Orphanet:399158"],"synonyms":[{"name":"aseptic necrosis","type":"exact"},{"name":"bone necrosis","type":"exact"},{"name":"ischaemic bone disease","type":"exact"},{"name":"ischemic bone disease","type":"exact"},{"name":"osteonecrosis","type":"exact"}],"termid":"MONDO:0005380","xrefs":{"Monarch":{"xref_id":"0005380"}}}


id: MONDO:0018911
data:
  {"annotated_genes":["SJAG_03247","SJAG_04334","SJAG_04495"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87037],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014674"},{"annotations":[84915,84914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007453"}]},"cv_name":"mondo","definition":"MODY (maturity-onset diabetes of the young) is a rare, familial, clinically and genetically heterogeneous form of diabetes characterized by young age of onset (generally 10-45 years of age) with maintenance of endogenous insulin production, lack of pancreatic beta-cell autoimmunity, absence of obesity and insulin resistance and extra-pancreatic manifestations in some subtypes.","definition_xrefs":["Orphanet:552"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monogenic diabetes","termid":"MONDO:0015967"},{"relation_name":"is_a","term_name":"disorder of glycolysis","termid":"MONDO:0017688"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03247":null,"SJAG_04334":null,"SJAG_04495":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005015"},{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0019254","MONDO:0005015","MONDO:0004335","MONDO:0037792"],"is_obsolete":false,"name":"maturity-onset diabetes of the young","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0050524","UMLS:C0342276","OMIM:606391","MESH:C562772","HP:0004904","NANDO:2200462","MEDGEN:87433","GARD:3697","NCIT:C114769","SCTID:609561005"],"synonyms":[{"name":"MODY","type":"exact"},{"name":"Mason type diabetes","type":"related"},{"name":"Mason-type diabetes","type":"exact"},{"name":"maturity onset diabetes of the young","type":"exact"},{"name":"maturity-onset diabetes of the young","type":"exact"},{"name":"maturity-onset diabetes of the young (disease)","type":"exact"}],"termid":"MONDO:0018911","terms_by_termid":{"MONDO:0007453":null,"MONDO:0014674":null},"xrefs":{"Monarch":{"xref_id":"0018911"}}}


id: MOD:00191
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts L-tyrosine to (Z)-2,3-didehydrotyrosine.","definition_xrefs":["PubMed:1347277","PubMed:9631087","RESID:AA0183"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dehydrogenated tyrosine","termid":"MOD:00706"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(Z)-2,3-didehydrotyrosine","synonyms":[{"name":"(2Z)-2-amino-3-(4-hydroxyphenyl)prop-2-enoic acid","type":"exact"},{"name":"(Z)-2,3-didehydrogenated tyrosine","type":"exact"},{"name":"(Z)-2,3-didehydrotyrosine","type":"exact"},{"name":"2-amino-3-oxo-butanoic_acid","type":"related"},{"name":"Didehydro","type":"related"},{"name":"MOD_RES (Z)-2,3-didehydrotyrosine","type":"exact"},{"name":"Z-dHTyr","type":"exact"},{"name":"amino-(para-hydroxybenzylidenyl)acetic acid","type":"exact"},{"name":"cis-dehydrotyrosine","type":"exact"},{"name":"green fluorescent protein chromophore","type":"exact"},{"name":"para-hydroxybenzylidene-imidazolidinone chromophore","type":"exact"},{"name":"red fluorescent protein chromophore","type":"exact"}],"termid":"MOD:00191"}


id: GO:1902848
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of neuronal signal transduction.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","GOC:sjp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of signal transduction","termid":"GO:0009968"},{"relation_name":"is_a","term_name":"regulation of neuronal signal transduction","termid":"GO:1902847"},{"relation_name":"negatively_regulates","term_name":"neuronal signal transduction","termid":"GO:0023041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of neuronal signal transduction","synonyms":[{"name":"down regulation of neuronal signal transduction","type":"exact"},{"name":"down-regulation of neuronal signal transduction","type":"exact"},{"name":"downregulation of neuronal signal transduction","type":"exact"},{"name":"inhibition of neuronal signal transduction","type":"narrow"}],"termid":"GO:1902848"}


id: GO:0099639
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of neurotransmitter receptor from the endosome to the plasma membrane in transport vesicles.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurotransmitter receptor transport to plasma membrane","termid":"GO:0098877"},{"relation_name":"is_a","term_name":"endosome to plasma membrane protein transport","termid":"GO:0099638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0016192","GO:0006810"],"is_obsolete":false,"name":"neurotransmitter receptor transport, endosome to plasma membrane","termid":"GO:0099639"}


id: PBO:0079253
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TTC23L antisense RNA 1","termid":"PBO:0079253"}


id: PR:P17609
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ypt2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P17609"],"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":"GTP-binding protein ypt2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC9E9.07c","synonyms":[{"name":"SEC4 homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ypt2","type":"exact"}],"termid":"PR:P17609"}


id: GO:0102238
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2E)-geraniol + ATP = (2E)-geranyl phosphate + ADP + H+.","definition_xrefs":["RHEA:61660"],"direct_ancestors":[{"relation_name":"is_a","term_name":"geraniol kinase activity","termid":"GO:0052670"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"ATP:geraniol kinase activity","secondary_identifiers":["MetaCyc:RXN-12307"],"synonyms":[{"name":"geraniol kinase activity (ATP-dependent) activity","type":"exact"}],"termid":"GO:0102238"}


id: GO:0102942
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 3,5-dimethoxyphenol + S-adenosyl-L-methionine = H+ + 1,3,5-trimethoxybenzene + S-adenosyl-L-homocysteine.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 3,5-dimethoxyphenol O-methyltransferase activity (obsolete GO:0102942)","termid":"GO:0102942"}


id: PBO:0066501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"raftlin family member 2","termid":"PBO:0066501"}


id: MONDO:1011749
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"linear IgA disease, non-human animal","secondary_identifiers":["OMIA:001330"],"termid":"MONDO:1011749","xrefs":{"Monarch":{"xref_id":"1011749"}}}


id: PR:Q9HDW1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR12586:SF0","OMA:SCHPO03262","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":"CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP18G5.02","secondary_identifiers":["UniProtKB:Q9HDW1"],"synonyms":[{"name":"PGP synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PGS1","type":"exact"},{"name":"phosphatidylglycerophosphate synthase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9HDW1"}


id: MONDO:0030747
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"junctional epidermolysis bullosa","termid":"MONDO:0017612"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"epidermolysis bullosa, junctional 2B, severe","secondary_identifiers":["UMLS:C5676937","OMIM:619784","MEDGEN:1805467"],"synonyms":[{"name":"JEB2B","type":"exact"},{"name":"epidermolysis bullosa, junctional 2B, generalised severe","type":"exact"},{"name":"epidermolysis bullosa, junctional 2B, generalized severe","type":"exact"},{"name":"epidermolysis bullosa, junctional 2B, herlitz IIA","type":"exact"},{"name":"epidermolysis bullosa, junctional 2B, severe","type":"exact"}],"termid":"MONDO:0030747","xrefs":{"Monarch":{"xref_id":"0030747"}}}


id: PBO:0088805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protor homolog, Bit61","termid":"PBO:0088805"}


id: GO:0033800
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + a 7-hydroxyisoflavone = S-adenosyl-L-homocysteine + a 7-methoxyisoflavone.","definition_xrefs":["EC:2.1.1.150"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-methyltransferase activity","termid":"GO:0008171"},{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674","GO:0016741"],"is_obsolete":false,"name":"isoflavone 7-O-methyltransferase activity","secondary_identifiers":["MetaCyc:RXN-6241","RHEA:17933"],"synonyms":[{"name":"S-adenosyl-L-methionine:hydroxyisoflavone 7-O-methyltransferase activity","type":"related"}],"termid":"GO:0033800"}


id: PBO:0054470
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 1870","termid":"PBO:0054470"}


id: GO:0006174
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of introducing a phosphate group into dADP, deoxyadenosine diphosphate, to produce dATP.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete dADP phosphorylation (obsolete GO:0006174)","termid":"GO:0006174"}


id: MONDO:0020855
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 32","secondary_identifiers":["GARD:16292","UMLS:C4748253","DOID:0111925","MEDGEN:1648444","OMIM:618115"],"synonyms":[{"name":"SPGF32","type":"exact"},{"name":"spermatogenic failure 32","type":"exact"}],"termid":"MONDO:0020855","xrefs":{"Monarch":{"xref_id":"0020855"}}}


id: GO:2000362
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of prostaglandin-E synthase activity.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of prostaglandin-E synthase activity (obsolete GO:2000362)","synonyms":[{"name":"negative regulation of (5Z,13E)-(15S)-9alpha,11alpha-epidioxy-15-hydroxyprosta-5,13-dienoate E-isomerase activity","type":"exact"},{"name":"negative regulation of PGE isomerase activity","type":"exact"},{"name":"negative regulation of PGE2 isomerase activity","type":"exact"},{"name":"negative regulation of PGH-PGE isomerase activity","type":"exact"},{"name":"negative regulation of Prostaglandin-H(2) E-isomerase activity","type":"exact"},{"name":"negative regulation of endoperoxide isomerase activity","type":"exact"},{"name":"negative regulation of prostaglandin H-E isomerase activity","type":"exact"},{"name":"negative regulation of prostaglandin R-prostaglandin E isomerase activity","type":"exact"},{"name":"negative regulation of prostaglandin endoperoxide E isomerase activity","type":"exact"},{"name":"negative regulation of prostaglandin endoperoxide E2 isomerase activity","type":"exact"},{"name":"negative regulation of prostaglandin-H2 E-isomerase activity","type":"exact"}],"termid":"GO:2000362"}


id: MONDO:0008526
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":"talonavicular coalition","secondary_identifiers":["UMLS:C1861296","MEDGEN:350002","OMIM:186750","MESH:C536895"],"synonyms":[{"name":"talonavicular coalition","type":"exact"}],"termid":"MONDO:0008526","xrefs":{"Monarch":{"xref_id":"0008526"}}}


id: PBO:0059951
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND2 pseudogene 37","termid":"PBO:0059951"}


id: GO:0036073
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Intramembranous ossification from the surface of a cartilage element as the perichondrium becomes a periosteum, without replacement of cartilage.","definition_xrefs":["GO_REF:0000034"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramembranous ossification","termid":"GO:0001957"}],"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":"perichondral ossification","termid":"GO:0036073"}


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


id: PBO:0090145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pex16 family peroxisome import protein Pex16","termid":"PBO:0090145"}


id: GO:0035522
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The removal of the ubiquitin group from a monoubiquitinated histone H2A protein.","definition_xrefs":["GOC:bf","PMID:18226187","PMID:20436459"],"gene_count":0,"genotype_count":0,"name":"obsolete monoubiquitinated histone H2A deubiquitination (obsolete GO:0035522)","synonyms":[{"name":"monoubiquitinated histone H2A deubiquitinylation","type":"exact"},{"name":"monoubiquitinated histone H2A deubiquitylation","type":"exact"}],"termid":"GO:0035522"}


id: PBO:0004045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA export receptor, Tap, nucleoporin Mex67","termid":"PBO:0004045"}


id: MONDO:0006911
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete placental site trophoblastic tumor (obsolete MONDO:0006911)","termid":"MONDO:0006911","xrefs":{"Monarch":{"xref_id":"0006911"}}}


id: PBO:0076619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin folding cofactor B","termid":"PBO:0076619"}


id: GO:0010639
data:
  {"annotated_genes":["SJAG_04999","SJAG_02700","SJAG_00823","SJAG_00369","SJAG_04203","SJAG_01297","SJAG_03438","SJAG_00460","SJAG_01330","SJAG_03591","SJAG_03072","SJAG_04699","SJAG_02451","SJAG_00304","SJAG_05978","SJAG_03126","SJAG_02336","SJAG_00266","SJAG_01894","SJAG_03353","SJAG_01825","SJAG_04884","SJAG_00279","SJAG_01993","SJAG_01679","SJAG_04259","SJAG_00364","SJAG_03681","SJAG_04287","SJAG_03455","SJAG_02795","SJAG_00855","SJAG_03327","SJAG_02169","SJAG_01716","SJAG_04126","SJAG_01680","SJAG_00883","SJAG_01837","SJAG_01082","SJAG_04638","SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78930,79827,92089,75443],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051016"},{"annotations":[114011,90486,103647,99350,115643,111706,113524,106987,108006],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[106075,114241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905318"},{"annotations":[106373,88819,115802,114001],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051598"},{"annotations":[115298,114244,99194,101551,106077,109656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007094"},{"annotations":[74266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034316"},{"annotations":[98032],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000432"},{"annotations":[117690],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905560"},{"annotations":[116046],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090258"},{"annotations":[101800,106211],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010637"},{"annotations":[102118],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903500"},{"annotations":[103031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000816"},{"annotations":[93960],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[107724],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045128"},{"annotations":[107158,115080,91504,106018,106114,106336],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045875"},{"annotations":[101208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061192"},{"annotations":[113529],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905326"},{"annotations":[116417],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090267"},{"annotations":[101093],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905325"}]},"cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of a process involved in the formation, arrangement of constituent parts, or disassembly of an organelle.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of organelle organization","termid":"GO:0033043"},{"relation_name":"is_a","term_name":"negative regulation of cellular component organization","termid":"GO:0051129"},{"relation_name":"negatively_regulates","term_name":"organelle organization","termid":"GO:0006996"}],"gene_count":42,"genes_by_uniquename":{"SJAG_00266":null,"SJAG_00279":null,"SJAG_00304":null,"SJAG_00364":null,"SJAG_00369":null,"SJAG_00460":null,"SJAG_00823":null,"SJAG_00855":null,"SJAG_00883":null,"SJAG_01082":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01716":null,"SJAG_01825":null,"SJAG_01837":null,"SJAG_01894":null,"SJAG_01993":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02451":null,"SJAG_02700":null,"SJAG_02795":null,"SJAG_03048":null,"SJAG_03072":null,"SJAG_03126":null,"SJAG_03327":null,"SJAG_03353":null,"SJAG_03438":null,"SJAG_03455":null,"SJAG_03591":null,"SJAG_03681":null,"SJAG_04126":null,"SJAG_04203":null,"SJAG_04259":null,"SJAG_04287":null,"SJAG_04638":null,"SJAG_04699":null,"SJAG_04884":null,"SJAG_04999":null,"SJAG_05978":null},"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 organelle organization","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"negative regulation of organelle organisation","type":"exact"},{"name":"negative regulation of organelle organization and biogenesis","type":"related"}],"termid":"GO:0010639","terms_by_termid":{"GO:0007094":null,"GO:0010637":null,"GO:0034316":null,"GO:0045128":null,"GO:0045875":null,"GO:0051016":null,"GO:0051598":null,"GO:0061192":null,"GO:0090258":null,"GO:0090267":null,"GO:0140499":null,"GO:1902426":null,"GO:1903500":null,"GO:1905318":null,"GO:1905325":null,"GO:1905326":null,"GO:1905560":null,"GO:2000432":null,"GO:2000816":null}}


id: MONDO:0020184
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare eyebrow/eyelashes anomaly (obsolete MONDO:0020184)","secondary_identifiers":["Orphanet:98594"],"termid":"MONDO:0020184","xrefs":{"Monarch":{"xref_id":"0020184"}}}


id: GO:0005571
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete untranslated RNA (obsolete GO:0005571)","synonyms":[{"name":"untranslated RNA","type":"exact"}],"termid":"GO:0005571"}


id: PBO:0082924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytochrome c oxidase subunit; required for assembly of the Complex III-Complex IV supercomplex, and for assembly of Cox13p and Rcf2p into cytochrome c oxidase; similar to Rcf2p, and either Rcf1p or Rcf2p is required for late-stage assembly of the Cox12p and Cox13p subunits and for cytochrome c oxidase activity; required for growth under hypoxic conditions; member of the hypoxia induced gene family; C. elegans and human orthologs are functional in yeast","termid":"PBO:0082924"}


id: PBO:0001258
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulated by Prr1","termid":"PBO:0001258"}


id: MONDO:0012160
data:
  {"annotated_genes":["SJAG_00946"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85977],"is_not":false,"summary":null,"term":"MONDO:0012160"}]},"cv_name":"mondo","definition":"Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome is characterized by the association of spondylometaphyseal dysplasia (marked by platyspondyly, shortening of the tubular bones and progressive metaphyseal irregularity and cupping), with postnatal growth retardation and progressive visual impairment due to cone-rod dystrophy. So far, it has been described in eight individuals. Transmission appears to be autosomal recessive.","definition_xrefs":["Orphanet:85167"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spondylometaphyseal dysplasia","termid":"MONDO:0016763"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00946":null},"genotype_count":0,"is_obsolete":false,"name":"spondylometaphyseal dysplasia-cone-rod dystrophy syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:10647","DOID:0112300","MESH:C563825","OMIM:608940","UMLS:C1837073","MEDGEN:324684"],"synonyms":[{"name":"SMD-CRD","type":"exact"},{"name":"SMDCRD","type":"related"},{"name":"SmD-CRD","type":"exact"},{"name":"spondylometaphyseal dysplasia with cone-rod dystrophy","type":"related"},{"name":"spondylometaphyseal dysplasia-cone-rod dystrophy syndrome","type":"exact"}],"termid":"MONDO:0012160","terms_by_termid":{"MONDO:0012160":null},"xrefs":{"Monarch":{"xref_id":"0012160"}}}


id: GO:0075208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont modulates the frequency, rate or extent of cAMP-mediated signal transduction in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by symbiont of host cAMP-mediated signal transduction (obsolete GO:0075208)","synonyms":[{"name":"modulation by symbiont of host cAMP-mediated signaling","type":"exact"}],"termid":"GO:0075208"}


id: GO:0036527
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of a sugar or dicarbonyl from an arginine residue of a glycated protein.","definition_xrefs":["GOC:bf","PMID:14568004","PMID:25416785","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-arginine modification","termid":"GO:0018195"},{"relation_name":"is_a","term_name":"protein deglycation","termid":"GO:0036525"}],"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":"peptidyl-arginine deglycation","synonyms":[{"name":"deglycation of N-acetylarginine","type":"related"}],"termid":"GO:0036527"}


id: GO:1990848
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of removal of reactive oxygen species in a cell.","definition_xrefs":["PMID:24118096"],"gene_count":0,"genotype_count":0,"name":"obsolete Positive regulation of removal of reactive oxygen species (obsolete GO:1990848)","termid":"GO:1990848"}


id: PBO:0113480
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tail-anchored plasma membrane (PM) protein; C-terminal palmitoylation is required for membrane anchoring and protein stability; PM localization is polarized to the daughter cell; contains a conserved cysteine rich palmitoylated domain (CYSPD, aka CYSTM); related proteins in other organisms may be involved in response to stress","termid":"PBO:0113480"}


id: GO:1901540
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of ent-pimara-8(14),15-diene.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terpene catabolic process","termid":"GO:0046247"},{"relation_name":"is_a","term_name":"ent-pimara-8(14),15-diene metabolic process","termid":"GO:1901539"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"ent-pimara-8(14),15-diene catabolic process","synonyms":[{"name":"ent-pimara-8(14),15-diene breakdown","type":"exact"},{"name":"ent-pimara-8(14),15-diene catabolism","type":"exact"},{"name":"ent-pimara-8(14),15-diene degradation","type":"exact"}],"termid":"GO:1901540"}


id: GO:1904472
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of endothelin production.","definition_xrefs":["GO_REF:0000058","PMID:15560120","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cytokine production","termid":"GO:0001819"},{"relation_name":"is_a","term_name":"regulation of endothelin production","termid":"GO:1904470"},{"relation_name":"positively_regulates","term_name":"endothelin production","termid":"GO:1990775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of endothelin production","synonyms":[{"name":"activation of EDN1 secretion","type":"narrow"},{"name":"activation of EDN2 secretion","type":"narrow"},{"name":"activation of EDN3 secretion","type":"narrow"},{"name":"activation of endothelin secretion","type":"narrow"},{"name":"activation of endothelin-1 secretion","type":"narrow"},{"name":"activation of endothelin-2 secretion","type":"narrow"},{"name":"activation of endothelin-3 secretion","type":"narrow"},{"name":"positive regulation of EDN1 secretion","type":"narrow"},{"name":"positive regulation of EDN2 secretion","type":"narrow"},{"name":"positive regulation of EDN3 secretion","type":"narrow"},{"name":"positive regulation of endothelin secretion","type":"narrow"},{"name":"positive regulation of endothelin-1 secretion","type":"narrow"},{"name":"positive regulation of endothelin-2 secretion","type":"narrow"},{"name":"positive regulation of endothelin-3 secretion","type":"narrow"},{"name":"up regulation of EDN1 secretion","type":"narrow"},{"name":"up regulation of EDN2 secretion","type":"narrow"},{"name":"up regulation of EDN3 secretion","type":"narrow"},{"name":"up regulation of endothelin secretion","type":"exact"},{"name":"up regulation of endothelin-1 secretion","type":"narrow"},{"name":"up regulation of endothelin-2 secretion","type":"narrow"},{"name":"up regulation of endothelin-3 secretion","type":"narrow"},{"name":"up-regulation of EDN1 secretion","type":"narrow"},{"name":"up-regulation of EDN2 secretion","type":"narrow"},{"name":"up-regulation of EDN3 secretion","type":"narrow"},{"name":"up-regulation of endothelin secretion","type":"exact"},{"name":"up-regulation of endothelin-1 secretion","type":"narrow"},{"name":"up-regulation of endothelin-2 secretion","type":"narrow"},{"name":"up-regulation of endothelin-3 secretion","type":"narrow"},{"name":"upregulation of EDN1 secretion","type":"narrow"},{"name":"upregulation of EDN2 secretion","type":"narrow"},{"name":"upregulation of EDN3 secretion","type":"narrow"},{"name":"upregulation of endothelin secretion","type":"exact"},{"name":"upregulation of endothelin-1 secretion","type":"narrow"},{"name":"upregulation of endothelin-2 secretion","type":"narrow"},{"name":"upregulation of endothelin-3 secretion","type":"narrow"}],"termid":"GO:1904472"}


id: PBO:0083939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Gamma-adaptin; large subunit of the clathrin-associated protein (AP-1) complex; binds clathrin; involved in vesicle mediated transport","termid":"PBO:0083939"}


id: PBO:0045291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynamin 1 pseudogene 43","termid":"PBO:0045291"}


id: PBO:0085628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in Fe-S cluster transfer to mitochondrial clients; protects [4Fe-4S] clusters from damage due to oxidative stress; acts along with Bol3 at a late step in the transfer of [4Fe-4S] clusters from the ISA complex to client proteins; Fe-S loaded homodimer at steady state; similar to NifU, a bacterial protein required for Fe/S cluster maturation; ortholog of the human NFU1, mutations of which are associated with Multiple Mitochondria Dysfunctions Syndrome (MMDS1)","termid":"PBO:0085628"}


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


id: GO:0003851
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-acylsphing-4-enine + UDP-alpha-D-galactose = a beta-D-galactosyl-(1<->1')-N-acylsphing-4-enine + H+ + UDP.","definition_xrefs":["EC:2.4.1.47"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-galactosyltransferase activity","termid":"GO:0035250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016757","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"N-acylsphingosine galactosyltransferase activity","secondary_identifiers":["RHEA:13093","MetaCyc:2.4.1.47-RXN","Reactome:R-HSA-6785933"],"synonyms":[{"name":"2-hydroxyacylsphingosine 1-beta-galactosyltransferase activity","type":"exact"}],"termid":"GO:0003851"}


id: MONDO:0035344
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare neurologic disease characterized by lethargy, hypotonia, poor feeding, opisthotonus, and a typical high-pitched cry due to bilirubin accumulation in the globus pallidus, sub-thalamic nuclei, and other brain regions, resulting from severe neonatal unconjugated hyperbilirubinemia. Onset of symptoms is typically within the first three to five days of life. Additional features include fever, apnea, seizures, and coma. Especially respiratory failure or refractory seizures may lead to a fatal outcome.","definition_xrefs":["Orphanet:529799"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute bilirubin encephalopathy","secondary_identifiers":["GARD:22197","MEDGEN:1808922","UMLS:C5671282"],"synonyms":[{"name":"ABE","type":"exact"},{"name":"Acute kernicterus","type":"exact"}],"termid":"MONDO:0035344","xrefs":{"Monarch":{"xref_id":"0035344"}}}


id: GO:0038068
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the concomitant phosphorylation of threonine (T) and tyrosine (Y) residues in a Thr-Glu-Tyr (TEY) thiolester sequence in a MAP kinase (MAPK) substrate, as part of a MAPK signaling cascade that contributes to cell wall organization or biogenesis.","definition_xrefs":["GOC:signaling"],"gene_count":0,"genotype_count":0,"name":"obsolete MAP kinase kinase activity involved in cell wall organization or biogenesis (obsolete GO:0038068)","synonyms":[{"name":"MAP kinase kinase activity involved in cell wall biogenesis","type":"narrow"},{"name":"MAP2K activity involved in cell wall integrity","type":"exact"},{"name":"MAPKK activity involved in cell wall integrity","type":"exact"}],"termid":"GO:0038068"}


id: GO:0046803
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the severity of viral infection and subsequent disease.","definition_xrefs":["PMID:10982346"],"gene_count":0,"genotype_count":0,"name":"obsolete reduction of virulence (obsolete GO:0046803)","synonyms":[{"name":"reduction of virulence","type":"exact"}],"termid":"GO:0046803"}


id: PBO:0044516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"D-2-hydroxyglutarate dehydrogenase","termid":"PBO:0044516"}


id: PBO:0031305
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_amiloride","termid":"PBO:0031305"}


id: GO:0050472
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dihydrozeatin + NADP+ = H+ + NADPH + zeatin.","definition_xrefs":["EC:1.3.1.69","RHEA:12757"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO: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":"zeatin reductase activity","secondary_identifiers":["MetaCyc:ZEATIN-REDUCTASE-RXN","KEGG_REACTION:R05702"],"synonyms":[{"name":"dihydrozeatin:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0050472"}


id: MONDO:0016654
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ring chromosome 5 syndrome is a rare chromosomal anomaly syndrome, with high phenotypic variability, principally characterized by a neonatal mewing cry, severe developmental delay and intellectual disability, short stature, hypotonia, dysmorphic features (incl. microcephaly, facial asymmetry, hypertelorism, epicanthal folds, abnormal ears, micro/retrognathia), congenital cardiac anomalies (such as atrial and ventricular septal defect, tricuspid insufficiency, hypoplastic aorta) and skeletal abnormalities (e.g. hypoplastic thumbs, anomalous ulna/radius, dysplastic metacarpals and phalanges).","definition_xrefs":["Orphanet:251043"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 5 disorder","termid":"MONDO:0700012"},{"relation_name":"is_a","term_name":"ring chromosome disorder","termid":"MONDO:0700091"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring chromosome 5","secondary_identifiers":["GARD:10841","MEDGEN:881956","UMLS:C4050064","SCTID:765487008","NCIT:C121984"],"synonyms":[{"name":"R5","type":"related"},{"name":"Ring 5","type":"related"},{"name":"Ring chromosome 5 syndrome","type":"related"},{"name":"Ring chromosome type 5","type":"exact"},{"name":"chromosome 5 ring","type":"related"},{"name":"rose cluster 5","type":"exact"}],"termid":"MONDO:0016654","xrefs":{"Monarch":{"xref_id":"0016654"}}}


id: GO:0021570
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of rhombomere 4 over time, from its formation to the mature structure. Rhombomeres are transverse segments of the developing rhombencephalon. Rhombomeres are lineage restricted, express different genes from one another, and adopt different developmental fates. Rhombomeres are numbered in anterior to posterior order.","definition_xrefs":["GOC:jid","GOC:curators","GOC:cls","GOC:dgh","GO_REF:0000021","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhombomere development","termid":"GO:0021546"}],"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":"rhombomere 4 development","termid":"GO:0021570"}


id: GO:0036529
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of glyoxal from a glycated protein, to form glycolate and a deglycated protein.","definition_xrefs":["GOC:PARL","PMID:25416785","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein deglycation","termid":"GO:0036525"},{"relation_name":"is_a","term_name":"glycolate biosynthetic process","termid":"GO:0046295"},{"relation_name":"is_a","term_name":"glyoxal metabolic process","termid":"GO:1903189"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"protein deglycation, glyoxal removal","synonyms":[{"name":"protein deglycation of glyoxal-glycated protein","type":"related"}],"termid":"GO:0036529"}


id: PBO:0056871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MHC class I polypeptide-related sequence B","termid":"PBO:0056871"}


id: PBO:0045000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dicer 1, ribonuclease III","termid":"PBO:0045000"}


id: PBO:0062114
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily C member 13","termid":"PBO:0062114"}


id: PBO:0017471
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-encompasses","termid":"PBO:0017471"}


id: PBO:0090478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA processing protein Enp2","termid":"PBO:0090478"}


id: GO:0106296
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of resolvin family D-series, hydroxy fatty acids derived from docosahexaenoic acid.","definition_xrefs":["PMID:12391014"],"direct_ancestors":[{"relation_name":"is_a","term_name":"resolvin biosynthetic process","termid":"GO:0106295"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"D-series resolvin biosynthetic process","termid":"GO:0106296"}


id: GO:0009458
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. A hemeprotein whose characteristic mode of action involves transfer of reducing equivalents associated with a reversible change in oxidation state of the prosthetic group. This redox change involves a single electron, reversible equilibrium between the Fe(II) and Fe(III) states of the central iron atom.","definition_xrefs":["PMID:1655423"],"gene_count":0,"genotype_count":0,"name":"obsolete cytochrome (obsolete GO:0009458)","synonyms":[{"name":"cytochrome","type":"exact"}],"termid":"GO:0009458"}


id: PR:Q09829
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- puf5 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09829"],"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":"pumilio domain-containing protein C4G8.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4G8.03c","synonyms":[{"name":"Spom972h-puf5","type":"exact"}],"termid":"PR:Q09829"}


id: PBO:0068192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 499","termid":"PBO:0068192"}


id: MONDO:1011546
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Intervertebral disc disease that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intervertebral disc disease, non-human animal","termid":"MONDO:1011452"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intervertebral disc disease, dog","secondary_identifiers":["OMIA:000157-9615"],"termid":"MONDO:1011546","xrefs":{"Monarch":{"xref_id":"1011546"}}}


id: GO:0044349
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The removal of a section of DNA from a larger DNA molecule by the making of dual incisions that flank the section to be excised.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA excision (obsolete GO:0044349)","termid":"GO:0044349"}


id: PBO:0059671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 37","termid":"PBO:0059671"}


id: PBO:0074593
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 7A","termid":"PBO:0074593"}


id: MONDO:0010307
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic X-linked intellectual disability","termid":"MONDO:0019181"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability, X-linked 73","secondary_identifiers":["OMIM:300355","DOID:0112017","GARD:22673","MEDGEN:335293","UMLS:C1845860","MESH:C564528"],"synonyms":[{"name":"MRX73","type":"exact"},{"name":"intellectual disability, X-linked 73","type":"exact"},{"name":"mental retardation, X-linked 73","type":"related"},{"name":"mental retardation, X-linked 73, X-linked recessive","type":"exact"}],"termid":"MONDO:0010307","xrefs":{"Monarch":{"xref_id":"0010307"}}}


id: GO:0035702
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of regulating the proliferation and elimination of monocytes such that the total number of monocytes within a whole or part of an organism is stable over time in the absence of an outside stimulus.","definition_xrefs":["CL:0000576","GOC:BHF","PMID:18832716"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte homeostasis","termid":"GO:0001776"},{"relation_name":"is_a","term_name":"myeloid cell homeostasis","termid":"GO:0002262"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"monocyte homeostasis","termid":"GO:0035702"}


id: GO:0000907
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: sulfonate + 2-oxoglutarate + O2 = sulfite + aminoacetaldehyde + succinate + CO2.","definition_xrefs":["GOC:clt","PMID:10482536"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxoglutarate-dependent dioxygenase activity","termid":"GO:0016706"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"sulfonate dioxygenase activity","synonyms":[{"name":"sulfonate/alpha-ketoglutarate dioxygenase activity","type":"exact"},{"name":"sulphonate dioxygenase activity","type":"exact"}],"termid":"GO:0000907"}


id: GO:0010155
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of proton transport into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of monoatomic cation transmembrane transport","termid":"GO:1904062"},{"relation_name":"regulates","term_name":"proton transmembrane transport","termid":"GO:1902600"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of proton transport","termid":"GO:0010155"}


id: PBO:0002214
data:
  {"annotation_feature_type":"gene","cv_name":"genome_org","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alternative transcript, alternative start","termid":"PBO:0002214"}


id: PBO:0080203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vascular endothelial zinc finger 1 pseudogene 1","termid":"PBO:0080203"}


id: GO:0043126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the activity of the enzyme 1-phosphatidylinositol 4-kinase.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of 1-phosphatidylinositol 4-kinase activity (obsolete GO:0043126)","synonyms":[{"name":"regulation of PI4K activity","type":"exact"}],"termid":"GO:0043126"}


id: PBO:0053462
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 423","termid":"PBO:0053462"}


id: PBO:0056067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"latexin","termid":"PBO:0056067"}


id: PBO:0054576
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 1978","termid":"PBO:0054576"}


id: PBO:0059044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MMS19 homolog, cytosolic iron-sulfur assembly component","termid":"PBO:0059044"}


id: GO:0031056
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the covalent alteration of a histone.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone modification (obsolete GO:0031056)","termid":"GO:0031056"}


id: PBO:0001859
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.4.1.34","termid":"PBO:0001859"}


id: PBO:0055485
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 2918","termid":"PBO:0055485"}


id: GO:1905336
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of aggrephagy.","definition_xrefs":["GOC:pad","GOC:PARL","GOC:TermGenie","GO_REF:0000058","PMID:25686248"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of macroautophagy","termid":"GO:0016242"},{"relation_name":"is_a","term_name":"regulation of aggrephagy","termid":"GO:1905335"},{"relation_name":"negatively_regulates","term_name":"aggrephagy","termid":"GO:0035973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006914"},{"rel_name":"negatively_regulates","termid":"GO:0006914"}],"interesting_parent_ids":["GO:0006914","GO:0008150"],"is_obsolete":false,"name":"negative regulation of aggrephagy","synonyms":[{"name":"down regulation of aggrephagy","type":"exact"},{"name":"down-regulation of aggrephagy","type":"exact"},{"name":"downregulation of aggrephagy","type":"exact"},{"name":"inhibition of aggrephagy","type":"narrow"}],"termid":"GO:1905336"}


id: PR:O94556
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cell division cycle protein 23 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00543","PRO:DNx","PANTHER:PTHR12558:SF10"],"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":"anaphase-promoting complex subunit 8 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6F12.14","secondary_identifiers":["UniProtKB:O94556"],"synonyms":[{"name":"20S cyclosome/APC complex protein apc8 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-CDC23","type":"exact"},{"name":"cell untimely torn protein 23 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94556"}


id: GO:0018065
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The covalent attachment of a cofactor to a protein.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete protein-cofactor linkage (obsolete GO:0018065)","termid":"GO:0018065"}


id: GO:0051500
data:
  {"annotated_genes":["SJAG_01248"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73239],"is_not":false,"summary":null,"term":"GO:0051500"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-tyrosyl-tRNATyr + H2O = D-tyrosine + tRNATyr. Removal of a D-tyrosine from a charged tRNA(Tyr).","definition_xrefs":["PMID:14527667","RHEA:25347"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-aminoacyl-tRNA deacylase activity","termid":"GO:0051499"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01248":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0016788","GO:0003674","GO:0140098","GO:0140101"],"is_obsolete":false,"name":"D-tyrosyl-tRNA(Tyr) deacylase activity","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0051500","terms_by_termid":{"GO:0051500":null}}


id: GO:0016574
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histones by addition of ubiquitin groups.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete histone ubiquitination (obsolete GO:0016574)","synonyms":[{"name":"histone ubiquitinylation","type":"exact"},{"name":"histone ubiquitylation","type":"exact"}],"termid":"GO:0016574"}


id: GO:0031942
data:
  {"annotated_genes":["SJAG_00354","SJAG_01816"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[76941,118471],"is_not":false,"summary":null,"term":"GO:0031942"}]},"cv_name":"cellular_component","definition":"Protease complex of the mitochondrial inner membrane whose catalytic residues lie on the intermembrane space side of the inner membrane; involved in mitochondrial protein turnover. Contains a subunit belonging to the AAA family of ATP-dependent metalloproteases.","definition_xrefs":["PMID:16247555","PMID:16267274"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inner mitochondrial membrane protein complex","termid":"GO:0098800"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00354":null,"SJAG_01816":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005739"}],"interesting_parent_ids":["GO:0005575","GO:0005739","GO:0032991","GO:0005737"],"is_obsolete":false,"name":"i-AAA complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0031942","terms_by_termid":{"GO:0031942":null}}


id: PBO:0005367
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polycystic liver disease","termid":"PBO:0005367"}


id: PATO:0002229
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quadrangular shape quality inhering in a bearer by virtue of the bearer's being approximately rectangular.","direct_ancestors":[{"relation_name":"is_a","term_name":"quadrangular","termid":"PATO:0001988"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subrectangular","termid":"PATO:0002229"}


id: PBO:0042861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 91","termid":"PBO:0042861"}


id: PBO:0039469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 17","termid":"PBO:0039469"}


id: GO:0086091
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A cardiac conduction process that modulates the frequency or rate of heart contraction.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of heart rate","termid":"GO:0002027"},{"relation_name":"is_a","term_name":"cardiac conduction","termid":"GO:0061337"}],"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 heart rate by cardiac conduction","termid":"GO:0086091"}


id: GO:0017195
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The acetylation of the N-terminal lysine of proteins to form the derivative N2-acetyl-L-lysine. The occurrence of this modification has not been confirmed.","definition_xrefs":["RESID:AA0048"],"gene_count":0,"genotype_count":0,"name":"obsolete N-terminal peptidyl-lysine N2-acetylation (obsolete GO:0017195)","termid":"GO:0017195"}


id: MONDO:0011179
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leishmaniasis, tegumentary, susceptibility to","secondary_identifiers":["MEDGEN:412566","OMIM:602068","UMLS:C2748501"],"synonyms":[{"name":"leishmaniasis, tegumentary, susceptibility to","type":"exact"}],"termid":"MONDO:0011179","xrefs":{"Monarch":{"xref_id":"0011179"}}}


id: PBO:0078716
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Leu (anticodon TAA) 1-1","termid":"PBO:0078716"}


id: MONDO:0024463
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"46 XX gonadal dysgenesis","termid":"MONDO:0009299"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"ovarian dysgenesis 1","secondary_identifiers":["DOID:0080493","GARD:18039","OMIM:233300","UMLS:C0949595","MEDGEN:215397"],"synonyms":[{"name":"ODG1","type":"exact"},{"name":"XX gonadal dysgenesis","type":"related"},{"name":"XXGD","type":"related"},{"name":"gonadal dysgenesis, 20 type","type":"related"},{"name":"gonadal dysgenesis, XX type","type":"related"},{"name":"ovarian dysgenesis 1","type":"exact"},{"name":"ovarian dysgenesis, hypergonadotropic, autosomal recessive","type":"related"},{"name":"ovarian dysgenesis, hypergonadotropic, with normal karyotype","type":"related"},{"name":"ovarian failure, hypergonadotropic","type":"related"}],"termid":"MONDO:0024463","xrefs":{"Monarch":{"xref_id":"0024463"}}}


id: PBO:0083778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential nucleolar protein involved in pre-18S rRNA processing; binds to RNA and stimulates ATPase activity of Dbp8; involved in assembly of the small subunit (SSU) processome","termid":"PBO:0083778"}


id: MONDO:0005427
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete vasuclar dementia (obsolete MONDO:0005427)","termid":"MONDO:0005427","xrefs":{"Monarch":{"xref_id":"0005427"}}}


id: PBO:0038332
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-connecting_branch_of","termid":"PBO:0038332"}


id: PBO:0071511
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L34 pseudogene 14","termid":"PBO:0071511"}


id: PBO:0062674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 14 subfamily A member 16","termid":"PBO:0062674"}


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


id: MONDO:1011202
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited disorder affecting the structure, composition, and quantity of tooth enamel in dogs due to a variation in the ENAM gene.","definition_xrefs":["PMID:30877375"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amelogenesis imperfecta, non-human animal","termid":"MONDO:1012952"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amelogenesis imperfecta, ENAM-related, dog","secondary_identifiers":["OMIA:001805-9615"],"termid":"MONDO:1011202","xrefs":{"Monarch":{"xref_id":"1011202"}}}


id: MONDO:0859169
data:
  {"annotated_genes":["SJAG_03454"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86109],"is_not":false,"summary":null,"term":"MONDO:0859169"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03454":null},"genotype_count":0,"is_obsolete":false,"name":"White-Kernohan syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1785087","OMIM:619426","UMLS:C5543635"],"termid":"MONDO:0859169","terms_by_termid":{"MONDO:0859169":null},"xrefs":{"Monarch":{"xref_id":"0859169"}}}


id: GO:0015099
data:
  {"annotated_genes":["SJAG_04830"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79738],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044750"}]},"cv_name":"molecular_function","definition":"Enables the transfer of nickel (Ni) cations from one side of a membrane to the other.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transition metal ion transmembrane transporter activity","termid":"GO:0046915"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04830":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"nickel cation transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:TRANS-RXN-141B"],"synonyms":[{"name":"zinc, cadmium, cobalt, nickel, lead-efflux ATPase activity","type":"related"}],"termid":"GO:0015099","terms_by_termid":{"GO:0044750":null}}


id: GO:0018647
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: phenanthrene + O2 + NADH + H+ = H2O + NAD+ + phenanthrene-1,2-oxide.","definition_xrefs":["PMID:1599252","UM-BBD_enzymeID:e0333"],"gene_count":0,"genotype_count":0,"name":"obsolete phenanthrene 1,2-monooxygenase activity (obsolete GO:0018647)","termid":"GO:0018647"}


id: PBO:0080224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vir like m6A methyltransferase associated","termid":"PBO:0080224"}


id: MONDO:0021169
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioma characterized by the presence of epithelioid endothelial cells.","definition_xrefs":["NCIT:C4298"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemangioma","termid":"MONDO:0006500"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epithelioid hemangioma","secondary_identifiers":["UMLS:C0205788","DOID:474","ICDO:9125/0","MEDGEN:61449","Orphanet:675396"],"synonyms":[{"name":"epithelioid haemangioma","type":"exact"},{"name":"epithelioid hemangioma","type":"exact"},{"name":"histiocytoid hemangioma","type":"exact"}],"termid":"MONDO:0021169","xrefs":{"Monarch":{"xref_id":"0021169"}}}


id: GO:0031722
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a hemoglobin beta chain.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemoglobin binding","termid":"GO:0030492"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"hemoglobin beta binding","termid":"GO:0031722"}


id: PBO:0002668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-directed RNA polymerase II complex subunit Rpb9","termid":"PBO:0002668"}


id: MONDO:0020093
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Autosomal dominant form of isolated diffuse palmoplantar keratoderma.","definition_xrefs":["MONDO:patterns/autosomal_dominant"],"gene_count":0,"genotype_count":0,"name":"obsolete autosomal dominant isolated diffuse palmoplantar keratoderma (obsolete MONDO:0020093)","secondary_identifiers":["Orphanet:98349"],"synonyms":[{"name":"autosomal dominant isolated diffuse palmoplantar hyperkeratosis","type":"exact"},{"name":"isolated diffuse palmoplantar keratoderma, autosomal dominant","type":"exact"}],"termid":"MONDO:0020093","xrefs":{"Monarch":{"xref_id":"0020093"}}}


id: PBO:0041785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcyphosine like","termid":"PBO:0041785"}


id: PBO:0041826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cysteinyl-tRNA synthetase 1 pseudogene 2","termid":"PBO:0041826"}


id: GO:0047979
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: hexose + O2 = aldono-1,5-lactone + H202.","definition_xrefs":["EC:1.1.3.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor","termid":"GO:0016899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"hexose oxidase activity","synonyms":[{"name":"D-hexose:oxygen 1-oxidoreductase activity","type":"related"}],"termid":"GO:0047979"}


id: PBO:0029125
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_saccharopine_dehydrogenase_activity","termid":"PBO:0029125"}


id: PBO:0040564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beta-1,4-N-acetyl-galactosaminyltransferase 4","termid":"PBO:0040564"}


id: MONDO:0012515
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"juvenile open angle glaucoma","termid":"MONDO:0020367"}],"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":"glaucoma 1, open angle, M","secondary_identifiers":["OMIM:610535","GARD:18230","MESH:C566436","UMLS:C1864653","MEDGEN:400584"],"synonyms":[{"name":"GLC1M","type":"exact"},{"name":"JOAG1M","type":"exact"},{"name":"glaucoma 1, open angle, M","type":"exact"}],"termid":"MONDO:0012515","xrefs":{"Monarch":{"xref_id":"0012515"}}}


id: PBO:0012841
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Perlman syndrome","termid":"PBO:0012841"}


id: GO:0010466
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops or reduces the rate of peptidase activity, the hydrolysis of peptide bonds within proteins.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of proteolysis","termid":"GO:0045861"},{"relation_name":"is_a","term_name":"negative regulation of hydrolase activity","termid":"GO:0051346"},{"relation_name":"is_a","term_name":"regulation of peptidase activity","termid":"GO:0052547"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of peptidase activity","termid":"GO:0010466"}


id: GO:0044504
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism effects a change in the activity of a receptor in a second organism.","definition_xrefs":["GOC:jl","GOC:fj","PMID:8405712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation of molecular function in another organism","termid":"GO:0044359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"modulation of receptor activity in another organism","synonyms":[{"name":"modulation of receptor activity in other organism","type":"exact"}],"termid":"GO:0044504"}


id: MONDO:1030016
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A schwannomatosis that causes a predisposition to develop multiple schwannoma. It is diagnosed when an individual does not meet criteria for NF2-related schwannomatosis, SMARCB1-related schwannomatosis, or LTZR1-related schwannomatosis and both of the following molecular features exist: a loss of heterozygosity (LOH) of the same chromosome 22q markers in two anatomically distinct tumors or hybrid nerve sheath tumors and a different NF2 pathogenic variant in each tumor which cannot be detected in unaffected tissue.","definition_xrefs":["PMID:35674741"],"direct_ancestors":[{"relation_name":"is_a","term_name":"schwannomatosis","termid":"MONDO:0008075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005093"],"is_obsolete":false,"name":"22q-related schwannomatosis","termid":"MONDO:1030016","xrefs":{"Monarch":{"xref_id":"1030016"}}}


id: FYPO:0004813
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the termination of transcription by RNA polymerase II at tRNA genes (tDNA) is abnormal.","definition_xrefs":["PMID:25417108","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal termination of RNA polymerase II transcription","termid":"FYPO:0004811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000294"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000294","FYPO:0005447","FYPO:0000002","FYPO:0006551","FYPO:0001985"],"is_obsolete":false,"name":"abnormal termination of RNA polymerase II transcription at tDNA","synonyms":[{"name":"abnormal RNA polymerase II release at tDNA","type":"related"},{"name":"abnormal RNA polymerase II transcription termination at tDNA","type":"exact"},{"name":"abnormal termination of RNA polymerase II transcription at tDNA during mitotic cell cycle","type":"related"},{"name":"abnormal termination of RNA polymerase II transcription at tDNA during vegetative growth","type":"exact"},{"name":"abnormal termination of RNA polymerase II transcription at transfer RNA genes","type":"related"}],"termid":"FYPO:0004813"}


id: PBO:0035909
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_acetylation_at_centromere_during_vegetative_growth","termid":"PBO:0035909"}


id: FYPO:0006863
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 bleomycin.","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:0002057"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"loss of viability following cellular response to bleomycin","synonyms":[{"name":"decreased viability following cellular response to bleomycin","type":"exact"},{"name":"loss of cell population viability following cellular response to bleomycin","type":"exact"},{"name":"loss of viability following bleomycin exposure","type":"exact"},{"name":"reduced viability following cellular response to bleomycin","type":"related"}],"termid":"FYPO:0006863"}


id: PBO:0043831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cleavage and polyadenylation specific factor 3","termid":"PBO:0043831"}


id: PR:P87177
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A WD repeat-containing protein 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02804"],"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 WD repeat-containing protein C3D6.12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3D6.12","secondary_identifiers":["UniProtKB:P87177"],"synonyms":[{"name":"Spom972h-WDR3","type":"exact"}],"termid":"PR:P87177"}


id: GO:0046080
data:
  {"annotated_genes":["SJAG_04487"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046081"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving dUTP, deoxyuridine (5'-)triphosphate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleoside triphosphate metabolic process","termid":"GO:0009211"},{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleotide metabolic process","termid":"GO:0009219"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04487":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"dUTP metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"dUTP metabolism","type":"exact"}],"termid":"GO:0046080","terms_by_termid":{"GO:0046081":null}}


id: PBO:0079531
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U2 small nuclear RNA auxiliary factor 1","termid":"PBO:0079531"}


id: PBO:0053311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lin-54 DREAM MuvB core complex component","termid":"PBO:0053311"}


id: FYPO:0003410
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 chromatin containing the histone H3 variant CenH3 (also called CENP-A; Cnp1 in S. pombe) are assembled over a larger portion of the centromeric region of the chromosome than normal. CENP-A-containing nucleosomes are normally assembled into chromatin at the centromeres, encompassing the central core and centromeric inner repeat regions.","definition_xrefs":["PomBase:mah","PomBase:vw","GO:0034080","PMID:24710126"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal CENP-A containing chromatin assembly","termid":"FYPO:0003409"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000641","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"increased spatial extent of CENP-A containing chromatin assembly","synonyms":[{"name":"CENP-A containing nucleosome spreading","type":"related"},{"name":"increased extent of CENP-A containing nucleosome","type":"related"},{"name":"increased spatial extent of CENP-A containing nucleosome assembly","type":"related"},{"name":"increased spatial extent of CENP-A containing nucleosome assembly at centromere","type":"exact"},{"name":"increased spatial extent of CENP-A containing nucleosome assembly during mitotic cell cycle","type":"related"},{"name":"increased spatial extent of CENP-A containing nucleosome assembly during vegetative growth","type":"exact"},{"name":"increased spatial extent of CENP-A deposition","type":"related"},{"name":"increased spatial extent of CENP-A loading","type":"related"},{"name":"increased spatial extent of CenH3-containing nucleosome assembly at centromere","type":"related"},{"name":"increased spatial extent of DNA replication-independent nucleosome assembly at centromere","type":"exact"},{"name":"increased spatial extent of centromere-specific histone exchange","type":"exact"},{"name":"increased spatial extent of centromere-specific nucleosome assembly","type":"exact"},{"name":"increased spatial extent of centromeric DNA replication-independent nucleosome assembly","type":"exact"}],"termid":"FYPO:0003410"}


id: SO:0001176
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Non-base-paired sequence of nucleotide bases in tRNA. It contains several dihydrouracil residues.","definition_xrefs":["ISBN:071671920"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA_region","termid":"SO:0001172"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DHU_loop","synonyms":[{"name":"D loop","type":"related"},{"name":"DHU loop","type":"exact"}],"termid":"SO:0001176"}


id: PBO:0026781
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_cell_cycle_progression_following_cellular_response_to_hydroxyurea","termid":"PBO:0026781"}


id: PBO:0068523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 119, pseudogene","termid":"PBO:0068523"}


id: MONDO:0045037
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An opportunistic infection caused by a heterogeneous group of mitosporic fungi with clear (hyalo-) hyphae in the host. Common causative agents include acremonium; aspergillus; chrysosporium; fusarium; paecilomyces; penicillium; pseudallescheria; scedosporium; and scopulariopsis. Normally a dermatomycoses, it can become invasive in the immunocompromised host.","definition_xrefs":["MESH:D060605"],"direct_ancestors":[{"relation_name":"is_a","term_name":"opportunistic mycosis","termid":"MONDO:0002312"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyalohyphomycosis","secondary_identifiers":["MEDGEN:452455","SCTID:240773008","UMLS:C0343952"],"synonyms":[{"name":"hyalohyphomycosis","type":"exact"}],"termid":"MONDO:0045037","xrefs":{"Monarch":{"xref_id":"0045037"}}}


id: PBO:0074644
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 36A","termid":"PBO:0074644"}


id: PR:O75011
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A CaM kinase-like vesicle-associated protein that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03293"],"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":"serine/threonine-protein kinase nak1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17F3.02","secondary_identifiers":["UniProtKB:O75011"],"synonyms":[{"name":"N-rich kinase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-CAMKV","type":"exact"}],"termid":"PR:O75011"}


id: MONDO:0019820
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital heart malformation","termid":"MONDO:0019512"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"univentricular cardiopathy","secondary_identifiers":["UMLS:C5681576","GARD:19269","MEDGEN:1843389","Orphanet:95483"],"termid":"MONDO:0019820","xrefs":{"Monarch":{"xref_id":"0019820"}}}


id: MONDO:0011172
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":"otofacioosseous-gonadal syndrome","secondary_identifiers":["OMIM:601976","UMLS:C1865988","MEDGEN:356416","MESH:C566597"],"synonyms":[{"name":"otofacioosseous-gonadal syndrome","type":"exact"}],"termid":"MONDO:0011172","xrefs":{"Monarch":{"xref_id":"0011172"}}}


id: GO:0048516
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Processes causing the differentiation of an epidermal cell into a trichome cell; as in, but not restricted to, the flowering plants (Magnoliophyta, ncbi_taxonomy_id:3398).","definition_xrefs":["GOC:lr"],"gene_count":0,"genotype_count":0,"name":"obsolete trichome initiation (sensu Magnoliophyta) (obsolete GO:0048516)","synonyms":[{"name":"trichome initiation (sensu Magnoliophyta)","type":"exact"}],"termid":"GO:0048516"}


id: MONDO:0002452
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign smooth muscle neoplasm arising from the prostate. It is characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.","definition_xrefs":["NCIT:C5544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"},{"relation_name":"is_a","term_name":"benign neoplasm of prostate","termid":"MONDO:0021510"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostate leiomyoma","secondary_identifiers":["DOID:2887","MEDGEN:233875","UMLS:C1335510"],"synonyms":[{"name":"leiomyoma of prostate","type":"exact"},{"name":"leiomyoma of prostate gland","type":"exact"},{"name":"leiomyoma of the prostate","type":"exact"},{"name":"prostate gland leiomyoma","type":"exact"},{"name":"prostate leiomyoma","type":"exact"},{"name":"prostatic leiomyoma","type":"exact"}],"termid":"MONDO:0002452","xrefs":{"Monarch":{"xref_id":"0002452"}}}


id: PBO:0073328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serpin family A member 4","termid":"PBO:0073328"}


id: GO:2001173
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of histone H2B conserved C-terminal lysine ubiquitination.","definition_xrefs":["PMID:17576814"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone H2B conserved C-terminal lysine ubiquitination (obsolete GO:2001173)","synonyms":[{"name":"regulation of budding yeast H2B K123 ubiquitination","type":"related"},{"name":"regulation of fission yeast H2B K119 ubiquitination","type":"related"},{"name":"regulation of mammalian H2B K120 ubiquitination","type":"related"}],"termid":"GO:2001173"}


id: FYPO:0001935
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of proton-transporting ATP synthase activity by a rotational mechanism is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"},{"relation_name":"is_a","term_name":"abnormal metabolic process","termid":"FYPO:0000860"},{"relation_name":"is_a","term_name":"abnormal transmembrane transporter activity","termid":"FYPO:0002116"},{"relation_name":"is_a","term_name":"abnormal proton transport","termid":"FYPO:0005971"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0002114"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0000002","FYPO:0000652","FYPO:0000654","FYPO:0002114","FYPO:0000707","FYPO:0001985","FYPO:0000661"],"is_obsolete":false,"name":"abnormal proton-transporting ATP synthase activity, rotational mechanism","synonyms":[{"name":"abnormal hydrogen ion transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"abnormal mitochondrial proton-transporting ATP synthase activity","type":"narrow"},{"name":"abnormal proton-transporting ATP synthase activity","type":"related"}],"termid":"FYPO:0001935"}


id: MONDO:0018614
data:
  {"annotated_genes":["SJAG_02384","SJAG_01059","SJAG_01851","SJAG_02848","SJAG_02180","SJAG_04157","SJAG_02084","SJAG_01797"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86162],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014392"},{"annotations":[85029],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014593"},{"annotations":[85040,85039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014598"},{"annotations":[85004,85003,85005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014625"},{"annotations":[86925],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014933"}]},"cv_name":"mondo","definition":"A rare infantile epilepsy syndrome characterized by early onset of seizures of variable type and severity, potentially associated with a spectrum of clinical signs and symptoms including delay or lack of psychomotor development, intellectual disability, poor or absent speech development, behavioral abnormalities, hypotonia, movement disorders, spasticity, microcephaly, and dysmorphic facial features, among others. Brain imaging findings are also variable and may include cerebral atrophy or white matter abnormalities.","definition_xrefs":["Orphanet:442835"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of amino acid transport","termid":"MONDO:0019216"},{"relation_name":"is_a","term_name":"neonatal epilepsy syndrome","termid":"MONDO:0020070"},{"relation_name":"is_a","term_name":"infantile epilepsy syndrome","termid":"MONDO:0020071"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":8,"genes_by_uniquename":{"SJAG_01059":null,"SJAG_01797":null,"SJAG_01851":null,"SJAG_02084":null,"SJAG_02180":null,"SJAG_02384":null,"SJAG_02848":null,"SJAG_04157":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005027","MONDO:0005066"],"is_obsolete":false,"name":"undetermined early-onset epileptic encephalopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5680057","GARD:15028","MEDGEN:1826068"],"synonyms":[{"name":"non-specific early-onset epileptic encephalopathy","type":"exact"},{"name":"undetermined EOEE","type":"exact"},{"name":"undetermined early-onset epileptic encephalopathy","type":"exact"}],"termid":"MONDO:0018614","terms_by_termid":{"MONDO:0014392":null,"MONDO:0014593":null,"MONDO:0014598":null,"MONDO:0014625":null,"MONDO:0014933":null},"xrefs":{"Monarch":{"xref_id":"0018614"}}}


id: GO:0006935
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a motile cell or organism, or the directed growth of a cell guided by a specific chemical concentration gradient. Movement may be towards a higher concentration (positive chemotaxis) or towards a lower concentration (negative chemotaxis).","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"taxis","termid":"GO:0042330"},{"relation_name":"part_of","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":"chemotaxis","secondary_identifiers":["Wikipedia:Chemotaxis"],"synonyms":[{"name":"taxis in response to chemical stimulus","type":"exact"}],"termid":"GO:0006935"}


id: PBO:0056286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MANEA divergent transcript","termid":"PBO:0056286"}


id: PBO:0083789
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential protein involved in rRNA processing and ribosome biogenesis; forms a complex with Utp22p; protein abundance increases in response to DNA replication stress","termid":"PBO:0083789"}


id: GO:0070328
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the maintenance of an internal steady state of triglyceride within an organism or cell.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acylglycerol homeostasis","termid":"GO:0055090"}],"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":"triglyceride homeostasis","synonyms":[{"name":"triacylglycerol homeostasis","type":"exact"}],"termid":"GO:0070328"}


id: GO:0016580
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A multiprotein complex that functions broadly in eukaryotic organisms as a transcriptional repressor of protein-coding genes, through the gene-specific deacetylation of histones. Amongst its subunits, the Sin3 complex contains Sin3-like proteins, and a number of core proteins that are shared with the NuRD complex (including histone deacetylases and histone binding proteins). The Sin3 complex does not directly bind DNA itself, but is targeted to specific genes through protein-protein interactions with DNA-binding proteins.","definition_xrefs":["PMID:10589671","PMID:11743021","PMID:12865422"],"gene_count":0,"genotype_count":0,"name":"obsolete Sin3 complex (obsolete GO:0016580)","termid":"GO:0016580"}


id: GO:0098908
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of action potential creation, propagation or termination in a neuron. This typically occurs via modulation of the activity or expression of voltage-gated ion channels.","definition_xrefs":["GOC:tb","GOC:dph","GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transmission of nerve impulse","termid":"GO:0051969"},{"relation_name":"is_a","term_name":"regulation of action potential","termid":"GO:0098900"},{"relation_name":"regulates","term_name":"neuronal action potential","termid":"GO:0019228"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of neuronal action potential","synonyms":[{"name":"generation of action potential","type":"related"}],"termid":"GO:0098908"}


id: GO:0007614
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The memory process that deals with the storage, retrieval and modification of information received a short time (up to about 30 minutes) ago. This type of memory is typically dependent on direct, transient effects of second messenger activation.","definition_xrefs":["ISBN:0582227089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"memory","termid":"GO:0007613"}],"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":"short-term memory","secondary_identifiers":["Wikipedia:Short-term_memory"],"termid":"GO:0007614"}


id: PBO:0043635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COPI coat complex subunit gamma 2","termid":"PBO:0043635"}


id: PBO:0052887
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 9-10, pseudogene","termid":"PBO:0052887"}


id: GO:0150022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an apical dendrite over time, from its formation to the mature structure.","definition_xrefs":["GOC:aruk","GOC:bc","PMID:22683681"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dendrite development","termid":"GO:0016358"}],"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":"apical dendrite development","termid":"GO:0150022"}


id: MONDO:0011146
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pallister-Killian syndrome (PKS) is a rare multiple congenital anomaly/intellectual deficit syndrome caused by mosaic tissue-limited tetrasomy for chromosome 12p.","definition_xrefs":["Orphanet:884"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"epilepsy","termid":"MONDO:0005027"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"partial trisomy/tetrasomy of the short arm of chromosome 12","termid":"MONDO:0016933"},{"relation_name":"is_a","term_name":"overgrowth syndrome","termid":"MONDO:0019716"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetrasomy 12p","secondary_identifiers":["NCIT:C75458","GARD:8421","ICD9:758.81","MESH:C538105","NORD:1546","OMIM:601803","SCTID:9527009","UMLS:C0265449","MEDGEN:120540"],"synonyms":[{"name":"Hexasomy 12P, Mosaic","type":"related"},{"name":"Isochromosome 12P syndrome","type":"related"},{"name":"Isochromosome 12p mosaicism","type":"exact"},{"name":"Isochromosome 12p syndrome","type":"exact"},{"name":"Killian Teschler-Nicola syndrome","type":"related"},{"name":"Killian syndrome","type":"related"},{"name":"PKS","type":"related"},{"name":"Pallister Killian Mosaic Syndrome","type":"exact"},{"name":"Pallister Killian syndrome","type":"related"},{"name":"Pallister mosaic syndrome","type":"related"},{"name":"Pallister-Killian mosaic syndrome","type":"related"},{"name":"Pallister-Killian syndrome","type":"exact"},{"name":"Pallister-Killian syndrome, Somatic mosaicism","type":"exact"},{"name":"Teschler-Nicola Killian syndrome","type":"related"},{"name":"chromosome 12, Isochromosome 12p syndrome","type":"related"},{"name":"tetrasomy 12P, Mosaic","type":"related"},{"name":"tetrasomy type 12p","type":"exact"}],"termid":"MONDO:0011146","xrefs":{"Monarch":{"xref_id":"0011146"}}}


id: MONDO:0851095
data:
  {"annotated_genes":["SJAG_02238"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86356],"is_not":false,"summary":null,"term":"MONDO:0851095"}]},"cv_name":"mondo","definition":"A syndrome characterized by developmental delay, impaired intellectual development, seizures, mesomelic dysplasia, dysmorphic facial features, horseshoe or hypoplastic kidney, and failure to thrive that has material basis in heterozygous mutation in AFF3 on chromosome 2q11.2.","definition_xrefs":["DOID:0112383"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02238":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"KINSSHIP syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1779339","OMIM:619297","UMLS:C5543317"],"termid":"MONDO:0851095","terms_by_termid":{"MONDO:0851095":null},"xrefs":{"Monarch":{"xref_id":"0851095"}}}


id: PR:P87118
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An inorganic pyrophosphatase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00572"],"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":"inorganic pyrophosphatase C3A12.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3A12.02","secondary_identifiers":["UniProtKB:P87118"],"synonyms":[{"name":"PPase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PPA1","type":"exact"},{"name":"pyrophosphate phosphohydrolase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P87118"}


id: PBO:0049910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hexosaminidase subunit beta","termid":"PBO:0049910"}


id: MONDO:0020409
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"univentricular heart","termid":"MONDO:0015451"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"univentricular heart with single atrio-ventricular valve","secondary_identifiers":["Orphanet:99069"],"termid":"MONDO:0020409","xrefs":{"Monarch":{"xref_id":"0020409"}}}


id: GO:0019238
data:
  {"annotated_genes":["SJAG_04156","SJAG_03275","SJAG_00376","SJAG_04711","SJAG_00106","SJAG_02400","SJAG_04681"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[69671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003934"},{"annotations":[58661,60065],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003935"},{"annotations":[69583],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003937"},{"annotations":[75628,76338],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004477"},{"annotations":[60024],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004635"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of any non-peptide carbon-nitrogen bond in a cyclic amidine, a compound of the form R-C(=NH)-NH2, in a reaction that involves the opening of a ring.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines","termid":"GO:0016814"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00106":null,"SJAG_00376":null,"SJAG_02400":null,"SJAG_03275":null,"SJAG_04156":null,"SJAG_04681":null,"SJAG_04711":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"}],"interesting_parent_ids":["GO:0016810","GO:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"cyclohydrolase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null},"termid":"GO:0019238","terms_by_termid":{"GO:0003934":null,"GO:0003935":null,"GO:0003937":null,"GO:0004477":null,"GO:0004635":null}}


id: PBO:0075611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPOPL divergent transcript","termid":"PBO:0075611"}


id: PBO:0072738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S100 calcium binding protein A3","termid":"PBO:0072738"}


id: GO:0000105
data:
  {"annotated_genes":["SJAG_00592","SJAG_00248","SJAG_04747","SJAG_03055","SJAG_03775","SJAG_01346","SJAG_01137","SJAG_02400"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[57836,60026,64152,70902,75501,76378,78222,79941],"is_not":false,"summary":null,"term":"GO:0000105"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of L-histidine, 2-amino-3-(1H-imidazol-4-yl)propanoic acid.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-histidine metabolic process","termid":"GO:0006547"},{"relation_name":"is_a","term_name":"aromatic amino acid family biosynthetic process","termid":"GO:0009073"},{"relation_name":"is_a","term_name":"L-amino acid biosynthetic process","termid":"GO:0170034"},{"relation_name":"is_a","term_name":"proteinogenic amino acid biosynthetic process","termid":"GO:0170038"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00248":null,"SJAG_00592":null,"SJAG_01137":null,"SJAG_01346":null,"SJAG_02400":null,"SJAG_03055":null,"SJAG_03775":null,"SJAG_04747":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006520"],"is_obsolete":false,"name":"L-histidine biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null},"secondary_identifiers":["MetaCyc:HISTSYN-PWY"],"synonyms":[{"name":"histidine anabolism","type":"exact"},{"name":"histidine biosynthesis","type":"exact"},{"name":"histidine biosynthetic process","type":"broad"},{"name":"histidine formation","type":"exact"},{"name":"histidine synthesis","type":"exact"}],"termid":"GO:0000105","terms_by_termid":{"GO:0000105":null}}


id: PBO:0069848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1134, pseudogene","termid":"PBO:0069848"}


id: GO:0043200
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an amino acid stimulus. An amino acid is a carboxylic acids containing one or more amino groups.","definition_xrefs":["GOC:mlg","GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to acid chemical","termid":"GO:0001101"}],"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 amino acid","secondary_identifiers":["GO:0010237"],"synonyms":[{"name":"response to amino acid stimulus","type":"exact"}],"termid":"GO:0043200"}


id: PBO:0071100
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 102","termid":"PBO:0071100"}


id: PBO:0082588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cis-golgi localized monothiol glutaredoxin; more similar in activity to dithiol than other monothiol glutaredoxins; involved in the oxidative stress response; does not bind metal ions; GRX7 has a paralog, GRX6, that arose from the whole genome duplication","termid":"PBO:0082588"}


id: PBO:0078254
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 29-1","termid":"PBO:0078254"}


id: PR:O14017
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC29A4.14c gene.","definition_xrefs":["UniProtKB:O14017","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 C29A4.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29A4.14c","synonyms":[{"name":"Spom972h-SPAC29A4.14c","type":"exact"}],"termid":"PR:O14017"}


id: GO:0071154
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex formed by the association of the guanine nucleotide exchange factor synembrin with the alpha(i)1 subunit of a heterotrimeric G protein.","definition_xrefs":["GOC:mah","PMID:12509430"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"G-protein alpha(i)1-synembrin complex","synonyms":[{"name":"Ric-8A G(i) alpha-1 subunit complex","type":"narrow"},{"name":"Ric-8A G(i) alpha-2 subunit complex","type":"related"}],"termid":"GO:0071154"}


id: PBO:0051284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 1-27","termid":"PBO:0051284"}


id: FYPO:0004052
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell is too low to detect during a cellular response to hydrogen peroxide. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during cellular response to hydrogen peroxide","termid":"FYPO:0001116"},{"relation_name":"is_a","term_name":"RNA absent from cell during cellular response to oxidative stress","termid":"FYPO:0007794"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0006551","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"RNA absent from cell during cellular response to hydrogen peroxide","synonyms":[{"name":"RNA absent from cell during cellular response to H2O2","type":"exact"},{"name":"RNA absent from cell during cellular response to hydrogen peroxide during mitotic cell cycle","type":"related"},{"name":"RNA absent from cell during cellular response to hydrogen peroxide during vegetative growth","type":"exact"},{"name":"transcripts absent from cell during cellular response to hydrogen peroxide","type":"exact"},{"name":"undetectable RNA level during cellular response to hydrogen peroxide","type":"exact"}],"termid":"FYPO:0004052"}


id: GO:0060958
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of an endocardial cell over time, from its formation to the mature cell. An endocardial cell is a specialized endothelial cell that makes up the endocardium portion of the heart.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endothelial cell development","termid":"GO:0001885"},{"relation_name":"is_a","term_name":"cardiac cell development","termid":"GO:0055006"},{"relation_name":"part_of","term_name":"endocardial cell differentiation","termid":"GO:0060956"}],"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":"endocardial cell development","termid":"GO:0060958"}


id: PBO:0046396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"erythrocyte membrane protein band 4.1 like 2","termid":"PBO:0046396"}


id: GO:0103009
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + 3-chlorotoluene + NADH + O2 = 3-chlorobenzyl alcohol + NAD + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-chlorotoluene monooxygenase activity (obsolete GO:0103009)","termid":"GO:0103009"}


id: GO:0042663
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that mediates the specification of a cell into an endoderm cell.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell fate specification","termid":"GO:0042659"},{"relation_name":"is_a","term_name":"regulation of endodermal cell differentiation","termid":"GO:1903224"},{"relation_name":"regulates","term_name":"endodermal cell fate specification","termid":"GO:0001714"}],"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 endodermal cell fate specification","synonyms":[{"name":"regulation of endoderm cell fate specification","type":"exact"}],"termid":"GO:0042663"}


id: PBO:0017030
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human MARK4","termid":"PBO:0017030"}


id: GO:1903572
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of protein kinase D signaling.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","GOC:BHF","PMID:20497126","GOC:rl"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of protein kinase D signaling (obsolete GO:1903572)","synonyms":[{"name":"activation of PKD signal transduction","type":"narrow"},{"name":"activation of PKD signaling cascade","type":"related"},{"name":"activation of protein kinase D signal transduction","type":"narrow"},{"name":"activation of protein kinase D signaling","type":"narrow"},{"name":"activation of protein kinase D signaling cascade","type":"related"},{"name":"activation of protein kinase D signalling cascade","type":"related"},{"name":"positive regulation of PKD signal transduction","type":"exact"},{"name":"positive regulation of PKD signaling cascade","type":"related"},{"name":"positive regulation of protein kinase D signal transduction","type":"exact"},{"name":"positive regulation of protein kinase D signaling cascade","type":"related"},{"name":"positive regulation of protein kinase D signalling cascade","type":"related"},{"name":"up regulation of PKD signal transduction","type":"exact"},{"name":"up regulation of PKD signaling cascade","type":"related"},{"name":"up regulation of protein kinase D signal transduction","type":"exact"},{"name":"up regulation of protein kinase D signaling","type":"exact"},{"name":"up regulation of protein kinase D signaling cascade","type":"related"},{"name":"up regulation of protein kinase D signalling cascade","type":"related"},{"name":"up-regulation of PKD signal transduction","type":"exact"},{"name":"up-regulation of PKD signaling cascade","type":"related"},{"name":"up-regulation of protein kinase D signal transduction","type":"exact"},{"name":"up-regulation of protein kinase D signaling","type":"exact"},{"name":"up-regulation of protein kinase D signaling cascade","type":"related"},{"name":"up-regulation of protein kinase D signalling cascade","type":"related"},{"name":"upregulation of PKD signal transduction","type":"exact"},{"name":"upregulation of PKD signaling cascade","type":"related"},{"name":"upregulation of protein kinase D signal transduction","type":"exact"},{"name":"upregulation of protein kinase D signaling","type":"exact"},{"name":"upregulation of protein kinase D signaling cascade","type":"related"},{"name":"upregulation of protein kinase D signalling cascade","type":"related"}],"termid":"GO:1903572"}


id: PBO:0061841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoglycin","termid":"PBO:0061841"}


id: GO:0051466
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the regulated release of corticotropin-releasing hormone from a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of corticotropin-releasing hormone secretion","termid":"GO:0043397"},{"relation_name":"is_a","term_name":"positive regulation of peptide hormone secretion","termid":"GO:0090277"},{"relation_name":"positively_regulates","term_name":"corticotropin-releasing hormone secretion","termid":"GO:0043396"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0006810","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of corticotropin-releasing hormone secretion","synonyms":[{"name":"activation of corticotropin-releasing hormone secretion","type":"narrow"},{"name":"positive regulation of CRF secretion","type":"exact"},{"name":"positive regulation of CRH secretion","type":"exact"},{"name":"positive regulation of corticotropin-releasing factor secretion","type":"exact"},{"name":"stimulation of corticotropin-releasing hormone secretion","type":"narrow"},{"name":"up regulation of corticotropin-releasing hormone secretion","type":"exact"},{"name":"up-regulation of corticotropin-releasing hormone secretion","type":"exact"},{"name":"upregulation of corticotropin-releasing hormone secretion","type":"exact"}],"termid":"GO:0051466"}


id: PBO:0066290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein Y-linked family 2 member Q, pseudogene","termid":"PBO:0066290"}


id: FYPO:0000914
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of glutamate-ammonia ligase (also known as glutamine synthetase) activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal catalytic activity","termid":"FYPO:0000660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000654","FYPO:0000652"],"is_obsolete":false,"name":"normal glutamate-ammonia ligase activity","synonyms":[{"name":"normal GS activity","type":"exact"},{"name":"normal glutamine synthetase activity","type":"exact"},{"name":"normal glutamylhydroxamic synthetase activity","type":"exact"}],"termid":"FYPO:0000914"}


id: PBO:0000503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDZ domain protein","termid":"PBO:0000503"}


id: PBO:0002807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"superoxide dismutase copper chaperone Ccs1","termid":"PBO:0002807"}


id: PBO:0001107
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulated by temperature","termid":"PBO:0001107"}


id: MOD:00327
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-tryptophan residue to a 3-hydroxy-L-tryptophan.","definition_xrefs":["PubMed:11457355","RESID:AA0322","ChEBI:141794","PubMed:10024453"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monohydroxylated tryptophan","termid":"MOD:01622"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-hydroxy-L-tryptophan","synonyms":[{"name":"(2S,3S)-2-amino-3-hydroxy-3-(1H-indol-3-yl)propanoic acid","type":"exact"},{"name":"3-hydroxy-L-tryptophan","type":"exact"},{"name":"3-hydroxylated L-tryptophan","type":"exact"},{"name":"3-hydroxytryptophan","type":"exact"},{"name":"3HyTrp","type":"exact"},{"name":"MOD_RES 3-hydroxytryptophan","type":"exact"},{"name":"beta-hydroxytryptophan","type":"exact"}],"termid":"MOD:00327"}


id: PBO:0055899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 20","termid":"PBO:0055899"}


id: PBO:0000972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II complex subunit Rpb11","termid":"PBO:0000972"}


id: PBO:0091499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PI31 proteasome inhibitor Fub1","termid":"PBO:0091499"}


id: PBO:0055370
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 2799","termid":"PBO:0055370"}


id: GO:0010171
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the soma are generated and organized.","definition_xrefs":["ISBN:0140512888","GOC:ems"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"body morphogenesis","termid":"GO:0010171"}


id: PBO:0059852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase pseudogene 5","termid":"PBO:0059852"}


id: PBO:0043083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholinergic receptor nicotinic beta 3 subunit","termid":"PBO:0043083"}


id: PBO:0047453
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FCHO2 divergent transcript","termid":"PBO:0047453"}


id: PR:000037033
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mitotic cohesin complex subunit Psm3/Smc3 (Schizosaccharomyces pombe) that has been acetylated on two Lys residues equivalent to Lys-105 and Lys-106 of the amino acid sequence represented by UniProtKB:O42649. Example: UniProtKB:O42649, Lys-105/Lys-106, MOD:00723.","definition_xrefs":["PMID:26687354","PomBase:VW","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic cohesin complex subunit Psm3/Smc3 (Schizosaccharomyces pombe)","termid":"PR:000037032"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"psm3/Ac(K105,K106)","pombase_gene_id":"SPAC10F6.09c","synonyms":[{"name":"PomBase_original_PRO_term_name: mitotic cohesin complex subunit Psm3/Smc3 acetylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-psm3/Ac:1","type":"exact"},{"name":"UniProtKB:O42649, Lys-105/Lys-106, MOD:00723","type":"narrow"},{"name":"cohesin complex Psm3 subunit acetylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"psm3/Ac(K105,K106)","type":"exact"},{"name":"structural maintenance of chromosomes protein 3 acetylated 1 (Schizosaccharomyces pombe)","type":"exact"}],"termid":"PR:000037033"}


id: PBO:0038418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-1-B glycoprotein","termid":"PBO:0038418"}


id: MOD:00178
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-(ADP-ribosyl)-L-cysteine.","definition_xrefs":["Unimod:213#C","PubMed:3863818","DeltaMass:0","PubMed:15842200","RESID:AA0169"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenosine diphosphoribosyl (ADP-ribosyl) modified residue","termid":"MOD:00752"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-(ADP-ribosyl)-L-cysteine","synonyms":[{"name":"(R)-2-amino-3-([adenosine 5'-(trihydrogen diphosphate) 5'->5'-ester with alpha-D-ribofuranosyl]sulfanyl)propanoic acid","type":"exact"},{"name":"ADP Ribose addition","type":"related"},{"name":"ADP-Ribosyl","type":"related"},{"name":"ADPRibCys","type":"exact"},{"name":"MOD_RES ADP-ribosylcysteine","type":"exact"},{"name":"S-(ADP-ribosyl)- (on Cysteine)","type":"exact"},{"name":"S-(ADP-ribosyl)-L-cysteine","type":"exact"},{"name":"S-L-cysteine alpha-D-ribofuranoside 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)","type":"exact"},{"name":"S-alpha-D-ribofuranosyl-L-cysteine 5'->5'-ester with adenosine 5'-(trihydrogen diphosphate)","type":"exact"}],"termid":"MOD:00178"}


id: MONDO:0032889
data:
  {"annotated_genes":["SJAG_03931","SJAG_00142"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86586,86587],"is_not":false,"summary":null,"term":"MONDO:0032889"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00142":null,"SJAG_03931":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"Poirier-Bienvenu neurodevelopmental syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1684718","OMIM:618732","UMLS:C5231482"],"synonyms":[{"name":"POBINDS","type":"related"},{"name":"POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME","type":"related"}],"termid":"MONDO:0032889","terms_by_termid":{"MONDO:0032889":null},"xrefs":{"Monarch":{"xref_id":"0032889"}}}


id: MONDO:0016072
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An instance of anomaly of puberty or/and menstrual cycle that is caused by a modification of the individual's genome.","definition_xrefs":["MONDO:patterns/genetic"],"gene_count":0,"genotype_count":0,"name":"obsolete anomaly of puberty or/and menstrual cycle of genetic origin (obsolete MONDO:0016072)","secondary_identifiers":["Orphanet:202940"],"synonyms":[{"name":"genetic anomaly of puberty or/and menstrual cycle","type":"exact"}],"termid":"MONDO:0016072","xrefs":{"Monarch":{"xref_id":"0016072"}}}


id: GO:0006559
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of phenylalanine, 2-amino-3-phenylpropanoic acid.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-phenylalanine metabolic process","termid":"GO:0006558"},{"relation_name":"is_a","term_name":"aromatic amino acid family catabolic process","termid":"GO:0009074"},{"relation_name":"is_a","term_name":"erythrose 4-phosphate/phosphoenolpyruvate family amino acid catabolic process","termid":"GO:1902222"}],"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:0006520"},{"rel_name":"is_a","termid":"GO:0044248"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044248","GO:0044281"],"is_obsolete":false,"name":"L-phenylalanine catabolic process","synonyms":[{"name":"L-phenylalanine breakdown","type":"exact"},{"name":"L-phenylalanine catabolism","type":"exact"},{"name":"L-phenylalanine degradation","type":"exact"},{"name":"phenylalanine catabolic process","type":"broad"},{"name":"phenylalanine catabolism","type":"broad"}],"termid":"GO:0006559"}


id: MONDO:0006927
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with bacteria of the family rickettsiaceae.","definition_xrefs":["MESH:D012288"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Rickettsiosis","termid":"MONDO:0006956"},{"relation_name":"is_a","term_name":"gram-negative bacterial infections","termid":"MONDO:0021678"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rickettsiaceae infectious disease","secondary_identifiers":["EFO:1001128"],"synonyms":[{"name":"Rickettsiaceae caused disease or disorder","type":"exact"},{"name":"Rickettsiaceae disease or disorder","type":"exact"},{"name":"Rickettsiaceae infection","type":"related"},{"name":"infection, Rickettsiaceae","type":"related"},{"name":"infections, Rickettsiaceae","type":"related"},{"name":"rickettsialpox","type":"related"}],"termid":"MONDO:0006927","xrefs":{"Monarch":{"xref_id":"0006927"}}}


id: GO:1902742
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any apoptotic process that is involved in anatomical structure development.","definition_xrefs":["GOC:pg","GO_REF:0000060","GOC:mtg_apoptosis","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apoptotic process","termid":"GO:0006915"},{"relation_name":"part_of","term_name":"anatomical structure development","termid":"GO:0048856"}],"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":"apoptotic process involved in development","synonyms":[{"name":"activation of apoptosis involved in anatomical structure development","type":"narrow"},{"name":"activation of apoptosis involved in development of an anatomical structure","type":"narrow"},{"name":"apoptosis activator activity involved in anatomical structure development","type":"related"},{"name":"apoptosis activator activity involved in development of an anatomical structure","type":"related"},{"name":"apoptosis involved in anatomical structure development","type":"narrow"},{"name":"apoptosis involved in development of an anatomical structure","type":"narrow"},{"name":"apoptosis signaling involved in anatomical structure development","type":"narrow"},{"name":"apoptosis signaling involved in development of an anatomical structure","type":"narrow"},{"name":"apoptotic cell death involved in anatomical structure development","type":"exact"},{"name":"apoptotic cell death involved in development of an anatomical structure","type":"exact"},{"name":"apoptotic process involved in anatomical structure development","type":"exact"},{"name":"apoptotic process involved in development of an anatomical structure","type":"exact"},{"name":"apoptotic program involved in anatomical structure development","type":"narrow"},{"name":"apoptotic program involved in development of an anatomical structure","type":"narrow"},{"name":"apoptotic programmed cell death involved in anatomical structure development","type":"exact"},{"name":"apoptotic programmed cell death involved in development of an anatomical structure","type":"exact"},{"name":"commitment to apoptosis involved in anatomical structure development","type":"related"},{"name":"commitment to apoptosis involved in development of an anatomical structure","type":"related"},{"name":"induction of apoptosis by p53 involved in anatomical structure development","type":"related"},{"name":"induction of apoptosis by p53 involved in development of an anatomical structure","type":"related"},{"name":"induction of apoptosis involved in anatomical structure development","type":"related"},{"name":"induction of apoptosis involved in development of an anatomical structure","type":"related"},{"name":"programmed cell death by apoptosis involved in anatomical structure development","type":"exact"},{"name":"programmed cell death by apoptosis involved in development of an anatomical structure","type":"exact"},{"name":"signaling (initiator) caspase activity involved in anatomical structure development","type":"related"},{"name":"signaling (initiator) caspase activity involved in development of an anatomical structure","type":"related"},{"name":"type I programmed cell death involved in anatomical structure development","type":"narrow"},{"name":"type I programmed cell death involved in development of an anatomical structure","type":"narrow"}],"termid":"GO:1902742"}


id: MONDO:0958137
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autoinflammatory disease, multisystem, with immune dysregulation, X-linked","termid":"MONDO:0957494"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"early-onset autoimmune disorder due to DOCK11 partial deficiency","secondary_identifiers":["MEDGEN:1864045","Orphanet:658946","UMLS:C5925146"],"termid":"MONDO:0958137","xrefs":{"Monarch":{"xref_id":"0958137"}}}


id: PBO:0003011
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.1.1.27","termid":"PBO:0003011"}


id: PBO:0078854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRPC6 pseudogene 2","termid":"PBO:0078854"}


id: PR:Q9UTE5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- hri2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UTE5"],"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":"eukaryotic translation initiation factor 2-alpha kinase 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC222.07c","synonyms":[{"name":"Spom972h-hri2","type":"exact"},{"name":"heme-regulated eukaryotic initiation factor eIF-2-alpha kinase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"heme-regulated inhibitor 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UTE5"}


id: MONDO:1012802
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neuroaxonal dystrophy that occurs in dogs due to a mutation in the VPS11 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"neuroaxonal dystrophy, dog","termid":"MONDO:1011561"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroaxonal dystrophy, VPS11-related, dog","secondary_identifiers":["OMIA:002152-9615"],"termid":"MONDO:1012802","xrefs":{"Monarch":{"xref_id":"1012802"}}}


id: PBO:0050481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox A10","termid":"PBO:0050481"}


id: GO:0019842
data:
  {"annotated_genes":["SJAG_00673","SJAG_03102","SJAG_03434","SJAG_00937","SJAG_02791","SJAG_00432","SJAG_04145","SJAG_00097","SJAG_00830","SJAG_00706","SJAG_04031","SJAG_03055","SJAG_03671","SJAG_00869","SJAG_03312","SJAG_04988","SJAG_03914","SJAG_00582","SJAG_04149","SJAG_03362","SJAG_02464","SJAG_02734","SJAG_02305","SJAG_03861","SJAG_02972","SJAG_04678","SJAG_01019","SJAG_00186","SJAG_00714","SJAG_02205","SJAG_01766","SJAG_03306","SJAG_04178","SJAG_05230","SJAG_03743","SJAG_00495","SJAG_03985","SJAG_04842","SJAG_03961"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[64728,59097],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031177"},{"annotations":[65573,57835,65212,67753,110190,67257,68335,78079,73185,67589,65867,58233,64488,70319,66065,65295,60064,63413,69570,57217,72195,64910,68666,79362,74024,74204,61597,79141,71773,66157],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030170"},{"annotations":[66952],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030975"},{"annotations":[57592,64384,61663,72965,58855,58566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030976"}]},"cv_name":"molecular_function","definition":"Binding to a vitamin, one of a number of unrelated organic substances that occur in many foods in small amounts and that are necessary in trace amounts for the normal metabolic functioning of the body.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small molecule binding","termid":"GO:0036094"}],"gene_count":39,"genes_by_uniquename":{"SJAG_00097":null,"SJAG_00186":null,"SJAG_00432":null,"SJAG_00495":null,"SJAG_00582":null,"SJAG_00673":null,"SJAG_00706":null,"SJAG_00714":null,"SJAG_00830":null,"SJAG_00869":null,"SJAG_00937":null,"SJAG_01019":null,"SJAG_01766":null,"SJAG_02205":null,"SJAG_02305":null,"SJAG_02464":null,"SJAG_02734":null,"SJAG_02791":null,"SJAG_02972":null,"SJAG_03055":null,"SJAG_03102":null,"SJAG_03306":null,"SJAG_03312":null,"SJAG_03362":null,"SJAG_03434":null,"SJAG_03671":null,"SJAG_03743":null,"SJAG_03861":null,"SJAG_03914":null,"SJAG_03961":null,"SJAG_03985":null,"SJAG_04031":null,"SJAG_04145":null,"SJAG_04149":null,"SJAG_04178":null,"SJAG_04678":null,"SJAG_04842":null,"SJAG_04988":null,"SJAG_05230":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"vitamin binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0019842","terms_by_termid":{"GO:0030170":null,"GO:0030975":null,"GO:0030976":null,"GO:0031177":null}}


id: GO:0034800
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: trinitrophenol dihydride Meisenheimer complex (aci form) = 2,4-dinitrophenol hydride Meisenheimer complex + NO2. Trinitrophenol is also known as TNP and dinitrophenol is also known as DNP.","definition_xrefs":["UM-BBD_reactionID:r1067"],"gene_count":0,"genotype_count":0,"name":"obsolete trinitrophenol dihydride denitratase activity (obsolete GO:0034800)","synonyms":[{"name":"2,4,6-trinitrophenol dihydride denitratase activity","type":"exact"},{"name":"TNP dihydride denitratase activity","type":"exact"}],"termid":"GO:0034800"}


id: GO:0017194
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The acetylation of the N-terminal isoleucine of proteins to form the derivative N-acetyl-L-isoleucine. The occurrence of this modification has not been confirmed.","definition_xrefs":["RESID:AA0047"],"gene_count":0,"genotype_count":0,"name":"obsolete N-terminal peptidyl-isoleucine acetylation (obsolete GO:0017194)","termid":"GO:0017194"}


id: GO:0044426
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Any constituent part of the cell wall, the rigid or semi-rigid envelope lying outside the cell membrane of plant, fungal, and most prokaryotic cells, maintaining their shape and protecting them from osmotic lysis.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete cell wall part (obsolete GO:0044426)","termid":"GO:0044426"}


id: MONDO:0020239
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete color-vision disease (obsolete MONDO:0020239)","termid":"MONDO:0020239","xrefs":{"Monarch":{"xref_id":"0020239"}}}


id: PR:P22192
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pac1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P22192"],"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":"double-strand-specific pac1 ribonuclease (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC119.11c","synonyms":[{"name":"Spom972h-pac1","type":"exact"},{"name":"protein hcs (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P22192"}


id: GO:0102931
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,6-trans-farnesyl diphosphate = (Z,E)-alpha-farnesene + diphosphoric acid.","definition_xrefs":["PMID:17140613","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"(Z,E)-alpha- farnesene synthase activity","secondary_identifiers":["MetaCyc:RXN-8931"],"termid":"GO:0102931"}


id: PBO:0044566
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DAZ associated protein 2 pseudogene 1","termid":"PBO:0044566"}


id: PBO:0001655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IQGAP","termid":"PBO:0001655"}


id: MONDO:0044279
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete bone mineral density quantitative trait locus 15 (obsolete MONDO:0044279)","secondary_identifiers":["OMIM:613418"],"synonyms":[{"name":"BMND15","type":"related"},{"name":"bone mineral density QTL 15","type":"exact"},{"name":"bone mineral density quantitative trait locus 15","type":"related"},{"name":"compression fracture, susceptibility to","type":"related"},{"name":"metaphyseal fracture, susceptibility to","type":"related"},{"name":"osteoporosis, susceptibility to","type":"related"}],"termid":"MONDO:0044279","xrefs":{"Monarch":{"xref_id":"0044279"}}}


id: PBO:0056396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAPRE1 pseudogene 3","termid":"PBO:0056396"}


id: PBO:0068116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 423","termid":"PBO:0068116"}


id: GO:1902787
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 dodecane stimulus.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie","GO_REF:0000071","PMID:23826995"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to alkane","termid":"GO:1902779"},{"relation_name":"is_a","term_name":"response to dodecane","termid":"GO:1902786"}],"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 dodecane","termid":"GO:1902787"}


id: GO:0001880
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the Mullerian ducts, primordia of the oviducts, uterus and upper vagina, undergo regression in male embryos.","definition_xrefs":["GOC:dph","PMID:12368913"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"anatomical structure regression","termid":"GO:0060033"},{"relation_name":"part_of","term_name":"male sex differentiation","termid":"GO:0046661"}],"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":"Mullerian duct regression","termid":"GO:0001880"}


id: PBO:0052493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KLHL6 antisense RNA 1","termid":"PBO:0052493"}


id: PBO:0065832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB7B, member RAS oncogene family","termid":"PBO:0065832"}


id: PBO:0009498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA hydrolase (predicted)","termid":"PBO:0009498"}


id: PBO:0050148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 3 pseudogene 4","termid":"PBO:0050148"}


id: GO:2000058
data:
  {"annotated_genes":["SJAG_00642","SJAG_00475","SJAG_00052","SJAG_02485","SJAG_03048","SJAG_03699","SJAG_02723","SJAG_00071","SJAG_01210"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905785"},{"annotations":[77033,106708],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032435"},{"annotations":[88705],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905786"},{"annotations":[108648,106415,102134,116814,111460],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032436"},{"annotations":[114374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032434"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of ubiquitin-dependent protein catabolic process.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of catabolic process","termid":"GO:0009894"},{"relation_name":"is_a","term_name":"regulation of proteolysis involved in protein catabolic process","termid":"GO:1903050"},{"relation_name":"regulates","term_name":"ubiquitin-dependent protein catabolic process","termid":"GO:0006511"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00052":null,"SJAG_00071":null,"SJAG_00475":null,"SJAG_00642":null,"SJAG_01210":null,"SJAG_02485":null,"SJAG_02723":null,"SJAG_03048":null,"SJAG_03699":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 ubiquitin-dependent protein catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"regulation of myofibrillar protein ubiquitination during ubiquitin-dependent protein breakdown","type":"related"},{"name":"regulation of myofibrillar protein ubiquitination during ubiquitin-dependent protein catabolic process","type":"related"},{"name":"regulation of myofibrillar protein ubiquitination during ubiquitin-dependent protein catabolism","type":"related"},{"name":"regulation of myofibrillar protein ubiquitination during ubiquitin-dependent protein degradation","type":"related"},{"name":"regulation of protein degradation tagging activity","type":"related"},{"name":"regulation of protein ubiquitination during ubiquitin-dependent protein breakdown","type":"exact"},{"name":"regulation of protein ubiquitination during ubiquitin-dependent protein catabolic process","type":"related"},{"name":"regulation of protein ubiquitination during ubiquitin-dependent protein catabolism","type":"exact"},{"name":"regulation of protein ubiquitination during ubiquitin-dependent protein degradation","type":"exact"},{"name":"regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process","type":"narrow"},{"name":"regulation of protein ubiquitinylation during ubiquitin-dependent protein catabolic process","type":"exact"},{"name":"regulation of protein ubiquitinylation during ubiquitin-dependent protein catabolism","type":"exact"},{"name":"regulation of protein ubiquitylation during ubiquitin-dependent protein catabolic process","type":"exact"},{"name":"regulation of protein ubiquitylation during ubiquitin-dependent protein catabolism","type":"exact"}],"termid":"GO:2000058","terms_by_termid":{"GO:0032434":null,"GO:0032435":null,"GO:0032436":null,"GO:1905785":null,"GO:1905786":null}}


id: MONDO:0014340
data:
  {"annotated_genes":["SJAG_02757"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86405],"is_not":false,"summary":null,"term":"MONDO:0014340"}]},"cv_name":"mondo","definition":"Any familial atrial fibrillation in which the cause of the disease is a mutation in the NUP155 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial atrial fibrillation","termid":"MONDO:0018054"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02757":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"atrial fibrillation, familial, 15","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:16010","UMLS:C4014269","MEDGEN:862706","OMIM:615770"],"synonyms":[{"name":"ATFB15","type":"related"},{"name":"NUP155 familial atrial fibrillation","type":"exact"},{"name":"atrial fibrillation 15","type":"exact"},{"name":"atrial fibrillation, familial, 15","type":"exact"},{"name":"atrial fibrillation, familial, type 15","type":"exact"},{"name":"familial atrial fibrillation caused by mutation in NUP155","type":"exact"}],"termid":"MONDO:0014340","terms_by_termid":{"MONDO:0014340":null},"xrefs":{"Monarch":{"xref_id":"0014340"}}}


id: PBO:0090238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lipid particle hydrolase","termid":"PBO:0090238"}


id: MONDO:0008991
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Verloove Vanhorick-Brubakk syndrome is a multiple congenital anomalies/dysmorphic syndrome characterized by multiple skeletal malformations (short femora and humeri, bilateral absence of metatarsal and metacarpal bone in hands and feet, bilateral partial syndactyly of fingers and toes or oligopolysyndactyly, deformed lumbosacral spine), congenital heart disease (truncus arteriosus), lung and urogenital malformations (bilateral bilobar lungs, horseshoe kidney, cryptorchidism), and facial malformations (bilateral cleft lip and palate, micrognathia, small, low-set ears without external meatus). It is lethal in the neonatal period. There have been no further descriptions in the literature since 1981.","definition_xrefs":["Orphanet:3429"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Verloove Vanhorick-Brubakk syndrome","secondary_identifiers":["GARD:5482","MESH:C536541","OMIM:215850","UMLS:C1859082","MEDGEN:395171","SCTID:764697003"],"synonyms":[{"name":"Clh syndrome","type":"related"},{"name":"Verloove Vanhorick Brubakk syndrome","type":"related"},{"name":"cleft limb heart malformation syndrome","type":"related"},{"name":"cleft lip-limb and heart malformations syndrome","type":"exact"},{"name":"cleft-limb-heart malformation syndrome","type":"related"},{"name":"cleft-limb-heart malformation syndrome syndrome","type":"exact"}],"termid":"MONDO:0008991","xrefs":{"Monarch":{"xref_id":"0008991"}}}


id: GO:0071128
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alpha5-beta1 integrin complex bound to osteopontin.","definition_xrefs":["PMID:16005200"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005886"],"is_obsolete":false,"name":"alpha5-beta1 integrin-osteopontin complex","synonyms":[{"name":"ITGA5-ITGB1-SPP1 complex","type":"narrow"}],"termid":"GO:0071128"}


id: GO:0071119
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alpha7-beta1 integrin complex bound to nicotinamide riboside kinase 2 (also known as muscle integrin binding protein, MIBP).","definition_xrefs":["PMID:12941630"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005886"],"is_obsolete":false,"name":"alpha7-beta1 integrin-nicotinamide riboside kinase complex","synonyms":[{"name":"ITGA7-ITGB1-ITGB1BP3 complex","type":"narrow"}],"termid":"GO:0071119"}


id: MOD:00138
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue into 2-oxobutanoic acid.","definition_xrefs":["Unimod:385#T","ChEBI:149508","PubMed:2253617","PubMed:15023056","PubMed:1680314","PubMed:2764678","RESID:AA0129"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-threonine residue","termid":"MOD:00917"},{"relation_name":"is_a","term_name":"deaminated residue","termid":"MOD:01160"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2-oxobutanoic acid","synonyms":[{"name":"2-ketobutyric acid","type":"exact"},{"name":"2-oxobutanoic acid","type":"exact"},{"name":"2-oxobutyric acid","type":"exact"},{"name":"Ammonia-loss","type":"related"},{"name":"Loss of ammonia","type":"related"},{"name":"MOD_RES 2-oxobutanoic acid","type":"exact"}],"termid":"MOD:00138"}


id: GO:0009496
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 H+[side 1] + 2 oxidized plastocyanin + plastoquinol-1 = 2 H+[side 2] + 2 reduced plastocyanin + plastoquinone. This reaction involves the concomitant transfer of 2 H+ ions across a membrane.","definition_xrefs":["RHEA:22148"],"direct_ancestors":[{"relation_name":"is_a","term_name":"electron transfer activity","termid":"GO:0009055"},{"relation_name":"is_a","term_name":"oxidoreduction-driven active transmembrane transporter activity","termid":"GO:0015453"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on diphenols and related substances as donors, with copper protein as acceptor","termid":"GO:0052880"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"plastoquinol--plastocyanin reductase activity","secondary_identifiers":["MetaCyc:PLASTOQUINOL--PLASTOCYANIN-REDUCTASE-RXN","EC:7.1.1.6","KEGG_REACTION:R03817"],"synonyms":[{"name":"cytochrome b6f","type":"narrow"},{"name":"cytochrome b6f complex activity","type":"related"},{"name":"plastoquinol-plastocyanin reductase activity","type":"related"},{"name":"plastoquinol/plastocyanin oxidoreductase activity","type":"related"},{"name":"plastoquinol:oxidized-plastocyanin oxidoreductase activity","type":"related"}],"termid":"GO:0009496"}


id: PR:Q10320
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A transmembrane protein 165 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00979","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":"GDT1-like protein C17G8.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17G8.08c","secondary_identifiers":["UniProtKB:Q10320"],"synonyms":[{"name":"Spom972h-TMEM165","type":"exact"}],"termid":"PR:Q10320"}


id: GO:0140826
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of zinc from one side of a membrane to the other according to the reaction: H+(out) + Zn2+(in) = H+(in) + Zn2+(out).","definition_xrefs":["PMID:19366695","PMID:30893306"],"direct_ancestors":[{"relation_name":"is_a","term_name":"zinc ion transmembrane transporter activity","termid":"GO:0005385"},{"relation_name":"is_a","term_name":"metal cation:proton antiporter activity","termid":"GO:0051139"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"zinc:proton antiporter activity","termid":"GO:0140826"}


id: PBO:0000953
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.5.5.1","termid":"PBO:0000953"}


id: FYPO:0002633
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 dTTP measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"increased cellular dTTP level","synonyms":[{"name":"increased cellular dTTP level during mitotic cell cycle","type":"related"},{"name":"increased cellular dTTP level during vegetative growth","type":"exact"},{"name":"increased dTTP accumulation","type":"related"}],"termid":"FYPO:0002633"}


id: MOD:01126
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5'phos Cytidinyl","termid":"MOD:01126"}


id: PATO:0000938
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's exhibiting organisation.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organization quality","termid":"PATO:0002264"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"organized","termid":"PATO:0000938"}


id: GO:0090654
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Tubulo-vesicular structure located in the basolateral cytoplasm that participates in basolateral cargo recycling in polarized epithelial cells.","definition_xrefs":["PMID:11389442","PMID:21170358","PMID:9405315","PMID:17494872","PMID:16394106"],"direct_ancestors":[{"relation_name":"is_a","term_name":"recycling endosome","termid":"GO:0055037"},{"relation_name":"part_of","term_name":"basolateral cytoplasm","termid":"GO:0090652"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005768"},{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005768","GO:0031410"],"is_obsolete":false,"name":"basolateral recycling endosome","termid":"GO:0090654"}


id: PBO:0117038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MARCHF4 antisense RNA 1","termid":"PBO:0117038"}


id: FYPO:0006737
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which the proportion of cells in the population remains viable after entering stationary phase does not change in the presence of alpha-hibitakanine. Normally, wild-type cell populations survive longer in the presence of alpha-hibitakanine than in its absence.","definition_xrefs":["PMID:29900664","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population phenotype","termid":"FYPO:0000003"},{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"stationary phase viability unaffected by alpha-hibitakanine","synonyms":[{"name":"chronological lifespan unaffected by alpha-hibitakanine","type":"related"},{"name":"loss of chronological lifespan extension by alpha-hibitakanine","type":"related"},{"name":"loss of stationary phase viability extension in presence of alpha-hibitakanine","type":"exact"}],"termid":"FYPO:0006737"}


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


id: MONDO:0015814
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary lymphoma of the skin composed of various numbers of small and large irregular neoplastic follicle center cells. Its morphologic pattern can be nodular, diffuse, or nodular and diffuse. It presents with solitary or grouped plaques and tumors, and it usually involves the scalp, forehead, or trunk. It rarely involves the legs. This type of cutaneous lymphoma tends to remain localized to the skin.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"indolent primary cutaneous B-cell lymphoma","termid":"MONDO:0015819"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005093","MONDO:0005046","MONDO:0004992"],"is_obsolete":false,"name":"primary cutaneous follicle center lymphoma","secondary_identifiers":["GARD:13701","UMLS:C1333171","MEDGEN:234180","icd11.foundation:77501812","ONCOTREE:PCFCL","NCIT:C7217","SCTID:404143002","Orphanet:178540","ICDO:9597/3"],"synonyms":[{"name":"Crosti's disease","type":"exact"},{"name":"PCFCL","type":"exact"},{"name":"Reticulohistiocytoma of the dorsum","type":"exact"},{"name":"cutaneous follicle center lymphoma","type":"exact"},{"name":"cutaneous follicle centre lymphoma","type":"exact"}],"termid":"MONDO:0015814","xrefs":{"Monarch":{"xref_id":"0015814"}}}


id: GO:1901796
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of signal transduction by p53 class mediator.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular signal transduction","termid":"GO:1902531"},{"relation_name":"regulates","term_name":"signal transduction by p53 class mediator","termid":"GO:0072331"}],"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:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of signal transduction by p53 class mediator","secondary_identifiers":["Reactome:R-HSA-5633007"],"termid":"GO:1901796"}


id: MONDO:0018660
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hemophilia is a genetic disorder characterized by spontaneous hemorrhage or prolonged bleeding due to factor VIII or IX deficiency.","definition_xrefs":["Orphanet:448"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare hemorrhagic disorder due to a constitutional coagulation factors defect (obsolete MONDO:0019039)","termid":"MONDO:0019039"},{"relation_name":"is_a","term_name":"coagulation protein disease","termid":"MONDO:0002242"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"hemophilia","secondary_identifiers":["MEDGEN:146334","GARD:10418","NCIT:C3093","MedDRA:10061992","SCTID:90935002","UMLS:C0684275"],"synonyms":[{"name":"hemophilia","type":"exact"}],"termid":"MONDO:0018660","xrefs":{"Monarch":{"xref_id":"0018660"}}}


id: PBO:0067035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 49, pseudogene","termid":"PBO:0067035"}


id: MONDO:0004127
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lung adenocarcinoma detectable by sputum cytology only. The primary tumor is undetectable radiographically or during bronchoscopy; therefore, it can not be assessed.","definition_xrefs":["NCIT:C6699"],"direct_ancestors":[{"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 occult adenocarcinoma","secondary_identifiers":["MEDGEN:277443","UMLS:C1335096","DOID:7168"],"synonyms":[{"name":"occult adenocarcinoma of lung","type":"related"},{"name":"occult adenocarcinoma of the lung","type":"exact"},{"name":"occult lung adenocarcinoma","type":"related"}],"termid":"MONDO:0004127","xrefs":{"Monarch":{"xref_id":"0004127"}}}


id: MONDO:0009523
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lichstenstein syndrome is characterized by frequent infections associated with osteoporosis, a tendency for fractures and osseous anomalies. It has been described in two monozygotic twin brothers. Transmission is autosomal recessive.","definition_xrefs":["Orphanet:2390"],"direct_ancestors":[{"relation_name":"is_a","term_name":"constitutional neutropenia","termid":"MONDO:0015134"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"Lichtenstein syndrome","secondary_identifiers":["UMLS:C1855502","GARD:3248","MESH:C535894","MEDGEN:340889","OMIM:246550","SCTID:763668009"],"synonyms":[{"name":"Lichtenstein syndrome","type":"exact"},{"name":"neutropenia immunoglobulin deficiency peculiar facies and bony anomalies","type":"related"}],"termid":"MONDO:0009523","xrefs":{"Monarch":{"xref_id":"0009523"}}}


id: PBO:0040897
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMS1 ribosome biogenesis factor","termid":"PBO:0040897"}


id: MONDO:0009112
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any rhizomelic chondrodysplasia punctata in which the cause of the disease is a mutation in the GNPAT gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhizomelic chondrodysplasia punctata","termid":"MONDO:0015776"},{"relation_name":"is_a","term_name":"glyceronephosphate O-acyltransferase deficiency","termid":"MONDO:0100273"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005328","MONDO:0002525","MONDO:0019053"],"is_obsolete":false,"name":"rhizomelic chondrodysplasia punctata type 2","secondary_identifiers":["OMIM:222765","icd11.foundation:179969811","MESH:C537607","Orphanet:309796","MEDGEN:341734","UMLS:C1857242","DOID:0110852","GARD:9429","NANDO:1200771"],"synonyms":[{"name":"Dhapat deficiency","type":"exact"},{"name":"Dihydroxyacetonephosphate acyltransferase deficiency","type":"exact"},{"name":"GNPAT rhizomelic chondrodysplasia punctata","type":"exact"},{"name":"Glyceronephosphate O-acyltransferase deficiency","type":"exact"},{"name":"Gnpat deficiency","type":"exact"},{"name":"RCDP2","type":"exact"},{"name":"Rcdp2","type":"exact"},{"name":"chondrodysplasia punctata, rhizomelic, due to Dihydroxyacetonephosphate acyltransferase deficiency","type":"exact"},{"name":"chondrodysplasia punctata, rhizomelic, due to dihydroxyacetonephosphate","type":"related"},{"name":"peroxisomal dihydroxyacetonephosphate acyltransferase deficiency","type":"exact"},{"name":"rhizomelic chondrodysplasia punctata caused by mutation in GNPAT","type":"exact"},{"name":"rhizomelic chondrodysplasia punctata type 2","type":"exact"},{"name":"rhizomelic chondrodysplasia punctata, type 2","type":"exact"},{"name":"type 2 rhizomelic chondrodysplasia punctata","type":"exact"}],"termid":"MONDO:0009112","xrefs":{"Monarch":{"xref_id":"0009112"}}}


id: PBO:0077476
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 198B (pseudogene)","termid":"PBO:0077476"}


id: PBO:0091357
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Catabolism of ARginine, after S. cerevisiae","termid":"PBO:0091357"}


id: PBO:0048099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferritin mitochondrial","termid":"PBO:0048099"}


id: MONDO:1012923
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cataract that occurs in cattle due to a mutation in the ADAMTSL4 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cataract, non-human animal","termid":"MONDO:1012962"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cataract, ADAMTSL4-related, cattle","secondary_identifiers":["OMIA:002535-9913"],"termid":"MONDO:1012923","xrefs":{"Monarch":{"xref_id":"1012923"}}}


id: PBO:0047078
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 133 member G, pseudogene","termid":"PBO:0047078"}


id: MONDO:1012897
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any heart disorder characterized by pathologically accelerated cardiac repolarization and increased ventricular tachycardia/fibrillation inducibility that occurs in rabbits due to a mutation in the KCNH2 gene created by genetic engineering or gene editing.","definition_xrefs":["PMID:30496390"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"heart disorder, non-human animal","termid":"MONDO:1012982"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"short QT syndrome, KCNH2-related, rabbit","secondary_identifiers":["OMIA:002441-9986"],"termid":"MONDO:1012897","xrefs":{"Monarch":{"xref_id":"1012897"}}}


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


id: PBO:0002951
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent DNA helicase Hrp3","termid":"PBO:0002951"}


id: PATO:0002393
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A tolerance quality inhering in a bearer by virtue of the bearer's increased ability to endure a stimulus.","definition_xrefs":["PATOC:LC"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"tolerant to","termid":"PATO:0000515"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased tolerance to","termid":"PATO:0002393"}


id: GO:1903264
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any nitrate reductase activity that is involved in anaerobic electron transport chain.","definition_xrefs":["PMID:12910261","GOC:TermGenie","GOC:dos","GO_REF:0000061"],"gene_count":0,"genotype_count":0,"name":"obsolete nitrate reductase activity involved in anaerobic electron transport chain (obsolete GO:1903264)","synonyms":[{"name":"nitrate reductase (acceptor) involved in anaerobic electron transport chain","type":"exact"},{"name":"nitrite:(acceptor) oxidoreductase involved in anaerobic electron transport chain","type":"exact"},{"name":"nitrite:acceptor oxidoreductase involved in anaerobic electron transport chain","type":"exact"},{"name":"respiratory nitrate reductase activity involved in anaerobic electron transport chain","type":"narrow"}],"termid":"GO:1903264"}


id: PBO:0027718
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_level_of_amino_acid_biosynthesis_gene_mRNA_during_vegetative_growth","termid":"PBO:0027718"}


id: GO:1905852
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of backward locomotion.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:11717360"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of locomotion","termid":"GO:0040017"},{"relation_name":"is_a","term_name":"regulation of backward locomotion","termid":"GO:0043058"},{"relation_name":"positively_regulates","term_name":"backward locomotion","termid":"GO:0043057"}],"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 backward locomotion","synonyms":[{"name":"activation of backward locomotion","type":"narrow"},{"name":"up regulation of backward locomotion","type":"exact"},{"name":"up-regulation of backward locomotion","type":"exact"},{"name":"upregulation of backward locomotion","type":"exact"}],"termid":"GO:1905852"}


id: MONDO:0013730
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An immune system disorder that occurs after allogeneic hematopoietic stem cell transplant and is a reaction of donor immune cells against host tissues. Activated donor T cells damage host epithelial cells after an inflammatory cascade that begins with the preparative regimen.","definition_xrefs":["Orphanet:39812"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"},{"relation_name":"is_a","term_name":"disease related to hematopoietic stem cell transplant","termid":"MONDO:0700222"}],"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":"graft versus host disease","secondary_identifiers":["DOID:0081267","ICD9:279.50","GARD:16642","MESH:D006086","UMLS:C0018133","icd11.foundation:437372167","MedDRA:10018651","MEDGEN:9082","SCTID:234646005","NCIT:C3063","NORD:1203"],"synonyms":[{"name":"GVH","type":"exact"},{"name":"GVHD","type":"exact"},{"name":"GvHD","type":"exact"},{"name":"disease, graft-versus-host","type":"exact"},{"name":"disease, graft-vs-host","type":"exact"},{"name":"disease, homologous wasting","type":"related"},{"name":"disease, runt","type":"related"},{"name":"diseases, graft-versus-host","type":"exact"},{"name":"diseases, graft-vs-host","type":"exact"},{"name":"graft versus host disease","type":"exact"},{"name":"graft vs host disease","type":"exact"},{"name":"graft vs. host disease","type":"exact"},{"name":"graft-VS-host diseases","type":"related"},{"name":"graft-versus-host disease","type":"exact"},{"name":"graft-versus-host disease, resistance to","type":"related"},{"name":"graft-versus-host disease, susceptibility to","type":"related"},{"name":"graft-versus-host diseases","type":"related"},{"name":"graft-versus-host-disease","type":"exact"},{"name":"graft-vs-host disease","type":"exact"},{"name":"homologous wasting disease","type":"related"},{"name":"runt disease","type":"exact"}],"termid":"MONDO:0013730","xrefs":{"Monarch":{"xref_id":"0013730"}}}


id: GO:0006436
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of coupling tryptophan to tryptophanyl-tRNA, catalyzed by tryptophanyl-tRNA synthetase. The tryptophanyl-tRNA synthetase is a class-I synthetase. The activated amino acid is transferred to the 2'-OH group of a tryptophan-accetping tRNA. The 2'-O-aminoacyl-tRNA will ultimately migrate to the 3' position via transesterification.","definition_xrefs":["ISBN:0716730510","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA aminoacylation for protein translation","termid":"GO:0006418"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0006399","GO:0010467","GO:0006520"],"is_obsolete":false,"name":"tryptophanyl-tRNA aminoacylation","termid":"GO:0006436"}


id: PBO:0056843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B","termid":"PBO:0056843"}


id: SO:0000491
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Genomic DNA of immunoglobulin/T-cell receptor gene in rearranged configuration including at least one VJ-gene and one J-gene.","direct_ancestors":[{"relation_name":"has_part","term_name":"J_gene_segment","termid":"SO:0000470"},{"relation_name":"has_part","term_name":"VJ_gene_segment","termid":"SO:0000576"},{"relation_name":"is_a","term_name":"vertebrate_immunoglobulin_T_cell_receptor_rearranged_gene_cluster","termid":"SO:0000938"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VJ_J_cluster","synonyms":[{"name":"(VJ)-J-CLUSTER","type":"exact"},{"name":"VJ J cluster","type":"exact"}],"termid":"SO:0000491"}


id: PBO:0045492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Down syndrome critical region 10","termid":"PBO:0045492"}


id: GO:0140250
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the breakdown of a protein at the synapse.","definition_xrefs":["PMID:23083742"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of catabolic process","termid":"GO:0009894"}],"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 protein catabolic process at synapse","termid":"GO:0140250"}


id: PBO:0086744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; possibly involved in zinc homeostasis; Bdf1p-dependent transcription induced by salt stress; green fluorescent protein (GFP)-fusion protein localizes to both the cytoplasm and the nucleus","termid":"PBO:0086744"}


id: PBO:0029130
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_DNA_recombination_at_mating_type_locus","termid":"PBO:0029130"}


id: PBO:0004844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar membrane alkaline phosphatase (predicted)","termid":"PBO:0004844"}


id: MOD:00835
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to L-oxoalanine.","definition_xrefs":["DeltaMass:349","PubMed:9276974","RESID:AA0185#SER","PubMed:7628016","PubMed:8681943","PubMed:14563551","Unimod:401#S","PubMed:9478923"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"},{"relation_name":"is_a","term_name":"L-3-oxoalanine","termid":"MOD:01169"},{"relation_name":"is_a","term_name":"didehydrogenated residue","termid":"MOD:01888"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-3-oxoalanine (Ser)","synonyms":[{"name":"(S)-2-amino-3-oxopropanoic acid","type":"exact"},{"name":"2-amino-3-oxopropionic acid","type":"exact"},{"name":"C(alpha)-formylglycine","type":"related"},{"name":"Didehydro","type":"related"},{"name":"L-3-oxoalanine","type":"exact"},{"name":"L-amino-malonic acid semialdehyde","type":"exact"},{"name":"L-aminomalonaldehydic acid","type":"exact"},{"name":"L-serinesemialdehyde","type":"related"},{"name":"MOD_RES 3-oxoalanine (Ser)","type":"exact"},{"name":"dehydrogenated serine residue","type":"related"},{"name":"formylglycine","type":"related"},{"name":"formylglycine (from serine)","type":"exact"},{"name":"oxoalanine","type":"related"}],"termid":"MOD:00835"}


id: PBO:0056270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mannosidase alpha class 1A member 1","termid":"PBO:0056270"}


id: MONDO:0016449
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dermis disorder","termid":"MONDO:0021154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"mid-dermal elastolysis","secondary_identifiers":["MEDGEN:1672488","UMLS:C4728147","Orphanet:228299","GARD:20589","icd11.foundation:1379952112"],"termid":"MONDO:0016449","xrefs":{"Monarch":{"xref_id":"0016449"}}}


id: GO:0150116
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell-substrate junction organization.","definition_xrefs":["GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"regulates","term_name":"cell-substrate junction organization","termid":"GO:0150115"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cell-substrate junction organization","termid":"GO:0150116"}


id: PBO:0044170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"catenin alpha 1","termid":"PBO:0044170"}


id: PBO:0077841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tumor protein D52","termid":"PBO:0077841"}


id: PBO:0001829
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Delayed minus-Nitrogen Induction","termid":"PBO:0001829"}


id: PBO:0089117
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER-associated lipid droplet biogenesis protein, seipin Sei1","termid":"PBO:0089117"}


id: FYPO:0000010
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell adhesion phenotype observed in the vegetative growth phase of the life cycle in which cells fail to adhere to a substrate.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell adhesion during vegetative growth","termid":"FYPO:0000009"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abolished cell-substrate adhesion","synonyms":[{"name":"abolished cell-substrate adhesion during mitotic cell cycle","type":"related"},{"name":"cell-substrate adhesion abolished","type":"exact"},{"name":"cell-substrate adhesion abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0000010"}


id: MONDO:0001886
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"prolapse of female genital organ","termid":"MONDO:0001592"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"midline cystocele","secondary_identifiers":["MEDGEN:733480","SCTID:423633003","UMLS:C1456248","ICD10CM:N81.11","ICD9:618.01","DOID:14131"],"termid":"MONDO:0001886","xrefs":{"Monarch":{"xref_id":"0001886"}}}


id: PBO:0042150
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 11","termid":"PBO:0042150"}


id: GO:0160240
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that promotes premature RNA polymerase II transcription termination of transcripts that are unfavorably configured for transcriptional elongation by releasing RNA polymerase II from bound DNA or promoting RNA polymerase II degradation.","definition_xrefs":["PMID:34762484","PMID:33385327"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear RNA surveillance","termid":"GO:0071027"},{"relation_name":"part_of","term_name":"transcription initiation at RNA polymerase II promoter","termid":"GO:0006367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0006351","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"RNA polymerase II transcription initiation surveillance","termid":"GO:0160240"}


id: PBO:0086709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; member of the seripauperin multigene family encoded mainly in subtelomeric regions; mRNA expression appears to be regulated by SUT1 and UPC2","termid":"PBO:0086709"}


id: GO:0006828
data:
  {"annotated_genes":["SJAG_04867","SJAG_01007","SJAG_04096","SJAG_03850"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70430,61336,63794,108421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071421"}]},"cv_name":"biological_process","definition":"The directed movement of manganese (Mn) ions into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transition metal ion transport","termid":"GO:0000041"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01007":null,"SJAG_03850":null,"SJAG_04096":null,"SJAG_04867":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"manganese ion transport","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"termid":"GO:0006828","terms_by_termid":{"GO:0071421":null}}


id: PBO:0075206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide G pseudogene 18","termid":"PBO:0075206"}


id: GO:0047233
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-acetylneuraminyl-2,3-alpha-D-galactosyl-1,4-beta-D-glucosylceramide + UDP-N-acetylgalactosamine = N-acetyl-beta-D-galactosaminyl-1,4-(N-acetyl-alpha-neuraminyl-2,3)-beta-D-galactosyl-1,4-beta-D-glucosylceramide + UDP.","definition_xrefs":["EC:2.4.1.165","MetaCyc:2.4.1.165-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylgalactosaminyltransferase activity","termid":"GO:0008376"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016757","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"N-acetylneuraminylgalactosylglucosylceramide beta-1,4-N-acetylgalactosaminyltransferase activity","secondary_identifiers":["RHEA:13569"],"synonyms":[{"name":"UDP-N-acetyl-D-galactosamine:N-acetylneuraminyl-2,3-alpha-D-galactosyl-1,4-beta-D-glucosylceramide beta-1,4-N-acetylgalactosaminyltransferase activity","type":"related"},{"name":"uridine diphosphoacetylgalactosamine-acetylneuraminyl(alpha2->3)galactosyl(beta1->4)glucosyl beta1->4-acetylgalactosaminyltransferase activity","type":"related"}],"termid":"GO:0047233"}


id: MONDO:0012324
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare partial deletion of the long arm of chromosome 14 characterized by ocular anomalies (anopthalmia/microphthalmia, ptosis, hypertelorism, exophthalmos), pituitary anomalies (pituitary hypoplasia/aplasia with growth hormone deficiency and growth retardation) and hand/foot anomalies (polydactyly, short digits, pes cavus). Other clinical features may include muscular hypotonia, psychomotor development delay/intellectual disability, dysmorphic signs (facial asymmetry, microretrognathia, high-arched palate, ear anomalies), congenital genitourinary malformations, hearing impairment. Smaller 14q22 deletions may have variable expression.","definition_xrefs":["Orphanet:264200"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"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":"Frias syndrome","secondary_identifiers":["Orphanet:2055","UMLS:C1864825","GARD:2384","MEDGEN:400621","OMIM:609640","MESH:C535639"],"synonyms":[{"name":"14q22-q23 microdeletion syndrome","type":"exact"},{"name":"14q22q23 microdeletion syndrome","type":"exact"},{"name":"Del(14)(q22q23)","type":"exact"},{"name":"Frias syndrome","type":"exact"},{"name":"Growth deficiency, Facial anomalies, and brachydactyly","type":"related"},{"name":"chromosome 14Q22 deletion syndrome","type":"related"},{"name":"monosomy 14q22-q23","type":"exact"},{"name":"monosomy 14q22q23","type":"exact"}],"termid":"MONDO:0012324","xrefs":{"Monarch":{"xref_id":"0012324"}}}


id: PBO:0062347
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily K member 6","termid":"PBO:0062347"}


id: PBO:0001416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L15b (predicted)","termid":"PBO:0001416"}


id: PBO:0068469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 46, pseudogene","termid":"PBO:0068469"}


id: GO:0003402
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by binding of a Wnt protein to a receptor on the surface of the target cell where activated receptors signal to modulate cytoskeletal elements and control cell polarity that contributes to axis elongation.","definition_xrefs":["GOC:dph","GOC:ascb_2009","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete planar cell polarity pathway involved in axis elongation (obsolete GO:0003402)","termid":"GO:0003402"}


id: PBO:0039513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 30B pseudogene 1","termid":"PBO:0039513"}


id: PATO:0001293
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A scalar EM radiation quality which obtains by the capacity of the bearer to retain radiation.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"full-spectrum EM radiation quality","termid":"PATO:0001292"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"absorption quality","termid":"PATO:0001293"}


id: PBO:0075210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syntrophin alpha 1","termid":"PBO:0075210"}


id: MONDO:0800488
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An epilepsy syndrome characterized by the onset of seizures in neonates/infants where there is a high likelihood of spontaneously remitting at a predictable age.","direct_ancestors":[{"relation_name":"is_a","term_name":"neonatal/infantile epilepsy syndrome","termid":"MONDO:0100022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"neonatal/infantile-onset self-limited epilepsy syndrome","termid":"MONDO:0800488","xrefs":{"Monarch":{"xref_id":"0800488"}}}


id: FYPO:0006573
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of protein measured in a cell during a cellular response to a pheromone is normal (i.e. indistinguishable from wild type). Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein level","termid":"FYPO:0004083"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal protein level during cellular response to pheromone","synonyms":[{"name":"normal protein accumulation during cellular response to pheromone","type":"related"}],"termid":"FYPO:0006573"}


id: PBO:0027416
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cell_population_growth_during_glucose_starvation","termid":"PBO:0027416"}


id: PBO:0054642
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 2047","termid":"PBO:0054642"}


id: GO:1905194
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of chloroplast fission.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:26862170"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organelle organization","termid":"GO:0010638"},{"relation_name":"is_a","term_name":"regulation of chloroplast fission","termid":"GO:1905192"},{"relation_name":"positively_regulates","term_name":"chloroplast fission","termid":"GO:0010020"}],"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 chloroplast fission","synonyms":[{"name":"activation of chloroplast division","type":"narrow"},{"name":"activation of chloroplast fission","type":"narrow"},{"name":"positive regulation of chloroplast division","type":"exact"},{"name":"up regulation of chloroplast division","type":"exact"},{"name":"up regulation of chloroplast fission","type":"exact"},{"name":"up-regulation of chloroplast division","type":"exact"},{"name":"up-regulation of chloroplast fission","type":"exact"},{"name":"upregulation of chloroplast division","type":"exact"},{"name":"upregulation of chloroplast fission","type":"exact"}],"termid":"GO:1905194"}


id: PBO:0082946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic isoleucine-tRNA synthetase; target of the G1-specific inhibitor reveromycin A","termid":"PBO:0082946"}


id: PBO:0071221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 62","termid":"PBO:0071221"}


id: SO:0000654
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A mitochondrial gene located in a maxicircle.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinetoplast_gene","termid":"SO:0000089"},{"relation_name":"part_of","term_name":"maxicircle","termid":"SO:0000742"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maxicircle_gene","synonyms":[{"name":"maxi-circle gene","type":"exact"},{"name":"maxicircle gene","type":"exact"}],"termid":"SO:0000654"}


id: PBO:0074789
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 10","termid":"PBO:0074789"}


id: PBO:0057683
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1272","termid":"PBO:0057683"}


id: SO:0000338
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A highly repetitive and short (100-500 base pair) transposable element with terminal inverted repeats (TIR) and target site duplication (TSD). MITEs do not encode proteins.","direct_ancestors":[{"relation_name":"is_a","term_name":"terminal_inverted_repeat_element","termid":"SO:0000208"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MITE","synonyms":[{"name":"miniature inverted repeat transposable element","type":"exact"}],"termid":"SO:0000338"}


id: PR:O13681
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ima1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13681"],"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":"integral inner nuclear membrane protein ima1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC737.03c","synonyms":[{"name":"Spom972h-ima1","type":"exact"}],"termid":"PR:O13681"}


id: GO:0044316
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A specialized axon terminus which is produced by retinal cone cells. Pedicles are large, conical, flat end-feet (8-10 micrometers diameter) of the retinal cone axon that lie more or less side by side on the same plane at the outer edge of the outer plexiform layer (OPL).","definition_xrefs":["PMID:10939333"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axon terminus","termid":"GO:0043679"}],"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":"cone cell pedicle","synonyms":[{"name":"cone pedicle","type":"exact"}],"termid":"GO:0044316"}


id: FYPO:0007297
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 from a promoter that contains one or more SRE elements occurs to a greater extent than normal.","definition_xrefs":["PMID:32053662","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased transcription during vegetative growth","termid":"FYPO:0000780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"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:0006551"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0006551","FYPO:0000002","FYPO:0000294","FYPO:0001985"],"is_obsolete":false,"name":"increased transcription from SRE promoter","synonyms":[{"name":"expression of SRE target genes increased","type":"related"},{"name":"increased transcription from SRE promoter during mitotic cell cycle","type":"related"},{"name":"increased transcription from SRE promoter during vegetative growth","type":"exact"}],"termid":"FYPO:0007297"}


id: GO:0097363
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-N-acetyl-D-glucosamine + [protein]-L-serine = UDP + [protein]-3-O-(N-acetyl-D-glucosaminyl)-L-serine, or UDP-N-acetyl-D-glucosamine + [protein]-L-threonine = UDP + [protein]-3-O-(N-acetyl-D-glucosaminyl)-L-threonine.","definition_xrefs":["PMID:22158438","GOC:sart","GOC:jsg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylglucosaminyltransferase activity","termid":"GO:0008375"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a protein","termid":"GO:0140096"}],"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:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0140096","GO:0016740","GO:0016757","GO:0003674"],"is_obsolete":false,"name":"protein O-acetylglucosaminyltransferase activity","secondary_identifiers":["EC:2.4.1.255","Reactome:R-HSA-9687828"],"synonyms":[{"name":"O-GlcNAc transferase","type":"exact"},{"name":"O-linked N-acetylglucosaminyltransferase","type":"exact"},{"name":"OGTase","type":"exact"},{"name":"UDP-N-acetyl-D-glucosamine:protein-O-beta-N-acetyl-D-glucosaminyl transferase","type":"exact"},{"name":"protein O-GlcNAc transferase activity","type":"exact"}],"termid":"GO:0097363"}


