# terms

id: PBO:0110352
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DBF4-CDC7 kinase regulatory subunit","termid":"PBO:0110352"}


id: PBO:0077955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ala (anticodon AGC) 12-2","termid":"PBO:0077955"}


id: PBO:0063368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proprotein convertase subtilisin/kexin type 7","termid":"PBO:0063368"}


id: PBO:0030880
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cellular_component_organization_during_vegetative_growth","termid":"PBO:0030880"}


id: PBO:0079411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin beta 8 class VIII pseudogene 5","termid":"PBO:0079411"}


id: MONDO:0005021
data:
  {"annotated_genes":["SJAG_04567","SJAG_01209","SJAG_03703","SJAG_01671","SJAG_MIT13","SJAG_02611","SJAG_03145","SJAG_MIT15","SJAG_01240","SJAG_01322","SJAG_03815","SJAG_02431","SJAG_01139","SJAG_01754","SJAG_MIT03","SJAG_04231","SJAG_04621","SJAG_02919"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88110],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032592"},{"annotations":[88395,88396],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030300"},{"annotations":[87388],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859358"},{"annotations":[88210],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957545"},{"annotations":[87716,87715],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008409"},{"annotations":[88030],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012808"},{"annotations":[88300,88301],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013198"},{"annotations":[88902],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013339"},{"annotations":[86981,86979,86980],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014073"},{"annotations":[88010],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013261"},{"annotations":[88012,88011],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013262"},{"annotations":[87520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012556"},{"annotations":[87380,87381,87382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010788"},{"annotations":[89061],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013968"}]},"cv_name":"mondo","definition":"Cardiomyopathy which is characterized by dilation and contractile dysfunction of the left and right ventricles. It may be idiopathic, or it may result from a myocardial infarction, myocardial infection, or alcohol abuse. It is a cause of congestive heart failure.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intrinsic cardiomyopathy","termid":"MONDO:0000591"}],"gene_count":18,"genes_by_uniquename":{"SJAG_01139":null,"SJAG_01209":null,"SJAG_01240":null,"SJAG_01322":null,"SJAG_01671":null,"SJAG_01754":null,"SJAG_02431":null,"SJAG_02611":null,"SJAG_02919":null,"SJAG_03145":null,"SJAG_03703":null,"SJAG_03815":null,"SJAG_04231":null,"SJAG_04567":null,"SJAG_04621":null,"SJAG_MIT03":null,"SJAG_MIT13":null,"SJAG_MIT15":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"dilated cardiomyopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:2880","HP:0001644","icd11.foundation:1916294688","GARD:221","ICD9:425.4","MedDRA:10056370","SCTID:195021004","ICD10CM:I42.0","DOID:12930","NANDO:2200232","UMLS:C0007193","Orphanet:217604","NANDO:2100057","EFO:0000407","NCIT:C84673","MESH:D002311"],"synonyms":[{"name":"congestive cardiomyopathy","type":"related"},{"name":"dilated cardiomyopathy","type":"exact"},{"name":"familial dilated cardiomyopathy","type":"related"},{"name":"idiopathic dilation cardiomyopathy","type":"related"},{"name":"primary dilated cardiomyopathy","type":"related"}],"termid":"MONDO:0005021","terms_by_termid":{"MONDO:0008409":null,"MONDO:0010788":null,"MONDO:0012556":null,"MONDO:0012808":null,"MONDO:0013198":null,"MONDO:0013261":null,"MONDO:0013262":null,"MONDO:0013339":null,"MONDO:0013968":null,"MONDO:0014073":null,"MONDO:0030300":null,"MONDO:0032592":null,"MONDO:0859358":null,"MONDO:0957545":null},"xrefs":{"Monarch":{"xref_id":"0005021"}}}


id: PBO:0080185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"voltage dependent anion channel 3","termid":"PBO:0080185"}


id: PBO:0051635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inner membrane mitochondrial protein","termid":"PBO:0051635"}


id: GO:2000194
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of female gonad development.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of gonad development","termid":"GO:1905939"},{"relation_name":"is_a","term_name":"regulation of multicellular organismal development","termid":"GO:2000026"},{"relation_name":"regulates","term_name":"female gonad development","termid":"GO:0008585"}],"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 female gonad development","synonyms":[{"name":"regulation of ovarian development","type":"exact"},{"name":"regulation of ovary development","type":"exact"}],"termid":"GO:2000194"}


id: MONDO:0016744
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete primary melanocytic tumor of central nervous system (obsolete MONDO:0016744)","secondary_identifiers":["Orphanet:252028"],"synonyms":[{"name":"primary melanocytic lesion of CNS","type":"exact"},{"name":"primary melanocytic lesion of central nervous system","type":"exact"},{"name":"primary melanocytic tumor of CNS","type":"exact"},{"name":"primary melanocytic tumour of CNS","type":"exact"}],"termid":"MONDO:0016744","xrefs":{"Monarch":{"xref_id":"0016744"}}}


id: PBO:0012254
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"octameric","termid":"PBO:0012254"}


id: GO:0140725
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that reduces or removes the toxicity of free heme. These include transport of heme away from sensitive areas and to compartments or complexes whose purpose is sequestration of heme.","definition_xrefs":["PMID:32983129","PMID:26741528"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detoxification","termid":"GO:0098754"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098754"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0098754"],"is_obsolete":false,"name":"detoxification of free heme","synonyms":[{"name":"free heme detoxification","type":"exact"}],"termid":"GO:0140725"}


id: PBO:0065570
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostaglandin reductase 1","termid":"PBO:0065570"}


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


id: PBO:0062948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proliferation-associated 2G4 pseudogene 6","termid":"PBO:0062948"}


id: PBO:0005223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAGA complex subunit/TATA-binding protein associated factor/transcription factor TFIID complex subunit Taf5","termid":"PBO:0005223"}


id: PR:P0CT67
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rps1802 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P0CT67"],"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":"40S ribosomal protein S18-B (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1259.01c","synonyms":[{"name":"Spom972h-rps1802","type":"exact"}],"termid":"PR:P0CT67"}


id: GO:0042278
data:
  {"annotated_genes":["SJAG_02959","SJAG_03881","SJAG_02580","SJAG_00885","SJAG_02582","SJAG_00044","SJAG_01359","SJAG_04927","SJAG_00957","SJAG_01859","SJAG_01070","SJAG_00134","SJAG_03096","SJAG_06634"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109231],"is_not":false,"summary":null,"term":"GO:0042278"},{"annotations":[90755],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046086"},{"annotations":[89452,89451],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006154"},{"annotations":[92427],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046085"},{"annotations":[118863],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006169"},{"annotations":[71666],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006190"},{"annotations":[92961,114177,77037],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006152"},{"annotations":[62512,67880,75203,95652],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006166"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving one of a family of organic molecules consisting of a purine base covalently bonded to a sugar ribose (a ribonucleoside) or deoxyribose (a deoxyribonucleoside).","definition_xrefs":["ISBN:0140512713","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside metabolic process","termid":"GO:0009116"},{"relation_name":"is_a","term_name":"purine-containing compound metabolic process","termid":"GO:0072521"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00044":null,"SJAG_00134":null,"SJAG_00885":null,"SJAG_00957":null,"SJAG_01070":null,"SJAG_01359":null,"SJAG_01859":null,"SJAG_02580":null,"SJAG_02582":null,"SJAG_02959":null,"SJAG_03096":null,"SJAG_03881":null,"SJAG_04927":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"purine nucleoside metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000107":null},"synonyms":[{"name":"purine metabolic process","type":"broad"},{"name":"purine metabolism","type":"broad"},{"name":"purine nucleoside metabolism","type":"exact"}],"termid":"GO:0042278","terms_by_termid":{"GO:0006152":null,"GO:0006154":null,"GO:0006166":null,"GO:0006169":null,"GO:0006190":null,"GO:0042278":null,"GO:0046085":null,"GO:0046086":null}}


id: GO:0009723
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 ethylene (ethene) stimulus.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to hormone","termid":"GO:0009725"}],"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 ethylene","synonyms":[{"name":"response to ethene stimulus","type":"exact"},{"name":"response to ethylene stimulus","type":"exact"}],"termid":"GO:0009723"}


id: FYPO:0001852
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which transcription occurs to a lower extent than normal when the cell is subject to iron ion starvation. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"decreased RNA level during cellular response to iron ion starvation","termid":"FYPO:0002042"},{"relation_name":"is_a","term_name":"decreased transcription during vegetative growth","termid":"FYPO:0000781"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000294","FYPO:0001320","FYPO:0006551","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased transcription during iron starvation","synonyms":[{"name":"decreased transcription during iron depletion","type":"exact"},{"name":"decreased transcription during iron deprivation","type":"exact"},{"name":"decreased transcription during iron ion starvation","type":"exact"},{"name":"decreased transcription during iron starvation during mitotic cell cycle","type":"related"},{"name":"decreased transcription during iron starvation during vegetative growth","type":"exact"},{"name":"reduced transcription during iron starvation","type":"exact"}],"termid":"FYPO:0001852"}


id: PBO:0026935
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_duration_of_horsetail_movement","termid":"PBO:0026935"}


id: PR:O94706
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A transcription initiation factor TFIID subunit 8 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR23307: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":"transcription initiation factor TFIID subunit 8 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1259.06","secondary_identifiers":["UniProtKB:O94706"],"synonyms":[{"name":"SPCC1259.06","type":"related"},{"name":"Spom972h-TAF8","type":"exact"},{"name":"TBP-associated factor 8 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94706"}


id: MONDO:0054550
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial avascular necrosis of femoral head","termid":"MONDO:0012126"},{"relation_name":"is_a","term_name":"dysplasia of the proximal femoral epiphyses","termid":"MONDO:1030002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"avascular necrosis of femoral head, primary, 1","secondary_identifiers":["UMLS:C4551562","OMIM:608805","MEDGEN:1639295"],"synonyms":[{"name":"ANFH1","type":"related"},{"name":"Femoral head, avascular necrosis of","type":"related"},{"name":"avascular necrosis of femoral head, primary, 1","type":"exact"},{"name":"avascular necrosis of the femoral head","type":"exact"},{"name":"femoral head, aseptic necrosis of","type":"related"},{"name":"ischaemic necrosis of femoral head","type":"related"},{"name":"ischemic necrosis of femoral head","type":"related"},{"name":"osteonecrosis of femoral head","type":"related"}],"termid":"MONDO:0054550","xrefs":{"Monarch":{"xref_id":"0054550"}}}


id: GO:0047530
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2,4-diaminopentanoate + H2O + NAD(P)+ = 2-amino-4-oxopentanoate + NH3 + NAD(P)H + H+.","definition_xrefs":["MetaCyc:24-DIAMINOPENTANOATE-DEHYDROGENASE-RXN","EC:1.4.1.12"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor","termid":"GO:0016639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"2,4-diaminopentanoate dehydrogenase activity","synonyms":[{"name":"2,4-diaminopentanoate:NAD(P)+ oxidoreductase (deaminating)","type":"related"},{"name":"2,4-diaminopentanoic acid C4 dehydrogenase activity","type":"related"}],"termid":"GO:0047530"}


id: MONDO:0042973
data:
  {"annotated_genes":["SJAG_01181","SJAG_01183","SJAG_00993","SJAG_00516","SJAG_02342"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88234],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009815"},{"annotations":[87320,87321,87322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007970"},{"annotations":[88403],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957262"}]},"cv_name":"mondo","definition":"An instance of osteosclerosis that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteosclerosis","termid":"MONDO:0002933"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00516":null,"SJAG_00993":null,"SJAG_01181":null,"SJAG_01183":null,"SJAG_02342":null},"genotype_count":0,"is_obsolete":false,"name":"familial osteosclerosis","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"hereditary osteosclerosis","type":"exact"}],"termid":"MONDO:0042973","terms_by_termid":{"MONDO:0007970":null,"MONDO:0009815":null,"MONDO:0957262":null},"xrefs":{"Monarch":{"xref_id":"0042973"}}}


id: FYPO:0002174
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of an RNA catabolic process that specifically degrades DSR-containing RNA molecules is decreased. A DSR (determinant of selective removal) is a region that is often found near the 3' end of meiosis-specific transcripts, usually contains one or more copies of the motif U(U/C/G)AAAC, and targets RNAs for degradation in vegetatively growing cells.","definition_xrefs":["PMID:22046364","PomBase:mah","PMID:22645662"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA catabolic process during vegetative growth","termid":"FYPO:0002137"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000294","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased degradation of DSR-containing RNA","synonyms":[{"name":"decreased RNA catabolic process, DSR-containing RNA","type":"exact"},{"name":"decreased catabolism of DSR-containing RNA","type":"exact"},{"name":"decreased degradation of DSR-containing RNA during mitotic cell cycle","type":"related"},{"name":"decreased degradation of DSR-containing RNA during vegetative growth","type":"exact"},{"name":"reduced degradation of DSR-containing RNA","type":"exact"}],"termid":"FYPO:0002174"}


id: PBO:0030422
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_sterol_binding","termid":"PBO:0030422"}


id: PBO:0029676
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_septum_morphology_during_vegetative_growth","termid":"PBO:0029676"}


id: PBO:0043786
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carboxypeptidase D pseudogene 1","termid":"PBO:0043786"}


id: GO:0002053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of activating or increasing the rate or extent of mesenchymal cell proliferation. Mesenchymal cells are loosely organized embryonic cells.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell population proliferation","termid":"GO:0008284"},{"relation_name":"is_a","term_name":"regulation of mesenchymal cell proliferation","termid":"GO:0010464"},{"relation_name":"positively_regulates","term_name":"mesenchymal cell proliferation","termid":"GO:0010463"}],"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 mesenchymal cell proliferation","synonyms":[{"name":"activation of mesenchymal cell proliferation","type":"narrow"},{"name":"stimulation of mesenchymal cell proliferation","type":"narrow"},{"name":"up regulation of mesenchymal cell proliferation","type":"exact"},{"name":"up-regulation of mesenchymal cell proliferation","type":"exact"},{"name":"upregulation of mesenchymal cell proliferation","type":"exact"}],"termid":"GO:0002053"}


id: PBO:0002854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase I upstream activation factor complex subunit Rrn5","termid":"PBO:0002854"}


id: PATO:0001218
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001218 substance_unit (obsolete PATO:0001218)","termid":"PATO:0001218"}


id: GO:1900324
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of maltotriulose transport.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"maltotriulose transport","termid":"GO:2001090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of maltotriulose transport","termid":"GO:1900324"}


id: GO:0047115
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADP+ + trans-1,2-dihydrobenzene-1,2-diol = NADPH + catechol.","definition_xrefs":["EC:1.3.1.20","MetaCyc:1.3.1.20-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"trans-1,2-dihydrobenzene-1,2-diol dehydrogenase activity","secondary_identifiers":["RHEA:16729"],"synonyms":[{"name":"dihydrodiol dehydrogenase activity","type":"related"},{"name":"trans-1,2-dihydrobenzene-1,2-diol:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0047115"}


id: PBO:0041666
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDK2 associated cullin domain 1","termid":"PBO:0041666"}


id: PBO:0079561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBA like domain containing 2","termid":"PBO:0079561"}


id: PBO:0059243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L14","termid":"PBO:0059243"}


id: SO:0002090
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A UTR variant of intronic sequence of the 3' UTR.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"3_prime_UTR_variant","termid":"SO:0001624"},{"relation_name":"is_a","term_name":"coding_transcript_intron_variant","termid":"SO:0001969"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3_prime_UTR_intron_variant","synonyms":[{"name":"3 prime UTR intron variant","type":"exact"}],"termid":"SO:0002090"}


id: PBO:0109320
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAR adaptor protein, human endophilin A1-like ortholog","termid":"PBO:0109320"}


id: PBO:0067317
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 403, pseudogene","termid":"PBO:0067317"}


id: MONDO:0018646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A chronic, autoimmune inflammatory liver disorder characterized by narrowing and scarring of the lumen of the bile ducts. It is often seen in patients with ulcerative colitis. Signs and symptoms include jaundice, fatigue, and malabsorption. It may lead to cirrhosis and liver failure.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cholangitis","termid":"MONDO:0004789"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"sclerosing cholangitis","secondary_identifiers":["Orphanet:447771","HP:0030991","NCIT:C4828","GARD:21868","SCTID:235917005","DOID:14268","EFO:0004268","MEDGEN:3036","NANDO:1200440","NANDO:2100265","UMLS:C0008313"],"synonyms":[{"name":"Primary sclerosing cholangitis","type":"exact"},{"name":"fibrosing cholangitis","type":"exact"},{"name":"primary sclerosing cholangitis (PSC)","type":"exact"},{"name":"sclerosing cholangitis","type":"exact"},{"name":"sclerosing cholangitis (disease)","type":"exact"}],"termid":"MONDO:0018646","xrefs":{"Monarch":{"xref_id":"0018646"}}}


id: GO:0102083
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 7,8-dihydromonapterin = glycolaldehyde + 2-amino-6-(hydroxymethyl)-7,8-dihydropteridin-4-ol.","definition_xrefs":["GOC:pz","PMID:15107504"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde-lyase activity","termid":"GO:0016832"}],"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:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"7,8-dihydromonapterin aldolase activity","secondary_identifiers":["MetaCyc:RXN-10857"],"termid":"GO:0102083"}


id: PBO:0041277
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1QTNF3-AMACR readthrough (NMD candidate)","termid":"PBO:0041277"}


id: GO:1905896
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of cellular response to tunicamycin.","definition_xrefs":["PMID:21803450","GO_REF:0000058","GOC:aruk","GOC:TermGenie","GOC:bc"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of cellular response to tunicamycin (obsolete GO:1905896)","synonyms":[{"name":"activation of cellular response to tunicamycin","type":"narrow"},{"name":"up regulation of cellular response to tunicamycin","type":"exact"},{"name":"up-regulation of cellular response to tunicamycin","type":"exact"},{"name":"upregulation of cellular response to tunicamycin","type":"exact"}],"termid":"GO:1905896"}


id: PBO:0062979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PABPN1 pseudogene 1","termid":"PBO:0062979"}


id: FYPO:0007342
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of one or more triglycerides measured in lipid droplets is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell","termid":"FYPO:0000991"},{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype during vegetative growth","termid":"FYPO:0004639"}],"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:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased triglyceride level in lipid droplet","synonyms":[{"name":"decreased TAG level in lipid droplet","type":"exact"},{"name":"decreased lipid droplet triglyceride level","type":"exact"},{"name":"decreased triacylglycerol level in lipid droplet","type":"exact"},{"name":"decreased triglyceride accumulation in lipid droplet","type":"related"},{"name":"reduced cellular triglyceride level in lipid droplet","type":"exact"}],"termid":"FYPO:0007342"}


id: PBO:0054651
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 2056","termid":"PBO:0054651"}


id: PBO:0004811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dolichyl-phosphate beta-glucosyltransferase Alg5 (predicted)","termid":"PBO:0004811"}


id: MONDO:0016856
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mowat-Wilson syndrome","termid":"MONDO:0009341"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0002320","MONDO:0000426"],"is_obsolete":false,"name":"Mowat-Wilson syndrome due to a ZEB2 point mutation","secondary_identifiers":["GARD:17249","Orphanet:261552","UMLS:C5679681","MEDGEN:1842263"],"synonyms":[{"name":"Hirschsprung disease and intellectual disability due to a ZEB2 point mutation","type":"exact"}],"termid":"MONDO:0016856","xrefs":{"Monarch":{"xref_id":"0016856"}}}


id: PBO:0046686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"electron transfer flavoprotein subunit alpha","termid":"PBO:0046686"}


id: PBO:0050332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 34","termid":"PBO:0050332"}


id: PBO:0049904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hes family bHLH transcription factor 5","termid":"PBO:0049904"}


id: MONDO:0003175
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenoid cystic carcinoma arising from the salivary gland. It is characterized by the presence of epithelial and myoepithelial cells forming tubular, cribriform, and solid patterns. It usually presents as a slow growing mass. Patients may experience pain because of the tumor propensity for perineural invasion. The tumor may follow an aggressive clinical course with recurrences and mestastases to distant sites including lungs, bones, brain, and liver.","definition_xrefs":["NCIT:C8026"],"direct_ancestors":[{"relation_name":"is_a","term_name":"salivary gland carcinoma","termid":"MONDO:0000521"},{"relation_name":"is_a","term_name":"adenoid cystic carcinoma","termid":"MONDO:0004971"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"salivary gland adenoid cystic carcinoma","secondary_identifiers":["DOID:4866","UMLS:C0279751","MEDGEN:79034","SCTID:422833009"],"synonyms":[{"name":"adenoid cystic cancer","type":"broad"},{"name":"adenoid cystic carcinoma (morphologic abnormality)","type":"broad"},{"name":"adenoid cystic carcinoma of salivary gland","type":"exact"},{"name":"adenoid cystic carcinoma of the salivary gland","type":"exact"},{"name":"cylindroma (morphologic abnormality)","type":"exact"},{"name":"saliva-secreting gland adenoid cystic carcinoma","type":"exact"},{"name":"salivary gland adenoid cystic cancer","type":"exact"},{"name":"salivary gland adenoid cystic carcinoma","type":"exact"}],"termid":"MONDO:0003175","xrefs":{"Monarch":{"xref_id":"0003175"}}}


id: PBO:0043902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cysteine rich secretory protein 2","termid":"PBO:0043902"}


id: PBO:0049016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycoprotein M6B pseudogene 1","termid":"PBO:0049016"}


id: MONDO:0008349
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":"pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities","secondary_identifiers":["UMLS:C1867407","OMIM:178650","MEDGEN:357274","MESH:C566733"],"synonyms":[{"name":"Ciuffo syndrome","type":"related"},{"name":"pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities","type":"exact"}],"termid":"MONDO:0008349","xrefs":{"Monarch":{"xref_id":"0008349"}}}


id: MONDO:1010306
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Osteochondrodysplasia that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis, non-human animal","termid":"MONDO:1011313"},{"relation_name":"is_a","term_name":"skeletal dysplasia, non-human animal","termid":"MONDO:1012973"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteochondrodysplasia, non-human animal","secondary_identifiers":["OMIA:001315"],"termid":"MONDO:1010306","xrefs":{"Monarch":{"xref_id":"1010306"}}}


id: PBO:0043100
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carbohydrate sulfotransferase 12","termid":"PBO:0043100"}


id: GO:2000949
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of xyloglucan metabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of macromolecule metabolic process","termid":"GO:0010605"},{"relation_name":"is_a","term_name":"negative regulation of carbohydrate metabolic process","termid":"GO:0045912"},{"relation_name":"is_a","term_name":"regulation of xyloglucan metabolic process","termid":"GO:2000948"},{"relation_name":"negatively_regulates","term_name":"xyloglucan metabolic process","termid":"GO:0010411"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"negative regulation of xyloglucan metabolic process","synonyms":[{"name":"negative regulation of xyloglucan metabolism","type":"exact"}],"termid":"GO:2000949"}


id: PBO:0029686
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_oxidation","termid":"PBO:0029686"}


id: PBO:0057813
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3134","termid":"PBO:0057813"}


id: MONDO:0100202
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":"lumbar disk herniation, susceptibility to","secondary_identifiers":["MEDGEN:393597","UMLS:C2676840"],"termid":"MONDO:0100202","xrefs":{"Monarch":{"xref_id":"0100202"}}}


id: PBO:0057232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 411","termid":"PBO:0057232"}


id: GO:0043665
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The soluble material inside the peribacteroid membrane, but outside of the bacteroid, within a bacteroid-containing symbiosome of a host cell.","definition_xrefs":["GOC:cc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell part","termid":"GO:0033643"},{"relation_name":"part_of","term_name":"host bacteroid-containing symbiosome","termid":"GO:0043663"}],"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":"host peribacteroid fluid","termid":"GO:0043665"}


id: GO:0061065
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of dauer larval development, the process whose specific outcome is the progression of the dauer larva over time, through the facultative diapause of the dauer (enduring) larval stage, with specialized traits adapted for dispersal and long-term survival, with elevated stress resistance and without feeding.","definition_xrefs":["GOC:dph","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nematode larval development","termid":"GO:0061062"},{"relation_name":"regulates","term_name":"dauer larval development","termid":"GO:0040024"}],"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 dauer larval development","termid":"GO:0061065"}


id: PBO:0063019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phenylalanine hydroxylase","termid":"PBO:0063019"}


id: PBO:0057676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1267","termid":"PBO:0057676"}


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


id: PBO:0054950
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 2364","termid":"PBO:0054950"}


id: GO:0018263
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The formation of an isopeptide cross-link between peptidyl-asparagine and peptidyl-cysteine to produce N-(L-isoaspartyl)-L-cysteine.","definition_xrefs":["RESID:AA0216"],"gene_count":0,"genotype_count":0,"name":"obsolete isopeptide cross-linking via N-(L-isoaspartyl)-L-cysteine (obsolete GO:0018263)","termid":"GO:0018263"}


id: PBO:0002485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endo-1,3-beta-glucanase Eng2","termid":"PBO:0002485"}


id: PBO:0038382
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_exposure_stressor","termid":"PBO:0038382"}


id: SO:0001781
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A variant arising in the offspring that is not found in either of the parents.","direct_ancestors":[{"relation_name":"is_a","term_name":"variant_origin","termid":"SO:0001762"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"de_novo_variant","synonyms":[{"name":"de novo variant","type":"exact"}],"termid":"SO:0001781"}


id: MONDO:0010155
data:
  {"annotated_genes":["SJAG_04323"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86827],"is_not":false,"summary":null,"term":"MONDO:0010155"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete autosomal ichthyosis syndrome (obsolete MONDO:0017270)","termid":"MONDO:0017270"},{"relation_name":"is_a","term_name":"neutral lipid storage disease","termid":"MONDO:0015611"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04323":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002561","MONDO:0002525"],"is_obsolete":false,"name":"Dorfman-Chanarin disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:690728790","NANDO:1200622","NANDO:1200623","Orphanet:98907","GARD:3979","NORD:1283","MEDGEN:82780","NANDO:2200997","SCTID:19604005","OMIM:275630","UMLS:C0268238"],"synonyms":[{"name":"CDS","type":"related"},{"name":"Chanarin-Dorfman Syndrome","type":"exact"},{"name":"Chanarin-Dorfman disease","type":"related"},{"name":"Chanarin-Dorfman syndrome","type":"exact"},{"name":"DCs","type":"related"},{"name":"Dorfman Chanarin syndrome","type":"related"},{"name":"Dorfman-Chanarin syndrome","type":"related"},{"name":"NLSDI","type":"exact"},{"name":"disorder of cornification 12 (neutral lipid storage type)","type":"related"},{"name":"ichthyosiform erythroderma with leukocyte vacuolation","type":"related"},{"name":"ichthyotic neutral Lipid storage disease","type":"related"},{"name":"neutral Lipid storage disease with ichthyosis","type":"related"},{"name":"neutral lipid storage disease with ichthyosis","type":"exact"},{"name":"neutral lipid storage disease with ichthyotic","type":"related"},{"name":"triglyceride storage disease with impaired long-chain fatty acid oxidation","type":"related"}],"termid":"MONDO:0010155","terms_by_termid":{"MONDO:0010155":null},"xrefs":{"Monarch":{"xref_id":"0010155"}}}


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: PBO:0036254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KH domain RNA-binding protein (predicted)","termid":"PBO:0036254"}


id: PBO:0108921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMX1 pseudogene 1","termid":"PBO:0108921"}


id: PR:O13966
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An aconitate hydratase, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01274","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":"aconitate hydratase, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24C9.06c","secondary_identifiers":["UniProtKB:O13966"],"synonyms":[{"name":"Aconitase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ACO2","type":"exact"},{"name":"citrate hydro-lyase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13966"}


id: PBO:0087716
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the RNA polymerase II mediator complex; associates with core polymerase subunits to form the RNA polymerase II holoenzyme; involved in telomere maintenance; conserved with other metazoan MED31 subunits","termid":"PBO:0087716"}


id: PBO:0055772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LNX1 antisense RNA 1","termid":"PBO:0055772"}


id: GO:0052884
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + all-trans-retinyl palmitate = 11-cis-retinol + H+ + palmitate.","definition_xrefs":["RHEA:31775"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinyl-palmitate esterase activity","termid":"GO:0050253"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016788","GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"all-trans-retinyl-palmitate hydrolase, 11-cis retinol forming activity","secondary_identifiers":["Reactome:R-HSA-2453833"],"synonyms":[{"name":"all-trans-retinol isomerase:hydrolase activity","type":"broad"},{"name":"all-trans-retinyl-palmitate hydrolase activity","type":"broad"},{"name":"retinoid isomerohydrolase activity","type":"broad"},{"name":"retinol isomerase activity","type":"broad"}],"termid":"GO:0052884"}


id: GO:0098638
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Any laminin protein binding that occurs as part of cell-matrix adhesion.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"laminin binding","termid":"GO:0043236"},{"relation_name":"is_a","term_name":"cell-matrix adhesion mediator activity","termid":"GO:0098634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0098631"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0098631","GO:0005488"],"is_obsolete":false,"name":"laminin binding involved in cell-matrix adhesion","termid":"GO:0098638"}


id: MONDO:0004369
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"}],"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 infectious disease","secondary_identifiers":["ICD9:590.9","DOID:782","ICD9:590","UMLS:C0021313","MEDGEN:507844"],"termid":"MONDO:0004369","xrefs":{"Monarch":{"xref_id":"0004369"}}}


id: PBO:0027699
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_rDNA_separation","termid":"PBO:0027699"}


id: GO:1905632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within an euchromatin.","definition_xrefs":["GO_REF:0000087","GOC:TermGenie","PMID:20889714"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to chromatin","termid":"GO:0071168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to euchromatin","synonyms":[{"name":"protein localisation in euchromatin","type":"exact"},{"name":"protein localisation to euchromatin","type":"exact"},{"name":"protein localization in euchromatin","type":"exact"}],"termid":"GO:1905632"}


id: GO:0071620
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of introducing a phosphate group onto a serine residue at position 5 within the heptapeptide repeat (YSPTSPS) of the C-terminal domain of RNA polymerase II. Typically, phosphorylation of serine 5 (Ser5) occurs near the 5' ends of genes. It is generally still observed in the middle of genes, overlapping with phosphorylation of serine 2, but is generally not present at the 3' ends of genes. In vivo, Ser5 phosphorylation occurs primarily through the action of TFIIH (KIN28 in S. cerevisiae, CKD7 in metazoans).","definition_xrefs":["GOC:krc","PMID:17079683"],"gene_count":0,"genotype_count":0,"name":"obsolete phosphorylation of RNA polymerase II C-terminal domain serine 5 residues (obsolete GO:0071620)","termid":"GO:0071620"}


id: PBO:0055336
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 2764","termid":"PBO:0055336"}


id: PBO:0035881
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_rate_of_protein_transport_during_vegetative_growth","termid":"PBO:0035881"}


id: PBO:0043097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carbohydrate sulfotransferase 9","termid":"PBO:0043097"}


id: GO:0000210
data:
  {"annotated_genes":["SJAG_03091"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[107082],"is_not":false,"summary":null,"term":"GO:0000210"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: NAD+ + H2O = AMP + NMN.","definition_xrefs":["RHEA:11800"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dinucleotide phosphatase activity","termid":"GO:0004551"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03091":null},"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:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"NAD+ diphosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:NADPYROPHOSPHAT-RXN"],"synonyms":[{"name":"NAD diphosphatase activity","type":"broad"},{"name":"NAD pyrophosphatase activity","type":"broad"},{"name":"NAD(+) pyrophosphatase activity","type":"exact"},{"name":"NAD+ phosphohydrolase activity","type":"exact"},{"name":"NAD+ pyrophosphatase activity","type":"exact"},{"name":"NADP pyrophosphatase activity","type":"related"},{"name":"nicotinamide adenine dinucleotide pyrophosphatase activity","type":"related"}],"termid":"GO:0000210","terms_by_termid":{"GO:0000210":null}}


id: PR:G2TRK2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC29A4.22 gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRK2"],"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 C29A4.22 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29A4.22","synonyms":[{"name":"Spom972h-SPAC29A4.22","type":"exact"}],"termid":"PR:G2TRK2"}


id: RO:0009002
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"\\\"has substance removed\\\" is a relation existing between two physical entities in which the first entity has had the second entity (a substance) removed from it at some point in time.","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_substance_removed","termid":"RO:0009002"}


id: PATO:0002394
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A tolerance quality inhering in a bearer by virtue of the bearer's decreased ability to endure a stimulus.","definition_xrefs":["PATOC:LC"],"direct_ancestors":[{"relation_name":"decreased_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":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased tolerance to","termid":"PATO:0002394"}


id: GO:0014059
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of dopamine.","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of catecholamine secretion","termid":"GO:0050433"},{"relation_name":"regulates","term_name":"dopamine secretion","termid":"GO:0014046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of dopamine secretion","termid":"GO:0014059"}


id: GO:1900780
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of fumiquinazoline C.","definition_xrefs":["GOC:di","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete fumiquinazoline C catabolic process (obsolete GO:1900780)","synonyms":[{"name":"fumiquinazoline C breakdown","type":"exact"},{"name":"fumiquinazoline C catabolism","type":"exact"},{"name":"fumiquinazoline C degradation","type":"exact"}],"termid":"GO:1900780"}


id: PBO:0017940
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Long Chain Fatty acyl-CoA synthetase","termid":"PBO:0017940"}


id: MONDO:0017465
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital pseudoarthrosis of the limbs","termid":"MONDO:0015525"}],"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":"congenital pseudoarthrosis of the radius","secondary_identifiers":["UMLS:C5679936","MEDGEN:1842721","GARD:21206","Orphanet:295024"],"synonyms":[{"name":"congenital pseudarthrosis of the radius","type":"exact"}],"termid":"MONDO:0017465","xrefs":{"Monarch":{"xref_id":"0017465"}}}


id: PBO:0083204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps the verified gene YJL020C/BBC1","termid":"PBO:0083204"}


id: GO:0031340
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of vesicle fusion.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organelle organization","termid":"GO:0010638"},{"relation_name":"is_a","term_name":"regulation of vesicle fusion","termid":"GO:0031338"},{"relation_name":"is_a","term_name":"positive regulation of transport","termid":"GO:0051050"},{"relation_name":"positively_regulates","term_name":"vesicle fusion","termid":"GO:0006906"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0061024"},{"rel_name":"positively_regulates","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0061024","GO:0016192"],"is_obsolete":false,"name":"positive regulation of vesicle fusion","synonyms":[{"name":"activation of vesicle fusion","type":"narrow"},{"name":"stimulation of vesicle fusion","type":"narrow"},{"name":"up regulation of vesicle fusion","type":"exact"},{"name":"up-regulation of vesicle fusion","type":"exact"},{"name":"upregulation of vesicle fusion","type":"exact"}],"termid":"GO:0031340"}


id: PBO:0069886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1175, pseudogene","termid":"PBO:0069886"}


id: PBO:0058481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5588","termid":"PBO:0058481"}


id: GO:0140036
data:
  {"annotated_genes":["SJAG_04574"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[112496],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061649"}]},"cv_name":"molecular_function","definition":"A molecular adaptor recognizes and binds a target protein containing a ubiquitination modification and brings the target protein into contact with another protein to allow those proteins to function in a coordinated way.","definition_xrefs":["PMID:26060076"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-like protein reader activity","termid":"GO:0140035"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04574":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0030674","GO:0003674","GO:0060090"],"is_obsolete":false,"name":"ubiquitin-modified protein reader activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"ubiquitin-dependent protein binding","type":"exact"}],"termid":"GO:0140036","terms_by_termid":{"GO:0061649":null}}


id: PBO:0039776
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aquaporin 7 pseudogene 1","termid":"PBO:0039776"}


id: PBO:0051303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 1D-43","termid":"PBO:0051303"}


id: PBO:0043956
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crystallin gamma A","termid":"PBO:0043956"}


id: GO:0006059
data:
  {"annotated_genes":["SJAG_00237"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74383],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006062"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving hexitols, any alditol with a chain of six carbon atoms in the molecule.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alditol metabolic process","termid":"GO:0019400"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00237":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0005975","GO:0044281"],"is_obsolete":false,"name":"hexitol metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"hexitol metabolism","type":"exact"},{"name":"sugar alcohol (hexitol) metabolic process","type":"exact"},{"name":"sugar alcohol (hexitol) metabolism","type":"exact"}],"termid":"GO:0006059","terms_by_termid":{"GO:0006062":null}}


id: MONDO:0859265
data:
  {"annotated_genes":["SJAG_00516"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88695],"is_not":false,"summary":null,"term":"MONDO:0859265"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00516":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with epilepsy and brain atrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1823957","OMIM:619971","UMLS:C5774184"],"termid":"MONDO:0859265","terms_by_termid":{"MONDO:0859265":null},"xrefs":{"Monarch":{"xref_id":"0859265"}}}


id: PBO:0082757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the septin ring that is required for cytokinesis; septins are GTP-binding proteins that assemble into rod-like hetero-oligomers that can associate with other rods to form filaments; septin rings at the mother-bud neck act as scaffolds for recruiting cell division factors and as barriers to prevent diffusion of specific proteins between mother and daughter cells","termid":"PBO:0082757"}


id: GO:0060668
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of salivary gland branching as a result of the transfer of information from the extracellular matrix to the epithelium of the salivary gland.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular matrix-cell signaling","termid":"GO:0035426"},{"relation_name":"is_a","term_name":"regulation of branching involved in salivary gland morphogenesis","termid":"GO:0060693"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of branching involved in salivary gland morphogenesis by extracellular matrix-epithelial cell signaling","synonyms":[{"name":"regulation of branching involved in salivary gland morphogenesis by extracellular matrix-epithelial cell signalling","type":"exact"}],"termid":"GO:0060668"}


id: MONDO:0017621
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital sucrase-isomaltase deficiency","termid":"MONDO:0009114"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"congenital sucrase-isomaltase deficiency with starch and lactose intolerance","secondary_identifiers":["Orphanet:306474"],"synonyms":[{"name":"CSID with starch and lactose intolerance","type":"exact"},{"name":"congenital sucrase-isomaltose malabsorption with starch and lactose intolerance","type":"exact"},{"name":"congenital sucrose intolerance with starch and lactose intolerance","type":"exact"},{"name":"disaccharide intolerance with starch and lactose intolerance","type":"exact"}],"termid":"MONDO:0017621","xrefs":{"Monarch":{"xref_id":"0017621"}}}


id: MOD:01444
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to L-3,3-dihydroxyoalanine.","definition_xrefs":["RESID:AA0492#CYS","PubMed:11435113","PubMed:17558559"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"},{"relation_name":"is_a","term_name":"L-3,3-dihydroxyoalanine","termid":"MOD:01448"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"L-3,3-dihydroxyoalanine (Cys)","synonyms":[{"name":"(S)-2-amino-3,3-dihydroxypropanoic acid","type":"exact"},{"name":"2-(dihydroxymethyl)glycine","type":"exact"},{"name":"3,3-dihydroxy-L-alanine","type":"exact"},{"name":"3,3-dihydroxyalanine","type":"exact"},{"name":"3-hydroxy-L-serine","type":"exact"},{"name":"3-oxoalanine hydrate","type":"exact"},{"name":"C(alpha)-formylglycine hydrate","type":"related"}],"termid":"MOD:01444"}


id: GO:0000108
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A stable complex of proteins that carry out the DNA damage recognition and incision reactions characteristic of nucleotide excision repair (NER), such as DNA damage recognition, DNA helix unwinding, and endonucleolytic cleavage at sites flanking damaged DNA; includes TFIIH subunits and additional polypeptides; may form in the absence of DNA damage.","definition_xrefs":["PMID:10681587","PMID:9852079"],"gene_count":0,"genotype_count":0,"name":"obsolete repairosome (obsolete GO:0000108)","synonyms":[{"name":"repairosome","type":"exact"}],"termid":"GO:0000108"}


id: PBO:0030823
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_chlorpromazine","termid":"PBO:0030823"}


id: GO:0039508
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus stops, prevents, or reduces the frequency, rate or extent of the functional activity of a host receptor.","definition_xrefs":["GOC:bf","GOC:sp"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host receptor activity (obsolete GO:0039508)","synonyms":[{"name":"down-regulation by virus of host receptor activity","type":"exact"},{"name":"downregulation by virus of host receptor activity","type":"exact"},{"name":"inhibition by virus of host receptor activity","type":"narrow"},{"name":"negative regulation by virus of host receptor activity","type":"exact"},{"name":"suppression by virus of host receptor function","type":"exact"},{"name":"viral inhibition of host receptor","type":"exact"}],"termid":"GO:0039508"}


id: PBO:0116756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMARCE1 pseudogene 2","termid":"PBO:0116756"}


id: GO:0016174
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NAD(P)H + H+ + O2 = NAD(P)+ + hydrogen peroxide.","definition_xrefs":["PMID:10601291","EC:1.6.3.1","PMID:11822874","PMID:10401672"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on NAD(P)H, oxygen as acceptor","termid":"GO:0050664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"NAD(P)H oxidase H2O2-forming activity","secondary_identifiers":["Reactome:R-HSA-5693681","Reactome:R-HSA-9698758"],"synonyms":[{"name":"NAD(P)H oxidase activity","type":"broad"},{"name":"NAD(P)H:oxygen oxidoreductase activity","type":"related"},{"name":"NADPH oxidase","type":"broad"},{"name":"THOX2 activity","type":"narrow"},{"name":"ThOX activity","type":"narrow"},{"name":"dual oxidase activity","type":"related"},{"name":"p138tox","type":"related"},{"name":"thyroid NADPH oxidase activity","type":"narrow"},{"name":"thyroid oxidase 2 activity","type":"narrow"},{"name":"thyroid oxidase activity","type":"narrow"}],"termid":"GO:0016174"}


id: GO:1902295
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any DNA replication, synthesis of RNA primer that is involved in cell cycle DNA replication.","definition_xrefs":["GOC:TermGenie","GOC:mtg_cell_cycle"],"gene_count":0,"genotype_count":0,"name":"obsolete synthesis of RNA primer involved in cell cycle DNA replication (obsolete GO:1902295)","synonyms":[{"name":"DNA replication, synthesis of RNA primer involved in cell cycle DNA replication","type":"exact"},{"name":"replication priming involved in cell cycle DNA replication","type":"related"}],"termid":"GO:1902295"}


id: PBO:0060957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NFKB inhibitor delta","termid":"PBO:0060957"}


id: MOD:01852
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-cysteine residue and an L-lysine residue to release hydrogen sulfide and form 2-amino-6-(2-amino-2-carboxyethylamino)hexanoic acid.","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uncategorized crosslinked residues","termid":"MOD:00692"},{"relation_name":"is_a","term_name":"L-lysinoalanine","termid":"MOD:01853"},{"relation_name":"is_a","term_name":"crosslinked L-cysteine residue","termid":"MOD:02044"},{"relation_name":"is_a","term_name":"crosslinked L-lysine residue","termid":"MOD:02051"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"L-lysinoalanine (Lys-Cys)","synonyms":[{"name":"Lysinoalanine (from Cysteine)","type":"exact"}],"termid":"MOD:01852"}


id: GO:0032814
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of natural killer cell activation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lymphocyte activation","termid":"GO:0051249"},{"relation_name":"regulates","term_name":"natural killer cell activation","termid":"GO:0030101"}],"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 natural killer cell activation","synonyms":[{"name":"regulation of NK cell activation","type":"exact"}],"termid":"GO:0032814"}


id: MOD:01761
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom of a protein N-terminal with the Proteome Sciences TMT6plex-131 reporter+balance group.","definition_xrefs":["Unimod:737#N-term"],"direct_ancestors":[{"relation_name":"is_a","term_name":"TMT6plex reporter+balance reagent acylated N-terminal","termid":"MOD:01718"},{"relation_name":"is_a","term_name":"TMT6plex-131 reporter+balance reagent acylated residue","termid":"MOD:01760"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMT6plex-131 reporter+balance reagent acylated N-terminal","synonyms":[{"name":"3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl","type":"exact"},{"name":"Sixplex Tandem Mass Tag(TM)","type":"related"},{"name":"TMT6plex","type":"related"}],"termid":"MOD:01761"}


id: PBO:0042018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 74B","termid":"PBO:0042018"}


id: PBO:0073627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sialic acid binding Ig like lectin 11","termid":"PBO:0073627"}


id: PBO:0088393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-hydroxyacyl-ACP dehydratase Htd2","termid":"PBO:0088393"}


id: GO:0015348
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete prostaglandin/thromboxane transporter activity (obsolete GO:0015348)","synonyms":[{"name":"prostaglandin/thromboxane transporter activity","type":"exact"}],"termid":"GO:0015348"}


id: PBO:0055104
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 2522","termid":"PBO:0055104"}


id: PBO:0091660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isocitrate lyase Icl1","termid":"PBO:0091660"}


id: MONDO:0015245
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare intestinal disease.","gene_count":0,"genotype_count":0,"name":"obsolete rare intestinal disease (obsolete MONDO:0015245)","secondary_identifiers":["Orphanet:117569"],"synonyms":[{"name":"rare intestinal disease","type":"exact"}],"termid":"MONDO:0015245","xrefs":{"Monarch":{"xref_id":"0015245"}}}


id: GO:1990670
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The joining of the lipid bilayer membrane around a vesicle to the lipid bilayer membrane around the Golgi cis cisterna. This can involve anterograde or retrograde transport vesicles.","definition_xrefs":["GOC:bhm","PMID:16038056","PMID:24119662"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle fusion","termid":"GO:0006906"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0016192","GO:0006810","GO:0061024","GO:0008150"],"is_obsolete":false,"name":"vesicle fusion with Golgi cis cisterna membrane","termid":"GO:1990670"}


id: PBO:0082192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Aldehyde reductase; substrates include both aromatic and aliphatic aldehydes; uses NADPH as cofactor; SWAT-GFP and mCherry fusion proteins localize to the endoplasmic reticulum and vacuole respectively","termid":"PBO:0082192"}


id: GO:0043407
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of MAP kinase activity.","definition_xrefs":["GOC:dph","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of MAP kinase activity","termid":"GO:0043405"},{"relation_name":"is_a","term_name":"negative regulation of MAPK cascade","termid":"GO:0043409"},{"relation_name":"is_a","term_name":"negative regulation of protein serine/threonine kinase activity","termid":"GO:0071901"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of MAP kinase activity","synonyms":[{"name":"down regulation of MAPK activity","type":"exact"},{"name":"down-regulation of MAPK activity","type":"exact"},{"name":"downregulation of MAPK activity","type":"exact"},{"name":"inhibition of MAPK activity","type":"narrow"},{"name":"negative regulation of mitogen activated protein kinase activity","type":"exact"},{"name":"negative regulation of mitogen-activated protein kinase activity","type":"exact"}],"termid":"GO:0043407"}


id: PBO:0002104
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DRE Element Binding","termid":"PBO:0002104"}


id: PBO:0113313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in proteolytic activation of Rim101p; part of response to alkaline pH; PalA/AIP1/Alix family member; interaction with the ESCRT-III subunit Snf7p suggests a relationship between pH response and multivesicular body formation; localizes to cytosol, nucleus and peroxisomes","termid":"PBO:0113313"}


id: PBO:0064583
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POTE ankyrin domain family member D","termid":"PBO:0064583"}


id: PBO:0074638
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 31","termid":"PBO:0074638"}


id: MONDO:0018081
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hemorrhagic fever with renal syndrome (HFRS) is a rodent-borne potentially severe hemorrhagic disease caused by Old World Hantaviruses characterized by high fever, malaise, headache, myalgia, arthralgia, backache, abdominal pain, oliguria/renal failure and systemic hemorrhagic manifestations.","definition_xrefs":["Orphanet:340"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral hemorrhagic fever","termid":"MONDO:0018087"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemorrhagic fever-renal syndrome","secondary_identifiers":["GARD:18689","ICD10EXP:N08.0*","MEDGEN:42408","ICD10EXP:A98.5+","icd11.foundation:1059069619","MESH:C535630","UMLS:C0019101","MedDRA:10023484"],"synonyms":[{"name":"Hantavirosis","type":"exact"},{"name":"Hantavirus fever","type":"exact"}],"termid":"MONDO:0018081","xrefs":{"Monarch":{"xref_id":"0018081"}}}


id: GO:0071126
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alphaV-beta6 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":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"alphaV-beta6 integrin-osteopontin complex","synonyms":[{"name":"ITGAV-ITGB6-SPP1 complex","type":"narrow"}],"termid":"GO:0071126"}


id: PBO:0071889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 27","termid":"PBO:0071889"}


id: PBO:0067932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 234","termid":"PBO:0067932"}


id: PBO:0117243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycine cleavage complex subunit T, Gcv1","termid":"PBO:0117243"}


id: PBO:0059463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MSH2 overlapping transcript 1","termid":"PBO:0059463"}


id: PR:C6Y4A4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC688.16 gene.","definition_xrefs":["PRO:DNx","UniProtKB:C6Y4A4"],"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 membrane protein C688.16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC688.16","synonyms":[{"name":"Spom972h-SPAC688.16","type":"exact"}],"termid":"PR:C6Y4A4"}


id: PBO:0035882
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_N-linked_glycosylation_during_vegetative_growth","termid":"PBO:0035882"}


id: GO:0039724
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont interferes with, inhibits or disrupts a cytoplasmic pattern recognition receptor signaling pathway by reducing the activity of host I-kappa-B kinase epsilon (IKBKE/IKK-epsilon/IKK-E).","definition_xrefs":["PMID:24173023","PMID:19153231","PMID:22532683"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of cytoplasmic pattern recognition receptor signaling pathway","termid":"GO:0039537"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host cytoplasmic pattern recognition receptor signaling pathway via inhibition of IKBKE activity","secondary_identifiers":["VZ:4478"],"synonyms":[{"name":"inhibition of host IKBKE by virus","type":"related"},{"name":"suppression by virus of host IKBKE activity","type":"related"},{"name":"suppression by virus of host viral-induced cytoplasmic pattern recognition receptor signaling pathway via inhibition of IKBKE activity","type":"narrow"}],"termid":"GO:0039724"}


id: MONDO:0003661
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lymphoma that arises from the breast. There is no history of extramammary breast lymphoma and ipsilateral axillary lymph node involvement does not exclude the diagnosis of primary breast lymphoma. Most patients present with a painless breast lump. The vast majority of cases are B-cell non-Hodgkin lymphomas. Diffuse large B-cell lymphoma, follicular lymphoma, and extranodal marginal zone B-cell lymphoma of mucosa associated lymphoid tissue are the most common types of primary non-Hodgkin lymphoma of the breast. Primary Hodgkin lymphoma of the breast is rare.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoma","termid":"MONDO:0005062"},{"relation_name":"is_a","term_name":"breast cancer","termid":"MONDO:0007254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570"],"is_obsolete":false,"name":"breast lymphoma","secondary_identifiers":["UMLS:C1704251","DOID:5826","SCTID:278052009","MEDGEN:309939","NCIT:C4671"],"synonyms":[{"name":"breast lymphoma","type":"exact"},{"name":"lymphoma of breast","type":"exact"},{"name":"lymphoma of the breast","type":"exact"},{"name":"malignant lymphoma of breast","type":"exact"},{"name":"primary breast lymphoma","type":"exact"}],"termid":"MONDO:0003661","xrefs":{"Monarch":{"xref_id":"0003661"}}}


id: PR:O94268
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nop2 gene.","definition_xrefs":["UniProtKB:O94268","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":"25S rRNA (cytosine-C(5))-methyltransferase nop2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP8B7.20c","synonyms":[{"name":"Spom972h-nop2","type":"exact"},{"name":"nucleolar protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94268"}


id: PBO:0056507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mannose binding lectin 2","termid":"PBO:0056507"}


id: MONDO:0006741
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Localized atrophy of the brain parenchyma due to aging, hemorrhage, infarct, or inflammation.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"encephalomalacia","secondary_identifiers":["MEDGEN:4936","NCIT:C98920","DOID:2034","MedDRA:10051818","MESH:D004678","UMLS:C0014068","icd11.foundation:689481271","EFO:1000915","SCTID:58762006"],"termid":"MONDO:0006741","xrefs":{"Monarch":{"xref_id":"0006741"}}}


id: MONDO:0011112
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Wilms tumor in which the cause of the disease is a mutation in the POU6F2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary Wilms tumor","termid":"MONDO:0003321"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0004992"],"is_obsolete":false,"name":"Wilms tumor 5","secondary_identifiers":["UMLS:C1832099","MEDGEN:316905","MESH:C536707","OMIM:601583","GARD:15336"],"synonyms":[{"name":"WT5","type":"related"},{"name":"Wilms tumor 5","type":"exact"},{"name":"Wilms tumor and radial bilateral aplasia","type":"related"},{"name":"Wilms tumor susceptibility-5, autosomal dominant, somatic mutation","type":"exact"},{"name":"Wilms tumor type 5","type":"exact"},{"name":"Wilms tumor, susceptibility to","type":"related"},{"name":"Wilms tumour and radial bilateral aplasia","type":"related"},{"name":"Wilms tumour susceptibility-5, autosomal dominant, somatic mutation","type":"exact"},{"name":"Wilms tumour type 5","type":"exact"},{"name":"bilateral radial aplasia with Wilms tumor","type":"related"},{"name":"bilateral radial aplasia with Wilms tumour","type":"related"}],"termid":"MONDO:0011112","xrefs":{"Monarch":{"xref_id":"0011112"}}}


id: GO:0097572
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"One of the two nuclei found in Giardia species (trophozoite stage). It is located on the right side of the cell when viewed from the dorsal side.","definition_xrefs":["GOC:giardia","ISBN:0-444-81258-X"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus","termid":"GO:0005634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005634"],"is_obsolete":false,"name":"right nucleus","termid":"GO:0097572"}


id: GO:0021803
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The extension of a long process to the pial surface as a cell leaves the ventricular zone.","definition_xrefs":["GOC:cls","GOC:dph","GOC:dgh","GO_REF:0000021","GOC:jid","PMID:12626695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection assembly","termid":"GO:0120031"},{"relation_name":"part_of","term_name":"somal translocation","termid":"GO:0021802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"extension of leading cell process to pial surface","termid":"GO:0021803"}


id: GO:0022008
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Generation of cells within the nervous system.","definition_xrefs":["GOC:curators","GO_REF:0000021","GOC:dph","GOC:cls","GOC:dgh","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"nervous system development","termid":"GO:0007399"}],"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":"neurogenesis","secondary_identifiers":["Wikipedia:Neurogenesis"],"synonyms":[{"name":"nervous system cell generation","type":"exact"},{"name":"neural cell differentiation","type":"related"}],"termid":"GO:0022008"}


id: PBO:0088257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylyl-sulfate kinase","termid":"PBO:0088257"}


id: PBO:0027632
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_subtelomere","termid":"PBO:0027632"}


id: MONDO:0019153
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Goossens-Devriendt syndrome is characterized by intrauterine growth retardation, a congenital heart defect, postaxial polydactyly, a brain malformation, abnormal hair with temporal balding, and marked facial dysmorphism. It has been reported in two siblings from unrelated parents. One of the siblings died and the surviving patient showed postnatal growth retardation and severe developmental delay.","definition_xrefs":["Orphanet:75389"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"heart disorder","termid":"MONDO:0005267"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain malformation-congenital heart disease-postaxial polydactyly syndrome","secondary_identifiers":["UMLS:C4303545","MEDGEN:929214","SCTID:717943008","GARD:18926"],"synonyms":[{"name":"Goossens-Devriendt syndrome","type":"exact"}],"termid":"MONDO:0019153","xrefs":{"Monarch":{"xref_id":"0019153"}}}


id: PBO:0003795
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beige protein homolog (predicted)","termid":"PBO:0003795"}


id: GO:0019596
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of mandelate, the anion of mandelic acid. Mandelic acid (alpha-hydroxybenzeneacetic acid) is an 8-carbon alpha-hydroxy acid (AHA) that is used in organic chemistry and as a urinary antiseptic.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mandelate metabolic process","termid":"GO:0018924"},{"relation_name":"is_a","term_name":"monocarboxylic acid catabolic process","termid":"GO:0072329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"mandelate catabolic process","synonyms":[{"name":"mandelate breakdown","type":"exact"},{"name":"mandelate catabolism","type":"exact"},{"name":"mandelate degradation","type":"exact"}],"termid":"GO:0019596"}


id: SO:0000036
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A DNA region that is required for the binding of chromatin to the nuclear matrix.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosomal_regulatory_element","termid":"SO:0000626"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"matrix_attachment_site","secondary_identifiers":["http://en.wikipedia.org/wiki/Matrix_attachment_site"],"synonyms":[{"name":"INSDC_feature:regulatory","type":"broad"},{"name":"INSDC_qualifier:matrix_attachment_region","type":"exact"},{"name":"MAR","type":"exact"},{"name":"S/MAR","type":"exact"},{"name":"S/MAR element","type":"related"},{"name":"SMAR","type":"exact"},{"name":"matrix association region","type":"exact"},{"name":"matrix attachment region","type":"exact"},{"name":"matrix attachment site","type":"exact"},{"name":"nuclear matrix association region","type":"exact"},{"name":"nuclear matrix attachment site","type":"exact"},{"name":"scaffold attachment site","type":"exact"},{"name":"scaffold matrix attachment region","type":"exact"}],"termid":"SO:0000036"}


id: PBO:0051963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ITPRIP like 1","termid":"PBO:0051963"}


id: PBO:0078597
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 60 pseudogene 10, Y-linked","termid":"PBO:0078597"}


id: GO:1901385
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of voltage-gated calcium channel activity.","definition_xrefs":["GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cation channel activity","termid":"GO:2001257"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"regulation of voltage-gated calcium channel activity","synonyms":[{"name":"regulation of depolarization-activated calcium channel","type":"broad"},{"name":"regulation of depolarization-activated voltage gated calcium channel activity","type":"exact"},{"name":"regulation of depolarization-activated voltage-gated calcium channel","type":"exact"},{"name":"regulation of depolarization-activated voltage-gated calcium channel activity","type":"exact"},{"name":"regulation of dihydropyridine-sensitive calcium channel activity","type":"narrow"},{"name":"regulation of voltage gated calcium channel activity","type":"exact"},{"name":"regulation of voltage-dependent calcium channel activity","type":"exact"},{"name":"regulation of voltage-gated calcium ion channel activity","type":"exact"},{"name":"regulation of voltage-sensitive calcium channel","type":"exact"}],"termid":"GO:1901385"}


id: GO:0140504
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Degradation of a lipid droplet by microautophagy.","definition_xrefs":["PMID:29601311","PMID:25070953","PMID:28838958","PMID:29293450","PMID:28394250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microautophagy","termid":"GO:0016237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006914"}],"interesting_parent_ids":["GO:0008150","GO:0006914"],"is_obsolete":false,"name":"microlipophagy","synonyms":[{"name":"lipid droplet autophagy","type":"exact"}],"termid":"GO:0140504"}


id: PBO:0081362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 197","termid":"PBO:0081362"}


id: PBO:0082521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cdc42p-activated signal transducing kinase; member of the PAK (p21-activated kinase) family, along with Ste20p and Skm1p; involved in septin ring assembly, vacuole inheritance, cytokinesis, sterol uptake regulation; phosphorylates Cdc3p and Cdc10p; CLA4 has a paralog, SKM1, that arose from the whole genome duplication","termid":"PBO:0082521"}


id: PBO:0053930
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 1229","termid":"PBO:0053930"}


id: PBO:0040731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL6 corepressor","termid":"PBO:0040731"}


id: PBO:0114496
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-like protein involved in thiolation of cytoplasmic tRNAs; receives sulfur from the E1-like enzyme Uba4p and transfers it to tRNA; functions as a protein tag involved in the urmylation of proteins involved in nutrient sensing and the oxidative stress response; regulates stress-dependent condensate formation, promoting phase separation of numerous proteins to promote stress resilience and survival; forms co-condensates with Uba4p resulting in increased target urmylation","termid":"PBO:0114496"}


id: PBO:0080555
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WBP1 pseudogene 2","termid":"PBO:0080555"}


id: MONDO:0000811
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital coronary vessel anomaly in which the left main coronary artery originates from the pulmonary artery instead of from aorta. The congenital heart defect typically results in coronary artery fistula; left-sided heart failure and mitral valve insufficiency during the first months of life.","definition_xrefs":["MESH:D063748"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital coronary artery anomaly","termid":"MONDO:0001389"}],"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":"anomalous left coronary artery from the pulmonary artery","secondary_identifiers":["MEDGEN:760471","NANDO:2200242","UMLS:C1735886","DOID:0060562"],"synonyms":[{"name":"ALCAPA","type":"exact"},{"name":"ALCAPA disorder","type":"exact"},{"name":"BWGS","type":"exact"},{"name":"Bland-White-Garland syndrome","type":"exact"},{"name":"White-Garland syndrome","type":"exact"}],"termid":"MONDO:0000811","xrefs":{"Monarch":{"xref_id":"0000811"}}}


id: PBO:0044974
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAH-box helicase 9 pseudogene 1","termid":"PBO:0044974"}


id: PBO:0062297
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 M member 8","termid":"PBO:0062297"}


id: MONDO:0001409
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute or chronic inflammatory disease affecting the esophageal wall.","definition_xrefs":["NCIT:C9224"],"direct_ancestors":[{"relation_name":"is_a","term_name":"esophageal disorder","termid":"MONDO:0003749"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"esophagitis","secondary_identifiers":["MESH:D004941","UMLS:C0014868","HP:0100633","DOID:11963","ICD9:530.1","ICD9:530.12","MEDGEN:4549","SCTID:16761005","ICD9:530.10"],"synonyms":[{"name":"acute esophagitis","type":"narrow"},{"name":"esophagitis","type":"exact"},{"name":"esophagitis (disease)","type":"exact"},{"name":"esophagus inflammation","type":"exact"},{"name":"inflammation of esophagus","type":"exact"},{"name":"inflammation of oesophagus","type":"exact"},{"name":"oesophagus inflammation","type":"exact"}],"termid":"MONDO:0001409","xrefs":{"Monarch":{"xref_id":"0001409"}}}


id: GO:0039686
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A viral DNA replication process where replication occurs in both directions from the starting point. This creates two replication forks, moving in opposite directions.","definition_xrefs":["GOC:bf","VZ:1939","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral DNA genome replication","termid":"GO:0039693"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0008150","GO:0006259"],"is_obsolete":false,"name":"bidirectional double-stranded viral DNA replication","synonyms":[{"name":"viral bidirectional dsDNA replication","type":"exact"}],"termid":"GO:0039686"}


id: MONDO:0002712
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An uncommon lipoma characterized by prominent vascularity that arises in the epidural space of the spinal canal.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"spinal cord lipoma","termid":"MONDO:0001790"},{"relation_name":"is_a","term_name":"epidural spinal canal neoplasm","termid":"MONDO:0002713"},{"relation_name":"is_a","term_name":"angiolipoma","termid":"MONDO:0006085"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epidural spinal canal angiolipoma","secondary_identifiers":["DOID:3617","NCIT:C5424","UMLS:C1333416","MEDGEN:232461"],"synonyms":[{"name":"angiolipoma of epidural space","type":"exact"},{"name":"angiolipoma of epidural spinal canal","type":"exact"},{"name":"angiolipoma of extradural spinal canal","type":"exact"},{"name":"angiolipoma of the epidural spinal canal","type":"exact"},{"name":"angiolipoma of the extradural spinal canal","type":"exact"},{"name":"epidural space angiolipoma","type":"exact"},{"name":"extradural spinal canal angiolipoma","type":"exact"}],"termid":"MONDO:0002712","xrefs":{"Monarch":{"xref_id":"0002712"}}}


id: MONDO:0003305
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neurofibroma characterized by the presence of areas with increased cellularity.","definition_xrefs":["NCIT:C41427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurofibroma","termid":"MONDO:0016755"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cellular neurofibroma","secondary_identifiers":["MEDGEN:275699","DOID:5152","UMLS:C1516371"],"synonyms":[{"name":"cellular neurofibroma","type":"exact"}],"termid":"MONDO:0003305","xrefs":{"Monarch":{"xref_id":"0003305"}}}


id: CHEBI:17326
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoside triphosphate","termid":"CHEBI:17326"}


id: GO:1902262
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any apoptotic process that is involved in blood vessel morphogenesis.","definition_xrefs":["GOC:TermGenie","GOC:dph","GOC:mtg_apoptosis","PMID:16163358"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apoptotic process involved in morphogenesis","termid":"GO:0060561"},{"relation_name":"part_of","term_name":"blood vessel morphogenesis","termid":"GO:0048514"}],"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 blood vessel morphogenesis","synonyms":[{"name":"apoptosis involved in patterning of blood vessels","type":"narrow"},{"name":"apoptotic cell death involved in patterning of blood vessels","type":"exact"},{"name":"apoptotic program involved in patterning of blood vessels","type":"narrow"},{"name":"apoptotic programmed cell death involved in patterning of blood vessels","type":"exact"},{"name":"programmed cell death by apoptosis involved in patterning of blood vessels","type":"exact"},{"name":"signaling (initiator) caspase activity involved in patterning of blood vessels","type":"related"},{"name":"type I programmed cell death involved in patterning of blood vessels","type":"narrow"}],"termid":"GO:1902262"}


id: MONDO:0850353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A prostate carcinoma that is characterized by continued growth and spread despite the surgical removal of the testes or medical intervention to block androgen production.","definition_xrefs":["DOID:0080909"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostate carcinoma","termid":"MONDO:0005159"}],"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":"castration-resistant prostate carcinoma","secondary_identifiers":["UMLS:C1328504","NCIT:C130234","MEDGEN:730224"],"termid":"MONDO:0850353","xrefs":{"Monarch":{"xref_id":"0850353"}}}


id: PBO:0048676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucuronic acid epimerase","termid":"PBO:0048676"}


id: PBO:0028664
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-loss_of_gross_chromosomal_rearrangement_during_replication_fork_processing","termid":"PBO:0028664"}


id: PBO:0083066
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dihydrosphingosine phosphate lyase; regulates intracellular levels of sphingolipid long-chain base phosphates (LCBPs), degrades phosphorylated long chain bases, prefers C16 dihydrosphingosine-l-phosphate as a substrate","termid":"PBO:0083066"}


id: PBO:0090008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein phosphatase PP2C catalytic subunit Ptc1","termid":"PBO:0090008"}


id: PBO:0062311
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 T member 3","termid":"PBO:0062311"}


id: MONDO:0021358
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the hypopharynx.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"head and neck neoplasm","termid":"MONDO:0005586"},{"relation_name":"is_a","term_name":"disorder of pharynx","termid":"MONDO:0020592"},{"relation_name":"is_a","term_name":"pharynx neoplasm","termid":"MONDO:0021246"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neoplasm of hypopharynx","secondary_identifiers":["MEDGEN:43797","NCIT:C3127","SCTID:126686005","UMLS:C0020627"],"synonyms":[{"name":"hypopharyngeal neoplasm","type":"exact"},{"name":"hypopharyngeal neoplasms","type":"exact"},{"name":"hypopharyngeal tumor","type":"exact"},{"name":"hypopharyngeal tumour","type":"exact"},{"name":"hypopharynx neoplasm","type":"exact"},{"name":"hypopharynx neoplasm (disease)","type":"exact"},{"name":"hypopharynx tumor","type":"exact"},{"name":"hypopharynx tumour","type":"exact"},{"name":"neoplasm of hypopharynx","type":"exact"},{"name":"neoplasm of the hypopharynx","type":"exact"},{"name":"tumor of hypopharynx","type":"exact"},{"name":"tumor of the hypopharynx","type":"exact"},{"name":"tumour of hypopharynx","type":"exact"},{"name":"tumour of the hypopharynx","type":"exact"}],"termid":"MONDO:0021358","xrefs":{"Monarch":{"xref_id":"0021358"}}}


id: PBO:0001125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIM23 translocase complex subunit Tim14 (predicted)","termid":"PBO:0001125"}


id: GO:0044262
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving carbohydrates, any of a group of organic compounds based of the general formula Cx(H2O)y, as carried out by individual cells.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete cellular carbohydrate metabolic process (obsolete GO:0044262)","synonyms":[{"name":"cellular carbohydrate metabolism","type":"exact"},{"name":"main pathways of carbohydrate metabolic process","type":"narrow"},{"name":"main pathways of carbohydrate metabolism","type":"narrow"}],"termid":"GO:0044262"}


id: GO:1900360
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of pentasaccharide transport.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"pentasaccharide transport","termid":"GO:2001100"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of pentasaccharide transport","termid":"GO:1900360"}


id: MONDO:0006014
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infection of the vulva and vagina with a fungus of the genus CANDIDA. It is a disease associated with HIV infection.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cutaneous candidiasis","termid":"MONDO:0000879"},{"relation_name":"is_a","term_name":"vulvovaginitis","termid":"MONDO:0007019"},{"relation_name":"is_a","term_name":"infective vaginitis","termid":"MONDO:0023557"}],"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":"vulvovaginal candidiasis","secondary_identifiers":["NCIT:C2914","DOID:2272","UMLS:C0700345","ICD9:112.1","MESH:D002181","EFO:0007543","MEDGEN:195979","SCTID:72605008","ICD10CM:B37.3"],"synonyms":[{"name":"candidal vulvovaginitis","type":"exact"},{"name":"candidal: [vulvovaginitis NOS] or [cervix]","type":"exact"},{"name":"candidal: cervix","type":"exact"},{"name":"candidiasis of vulva and vagina","type":"exact"},{"name":"monilial vulvovaginitis","type":"exact"},{"name":"vaginal candidiasis","type":"exact"},{"name":"vulvovaginal candidiasis","type":"exact"}],"termid":"MONDO:0006014","xrefs":{"Monarch":{"xref_id":"0006014"}}}


id: MONDO:0800328
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":0,"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:0005328"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005328","MONDO:0005066"],"is_obsolete":false,"name":"retinitis pigmentosa 94, variable age at onset","secondary_identifiers":["UMLS:C5676889","MEDGEN:1805655"],"synonyms":[{"name":"RP94","type":"exact"}],"termid":"MONDO:0800328","xrefs":{"Monarch":{"xref_id":"0800328"}}}


id: PBO:0048148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FXYD domain containing ion transport regulator 7","termid":"PBO:0048148"}


id: GO:0047596
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 6-methylsalicylate + H+ = 3-cresol + CO2.","definition_xrefs":["EC:4.1.1.52","RHEA:23112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"6-methylsalicylate decarboxylase activity","secondary_identifiers":["MetaCyc:6-METHYLSALICYLATE-DECARBOXYLASE-RXN","KEGG_REACTION:R03567"],"synonyms":[{"name":"6-MSA decarboxylase activity","type":"related"},{"name":"6-methylsalicylate carboxy-lyase (3-cresol-forming)","type":"related"},{"name":"6-methylsalicylate carboxy-lyase activity","type":"related"},{"name":"6-methylsalicylic acid (2,6-cresotic acid) decarboxylase activity","type":"related"}],"termid":"GO:0047596"}


id: GO:0072215
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of metanephros development. Metanephros development is the process whose specific outcome is the progression of the metanephros over time, from its formation to the mature structure. The metanephros is an endocrine and metabolic organ that filters the blood and excretes the end products of body metabolism in the form of urine.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of kidney development","termid":"GO:0090183"},{"relation_name":"regulates","term_name":"metanephros development","termid":"GO:0001656"}],"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 metanephros development","termid":"GO:0072215"}


id: PBO:0054763
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 2175","termid":"PBO:0054763"}


id: PBO:0013838
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PhosphoPantothenate-Cysteine","termid":"PBO:0013838"}


id: PBO:0085942
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; mutant sensitive to 6-azauracil (6AU) and mycophenolic acid (MPA)","termid":"PBO:0085942"}


id: MONDO:0018965
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare renal disease characterized by glomerular nephropathy with hematuria progressing to end-stage renal disease (ESRD), frequently associated with sensorineural deafness, and occasionally with ocular anomalies.","definition_xrefs":["Orphanet:63"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete lens shape anomaly (obsolete MONDO:0020237)","termid":"MONDO:0020237"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary nephritis","termid":"MONDO:0005334"}],"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":"Alport syndrome","secondary_identifiers":["OMIMPS:301050","UMLS:C1567741","MedDRA:10001843","ICD10CM:Q87.81","icd11.foundation:1170919425","NANDO:1200712","NANDO:2200126","NCIT:C34842","DOID:10983","MEDGEN:339209","MESH:D009394","GARD:5785","NORD:756"],"synonyms":[{"name":"Alport deafness-nephropathy","type":"exact"},{"name":"Alport syndrome","type":"exact"},{"name":"Alport's syndrome","type":"exact"},{"name":"hereditary nephritis","type":"broad"}],"termid":"MONDO:0018965","xrefs":{"Monarch":{"xref_id":"0018965"}}}


id: PBO:0001553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA U24b (predicted)","termid":"PBO:0001553"}


id: PBO:0109026
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 3102","termid":"PBO:0109026"}


id: GO:0004061
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-formyl-L-kynurenine + H2O = formate + L-kynurenine.","definition_xrefs":["EC:3.5.1.9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016810","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"arylformamidase activity","secondary_identifiers":["Reactome:R-HSA-71189","RHEA:13009","MetaCyc:ARYLFORMAMIDASE-RXN"],"synonyms":[{"name":"aryl-formylamine amidohydrolase activity","type":"related"},{"name":"formamidase I","type":"related"},{"name":"formamidase II","type":"related"},{"name":"formylase activity","type":"related"},{"name":"formylkynureninase activity","type":"related"},{"name":"formylkynurenine formamidase activity","type":"related"},{"name":"kynurenine formamidase activity","type":"related"}],"termid":"GO:0004061"}


id: PBO:0070993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L19 pseudogene 17","termid":"PBO:0070993"}


id: MONDO:1012112
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypoadrenocorticism, non-human animal","termid":"MONDO:1011675"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypoadrenocorticism, goat","secondary_identifiers":["OMIA:000519-9925"],"termid":"MONDO:1012112","xrefs":{"Monarch":{"xref_id":"1012112"}}}


id: PomGeneEx:0000017
data:
  {"annotation_feature_type":"gene","cv_name":"PomGeneExRNA","definition":"A gene expression qualifier that indicates that an RNA is present at levels that vary under two or more sets of conditions or over a time course.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fluctuates","termid":"PomGeneEx:0000008"},{"relation_name":"is_a","term_name":"RNA expression level","termid":"PomGeneEx:0000009"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA level fluctuates","synonyms":[{"name":"RNA expression fluctuates","type":"exact"},{"name":"fluctuating RNA level","type":"exact"}],"termid":"PomGeneEx:0000017"}


id: PBO:0038920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adhesion G protein-coupled receptor G2","termid":"PBO:0038920"}


id: GO:0032727
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of interferon-alpha production.","definition_xrefs":["PMID:15546383","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of type I interferon production","termid":"GO:0032481"},{"relation_name":"is_a","term_name":"regulation of interferon-alpha production","termid":"GO:0032647"},{"relation_name":"positively_regulates","term_name":"interferon-alpha production","termid":"GO:0032607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of interferon-alpha production","secondary_identifiers":["GO:1902741","GO:0045356"],"synonyms":[{"name":"activation of interferon-alpha production","type":"narrow"},{"name":"positive regulation of interferon-alpha biosynthetic process","type":"narrow"},{"name":"positive regulation of interferon-alpha secretion","type":"narrow"},{"name":"stimulation of interferon-alpha production","type":"narrow"},{"name":"up regulation of interferon-alpha production","type":"exact"},{"name":"up-regulation of interferon-alpha production","type":"exact"},{"name":"upregulation of interferon-alpha production","type":"exact"}],"termid":"GO:0032727"}


id: PBO:0054010
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 1340","termid":"PBO:0054010"}


id: PBO:0061114
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NLR family pyrin domain containing 5","termid":"PBO:0061114"}


id: PBO:0088531
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uridine kinase Yfh7","termid":"PBO:0088531"}


id: MONDO:0022574
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"biliary atresia","termid":"MONDO:0008867"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"biliary atresia intrahepatic syndromic form","secondary_identifiers":["GARD:888"],"termid":"MONDO:0022574","xrefs":{"Monarch":{"xref_id":"0022574"}}}


id: MONDO:0033199
data:
  {"annotated_genes":["SJAG_00164"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87217],"is_not":false,"summary":null,"term":"MONDO:0033199"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00164":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"hearing loss, autosomal recessive 107","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4539964","GARD:22657","MEDGEN:1622558","OMIM:617639","DOID:0080262"],"synonyms":[{"name":"DFNB107","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 107","type":"narrow"},{"name":"deafness, autosomal recessive 107","type":"narrow"}],"termid":"MONDO:0033199","terms_by_termid":{"MONDO:0033199":null},"xrefs":{"Monarch":{"xref_id":"0033199"}}}


id: MONDO:0008913
data:
  {"annotated_genes":["SJAG_01519"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86840],"is_not":false,"summary":null,"term":"MONDO:0008913"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"},{"relation_name":"is_a","term_name":"cardiac valvular defect","termid":"MONDO:0031323"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01519":null},"genotype_count":0,"is_obsolete":false,"name":"cardiac valvular defect, developmental","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1823949","UMLS:C5774175","MESH:C565882","DOID:0080633","OMIM:212093"],"synonyms":[{"name":"CARDIAC valvular defect, developmental","type":"related"},{"name":"CVDD","type":"related"},{"name":"cardiac valvular defect, developmental","type":"exact"}],"termid":"MONDO:0008913","terms_by_termid":{"MONDO:0008913":null},"xrefs":{"Monarch":{"xref_id":"0008913"}}}


id: MONDO:0009122
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":"Dohle bodies and leukemia","secondary_identifiers":["MESH:C565617","OMIM:223350","MEDGEN:346548","UMLS:C1857225"],"synonyms":[{"name":"Dohle bodies and leukemia","type":"exact"}],"termid":"MONDO:0009122","xrefs":{"Monarch":{"xref_id":"0009122"}}}


id: MONDO:0022653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cardiomyopathy","termid":"MONDO:0004994"}],"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":"cardiomyopathy due to anthracyclines","secondary_identifiers":["UMLS:C5437452","GARD:1107","MEDGEN:1755373"],"termid":"MONDO:0022653","xrefs":{"Monarch":{"xref_id":"0022653"}}}


id: MONDO:0018207
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"2p13.2 microdeletion syndrome is a rare partial autosomal monosomy characterized by global development delay, intellectual disability, behavioral abnormalities (hyperactivity, attention deficit and autistic behaviors), brachycephaly and variable facial dysmorphism. Other associated features may include vertebral fusions, mild contractures of knees and elbows, and feeding difficulties during infancy.","definition_xrefs":["Orphanet:363680"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"partial deletion of the short arm of chromosome 2","termid":"MONDO:0016884"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2p13.2 microdeletion syndrome","secondary_identifiers":["UMLS:C4749460","GARD:21557","MEDGEN:1662313"],"synonyms":[{"name":"Del(2)(p13.2)","type":"exact"}],"termid":"MONDO:0018207","xrefs":{"Monarch":{"xref_id":"0018207"}}}


id: PBO:0077400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMEM132E divergent transcript","termid":"PBO:0077400"}


id: MONDO:0005737
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A viral hemorrhagic fever that is caused by the Ebola virus, which is transmitted by contact with infected animals or humans; it is characterized by high fever, unexplained bleeding, and a high mortality rate.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Filoviridae infectious disease","termid":"MONDO:0005762"},{"relation_name":"is_a","term_name":"viral hemorrhagic fever","termid":"MONDO:0018087"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ebola hemorrhagic fever","secondary_identifiers":["MEDGEN:129219","EFO:0007243","MESH:D019142","DOID:4325","UMLS:C0282687","Orphanet:319218","icd11.foundation:792755706","GARD:2035","MedDRA:10014071","NCIT:C36171","SCTID:37109004"],"synonyms":[{"name":"EHF","type":"exact"},{"name":"Ebola","type":"exact"},{"name":"Ebola fever","type":"exact"},{"name":"Ebola virus disease","type":"exact"},{"name":"Ebolavirus caused disease or disorder","type":"exact"},{"name":"Ebolavirus disease or disorder","type":"exact"},{"name":"Ebolavirus infectious disease","type":"exact"}],"termid":"MONDO:0005737","xrefs":{"Monarch":{"xref_id":"0005737"}}}


id: PBO:0086922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pyridoxal-5'-phosphate synthase; involved in thiamine and pyridoxine biosynthesis; member of a stationary phase-induced gene family where transcriptional induction precedes the diauxic shift; induced in the absence of thiamine in a Thi2/3p-dependent manner and repressed in its presence; forms a co-regulated gene pair with SNO3; paralog of SNZ1 and SNZ2","termid":"PBO:0086922"}


id: PBO:0011154
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Metachromatic leukodystrophy","termid":"PBO:0011154"}


id: MONDO:0007962
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition in which a finger or toe is larger than normal size secondary to excessive growth of the anatomical structures or abnormal accumulation of substances.","definition_xrefs":["NCIT:C48900"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"megalodactyly","secondary_identifiers":["UMLS:C0265552","MESH:C562546","MEDGEN:78564","OMIM:155500","SCTID:48449000"],"synonyms":[{"name":"Megalodactyly","type":"exact"},{"name":"macrodactyly","type":"related"},{"name":"macrodactyly, somatic, (3), cerebral cavernous malformations 4, somatic","type":"exact"}],"termid":"MONDO:0007962","xrefs":{"Monarch":{"xref_id":"0007962"}}}


id: PBO:0047272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 247 member D","termid":"PBO:0047272"}


id: PBO:0080529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WASH complex subunit 2A","termid":"PBO:0080529"}


id: GO:0047174
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: caffeoyl-CoA + putrescine = N-caffeoylputrescine + CoA + H+.","definition_xrefs":["EC:2.3.1.138","RHEA:12436"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acyltransferase activity","termid":"GO:0016410"},{"relation_name":"is_a","term_name":"hydroxycinnamoyltransferase activity","termid":"GO:0050734"}],"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"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"putrescine N-hydroxycinnamoyltransferase activity","secondary_identifiers":["KEGG_REACTION:R01944","MetaCyc:2.3.1.138-RXN"],"synonyms":[{"name":"PHT","type":"related"},{"name":"caffeoyl-CoA putrescine N-caffeoyl transferase activity","type":"related"},{"name":"caffeoyl-CoA:putrescine N-(3,4-dihydroxycinnamoyl)transferase activity","type":"related"},{"name":"hydroxycinnamoyl-CoA:putrescine hydroxycinnamoyltransferase activity","type":"related"},{"name":"putrescine hydroxycinnamoyl transferase activity","type":"related"},{"name":"putrescine hydroxycinnamoyltransferase activity","type":"related"}],"termid":"GO:0047174"}


id: GO:0042015
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to interleukin-20.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine binding","termid":"GO:0019955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"interleukin-20 binding","synonyms":[{"name":"IL-20 binding","type":"exact"}],"termid":"GO:0042015"}


id: PBO:0073413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SET pseudogene 17","termid":"PBO:0073413"}


id: PBO:0059818
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 44","termid":"PBO:0059818"}


id: PBO:0036468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial F1-F0 ATPase synthase peripheral stalk assembly factor Ina17 (predicted)","termid":"PBO:0036468"}


id: MONDO:0600017
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acinar dysplasia in which the cause of the disease is a mutation in the FGF10 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"acinar dysplasia","termid":"MONDO:0600016"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acinar dysplasia caused by mutation in FGF10","synonyms":[{"name":"FGF10 acinar dysplasia","type":"exact"},{"name":"FGF10 related acinar dysplasia","type":"exact"}],"termid":"MONDO:0600017","xrefs":{"Monarch":{"xref_id":"0600017"}}}


id: PBO:0000011
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-localization_dependent_on","termid":"PBO:0000011"}


id: GO:1901075
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of engulfment of apoptotic cell.","definition_xrefs":["GOC:TermGenie","GO:kmv","PMID:19402756"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of phagocytosis, engulfment","termid":"GO:0060101"},{"relation_name":"is_a","term_name":"regulation of engulfment of apoptotic cell","termid":"GO:1901074"},{"relation_name":"is_a","term_name":"negative regulation of apoptotic cell clearance","termid":"GO:2000426"},{"relation_name":"negatively_regulates","term_name":"engulfment of apoptotic cell","termid":"GO:0043652"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0061024"},{"rel_name":"negatively_regulates","termid":"GO:0016192"},{"rel_name":"negatively_regulates","termid":"GO:0061024"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0016192","GO:0008150","GO:0061024","GO:0006810"],"is_obsolete":false,"name":"negative regulation of engulfment of apoptotic cell","synonyms":[{"name":"down regulation of engulfment of apoptotic cell","type":"exact"},{"name":"down regulation of engulfment of apoptotic cell corpse","type":"exact"},{"name":"down regulation of engulfment of cell corpse","type":"exact"},{"name":"down-regulation of engulfment of apoptotic cell","type":"exact"},{"name":"down-regulation of engulfment of apoptotic cell corpse","type":"exact"},{"name":"down-regulation of engulfment of cell corpse","type":"exact"},{"name":"downregulation of engulfment of apoptotic cell","type":"exact"},{"name":"downregulation of engulfment of apoptotic cell corpse","type":"exact"},{"name":"downregulation of engulfment of cell corpse","type":"exact"},{"name":"inhibition of engulfment of apoptotic cell","type":"narrow"},{"name":"inhibition of engulfment of apoptotic cell corpse","type":"narrow"},{"name":"inhibition of engulfment of cell corpse","type":"narrow"},{"name":"negative regulation of engulfment of apoptotic cell corpse","type":"exact"},{"name":"negative regulation of engulfment of cell corpse","type":"exact"}],"termid":"GO:1901075"}


id: PBO:0040321
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase F1 subunit epsilon","termid":"PBO:0040321"}


id: GO:0006630
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete lipid binding (obsolete GO:0006630)","synonyms":[{"name":"lipid binding","type":"exact"}],"termid":"GO:0006630"}


id: PBO:0027027
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_level_of_iron_homeostasis_gene_mRNA_during_vegetative_growth","termid":"PBO:0027027"}


id: FYPO:0000375
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which programmed cell death by apoptosis does not occur. Apoptosis is a form of cell death characterized by rounding-up of the cell, retraction of pseudopodes, reduction of cellular volume (pyknosis), chromatin condensation, nuclear fragmentation (karyorrhexis), plasma membrane blebbing and fragmentation of the cell into apoptotic bodies.","definition_xrefs":["GO:0006915","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal apoptotic process","termid":"FYPO:0000629"},{"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abolished apoptotic process","synonyms":[{"name":"abolished apoptosis","type":"narrow"},{"name":"absent apoptotic process","type":"exact"},{"name":"apoptosis: absent","type":"related"},{"name":"apoptotic process abolished","type":"exact"}],"termid":"FYPO:0000375"}


id: GO:0052818
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: heteroglycan + GDP-mannose = (1->3)-alpha-D-mannosylheteroglycan + GDP.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete heteroglycan 3-alpha-mannosyltransferase activity (obsolete GO:0052818)","synonyms":[{"name":"heteropolysaccharide 3-alpha-mannosyltransferase activity","type":"exact"}],"termid":"GO:0052818"}


id: GO:0070288
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that binds iron and acts as a major iron storage system. There are three major subclasses of ferritins: the classical ferritins (Ftn), the heme-containing bacterioferritins (Bfr) and the DNA-binding proteins from starved cells (Dps). Ftn and Bfr are made of 24 subunits, whereas Dps are smaller with 12 subunits. Ftn is found in most kindoms, while Bfr and Dps are restricted to prokaryotes.","definition_xrefs":["PMID:33881539","PMID:19154717"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"ferritin complex","termid":"GO:0070288"}


id: GO:0004070
data:
  {"annotated_genes":["SJAG_00964"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73663],"is_not":false,"summary":null,"term":"GO:0004070"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-aspartate + carbamoyl phosphate = N-carbamoyl-L-aspartate + H+ + phosphate.","definition_xrefs":["EC:2.1.3.2","RHEA:20013"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxyl- or carbamoyltransferase activity","termid":"GO:0016743"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00964":null},"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:0016740"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0016741","GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"aspartate carbamoyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:ASPCARBTRANS-RXN","Reactome:R-HSA-73573","KEGG_REACTION:R01397"],"synonyms":[{"name":"ATCase activity","type":"related"},{"name":"L-aspartate transcarbamoylase activity","type":"related"},{"name":"L-aspartate transcarbamylase activity","type":"related"},{"name":"aspartate carbamyltransferase activity","type":"related"},{"name":"aspartate transcarbamoylase activity","type":"related"},{"name":"aspartate transcarbamylase activity","type":"related"},{"name":"aspartic acid transcarbamoylase activity","type":"related"},{"name":"aspartic carbamyltransferase activity","type":"related"},{"name":"aspartic transcarbamylase activity","type":"related"},{"name":"carbamoyl-phosphate:L-aspartate carbamoyltransferase activity","type":"related"},{"name":"carbamoylaspartotranskinase activity","type":"related"},{"name":"carbamylaspartotranskinase activity","type":"related"}],"termid":"GO:0004070","terms_by_termid":{"GO:0004070":null}}


id: GO:0075036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of symbiont appressorium maturation.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of appressorium maturation (obsolete GO:0075036)","synonyms":[{"name":"regulation of appressorium maturation on or near host","type":"related"},{"name":"regulation of maturation of appressorium on or near host","type":"exact"}],"termid":"GO:0075036"}


id: PBO:0063714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoglucomutase 5 pseudogene 3","termid":"PBO:0063714"}


id: GO:0032470
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the concentration of calcium ions in the endoplasmic reticulum.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endoplasmic reticulum calcium ion homeostasis","termid":"GO:0032469"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098771"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0098771","GO:0008150"],"is_obsolete":false,"name":"positive regulation of endoplasmic reticulum calcium ion concentration","synonyms":[{"name":"elevation of ER calcium ion concentration","type":"exact"},{"name":"elevation of calcium ion concentration in endoplasmic reticulum","type":"exact"},{"name":"elevation of endoplasmic reticulum calcium ion concentration","type":"exact"},{"name":"endoplasmic reticulum calcium ion concentration elevation","type":"exact"}],"termid":"GO:0032470"}


id: PBO:0065556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostaglandin E synthase 2","termid":"PBO:0065556"}


id: PBO:0088553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Utp1","termid":"PBO:0088553"}


id: PBO:0038646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA oxidase 1","termid":"PBO:0038646"}


id: PBO:0060652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NCOR1 pseudogene 1","termid":"PBO:0060652"}


id: PBO:0055366
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 2795","termid":"PBO:0055366"}


id: PBO:0085244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peptidyl-prolyl cis-trans isomerase (cyclophilin) of the ER; catalyzes the cis-trans isomerization of peptide bonds N-terminal to proline residues; transcriptionally induced in response to unfolded proteins in the ER; CPR5 has a paralog, CPR2, that arose from the whole genome duplication","termid":"PBO:0085244"}


id: PBO:0030412
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_purvalanol_A","termid":"PBO:0030412"}


id: PBO:0047497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fem-1 homolog B","termid":"PBO:0047497"}


id: GO:0004339
data:
  {"annotated_genes":["SJAG_02076"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[60490],"is_not":false,"summary":null,"term":"GO:0004339"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of terminal (1->4)-linked alpha-D-glucose residues successively from non-reducing ends of the chains with release of beta-D-glucose.","definition_xrefs":["EC:3.2.1.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-glucosidase activity","termid":"GO:0090599"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02076":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016798","GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"glucan 1,4-alpha-glucosidase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["MetaCyc:3.2.1.3-RXN"],"synonyms":[{"name":"1,4-alpha-D-glucan glucohydrolase activity","type":"related"},{"name":"amyloglucosidase activity","type":"related"},{"name":"exo-1,4-alpha-glucosidase activity","type":"related"},{"name":"gamma-1,4-glucan glucohydrolase activity","type":"related"},{"name":"gamma-amylase activity","type":"related"},{"name":"glucoamylase activity","type":"exact"},{"name":"glucose amylase activity","type":"related"},{"name":"lysosomal alpha-glucosidase activity","type":"broad"}],"termid":"GO:0004339","terms_by_termid":{"GO:0004339":null}}


id: FYPO:0004554
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 phosphorylation of one or more specific proteins, or of specific protein sites, occurs to a lower extent than normal during S phase of the mitotic cell cycle and during a cellular response to ionizing radiation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein phosphorylation during mitotic G2 phase during cellular response to ionizing radiation","termid":"FYPO:0004261"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0002494"],"is_obsolete":false,"name":"decreased protein phosphorylation during mitotic S phase during cellular response to ionizing radiation","synonyms":[{"name":"decreased protein phosphorylation during cellular response to ionizing radiation during S phase of mitotic cell cycle","type":"exact"},{"name":"decreased protein phosphorylation during cellular response to ionizing radiation during mitotic S phase","type":"exact"},{"name":"decreased protein phosphorylation during mitotic S phase during cellular response to IR","type":"exact"},{"name":"decreased protein phosphorylation during mitotic S phase during cellular response to ionizing radiation during vegetative growth","type":"exact"},{"name":"reduced protein phosphorylation during cellular response to IR during mitotic S phase","type":"exact"},{"name":"reduced protein phosphorylation during mitotic S phase during cellular response to ionizing radiation","type":"exact"}],"termid":"FYPO:0004554"}


id: PBO:0077169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tousled like kinase 2","termid":"PBO:0077169"}


id: PBO:0078729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Met (anticodon CAT) 4-1","termid":"PBO:0078729"}


id: PBO:0108919
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STAG3 cohesin complex component like 5, pseudogene","termid":"PBO:0108919"}


id: MONDO:0013946
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the HS6ST1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Kallmann syndrome","termid":"MONDO:0018800"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadotropic hypogonadism 15 with or without anosmia","secondary_identifiers":["MEDGEN:766891","GARD:15872","OMIM:614880","UMLS:C3553977","DOID:0090075"],"synonyms":[{"name":"HH15","type":"related"},{"name":"HS6ST1 hypogonadotropic hypogonadism","type":"exact"},{"name":"hypogonadotropic hypogonadism 15 with or without anosmia","type":"exact"},{"name":"hypogonadotropic hypogonadism caused by mutation in HS6ST1","type":"exact"}],"termid":"MONDO:0013946","xrefs":{"Monarch":{"xref_id":"0013946"}}}


id: MONDO:0044881
data:
  {"annotated_genes":["SJAG_02527","SJAG_02460","SJAG_00980","SJAG_03453","SJAG_01013","SJAG_01349","SJAG_01748","SJAG_05979","SJAG_03905"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89073,89230,89075,89074,89076,89231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018874"},{"annotations":[88019,88020],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011508"},{"annotations":[89195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009693"}]},"cv_name":"mondo","definition":"A neoplasm arising from hematopoietic cells found in the bone marrow, peripheral blood, lymph nodes and spleen (organs of the hematopoietic system). Hematopoietic cell neoplasms can also involve other anatomic sites (e.g. central nervous system, gastrointestinal tract), either by metastasis, direct tumor infiltration, or neoplastic transformation of extranodal lymphoid tissues. The commonest forms are the various types of leukemia, Hodgkin and non-Hodgkin lymphomas, myeloproliferative neoplasms, and myelodysplastic syndromes.","definition_xrefs":["NCIT:C27134"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hematopoietic and lymphoid system neoplasm","termid":"MONDO:0002334"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00980":null,"SJAG_01013":null,"SJAG_01349":null,"SJAG_01748":null,"SJAG_02460":null,"SJAG_02527":null,"SJAG_03453":null,"SJAG_03905":null,"SJAG_05979":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"hematopoietic and lymphoid cell neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0376544","MEDGEN:91264"],"synonyms":[{"name":"HEMOLYMPHORETICULAR tumor, malignant","type":"exact"},{"name":"haematological neoplasm","type":"exact"},{"name":"haematological tumour","type":"exact"},{"name":"haematopoietic and lymphoid neoplasms","type":"exact"},{"name":"haematopoietic cancer","type":"exact"},{"name":"haematopoietic cell tumour","type":"exact"},{"name":"haematopoietic malignancy, NOS","type":"exact"},{"name":"haematopoietic neoplasm","type":"exact"},{"name":"haematopoietic neoplasms including lymphomas","type":"exact"},{"name":"haematopoietic tumour","type":"exact"},{"name":"hematologic cancer","type":"exact"},{"name":"hematologic malignancy","type":"exact"},{"name":"hematologic neoplasm","type":"exact"},{"name":"hematological neoplasm","type":"exact"},{"name":"hematological tumor","type":"exact"},{"name":"hematopoietic and lymphoid cell neoplasm","type":"exact"},{"name":"hematopoietic and lymphoid neoplasms","type":"exact"},{"name":"hematopoietic cancer","type":"exact"},{"name":"hematopoietic cell tumor","type":"exact"},{"name":"hematopoietic malignancy, NOS","type":"exact"},{"name":"hematopoietic neoplasm","type":"exact"},{"name":"hematopoietic neoplasms including lymphomas","type":"exact"},{"name":"hematopoietic tumor","type":"exact"},{"name":"hematopoietic, Including myeloma","type":"exact"},{"name":"malignant haematopoietic neoplasm","type":"exact"},{"name":"malignant hematologic neoplasm","type":"exact"},{"name":"malignant hematopoietic neoplasm","type":"exact"}],"termid":"MONDO:0044881","terms_by_termid":{"MONDO:0009693":null,"MONDO:0011508":null,"MONDO:0018874":null},"xrefs":{"Monarch":{"xref_id":"0044881"}}}


id: PBO:0044910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA fragmentation factor subunit beta","termid":"PBO:0044910"}


id: GO:0007540
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process in which an organism senses the number of X chromosomes and autosomes in its genomic complement and responds to it.","definition_xrefs":["GOC:mr","Wikipedia:XY_sex-determination_system","GOC:isa_complete","PMID:20622855"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"part_of","term_name":"primary sex determination, soma","termid":"GO:0007539"}],"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":"sex determination, establishment of X:A ratio","termid":"GO:0007540"}


id: GO:0018542
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2,3-dihydroxy DDT + O2 = 6-oxo-2-hydroxy-7-(4-chlorophenyl)-3,8,8,8-tetrachloroocta-2E,4E-dienoate.","definition_xrefs":["UM-BBD_reactionID:r0452"],"gene_count":0,"genotype_count":0,"name":"obsolete 2,3-dihydroxy DDT 1,2-dioxygenase activity (obsolete GO:0018542)","termid":"GO:0018542"}


id: MONDO:0016436
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete acquired dermis elastic tissue disorder with increased elastic tissue (obsolete MONDO:0016436)","secondary_identifiers":["Orphanet:228224"],"termid":"MONDO:0016436","xrefs":{"Monarch":{"xref_id":"0016436"}}}


id: PBO:0068721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4atac small nuclear 10, pseudogene","termid":"PBO:0068721"}


id: PBO:0013123
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sequence orphan, localizing to double strand breaks Dbl1","termid":"PBO:0013123"}


id: GO:0018316
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The oxidation of two peptidyl-cysteine residues to form a peptidyl-L-cystine (dicysteine) in which segments of peptide chain are linked by a disulfide bond; the cross-link may be between different or the same peptide chain.","definition_xrefs":["RESID:AA0025"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide cross-linking","termid":"GO:0018149"},{"relation_name":"is_a","term_name":"peptidyl-cysteine modification","termid":"GO:0018198"}],"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":"peptide cross-linking via L-cystine","termid":"GO:0018316"}


id: MONDO:0018547
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute tricyclic antidepressant (TCA) poisoning is a potentially lethal intoxication that is characterized by life-threatening arrhythmias (sinus tachycardias, premature ventricular contractions, ventricular arrhythmias), anticholinergic toxidrome (mydriasis, dry mucous membrane, tachycardia, hypertension), central nervous system toxicity (lethargy, coma, myoclonic jerks), refractory hypotension, and sudden death.","definition_xrefs":["Orphanet:43117"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute tricyclic antidepressant poisoning","secondary_identifiers":["MEDGEN:1830115","UMLS:C5681319"],"termid":"MONDO:0018547","xrefs":{"Monarch":{"xref_id":"0018547"}}}


id: PR:O42875
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A tryptophan--tRNA ligase, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10055:SF2","PRO:DNx","OMA:SCHPO01319"],"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":"tryptophan--tRNA ligase, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3G9.13c","secondary_identifiers":["UniProtKB:O42875"],"synonyms":[{"name":"Spom972h-WARS2","type":"exact"},{"name":"TrpRS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"tryptophanyl-tRNA synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O42875"}


id: MONDO:1011028
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ataxia telangiectasia that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ataxia telangiectasia, non-human animal","termid":"MONDO:1010249"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ataxia telangiectasia, pig","secondary_identifiers":["OMIA:002044-9823"],"termid":"MONDO:1011028","xrefs":{"Monarch":{"xref_id":"1011028"}}}


id: PBO:0087692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the Nup84p subcomplex of the nuclear pore complex (NPC); contributes to nucleocytoplasmic transport and NPC biogenesis and is involved in establishment of a normal nucleocytoplasmic concentration gradient of the GTPase Gsp1p; also plays roles in several processes that may require localization of genes or chromosomes at the nuclear periphery, including double-strand break repair, transcription and chromatin silencing; homologous to human NUP85 aka NUP75","termid":"PBO:0087692"}


id: PBO:0062494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily B member 10 pseudogene","termid":"PBO:0062494"}


id: GO:1904630
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 diterpene stimulus.","definition_xrefs":["GOC:TermGenie","PMID:19765580","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to lipid","termid":"GO:0071396"},{"relation_name":"is_a","term_name":"response to diterpene","termid":"GO:1904629"}],"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 diterpene","termid":"GO:1904630"}


id: MONDO:0009098
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":"dextrocardia with unusual facies and microphthalmia","secondary_identifiers":["MEDGEN:346559","OMIM:221950","MESH:C538269","UMLS:C1857298"],"synonyms":[{"name":"Aughton syndrome","type":"related"},{"name":"dextrocardia with unusual facies and microphthalmia","type":"exact"},{"name":"dextrocardia, microphthalmia, cleft palate, choreoathetosis and intellectual disability","type":"related"},{"name":"dextrocardia, microphthalmia, cleft palate, choreoathetosis and mental retardation","type":"related"}],"termid":"MONDO:0009098","xrefs":{"Monarch":{"xref_id":"0009098"}}}


id: GO:0070622
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that possesses UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase activity; the bovine complex contains disulfide-linked homodimers of 166- and 51-kDa subunits and two identical, noncovalently associated 56-kDa subunits.","definition_xrefs":["GOC:mah","PMID:8940155"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase complex, transferring phosphorus-containing groups","termid":"GO:0061695"},{"relation_name":"part_of","term_name":"lysosome","termid":"GO:0005764"}],"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:0005737"},{"rel_name":"part_of","termid":"GO:0005773"}],"interesting_parent_ids":["GO:0005737","GO:0032991","GO:0005773","GO:0005575"],"is_obsolete":false,"name":"UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase complex","synonyms":[{"name":"N-acetylglucosamine-1-phosphotransferase complex","type":"related"},{"name":"UDP-N-acetylglucosamine:lysosomal-enzyme N-acetylglucosamine-1-phosphotransferase complex","type":"exact"}],"termid":"GO:0070622"}


id: PBO:0084465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAP kinase-responsive inhibitor of the Ste12p transcription factor; involved in the regulation of mating-specific genes and the invasive growth pathway; related regulators Dig1p and Dig2p bind to Ste12p; DIG1 has a paralog, DIG2, that arose from the whole genome duplication","termid":"PBO:0084465"}


id: FYPO:0004879
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the occurrence of chromatin binding by a gene product (usually a protein) in a mutant is normal (i.e. indistinguishable from wild type) at the centromere central core.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal chromatin binding","termid":"FYPO:0003086"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000257"],"is_obsolete":false,"name":"normal chromatin binding at centromere central core","termid":"FYPO:0004879"}


id: GO:0042858
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of the siderophore chrysobactin (alpha-N-(2,3-dihydroxybenzoyl)-D-lysyl-L-serine).","definition_xrefs":["GOC:jl","PMID:8837459"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catechol-containing compound biosynthetic process","termid":"GO:0009713"},{"relation_name":"is_a","term_name":"siderophore biosynthetic process","termid":"GO:0019290"},{"relation_name":"is_a","term_name":"primary alcohol biosynthetic process","termid":"GO:0034309"},{"relation_name":"is_a","term_name":"chrysobactin metabolic process","termid":"GO:0042857"},{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"},{"relation_name":"is_a","term_name":"carboxylic acid biosynthetic process","termid":"GO:0046394"},{"relation_name":"is_a","term_name":"primary amino compound biosynthetic process","termid":"GO:1901162"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0019748"],"is_obsolete":false,"name":"chrysobactin biosynthetic process","secondary_identifiers":["GO:0031183","GO:0031184"],"synonyms":[{"name":"chrysobactin anabolism","type":"exact"},{"name":"chrysobactin biosynthesis","type":"exact"},{"name":"chrysobactin biosynthetic process, peptide formation","type":"narrow"},{"name":"chrysobactin biosynthetic process, peptide modification","type":"narrow"},{"name":"chrysobactin formation","type":"exact"},{"name":"chrysobactin synthesis","type":"exact"}],"termid":"GO:0042858"}


id: MONDO:1010689
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"AA amyloidosis that occurs in Sumatran tiger.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"AA amyloidosis, non-human animal","termid":"MONDO:1010092"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AA amyloidosis, Sumatran tiger","secondary_identifiers":["OMIA:000038-9695"],"termid":"MONDO:1010689","xrefs":{"Monarch":{"xref_id":"1010689"}}}


id: PBO:0085976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; proposed involvement in transport based on mass spectrometry analysis of copurifying proteins; null mutant is viable","termid":"PBO:0085976"}


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


id: PBO:0013793
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IRC1-R/borderline right","termid":"PBO:0013793"}


id: PR:Q9UTK1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cox16 gene.","definition_xrefs":["UniProtKB:Q9UTK1","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":"cytochrome c oxidase assembly protein cox16, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1486.08","synonyms":[{"name":"Spom972h-cox16","type":"exact"}],"termid":"PR:Q9UTK1"}


id: GO:0140822
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of ADP-ribose groups to the glutamate-35 residue of the N-terminal tail of histone H2B (or an equivalent residue).","definition_xrefs":["PMID:32822587"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NAD+-protein-glutamate ADP-ribosyltransferase activity","termid":"GO:0140807"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"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:0016757","GO:0140096","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"NAD+-histone H2BE35 glutamate ADP-ribosyltransferase activity","synonyms":[{"name":"NAD+-histone H2B-E35 glutamate ADP-ribosyltransferase activity","type":"exact"},{"name":"NAD+-histone-glutamate ADP-ribosyltransferase activity (H2B-E35 specific)","type":"exact"}],"termid":"GO:0140822"}


id: GO:0007574
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Process associated with continued cell division (budding) by the mother cell. Age is often measured by counting the number of bud scars on the cell.","definition_xrefs":["GOC:sgd_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete cell aging (sensu Saccharomyces) (obsolete GO:0007574)","synonyms":[{"name":"cell aging (sensu Saccharomyces)","type":"exact"}],"termid":"GO:0007574"}


id: GO:0018182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The covalent linkage of heme and a protein via 3'-L-histidine (otherwise known as pi-heme-histidine, pros-heme-histidine).","definition_xrefs":["RESID:AA0276"],"gene_count":0,"genotype_count":0,"name":"obsolete protein-heme linkage via 3'-L-histidine (obsolete GO:0018182)","synonyms":[{"name":"protein-haem linkage via 3'-L-histidine","type":"exact"}],"termid":"GO:0018182"}


id: GO:0051316
data:
  {"annotated_genes":["SJAG_00678","SJAG_04508","SJAG_01211","SJAG_04076","SJAG_01278","SJAG_05220","SJAG_01837","SJAG_02814","SJAG_00418","SJAG_03217","SJAG_05266","SJAG_05319","SJAG_01775","SJAG_02731","SJAG_03327","SJAG_02346","SJAG_03926","SJAG_03989","SJAG_03437","SJAG_00794","SJAG_01371","SJAG_03683","SJAG_03220","SJAG_00918","SJAG_01224","SJAG_01805"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89734,95725],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051456"},{"annotations":[118706],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1904967"},{"annotations":[111132,111885,117948,107442,110875,115240,112309,109482,91628,97227,99830,97473,116115,100552,112353,95706,102462,104384,118944,103284,109800,91021,92866],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051455"}]},"cv_name":"biological_process","definition":"The cellular process in which spindle microtubules become physically associated with the proteins making up the kinetochore complex in meiosis.","definition_xrefs":["GOC:dph","GOC:tb","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"attachment of spindle microtubules to kinetochore","termid":"GO:0008608"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"},{"relation_name":"part_of","term_name":"meiotic metaphase chromosome alignment","termid":"GO:0051311"}],"gene_count":26,"genes_by_uniquename":{"SJAG_00418":null,"SJAG_00678":null,"SJAG_00794":null,"SJAG_00918":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01278":null,"SJAG_01371":null,"SJAG_01775":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_02346":null,"SJAG_02731":null,"SJAG_02814":null,"SJAG_03217":null,"SJAG_03220":null,"SJAG_03327":null,"SJAG_03437":null,"SJAG_03683":null,"SJAG_03926":null,"SJAG_03989":null,"SJAG_04076":null,"SJAG_04508":null,"SJAG_05220":null,"SJAG_05266":null,"SJAG_05319":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0140013","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"attachment of meiotic spindle microtubules to kinetochore","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0051317"],"synonyms":[{"name":"attachment of spindle microtubules to kinetochore during meiosis","type":"related"},{"name":"attachment of spindle microtubules to kinetochore during meiotic chromosome segregation","type":"related"},{"name":"attachment of spindle microtubules to meiotic chromosome","type":"exact"}],"termid":"GO:0051316","terms_by_termid":{"GO:0051455":null,"GO:0051456":null,"GO:1904967":null}}


id: PBO:0034390
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_eggs_laid_in_by","termid":"PBO:0034390"}


id: GO:2000876
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of glyoxylate cycle.","definition_xrefs":["GOC:dgf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of carbohydrate metabolic process","termid":"GO:0045913"},{"relation_name":"is_a","term_name":"positive regulation of small molecule metabolic process","termid":"GO:0062013"},{"relation_name":"is_a","term_name":"regulation of glyoxylate cycle","termid":"GO:2000874"},{"relation_name":"positively_regulates","term_name":"glyoxylate cycle","termid":"GO:0006097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0005975"],"is_obsolete":false,"name":"positive regulation of glyoxylate cycle","synonyms":[{"name":"positive regulation of glyoxylate bypass","type":"exact"}],"termid":"GO:2000876"}


id: PBO:0045064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DLG3 antisense RNA 1","termid":"PBO:0045064"}


id: FYPO:0004473
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a cell that enters the cell cycle but then undergoes cell cycle arrest with unreplicated DNA, and eventually dies.","definition_xrefs":["PMID:9356477","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle arrest with unreplicated DNA","termid":"FYPO:0001430"},{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division, cell cycle arrest","termid":"FYPO:0001924"}],"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:0000004"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000004","FYPO:0000631","FYPO:0000002"],"is_obsolete":false,"name":"inviable after spore germination, without cell division, cell cycle arrest with unreplicated DNA","synonyms":[{"name":"inviable following spore germination, without cell division, cell cycle arrest with unreplicated DNA","type":"exact"},{"name":"inviable germinated spore, without cell division, cell cycle arrest with unreplicated DNA","type":"exact"},{"name":"lethal after spore germination, without cell division, cell cycle arrest with unreplicated DNA","type":"exact"}],"termid":"FYPO:0004473"}


id: PBO:0070933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 41","termid":"PBO:0070933"}


id: PBO:0046092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 4A2 pseudogene 3","termid":"PBO:0046092"}


id: PATO:0001841
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An intensity which is characterized by temporary abatement in severity.","definition_xrefs":["answers.com:answers.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intensity","termid":"PATO:0000049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"remittent intensity","termid":"PATO:0001841"}


id: PATO:0001095
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001095 force value (obsolete PATO:0001095)","termid":"PATO:0001095"}


id: PBO:0080924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 2","termid":"PBO:0080924"}


id: PBO:0056689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple EGF like domains 10","termid":"PBO:0056689"}


id: MONDO:1011952
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":"polyarthritis, non-human animal","secondary_identifiers":["OMIA:000805"],"termid":"MONDO:1011952","xrefs":{"Monarch":{"xref_id":"1011952"}}}


id: GO:0045123
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The migration of a leukocyte from the blood vessels into the surrounding tissue.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte migration","termid":"GO:0050900"}],"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 extravasation","secondary_identifiers":["Wikipedia:Leukocyte_extravasation"],"synonyms":[{"name":"immune cell cellular extravasation","type":"exact"},{"name":"leucocyte cellular extravasation","type":"exact"},{"name":"leukocyte cellular extravasation","type":"exact"},{"name":"transendothelial leukocyte migration","type":"exact"}],"termid":"GO:0045123"}


id: PBO:0076178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfotransferase family 2A member 1","termid":"PBO:0076178"}


id: MONDO:0007863
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Kleine-Levin syndrome (KLS) is a rare neurological disorder of unknown origin characterized by relapsing-remitting episodes of hypersomnia in association with cognitive and behavioral disturbances.","definition_xrefs":["Orphanet:33543"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"recurrent hypersomnia","termid":"MONDO:0004617"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Kleine-Levin syndrome","secondary_identifiers":["MEDGEN:61511","icd11.foundation:1180849398","UMLS:C0206085","NCIT:C84800","GARD:3117","NORD:1334","MESH:D017593","MedDRA:10053712","SCTID:111488004","DOID:0060165","EFO:1001354","OMIM:148840"],"synonyms":[{"name":"Kleine Levin syndrome","type":"related"},{"name":"Kleine-LEVIN hibernation syndrome","type":"related"},{"name":"Kleine-Levin syndrome","type":"exact"},{"name":"familial Kleine-Levin syndrome","type":"related"},{"name":"familial hibernation syndrome","type":"related"}],"termid":"MONDO:0007863","xrefs":{"Monarch":{"xref_id":"0007863"}}}


id: PBO:0086189
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein similar to GDP/GTP exchange factors; without detectable GEF activity; required for asymmetric localization of Bfa1p at daughter-directed spindle pole bodies and for mitotic exit at low temperatures","termid":"PBO:0086189"}


id: GO:1901265
data:
  {"annotated_genes":["SJAG_03660","SJAG_04394","SJAG_04042","SJAG_04743","SJAG_01018","SJAG_02838","SJAG_04167","SJAG_04351","SJAG_00529","SJAG_01080","SJAG_03342","SJAG_05276","SJAG_02686","SJAG_00963","SJAG_00616","SJAG_02429","SJAG_03096","SJAG_03336","SJAG_03451","SJAG_02564","SJAG_02206","SJAG_00516","SJAG_00004","SJAG_01944","SJAG_02615","SJAG_03077","SJAG_00964","SJAG_01510","SJAG_01831","SJAG_03562","SJAG_00169","SJAG_06621","SJAG_00042","SJAG_02148","SJAG_02142","SJAG_00661","SJAG_01352","SJAG_02723","SJAG_04734","SJAG_03421","SJAG_05025","SJAG_02977","SJAG_02199","SJAG_04343","SJAG_03290","SJAG_04366","SJAG_02509","SJAG_02233","SJAG_02945","SJAG_00208","SJAG_02895","SJAG_02421","SJAG_00378","SJAG_03461","SJAG_01435","SJAG_04692","SJAG_03209","SJAG_05010","SJAG_04265","SJAG_01148","SJAG_02180","SJAG_04186","SJAG_02200","SJAG_02287","SJAG_16455","SJAG_05105","SJAG_01466","SJAG_00609","SJAG_04362","SJAG_01680","SJAG_04285","SJAG_01449","SJAG_02084","SJAG_03436","SJAG_03495","SJAG_02599","SJAG_02249","SJAG_02104","SJAG_05030","SJAG_04147","SJAG_03708","SJAG_01471","SJAG_05340","SJAG_03898","SJAG_00502","SJAG_01254","SJAG_03720","SJAG_01671","SJAG_02558","SJAG_00857","SJAG_04757","SJAG_01664","SJAG_02394","SJAG_02353","SJAG_04573","SJAG_03567","SJAG_00980","SJAG_04367","SJAG_00956","SJAG_02704","SJAG_03730","SJAG_01339","SJAG_04599","SJAG_00420","SJAG_04544","SJAG_01010","SJAG_01863","SJAG_04862","SJAG_00690","SJAG_02015","SJAG_01774","SJAG_00430","SJAG_00766","SJAG_02879","SJAG_00599","SJAG_01522","SJAG_04000","SJAG_04537","SJAG_03409","SJAG_04320","SJAG_04154","SJAG_00359","SJAG_02038","SJAG_05173","SJAG_03345","SJAG_04622","SJAG_04509","SJAG_00402","SJAG_00344","SJAG_00235","SJAG_01186","SJAG_01909","SJAG_02384","SJAG_05015","SJAG_03602","SJAG_01215","SJAG_00412","SJAG_00500","SJAG_05353","SJAG_05231","SJAG_06597","SJAG_00650","SJAG_02696","SJAG_04282","SJAG_04435","SJAG_01474","SJAG_00995","SJAG_01235","SJAG_01000","SJAG_04552","SJAG_01881","SJAG_01769","SJAG_01797","SJAG_00111","SJAG_00881","SJAG_04081","SJAG_00863","SJAG_03526","SJAG_01221","SJAG_04777","SJAG_00669","SJAG_03679","SJAG_04761","SJAG_01885","SJAG_03240","SJAG_00790","SJAG_03570","SJAG_00855","SJAG_03832","SJAG_00252","SJAG_05372","SJAG_04597","SJAG_00443","SJAG_03846","SJAG_04312","SJAG_01964","SJAG_04230","SJAG_00875","SJAG_00168","SJAG_03453","SJAG_04459","SJAG_05027","SJAG_02595","SJAG_02302","SJAG_02295","SJAG_01929","SJAG_04738","SJAG_03374","SJAG_01432","SJAG_04772","SJAG_04482","SJAG_00605","SJAG_02656","SJAG_03320","SJAG_03017","SJAG_01179","SJAG_03141","SJAG_02906","SJAG_02288","SJAG_03798","SJAG_00999","SJAG_01315","SJAG_01718","SJAG_00678","SJAG_04457","SJAG_02991","SJAG_01575","SJAG_03236","SJAG_01945","SJAG_00392","SJAG_04874","SJAG_02077","SJAG_01684","SJAG_00801","SJAG_02426","SJAG_02889","SJAG_03658","SJAG_01859","SJAG_04657","SJAG_02342","SJAG_01595","SJAG_00704","SJAG_00329","SJAG_00342","SJAG_03545","SJAG_03585","SJAG_00360","SJAG_02856","SJAG_03471","SJAG_02643","SJAG_05313","SJAG_04355","SJAG_04810","SJAG_03799","SJAG_02610","SJAG_00039","SJAG_01587","SJAG_03626","SJAG_04187","SJAG_03237","SJAG_02563","SJAG_01571","SJAG_04612","SJAG_03613","SJAG_04473","SJAG_04486","SJAG_02872","SJAG_03449","SJAG_03501","SJAG_04465","SJAG_00906","SJAG_00933","SJAG_03897","SJAG_01438","SJAG_02176","SJAG_01878","SJAG_03152","SJAG_00757","SJAG_02236","SJAG_00331","SJAG_04666","SJAG_00364","SJAG_00660","SJAG_01644","SJAG_04507","SJAG_01311","SJAG_04150","SJAG_04946","SJAG_04114","SJAG_03206","SJAG_02399","SJAG_02712","SJAG_05209","SJAG_00114","SJAG_03689","SJAG_02760","SJAG_02835","SJAG_04126","SJAG_03457","SJAG_00244","SJAG_00636","SJAG_00712","SJAG_04700","SJAG_00984","SJAG_00968","SJAG_00414","SJAG_02994","SJAG_02571","SJAG_02521","SJAG_00533","SJAG_03927","SJAG_02808","SJAG_02640","SJAG_02242","SJAG_02738","SJAG_03277","SJAG_02135","SJAG_01373","SJAG_02575","SJAG_02183","SJAG_00996","SJAG_00583","SJAG_04665","SJAG_02378","SJAG_04480","SJAG_03193","SJAG_01668","SJAG_04280","SJAG_03533","SJAG_01558","SJAG_02082","SJAG_04268","SJAG_03811","SJAG_01696","SJAG_02489","SJAG_02292","SJAG_02444","SJAG_00337","SJAG_04650","SJAG_01040","SJAG_01277","SJAG_00931","SJAG_03732","SJAG_03592","SJAG_03384","SJAG_04468","SJAG_03061","SJAG_05194","SJAG_02876","SJAG_03188","SJAG_04233","SJAG_04032","SJAG_00541","SJAG_04288","SJAG_00718","SJAG_02022","SJAG_04589","SJAG_02923","SJAG_02878","SJAG_04980","SJAG_00265","SJAG_04608","SJAG_03950","SJAG_02725","SJAG_02370","SJAG_04054","SJAG_01082","SJAG_01197","SJAG_03145","SJAG_01259","SJAG_02297","SJAG_01787","SJAG_04156","SJAG_03475","SJAG_00633","SJAG_03496","SJAG_03257","SJAG_02721","SJAG_03349","SJAG_00947","SJAG_04974","SJAG_00564","SJAG_01799","SJAG_03804","SJAG_05024","SJAG_00845","SJAG_04762","SJAG_05022","SJAG_04461","SJAG_03157","SJAG_03852","SJAG_03115","SJAG_05295","SJAG_04549","SJAG_02785","SJAG_03712","SJAG_04189","SJAG_03785","SJAG_00610","SJAG_00330","SJAG_02858","SJAG_01620","SJAG_00370","SJAG_06642","SJAG_01534","SJAG_03923","SJAG_04856","SJAG_03213","SJAG_01731","SJAG_03275","SJAG_16456","SJAG_01679","SJAG_05304","SJAG_01075","SJAG_04849","SJAG_01544","SJAG_01489","SJAG_00424","SJAG_01240","SJAG_04477","SJAG_00729","SJAG_03355","SJAG_00649","SJAG_01181","SJAG_03067","SJAG_02887","SJAG_01447","SJAG_01530","SJAG_00663","SJAG_03982","SJAG_01391","SJAG_02517","SJAG_02596","SJAG_00475","SJAG_01383","SJAG_01618","SJAG_04287","SJAG_03386","SJAG_01837","SJAG_01677","SJAG_03438","SJAG_02897","SJAG_01938","SJAG_04469","SJAG_01245","SJAG_01063","SJAG_01358","SJAG_00938","SJAG_00466","SJAG_00779","SJAG_03371","SJAG_01084","SJAG_01669","SJAG_01693","SJAG_03887","SJAG_04845","SJAG_00851","SJAG_02950","SJAG_01816","SJAG_06622","SJAG_01653","SJAG_04577","SJAG_02074","SJAG_03985","SJAG_04857","SJAG_04970","SJAG_00203","SJAG_00356","SJAG_00884","SJAG_00447","SJAG_01198","SJAG_00972","SJAG_00773","SJAG_05332","SJAG_02602","SJAG_01704","SJAG_03915","SJAG_02708","SJAG_05249","SJAG_00231","SJAG_04157","SJAG_00604","SJAG_02713","SJAG_01129","SJAG_01268","SJAG_00653","SJAG_03659","SJAG_02336","SJAG_03486","SJAG_00234","SJAG_00027","SJAG_04064","SJAG_01081","SJAG_01855","SJAG_01002","SJAG_03479","SJAG_03036","SJAG_02736","SJAG_03909","SJAG_01410","SJAG_04258","SJAG_01918","SJAG_01297","SJAG_02382","SJAG_02364","SJAG_02690","SJAG_04121","SJAG_01953","SJAG_01176","SJAG_02698","SJAG_00048","SJAG_04634","SJAG_01012","SJAG_04387","SJAG_01903","SJAG_01070","SJAG_03485","SJAG_03903","SJAG_02267","SJAG_04470","SJAG_03828","SJAG_02286","SJAG_03476","SJAG_02058","SJAG_01942","SJAG_02331","SJAG_02496","SJAG_03780","SJAG_01354","SJAG_01400","SJAG_04375","SJAG_03069","SJAG_04118","SJAG_03987","SJAG_00798","SJAG_03813","SJAG_00871","SJAG_01611","SJAG_00136","SJAG_04270","SJAG_00988","SJAG_02400","SJAG_01456","SJAG_03728","SJAG_01458","SJAG_00403","SJAG_01762","SJAG_02997","SJAG_03071","SJAG_05213","SJAG_00293","SJAG_01351","SJAG_00198","SJAG_02848","SJAG_00659","SJAG_03363","SJAG_01874","SJAG_04755","SJAG_02294","SJAG_01789","SJAG_00174","SJAG_03497","SJAG_00044","SJAG_01937","SJAG_01024","SJAG_01577","SJAG_01613","SJAG_04865","SJAG_04094","SJAG_04038","SJAG_02061","SJAG_01344","SJAG_02697","SJAG_01405","SJAG_01159","SJAG_02498","SJAG_03703","SJAG_01379","SJAG_01419","SJAG_02187","SJAG_02468","SJAG_02313","SJAG_01131","SJAG_02827","SJAG_02431","SJAG_01041","SJAG_02460","SJAG_02226","SJAG_00898","SJAG_00786","SJAG_03892","SJAG_04669","SJAG_03932","SJAG_01499","SJAG_00103","SJAG_00031","SJAG_01695","SJAG_01724","SJAG_02520","SJAG_03959","SJAG_00106","SJAG_02428","SJAG_00409","SJAG_00815","SJAG_00707","SJAG_04210","SJAG_00638","SJAG_01877","SJAG_05290","SJAG_04693","SJAG_04940","SJAG_04840","SJAG_02619","SJAG_03140","SJAG_01162","SJAG_02824","SJAG_00853","SJAG_03684","SJAG_00983","SJAG_03789","SJAG_01791","SJAG_02488","SJAG_01182","SJAG_03896","SJAG_04745","SJAG_00150","SJAG_04003","SJAG_02598","SJAG_00358","SJAG_03072","SJAG_00118","SJAG_04511","SJAG_00993","SJAG_03174","SJAG_01616","SJAG_00930","SJAG_04655","SJAG_03669","SJAG_04004","SJAG_00353","SJAG_01615","SJAG_00084","SJAG_03313","SJAG_01137","SJAG_02720","SJAG_01825","SJAG_00381","SJAG_00226","SJAG_03676","SJAG_01047","SJAG_00332","SJAG_01546","SJAG_01402","SJAG_03866","SJAG_02875","SJAG_03709","SJAG_02822","SJAG_01500","SJAG_02605","SJAG_00840","SJAG_02926","SJAG_02392","SJAG_03362","SJAG_04039","SJAG_01152","SJAG_02545","SJAG_00390","SJAG_05018","SJAG_03967","SJAG_02366","SJAG_04410","SJAG_03376","SJAG_04495","SJAG_05019","SJAG_02604","SJAG_01052","SJAG_02825","SJAG_01164","SJAG_00464","SJAG_02748","SJAG_03129","SJAG_00887","SJAG_00486","SJAG_00878","SJAG_04882","SJAG_00597","SJAG_00281","SJAG_03137","SJAG_02457","SJAG_02374","SJAG_04183","SJAG_01805","SJAG_02592","SJAG_00427","SJAG_03011","SJAG_01851","SJAG_02601","SJAG_00986","SJAG_04203","SJAG_03753","SJAG_04001","SJAG_02618","SJAG_03224","SJAG_02796","SJAG_03557","SJAG_00436","SJAG_04760","SJAG_04551","SJAG_03534","SJAG_03048","SJAG_04206","SJAG_04652","SJAG_00256","SJAG_01376","SJAG_04055","SJAG_04566","SJAG_04372","SJAG_04276","SJAG_02348","SJAG_04334","SJAG_00488","SJAG_02420","SJAG_03886","SJAG_04409","SJAG_03529","SJAG_00243","SJAG_03948","SJAG_02527","SJAG_02684","SJAG_02741","SJAG_03688","SJAG_04232","SJAG_02182","SJAG_03850","SJAG_04627","SJAG_02171","SJAG_04125","SJAG_00457","SJAG_01807","SJAG_03946","SJAG_02661","SJAG_03160","SJAG_04277","SJAG_00300","SJAG_02680","SJAG_04747","SJAG_04052","SJAG_03854"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74500,71714,94748,91095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043531"},{"annotations":[71768,90760,70354,75704],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016208"},{"annotations":[70997,68014,68815,69450,57380,70005,65070,71416,70861,59330,66056,71120,63945,57364,61156,58654,99422,70863,59011,70707,61591,61729,115433,120018,66147,106274,109922,69776,59129,66239,58307,63077,68256,57505,59345,66388,65383,58823,64357,71129,58830,91097,70087,69067,57356,62615,68787,57459,57756,73864,61125,61688,64568,64849,70979,66287,69581,67656,62008,71311,90252,71137,59444,64625,69790,69346,61641,59867,67891,58614,63146,110529,57940,70667,69393,69460,67149,65893,69021,58343,68367,59342,58737,58183,62501,63009,63463,63636,69632,59645,70471,103046,68410,62486,110147,70043,60317,57495,90679,61224,66835,64057,58540,70501,116130,59621,70358,63043,70081,65130,71276,63676,66773,116535,66894,69126,61480,105775,62031,57410,66605,59619,59065,59409,63400,58935,66582,65993,67428,70576,57730,71260,60759,66172,67927,65806,60300,57589,59192,71317,58761,66390,69438,58304,65330,62437,61855,62359,58913,65766,66476,58968,65093,66672,69813,70309,64742,70946,57280,94040,65539,59321,70361,57415,60637,107560,71061,69850,66531,67486,71715,68983,67815,68035,63417,60482,62425,66436,61790,58661,57029,60996,65588,59579,66085,64378,60922,66442,71191,65614,67718,61372,78241,104618,60824,57072,60357,65694,68880,68710,58944,107462,57660,69719,60400,57718,64949,64230,65395,59864,57676,71398,57523,61101,61314,68179,59517,59216,64209,64545,64327,70871,64316,65230,67507,79564,64578,62052,64980,68850,60000,70403,64405,65788,67672,60702,57572,65214,58784,57164,61026,60309,64799,67822,66275,67263,70228,68266,58076,70639,70711,107201,65043,67399,116076,106601,63082,59161,66838,68241,64880,117721,70747,57120,58268,60038,115188,70348,60725,62045,101621,60454,67002,57918,74434,63517,119957,57329,68543,69114,62055,66828,67534,63995,69217,60096,118043,68286,67993,70189,65583,74214,69567,65874,67135,63308,67506,61666,69435,62197,60593,59874,71263,67237,64216,58509,67969,63459,57958,104209,67381,61705,68499,69562,67171,63645,71270,60155,59000,69351,64148,98411,63071,57469,58893,117786,57832,60658,69726,58703,59420,61571,66468,100725,62771,57196,67366,60422,67145,58490,61307,66992,57930,69540,59662,62666,64242,74501,60548,66506,62711,114964,58954,60438,68394,67446,60210,90954,67309,59041,57002,58137,61694,68600,58711,101070,59353,57654,70427,58223,59028,68343,57536,63770,60744,58536,69086,61058,58253,64046,69492,62183,70300,93051,62383,62274,114963,67735,62586,58856,113083,61971,71163,63017,62039,67325,68090,65724,62854,70838,57906,66679,58430,115099,62026,68463,66300,58628,61273,66639,114967,57435,62548,68962,68102,60293,70532,63526,115602,61085,59272,61377,69149,69834,69861,61300,69037,59598,59199,59286,64390,60273,63332,69006,67218,59257,60787,71485,102033,64857,61840,63668,95594,59564,63575,64123,64859,66431,69597,63199,75862,105272,110487,91380,58486,70164,59857,68975,71499,63541,59771,69585,64719,65241,58082,67723,60135,73485,113389,60631,58154,59666,68325,59476,65997,67915,70604,70330,70660,66154,76095,61279,63550,62836,64129,59053,64866,68056,57618,69604,71153,65556,67020,62635,70328,71516,62332,63832,68823,62497,62213,59751,62919,63591,64164,57474,69778,62999,74718,82012,66016,60527,58334,57770,58638,67519,101271,67841,57188,59655,57861,60174,66409,66808,70157,69371,65640,66935,61755,62767,61607,57271,65354,67527,67862,64434,69524,69933,60058,70449,91727,112529,65706,59155,65220,70069,93447,60945,66104,57671,64694,71512,60022,79215,69001,60131,58585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005524"},{"annotations":[72736],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030552"},{"annotations":[92736,89605],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002135"},{"annotations":[59843,65657,73617,111674,72674,115021,94236,71431,71466,72014,78044,61188,70686],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071949"},{"annotations":[80855,63310,67190,73517,60113,66092,78001,80887,61136,67091,78016,120829,77839,114807,96008,76325,80114,79012,77786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050660"},{"annotations":[78014,80851,65972,59963,74486,76321,80111,91257,61179,66880,57516,65178,79011,68856,71018,60108,63813],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010181"},{"annotations":[74013,76971,93595,94321],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019003"},{"annotations":[117712,90761],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019002"},{"annotations":[57343,59249,61526,62616,71087,68726,76180,59086,76968,82172,75805,115546,60502,72065,79228,98431,71522,58204,58159,58210,65318,67234,98193,103182,74134,79279,65917,80319,110451,119520,74291,67874,65665,64777,67437,74521,95346,75059,78214,68184,62559,121008,93822,66400,70672,59897,69587,63870,65306,77640,62106,75174,72810,58320,74010,62868,67629,75090,81738,81921,95293,58291,105614,63784,64078,66872,70544,107029,69501,61864,70646,61041,76190,59300,63498,71635,120526,79722,60375,69997,81949,64604,65786,79604,79732,92970,60791,96127,97672,68960,57295,73458,63630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005525"},{"annotations":[77698],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036042"},{"annotations":[61566,58252,65474,59187,63535,71363,71475,111397,120830,64411,62401,63825,63714,64225,70830,111398,111395,65959,111399,60586],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051287"},{"annotations":[67254,58517,60472,80531,113977],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070403"},{"annotations":[71474,63490,65472,65974,72832,82163,96009,106417,111402,111404,58803,111406,63534,116825,111405,65684,67111,57689,60255,69677,69686,60585,65746],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050661"},{"annotations":[59180],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070401"},{"annotations":[104992,76155,116808],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070402"},{"annotations":[92742,93573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002134"}]},"cv_name":"molecular_function","definition":"Binding to nucleoside phosphate.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding","termid":"GO:0005488"}],"gene_count":728,"genes_by_uniquename":{"SJAG_00004":null,"SJAG_00027":null,"SJAG_00031":null,"SJAG_00039":null,"SJAG_00042":null,"SJAG_00044":null,"SJAG_00048":null,"SJAG_00084":null,"SJAG_00103":null,"SJAG_00106":null,"SJAG_00111":null,"SJAG_00114":null,"SJAG_00118":null,"SJAG_00136":null,"SJAG_00150":null,"SJAG_00168":null,"SJAG_00169":null,"SJAG_00174":null,"SJAG_00198":null,"SJAG_00203":null,"SJAG_00208":null,"SJAG_00226":null,"SJAG_00231":null,"SJAG_00234":null,"SJAG_00235":null,"SJAG_00243":null,"SJAG_00244":null,"SJAG_00252":null,"SJAG_00256":null,"SJAG_00265":null,"SJAG_00281":null,"SJAG_00293":null,"SJAG_00300":null,"SJAG_00329":null,"SJAG_00330":null,"SJAG_00331":null,"SJAG_00332":null,"SJAG_00337":null,"SJAG_00342":null,"SJAG_00344":null,"SJAG_00353":null,"SJAG_00356":null,"SJAG_00358":null,"SJAG_00359":null,"SJAG_00360":null,"SJAG_00364":null,"SJAG_00370":null,"SJAG_00378":null,"SJAG_00381":null,"SJAG_00390":null,"SJAG_00392":null,"SJAG_00402":null,"SJAG_00403":null,"SJAG_00409":null,"SJAG_00412":null,"SJAG_00414":null,"SJAG_00420":null,"SJAG_00424":null,"SJAG_00427":null,"SJAG_00430":null,"SJAG_00436":null,"SJAG_00443":null,"SJAG_00447":null,"SJAG_00457":null,"SJAG_00464":null,"SJAG_00466":null,"SJAG_00475":null,"SJAG_00486":null,"SJAG_00488":null,"SJAG_00500":null,"SJAG_00502":null,"SJAG_00516":null,"SJAG_00529":null,"SJAG_00533":null,"SJAG_00541":null,"SJAG_00564":null,"SJAG_00583":null,"SJAG_00597":null,"SJAG_00599":null,"SJAG_00604":null,"SJAG_00605":null,"SJAG_00609":null,"SJAG_00610":null,"SJAG_00616":null,"SJAG_00633":null,"SJAG_00636":null,"SJAG_00638":null,"SJAG_00649":null,"SJAG_00650":null,"SJAG_00653":null,"SJAG_00659":null,"SJAG_00660":null,"SJAG_00661":null,"SJAG_00663":null,"SJAG_00669":null,"SJAG_00678":null,"SJAG_00690":null,"SJAG_00704":null,"SJAG_00707":null,"SJAG_00712":null,"SJAG_00718":null,"SJAG_00729":null,"SJAG_00757":null,"SJAG_00766":null,"SJAG_00773":null,"SJAG_00779":null,"SJAG_00786":null,"SJAG_00790":null,"SJAG_00798":null,"SJAG_00801":null,"SJAG_00815":null,"SJAG_00840":null,"SJAG_00845":null,"SJAG_00851":null,"SJAG_00853":null,"SJAG_00855":null,"SJAG_00857":null,"SJAG_00863":null,"SJAG_00871":null,"SJAG_00875":null,"SJAG_00878":null,"SJAG_00881":null,"SJAG_00884":null,"SJAG_00887":null,"SJAG_00898":null,"SJAG_00906":null,"SJAG_00930":null,"SJAG_00931":null,"SJAG_00933":null,"SJAG_00938":null,"SJAG_00947":null,"SJAG_00956":null,"SJAG_00963":null,"SJAG_00964":null,"SJAG_00968":null,"SJAG_00972":null,"SJAG_00980":null,"SJAG_00983":null,"SJAG_00984":null,"SJAG_00986":null,"SJAG_00988":null,"SJAG_00993":null,"SJAG_00995":null,"SJAG_00996":null,"SJAG_00999":null,"SJAG_01000":null,"SJAG_01002":null,"SJAG_01010":null,"SJAG_01012":null,"SJAG_01018":null,"SJAG_01024":null,"SJAG_01040":null,"SJAG_01041":null,"SJAG_01047":null,"SJAG_01052":null,"SJAG_01063":null,"SJAG_01070":null,"SJAG_01075":null,"SJAG_01080":null,"SJAG_01081":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01129":null,"SJAG_01131":null,"SJAG_01137":null,"SJAG_01148":null,"SJAG_01152":null,"SJAG_01159":null,"SJAG_01162":null,"SJAG_01164":null,"SJAG_01176":null,"SJAG_01179":null,"SJAG_01181":null,"SJAG_01182":null,"SJAG_01186":null,"SJAG_01197":null,"SJAG_01198":null,"SJAG_01215":null,"SJAG_01221":null,"SJAG_01235":null,"SJAG_01240":null,"SJAG_01245":null,"SJAG_01254":null,"SJAG_01259":null,"SJAG_01268":null,"SJAG_01277":null,"SJAG_01297":null,"SJAG_01311":null,"SJAG_01315":null,"SJAG_01339":null,"SJAG_01344":null,"SJAG_01351":null,"SJAG_01352":null,"SJAG_01354":null,"SJAG_01358":null,"SJAG_01373":null,"SJAG_01376":null,"SJAG_01379":null,"SJAG_01383":null,"SJAG_01391":null,"SJAG_01400":null,"SJAG_01402":null,"SJAG_01405":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01432":null,"SJAG_01435":null,"SJAG_01438":null,"SJAG_01447":null,"SJAG_01449":null,"SJAG_01456":null,"SJAG_01458":null,"SJAG_01466":null,"SJAG_01471":null,"SJAG_01474":null,"SJAG_01489":null,"SJAG_01499":null,"SJAG_01500":null,"SJAG_01510":null,"SJAG_01522":null,"SJAG_01530":null,"SJAG_01534":null,"SJAG_01544":null,"SJAG_01546":null,"SJAG_01558":null,"SJAG_01571":null,"SJAG_01575":null,"SJAG_01577":null,"SJAG_01587":null,"SJAG_01595":null,"SJAG_01611":null,"SJAG_01613":null,"SJAG_01615":null,"SJAG_01616":null,"SJAG_01618":null,"SJAG_01620":null,"SJAG_01644":null,"SJAG_01653":null,"SJAG_01664":null,"SJAG_01668":null,"SJAG_01669":null,"SJAG_01671":null,"SJAG_01677":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01684":null,"SJAG_01693":null,"SJAG_01695":null,"SJAG_01696":null,"SJAG_01704":null,"SJAG_01718":null,"SJAG_01724":null,"SJAG_01731":null,"SJAG_01762":null,"SJAG_01769":null,"SJAG_01774":null,"SJAG_01787":null,"SJAG_01789":null,"SJAG_01791":null,"SJAG_01797":null,"SJAG_01799":null,"SJAG_01805":null,"SJAG_01807":null,"SJAG_01816":null,"SJAG_01825":null,"SJAG_01831":null,"SJAG_01837":null,"SJAG_01851":null,"SJAG_01855":null,"SJAG_01859":null,"SJAG_01863":null,"SJAG_01874":null,"SJAG_01877":null,"SJAG_01878":null,"SJAG_01881":null,"SJAG_01885":null,"SJAG_01903":null,"SJAG_01909":null,"SJAG_01918":null,"SJAG_01929":null,"SJAG_01937":null,"SJAG_01938":null,"SJAG_01942":null,"SJAG_01944":null,"SJAG_01945":null,"SJAG_01953":null,"SJAG_01964":null,"SJAG_02015":null,"SJAG_02022":null,"SJAG_02038":null,"SJAG_02058":null,"SJAG_02061":null,"SJAG_02074":null,"SJAG_02077":null,"SJAG_02082":null,"SJAG_02084":null,"SJAG_02104":null,"SJAG_02135":null,"SJAG_02142":null,"SJAG_02148":null,"SJAG_02171":null,"SJAG_02176":null,"SJAG_02180":null,"SJAG_02182":null,"SJAG_02183":null,"SJAG_02187":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02206":null,"SJAG_02226":null,"SJAG_02233":null,"SJAG_02236":null,"SJAG_02242":null,"SJAG_02249":null,"SJAG_02267":null,"SJAG_02286":null,"SJAG_02287":null,"SJAG_02288":null,"SJAG_02292":null,"SJAG_02294":null,"SJAG_02295":null,"SJAG_02297":null,"SJAG_02302":null,"SJAG_02313":null,"SJAG_02331":null,"SJAG_02336":null,"SJAG_02342":null,"SJAG_02348":null,"SJAG_02353":null,"SJAG_02364":null,"SJAG_02366":null,"SJAG_02370":null,"SJAG_02374":null,"SJAG_02378":null,"SJAG_02382":null,"SJAG_02384":null,"SJAG_02392":null,"SJAG_02394":null,"SJAG_02399":null,"SJAG_02400":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_02426":null,"SJAG_02428":null,"SJAG_02429":null,"SJAG_02431":null,"SJAG_02444":null,"SJAG_02457":null,"SJAG_02460":null,"SJAG_02468":null,"SJAG_02488":null,"SJAG_02489":null,"SJAG_02496":null,"SJAG_02498":null,"SJAG_02509":null,"SJAG_02517":null,"SJAG_02520":null,"SJAG_02521":null,"SJAG_02527":null,"SJAG_02545":null,"SJAG_02558":null,"SJAG_02563":null,"SJAG_02564":null,"SJAG_02571":null,"SJAG_02575":null,"SJAG_02592":null,"SJAG_02595":null,"SJAG_02596":null,"SJAG_02598":null,"SJAG_02599":null,"SJAG_02601":null,"SJAG_02602":null,"SJAG_02604":null,"SJAG_02605":null,"SJAG_02610":null,"SJAG_02615":null,"SJAG_02618":null,"SJAG_02619":null,"SJAG_02640":null,"SJAG_02643":null,"SJAG_02656":null,"SJAG_02661":null,"SJAG_02680":null,"SJAG_02684":null,"SJAG_02686":null,"SJAG_02690":null,"SJAG_02696":null,"SJAG_02697":null,"SJAG_02698":null,"SJAG_02704":null,"SJAG_02708":null,"SJAG_02712":null,"SJAG_02713":null,"SJAG_02720":null,"SJAG_02721":null,"SJAG_02723":null,"SJAG_02725":null,"SJAG_02736":null,"SJAG_02738":null,"SJAG_02741":null,"SJAG_02748":null,"SJAG_02760":null,"SJAG_02785":null,"SJAG_02796":null,"SJAG_02808":null,"SJAG_02822":null,"SJAG_02824":null,"SJAG_02825":null,"SJAG_02827":null,"SJAG_02835":null,"SJAG_02838":null,"SJAG_02848":null,"SJAG_02856":null,"SJAG_02858":null,"SJAG_02872":null,"SJAG_02875":null,"SJAG_02876":null,"SJAG_02878":null,"SJAG_02879":null,"SJAG_02887":null,"SJAG_02889":null,"SJAG_02895":null,"SJAG_02897":null,"SJAG_02906":null,"SJAG_02923":null,"SJAG_02926":null,"SJAG_02945":null,"SJAG_02950":null,"SJAG_02977":null,"SJAG_02991":null,"SJAG_02994":null,"SJAG_02997":null,"SJAG_03011":null,"SJAG_03017":null,"SJAG_03036":null,"SJAG_03048":null,"SJAG_03061":null,"SJAG_03067":null,"SJAG_03069":null,"SJAG_03071":null,"SJAG_03072":null,"SJAG_03077":null,"SJAG_03096":null,"SJAG_03115":null,"SJAG_03129":null,"SJAG_03137":null,"SJAG_03140":null,"SJAG_03141":null,"SJAG_03145":null,"SJAG_03152":null,"SJAG_03157":null,"SJAG_03160":null,"SJAG_03174":null,"SJAG_03188":null,"SJAG_03193":null,"SJAG_03206":null,"SJAG_03209":null,"SJAG_03213":null,"SJAG_03224":null,"SJAG_03236":null,"SJAG_03237":null,"SJAG_03240":null,"SJAG_03257":null,"SJAG_03275":null,"SJAG_03277":null,"SJAG_03290":null,"SJAG_03313":null,"SJAG_03320":null,"SJAG_03336":null,"SJAG_03342":null,"SJAG_03345":null,"SJAG_03349":null,"SJAG_03355":null,"SJAG_03362":null,"SJAG_03363":null,"SJAG_03371":null,"SJAG_03374":null,"SJAG_03376":null,"SJAG_03384":null,"SJAG_03386":null,"SJAG_03409":null,"SJAG_03421":null,"SJAG_03436":null,"SJAG_03438":null,"SJAG_03449":null,"SJAG_03451":null,"SJAG_03453":null,"SJAG_03457":null,"SJAG_03461":null,"SJAG_03471":null,"SJAG_03475":null,"SJAG_03476":null,"SJAG_03479":null,"SJAG_03485":null,"SJAG_03486":null,"SJAG_03495":null,"SJAG_03496":null,"SJAG_03497":null,"SJAG_03501":null,"SJAG_03526":null,"SJAG_03529":null,"SJAG_03533":null,"SJAG_03534":null,"SJAG_03545":null,"SJAG_03557":null,"SJAG_03562":null,"SJAG_03567":null,"SJAG_03570":null,"SJAG_03585":null,"SJAG_03592":null,"SJAG_03602":null,"SJAG_03613":null,"SJAG_03626":null,"SJAG_03658":null,"SJAG_03659":null,"SJAG_03660":null,"SJAG_03669":null,"SJAG_03676":null,"SJAG_03679":null,"SJAG_03684":null,"SJAG_03688":null,"SJAG_03689":null,"SJAG_03703":null,"SJAG_03708":null,"SJAG_03709":null,"SJAG_03712":null,"SJAG_03720":null,"SJAG_03728":null,"SJAG_03730":null,"SJAG_03732":null,"SJAG_03753":null,"SJAG_03780":null,"SJAG_03785":null,"SJAG_03789":null,"SJAG_03798":null,"SJAG_03799":null,"SJAG_03804":null,"SJAG_03811":null,"SJAG_03813":null,"SJAG_03828":null,"SJAG_03832":null,"SJAG_03846":null,"SJAG_03850":null,"SJAG_03852":null,"SJAG_03854":null,"SJAG_03866":null,"SJAG_03886":null,"SJAG_03887":null,"SJAG_03892":null,"SJAG_03896":null,"SJAG_03897":null,"SJAG_03898":null,"SJAG_03903":null,"SJAG_03909":null,"SJAG_03915":null,"SJAG_03923":null,"SJAG_03927":null,"SJAG_03932":null,"SJAG_03946":null,"SJAG_03948":null,"SJAG_03950":null,"SJAG_03959":null,"SJAG_03967":null,"SJAG_03982":null,"SJAG_03985":null,"SJAG_03987":null,"SJAG_04000":null,"SJAG_04001":null,"SJAG_04003":null,"SJAG_04004":null,"SJAG_04032":null,"SJAG_04038":null,"SJAG_04039":null,"SJAG_04042":null,"SJAG_04052":null,"SJAG_04054":null,"SJAG_04055":null,"SJAG_04064":null,"SJAG_04081":null,"SJAG_04094":null,"SJAG_04114":null,"SJAG_04118":null,"SJAG_04121":null,"SJAG_04125":null,"SJAG_04126":null,"SJAG_04147":null,"SJAG_04150":null,"SJAG_04154":null,"SJAG_04156":null,"SJAG_04157":null,"SJAG_04167":null,"SJAG_04183":null,"SJAG_04186":null,"SJAG_04187":null,"SJAG_04189":null,"SJAG_04203":null,"SJAG_04206":null,"SJAG_04210":null,"SJAG_04230":null,"SJAG_04232":null,"SJAG_04233":null,"SJAG_04258":null,"SJAG_04265":null,"SJAG_04268":null,"SJAG_04270":null,"SJAG_04276":null,"SJAG_04277":null,"SJAG_04280":null,"SJAG_04282":null,"SJAG_04285":null,"SJAG_04287":null,"SJAG_04288":null,"SJAG_04312":null,"SJAG_04320":null,"SJAG_04334":null,"SJAG_04343":null,"SJAG_04351":null,"SJAG_04355":null,"SJAG_04362":null,"SJAG_04366":null,"SJAG_04367":null,"SJAG_04372":null,"SJAG_04375":null,"SJAG_04387":null,"SJAG_04394":null,"SJAG_04409":null,"SJAG_04410":null,"SJAG_04435":null,"SJAG_04457":null,"SJAG_04459":null,"SJAG_04461":null,"SJAG_04465":null,"SJAG_04468":null,"SJAG_04469":null,"SJAG_04470":null,"SJAG_04473":null,"SJAG_04477":null,"SJAG_04480":null,"SJAG_04482":null,"SJAG_04486":null,"SJAG_04495":null,"SJAG_04507":null,"SJAG_04509":null,"SJAG_04511":null,"SJAG_04537":null,"SJAG_04544":null,"SJAG_04549":null,"SJAG_04551":null,"SJAG_04552":null,"SJAG_04566":null,"SJAG_04573":null,"SJAG_04577":null,"SJAG_04589":null,"SJAG_04597":null,"SJAG_04599":null,"SJAG_04608":null,"SJAG_04612":null,"SJAG_04622":null,"SJAG_04627":null,"SJAG_04634":null,"SJAG_04650":null,"SJAG_04652":null,"SJAG_04655":null,"SJAG_04657":null,"SJAG_04665":null,"SJAG_04666":null,"SJAG_04669":null,"SJAG_04692":null,"SJAG_04693":null,"SJAG_04700":null,"SJAG_04734":null,"SJAG_04738":null,"SJAG_04743":null,"SJAG_04745":null,"SJAG_04747":null,"SJAG_04755":null,"SJAG_04757":null,"SJAG_04760":null,"SJAG_04761":null,"SJAG_04762":null,"SJAG_04772":null,"SJAG_04777":null,"SJAG_04810":null,"SJAG_04840":null,"SJAG_04845":null,"SJAG_04849":null,"SJAG_04856":null,"SJAG_04857":null,"SJAG_04862":null,"SJAG_04865":null,"SJAG_04874":null,"SJAG_04882":null,"SJAG_04940":null,"SJAG_04946":null,"SJAG_04970":null,"SJAG_04974":null,"SJAG_04980":null,"SJAG_05010":null,"SJAG_05015":null,"SJAG_05018":null,"SJAG_05019":null,"SJAG_05022":null,"SJAG_05024":null,"SJAG_05025":null,"SJAG_05027":null,"SJAG_05030":null,"SJAG_05105":null,"SJAG_05173":null,"SJAG_05194":null,"SJAG_05209":null,"SJAG_05213":null,"SJAG_05231":null,"SJAG_05249":null,"SJAG_05276":null,"SJAG_05290":null,"SJAG_05295":null,"SJAG_05304":null,"SJAG_05313":null,"SJAG_05332":null,"SJAG_05340":null,"SJAG_05353":null,"SJAG_05372":null,"SJAG_06597":null,"SJAG_06621":null,"SJAG_06622":null,"SJAG_06642":null,"SJAG_16455":null,"SJAG_16456":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"nucleoside phosphate binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"termid":"GO:1901265","terms_by_termid":{"GO:0002134":null,"GO:0002135":null,"GO:0005524":null,"GO:0005525":null,"GO:0010181":null,"GO:0016208":null,"GO:0019002":null,"GO:0019003":null,"GO:0030552":null,"GO:0036042":null,"GO:0043531":null,"GO:0050660":null,"GO:0050661":null,"GO:0051287":null,"GO:0070401":null,"GO:0070402":null,"GO:0070403":null,"GO:0071949":null}}


id: PBO:0079873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UPF3A regulator of nonsense mediated mRNA decay","termid":"PBO:0079873"}


id: GO:1903893
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the ATF6-mediated unfolded protein response.","definition_xrefs":["GOC:TermGenie","GOC:PARL","GO_REF:0000058","GOC:bf","PMID:22013210"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of endoplasmic reticulum unfolded protein response","termid":"GO:1900103"},{"relation_name":"is_a","term_name":"regulation of ATF6-mediated unfolded protein response","termid":"GO:1903891"},{"relation_name":"positively_regulates","term_name":"ATF6-mediated unfolded protein response","termid":"GO:0036500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of ATF6-mediated unfolded protein response","synonyms":[{"name":"activation of ATF6 branch of UPR","type":"narrow"},{"name":"activation of ATF6 signaling in response to endoplasmic reticulum stress","type":"related"},{"name":"activation of ATF6-alpha UPR branch","type":"narrow"},{"name":"activation of ATF6-beta UPR branch","type":"narrow"},{"name":"activation of ATF6-mediated unfolded protein response","type":"narrow"},{"name":"activation of UPR signaling by ATF6 stress sensor","type":"narrow"},{"name":"activation of activating transcription factor 6 signaling in unfolded protein response","type":"narrow"},{"name":"activation of endoplasmic reticulum unfolded protein response; ATF6 signaling","type":"narrow"},{"name":"positive regulation of ATF6 branch of UPR","type":"exact"},{"name":"positive regulation of ATF6 signaling in response to endoplasmic reticulum stress","type":"related"},{"name":"positive regulation of ATF6-alpha UPR branch","type":"narrow"},{"name":"positive regulation of ATF6-beta UPR branch","type":"narrow"},{"name":"positive regulation of UPR signaling by ATF6 stress sensor","type":"exact"},{"name":"positive regulation of activating transcription factor 6 signaling in unfolded protein response","type":"exact"},{"name":"positive regulation of endoplasmic reticulum unfolded protein response; ATF6 signaling","type":"exact"},{"name":"up regulation of ATF6 branch of UPR","type":"exact"},{"name":"up regulation of ATF6 signaling in response to endoplasmic reticulum stress","type":"related"},{"name":"up regulation of ATF6-alpha UPR branch","type":"narrow"},{"name":"up regulation of ATF6-beta UPR branch","type":"narrow"},{"name":"up regulation of ATF6-mediated unfolded protein response","type":"exact"},{"name":"up regulation of UPR signaling by ATF6 stress sensor","type":"exact"},{"name":"up regulation of activating transcription factor 6 signaling in unfolded protein response","type":"exact"},{"name":"up regulation of endoplasmic reticulum unfolded protein response; ATF6 signaling","type":"exact"},{"name":"up-regulation of ATF6 branch of UPR","type":"exact"},{"name":"up-regulation of ATF6 signaling in response to endoplasmic reticulum stress","type":"related"},{"name":"up-regulation of ATF6-alpha UPR branch","type":"narrow"},{"name":"up-regulation of ATF6-beta UPR branch","type":"narrow"},{"name":"up-regulation of ATF6-mediated unfolded protein response","type":"exact"},{"name":"up-regulation of UPR signaling by ATF6 stress sensor","type":"exact"},{"name":"up-regulation of activating transcription factor 6 signaling in unfolded protein response","type":"exact"},{"name":"up-regulation of endoplasmic reticulum unfolded protein response; ATF6 signaling","type":"exact"},{"name":"upregulation of ATF6 branch of UPR","type":"exact"},{"name":"upregulation of ATF6 signaling in response to endoplasmic reticulum stress","type":"related"},{"name":"upregulation of ATF6-alpha UPR branch","type":"narrow"},{"name":"upregulation of ATF6-beta UPR branch","type":"narrow"},{"name":"upregulation of ATF6-mediated unfolded protein response","type":"exact"},{"name":"upregulation of UPR signaling by ATF6 stress sensor","type":"exact"},{"name":"upregulation of activating transcription factor 6 signaling in unfolded protein response","type":"exact"},{"name":"upregulation of endoplasmic reticulum unfolded protein response; ATF6 signaling","type":"exact"}],"termid":"GO:1903893"}


id: PBO:0002613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cofactor for methionyl-and glutamyl-tRNA synthetases (predicted)","termid":"PBO:0002613"}


id: PBO:0051144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 3-22 (pseudogene)","termid":"PBO:0051144"}


id: MONDO:0013918
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"15q overgrowth syndrome","termid":"MONDO:0017806"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal tetrasomy 15q","secondary_identifiers":["UMLS:C3553858","OMIM:614846","MEDGEN:766772","Orphanet:314588","GARD:17424"],"synonyms":[{"name":"distal tetrasomy type 15q","type":"exact"},{"name":"levy-Shanske syndrome","type":"related"},{"name":"tetrasomy 15(q25-qter)","type":"exact"},{"name":"tetrasomy 15q26","type":"exact"},{"name":"tetrasomy type 15Q26","type":"exact"}],"termid":"MONDO:0013918","xrefs":{"Monarch":{"xref_id":"0013918"}}}


id: GO:0004396
data:
  {"annotated_genes":["SJAG_04334","SJAG_04495"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77872,71971],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008865"},{"annotations":[71968,77869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004340"},{"annotations":[99925,77873],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019158"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + D-hexose = ADP + D-hexose 6-phosphate.","definition_xrefs":["EC:2.7.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"},{"relation_name":"is_a","term_name":"carbohydrate kinase activity","termid":"GO:0019200"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04334":null,"SJAG_04495":null},"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:0016740"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0003674","GO:0016301"],"is_obsolete":false,"name":"hexokinase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:HEXOKINASE-RXN","RHEA:22740"],"synonyms":[{"name":"ATP-dependent hexokinase activity","type":"related"},{"name":"ATP:D-hexose 6-phosphotransferase activity","type":"related"},{"name":"glucose ATP phosphotransferase activity","type":"related"},{"name":"hexokinase (phosphorylating)","type":"related"},{"name":"hexokinase D","type":"related"},{"name":"hexokinase type I activity","type":"narrow"},{"name":"hexokinase type II activity","type":"narrow"},{"name":"hexokinase type III activity","type":"narrow"},{"name":"hexokinase type IV","type":"related"},{"name":"hexokinase type IV (glucokinase) activity","type":"narrow"},{"name":"hexokinase type IV glucokinase activity","type":"related"}],"termid":"GO:0004396","terms_by_termid":{"GO:0004340":null,"GO:0008865":null,"GO:0019158":null}}


id: PBO:0088637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19S proteasome regulatory subunit Rpn6","termid":"PBO:0088637"}


id: GO:0046530
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specialization of organization of a photoreceptor, a cell that responds to incident electromagnetic radiation, particularly visible light. An example of this process is found in Drosophila melanogaster.","definition_xrefs":["ISBN:0198506732","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron differentiation","termid":"GO:0030182"}],"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":"photoreceptor cell differentiation","secondary_identifiers":["GO:0007467"],"termid":"GO:0046530"}


id: PBO:0039548
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD44 antisense RNA 1","termid":"PBO:0039548"}


id: GO:0060584
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the rate, frequency or prostaglandin-endoperoxide synthase activity. Prostaglandin-endoperoxide synthase activity is the catalysis of the reaction: arachidonate + donor-H2 + 2 O2 = prostaglandin H2 + acceptor + H2O.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of prostaglandin-endoperoxide synthase activity (obsolete GO:0060584)","synonyms":[{"name":"regulation of (PG)H synthase activity","type":"related"},{"name":"regulation of PG synthetase activity","type":"related"},{"name":"regulation of fatty acid cyclooxygenase activity","type":"related"},{"name":"regulation of prostaglandin synthetase activity","type":"related"}],"termid":"GO:0060584"}


id: GO:0010198
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Synergid cells undergo degeneration and death in response to penetration by the pollen tube. It is an active process that involves a dramatic decrease in cell volume, collapse of the vacuoles, and complete disintegration of the plasma membrane and most organelles.","definition_xrefs":["PMID:12215516","GOC:isa_complete","GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"programmed cell death involved in cell development","termid":"GO:0010623"},{"relation_name":"part_of","term_name":"pollination","termid":"GO:0009856"}],"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":"synergid death","secondary_identifiers":["GO:0048470"],"synonyms":[{"name":"synergid cell death","type":"exact"},{"name":"synergid degeneration","type":"exact"}],"termid":"GO:0010198"}


id: GO:0120286
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to and responding, e.g. by conformational change, to changes in the cellular level of tryptophan.","definition_xrefs":["GOC:krc","PMID:31498992"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid sensor activity","termid":"GO:0140785"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140299"}],"interesting_parent_ids":["GO:0098772","GO:0003674","GO:0140299"],"is_obsolete":false,"name":"tryptophan sensor activity","synonyms":[{"name":"tryptophan sensing activity","type":"exact"}],"termid":"GO:0120286"}


id: PBO:0113321
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase; implicated in activation of the plasma membrane H(+)-ATPase Pma1p in response to glucose metabolism and under acetic acid stress; plays a role in ion homeostasis; maintains pH homeostasis and modulates plasma membrane potential under acetic acid stress; protein abundance increases in response to DNA replication stress","termid":"PBO:0113321"}


id: PBO:0038604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetyl-CoA acetyltransferase 1","termid":"PBO:0038604"}


id: GO:0030911
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a tetratricopeptide repeat (TPR) domain of a protein, the consensus sequence of which is defined by a pattern of small and large hydrophobic amino acids and a structure composed of helices.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"TPR domain binding","synonyms":[{"name":"tetratricopeptide repeat domain binding","type":"exact"}],"termid":"GO:0030911"}


id: PBO:0070890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L15 pseudogene 22","termid":"PBO:0070890"}


id: FYPO:0006458
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype that affects histone modification.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein modification","termid":"FYPO:0002494"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002274","FYPO:0001985","FYPO:0000002","FYPO:0002494"],"is_obsolete":false,"name":"abnormal histone modification","termid":"FYPO:0006458"}


id: PR:O14322
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug100 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14322"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 100 protein, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16E9.07","synonyms":[{"name":"Spom972h-mug100","type":"exact"}],"termid":"PR:O14322"}


id: PBO:0082464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Calcium and manganese transporter with higher affinity for Ca2+; involved in Ca2+ and Mn2+ homeostasis; localizes to the cis- and medial-Golgi apparatus; GFP-fusion localizes to the vacuole; required for the Mn2+-dependent function of glycosylation enzymes; TMEM165, a human ortholog linked to Congenital Disorders of Glycosylation, functionally complements the null allele; expression pattern and physical interactions suggest a possible role in ribosome biogenesis; expression regulated by Gcr1p","termid":"PBO:0082464"}


id: GO:0097746
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the diameter of blood vessels.","definition_xrefs":["GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular process in circulatory system","termid":"GO:0003018"},{"relation_name":"is_a","term_name":"regulation of tube diameter","termid":"GO:0035296"},{"relation_name":"part_of","term_name":"blood circulation","termid":"GO:0008015"}],"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":"blood vessel diameter maintenance","secondary_identifiers":["GO:0042312","GO:0050880"],"synonyms":[{"name":"blood vessel diameter homeostasis","type":"exact"},{"name":"regulation of blood vessel diameter","type":"exact"},{"name":"regulation of blood vessel size","type":"related"},{"name":"regulation of vasodilatation","type":"related"},{"name":"regulation of vasodilation","type":"related"}],"termid":"GO:0097746"}


id: PBO:0011120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase type 2A regulator, PTPA family Ypa1","termid":"PBO:0011120"}


id: PBO:0045091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DLX2 divergent transcript","termid":"PBO:0045091"}


id: GO:0008732
data:
  {"annotated_genes":["SJAG_02450"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73884],"is_not":false,"summary":null,"term":"GO:0008732"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-allo-threonine = glycine + acetaldehyde.","definition_xrefs":["RHEA:26209","PMID:9228760"],"direct_ancestors":[{"relation_name":"is_a","term_name":"threonine aldolase activity","termid":"GO:0004793"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02450":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"L-allo-threonine aldolase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["EC:4.1.2.49","MetaCyc:LTAA-RXN"],"synonyms":[{"name":"L-allo-threonine acetaldehyde-lyase activity","type":"exact"},{"name":"LtaA","type":"related"}],"termid":"GO:0008732","terms_by_termid":{"GO:0008732":null}}


id: PBO:0080163
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"variable charge Y-linked","termid":"PBO:0080163"}


id: PBO:0054390
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 1786","termid":"PBO:0054390"}


id: PBO:0072285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S24 pseudogene 3","termid":"PBO:0072285"}


id: PBO:0077787
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA topoisomerase III alpha","termid":"PBO:0077787"}


id: GO:0044816
data:
  {"annotated_genes":["SJAG_01370"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[92873],"is_not":false,"summary":null,"term":"GO:0044816"}]},"cv_name":"cellular_component","definition":"A dimer of Nsk1 (nucleolus spindle kinetochore 1) and the dynein light chain, Dlc1. The dimers form an oligomeric chain structure. Functions in the regulation of kinetochore-microtubule interactions and chromosome segregation.","definition_xrefs":["PMID:22065639","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01370":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"Nsk1-Dlc1 complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0044816","terms_by_termid":{"GO:0044816":null}}


id: PBO:0043134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capicua transcriptional repressor pseudogene 2","termid":"PBO:0043134"}


id: GO:0003944
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: glycoprotein N-acetyl-D-glucosaminyl-phospho-D-mannose + H2O = N-acetyl-D-glucosamine + glycoprotein phospho-D-mannose.","definition_xrefs":["EC:3.1.4.45"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosaminidase activity","termid":"GO:0015929"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0016798","GO:0003674"],"is_obsolete":false,"name":"N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase activity","secondary_identifiers":["MetaCyc:3.1.4.45-RXN","RHEA:24372"],"synonyms":[{"name":"2-acetamido-2-deoxy-alpha-D-glucose 1-phosphodiester acetamidodeoxyglucohydrolase activity","type":"related"},{"name":"alpha-N-acetyl-D-glucosamine-1-phosphodiester N-acetylglucosaminidase activity","type":"related"},{"name":"alpha-N-acetylglucosaminyl phosphodiesterase activity","type":"related"},{"name":"glycoprotein-N-acetyl-D-glucosaminyl-phospho-D-mannose N-acetyl-D-glucosaminylphosphohydrolase activity","type":"related"},{"name":"lysosomal alpha-N-acetylglucosaminidase activity","type":"narrow"},{"name":"phosphodiester glycosidase activity","type":"related"}],"termid":"GO:0003944"}


id: PBO:0049363
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIi pseudogene 22","termid":"PBO:0049363"}


id: MONDO:0015033
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D) is a form of HCHWA, a group of familial central nervous system disorders, characterized by severe cerebral amyloid angiopathy (CAA), hemorrhagic and non-hemorrhagic strokes and dementia.","definition_xrefs":["Orphanet:100006"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral amyloid angiopathy, APP-related","termid":"MONDO:0011583"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0021179"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0021179"],"is_obsolete":false,"name":"ABeta amyloidosis, dutch type","secondary_identifiers":["SCTID:56453003","ICD10EXP:I68.0*","ICD10EXP:E85.4+","MEDGEN:419468","GARD:16929","ICD9:277.39","UMLS:C2931672"],"synonyms":[{"name":"ABetaE22Q amyloidosis","type":"exact"},{"name":"HCHWA, Dutch type","type":"exact"},{"name":"HCHWA-D","type":"exact"},{"name":"cerebral amyloid angiopathy, APP-related, Dutch variant","type":"exact"},{"name":"hereditary cerebral haemorrhage with amyloidosis, Dutch type","type":"exact"},{"name":"hereditary cerebral hemorrhage with amyloidosis, Dutch type","type":"exact"}],"termid":"MONDO:0015033","xrefs":{"Monarch":{"xref_id":"0015033"}}}


id: MOD:00010
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a source amino acid residue to an L-alanine.","definition_xrefs":["PubMed:6692818","RESID:AA0001","ChEBI:29948","DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"residues isobaric at 71.037114 Da","termid":"MOD:00570"},{"relation_name":"is_a","term_name":"modified residue that can arise from different natural residues","termid":"MOD:00859"},{"relation_name":"is_a","term_name":"natural, standard, encoded residue","termid":"MOD:01441"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-alanine residue","synonyms":[{"name":"(2S)-2-aminopropanoic acid","type":"exact"},{"name":"2-aminopropionic acid","type":"exact"},{"name":"2-azanylpropanoic acid","type":"exact"},{"name":"Ala","type":"exact"},{"name":"L-alanine","type":"exact"},{"name":"alpha-alanine","type":"exact"},{"name":"alpha-aminopropionic acid","type":"exact"}],"termid":"MOD:00010"}


id: PBO:0081138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZFP36 ring finger protein like 1","termid":"PBO:0081138"}


id: PBO:0042365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD163 molecule like 1","termid":"PBO:0042365"}


id: PBO:0041340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 3 putative open reading frame 36","termid":"PBO:0041340"}


id: PBO:0041400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 6 open reading frame 52","termid":"PBO:0041400"}


id: PBO:0066010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RALY antisense RNA 1","termid":"PBO:0066010"}


id: GO:0098800
data:
  {"annotated_genes":["SJAG_02028","SJAG_01179","SJAG_02567","SJAG_02501","SJAG_02809","SJAG_01816","SJAG_00404","SJAG_04237","SJAG_02398","SJAG_03648","SJAG_03560","SJAG_00354","SJAG_01442","SJAG_01865","SJAG_02077","SJAG_00373","SJAG_01879","SJAG_04014","SJAG_01615","SJAG_04568","SJAG_04218","SJAG_02002","SJAG_01120","SJAG_07008","SJAG_01640","SJAG_05241","SJAG_04128","SJAG_01597","SJAG_04432"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[93723,115758],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032478"},{"annotations":[120780,78990],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031942"},{"annotations":[111716],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990524"},{"annotations":[77649],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005745"},{"annotations":[119815],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140275"},{"annotations":[58020,109291,76829,80784],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061617"},{"annotations":[81760,78610],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042720"},{"annotations":[75784,72846,105229,113799,101168,78497],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0001405"},{"annotations":[75198,104871,115204],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042721"},{"annotations":[61686,76770,78833,71809,68108,77482,80539],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005744"}]},"cv_name":"cellular_component","definition":"Any protein complex that is part of the inner mitochondrial membrane.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"is_a","term_name":"mitochondrial protein-containing complex","termid":"GO:0098798"},{"relation_name":"part_of","term_name":"mitochondrial inner membrane","termid":"GO:0005743"}],"gene_count":29,"genes_by_uniquename":{"SJAG_00354":null,"SJAG_00373":null,"SJAG_00404":null,"SJAG_01120":null,"SJAG_01179":null,"SJAG_01442":null,"SJAG_01597":null,"SJAG_01615":null,"SJAG_01640":null,"SJAG_01816":null,"SJAG_01865":null,"SJAG_01879":null,"SJAG_02002":null,"SJAG_02028":null,"SJAG_02077":null,"SJAG_02398":null,"SJAG_02501":null,"SJAG_02567":null,"SJAG_02809":null,"SJAG_03560":null,"SJAG_03648":null,"SJAG_04014":null,"SJAG_04128":null,"SJAG_04218":null,"SJAG_04237":null,"SJAG_04432":null,"SJAG_04568":null,"SJAG_05241":null,"SJAG_07008":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005739"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005739","GO:0005737"],"is_obsolete":false,"name":"inner mitochondrial membrane protein complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"termid":"GO:0098800","terms_by_termid":{"GO:0001405":null,"GO:0005744":null,"GO:0005745":null,"GO:0031942":null,"GO:0032478":null,"GO:0042720":null,"GO:0042721":null,"GO:0061617":null,"GO:0140275":null,"GO:1990524":null}}


id: GO:0002184
data:
  {"annotated_genes":["SJAG_02812","SJAG_00338","SJAG_03949","SJAG_04283","SJAG_02189","SJAG_02601","SJAG_01696","SJAG_05265"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[60380,60794,75610,96716,98406,111149,111150,118049],"is_not":false,"summary":null,"term":"GO:0002184"}]},"cv_name":"biological_process","definition":"The process resulting in the release of a polypeptide chain from the ribosome in the cytoplasm, usually in response to a termination codon.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translational termination","termid":"GO:0006415"},{"relation_name":"part_of","term_name":"cytoplasmic translation","termid":"GO:0002181"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00338":null,"SJAG_01696":null,"SJAG_02189":null,"SJAG_02601":null,"SJAG_02812":null,"SJAG_03949":null,"SJAG_04283":null,"SJAG_05265":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0002181"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0002181"],"is_obsolete":false,"name":"cytoplasmic translational termination","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0002184","terms_by_termid":{"GO:0002184":null}}


id: MONDO:0010375
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked intellectual disability-epilepsy syndrome","termid":"MONDO:0016160"},{"relation_name":"is_a","term_name":"hereditary hyperekplexia","termid":"MONDO:0021022"},{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"},{"relation_name":"is_a","term_name":"X-linked complex neurodevelopmental disorder","termid":"MONDO:0100148"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 8","secondary_identifiers":["OMIM:300607","Orphanet:163985","UMLS:C1845102","MESH:C564474","GARD:17010","MEDGEN:375581","DOID:0080215"],"synonyms":[{"name":"DEE8","type":"exact"},{"name":"EIEE8","type":"exact"},{"name":"developmental and epileptic encephalopathy 8","type":"exact"},{"name":"early infantile epileptic encephalopathy 8","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 8","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 8","type":"exact"},{"name":"hyperekplexia and epilepsy","type":"related"},{"name":"hyperekplexia-epilepsy syndrome","type":"exact"}],"termid":"MONDO:0010375","xrefs":{"Monarch":{"xref_id":"0010375"}}}


id: PBO:0030977
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_H3-K9_dimethylation_at_centromere_inner_repeat","termid":"PBO:0030977"}


id: GO:1904847
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell chemotaxis to fibroblast growth factor.","definition_xrefs":["GOC:BHF","GOC:BHF_miRNA","GO_REF:0000058","GOC:rph","GOC:TermGenie","PMID:23233752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell migration","termid":"GO:0030334"},{"relation_name":"is_a","term_name":"regulation of chemotaxis","termid":"GO:0050920"},{"relation_name":"is_a","term_name":"regulation of cellular response to growth factor stimulus","termid":"GO:0090287"},{"relation_name":"regulates","term_name":"cell chemotaxis to fibroblast growth factor","termid":"GO:0035766"}],"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 chemotaxis to fibroblast growth factor","termid":"GO:1904847"}


id: GO:1990884
data:
  {"annotated_genes":["SJAG_01877","SJAG_01638"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904812"},{"annotations":[74147,109296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051391"}]},"cv_name":"biological_process","definition":"The posttranscriptional addition of one or more acetyl groups to specific residues in an RNA molecule.","definition_xrefs":["PMID:25402480"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA modification","termid":"GO:0009451"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01638":null,"SJAG_01877":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"RNA acetylation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:1990884","terms_by_termid":{"GO:0051391":null,"GO:1904812":null}}


id: PBO:0071193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 34","termid":"PBO:0071193"}


id: GO:0098804
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the plasma membrane surrounding a non-motile cilium.","definition_xrefs":["GOC:dos","GOC:cilia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliary membrane","termid":"GO:0060170"},{"relation_name":"part_of","term_name":"non-motile cilium","termid":"GO:0097730"}],"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":"non-motile cilium membrane","synonyms":[{"name":"nonmotile primary cilium membrane","type":"related"}],"termid":"GO:0098804"}


id: GO:0141109
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and increases the activity of a transporter.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular function activator activity","termid":"GO:0140677"},{"relation_name":"is_a","term_name":"transporter regulator activity","termid":"GO:0141108"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0140677","GO:0003674","GO:0098772"],"is_obsolete":false,"name":"transporter activator activity","termid":"GO:0141109"}


id: GO:0003433
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of a chondrocyte over time from after its commitment to its mature state where the chondrocyte will contribute to the shaping of an endochondral bone.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chondrocyte development","termid":"GO:0002063"},{"relation_name":"part_of","term_name":"chondrocyte differentiation involved in endochondral bone morphogenesis","termid":"GO:0003413"}],"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":"chondrocyte development involved in endochondral bone morphogenesis","termid":"GO:0003433"}


id: MONDO:0001438
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary fibrosis","termid":"MONDO:0002771"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postinflammatory pulmonary fibrosis","secondary_identifiers":["SCTID:266368002","UMLS:C0175999","DOID:12123","MEDGEN:511625","ICD9:515"],"synonyms":[{"name":"post-inflammatory pulmonary fibrosis","type":"exact"},{"name":"postinflammatory pulmonary fibrosis","type":"exact"}],"termid":"MONDO:0001438","xrefs":{"Monarch":{"xref_id":"0001438"}}}


id: PBO:0002385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucan beta-glucosidase Bgl2 (predicted)","termid":"PBO:0002385"}


id: PBO:0041010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"blepharophimosis, epicanthus inversus and ptosis candidate 1","termid":"PBO:0041010"}


id: PBO:0068916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 159, pseudogene","termid":"PBO:0068916"}


id: PBO:0063736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHB1 pseudogene 1","termid":"PBO:0063736"}


id: PBO:0005437
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATM checkpoint kinase","termid":"PBO:0005437"}


id: PR:Q9P777
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histidinol dehydrogenase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03156","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":"histidinol dehydrogenase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1711.13","secondary_identifiers":["UniProtKB:Q9P777"],"synonyms":[{"name":"HDH (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-hisD","type":"exact"}],"termid":"PR:Q9P777"}


id: PBO:0053280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukocyte immunoglobulin-like receptor pseudogene 1","termid":"PBO:0053280"}


id: PBO:0014606
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae Fen2","termid":"PBO:0014606"}


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","MEDGEN:573462","UMLS:C0339985","SCTID:233629001"],"termid":"MONDO:0018956","xrefs":{"Monarch":{"xref_id":"0018956"}}}


id: GO:0050588
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 8'-apo-beta-carotenol + O2 = (E,E)-7-hydroxy-6-methylhepta-3,5-dienal + 14'-apo-beta-carotenal.","definition_xrefs":["RHEA:26023","EC:1.13.11.67"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of one atom of oxygen (internal monooxygenases or internal mixed function oxidases)","termid":"GO:0016703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"apo-beta-carotenoid-14',13'-dioxygenase activity","secondary_identifiers":["KEGG_REACTION:R08889","MetaCyc:1.13.12.12-RXN"],"synonyms":[{"name":"8'-apo-beta-carotenol:O2 oxidoreductase activity","type":"related"},{"name":"apo-b-carotenoid-14',13'-dioxygenase activity","type":"exact"}],"termid":"GO:0050588"}


id: PBO:0075197
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 9","termid":"PBO:0075197"}


id: GO:0000257
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a nitrile + H2O = a carboxylate + NH3. Acts on a wide range of aromatic nitriles including (indole-3-yl)-acetonitrile and some aliphatic nitriles, and on the corresponding acid amides.","definition_xrefs":["GOC:kd","EC:3.5.5.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in nitriles","termid":"GO:0016815"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016810","GO:0016787"],"is_obsolete":false,"name":"nitrilase activity","secondary_identifiers":["RHEA:21724","UM-BBD_reactionID:r0701","KEGG_REACTION:R00540","UM-BBD_reactionID:r0377","MetaCyc:3.5.5.1-RXN"],"synonyms":[{"name":"acetonitrilase activity","type":"related"},{"name":"benzonitrilase activity","type":"related"},{"name":"nitrile aminohydrolase activity","type":"related"}],"termid":"GO:0000257"}


id: GO:0043221
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a protein from the structural maintenance of chromosomes (SMC) family, a group of chromosomal ATPases with a role in mitotic chromosome organization.","definition_xrefs":["GOC:jl","GOC:vw","InterPro:IPR024704","PMID:9640531"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"SMC family protein binding","synonyms":[{"name":"structural maintenance of chromosomes family protein binding","type":"exact"}],"termid":"GO:0043221"}


id: PBO:0087856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcriptional activator for GABA-dependent induction of GABA genes; binds to DNA elements found in the promoters of target genes and increases their expression in the presence of GABA (gamma-aminobutyrate); zinc finger transcription factor of the Zn(2)-Cys(6) binuclear cluster domain type; localized to the nucleus; examples of GABA genes include UGA1, UGA2, and UGA4","termid":"PBO:0087856"}


id: GO:0043622
data:
  {"annotated_genes":["SJAG_00918"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109479],"is_not":false,"summary":null,"term":"GO:0043622"}]},"cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of structures formed of microtubules and associated proteins in the cell cortex, i.e. just beneath the plasma membrane of a cell.","definition_xrefs":["GOC:dph","GOC:jl","GOC:curators","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cortical cytoskeleton organization","termid":"GO:0030865"},{"relation_name":"is_a","term_name":"cytoplasmic microtubule organization","termid":"GO:0031122"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00918":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0000226"},{"rel_name":"is_a","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0008150","GO:0007010","GO:0000226"],"is_obsolete":false,"name":"cortical microtubule organization","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"cortical microtubule cytoskeleton organization","type":"exact"},{"name":"cortical microtubule organisation","type":"exact"},{"name":"cortical microtubule organization and biogenesis","type":"related"}],"termid":"GO:0043622","terms_by_termid":{"GO:0043622":null}}


id: PBO:0074091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 26 member 6","termid":"PBO:0074091"}


id: GO:0004110
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 11-deoxycorticosterone = 20-hydroxy-3-oxopregn-4-en-21-al.","definition_xrefs":["RHEA:17861","EC:5.3.1.21"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, interconverting aldoses and ketoses","termid":"GO:0016861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016853"],"is_obsolete":false,"name":"corticosteroid side-chain-isomerase activity","secondary_identifiers":["MetaCyc:CORTICOSTEROID-SIDE-CHAIN-ISOMERASE-RXN","KEGG_REACTION:R04165"],"synonyms":[{"name":"11-deoxycorticosterone aldose-ketose-isomerase activity","type":"related"},{"name":"11-deoxycorticosterone ketol-isomerase activity","type":"related"}],"termid":"GO:0004110"}


id: MONDO:0032485
data:
  {"annotated_genes":["SJAG_01778"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88371],"is_not":false,"summary":null,"term":"MONDO:0032485"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant non-syndromic intellectual disability","termid":"MONDO:0015802"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01778":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"intellectual developmental disorder 61","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618009","UMLS:C5231400","MEDGEN:1684867","GARD:18514"],"synonyms":[{"name":"INTELLECTUAL DEVELOPMENTAL DISORDER 61","type":"related"},{"name":"MRD61","type":"related"},{"name":"Mental Retardation, Autosomal Dominant 61","type":"related"}],"termid":"MONDO:0032485","terms_by_termid":{"MONDO:0032485":null},"xrefs":{"Monarch":{"xref_id":"0032485"}}}


id: GO:0001178
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of a process involved in the selection of the specific location within the template strand of an RNA polymerase II promoter for hybridization of the cognate ribonucleotides and formation of first phosphodiester bond within the nascent transcript.","definition_xrefs":["GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transcription, start site selection","termid":"GO:0010630"},{"relation_name":"is_a","term_name":"regulation of transcription initiation by RNA polymerase II","termid":"GO:0060260"},{"relation_name":"regulates","term_name":"transcriptional start site selection at RNA polymerase II promoter","termid":"GO:0001174"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0006355","GO:0010467","GO:0006351","GO:0008150"],"is_obsolete":false,"name":"regulation of transcriptional start site selection at RNA polymerase II promoter","synonyms":[{"name":"regulation of transcription start site selection at RNA polymerase II promoter","type":"exact"}],"termid":"GO:0001178"}


id: PBO:0082468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Calmodulin; Ca2+ binding protein that regulates Ca2+ independent processes (mitosis, bud growth, actin organization, endocytosis, etc.) and Ca2+ dependent processes (stress-activated pathways), targets include Nuf1p, Myo2p and calcineurin; binds to the Hog1p MAPK in response to hyperosmotic stress; potentiates membrane tubulation and constriction mediated by the Rvs161p-Rvs167p complex; human CALM1 or CALM2 functionally complement repression induced inviability","termid":"PBO:0082468"}


id: PBO:0005042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENP-Q homolog Fta7","termid":"PBO:0005042"}


id: GO:0030939
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 a photoperiod, an intermittent cycle of light (day) and dark (night) photoperiod regimes, with the light phase being longer than the dark.","definition_xrefs":["GOC:pj"],"gene_count":0,"genotype_count":0,"name":"obsolete response to long-day photoperiod (obsolete GO:0030939)","synonyms":[{"name":"response to long-day photoperiod","type":"exact"}],"termid":"GO:0030939"}


id: MONDO:0006631
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Osteoarthritis of the foot generally affects the joint at the base of your big toe. It can cause your toe to: - become stiff over time, which can make it difficult and painful to walk – this is called hallux rigidus - become bent, which can lead to painful bunions (bony lumps at the base of your big toe) – this is called hallux valgus. Osteoarthritis of the mid-foot is also quite common, especially in older people, and may cause an obvious bony swelling (osteophyte) on the top of your mid-foot. Ankle osteoarthritis is least common and may cause your heel to move to an unusual angle.","definition_xrefs":["EFO:1000788"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteoarthritis","termid":"MONDO:0005178"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoarthritis, toe","secondary_identifiers":["UMLS:C0409929","MEDGEN:592722"],"termid":"MONDO:0006631","xrefs":{"Monarch":{"xref_id":"0006631"}}}


id: PR:P87127
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ATP synthase mitochondrial F1 complex assembly factor 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00582","PANTHER:PTHR13126: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":"protein atp11, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3A12.12","secondary_identifiers":["UniProtKB:P87127"],"synonyms":[{"name":"Spom972h-ATPAF1","type":"exact"}],"termid":"PR:P87127"}


id: PBO:0091909
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Domain of Unknown function protein at the Cortex","termid":"PBO:0091909"}


id: PBO:0089215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation regulator, PHD finger Bye1","termid":"PBO:0089215"}


id: MONDO:0004366
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A mixed glioma characterized by the presence of astrocytic, ependymal, and oligodendroglial neoplastic components.","definition_xrefs":["NCIT:C8272"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mixed glioma","termid":"MONDO:0003268"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mixed astrocytoma-ependymoma-oligodendroglioma","secondary_identifiers":["MEDGEN:79184","UMLS:C0280792","DOID:7817"],"synonyms":[{"name":"mixed astrocytoma-ependymoma-oligodendroglioma","type":"exact"}],"termid":"MONDO:0004366","xrefs":{"Monarch":{"xref_id":"0004366"}}}


id: FYPO:0004607
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the size, shape, or structure of the spindle pole body is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component","termid":"FYPO:0000287"}],"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:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal spindle pole body morphology","synonyms":[{"name":"abnormal SPB morphology","type":"exact"},{"name":"abnormal spindle pole body structure","type":"narrow"}],"termid":"FYPO:0004607"}


id: MONDO:0001131
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete duodenum adenocarcinoma (obsolete MONDO:0001131)","termid":"MONDO:0001131","xrefs":{"Monarch":{"xref_id":"0001131"}}}


id: GO:0060697
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of phospholipid catabolism, the chemical reactions and pathways resulting in the breakdown of phospholipids, any lipid containing phosphoric acid as a mono- or diester.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of lipid catabolic process","termid":"GO:0050996"},{"relation_name":"is_a","term_name":"regulation of phospholipid catabolic process","termid":"GO:0060696"},{"relation_name":"is_a","term_name":"positive regulation of phospholipid metabolic process","termid":"GO:1903727"},{"relation_name":"positively_regulates","term_name":"phospholipid catabolic process","termid":"GO:0009395"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"positively_regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"positive regulation of phospholipid catabolic process","termid":"GO:0060697"}


id: GO:0050153
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 10-hydroxydecanoate + NAD+ = 10-oxodecanoate + H+ + NADH.","definition_xrefs":["RHEA:20880","EC:1.1.1.66"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"omega-hydroxydecanoate dehydrogenase activity","secondary_identifiers":["MetaCyc:OMEGA-HYDROXYDECANOATE-DEHYDROGENASE-RXN","KEGG_REACTION:R03886"],"synonyms":[{"name":"10-hydroxydecanoate:NAD+ 10-oxidoreductase activity","type":"related"},{"name":"w-hydroxydecanoate dehydrogenase activity","type":"exact"}],"termid":"GO:0050153"}


id: GO:0032383
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the directed movement of cholesterol within cells.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cholesterol transport","termid":"GO:0032374"},{"relation_name":"is_a","term_name":"regulation of intracellular sterol transport","termid":"GO:0032380"},{"relation_name":"regulates","term_name":"intracellular cholesterol transport","termid":"GO:0032367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of intracellular cholesterol transport","termid":"GO:0032383"}


id: GO:0003240
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process pertaining to the initial formation of the conus arteriosus from unspecified parts. The conus arteriosus is a valved chamber with thick muscular walls stemming from the ventricle and connecting to the pulmonary trunk.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac chamber formation","termid":"GO:0003207"},{"relation_name":"part_of","term_name":"conus arteriosus morphogenesis","termid":"GO:0003239"}],"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":"conus arteriosus formation","termid":"GO:0003240"}


id: GO:0036371
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, the T-tubule. The T-tubule is an invagination of the plasma membrane of a muscle cell that extends inward from the cell surface around each myofibril.","definition_xrefs":["GOC:rl","PMID:16292983","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to plasma membrane","termid":"GO:0072659"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"protein localization to T-tubule","synonyms":[{"name":"protein localisation to T-tubule","type":"exact"},{"name":"protein localization to T tubule","type":"exact"},{"name":"protein localization to transverse tubule","type":"exact"}],"termid":"GO:0036371"}


id: GO:0002816
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of biosynthesis of antibacterial peptides active against Gram-positive bacteria.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of antibacterial peptide biosynthetic process","termid":"GO:0002808"},{"relation_name":"regulates","term_name":"biosynthetic process of antibacterial peptides active against Gram-positive bacteria","termid":"GO:0002815"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of biosynthetic process of antibacterial peptides active against Gram-positive bacteria","termid":"GO:0002816"}


id: _global:derives_from
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"'Entity A' derives_from 'Entity B' implies that 'Entity A' is chemically derived from 'Entity B'.","definition_xrefs":["PubMed:18688235"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"derives_from","termid":"_global:derives_from"}


id: PBO:0057882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3186","termid":"PBO:0057882"}


id: FYPO:0001057
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 is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transport","termid":"FYPO:0001720"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"abnormal amino acid import","synonyms":[{"name":"abnormal amino acid import across plasma membrane","type":"exact"},{"name":"abnormal amino acid import into cell","type":"exact"},{"name":"abnormal amino acid uptake","type":"exact"}],"termid":"FYPO:0001057"}


id: MONDO:0005004
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm composed of glandular epithelial clear cells. Various architectural patterns may be seen, including papillary, tubulocystic, and solid.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"}],"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":"clear cell adenocarcinoma","secondary_identifiers":["NCIT:C4072","DOID:4468","EFO:0000348","ICDO:8310/3","MEDGEN:64629","MESH:D018262","UMLS:C0206681","NCIT:C3766"],"synonyms":[{"name":"Wolffian duct neoplasm","type":"related"},{"name":"adenocarcinoma, clear cell, malignant","type":"exact"},{"name":"clear cell adenocarcinoma","type":"exact"},{"name":"clear cell adenocarcinoma (morphologic abnormality)","type":"exact"},{"name":"clear cell adenocarcinoma NOS (morphologic abnormality)","type":"exact"},{"name":"clear cell carcinoma","type":"related"},{"name":"malignant mesonephroma","type":"related"},{"name":"mesonephroid clear cell adenocarcinoma","type":"related"},{"name":"mesonephroid clear cell carcinoma","type":"related"},{"name":"mesonephroma NOS (morphologic abnormality)","type":"exact"},{"name":"mesonephroma, malignant","type":"related"},{"name":"mesonephroma, malignant (morphologic abnormality)","type":"related"},{"name":"water-clear cell adenocarcinoma","type":"exact"},{"name":"water-clear cell adenocarcinoma (morphologic abnormality)","type":"exact"},{"name":"water-clear cell carcinoma","type":"related"}],"termid":"MONDO:0005004","xrefs":{"Monarch":{"xref_id":"0005004"}}}


id: MONDO:0014470
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the TBC1D24 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 65","secondary_identifiers":["OMIM:616044","DOID:0110586","UMLS:C3892048","MEDGEN:856147","GARD:18140"],"synonyms":[{"name":"DFNA65","type":"narrow"},{"name":"TBC1D24 autosomal dominant nonsyndromic deafness","type":"narrow"},{"name":"autosomal dominant deafness 65","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 65","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness caused by mutation in TBC1D24","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 65","type":"narrow"},{"name":"deafness, autosomal dominant 65","type":"narrow"},{"name":"deafness, autosomal dominant type 65","type":"narrow"}],"termid":"MONDO:0014470","xrefs":{"Monarch":{"xref_id":"0014470"}}}


id: MONDO:0002069
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer that involves the UBERON:0035289.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"female breast carcinoma","termid":"MONDO:0004379"}],"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":"female breast axillary tail cancer","secondary_identifiers":["ICD9:174.6","MEDGEN:509328","ICD10CM:C50.6","UMLS:C0153554","DOID:1650","SCTID:188156001"],"synonyms":[{"name":"axillary tail of breast cancer","type":"exact"},{"name":"cancer of axillary tail of breast","type":"exact"},{"name":"malignant axillary tail of breast neoplasm","type":"exact"},{"name":"malignant neoplasm of axillary tail of breast","type":"exact"},{"name":"malignant neoplasm of axillary tail of female breast","type":"exact"}],"termid":"MONDO:0002069","xrefs":{"Monarch":{"xref_id":"0002069"}}}


id: PBO:0063711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PGM5 antisense RNA 1","termid":"PBO:0063711"}


id: GO:0097009
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the balance between food intake (energy input) and energy expenditure.","definition_xrefs":["PMID:15919751","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal-level homeostasis","termid":"GO:0048871"}],"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":"energy homeostasis","secondary_identifiers":["GO:2000506","GO:2000505","GO:2000507"],"synonyms":[{"name":"negative regulation of energy homeostasis","type":"related"},{"name":"positive regulation of energy homeostasis","type":"related"},{"name":"regulation of energy homeostasis","type":"related"}],"termid":"GO:0097009"}


id: GO:0009653
data:
  {"annotated_genes":["SJAG_00514","SJAG_03557","SJAG_04483","SJAG_02989","SJAG_02529","SJAG_04615","SJAG_04010","SJAG_04461","SJAG_01662","SJAG_00596","SJAG_03587","SJAG_01531","SJAG_02712","SJAG_04922","SJAG_00304","SJAG_04322","SJAG_01993","SJAG_03250","SJAG_02718","SJAG_04271","SJAG_03090","SJAG_04868","SJAG_03483","SJAG_04184","SJAG_02241","SJAG_03536","SJAG_04080","SJAG_02700","SJAG_00610","SJAG_04666","SJAG_01456","SJAG_03746","SJAG_04781","SJAG_03013","SJAG_04470","SJAG_00826","SJAG_02838","SJAG_00114","SJAG_00405","SJAG_04238","SJAG_01943","SJAG_00028","SJAG_02169","SJAG_02320","SJAG_00855","SJAG_00333","SJAG_03486","SJAG_02536","SJAG_01894","SJAG_00244","SJAG_00974","SJAG_04236","SJAG_01212","SJAG_02222","SJAG_00216","SJAG_02022","SJAG_00486","SJAG_04522","SJAG_03057","SJAG_01017","SJAG_00821","SJAG_00971","SJAG_02248","SJAG_04509","SJAG_04859","SJAG_03705","SJAG_04275","SJAG_03915","SJAG_02392","SJAG_02864","SJAG_04203","SJAG_00661","SJAG_03637","SJAG_00663","SJAG_01321","SJAG_01483","SJAG_01769","SJAG_03688","SJAG_05309","SJAG_04901","SJAG_01799","SJAG_03581","SJAG_00845","SJAG_00236","SJAG_04724"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91744,97759,96484],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0051519"},{"annotations":[98859,98443,102665,114720,107088,113512],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030437"},{"annotations":[95913,113317],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071998"},{"annotations":[96363],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034413"},{"annotations":[93665,90081,90575,92127],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030476"},{"annotations":[74763],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034412"},{"annotations":[119811,116098,119819,106120,111059],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070591"},{"annotations":[93391,74765,106941],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031321"},{"annotations":[99477,100754,101837,120884,121067,112107,99514,115945,93180,97285,103655,107253,109360,120583],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032120"},{"annotations":[98793,108805,101766,104867,115946,94183,106078,109691,101767,99478],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031322"},{"annotations":[95914,89756],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0042815"},{"annotations":[119934,112756,108826,89921,101671,105436,118504],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0051523"},{"annotations":[100907,116341,100212,90129,94406,100824],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904600"},{"annotations":[92607],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0051517"},{"annotations":[118326],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090258"},{"annotations":[103991,108427],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0010637"},{"annotations":[118610,109587],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000784"},{"annotations":[95636,107321,102114],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000247"},{"annotations":[105649],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0061361"},{"annotations":[110868],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090141"},{"annotations":[117069],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0051516"},{"annotations":[121690,121689],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0008360"},{"annotations":[97572,106492,96490,115056,120837,93028],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000100"},{"annotations":[104795,108079,89765,94318],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:2000769"},{"annotations":[101768,101769,102056,107983,96411,117992],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070583"}]},"cv_name":"biological_process","definition":"The process in which anatomical structures are generated and organized. Morphogenesis pertains to the creation of form.","definition_xrefs":["GOC:go_curators","ISBN:0521436125"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process","termid":"GO:0032502"},{"relation_name":"part_of","term_name":"anatomical structure development","termid":"GO:0048856"}],"gene_count":85,"genes_by_uniquename":{"SJAG_00028":null,"SJAG_00114":null,"SJAG_00216":null,"SJAG_00236":null,"SJAG_00244":null,"SJAG_00304":null,"SJAG_00333":null,"SJAG_00405":null,"SJAG_00486":null,"SJAG_00514":null,"SJAG_00596":null,"SJAG_00610":null,"SJAG_00661":null,"SJAG_00663":null,"SJAG_00821":null,"SJAG_00826":null,"SJAG_00845":null,"SJAG_00855":null,"SJAG_00971":null,"SJAG_00974":null,"SJAG_01017":null,"SJAG_01212":null,"SJAG_01321":null,"SJAG_01456":null,"SJAG_01483":null,"SJAG_01531":null,"SJAG_01662":null,"SJAG_01769":null,"SJAG_01799":null,"SJAG_01894":null,"SJAG_01943":null,"SJAG_01993":null,"SJAG_02022":null,"SJAG_02169":null,"SJAG_02222":null,"SJAG_02241":null,"SJAG_02248":null,"SJAG_02320":null,"SJAG_02392":null,"SJAG_02529":null,"SJAG_02536":null,"SJAG_02700":null,"SJAG_02712":null,"SJAG_02718":null,"SJAG_02838":null,"SJAG_02864":null,"SJAG_02989":null,"SJAG_03013":null,"SJAG_03057":null,"SJAG_03090":null,"SJAG_03250":null,"SJAG_03483":null,"SJAG_03486":null,"SJAG_03536":null,"SJAG_03557":null,"SJAG_03581":null,"SJAG_03587":null,"SJAG_03637":null,"SJAG_03688":null,"SJAG_03705":null,"SJAG_03746":null,"SJAG_03915":null,"SJAG_04010":null,"SJAG_04080":null,"SJAG_04184":null,"SJAG_04203":null,"SJAG_04236":null,"SJAG_04238":null,"SJAG_04271":null,"SJAG_04275":null,"SJAG_04322":null,"SJAG_04461":null,"SJAG_04470":null,"SJAG_04483":null,"SJAG_04509":null,"SJAG_04522":null,"SJAG_04615":null,"SJAG_04666":null,"SJAG_04724":null,"SJAG_04781":null,"SJAG_04859":null,"SJAG_04868":null,"SJAG_04901":null,"SJAG_04922":null,"SJAG_05309":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"anatomical structure morphogenesis","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"PMID:30664646":null},"secondary_identifiers":["Wikipedia:Morphogenesis"],"synonyms":[{"name":"anatomical structure organization","type":"exact"},{"name":"embryogenesis and morphogenesis","type":"broad"},{"name":"morphogenesis","type":"exact"}],"termid":"GO:0009653","terms_by_termid":{"GO:0008360":null,"GO:0010637":null,"GO:0030437":null,"GO:0030476":null,"GO:0031321":null,"GO:0031322":null,"GO:0032120":null,"GO:0034412":null,"GO:0034413":null,"GO:0042815":null,"GO:0051516":null,"GO:0051517":null,"GO:0051519":null,"GO:0051523":null,"GO:0061361":null,"GO:0070583":null,"GO:0070591":null,"GO:0071998":null,"GO:0090141":null,"GO:0090258":null,"GO:1904600":null,"GO:2000100":null,"GO:2000247":null,"GO:2000769":null,"GO:2000784":null}}


id: PBO:0017843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"purine transmembrane transporter (predicted)","termid":"PBO:0017843"}


id: MONDO:0006123
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well circumscribed benign tumor arising from cardiac muscle. It usually affects children and may be present in the fetus. Depending on tumor location and size, cardiac, respiratory, and hemodynamic parameters may be affected. There is an association between cardiac rhabdomyoma and tuberous sclerosis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign neoplasm of heart","termid":"MONDO:0021450"},{"relation_name":"is_a","term_name":"rhabdomyoma","termid":"MONDO:0036688"}],"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":"cardiac rhabdomyoma","secondary_identifiers":["EFO:1000150","HP:0009729","UMLS:C1332852","MEDGEN:232027","NCIT:C6739"],"synonyms":[{"name":"cardiac rhabdomyoma","type":"exact"},{"name":"cardiac rhabdomyoma (disease)","type":"exact"},{"name":"heart rhabdomyoma","type":"exact"},{"name":"rhabdomyoma of heart","type":"exact"},{"name":"rhabdomyoma of the heart","type":"exact"}],"termid":"MONDO:0006123","xrefs":{"Monarch":{"xref_id":"0006123"}}}


id: PR:P00332
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An alcohol dehydrogenase, propanol-preferring that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04737"],"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":"alcohol dehydrogenase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC13B11.01","secondary_identifiers":["UniProtKB:P00332"],"synonyms":[{"name":"Spom972h-adhP","type":"exact"}],"termid":"PR:P00332"}


id: PBO:0073084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate dehydrogenase complex assembly factor 4","termid":"PBO:0073084"}


id: MONDO:0060712
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete developmental delay, intellectual disability, obesity, and dysmorphic features (obsolete MONDO:0060712)","termid":"MONDO:0060712","xrefs":{"Monarch":{"xref_id":"0060712"}}}


id: RO:0002213
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Process(P1) postively regulates process(P2) iff: P1 initiates P2, or P1 increases the the frequency of initiation of P2 or the magnitude or rate of output of P2.","direct_ancestors":[{"relation_name":"is_a","term_name":"regulates","termid":"RO:0002211"},{"relation_name":"is_a","term_name":"causally_upstream_of,_positive_effect","termid":"RO:0002304"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"positively_regulates","termid":"RO:0002213"}


id: GO:0006338
data:
  {"annotated_genes":["SJAG_03630","SJAG_02319","SJAG_01599","SJAG_04186","SJAG_00440","SJAG_00184","SJAG_03752","SJAG_02768","SJAG_00411","SJAG_03776","SJAG_00441","SJAG_03487","SJAG_00743","SJAG_02119","SJAG_04396","SJAG_02329","SJAG_03680","SJAG_01513","SJAG_01675","SJAG_02254","SJAG_02756","SJAG_00170","SJAG_04755","SJAG_01579","SJAG_04205","SJAG_01230","SJAG_02409","SJAG_04141","SJAG_02466","SJAG_03627","SJAG_00335","SJAG_01540","SJAG_03576","SJAG_00349","SJAG_01082","SJAG_03905","SJAG_01385","SJAG_00336","SJAG_02927","SJAG_03006","SJAG_01110","SJAG_03286","SJAG_00746","SJAG_04596","SJAG_04194","SJAG_04213","SJAG_03042","SJAG_00259","SJAG_03047","SJAG_01658","SJAG_03041","SJAG_02906","SJAG_03542","SJAG_03603","SJAG_03619","SJAG_03668","SJAG_01046","SJAG_00341","SJAG_02439","SJAG_07011","SJAG_03118","SJAG_00676","SJAG_03694","SJAG_00160","SJAG_01111","SJAG_04613","SJAG_02416","SJAG_02592","SJAG_00914","SJAG_02541","SJAG_02701","SJAG_00943","SJAG_03366","SJAG_02817","SJAG_01075","SJAG_02382","SJAG_00756","SJAG_03193","SJAG_04257","SJAG_03356","SJAG_05313","SJAG_02342","SJAG_04696","SJAG_02198","SJAG_03997","SJAG_02873","SJAG_04355","SJAG_01745","SJAG_03036","SJAG_00684","SJAG_00581","SJAG_00896","SJAG_00058","SJAG_03599","SJAG_04274","SJAG_02066","SJAG_03916","SJAG_00925","SJAG_00769","SJAG_00142","SJAG_04039","SJAG_03982","SJAG_01009","SJAG_04030","SJAG_02908","SJAG_00584","SJAG_01005","SJAG_03255","SJAG_02846","SJAG_03839","SJAG_02170","SJAG_02659","SJAG_02314","SJAG_00320","SJAG_02629","SJAG_01804","SJAG_01016","SJAG_02981","SJAG_00307","SJAG_06641","SJAG_03787","SJAG_01878","SJAG_01325","SJAG_01193","SJAG_04097","SJAG_04793","SJAG_01836","SJAG_00266","SJAG_00414","SJAG_04547","SJAG_00596","SJAG_03548","SJAG_02773","SJAG_00303","SJAG_02589","SJAG_04576","SJAG_02165","SJAG_02447","SJAG_03431","SJAG_03884","SJAG_04692","SJAG_02698","SJAG_04879","SJAG_03230","SJAG_01622","SJAG_02401","SJAG_03183","SJAG_03758","SJAG_00293","SJAG_03867","SJAG_04389","SJAG_02500","SJAG_02458","SJAG_01610","SJAG_05192","SJAG_01992","SJAG_02303","SJAG_01823","SJAG_03128","SJAG_03844","SJAG_01873","SJAG_00678","SJAG_03689","SJAG_01611","SJAG_01867","SJAG_00868","SJAG_03941","SJAG_01938","SJAG_01511","SJAG_02869","SJAG_04670","SJAG_06608","SJAG_04005","SJAG_02571","SJAG_05193","SJAG_04038","SJAG_05161","SJAG_02723","SJAG_05020","SJAG_03942","SJAG_00735","SJAG_02549","SJAG_00739","SJAG_02621","SJAG_03635","SJAG_00913","SJAG_04942","SJAG_00641","SJAG_03387","SJAG_00302","SJAG_02778","SJAG_03441","SJAG_02798","SJAG_00942","SJAG_02872","SJAG_04061","SJAG_03546","SJAG_00873","SJAG_03792","SJAG_05273","SJAG_03394","SJAG_04574","SJAG_04989","SJAG_01926","SJAG_00545","SJAG_05282","SJAG_03543","SJAG_04253","SJAG_03628","SJAG_01465","SJAG_02381","SJAG_03145","SJAG_02347","SJAG_00961","SJAG_04114","SJAG_00187","SJAG_04369","SJAG_01707","SJAG_04758","SJAG_01008","SJAG_03579","SJAG_01601","SJAG_01653","SJAG_02576","SJAG_01475","SJAG_02725","SJAG_01837","SJAG_04272","SJAG_00934","SJAG_03624","SJAG_02035","SJAG_00510","SJAG_02622","SJAG_01204","SJAG_03033","SJAG_02594","SJAG_02385","SJAG_03900","SJAG_04768","SJAG_02990","SJAG_03945","SJAG_03537","SJAG_04190","SJAG_01711","SJAG_04815","SJAG_01331","SJAG_00045","SJAG_03664","SJAG_00087","SJAG_03944","SJAG_01146","SJAG_00783","SJAG_02311","SJAG_00701","SJAG_04581"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[58246,58754,58765,59034,59547,59623,60649,61615,62605,64190,64714,65887,66152,66540,66683,68546,68871,69028,69928,69936,71879,72180,72703,74690,78068,78283,90698,95848,97233,100070,100396,106386,106589,108487,109899,115091,115534,119748],"is_not":false,"summary":null,"term":"GO:0006338"},{"annotations":[96603,73115,90746,117101,119725,120865,118490,108335,116240,120901,101317,101065,109319,115123,97384,104011,94684,91941,104855,81624],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034080"},{"annotations":[111653,104350],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140898"},{"annotations":[115615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140719"},{"annotations":[106680,101318,96201,117621,120613,106172,75562,94265,108849,99142,96980,109702,96736,100890,111052,92575,96512,101066,94685,101605,105985,116735,115157,90747,100829,74177],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140861"},{"annotations":[118232,95282,120894,60192,66563,69829,93127],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0040029"},{"annotations":[95974,61249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140718"},{"annotations":[90025,105004,119153,114625,92635,114624,98075,95975,117273,61243,101048,100830,64598,101074,115062,119783],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033696"},{"annotations":[72095,121500,74654,81752,121501,74023,76557,75550,117427,78463,72132,74965],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031507"},{"annotations":[99249,95134,105067,95095,116163,99136],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045814"},{"annotations":[79125,108625],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0061188"},{"annotations":[110471],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0060906"},{"annotations":[80655,109705,93002,71626,62958,75032,93003,98372,74779,116560],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006334"},{"annotations":[99007,91944,118929],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006337"},{"annotations":[76574,113272,59176,115303],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034728"},{"annotations":[64601,94718,95337,114634,93967,114112,113273,74178,116004,116441,61247,96245,100177,95977,104729,106141,115304,110139,92092,106040,114633],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031508"},{"annotations":[93236],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140462"},{"annotations":[100891],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0031453"},{"annotations":[93072],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090053"},{"annotations":[93073,96271,112337],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090055"},{"annotations":[72710,114113,93968,106041,110140,74181,115305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000183"},{"annotations":[92695,100491],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0031445"},{"annotations":[99108,102239],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090052"},{"annotations":[119784],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0010964"},{"annotations":[120156,93760,99109,102240,119785],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902801"},{"annotations":[106042,113860,109757,111105,115064,109328],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031048"},{"annotations":[101055,113274,97434,94647,114216,115306,98654,110141,112480,61246,120133,106043,101494,73421,106142,109954,113210,116006,95978,114114,96247,117445,93162,118006,119727,115683,120016,120866],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030466"},{"annotations":[114115,92678,106143,89357,112481,118561],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902794"},{"annotations":[108280],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902795"},{"annotations":[116007],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141194"},{"annotations":[116587,90650,112649,115684,101056,118008,117446,101496,95990,97252,120017,120135,120867,112482,113211,119728,98655,108523,114217,90707,116326,93163],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140727"},{"annotations":[100178,114218,96248,93970,61248,115685,116008,119729,92093,110142,95979,74179,106044,79130,98656,60414,101057,113275,114116,115307,120868,112483,93164,120136],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031509"},{"annotations":[96516,110764,97395,110769,93130,115618,116562,94272,113276,118930,120895,118233,105513,95283,91945],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140673"},{"annotations":[93301,96016,115329,101069,117275,100426,119595,101319,109304,94686,61511,66090,105313,110444,107589,96203,89526,106992,118931,105797,67708,112605,119300,114561,100592,111461,97387,91946,64478,92577,109419,102916,116242,92591,117407,67654,117421,112469,97799,116418,96078,59022,109656,96030,98575,114985,111054,118562,115159,97362,95675,89848,116327,96548,99746,108875,105068,117728,115139,118370,94188,90028,111569,119644,100160,91676,99009,89670,107737,108723,117031,119997,119480,97806,90749,106526,103508,95404,95906,113754,116737,116253,98373,91162,119573,90213,111338,109856,90364,96050],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045815"},{"annotations":[118563],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141005"}]},"cv_name":"biological_process","definition":"A dynamic process of chromatin reorganization resulting in changes to chromatin structure. These changes allow DNA metabolic processes such as transcriptional regulation, DNA recombination, DNA repair, and DNA replication.","definition_xrefs":["GOC:vw","PMID:12697820","GOC:jid","PMID:12042764"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromatin organization","termid":"GO:0006325"}],"gene_count":255,"genes_by_uniquename":{"SJAG_00045":null,"SJAG_00058":null,"SJAG_00087":null,"SJAG_00142":null,"SJAG_00160":null,"SJAG_00170":null,"SJAG_00184":null,"SJAG_00187":null,"SJAG_00259":null,"SJAG_00266":null,"SJAG_00293":null,"SJAG_00302":null,"SJAG_00303":null,"SJAG_00307":null,"SJAG_00320":null,"SJAG_00335":null,"SJAG_00336":null,"SJAG_00341":null,"SJAG_00349":null,"SJAG_00411":null,"SJAG_00414":null,"SJAG_00440":null,"SJAG_00441":null,"SJAG_00510":null,"SJAG_00545":null,"SJAG_00581":null,"SJAG_00584":null,"SJAG_00596":null,"SJAG_00641":null,"SJAG_00676":null,"SJAG_00678":null,"SJAG_00684":null,"SJAG_00701":null,"SJAG_00735":null,"SJAG_00739":null,"SJAG_00743":null,"SJAG_00746":null,"SJAG_00756":null,"SJAG_00769":null,"SJAG_00783":null,"SJAG_00868":null,"SJAG_00873":null,"SJAG_00896":null,"SJAG_00913":null,"SJAG_00914":null,"SJAG_00925":null,"SJAG_00934":null,"SJAG_00942":null,"SJAG_00943":null,"SJAG_00961":null,"SJAG_01005":null,"SJAG_01008":null,"SJAG_01009":null,"SJAG_01016":null,"SJAG_01046":null,"SJAG_01075":null,"SJAG_01082":null,"SJAG_01110":null,"SJAG_01111":null,"SJAG_01146":null,"SJAG_01193":null,"SJAG_01204":null,"SJAG_01230":null,"SJAG_01325":null,"SJAG_01331":null,"SJAG_01385":null,"SJAG_01465":null,"SJAG_01475":null,"SJAG_01511":null,"SJAG_01513":null,"SJAG_01540":null,"SJAG_01579":null,"SJAG_01599":null,"SJAG_01601":null,"SJAG_01610":null,"SJAG_01611":null,"SJAG_01622":null,"SJAG_01653":null,"SJAG_01658":null,"SJAG_01675":null,"SJAG_01707":null,"SJAG_01711":null,"SJAG_01745":null,"SJAG_01804":null,"SJAG_01823":null,"SJAG_01836":null,"SJAG_01837":null,"SJAG_01867":null,"SJAG_01873":null,"SJAG_01878":null,"SJAG_01926":null,"SJAG_01938":null,"SJAG_01992":null,"SJAG_02035":null,"SJAG_02066":null,"SJAG_02119":null,"SJAG_02165":null,"SJAG_02170":null,"SJAG_02198":null,"SJAG_02254":null,"SJAG_02303":null,"SJAG_02311":null,"SJAG_02314":null,"SJAG_02319":null,"SJAG_02329":null,"SJAG_02342":null,"SJAG_02347":null,"SJAG_02381":null,"SJAG_02382":null,"SJAG_02385":null,"SJAG_02401":null,"SJAG_02409":null,"SJAG_02416":null,"SJAG_02439":null,"SJAG_02447":null,"SJAG_02458":null,"SJAG_02466":null,"SJAG_02500":null,"SJAG_02541":null,"SJAG_02549":null,"SJAG_02571":null,"SJAG_02576":null,"SJAG_02589":null,"SJAG_02592":null,"SJAG_02594":null,"SJAG_02621":null,"SJAG_02622":null,"SJAG_02629":null,"SJAG_02659":null,"SJAG_02698":null,"SJAG_02701":null,"SJAG_02723":null,"SJAG_02725":null,"SJAG_02756":null,"SJAG_02768":null,"SJAG_02773":null,"SJAG_02778":null,"SJAG_02798":null,"SJAG_02817":null,"SJAG_02846":null,"SJAG_02869":null,"SJAG_02872":null,"SJAG_02873":null,"SJAG_02906":null,"SJAG_02908":null,"SJAG_02927":null,"SJAG_02981":null,"SJAG_02990":null,"SJAG_03006":null,"SJAG_03033":null,"SJAG_03036":null,"SJAG_03041":null,"SJAG_03042":null,"SJAG_03047":null,"SJAG_03118":null,"SJAG_03128":null,"SJAG_03145":null,"SJAG_03183":null,"SJAG_03193":null,"SJAG_03230":null,"SJAG_03255":null,"SJAG_03286":null,"SJAG_03356":null,"SJAG_03366":null,"SJAG_03387":null,"SJAG_03394":null,"SJAG_03431":null,"SJAG_03441":null,"SJAG_03487":null,"SJAG_03537":null,"SJAG_03542":null,"SJAG_03543":null,"SJAG_03546":null,"SJAG_03548":null,"SJAG_03576":null,"SJAG_03579":null,"SJAG_03599":null,"SJAG_03603":null,"SJAG_03619":null,"SJAG_03624":null,"SJAG_03627":null,"SJAG_03628":null,"SJAG_03630":null,"SJAG_03635":null,"SJAG_03664":null,"SJAG_03668":null,"SJAG_03680":null,"SJAG_03689":null,"SJAG_03694":null,"SJAG_03752":null,"SJAG_03758":null,"SJAG_03776":null,"SJAG_03787":null,"SJAG_03792":null,"SJAG_03839":null,"SJAG_03844":null,"SJAG_03867":null,"SJAG_03884":null,"SJAG_03900":null,"SJAG_03905":null,"SJAG_03916":null,"SJAG_03941":null,"SJAG_03942":null,"SJAG_03944":null,"SJAG_03945":null,"SJAG_03982":null,"SJAG_03997":null,"SJAG_04005":null,"SJAG_04030":null,"SJAG_04038":null,"SJAG_04039":null,"SJAG_04061":null,"SJAG_04097":null,"SJAG_04114":null,"SJAG_04141":null,"SJAG_04186":null,"SJAG_04190":null,"SJAG_04194":null,"SJAG_04205":null,"SJAG_04213":null,"SJAG_04253":null,"SJAG_04257":null,"SJAG_04272":null,"SJAG_04274":null,"SJAG_04355":null,"SJAG_04369":null,"SJAG_04389":null,"SJAG_04396":null,"SJAG_04547":null,"SJAG_04574":null,"SJAG_04576":null,"SJAG_04581":null,"SJAG_04596":null,"SJAG_04613":null,"SJAG_04670":null,"SJAG_04692":null,"SJAG_04696":null,"SJAG_04755":null,"SJAG_04758":null,"SJAG_04768":null,"SJAG_04793":null,"SJAG_04815":null,"SJAG_04879":null,"SJAG_04942":null,"SJAG_04989":null,"SJAG_05020":null,"SJAG_05161":null,"SJAG_05192":null,"SJAG_05193":null,"SJAG_05273":null,"SJAG_05282":null,"SJAG_05313":null,"SJAG_06608":null,"SJAG_06641":null,"SJAG_07011":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006325"}],"interesting_parent_ids":["GO:0006325","GO:0008150"],"is_obsolete":false,"name":"chromatin remodeling","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null,"PMID:35226668":null},"secondary_identifiers":["GO:0043044"],"synonyms":[{"name":"ATP-dependent chromatin remodeling","type":"narrow"},{"name":"ATP-dependent chromatin remodelling","type":"narrow"},{"name":"chromatin modeling","type":"exact"},{"name":"chromatin modelling","type":"exact"},{"name":"chromatin remodelling","type":"exact"}],"termid":"GO:0006338","terms_by_termid":{"GO:0000183":null,"GO:0006334":null,"GO:0006337":null,"GO:0006338":null,"GO:0010964":null,"GO:0030466":null,"GO:0031048":null,"GO:0031445":null,"GO:0031453":null,"GO:0031507":null,"GO:0031508":null,"GO:0031509":null,"GO:0033696":null,"GO:0034080":null,"GO:0034728":null,"GO:0040029":null,"GO:0045814":null,"GO:0045815":null,"GO:0060906":null,"GO:0061188":null,"GO:0090052":null,"GO:0090053":null,"GO:0090055":null,"GO:0140462":null,"GO:0140673":null,"GO:0140718":null,"GO:0140719":null,"GO:0140727":null,"GO:0140861":null,"GO:0140898":null,"GO:0141005":null,"GO:0141194":null,"GO:1902794":null,"GO:1902795":null,"GO:1902801":null}}


id: MONDO:0010273
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Hodgkins lymphoma","termid":"MONDO:0004952"}],"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":"lymphoma, Hodgkin, X-linked pseudoautosomal","secondary_identifiers":["OMIM:300221","MESH:C538326","MEDGEN:335352","UMLS:C1846167"],"synonyms":[{"name":"Hodgkin disease susceptibility, pseudoautosomal","type":"exact"},{"name":"Hodgkin disease, X-linked Pseudoautosomal","type":"related"},{"name":"lymphoma, Hodgkin, X-linked pseudoautosomal","type":"exact"}],"termid":"MONDO:0010273","xrefs":{"Monarch":{"xref_id":"0010273"}}}


id: FYPO:0005909
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 formation of the mature 3' end of an RNA molecule is abnormal during a cellular response to endoplasmic reticulum stress.","definition_xrefs":["PomBase:mah","GO:0031123","PMID:23066505"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal RNA 3'-end processing","termid":"FYPO:0007918"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000294"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0006551"],"is_obsolete":false,"name":"abnormal RNA 3'-end processing during cellular response to endoplasmic reticulum stress","synonyms":[{"name":"abnormal RNA 3'-end processing during cellular response to ER stress","type":"exact"},{"name":"abnormal RNA 3'-end processing during cellular response to endoplasmic reticulum stress during mitotic cell cycle","type":"related"},{"name":"abnormal RNA 3'-end processing during cellular response to endoplasmic reticulum stress during vegetative growth","type":"exact"}],"termid":"FYPO:0005909"}


id: MONDO:0007100
data:
  {"annotated_genes":["SJAG_04300"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0971004"}]},"cv_name":"mondo","definition":"A rare genetic systemic disease characterized by adult onset, progressive sensorimotor and autonomic neuropathy and infiltrative cardiomyopathy. Neurological involvement usually starts with sensory loss in the extremities and progresses with motor neuropathy. Cardiomyopathy presents with rhythm abnormalities and heart failure. The disease also frequently manifests with a range of additional clinical signs and symptoms due to associated ocular, renal, central nervous system and gastrointestinal involvement.","definition_xrefs":["Orphanet:271861"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary amyloidosis","termid":"MONDO:0018634"},{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04300":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0021179"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0021179","MONDO:0005066"],"is_obsolete":false,"name":"familial amyloid neuropathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:807065795","OMIMPS:105210","DOID:0050761","MEDGEN:104815","NCIT:C84554","GARD:21017","EFO:0004129","ICD10EXP:E85.1+","ICD9:277.39","MESH:C567782","NANDO:1201060","SCTID:42295001","UMLS:C0206245","DOID:0050638","ICD10EXP:G63.3*","NANDO:1200214"],"synonyms":[{"name":"ATTRv amyloidosis","type":"exact"},{"name":"Corino de Andrade's disease","type":"exact"},{"name":"TTR amyloidosis","type":"exact"},{"name":"amyloid neuropathies, familial","type":"exact"},{"name":"amyloidosis, hereditary, transthyretin-related","type":"exact"},{"name":"familial TTR-related amyloidosis","type":"exact"},{"name":"familial amyloid neuropathy","type":"exact"},{"name":"familial amyloid polyneuropathy","type":"exact"},{"name":"familial transthyretin amyloidosis","type":"exact"},{"name":"familial transthyretin-related amyloidosis","type":"exact"},{"name":"hATTR","type":"exact"},{"name":"hereditary TTR amyloid polyneuropathy","type":"exact"},{"name":"hereditary TTR amyloidosis","type":"exact"},{"name":"hereditary amyloidosis, transthyretin-related","type":"related"},{"name":"hereditary transthyretin amyloid polyneuropathy","type":"exact"},{"name":"paramyloidosis","type":"exact"},{"name":"transthyretin-related hereditary amyloidosis","type":"exact"}],"termid":"MONDO:0007100","terms_by_termid":{"MONDO:0971004":null},"xrefs":{"Monarch":{"xref_id":"0007100"}}}


id: PBO:0027082
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_localization_to_nucleus_during_cellular_response_to_hydrogen_peroxide","termid":"PBO:0027082"}


id: PBO:0084521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of the ChAPs (Chs5p-Arf1p-binding proteins) family; part of the exomer complex that mediates export of specific cargo proteins, including Chs3p, from the Golgi to the plasma membrane; primary component of the Chs5/6 complex that binds directly to membranes; CHS6 has a paralog, BCH2, that arose from the whole genome duplication","termid":"PBO:0084521"}


id: PBO:0065867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB24, member RAS oncogene family","termid":"PBO:0065867"}


id: PBO:0053073
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lamin B receptor","termid":"PBO:0053073"}


id: GO:0042068
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving pteridine.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of metabolic process","termid":"GO:0019222"},{"relation_name":"regulates","term_name":"pteridine metabolic process","termid":"GO:0019889"}],"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 pteridine metabolic process","synonyms":[{"name":"regulation of pteridine metabolism","type":"exact"}],"termid":"GO:0042068"}


id: PBO:0058659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6787","termid":"PBO:0058659"}


id: GO:0036251
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of transcription from an RNA polymerase II promoter as a result of a stimulus indicating the organism is under salt stress. The stress is usually an increase or decrease in the concentration of salt (particularly but not exclusively sodium and chloride ions) in the environment.","definition_xrefs":["GOC:al"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter in response to salt stress (obsolete GO:0036251)","termid":"GO:0036251"}


id: PBO:0079810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UDP glycosyltransferase family 3 member A2","termid":"PBO:0079810"}


id: PBO:0067219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 286, pseudogene","termid":"PBO:0067219"}


id: GO:1902121
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to lithocholic acid.","definition_xrefs":["GOC:TermGenie","GOC:bf","PMID:20371703"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid binding","termid":"GO:0005496"},{"relation_name":"is_a","term_name":"bile acid binding","termid":"GO:0032052"}],"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:0008289"}],"interesting_parent_ids":["GO:0005488","GO:0008289","GO:0003674"],"is_obsolete":false,"name":"lithocholic acid binding","synonyms":[{"name":"LCA binding","type":"exact"}],"termid":"GO:1902121"}


id: PBO:0070926
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 34","termid":"PBO:0070926"}


id: _global:has_divisor_quality
data:
  {"annotation_feature_type":"gene","cv_name":"quality","direct_ancestors":[{"relation_name":"is_a","term_name":"has_ratio_quality","termid":"_global:has_ratio_quality"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_divisor_quality","termid":"_global:has_divisor_quality"}


id: PBO:0052242
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium channel tetramerization domain containing 12","termid":"PBO:0052242"}


id: PBO:0073875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 10 member 3","termid":"PBO:0073875"}


id: PBO:0078210
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 7-3","termid":"PBO:0078210"}


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


id: PBO:0057695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1284","termid":"PBO:0057695"}


id: GO:0097029
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which antigen-activated dendritic cells acquire the specialized features of a mature conventional dendritic cell. Mature conventional dendritic cells upregulate the surface expression of MHC molecules, chemokine receptors and adhesion molecules, and increase the number of dendrites (cytoplasmic protrusions) in preparation for migration to lymphoid organs where they present antigen to T cells.","definition_xrefs":["GOC:BHF","PMID:15845453"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid leukocyte differentiation","termid":"GO:0002573"},{"relation_name":"is_a","term_name":"dendritic cell differentiation","termid":"GO:0097028"}],"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":"mature conventional dendritic cell differentiation","termid":"GO:0097029"}


id: PBO:0069687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 966, pseudogene","termid":"PBO:0069687"}


id: PR:Q9C0Z3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- slx9 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9C0Z3"],"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":"ribosome biogenesis protein slx9 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB21F2.03","synonyms":[{"name":"Spom972h-slx9","type":"exact"}],"termid":"PR:Q9C0Z3"}


id: FYPO:0001269
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the kinetochore of a chromosome is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to centromere during vegetative growth","termid":"FYPO:0000634"},{"relation_name":"is_a","term_name":"decreased protein localization to kinetochore during vegetative growth","termid":"FYPO:0002902"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000138","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"abolished protein localization to kinetochore during vegetative growth","synonyms":[{"name":"abolished protein localisation to kinetochore during vegetative growth","type":"exact"},{"name":"abolished protein localization to kinetochore during mitotic cell cycle","type":"related"},{"name":"protein localization to kinetochore abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0001269"}


id: PR:Q9P6M5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC652.01 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P6M5"],"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 C652.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC652.01","synonyms":[{"name":"Spom972h-SPAC652.01","type":"exact"}],"termid":"PR:Q9P6M5"}


id: PBO:0012275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SIP/FAR complex subunit, Far11/Csc2","termid":"PBO:0012275"}


id: GO:2001194
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of lysine biosynthetic process via alpha-aminoadipate and saccharopine.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lysine biosynthetic process via aminoadipic acid","termid":"GO:1902986"},{"relation_name":"regulates","term_name":"lysine biosynthetic process via alpha-aminoadipate and saccharopine","termid":"GO:0051975"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"regulation of lysine biosynthetic process via alpha-aminoadipate and saccharopine","synonyms":[{"name":"regulation of lysine biosynthesis via aminoadipic acid and saccharopine","type":"exact"},{"name":"regulation of lysine biosynthetic process via aminoadipic acid and saccharopine","type":"exact"}],"termid":"GO:2001194"}


id: MONDO:0100460
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing nicotine dependence.","definition_xrefs":["MONDO:patterns/inherited_susceptibility"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tobacco addiction, susceptibility to","secondary_identifiers":["OMIM:188890","MEDGEN:348778","UMLS:C1861063"],"synonyms":[{"name":"cigarette habituation, susceptibility to","type":"exact"},{"name":"nicotine addiction, protection from","type":"exact"},{"name":"nicotine addiction, susceptibility to","type":"exact"},{"name":"nicotine dependence, protection against","type":"exact"},{"name":"nicotine dependence, susceptibility to","type":"exact"},{"name":"smoking habit, susceptibility to","type":"exact"},{"name":"susceptibility to tobacco addiction","type":"exact"},{"name":"tobacco addiction, susceptibility to","type":"exact"}],"termid":"MONDO:0100460","xrefs":{"Monarch":{"xref_id":"0100460"}}}


id: GO:0061836
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A macromolecular fiber consisting of actin and cofilin that is formed in the nucleus as a consequence of chemical or mechanical stress conditions.","definition_xrefs":["PMID:28074884"],"direct_ancestors":[{"relation_name":"is_a","term_name":"supramolecular fiber","termid":"GO:0099512"}],"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":"intranuclear rod","synonyms":[{"name":"intranuclear actin rod","type":"exact"}],"termid":"GO:0061836"}


id: GO:0009206
data:
  {"annotated_genes":["SJAG_02105","SJAG_03114","SJAG_07003","SJAG_MIT37","SJAG_MIT15","SJAG_00915","SJAG_02564","SJAG_04849","SJAG_04122","SJAG_03925","SJAG_05204","SJAG_00985","SJAG_01298","SJAG_00133","SJAG_00836","SJAG_04422","SJAG_MIT09","SJAG_02887","SJAG_00542","SJAG_00438","SJAG_02598"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[76675,65611,104183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006183"},{"annotations":[120038],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905707"},{"annotations":[94746,105601,121112,121118,117867,96754,91007,109785,110775,95764,105627,106977,121124,104984,103763,109877,95173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042776"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of purine ribonucleoside triphosphate, a compound consisting of a purine base linked to a ribose sugar esterified with triphosphate on the sugar.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleoside triphosphate biosynthetic process","termid":"GO:0009145"},{"relation_name":"is_a","term_name":"ribonucleoside triphosphate biosynthetic process","termid":"GO:0009201"},{"relation_name":"is_a","term_name":"purine ribonucleoside triphosphate metabolic process","termid":"GO:0009205"}],"gene_count":21,"genes_by_uniquename":{"SJAG_00133":null,"SJAG_00438":null,"SJAG_00542":null,"SJAG_00836":null,"SJAG_00915":null,"SJAG_00985":null,"SJAG_01298":null,"SJAG_02105":null,"SJAG_02564":null,"SJAG_02598":null,"SJAG_02887":null,"SJAG_03114":null,"SJAG_03925":null,"SJAG_04122":null,"SJAG_04422":null,"SJAG_04849":null,"SJAG_05204":null,"SJAG_07003":null,"SJAG_MIT09":null,"SJAG_MIT15":null,"SJAG_MIT37":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"purine ribonucleoside triphosphate biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"purine ribonucleoside triphosphate anabolism","type":"exact"},{"name":"purine ribonucleoside triphosphate biosynthesis","type":"exact"},{"name":"purine ribonucleoside triphosphate formation","type":"exact"},{"name":"purine ribonucleoside triphosphate synthesis","type":"exact"}],"termid":"GO:0009206","terms_by_termid":{"GO:0006183":null,"GO:0042776":null,"GO:1905707":null}}


id: PBO:0044151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTD nuclear envelope phosphatase 1","termid":"PBO:0044151"}


id: GO:1990110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process by which a callus is formed at a wound site. A plant callus is a portion of plant tissue that consists of mass of undifferentiated plant cells. It consists primarily of parenchyma cells but possibly contains other cell types as the callus begins to differentiate.","definition_xrefs":["ISBN:0070187517"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"part_of","term_name":"wound healing","termid":"GO:0042060"}],"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":"callus formation","termid":"GO:1990110"}


id: GO:1901865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of capsorubin.","definition_xrefs":["UniPathway:UPA00807","GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xanthophyll catabolic process","termid":"GO:0016124"},{"relation_name":"is_a","term_name":"capsorubin metabolic process","termid":"GO:1901864"}],"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":"capsorubin catabolic process","synonyms":[{"name":"capsorubin breakdown","type":"exact"},{"name":"capsorubin catabolism","type":"exact"},{"name":"capsorubin degradation","type":"exact"}],"termid":"GO:1901865"}


id: GO:0002790
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The controlled release of a peptide from a cell or a tissue.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide transport","termid":"GO:0015833"},{"relation_name":"is_a","term_name":"secretion","termid":"GO:0046903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"peptide secretion","termid":"GO:0002790"}


id: GO:0050936
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a xanthophore cell. Xanthophores are pigment cells derived from the neural crest. They contain pteridine and/or carotenoid pigments in structures called pterinosomes or xanthosomes. This makes them yellow to orange in appearance.","definition_xrefs":["GOC:jid","PMID:11858836","GOC:mh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pigment cell differentiation","termid":"GO:0050931"}],"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":"xanthophore differentiation","synonyms":[{"name":"xanthophore cell differentiation","type":"exact"}],"termid":"GO:0050936"}


id: GO:1904528
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of microtubule binding.","definition_xrefs":["GO_REF:0000059","PMID:24520051","GOC:als","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of microtubule binding (obsolete GO:1904528)","synonyms":[{"name":"activation of microtubule binding","type":"narrow"},{"name":"activation of microtubule severing activity","type":"related"},{"name":"activation of microtubule/chromatin interaction","type":"related"},{"name":"positive regulation of microtubule severing activity","type":"related"},{"name":"positive regulation of microtubule/chromatin interaction","type":"related"},{"name":"up regulation of microtubule binding","type":"exact"},{"name":"up regulation of microtubule severing activity","type":"related"},{"name":"up regulation of microtubule/chromatin interaction","type":"related"},{"name":"up-regulation of microtubule binding","type":"exact"},{"name":"up-regulation of microtubule severing activity","type":"related"},{"name":"up-regulation of microtubule/chromatin interaction","type":"related"},{"name":"upregulation of microtubule binding","type":"exact"},{"name":"upregulation of microtubule severing activity","type":"related"},{"name":"upregulation of microtubule/chromatin interaction","type":"related"}],"termid":"GO:1904528"}


id: GO:0047807
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 6-alkylaminopurine + UDP-D-glucose = 6-alkylamino-7-beta-D-glucosylpurine + H+ + UDP. This reaction is an N-glucosylation event.","definition_xrefs":["EC:2.4.1.118","MetaCyc:CYTOKININ-7-BETA-GLUCOSYLTRANSFERASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016757"],"is_obsolete":false,"name":"cytokinin 7-beta-glucosyltransferase activity","secondary_identifiers":["KEGG_REACTION:R04071","RHEA:23272"],"synonyms":[{"name":"UDP-glucose-zeatin 7-glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:zeatin 7-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:zeatin 7-glucosyltransferase activity","type":"related"},{"name":"cytokinin 7-b-glucosyltransferase activity","type":"exact"},{"name":"cytokinin 7-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-zeatin 7-glucosyltransferase activity","type":"related"}],"termid":"GO:0047807"}


id: GO:0010247
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a phosphate ion stimulus is received by a cell and converted into a molecular signal.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of chemical stimulus","termid":"GO:0009593"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of phosphate ion","synonyms":[{"name":"phosphate ion detection","type":"exact"},{"name":"phosphate ion perception","type":"related"},{"name":"phosphate ion sensing","type":"related"}],"termid":"GO:0010247"}


id: PR:Q9P4W1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cox8 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P4W1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase polypeptide VIII, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24C9.16c","synonyms":[{"name":"Spom972h-cox8","type":"exact"}],"termid":"PR:Q9P4W1"}


id: MONDO:0700112
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any visceral hetetotaxy in which the cause of the disease is a mutation in the NODAL gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"visceral heterotaxy","termid":"MONDO:0018677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterotaxy, visceral, 5, autosomal","secondary_identifiers":["UMLS:C3495537","MEDGEN:501198","OMIM:270100"],"synonyms":[{"name":"HTX5","type":"exact"},{"name":"NODAL visceral heterotaxy","type":"exact"},{"name":"SIV","type":"exact"},{"name":"situs inversus viscerum","type":"exact"},{"name":"visceral heterotaxy caused by mutation in NODAL","type":"exact"}],"termid":"MONDO:0700112","xrefs":{"Monarch":{"xref_id":"0700112"}}}


id: MONDO:0017426
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic polydactyly","termid":"MONDO:0011348"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postaxial polydactyly of fingers","secondary_identifiers":["Orphanet:294942","icd11.foundation:1146378807","SCTID:205131007","MEDGEN:609221","GARD:12460","UMLS:C0431904"],"synonyms":[{"name":"postaxial polydactyly of hand","type":"exact"}],"termid":"MONDO:0017426","xrefs":{"Monarch":{"xref_id":"0017426"}}}


id: GO:0014801
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the free sarcoplasmic reticulum consisting of longitudinal tubules that connect terminal cisternae.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"sarcoplasmic reticulum","termid":"GO:0016529"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005783","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"longitudinal sarcoplasmic reticulum","termid":"GO:0014801"}


id: GO:0140404
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process mediated by a molecule secreted by a symbiont that results in the modulation (either activation or suppression) of a host innate immune response. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:21467214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host innate immune response","termid":"GO:0052167"},{"relation_name":"is_a","term_name":"effector-mediated perturbation of host defenses by symbiont","termid":"GO:0140415"}],"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":"effector-mediated perturbation of host innate immune response by symbiont","synonyms":[{"name":"effector mediated modulation of host immune response by symbiont","type":"exact"},{"name":"effector triggered modulation of host immune response by symbiont","type":"exact"},{"name":"effector-dependent modulation of host immune response by symbiont","type":"exact"},{"name":"effector-mediated modulation of host immunity","type":"exact"},{"name":"effector-mediated modulation of host innate immune response by symbiont","type":"exact"},{"name":"effector-triggered modulation of host immune response by symbiont","type":"exact"}],"termid":"GO:0140404"}


id: FYPO:0002762
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce an inviable cell that does not divide, and that is shaped in the form of a spheroid. In spheroid cells, there is much less difference between the long and short axes of the cell than in wild type.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division","termid":"FYPO:0001991"},{"relation_name":"is_a","term_name":"inviable spheroid vegetative cell","termid":"FYPO:0002482"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0000005","FYPO:0000004"],"is_obsolete":false,"name":"inviable after spore germination, without cell division, spheroid cell","synonyms":[{"name":"inviable after spore germination, undivided spheroid cell","type":"exact"},{"name":"inviable following spore germination, without cell division, spheroid cell","type":"exact"},{"name":"inviable germinated spore, without cell division, spheroid cell","type":"exact"},{"name":"lethal after spore germination, without cell division, spheroid cell","type":"exact"}],"termid":"FYPO:0002762"}


id: PBO:0090928
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mevalonate kinase Erg12","termid":"PBO:0090928"}


id: PBO:0057653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1245b","termid":"PBO:0057653"}


id: MONDO:0024561
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any vitelliform macular dystrophy in which the cause of the disease is a mutation in the PRPH2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adult-onset foveomacular vitelliform dystrophy","termid":"MONDO:0011979"},{"relation_name":"is_a","term_name":"PRPH2-related retinopathy","termid":"MONDO:1040055"}],"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":"vitelliform macular dystrophy 3","secondary_identifiers":["OMIM:608161"],"synonyms":[{"name":"PRPH2 vitelliform macular dystrophy","type":"exact"},{"name":"VMD3","type":"related"},{"name":"foveomacular dystrophy, adult-onset","type":"related"},{"name":"foveomacular dystrophy, adult-onset, with or without choroidal neovascularization","type":"related"},{"name":"macular dystrophy, vitelliform, 3","type":"related"},{"name":"vitelliform macular dystrophy caused by mutation in PRPH2","type":"exact"},{"name":"vitelliform macular dystrophy, adult-onset","type":"related"}],"termid":"MONDO:0024561","xrefs":{"Monarch":{"xref_id":"0024561"}}}


id: PBO:0086016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; SWAT-GFP, seamless-GFP and mCherry fusion proteins localize to cytosol; conserved among Saccharomyces sensu stricto species","termid":"PBO:0086016"}


id: PBO:0030716
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_glucosyltransferase_activity","termid":"PBO:0030716"}


id: MONDO:0008279
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete familial adenomatous polyposis type 1 (obsolete MONDO:0008279)","termid":"MONDO:0008279","xrefs":{"Monarch":{"xref_id":"0008279"}}}


id: GO:0009133
data:
  {"annotated_genes":["SJAG_04657","SJAG_00885","SJAG_02038","SJAG_04665","SJAG_00779","SJAG_02874"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006172"},{"annotations":[82220],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046705"},{"annotations":[109229,94330,97401],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006240"},{"annotations":[72797],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006233"},{"annotations":[72796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006227"},{"annotations":[82219],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006225"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a nucleoside diphosphate, a compound consisting of a nucleobase linked to a deoxyribose or ribose sugar esterified with diphosphate on the sugar.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside diphosphate metabolic process","termid":"GO:0009132"},{"relation_name":"is_a","term_name":"nucleoside phosphate biosynthetic process","termid":"GO:1901293"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00779":null,"SJAG_00885":null,"SJAG_02038":null,"SJAG_02874":null,"SJAG_04657":null,"SJAG_04665":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"nucleoside diphosphate biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"nucleoside diphosphate anabolism","type":"exact"},{"name":"nucleoside diphosphate biosynthesis","type":"exact"},{"name":"nucleoside diphosphate formation","type":"exact"},{"name":"nucleoside diphosphate synthesis","type":"exact"}],"termid":"GO:0009133","terms_by_termid":{"GO:0006172":null,"GO:0006225":null,"GO:0006227":null,"GO:0006233":null,"GO:0006240":null,"GO:0046705":null}}


id: PBO:0051131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 2-70","termid":"PBO:0051131"}


id: GO:0008937
data:
  {"annotated_genes":["SJAG_01063"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[111675],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008860"},{"annotations":[111676],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004324"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: reduced ferredoxin + NAD(P)+ = oxidized ferredoxin + NAD(P)H + H+.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor","termid":"GO:0016731"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01063":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"ferredoxin-[NAD(P)H] reductase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"ferredoxin reductase activity","type":"broad"}],"termid":"GO:0008937","terms_by_termid":{"GO:0004324":null,"GO:0008860":null}}


id: PBO:0081160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger RNA binding protein","termid":"PBO:0081160"}


id: GO:0102449
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: kaempferol + S-adenosyl-L-methionine = 3-O-methylkaempferol + H+ + S-adenosyl-L-homocysteine.","definition_xrefs":["RHEA:74743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase activity","termid":"GO:0008168"}],"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:0016741"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016741","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"kaempferol 3-O-methyltransferase activity","secondary_identifiers":["MetaCyc:RXN-13935"],"termid":"GO:0102449"}


id: GO:0072104
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to a glomerular capillary. This process pertains to the initial formation of a structure from unspecified parts.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"angiogenesis","termid":"GO:0001525"},{"relation_name":"part_of","term_name":"glomerulus vasculature morphogenesis","termid":"GO:0072103"}],"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":"glomerular capillary formation","termid":"GO:0072104"}


id: GO:1903232
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a melanosome, a tissue-specific, membrane-bounded cytoplasmic organelle within which melanin pigments are synthesized and stored.","definition_xrefs":["GOC:PARL","GOC:bf","GO_REF:0000079","PMID:22511774","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanosome organization","termid":"GO:0032438"},{"relation_name":"is_a","term_name":"organelle assembly","termid":"GO:0070925"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"melanosome assembly","synonyms":[{"name":"melanosome formation","type":"exact"}],"termid":"GO:1903232"}


id: PBO:0089702
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glycoside Hydrolase family protein Gls1","termid":"PBO:0089702"}


id: MONDO:1011232
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Entropion that occurs in rabbit.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"entropion, non-human animal","termid":"MONDO:1010323"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"entropion, rabbit","secondary_identifiers":["OMIA:000337-9986"],"termid":"MONDO:1011232","xrefs":{"Monarch":{"xref_id":"1011232"}}}


id: PBO:0073707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SKI/DACH domain containing 1","termid":"PBO:0073707"}


id: PR:Q9UTQ7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- arp9 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UTQ7"],"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":"SWI/SNF and RSC complexes subunit arp9 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1071.06","synonyms":[{"name":"Spom972h-arp9","type":"exact"},{"name":"actin-like protein arp9 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"actin-related protein 9 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"chromatin structure-remodeling complex subunit arp9 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UTQ7"}


id: MONDO:0007072
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"ADULT (Acro-dermo-ungual-lacrimal-tooth) syndrome is a rare ectodermal dysplasia syndrome characterized by ectrodactyly, syndactyly, mammary hypoplasia, and excessive freckling as well as other typical ectodermal defects such as hypodontia, lacrimal duct anomalies, hypotrichosis, and onychodysplasia.","definition_xrefs":["Orphanet:978"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"},{"relation_name":"is_a","term_name":"TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations","termid":"MONDO:1040001"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0005093","MONDO:0000426"],"is_obsolete":false,"name":"ADULT syndrome","secondary_identifiers":["icd11.foundation:1445741645","DOID:0050601","MESH:C538052","OMIM:103285","MEDGEN:400232","SCTID:720464003","UMLS:C1863204","GARD:384"],"synonyms":[{"name":"ADULT syndrome","type":"exact"},{"name":"acro dermato ungual lacrimal tooth syndrome","type":"related"},{"name":"acro-dermato-ungual-lacrimal-Tooth syndrome","type":"related"},{"name":"acro-dermato-ungual-lacrimal-tooth syndrome","type":"exact"},{"name":"acrodermatounguallacrimaltooth syndrome","type":"exact"},{"name":"pigment anomaly-ectrodactyly-hypodontia syndrome","type":"exact"}],"termid":"MONDO:0007072","xrefs":{"Monarch":{"xref_id":"0007072"}}}


id: PR:O75001
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA replication licensing factor MCM7 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03822","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 replication licensing factor mcm7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC25D12.03c","secondary_identifiers":["UniProtKB:O75001"],"synonyms":[{"name":"Spom972h-MCM7","type":"exact"},{"name":"minichromosome maintenance protein 7 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O75001"}


id: PBO:0111894
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"armadillo repeat protein","termid":"PBO:0111894"}


id: PBO:0081499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 397","termid":"PBO:0081499"}


id: PBO:0076930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor binding to IGHM enhancer 3","termid":"PBO:0076930"}


id: PBO:0041341
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 3 open reading frame 38","termid":"PBO:0041341"}


id: PBO:0059832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metal response element binding transcription factor 2","termid":"PBO:0059832"}


id: PBO:0077829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TP53 target 3 family member H, pseudogene","termid":"PBO:0077829"}


id: PBO:0072226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S20 pseudogene 1","termid":"PBO:0072226"}


id: GO:0010814
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of the neuropeptide substance P.","definition_xrefs":["GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuropeptide catabolic process","termid":"GO:0010813"},{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"}],"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":"substance P catabolic process","termid":"GO:0010814"}


id: SO:0000552
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region in the 5' UTR that pairs with the 16S rRNA during formation of the preinitiation complex.","definition_xrefs":["SO:jh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribosome_entry_site","termid":"SO:0000139"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Shine_Dalgarno_sequence","secondary_identifiers":["http://en.wikipedia.org/wiki/Shine-Dalgarno_sequence"],"synonyms":[{"name":"RBS","type":"related"},{"name":"Shine Dalgarno sequence","type":"exact"},{"name":"Shine-Dalgarno sequence","type":"exact"},{"name":"five prime ribosome binding site","type":"exact"}],"termid":"SO:0000552"}


id: GO:0010570
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the process in which a multicellular organism or a group of unicellular organisms grow in a threadlike, filamentous shape.","definition_xrefs":["GOC:dph","GOC:jp","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of growth","termid":"GO:0040008"},{"relation_name":"regulates","term_name":"filamentous growth","termid":"GO:0030447"}],"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 filamentous growth","termid":"GO:0010570"}


id: GO:1902170
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 reactive nitrogen species stimulus.","definition_xrefs":["PMID:22504638","GOC:TermGenie","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"}],"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 reactive nitrogen species","secondary_identifiers":["GO:1990106"],"termid":"GO:1902170"}


id: PBO:0078695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Leu (anticodon AAG) 6-1","termid":"PBO:0078695"}


id: PBO:0003646
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDG-Ii","termid":"PBO:0003646"}


id: FYPO:0005878
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"Auxotrophy in which a cell is unable to synthesize tryptophan, and therefore requires tryptophan in the medium for vegetative cell growth.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auxotrophy","termid":"FYPO:0000128"},{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype","termid":"FYPO:0004638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"growth auxotrophic for tryptophan","synonyms":[{"name":"growth auxotrophic for tryptophan during mitotic cell cycle","type":"related"},{"name":"growth auxotrophic for tryptophan during vegetative growth","type":"exact"},{"name":"tryptophan auxotrophy","type":"exact"}],"termid":"FYPO:0005878"}


id: PR:O42953
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC19G7.04 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42953"],"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":"HMG box-containing protein C19G7.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19G7.04","synonyms":[{"name":"Spom972h-SPBC19G7.04","type":"exact"}],"termid":"PR:O42953"}


id: SO:1000074
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant causing a new (functional) splice site.","definition_xrefs":["EBI:www.ebi.ac.uk/mutations/recommendations/mutevent.html"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000074 sequence_variant_causing_cryptic_splice_activation (obsolete SO:1000074)","synonyms":[{"name":"cryptic splice activator sequence variant","type":"exact"},{"name":"mutation causing cryptic splice activator","type":"related"},{"name":"sequence variant causing cryptic splice activator","type":"exact"}],"termid":"SO:1000074"}


id: PBO:0087500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of GID complex; involved in proteasome-dependent catabolite inactivation of gluconeogenic enzymes FBPase, PEPCK, and c-MDH; forms dimer with Rmd5p that is then recruited to GID Complex by Gid8p; contains a degenerate RING finger motif needed for GID complex ubiquitin ligase activity in vivo, as well as CTLH and CRA domains; plays role in anti-apoptosis; required for survival upon exposure to K1 killer toxin","termid":"PBO:0087500"}


id: PBO:0044924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diacylglycerol kinase alpha","termid":"PBO:0044924"}


id: PBO:0034457
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_localization_to_chromatin_at_MCB_promoters","termid":"PBO:0034457"}


id: MONDO:0010697
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":"ophthalmoplegia, external, and myopia","secondary_identifiers":["MESH:C564087","UMLS:C1839577","MEDGEN:326916","OMIM:311000"],"synonyms":[{"name":"OPEM","type":"exact"},{"name":"myopia-ophthalmoplegia syndrome","type":"related"},{"name":"ophthalmoplegia, external, and myopia","type":"exact"}],"termid":"MONDO:0010697","xrefs":{"Monarch":{"xref_id":"0010697"}}}


id: SO:0002196
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A (unitary) pseudogene that is stable in the population but importantly it has a functional alternative allele also in the population. i.e., one strain may have the gene, another strain may have the pseudogene. MHC haplotypes have allelic pseudogenes.","direct_ancestors":[{"relation_name":"is_a","term_name":"pseudogenic_rRNA","termid":"SO:0000777"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"allelic_pseudogenic_rRNA","synonyms":[{"name":"INSDC_feature:rRNA","type":"broad"},{"name":"INSDC_qualifier:allelic","type":"exact"},{"name":"allelic pseudogenic rRNA","type":"exact"}],"termid":"SO:0002196"}


id: GO:0032799
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving low-density lipoprotein receptors.","definition_xrefs":["GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor metabolic process","termid":"GO:0043112"}],"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":"low-density lipoprotein receptor particle metabolic process","synonyms":[{"name":"LDL receptor metabolic process","type":"exact"},{"name":"low-density lipoprotein receptor metabolic process","type":"exact"},{"name":"low-density lipoprotein receptor metabolism","type":"exact"}],"termid":"GO:0032799"}


id: FYPO:0006717
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing sodium chloride, usually at a higher level than in standard media.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002058","FYPO:0000139","FYPO:0002060","FYPO:0000257","FYPO:0002057"],"is_obsolete":false,"name":"normal growth on sodium chloride","synonyms":[{"name":"normal cell population growth in presence of sodium chloride","type":"exact"},{"name":"normal cell population growth on sodium chloride","type":"exact"},{"name":"normal cellular response to sodium chloride","type":"related"},{"name":"normal growth on NaCl","type":"exact"},{"name":"normal vegetative cell population growth on sodium chloride","type":"exact"}],"termid":"FYPO:0006717"}


id: PBO:0072553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RRAD, Ras related glycolysis inhibitor and calcium channel regulator","termid":"PBO:0072553"}


id: GO:0047201
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 1-O-galloyl-beta-D-glucose = 1,6-bis-O-galloyl-beta-D-glucose + D-glucose.","definition_xrefs":["EC:2.3.1.90","RHEA:11416"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"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"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016746","GO:0003674"],"is_obsolete":false,"name":"beta-glucogallin O-galloyltransferase activity","secondary_identifiers":["MetaCyc:2.3.1.90-RXN","KEGG_REACTION:R00049"],"synonyms":[{"name":"1-O-galloyl-beta-D-glucose:1-O-galloyl-beta-D-glucose O-galloyltransferase activity","type":"related"}],"termid":"GO:0047201"}


id: PBO:0064928
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 6 regulatory subunit 2","termid":"PBO:0064928"}


id: GO:0140919
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The suite of morphological and architectural changes in an organism induced by high ambient temperatures, below the heat-stress range.","definition_xrefs":["PMID:27250752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to temperature stimulus","termid":"GO:0009266"},{"relation_name":"is_a","term_name":"post-embryonic development","termid":"GO:0009791"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"thermomorphogenesis","termid":"GO:0140919"}


id: PBO:0039115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha hemoglobin stabilizing protein","termid":"PBO:0039115"}


id: PBO:0068018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 323","termid":"PBO:0068018"}


id: GO:0046797
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The refolding and structural rearrangements of individual capsid subunits to transition from the intermediate procapsid, to the more stable capsid structure.","definition_xrefs":["PMID:10627558","GOC:bf","PMID:19204733"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"part_of","term_name":"viral capsid assembly","termid":"GO:0019069"},{"relation_name":"part_of","term_name":"virus maturation","termid":"GO:0019075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"viral procapsid maturation","secondary_identifiers":["UniProtKB-KW:KW-1273"],"synonyms":[{"name":"capsid maturation","type":"exact"},{"name":"viral capsid maturation","type":"exact"},{"name":"virion maturation","type":"broad"}],"termid":"GO:0046797"}


id: GO:0075054
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of symbiont penetration peg formation for entry into host. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"is_a","term_name":"modulation by symbiont of entry into host","termid":"GO:0052372"},{"relation_name":"regulates","term_name":"penetration peg formation","termid":"GO:0075053"}],"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 penetration peg formation","secondary_identifiers":["GO:0075058"],"synonyms":[{"name":"modulation of symbiont penetration peg formation for entry into host","type":"narrow"},{"name":"modulation of symbiont penetration peg initiation","type":"narrow"}],"termid":"GO:0075054"}


id: GO:0033897
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a ribonucleotidyl-ribonucleotide-RNA + H2O = a 3'-end 3'-phospho-ribonucleotide-RNA + a 5'-end dephospho-ribonucleoside-RNA + H+. This reaction is a two-stage endonucleolytic cleavage to nucleoside 3'-phosphates and 3'-phosphooligonucleotides with 2',3'-cyclic phosphate intermediates.","definition_xrefs":["RHEA:68052","EC:4.6.1.19"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA endonuclease activity","termid":"GO:0004521"},{"relation_name":"is_a","term_name":"phosphorus-oxygen lyase activity","termid":"GO:0016849"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674","GO:0140098"],"is_obsolete":false,"name":"ribonuclease T2 activity","secondary_identifiers":["MetaCyc:3.1.27.5-RXN"],"synonyms":[{"name":"Escherichia coli ribonuclease I' ribonuclease PP2 activity","type":"exact"},{"name":"Escherichia coli ribonuclease II activity","type":"related"},{"name":"RNAase CL activity","type":"exact"},{"name":"RNase (non-base specific) activity","type":"exact"},{"name":"RNase II activity","type":"broad"},{"name":"RNase M activity","type":"related"},{"name":"RNase Ms activity","type":"exact"},{"name":"RNase T2 activity","type":"related"},{"name":"acid RNase activity","type":"exact"},{"name":"acid ribonuclease activity","type":"exact"},{"name":"base-non-specific ribonuclease activity","type":"exact"},{"name":"non-base specific ribonuclease activity","type":"exact"},{"name":"nonbase-specific RNase activity","type":"exact"},{"name":"nonspecific RNase activity","type":"exact"},{"name":"ribonnuclease (non-base specific) activity","type":"exact"},{"name":"ribonuclease (non-base specific) activity","type":"related"},{"name":"ribonuclease II activity","type":"broad"},{"name":"ribonuclease M activity","type":"exact"},{"name":"ribonuclease N2 activity","type":"exact"},{"name":"ribonuclease PP3 activity","type":"related"},{"name":"ribonuclease U4 activity","type":"exact"},{"name":"ribonucleate 3'-oligonucleotide hydrolase activity","type":"exact"},{"name":"ribonucleate nucleotido-2'-transferase (cyclizing) activity","type":"broad"}],"termid":"GO:0033897"}


id: PBO:0033757
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitotic_spindle_pole_body_duplication","termid":"PBO:0033757"}


id: GO:1903780
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cardiac conduction.","definition_xrefs":["GOC:rph","GOC:TermGenie","PMID:12967627","GO_REF:0000058","GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biological process","termid":"GO:0048519"},{"relation_name":"is_a","term_name":"regulation of cardiac conduction","termid":"GO:1903779"},{"relation_name":"negatively_regulates","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":"negative regulation of cardiac conduction","synonyms":[{"name":"down regulation of cardiac conduction","type":"exact"},{"name":"down-regulation of cardiac conduction","type":"exact"},{"name":"downregulation of cardiac conduction","type":"exact"},{"name":"inhibition of cardiac conduction","type":"narrow"}],"termid":"GO:1903780"}


id: GO:0002643
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of tolerance induction.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of immune system process","termid":"GO:0002682"},{"relation_name":"regulates","term_name":"tolerance induction","termid":"GO:0002507"}],"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 tolerance induction","termid":"GO:0002643"}


id: PBO:0089094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear/mitochondrial metal-dependent protein hydrolase, human MYG1 ortholog","termid":"PBO:0089094"}


id: PBO:0081342
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 142","termid":"PBO:0081342"}


id: PBO:0108936
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL7L1 pseudogene 15","termid":"PBO:0108936"}


id: PBO:0073757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 2 member 11","termid":"PBO:0073757"}


id: PBO:0055161
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 2580","termid":"PBO:0055161"}


id: SO:0001323
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Archaeosine is a modified 7-deazoguanosine.","direct_ancestors":[{"relation_name":"is_a","term_name":"seven_deazaguanosine","termid":"SO:0001316"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"archaeosine","secondary_identifiers":["RNAMOD:049"],"synonyms":[{"name":"G+","type":"exact"}],"termid":"SO:0001323"}


id: PBO:0072019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S8 pseudogene 6","termid":"PBO:0072019"}


id: PBO:0083276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; not conserved in closely related Saccharomyces species; deletion mutation blocks replication of Brome mosaic virus in S. cerevisiae, but this is likely due to effects on the overlapping gene SCS2","termid":"PBO:0083276"}


id: PBO:0079261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TTC32 divergent transcript","termid":"PBO:0079261"}


id: PBO:0080305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 69 pseudogene","termid":"PBO:0080305"}


id: GO:0042170
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Either of the lipid bilayers that surround a plastid and form the plastid envelope.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle membrane","termid":"GO:0031090"},{"relation_name":"part_of","term_name":"plastid envelope","termid":"GO:0009526"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"plastid membrane","termid":"GO:0042170"}


id: SO:0001393
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A post translationally modified tryptophan amino acid feature.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified_amino_acid_feature","termid":"SO:0001385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modified_L_tryptophan","secondary_identifiers":["MOD:00918"],"synonyms":[{"name":"ModTrp","type":"exact"},{"name":"modified L tryptophan","type":"exact"},{"name":"modified L-tryptophan","type":"exact"}],"termid":"SO:0001393"}


id: PBO:0004040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDP-diacylglycerol-glycerol-3-phosphate3-phosphatidyltransferase(predicted)","termid":"PBO:0004040"}


id: PBO:0053286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIM and calponin homology domains 1","termid":"PBO:0053286"}


id: GO:0003953
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NAD+ + H2O = ADP-D-ribose + nicotinamide + H+.","definition_xrefs":["PMID:7805847","RHEA:16301","PMID:11866528"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing N-glycosyl compounds","termid":"GO:0016799"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0016798","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"NAD+ nucleosidase activity","secondary_identifiers":["MetaCyc:RXN-13859","EC:3.2.2.5"],"synonyms":[{"name":"DPNase activity","type":"exact"},{"name":"NAD glycohydrolase activity","type":"exact"},{"name":"NAD nucleosidase activity","type":"exact"},{"name":"NAD(+) glycohydrolase activity","type":"exact"},{"name":"NADase activity","type":"exact"},{"name":"beta-NAD(+) glycohydrolase activity","type":"exact"},{"name":"diphosphopyridine nucleosidase activity","type":"exact"},{"name":"nicotinamide adenine dinucleotide glycohydrolase activity","type":"exact"},{"name":"nicotinamide adenine dinucleotide nucleosidase activity","type":"exact"}],"termid":"GO:0003953"}


id: PBO:0088853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane TRP-like calcium ion channel Trp1322","termid":"PBO:0088853"}


id: MOD:00663
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to a methylated lysine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylated residue","termid":"MOD:00427"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"methylated lysine","synonyms":[{"name":"MeLys","type":"exact"}],"termid":"MOD:00663"}


id: MOD:00944
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label","definition_xrefs":["Unimod:477"],"direct_ancestors":[{"relation_name":"is_a","term_name":"4-trimethylammoniumbutanoyl derivatized residue","termid":"MOD:00943"},{"relation_name":"is_a","term_name":"(2)H deuterium tagged reagent","termid":"MOD:01431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"d9-4-trimethylammoniumbutanoyl derivatized residue","synonyms":[{"name":"TMAB:2H(9)","type":"related"},{"name":"d9-4-trimethyllammoniumbutyryl-","type":"related"}],"termid":"MOD:00944"}


id: MONDO:0017884
data:
  {"annotated_genes":["SJAG_01144"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87998],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0003789"}]},"cv_name":"mondo","definition":"A rare subtype of renal cell carcinoma, arising from the renal tubular epithelium and showing a papillary growth pattern, which typically manifests with hematuria, flank pain, palpable abdominal mass or nonspecific symptoms, such as fatigue, weight loss or fever. Symptoms related to metastatic spread, such as bone pain or persistent cough, are frequently associated since early diagnosis is not common. It is typically multifocal, bilateral, and in most cases sporadic, although different hereditary syndromes, such as Hereditary leiomyoma renal cell carcinoma, Birt-Hogg-DubC) syndrome and Tuberous sclerosis, may predispose to the development of papillary renal cell carcinoma.","definition_xrefs":["Orphanet:319298"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete inherited renal cancer-predisposing syndrome (obsolete MONDO:0017891)","termid":"MONDO:0017891"},{"relation_name":"is_a","term_name":"papillary adenocarcinoma","termid":"MONDO:0002512"},{"relation_name":"is_a","term_name":"renal cell adenocarcinoma","termid":"MONDO:0005549"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01144":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0004992"],"is_obsolete":false,"name":"papillary renal cell carcinoma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:4465","ONCOTREE:PRCC","UMLS:C1306837","EFO:0000640","GARD:9572","MEDGEN:266300","SCTID:733608000","NCIT:C6975"],"synonyms":[{"name":"HPRCC","type":"exact"},{"name":"RCCP","type":"related"},{"name":"RCCP1","type":"related"},{"name":"chromophil RCC","type":"related"},{"name":"chromophil carcinoma of kidney","type":"exact"},{"name":"chromophil carcinoma of the kidney","type":"exact"},{"name":"chromophil renal cell carcinoma","type":"exact"},{"name":"papillary (chromophil) renal cell carcinoma","type":"exact"},{"name":"papillary kidney carcinoma","type":"exact"},{"name":"papillary renal carcinoma, malignant - (subtype)","type":"related"},{"name":"papillary renal cell adenocarcinoma","type":"exact"},{"name":"papillary renal cell cancer","type":"exact"},{"name":"papillary renal cell carcinoma","type":"exact"},{"name":"papillary renal cell carcinoma, bilateral - (subtype)","type":"related"},{"name":"papillary renal cell carcinoma, familial - (subtype)","type":"related"},{"name":"papillary renal cell carcinoma, multiple - (subtype)","type":"related"},{"name":"papillary renal cell carcinoma, sporadic - (subtype)","type":"related"},{"name":"renal adenocarcinoma","type":"related"},{"name":"renal cell carcinoma, papillary, 1","type":"related"},{"name":"renal cell carcinoma, papillary, type 1","type":"exact"},{"name":"sporadic papillary renal cell carcinoma","type":"exact"}],"termid":"MONDO:0017884","terms_by_termid":{"MONDO:0003789":null},"xrefs":{"Monarch":{"xref_id":"0017884"}}}


id: PBO:0038573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin binding Rho activating protein","termid":"PBO:0038573"}


id: GO:0006658
data:
  {"annotated_genes":["SJAG_02100","SJAG_03076","SJAG_01233"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103362],"is_not":false,"summary":null,"term":"GO:0006658"},{"annotations":[68746],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006659"},{"annotations":[76114],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006660"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving phosphatidylserines, any of a class of glycerophospholipids in which the phosphatidyl group is esterified to the hydroxyl group of L-serine. They are important constituents of cell membranes.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified amino acid metabolic process","termid":"GO:0006575"},{"relation_name":"is_a","term_name":"glycerophospholipid metabolic process","termid":"GO:0006650"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01233":null,"SJAG_02100":null,"SJAG_03076":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":"phosphatidylserine metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"phosphatidylserine metabolism","type":"exact"}],"termid":"GO:0006658","terms_by_termid":{"GO:0006658":null,"GO:0006659":null,"GO:0006660":null}}


id: GO:0047536
data:
  {"annotated_genes":["SJAG_04678","SJAG_03312","SJAG_04988"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74305,78450,101312],"is_not":false,"summary":null,"term":"GO:0047536"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-oxoglutarate + L-2-aminoadipate = 2-oxoadipate + L-glutamate.","definition_xrefs":["EC:2.6.1.39","RHEA:12601"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03312":null,"SJAG_04678":null,"SJAG_04988":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016769","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"2-aminoadipate transaminase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-508561","MetaCyc:2-AMINOADIPATE-AMINOTRANSFERASE-RXN","Reactome:R-HSA-70952","KEGG_REACTION:R01939"],"synonyms":[{"name":"2-aminoadipate aminotransferase activity","type":"exact"},{"name":"2-aminoadipic aminotransferase activity","type":"related"},{"name":"L-2-aminoadipate:2-oxoglutarate aminotransferase activity","type":"related"},{"name":"alpha-aminoadipate aminotransferase activity","type":"related"},{"name":"glutamate-alpha-ketoadipate transaminase activity","type":"related"},{"name":"glutamic-ketoadipic transaminase activity","type":"related"}],"termid":"GO:0047536","terms_by_termid":{"GO:0047536":null}}


id: GO:0098841
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A cellular protein localization process in which a protein is transported to, or maintained at, the site of cell division following cytokinesis.","definition_xrefs":["PMID:25411334"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to cell division site","termid":"GO:0072741"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to cell division site after cytokinesis","termid":"GO:0098841"}


id: GO:0031471
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An organelle found in bacteria consisting of a proteinaceous coat containing enzymes for the degradation of ethanolamine whose purpose is the protection of the rest of the cell from the toxic acetaldehyde product of the enzyme ethanolamine ammonia lyase.","definition_xrefs":["GOC:js","PMID:11844753"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial microcompartment","termid":"GO:0031469"}],"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":"ethanolamine degradation polyhedral organelle","synonyms":[{"name":"ethanolamine metabolosome","type":"related"}],"termid":"GO:0031471"}


id: PBO:0031836
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_RNA_localization_during_vegetative_growth","termid":"PBO:0031836"}


id: PR:Q9Y7L0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A vesicle-trafficking protein SEC22b that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["UniProtKB:Q9Y7L0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein transport protein sec22 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2A9.08c","synonyms":[{"name":"Spom972h-SEC22B","type":"exact"}],"termid":"PR:Q9Y7L0"}


id: GO:0090340
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of secretion of lysosomal enzymes, the controlled release of lysosomal enzymes by a cell.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein secretion","termid":"GO:0050714"},{"relation_name":"is_a","term_name":"regulation of secretion of lysosomal enzymes","termid":"GO:0090182"},{"relation_name":"positively_regulates","term_name":"secretion of lysosomal enzymes","termid":"GO:0033299"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of secretion of lysosomal enzymes","termid":"GO:0090340"}


id: PBO:0084592
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Merged open reading frame; does not encode a discrete protein; YGL046W was originally annotated as an independent ORF, but as a result of a sequence change, it was merged with an adjacent ORF into a single reading frame, designated YGL045W","termid":"PBO:0084592"}


id: MONDO:0010724
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete RP6 (obsolete MONDO:0010724)","termid":"MONDO:0010724","xrefs":{"Monarch":{"xref_id":"0010724"}}}


id: PATO:0002460
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer being smaller and contracted, expecially due to loss of moisture.","definition_xrefs":["PATOC:JL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"shriveled","termid":"PATO:0002460"}


id: PBO:0004871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S3 (predicted)","termid":"PBO:0004871"}


id: MONDO:0032598
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 68","secondary_identifiers":["MEDGEN:1648479","DOID:0112204","GARD:16310","OMIM:618201","UMLS:C4748688"],"synonyms":[{"name":"DEE68","type":"exact"},{"name":"EIEE68","type":"exact"},{"name":"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68","type":"exact"},{"name":"developmental and epileptic encephalopathy 68","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 68","type":"exact"}],"termid":"MONDO:0032598","xrefs":{"Monarch":{"xref_id":"0032598"}}}


id: PBO:0041111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BSND pseudogene 4","termid":"PBO:0041111"}


id: PBO:0011458
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Changed Amiloride Resistance","termid":"PBO:0011458"}


id: PBO:0110478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GCM1 pseudogene 1","termid":"PBO:0110478"}


id: GO:0086015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An action potential that occurs in a sinoatrial node cardiac muscle cell.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac muscle cell action potential","termid":"GO:0086001"},{"relation_name":"part_of","term_name":"SA node cell to atrial cardiac muscle cell signaling","termid":"GO:0086018"}],"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":"SA node cell action potential","synonyms":[{"name":"SA node cardiac muscle cell action potential","type":"exact"},{"name":"SAN cardiac muscle cell action potential","type":"exact"},{"name":"sinoatrial node cardiac muscle cell action potential","type":"exact"},{"name":"sinus node cardiac muscle cell action potential","type":"narrow"}],"termid":"GO:0086015"}


id: MONDO:0005131
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma arising from either the exocervical squamous epithelium or the endocervical glandular epithelium. The major histologic types of cervical carcinoma are: squamous carcinoma, adenocarcinoma, adenosquamous carcinoma, adenoid cystic carcinoma and undifferentiated carcinoma.","definition_xrefs":["NCIT:C9039"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervical cancer","termid":"MONDO:0002974"},{"relation_name":"is_a","term_name":"uterine carcinoma","termid":"MONDO:0005213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"cervical carcinoma","secondary_identifiers":["EFO:0001061","UMLS:C0302592","icd11.foundation:1743710977","SCTID:285432005","DOID:2893","MEDGEN:86222"],"synonyms":[{"name":"cancer of cervix","type":"broad"},{"name":"cancer of the cervix","type":"broad"},{"name":"cancer of the uterine cervix","type":"broad"},{"name":"cancer of uterine cervix","type":"broad"},{"name":"carcinoma cervix uteri","type":"exact"},{"name":"carcinoma of cervix","type":"exact"},{"name":"carcinoma of cervix uteri","type":"exact"},{"name":"carcinoma of the cervix","type":"exact"},{"name":"carcinoma of the cervix uteri","type":"exact"},{"name":"carcinoma of the uterine cervix","type":"exact"},{"name":"carcinoma of uterine cervix","type":"exact"},{"name":"cervical cancer","type":"broad"},{"name":"cervical cancer, NOS","type":"broad"},{"name":"cervical carcinoma","type":"exact"},{"name":"cervix cancer","type":"broad"},{"name":"cervix carcinoma","type":"exact"},{"name":"cervix uteri carcinoma","type":"exact"},{"name":"uterine cervix cancer","type":"broad"},{"name":"uterine cervix carcinoma","type":"exact"}],"termid":"MONDO:0005131","xrefs":{"Monarch":{"xref_id":"0005131"}}}


