# terms

id: GO:0016553
data:
  {"annotated_genes":["SJAG_04380","SJAG_04189","SJAG_00352"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75492,102903,59428],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002100"}]},"cv_name":"biological_process","definition":"Any base modification or substitution events that result in alterations in the coding potential or structural properties of RNAs as a result of changes in the base-pairing properties of the modified ribonucleoside(s).","definition_xrefs":["PMID:11092837"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA modification","termid":"GO:0009451"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00352":null,"SJAG_04189":null,"SJAG_04380":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"base conversion or substitution editing","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"base conversion/substitution editing","type":"exact"}],"termid":"GO:0016553","terms_by_termid":{"GO:0002100":null}}


id: PR:Q9Y816
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1105.13c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y816"],"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 C1105.13c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1105.13c","synonyms":[{"name":"Spom972h-SPBC1105.13c","type":"exact"}],"termid":"PR:Q9Y816"}


id: PBO:0041651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium voltage-gated channel auxiliary subunit beta 1","termid":"PBO:0041651"}


id: GO:0002208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The somatic process that results in the generation of sequence diversity of immunoglobulins after induction, and contributes to an immune response.","definition_xrefs":["ISBN:0781735149","PMID:14991701","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatic diversification of immunoglobulins","termid":"GO:0016445"},{"relation_name":"part_of","term_name":"immunoglobulin production involved in immunoglobulin-mediated immune response","termid":"GO:0002381"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"somatic diversification of immunoglobulins involved in immune response","synonyms":[{"name":"somatic diversification of antibodies during immune response","type":"related"},{"name":"somatic diversification of immunoglobulins during immune response","type":"related"}],"termid":"GO:0002208"}


id: PBO:0011111
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deletion library version 2. has incorrect strain","termid":"PBO:0011111"}


id: GO:0005244
data:
  {"annotated_genes":["SJAG_05229","SJAG_00048"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76134],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008331"},{"annotations":[73368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008308"}]},"cv_name":"molecular_function","definition":"Enables the transmembrane transfer of an ion by a voltage-gated channel. An ion is an atom or group of atoms carrying an electric charge by virtue of having gained or lost one or more electrons. A voltage-gated channel is a channel whose open state is dependent on the voltage across the membrane in which it is embedded.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoatomic ion channel activity","termid":"GO:0005216"},{"relation_name":"is_a","term_name":"voltage-gated channel activity","termid":"GO:0022832"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00048":null,"SJAG_05229":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"voltage-gated monoatomic ion channel activity","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"voltage gated ion channel activity","type":"exact"},{"name":"voltage-dependent ion channel activity","type":"exact"},{"name":"voltage-gated ion channel activity","type":"broad"}],"termid":"GO:0005244","terms_by_termid":{"GO:0008308":null,"GO:0008331":null}}


id: PBO:0041095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BRWD1 intronic transcript 1","termid":"PBO:0041095"}


id: PBO:0089262
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(U)-specific exoribonuclease, producing 3' uridine cyclic phosphate ends Mpn1","termid":"PBO:0089262"}


id: PBO:0050249
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosomal binding domain 2 pseudogene 27","termid":"PBO:0050249"}


id: PBO:0075848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ssu-2 homolog","termid":"PBO:0075848"}


id: MONDO:0000473
data:
  {"annotated_genes":["SJAG_02218","SJAG_00210","SJAG_03081","SJAG_02977"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89070,89071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012011"},{"annotations":[89081],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007781"},{"annotations":[88666],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013458"}]},"cv_name":"mondo","definition":"An impairment of the structure or function of the blood vessels which carry blood away from the heart.","definition_xrefs":["NCIT:C35317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00210":null,"SJAG_02218":null,"SJAG_02977":null,"SJAG_03081":null},"genotype_count":0,"is_obsolete":false,"name":"arterial disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0050828","SCTID:359557001","MEDGEN:208875","ICD9:447.8","UMLS:C0852949","ICD9:447.9"],"synonyms":[{"name":"arterial disease","type":"exact"},{"name":"arterial disorder","type":"exact"},{"name":"arteriopathy","type":"exact"},{"name":"artery disease","type":"exact"},{"name":"artery disease or disorder","type":"exact"},{"name":"disease of artery","type":"exact"},{"name":"disease or disorder of artery","type":"exact"},{"name":"disorder of artery","type":"exact"}],"termid":"MONDO:0000473","terms_by_termid":{"MONDO:0007781":null,"MONDO:0012011":null,"MONDO:0013458":null},"xrefs":{"Monarch":{"xref_id":"0000473"}}}


id: PBO:0016997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FAS1 domain protein Mug57","termid":"PBO:0016997"}


id: GO:0140948
data:
  {"annotated_genes":["SJAG_04574"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[112320],"is_not":false,"summary":null,"term":"GO:0140948"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-lysyl9-[histone H3] + S-adenosyl-L-methionine = H+ + N6-methyl-L-lysyl9-[histone H3] + S-adenosyl-L-homocysteine. This reaction is the addition of a methyl group to the unmethylated lysine residue at position 9 of histone H3, producing histone H3K9me.","definition_xrefs":["RHEA:60280"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3K9 methyltransferase activity","termid":"GO:0046974"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04574":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0140096","GO:0016741","GO:0008276","GO:0016740"],"is_obsolete":false,"name":"histone H3K9 monomethyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:2.1.1.367"],"synonyms":[{"name":"histone H3-K9 methylation","type":"broad"},{"name":"histone H3K9 methylation","type":"broad"},{"name":"histone H3K9 monomethylase activity","type":"exact"},{"name":"histone lysine N-monomethyltransferase activity (H3-K9 specific)","type":"exact"}],"termid":"GO:0140948","terms_by_termid":{"GO:0140948":null}}


id: PBO:0030144
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_L-thialysine","termid":"PBO:0030144"}


id: PBO:0064946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PEAK1 related, kinase-activating pseudokinase 1","termid":"PBO:0064946"}


id: MONDO:0004077
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign well-circumscribed tumor, composed of lobules of mature adipocytes, that arises within the lumbosacral tissue of the spine.","definition_xrefs":["NCIT:C6500"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"bone benign neoplasm","termid":"MONDO:0000631"},{"relation_name":"is_a","term_name":"vertebral column disorder","termid":"MONDO:0000812"},{"relation_name":"is_a","term_name":"lipoma","termid":"MONDO:0005106"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lumbosacral lipoma","secondary_identifiers":["MEDGEN:232708","UMLS:C1334438","DOID:7017"],"synonyms":[{"name":"lipoma of sacral region of vertebral column","type":"exact"},{"name":"sacral region of vertebral column lipoma","type":"exact"}],"termid":"MONDO:0004077","xrefs":{"Monarch":{"xref_id":"0004077"}}}


id: PBO:0013117
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 Dbl6","termid":"PBO:0013117"}


id: PR:Q9UT45
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- eng1 gene.","definition_xrefs":["UniProtKB:Q9UT45","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":"endo-1,3(4)-beta-glucanase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC821.09","synonyms":[{"name":"Spom972h-eng1","type":"exact"},{"name":"endo-1,3-beta-glucanase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"endo-1,4-beta-glucanase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"laminarinase-1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UT45"}


id: GO:0043982
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H4 by the addition of an acetyl group to a lysine residue at position 8 of the histone.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H4-K8 acetylation (obsolete GO:0043982)","synonyms":[{"name":"histone H4 acetylation at K8","type":"exact"}],"termid":"GO:0043982"}


id: GO:0034280
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ent-copalyl diphosphate = ent-sandaracopimara-8(14),15-diene + diphosphate.","definition_xrefs":["RHEA:25536"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"ent-sandaracopimaradiene synthase activity","secondary_identifiers":["MetaCyc:RXN-4884","EC:4.2.3.29","KEGG_REACTION:R09120"],"synonyms":[{"name":"ent-copalyl-diphosphate diphosphate-lyase [ent-sandaracopimara-8(14),15-diene-forming] activity","type":"exact"},{"name":"ent-pimaradiene synthase activity","type":"broad"}],"termid":"GO:0034280"}


id: SO:0000298
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A feature where there has been exchange of genetic material in the event of mitosis or meiosis","direct_ancestors":[{"relation_name":"is_a","term_name":"biological_region","termid":"SO:0001411"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"recombination_feature","synonyms":[{"name":"INSDC_feature:misc_recomb","type":"broad"},{"name":"INSDC_qualifier:other","type":"exact"},{"name":"recombination feature","type":"exact"}],"termid":"SO:0000298"}


id: GO:0005031
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with tumor necrosis factor, a proinflammatory cytokine produced by monocytes and macrophages, to initiate a change in cell function.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"death receptor activity","termid":"GO:0005035"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"tumor necrosis factor receptor activity","secondary_identifiers":["GO:0005032","GO:0005033"],"synonyms":[{"name":"NGF/TNF (6 C-domain) receptor activity","type":"narrow"},{"name":"TNF receptor activity","type":"exact"},{"name":"TNF receptor activity, type I","type":"narrow"},{"name":"TNF receptor activity, type II","type":"narrow"},{"name":"tumor necrosis factor receptor activity, type I","type":"narrow"},{"name":"tumor necrosis factor receptor activity, type II","type":"narrow"},{"name":"tumor necrosis factor-activated receptor activity","type":"exact"}],"termid":"GO:0005031"}


id: GO:0102043
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: isopentenyl phosphate(2-) + ATP(4-) = isopentenyl diphosphate(3-) + ADP(3-).","definition_xrefs":["GOC:pz","RHEA:33963","PMID:19928876"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, phosphate group as acceptor","termid":"GO:0016776"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"isopentenyl phosphate kinase activity","secondary_identifiers":["EC:2.7.4.26","MetaCyc:RXN-10068"],"termid":"GO:0102043"}


id: PR:O42999
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mitochondrial import receptor subunit TOM7 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR16463: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":"mitochondrial import receptor subunit tom7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC27B12.10c","secondary_identifiers":["UniProtKB:O42999"],"synonyms":[{"name":"SPBC27B12.10c","type":"related"},{"name":"Spom972h-TOMM7","type":"exact"},{"name":"translocase of outer membrane 7 kDa subunit (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O42999"}


id: GO:0071691
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of proteins to form the actin-based thin filaments of myofibrils in cardiac muscle.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament organization","termid":"GO:0007015"},{"relation_name":"part_of","term_name":"cardiac myofibril assembly","termid":"GO:0055003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0030036"},{"rel_name":"part_of","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0030036","GO:0044085","GO:0007010","GO:0008150"],"is_obsolete":false,"name":"cardiac muscle thin filament assembly","termid":"GO:0071691"}


id: PBO:0008516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anamorsin family protein, involved in iron-sulfur cluster assembly (predicted)","termid":"PBO:0008516"}


id: GO:0002248
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events leading to growth of connective tissue when loss of tissues that are incapable of regeneration occurs, or when fibrinous exudate cannot be adequately cleared, as part of an inflammatory response.","definition_xrefs":["PMID:9639571","GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"connective tissue replacement","termid":"GO:0097709"},{"relation_name":"part_of","term_name":"wound healing involved in inflammatory response","termid":"GO:0002246"}],"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":"connective tissue replacement involved in inflammatory response wound healing","synonyms":[{"name":"connective tissue replacement during inflammatory response","type":"related"},{"name":"fibrosis during inflammatory response","type":"narrow"},{"name":"tissue fibrosis development","type":"narrow"}],"termid":"GO:0002248"}


id: GO:0070765
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that has aspartic-type endopeptidase activity and contains a presenilin catalytic subunit (either PSEN1 or PSEN2), an APH1 subunit (multiple genes and splice variants exist), nicastrin (NCT), and presenilin enhancer (aka PEN-2 or Psenen), as the core complex. Variants of the complex with different subunit compositions differ in localization and specific substrates. Additionally, variants of the complex exist that contain a additional regulatory subunit as well as the four core subunits; known regulatory subunits include gamma-secretase-activating protein (aka gSAP), TMP1 (aka TMED10), and CD147 antigen (aka basigin). Gamma-secretase cleaves type I transmembrane protein substrates, including the cell surface receptor Notch and the amyloid-beta precursor protein.","definition_xrefs":["PMID:17047368","PMID:15286082","PMID:15890777","GOC:krc","PMID:28320827","PMID:25565961","PMID:32616437","PMID:22122073"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"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:0005575","GO:0005886","GO:0032991"],"is_obsolete":false,"name":"gamma-secretase complex","synonyms":[{"name":"CD147-gamma-secretase complex (APH-1a, PS-1, PEN-2, NCT variant)","type":"narrow"},{"name":"PS1 complex","type":"narrow"},{"name":"PS2 complex","type":"narrow"},{"name":"gamma-secretase complex (APH1A, PSEN1, PSENEN, NCSTN variant)","type":"narrow"},{"name":"gamma-secretase complex (APH1A, PSEN2, PSENEN, NCSTN)","type":"narrow"},{"name":"gamma-secretase complex (APH1B, PSEN1, PSENEN, NCSTN)","type":"narrow"},{"name":"gamma-secretase complex (APH1B, PSEN2, PSENEN, NCSTN)","type":"narrow"},{"name":"presenilin complex","type":"exact"}],"termid":"GO:0070765"}


id: PR:P50531
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cell cycle checkpoint protein RAD17 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR12172: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":"checkpoint protein rad17 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC14C4.13","secondary_identifiers":["UniProtKB:P50531"],"synonyms":[{"name":"SPAC14C4.13","type":"related"},{"name":"Spom972h-RAD17","type":"exact"}],"termid":"PR:P50531"}


id: PBO:0041614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cdk5 and Abl enzyme substrate 2","termid":"PBO:0041614"}


id: MOD:00098
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-histidine residue to L-histidine amide.","definition_xrefs":["PubMed:2307683","PubMed:2153586","PubMed:2839478","RESID:AA0089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C1-amidated residue","termid":"MOD:00883"},{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-histidine amide","synonyms":[{"name":"(2S)-2-amino-3-(1H-imidazol-4-yl)propanamide","type":"exact"},{"name":"HisN","type":"exact"},{"name":"L-histidine amide","type":"exact"},{"name":"MOD_RES Histidine amide","type":"exact"},{"name":"amidated L-histidine","type":"exact"},{"name":"histidinamide","type":"exact"}],"termid":"MOD:00098"}


id: PBO:0084638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mevalonate pyrophosphate decarboxylase; essential enzyme involved in the biosynthesis of isoprenoids and sterols, including ergosterol; acts as a homodimer","termid":"PBO:0084638"}


id: PBO:0109226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spore wall alpha-1,3-glucan synthase Mok12","termid":"PBO:0109226"}


id: PBO:0046058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 subunit I","termid":"PBO:0046058"}


id: GO:1904477
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of small GTPase binding.","definition_xrefs":["GO_REF:0000059","GOC:TermGenie","PMID:15798216"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of small GTPase binding (obsolete GO:1904477)","synonyms":[{"name":"activation of Ras GTPase binding","type":"narrow"},{"name":"positive regulation of Ras GTPase binding","type":"narrow"},{"name":"up regulation of small GTPase binding","type":"exact"},{"name":"up-regulation of small GTPase binding","type":"exact"},{"name":"upregulation of small GTPase binding","type":"exact"}],"termid":"GO:1904477"}


id: GO:0008062
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The timing of the emergence of the adult fly from its pupal case, which usually occurs at dawn.","definition_xrefs":["PMID:11715043"],"direct_ancestors":[{"relation_name":"is_a","term_name":"circadian behavior","termid":"GO:0048512"},{"relation_name":"part_of","term_name":"eclosion","termid":"GO:0007562"}],"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":"eclosion rhythm","termid":"GO:0008062"}


id: GO:0016922
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a nuclear receptor protein. Nuclear receptor proteins are DNA-binding transcription factors which are regulated by binding to a ligand.","definition_xrefs":["PMID:7776974"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II-specific DNA-binding transcription factor binding","termid":"GO:0061629"}],"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":"nuclear receptor binding","secondary_identifiers":["GO:0035257","GO:0035258"],"synonyms":[{"name":"ligand-dependent nuclear receptor binding","type":"exact"},{"name":"ligand-dependent nuclear receptor interactor activity","type":"related"},{"name":"nuclear hormone receptor binding","type":"exact"},{"name":"steroid hormone receptor binding","type":"broad"}],"termid":"GO:0016922"}


id: PBO:0075613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secreted phosphoprotein 1","termid":"PBO:0075613"}


id: GO:1903551
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of extracellular vesicular exosome assembly.","definition_xrefs":["PMID:24105262","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of organelle assembly","termid":"GO:1902115"},{"relation_name":"regulates","term_name":"extracellular exosome assembly","termid":"GO:0071971"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"regulation of extracellular exosome assembly","synonyms":[{"name":"regulation of extracellular vesicular exosome assembly","type":"exact"}],"termid":"GO:1903551"}


id: MONDO:1012203
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"osteodystrophy, non-human animal","termid":"MONDO:1011951"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteodystrophy, domestic cat","secondary_identifiers":["OMIA:000753-9685"],"termid":"MONDO:1012203","xrefs":{"Monarch":{"xref_id":"1012203"}}}


id: PBO:0063494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDZ and LIM domain 2","termid":"PBO:0063494"}


id: MONDO:0005128
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A disease involving the sensory system.","gene_count":0,"genotype_count":0,"name":"obsolete sensory system disease (obsolete MONDO:0005128)","secondary_identifiers":["DOID:0050155"],"synonyms":[{"name":"disease of sensory system","type":"exact"},{"name":"disease or disorder of sensory system","type":"exact"},{"name":"disorder of sensory system","type":"exact"},{"name":"sensory disease","type":"exact"},{"name":"sensory system disease","type":"exact"},{"name":"sensory system disease or disorder","type":"exact"}],"termid":"MONDO:0005128","xrefs":{"Monarch":{"xref_id":"0005128"}}}


id: GO:0006303
data:
  {"annotated_genes":["SJAG_02237","SJAG_00823","SJAG_05372","SJAG_04199","SJAG_00640","SJAG_04372","SJAG_01677","SJAG_02527","SJAG_16460","SJAG_01076","SJAG_00441","SJAG_03048","SJAG_05373"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90312,90936,101730,106838,112776,113560,116124,118644],"is_not":false,"summary":null,"term":"GO:0006303"},{"annotations":[115730,118166],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097680"},{"annotations":[97659],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061674"},{"annotations":[104162],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:2001033"},{"annotations":[109221],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:2001034"}]},"cv_name":"biological_process","definition":"The repair of a double-strand break in DNA in which the two broken ends are rejoined with little or no sequence complementarity. Information at the DNA ends may be lost due to the modification of broken DNA ends. This term covers instances of separate pathways, called classical (or canonical) and alternative nonhomologous end joining (C-NHEJ and A-NHEJ). These in turn may further branch into sub-pathways, but evidence is still unclear.","definition_xrefs":["GOC:rph","PMID:10827453","PMID:24837021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"double-strand break repair","termid":"GO:0006302"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00441":null,"SJAG_00640":null,"SJAG_00823":null,"SJAG_01076":null,"SJAG_01677":null,"SJAG_02237":null,"SJAG_02527":null,"SJAG_03048":null,"SJAG_04199":null,"SJAG_04372":null,"SJAG_05372":null,"SJAG_05373":null,"SJAG_16460":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0006281"}],"interesting_parent_ids":["GO:0006259","GO:0006281","GO:0008150"],"is_obsolete":false,"name":"double-strand break repair via nonhomologous end joining","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5693571"],"synonyms":[{"name":"NHEJ","type":"exact"}],"termid":"GO:0006303","terms_by_termid":{"GO:0006303":null,"GO:0061674":null,"GO:0097680":null,"GO:2001033":null,"GO:2001034":null}}


id: GO:0008535
data:
  {"annotated_genes":["SJAG_02975","SJAG_04348","SJAG_04116","SJAG_03046","SJAG_05398","SJAG_00852","SJAG_02229","SJAG_02979","SJAG_05199","SJAG_06392","SJAG_05302","SJAG_01996","SJAG_04553","SJAG_00449","SJAG_06468","SJAG_04603","SJAG_03296","SJAG_03337","SJAG_03322","SJAG_06046","SJAG_02480","SJAG_01140"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74265,59210,96448,103492,62553,93430,90799,118902,109301,120216,108674,78412,105812,90996,61195,72053,96433,105557,94258,108983,80240,73647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033617"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form respiratory chain complex IV (also known as cytochrome c oxidase), the terminal member of the respiratory chain of the mitochondrion and some aerobic bacteria. Cytochrome c oxidases are multi-subunit enzymes containing from 13 subunits in the mammalian mitochondrial form to 3-4 subunits in the bacterial forms.","definition_xrefs":["PMID:32311046","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytochrome complex assembly","termid":"GO:0017004"}],"gene_count":22,"genes_by_uniquename":{"SJAG_00449":null,"SJAG_00852":null,"SJAG_01140":null,"SJAG_01996":null,"SJAG_02229":null,"SJAG_02480":null,"SJAG_02975":null,"SJAG_02979":null,"SJAG_03046":null,"SJAG_03296":null,"SJAG_03322":null,"SJAG_03337":null,"SJAG_04116":null,"SJAG_04348":null,"SJAG_04553":null,"SJAG_04603":null,"SJAG_05199":null,"SJAG_05302":null,"SJAG_05398":null,"SJAG_06046":null,"SJAG_06392":null,"SJAG_06468":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0008150","GO:0065003","GO:0044085"],"is_obsolete":false,"name":"respiratory chain complex IV assembly","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"cytochrome c oxidase biogenesis","type":"broad"},{"name":"cytochrome c oxidase complex assembly","type":"exact"}],"termid":"GO:0008535","terms_by_termid":{"GO:0033617":null}}


id: PBO:0054219
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 1600","termid":"PBO:0054219"}


id: MONDO:0023263
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"glucose metabolism disease","termid":"MONDO:0002908"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"glyceraldehyde-3-phosphate dehydrogenase deficiency","secondary_identifiers":["HGNC:4141","MEDGEN:224854","MESH:C536837","UMLS:C1291264"],"synonyms":[{"name":"GAPDH deficiency","type":"related"}],"termid":"MONDO:0023263","xrefs":{"Monarch":{"xref_id":"0023263"}}}


id: FYPO:0007800
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 endoplasmic reticulum is abolished, and some of the protein is present at the cell surface instead.","definition_xrefs":["PMID:33536395","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to endoplasmic reticulum during vegetative growth","termid":"FYPO:0003777"},{"relation_name":"is_a","term_name":"protein mislocalized to cell surface during vegetative growth","termid":"FYPO:0007799"},{"relation_name":"is_a","term_name":"abolished protein localization to endoplasmic reticulum","termid":"FYPO:0008405"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein localization to endoplasmic reticulum, with protein mislocalized to cell surface","synonyms":[{"name":"abolished luminal ER protein retention","type":"exact"},{"name":"abolished protein localization to ER, with protein mislocalized to cell surface","type":"exact"},{"name":"abolished protein localization to endoplasmic reticulum, with protein mislocalized to cell surface during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to endoplasmic reticulum, with protein mislocalized to cell surface during vegetative growth","type":"exact"}],"termid":"FYPO:0007800"}


id: GO:0036493
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, or increases the frequency, rate or extent of translation as a result of endoplasmic reticulum stress.","definition_xrefs":["GOC:PARL","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of translation in response to stress","termid":"GO:0032056"},{"relation_name":"is_a","term_name":"regulation of translation in response to endoplasmic reticulum stress","termid":"GO:0036490"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of translation in response to endoplasmic reticulum stress","synonyms":[{"name":"positive regulation of translation in response to ER stress","type":"exact"}],"termid":"GO:0036493"}


id: PBO:0073062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SDA1 domain containing 1 pseudogene 4","termid":"PBO:0073062"}


id: PBO:0066761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 59","termid":"PBO:0066761"}


id: PBO:0078606
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 19","termid":"PBO:0078606"}


id: PBO:0068512
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 103, pseudogene","termid":"PBO:0068512"}


id: MONDO:0010731
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Simpson-Golabi-Behmel syndrome is a rare X-linked multiple congenital anomalies syndrome, characterized by pre- and postnatal overgrowth, distinctive craniofacial features, variable congenital malformations, organomegaly and an increased tumor risk.","definition_xrefs":["Orphanet:373"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic diaphragmatic or abdominal wall malformation (obsolete MONDO:0015216)","termid":"MONDO:0015216"},{"relation_name":"excluded_subClassOf","term_name":"macroglossia","termid":"MONDO:0015496"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome or malformation associated with head and neck malformations (obsolete MONDO:0015501)","termid":"MONDO:0015501"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic diaphragmatic or thoracic malformation (obsolete MONDO:0015880)","termid":"MONDO:0015880"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic renal or urinary tract malformation (obsolete MONDO:0019721)","termid":"MONDO:0019721"},{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"overgrowth syndrome","termid":"MONDO:0019716"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Simpson-Golabi-Behmel syndrome","secondary_identifiers":["UMLS:C4317043","NCIT:C131002","ICD9:759.89","SCTID:439143004","NORD:1717","icd11.foundation:181316558","MEDGEN:1387611","MESH:C537340","GARD:7649","NANDO:2200978"],"synonyms":[{"name":"DGSX","type":"exact"},{"name":"Golabi-Rosen syndrome","type":"exact"},{"name":"SDYS","type":"exact"},{"name":"SGB syndrome","type":"exact"},{"name":"SGBS","type":"exact"},{"name":"Sara Angers syndrome","type":"exact"},{"name":"Sgbs","type":"related"},{"name":"Simpson-Golabi-Behmel syndrome","type":"exact"},{"name":"X-linked dysplasia gigantism syndrome","type":"exact"},{"name":"dysplasia gigantism syndrome, X-linked","type":"related"}],"termid":"MONDO:0010731","xrefs":{"Monarch":{"xref_id":"0010731"}}}


id: PBO:0092005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Lysine (uuu), mitochondrial","termid":"PBO:0092005"}


id: MONDO:0014376
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"autosomal dominant non-syndromic intellectual disability","termid":"MONDO:0015802"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"Coffin-Siris syndrome","termid":"MONDO:0015452"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism","secondary_identifiers":["DOID:0070057","MEDGEN:862965","OMIM:615866","GARD:16023","UMLS:C4014528"],"synonyms":[{"name":"CSS9","type":"exact"},{"name":"Coffin-Siris syndrome 9","type":"exact"},{"name":"MRD27","type":"exact"},{"name":"autosomal dominant intellectual disability 27","type":"exact"},{"name":"autosomal dominant mental retardation 27","type":"exact"},{"name":"autosomal dominant non-syndromic intellectual disability 27","type":"related"},{"name":"intellectual disability, autosomal dominant 27","type":"exact"},{"name":"intellectual disability, autosomal dominant type 27","type":"exact"},{"name":"mental retardation, autosomal dominant 27","type":"related"},{"name":"mental retardation, autosomal dominant type 27","type":"exact"}],"termid":"MONDO:0014376","xrefs":{"Monarch":{"xref_id":"0014376"}}}


id: GO:0031660
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of cyclin-dependent protein serine/threonine kinase activity contributing to the G2/M transition of the cell cycle.","definition_xrefs":["GOC:pr","GOC:tb","GOC:mah","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cyclin-dependent protein serine/threonine kinase activity involved in G2/M transition of mitotic cell cycle (obsolete GO:0031660)","synonyms":[{"name":"G2/M-specific regulation of cyclin-dependent protein kinase activity","type":"exact"},{"name":"regulation of cyclin-dependent protein kinase activity during G2/M","type":"related"},{"name":"regulation of cyclin-dependent protein kinase activity involved in G2/M","type":"broad"}],"termid":"GO:0031660"}


id: MONDO:0002969
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the ciliary body.","direct_ancestors":[{"relation_name":"is_a","term_name":"iris cancer","termid":"MONDO:0002658"},{"relation_name":"is_a","term_name":"ciliary body neoplasm","termid":"MONDO:0021229"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004992"],"is_obsolete":false,"name":"ciliary body cancer","secondary_identifiers":["DOID:4352","ICD10CM:C69.4","MEDGEN:99219","NCIT:C4766","SCTID:188263008","UMLS:C0496833"],"synonyms":[{"name":"cancer of ciliary body","type":"exact"},{"name":"ciliary body cancer","type":"exact"},{"name":"malignant ciliary body neoplasm","type":"exact"},{"name":"malignant ciliary body tumor","type":"exact"},{"name":"malignant ciliary body tumour","type":"exact"},{"name":"malignant neoplasm of ciliary body","type":"exact"},{"name":"malignant neoplasm of the ciliary body","type":"exact"},{"name":"malignant tumor of ciliary body","type":"exact"},{"name":"malignant tumor of the ciliary body","type":"exact"},{"name":"malignant tumour of ciliary body","type":"exact"},{"name":"malignant tumour of the ciliary body","type":"exact"},{"name":"tumor of the ciliary body","type":"broad"},{"name":"tumour of the ciliary body","type":"broad"}],"termid":"MONDO:0002969","xrefs":{"Monarch":{"xref_id":"0002969"}}}


id: MONDO:8000019
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral vertigo","termid":"MONDO:0004900"},{"relation_name":"is_a","term_name":"hereditary otorhinolaryngologic disease","termid":"MONDO:0018751"},{"relation_name":"is_a","term_name":"inherited auditory system disease","termid":"MONDO:0037940"},{"relation_name":"is_a","term_name":"hereditary neuromuscular disease","termid":"MONDO:0100546"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vertigo, benign recurrent, 1","secondary_identifiers":["MEDGEN:412807","MESH:C567620","UMLS:C2749845"],"synonyms":[{"name":"BRV1","type":"exact"},{"name":"vertigo, benign recurrent, 1","type":"exact"}],"termid":"MONDO:8000019","xrefs":{"Monarch":{"xref_id":"8000019"}}}


id: GO:0072379
data:
  {"annotated_genes":["SJAG_01496","SJAG_03865"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[81202,116934],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072380"}]},"cv_name":"cellular_component","definition":"A protein complex that is involved in the post-translational delivery of tail-anchored (TA) membrane proteins to the endoplasmic reticulum. TA membrane proteins, also called type II transmembrane proteins, contain a single C-terminal transmembrane region. Some ER membrane insertion complex subunits are conserved between different species such as mammals and budding yeast.","definition_xrefs":["PMID:20850366","GOC:mah","PMID:20676083"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cytosol","termid":"GO:0005829"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01496":null,"SJAG_03865":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005829"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0032991","GO:0005829","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"ER membrane insertion complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"endoplasmic reticulum membrane insertion complex","type":"exact"}],"termid":"GO:0072379","terms_by_termid":{"GO:0072380":null}}


id: PBO:0071345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L29 pseudogene 3","termid":"PBO:0071345"}


id: GO:0032599
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a protein out of a membrane raft. Membrane rafts are small (10-200 nm), heterogeneous, highly dynamic, sterol- and sphingolipid-enriched membrane domains that compartmentalize cellular processes.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein transport within lipid bilayer","termid":"GO:0032594"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0061024","GO:0051179"],"is_obsolete":false,"name":"protein transport out of membrane raft","synonyms":[{"name":"protein translocation out of membrane raft","type":"exact"},{"name":"protein transport out of lipid raft","type":"exact"},{"name":"receptor translocation out of membrane raft","type":"narrow"},{"name":"receptor transport out of membrane raft","type":"narrow"}],"termid":"GO:0032599"}


id: GO:0160162
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by the binding of the cell surface receptor CD27 to its physiological ligand CD70, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:26359318","PMID:8387892"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell surface receptor signaling pathway","termid":"GO:0007166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"CD27 signaling pathway","termid":"GO:0160162"}


id: PBO:0040043
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARNT2 divergent transcript","termid":"PBO:0040043"}


id: PR:O42968
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1E8.03c gene.","definition_xrefs":["UniProtKB:O42968","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C1E8.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1E8.03c","synonyms":[{"name":"Spom972h-SPBC1E8.03c","type":"exact"}],"termid":"PR:O42968"}


id: MONDO:0016082
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tracheo-esophageal fistula-hypospadias syndrome (obsolete MONDO:0016082)","secondary_identifiers":["Orphanet:2042"],"termid":"MONDO:0016082","xrefs":{"Monarch":{"xref_id":"0016082"}}}


id: GO:1902899
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of fatty acid methyl ester.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators","PMID:16570218","GO_REF:0000068"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid derivative biosynthetic process","termid":"GO:1901570"},{"relation_name":"is_a","term_name":"fatty acid methyl ester metabolic process","termid":"GO:1902898"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"fatty acid methyl ester biosynthetic process","synonyms":[{"name":"FAME biosynthetic process","type":"exact"},{"name":"fatty acid methyl ester anabolism","type":"exact"},{"name":"fatty acid methyl ester biosynthesis","type":"exact"},{"name":"fatty acid methyl ester formation","type":"exact"},{"name":"fatty acid methyl ester synthesis","type":"exact"}],"termid":"GO:1902899"}


id: MONDO:0019849
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"male reproductive system disorder","termid":"MONDO:0003150"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isolated micropenis","secondary_identifiers":["GARD:19292","Orphanet:95707","UMLS:C5681560","MEDGEN:1843275"],"termid":"MONDO:0019849","xrefs":{"Monarch":{"xref_id":"0019849"}}}


id: GO:0050284
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-glucose + sinapate = UDP + 1-sinapoyl-D-glucose.","definition_xrefs":["MetaCyc:SINAPATE-1-GLUCOSYLTRANSFERASE-RXN","EC:2.4.1.120"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016757","GO:0016740"],"is_obsolete":false,"name":"sinapate 1-glucosyltransferase activity","secondary_identifiers":["RHEA:13305"],"synonyms":[{"name":"UDP-glucose:sinapate D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:sinapate D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:sinapic acid glucosyltransferase activity","type":"related"},{"name":"uridine 5'-diphosphoglucose-hydroxycinnamic acid acylglucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-sinapate glucosyltransferase activity","type":"related"}],"termid":"GO:0050284"}


id: GO:0018876
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving benzonitrile. Benzonitrile is used as a solvent and chemical intermediate in the pharmaceutical, dyestuffs and rubber industries. It is highly toxic and harmful in contact with skin.","definition_xrefs":["UM-BBD_pathwayID:bzn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"},{"relation_name":"is_a","term_name":"nitrile metabolic process","termid":"GO:0050898"}],"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":"benzonitrile metabolic process","synonyms":[{"name":"benzonitrile metabolism","type":"exact"}],"termid":"GO:0018876"}


id: MONDO:0008396
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oculodental syndrome, Rutherfurd type is a rare genetic disorder that is primarily characterized by the classical triad of gingival fibromatosis, non-eruption of tooth and corneal dystrophy (bilateral corneal vascularization and opacity). Abnormally shaped teeth have also been reported. The syndrome is transmitted as an autosomal dominant trait.","definition_xrefs":["Orphanet:2709"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oculodental syndrome, Rutherfurd type","secondary_identifiers":["icd11.foundation:183543626","UMLS:C0796140","GARD:212","MEDGEN:163222","OMIM:180900","ICD9:759.89","MESH:C537732","SCTID:699754008"],"synonyms":[{"name":"Rutherfurd syndrome","type":"exact"},{"name":"corneal dystrophy with gum Hypertrophy","type":"exact"},{"name":"corneal dystrophy with gum hypertrophy","type":"exact"},{"name":"gingival Hypertrophy with corneal dystrophy","type":"exact"},{"name":"gingival hypertrophy corneal dystrophy","type":"exact"},{"name":"gingival hypertrophy-corneal dystrophy","type":"exact"}],"termid":"MONDO:0008396","xrefs":{"Monarch":{"xref_id":"0008396"}}}


id: PBO:0064498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II subunit B","termid":"PBO:0064498"}


id: PBO:0062371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily A member 10","termid":"PBO:0062371"}


id: PBO:0077040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"THOC7 antisense RNA 1","termid":"PBO:0077040"}


id: PBO:0061949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OR2A1 antisense RNA 1","termid":"PBO:0061949"}


id: PBO:0075821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SS nuclear autoantigen 1","termid":"PBO:0075821"}


id: PBO:0052652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 20","termid":"PBO:0052652"}


id: GO:0001153
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. The function of binding to an RNA polymerase III (RNAP III) transcription factor and recruiting it to the transcription machinery complex in order to modulate transcription by RNAP III.","definition_xrefs":["GOC:txnOH"],"gene_count":0,"genotype_count":0,"name":"obsolete transcription factor activity, RNA polymerase III transcription factor recruiting (obsolete GO:0001153)","synonyms":[{"name":"RNA polymerase III transcription factor recruiting transcription factor activity","type":"exact"}],"termid":"GO:0001153"}


id: MONDO:0020650
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"germ cell tumor","termid":"MONDO:0005040"},{"relation_name":"is_a","term_name":"vulvar neoplasm","termid":"MONDO:0021049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"germ cell tumor of the vulva","secondary_identifiers":["ONCOTREE:VGCT","NCIT:C128294","UMLS:C4288008","MEDGEN:925540"],"termid":"MONDO:0020650","xrefs":{"Monarch":{"xref_id":"0020650"}}}


id: PBO:0061072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"natural killer cell granule protein 7","termid":"PBO:0061072"}


id: FYPO:0005733
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of glutamate-ammonia ligase activity is increased during a cellular response to iron ion starvation.","definition_xrefs":["PomBase:mah","PMID:20435771"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased glutamate-ammonia ligase activity","termid":"FYPO:0002270"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000661","FYPO:0000707","FYPO:0001985","FYPO:0000654"],"is_obsolete":false,"name":"increased glutamate-ammonia ligase activity during cellular response to iron ion starvation","synonyms":[{"name":"increased GS activity during cellular response to iron ion starvation","type":"exact"},{"name":"increased glutamate-ammonia ligase activity during iron ion starvation","type":"exact"},{"name":"increased glutamine synthetase activity during cellular response to iron ion starvation","type":"exact"},{"name":"increased glutamylhydroxamic synthetase activity during cellular response to iron ion starvation","type":"exact"}],"termid":"FYPO:0005733"}


id: GO:1902459
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of stem cell population maintenance.","definition_xrefs":["GOC:hjd","GOC:TermGenie","PMID:22969033"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of stem cell population maintenance","termid":"GO:2000036"},{"relation_name":"positively_regulates","term_name":"stem cell population maintenance","termid":"GO:0019827"}],"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 stem cell population maintenance","synonyms":[{"name":"activation of maintenance of pluripotency","type":"related"},{"name":"activation of stem cell maintenance","type":"narrow"},{"name":"positive regulation of maintenance of pluripotency","type":"related"},{"name":"up regulation of maintenance of pluripotency","type":"related"},{"name":"up regulation of stem cell maintenance","type":"exact"},{"name":"up-regulation of maintenance of pluripotency","type":"related"},{"name":"up-regulation of stem cell maintenance","type":"exact"},{"name":"upregulation of maintenance of pluripotency","type":"related"},{"name":"upregulation of stem cell maintenance","type":"exact"}],"termid":"GO:1902459"}


id: MOD:02007
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to N6-palmitoleyl-L-lysine.","direct_ancestors":[{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"},{"relation_name":"is_a","term_name":"N-palmitoleylated residue","termid":"MOD:02008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"},{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01875","MOD:01155"],"is_obsolete":false,"name":"N6-palmitoleyl-L-lysine","termid":"MOD:02007"}


id: PBO:0039940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AT-rich interaction domain 3A","termid":"PBO:0039940"}


id: GO:0075298
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of zygospore formation, a process in which a thick-walled spore of some algae and fungi is formed by union of two similar sexual cells, usually serves as a resting spore, and produces the sporophytic phase.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sexual sporulation resulting in formation of a cellular spore","termid":"GO:0043940"},{"relation_name":"regulates","term_name":"zygospore formation","termid":"GO:0034296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of zygospore formation","termid":"GO:0075298"}


id: GO:1902120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of meiotic spindle elongation.","definition_xrefs":["PMID:23370392","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of meiotic nuclear division","termid":"GO:0045835"},{"relation_name":"is_a","term_name":"regulation of meiotic spindle elongation","termid":"GO:1902119"},{"relation_name":"negatively_regulates","term_name":"meiotic spindle elongation","termid":"GO:0051232"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0140013"},{"rel_name":"regulates","termid":"GO:0140013"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0140013","GO:0007049"],"is_obsolete":false,"name":"negative regulation of meiotic spindle elongation","synonyms":[{"name":"down regulation of meiotic spindle elongation","type":"exact"},{"name":"down regulation of spindle elongation during meiosis","type":"exact"},{"name":"down-regulation of meiotic spindle elongation","type":"exact"},{"name":"down-regulation of spindle elongation during meiosis","type":"exact"},{"name":"downregulation of meiotic spindle elongation","type":"exact"},{"name":"downregulation of spindle elongation during meiosis","type":"exact"},{"name":"inhibition of meiotic spindle elongation","type":"narrow"},{"name":"inhibition of spindle elongation during meiosis","type":"exact"},{"name":"negative regulation of spindle elongation during meiosis","type":"exact"}],"termid":"GO:1902120"}


id: MONDO:0007504
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Thickened earlobes-conductive deafness syndrome is characterized by microtia with thickened ear lobes, micrognathia and conductive hearing loss due to congenital ossicular anomalies. It has been described in two families. The mode of inheritance is autosomal dominant.","definition_xrefs":["Orphanet:2405"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thickened earlobes-conductive deafness syndrome","secondary_identifiers":["UMLS:C1851896","MEDGEN:343676","SCTID:722476007","OMIM:128980","GARD:2195"],"synonyms":[{"name":"Escher Hirt syndrome","type":"related"},{"name":"Escher-Hirt syndrome","type":"exact"},{"name":"earlobes, thickened, with conductive deafness from incudostapedial abnormalities","type":"related"}],"termid":"MONDO:0007504","xrefs":{"Monarch":{"xref_id":"0007504"}}}


id: GO:0098759
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an interleukin-8 stimulus.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to cytokine stimulus","termid":"GO:0071345"},{"relation_name":"is_a","term_name":"response to interleukin-8","termid":"GO:0098758"}],"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 interleukin-8","synonyms":[{"name":"cellular response to IL-8","type":"exact"}],"termid":"GO:0098759"}


id: PR:O13781
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC17G6.03 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13781"],"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 C17G6.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17G6.03","synonyms":[{"name":"Spom972h-SPAC17G6.03","type":"exact"}],"termid":"PR:O13781"}


id: MOD:00604
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to 2x(2)H labeled monomethylated L-lysine.","definition_xrefs":["PubMed:15525938","Unimod:284"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"N6-methyl-L-lysine","termid":"MOD:00085"},{"relation_name":"is_a","term_name":"(2)H deuterium labeled residue","termid":"MOD:00839"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2x(2)H monomethylated L-lysine","synonyms":[{"name":"Deuterium Methylation of Lysine","type":"related"},{"name":"Methyl:2H(2)","type":"related"}],"termid":"MOD:00604"}


id: PBO:0089690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FCP1 homology domain, HAD hydrolase superfamily","termid":"PBO:0089690"}


id: PBO:0005499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L6 (predicted)","termid":"PBO:0005499"}


id: MONDO:0017397
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete constitutional dyserythropoietic anemia (obsolete MONDO:0017397)","secondary_identifiers":["Orphanet:293830"],"termid":"MONDO:0017397","xrefs":{"Monarch":{"xref_id":"0017397"}}}


id: PBO:0026685
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cell_population_growth_at_high_temperature","termid":"PBO:0026685"}


id: PBO:0054485
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 1885","termid":"PBO:0054485"}


id: PBO:0110155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome-associated protein, implicated in ribosome assembly or ribosome quality control","termid":"PBO:0110155"}


id: FYPO:0005969
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of magnesium chloride than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000139","FYPO:0001985","FYPO:0002682","FYPO:0000003"],"is_obsolete":false,"name":"resistance to magnesium chloride","synonyms":[{"name":"resistance to MgCl2","type":"exact"},{"name":"resistance to magnesium chloride during mitotic cell cycle","type":"related"},{"name":"resistance to magnesium chloride during vegetative growth","type":"exact"},{"name":"resistance to magnesium dichloride","type":"exact"},{"name":"resistant to magnesium chloride","type":"exact"}],"termid":"FYPO:0005969"}


id: PBO:0084599
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; YKL199C 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 YKL198C","termid":"PBO:0084599"}


id: PBO:0050212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosome binding domain 1 pseudogene 29","termid":"PBO:0050212"}


id: PATO:0002438
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's being located or placed beneath the skin.","definition_xrefs":["thefreedictionary:thefreedictionary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subdermal","synonyms":[{"name":"subcutaneous","type":"exact"}],"termid":"PATO:0002438"}


id: MONDO:0001404
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An ulcerative pyoderma usually caused by group A beta-hemolytic streptococcal infection at the site of minor trauma. (Dorland, 27th ed)","definition_xrefs":["MESH:D004473"],"direct_ancestors":[{"relation_name":"is_a","term_name":"impetigo","termid":"MONDO:0004592"}],"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":"ecthyma","secondary_identifiers":["ICD9:686.8","MEDGEN:8541","UMLS:C0013568","SCTID:85791004","icd11.foundation:337308923","DOID:11907"],"termid":"MONDO:0001404","xrefs":{"Monarch":{"xref_id":"0001404"}}}


id: GO:0032211
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the addition of telomeric repeats by telomerase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of telomere maintenance via telomerase","termid":"GO:0032210"},{"relation_name":"is_a","term_name":"negative regulation of telomere maintenance via telomere lengthening","termid":"GO:1904357"},{"relation_name":"is_a","term_name":"negative regulation of DNA biosynthetic process","termid":"GO:2000279"},{"relation_name":"negatively_regulates","term_name":"telomere maintenance via telomerase","termid":"GO:0007004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0032200"},{"rel_name":"negatively_regulates","termid":"GO:0032200"},{"rel_name":"negatively_regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0032200"],"is_obsolete":false,"name":"negative regulation of telomere maintenance via telomerase","synonyms":[{"name":"down regulation of telomere maintenance via telomerase activity","type":"exact"},{"name":"down-regulation of telomere maintenance via telomerase activity","type":"exact"},{"name":"downregulation of telomere maintenance via telomerase activity","type":"exact"},{"name":"inhibition of telomere maintenance via telomerase","type":"narrow"}],"termid":"GO:0032211"}


id: GO:0070977
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A developmental process, independent of morphogenetic (shape) change, that is required for bone to attain its fully functional state.","definition_xrefs":["GOC:mah","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ maturation","termid":"GO:0048799"},{"relation_name":"part_of","term_name":"bone development","termid":"GO:0060348"}],"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":"bone maturation","termid":"GO:0070977"}


id: PBO:0002244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent DNA helicase, UvrD subfamily","termid":"PBO:0002244"}


id: PATO:0002193
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A molecular quality that inheres in a molecular entity by virtue of the overall electric charge of the molecule, which is due to a comparison between the total number of electrons and the total number of protons.","definition_xrefs":["PATOC:JH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular quality","termid":"PATO:0002182"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"electric charge","termid":"PATO:0002193"}


id: PBO:0050075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-hydroxymethylcytosine binding, ES cell specific","termid":"PBO:0050075"}


id: PBO:0081234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger MYND-type containing 19","termid":"PBO:0081234"}


id: MONDO:0015930
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete respiratory malformation (obsolete MONDO:0015930)","secondary_identifiers":["Orphanet:182111"],"termid":"MONDO:0015930","xrefs":{"Monarch":{"xref_id":"0015930"}}}


id: FYPO:0006181
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the cytoplasm is decreased, and some of the protein is present in the nucleus instead, during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to cytoplasm, with protein mislocalized to nucleus","termid":"FYPO:0006100"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to cytoplasm, with protein mislocalized to nucleus, during mitotic interphase","synonyms":[{"name":"decreased protein localisation to cytoplasm, with protein mislocalised to nucleus, during mitotic interphase","type":"exact"},{"name":"decreased protein localization in cytoplasm, with protein mislocalized to nucleus, during mitotic interphase","type":"exact"},{"name":"decreased protein localization to cytoplasm, with protein mislocalized to nucleus, during interphase of mitotic cell cycle","type":"exact"},{"name":"decreased protein localization to cytoplasm, with protein mislocalized to nucleus, during mitotic interphase, during vegetative growth","type":"exact"},{"name":"reduced protein localization to cytoplasm, with protein mislocalized to nucleus, during mitotic interphase","type":"exact"}],"termid":"FYPO:0006181"}


id: GO:1990776
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 angiotensin stimulus. Angiotensin is any of three physiologically active peptides (angiotensin II, III, or IV) processed from angiotensinogen.","definition_xrefs":["PMID:22982863"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to peptide hormone","termid":"GO:0043434"}],"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 angiotensin","termid":"GO:1990776"}


id: PBO:0076670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRPM8 channel associated factor 2C","termid":"PBO:0076670"}


id: PBO:0040624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BANF1 pseudogene 3","termid":"PBO:0040624"}


id: MONDO:0012266
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any preeclampsia in which the cause of the disease is a mutation in the STOX1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"preeclampsia","termid":"MONDO:0005081"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"preeclampsia/eclampsia 4","secondary_identifiers":["GARD:18392","MEDGEN:322874","MESH:C563724","OMIM:609404","UMLS:C1836255"],"synonyms":[{"name":"PEE4","type":"related"},{"name":"PREECLAMPSIA/eclampsia 4","type":"related"},{"name":"Preeclampsia/eclampsia type 4","type":"exact"},{"name":"STOX1 preeclampsia","type":"exact"},{"name":"preeclampsia caused by mutation in STOX1","type":"exact"},{"name":"preeclampsia/eclampsia 4","type":"exact"}],"termid":"MONDO:0012266","xrefs":{"Monarch":{"xref_id":"0012266"}}}


id: MONDO:1010951
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial adenomatous polyposis that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial adenomatous polyposis, non-human animal","termid":"MONDO:1010215"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial adenomatous polyposis, pig","secondary_identifiers":["OMIA:001916-9823"],"termid":"MONDO:1010951","xrefs":{"Monarch":{"xref_id":"1010951"}}}


id: GO:0007074
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 the cell leaves M phase. M phase is the part of the mitotic cell cycle during which mitosis and cytokinesis take place.","definition_xrefs":["GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription involved in exit from mitosis, from RNA polymerase II promoter (obsolete GO:0007074)","synonyms":[{"name":"activation of transcription on exit from mitosis, from Pol II promoter","type":"narrow"},{"name":"activation of transcription on exit from mitosis, from RNA polymerase II promoter","type":"narrow"}],"termid":"GO:0007074"}


id: GO:0140538
data:
  {"annotated_genes":["SJAG_00145"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96941],"is_not":false,"summary":null,"term":"GO:0140538"}]},"cv_name":"biological_process","definition":"A process that prevents a zygote from fusing an additional cell.","definition_xrefs":["PMID:30089908"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of conjugation with cellular fusion","termid":"GO:0031138"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00145":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0000747"},{"rel_name":"negatively_regulates","termid":"GO:0000747"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0000747","GO:0008150"],"is_obsolete":false,"name":"negative regulation of conjugation with zygote","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140538","terms_by_termid":{"GO:0140538":null}}


id: PBO:0005785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complexed with Cdc5 protein Cwf26","termid":"PBO:0005785"}


id: PBO:0087575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the 19S regulatory particle of the 26S proteasome lid; synthetically lethal with RPT1, which is an ATPase component of the 19S regulatory particle; physically interacts with Nob1p and Rpn3p; protein abundance increases in response to DNA replication stress","termid":"PBO:0087575"}


id: MOD:00819
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamic acid residue to L-2-aminobutanoic acid.","definition_xrefs":["PubMed:11740505","ChEBI:35619","RESID:AA0409","DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-glutamic acid residue","termid":"MOD:00906"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-2-aminobutanoic acid (Glu)","synonyms":[{"name":"(S)-2-aminobutanoic acid","type":"exact"},{"name":"Abu","type":"exact"},{"name":"L-2-amino-n-butyric acid","type":"exact"},{"name":"L-2-aminobutanoic acid","type":"exact"},{"name":"L-2-aminobutyric acid","type":"exact"},{"name":"L-alpha-amino-n-butyric acid","type":"exact"},{"name":"L-alpha-aminobutyric acid","type":"exact"},{"name":"L-butyrine","type":"exact"},{"name":"alpha-amino-n-butyric acid","type":"exact"},{"name":"alpha-aminobutyric acid","type":"exact"},{"name":"butyrine","type":"exact"},{"name":"dCbxGlu","type":"exact"}],"termid":"MOD:00819"}


id: PBO:0112753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"agmatinase 3, Agm3","termid":"PBO:0112753"}


id: PBO:0031225
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_response_to_cadmium_ion","termid":"PBO:0031225"}


id: GO:0075030
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of symbiont germ tube hook structure formation.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"regulates","term_name":"formation of appressorium germ tube hook structure","termid":"GO:0075029"}],"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 formation of symbiont germ tube hook structure for appressorium development","synonyms":[{"name":"modulation of germ tube tip of symbiont on or near the exterior of host","type":"exact"},{"name":"modulation of symbiont germ tube hook structure formation on or near host","type":"related"},{"name":"regulation of formation of symbiont germ tube hook structure on or near host","type":"exact"}],"termid":"GO:0075030"}


id: GO:0140971
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of AIM2 inflammasome complex assembly.","definition_xrefs":["PMID:33467177"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein-containing complex assembly","termid":"GO:0043254"},{"relation_name":"part_of","term_name":"regulation of inflammasome-mediated signaling pathway","termid":"GO:0141085"},{"relation_name":"regulates","term_name":"AIM2 inflammasome complex assembly","termid":"GO:0140970"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"regulation of AIM2 inflammasome complex assembly","termid":"GO:0140971"}


id: GO:1990741
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the non-selective, energy-independent passage of cations across a lipid bilayer down a concentration gradient.","definition_xrefs":["GOC:pr","Wikipedia:Ion_channel#Classification_by_type_of_ions","ISBN:0878937420"],"gene_count":0,"genotype_count":0,"name":"obsolete non-selective cation channel activity (obsolete GO:1990741)","synonyms":[{"name":"nonselective cation channel activity","type":"exact"}],"termid":"GO:1990741"}


id: MONDO:0002480
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, borderline, or malignant epithelial tumor of the female reproductive system characterized by the presence of glands and/or cysts lined by neoplastic cells that resemble endometrial cells.","definition_xrefs":["NCIT:C7113"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"female reproductive organ cancer","termid":"MONDO:0001416"},{"relation_name":"is_a","term_name":"epithelial neoplasm","termid":"MONDO:0005626"},{"relation_name":"is_a","term_name":"female reproductive system neoplasm","termid":"MONDO:0021148"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endometrioid tumor","secondary_identifiers":["UMLS:C0474809","MEDGEN:105374","DOID:3001"],"synonyms":[{"name":"endometrioid neoplasm","type":"exact"},{"name":"endometrioid neoplasm of female reproductive system","type":"exact"},{"name":"endometrioid neoplasm of the female reproductive system","type":"exact"},{"name":"endometrioid tumor","type":"exact"},{"name":"endometrioid tumor (morphologic abnormality)","type":"exact"},{"name":"endometrioid tumor of female reproductive system","type":"exact"},{"name":"endometrioid tumor of the female reproductive system","type":"exact"},{"name":"endometrioid tumour (morphologic abnormality)","type":"exact"},{"name":"endometrioid tumour of female reproductive system","type":"exact"},{"name":"endometrioid tumour of the female reproductive system","type":"exact"},{"name":"female reproductive endometrioid cancer","type":"related"},{"name":"female reproductive endometrioid neoplasm","type":"exact"},{"name":"female reproductive endometrioid tumor","type":"exact"},{"name":"female reproductive endometrioid tumour","type":"exact"}],"termid":"MONDO:0002480","xrefs":{"Monarch":{"xref_id":"0002480"}}}


id: PBO:0088662
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aspartic protease, yapsin family, unknown specificity Yps1","termid":"PBO:0088662"}


id: PBO:0069710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 990, pseudogene","termid":"PBO:0069710"}


id: PBO:0063914
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta","termid":"PBO:0063914"}


id: PBO:0051709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol polyphosphate phosphatase like 1","termid":"PBO:0051709"}


id: PBO:0089388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S8","termid":"PBO:0089388"}


id: GO:0010483
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An interaction between the pollen tube, part of the male gametophyte, and the female gametophyte (typically the synergid cells), that results in the arrest of pollen tube growth, rupture of the pollen tube and the release of the sperm cells.","definition_xrefs":["PMID:37640641"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological process involved in intraspecies interaction between organisms","termid":"GO:0051703"},{"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":"pollen tube reception","termid":"GO:0010483"}


id: PBO:0063535
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDZRN3 antisense RNA 1","termid":"PBO:0063535"}


id: GO:0102817
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: delphinidin 3-O-glucosyl-5-O-(caffeoylglucoside-3'-O-glucoside) + caffeoyl-CoA = gentiodelphin + coenzyme A.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete caffeoyl-CoA:3-O-glucosyl-5-O-(caffeoylglucoside-3'-O-glucoside) 3'-O-hydroxycinnamoyltransferase activity (obsolete GO:0102817)","termid":"GO:0102817"}


id: MONDO:0020271
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete phakomatosis with eye involvement (obsolete MONDO:0020271)","secondary_identifiers":["Orphanet:98701"],"termid":"MONDO:0020271","xrefs":{"Monarch":{"xref_id":"0020271"}}}


id: PBO:0049083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 137C","termid":"PBO:0049083"}


id: PBO:0078488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ile (anticodon AAT) 7-2","termid":"PBO:0078488"}


id: GO:0004879
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A DNA-binding transcription factor activity regulated by binding to a ligand that modulates the transcription of specific gene sets transcribed by RNA polymerase II. Nuclear receptor ligands are usually lipid-based (such as a steroid hormone) and the binding of the ligand to its receptor often occurs in the cytosol, which leads to its translocation to the nucleus.","definition_xrefs":["GOC:txnOH-2018","PMID:23457262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-binding transcription factor activity, RNA polymerase II-specific","termid":"GO:0000981"},{"relation_name":"is_a","term_name":"signaling receptor activity","termid":"GO:0038023"},{"relation_name":"is_a","term_name":"ligand-modulated transcription factor activity","termid":"GO:0098531"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140110"},{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003700"}],"interesting_parent_ids":["GO:0038023","GO:0003674","GO:0140110","GO:0003700"],"is_obsolete":false,"name":"nuclear receptor activity","secondary_identifiers":["GO:0038050","GO:0004884","GO:0004882","GO:0004886","GO:0038052","GO:0004887","GO:0003708","GO:0008434","GO:0038051","GO:0004880"],"synonyms":[{"name":"1,25-(OH)2D3 receptor activity","type":"narrow"},{"name":"9-cis retinoic acid receptor activity","type":"narrow"},{"name":"RNA polymerase II transcription factor activity, estrogen-activated sequence-specific DNA binding","type":"narrow"},{"name":"RNA polymerase II transcription factor activity, glucocorticoid-activated sequence-specific DNA binding","type":"narrow"},{"name":"RNA polymerase II transcription factor activity, ligand-activated sequence-specific DNA binding","type":"exact"},{"name":"RXR","type":"narrow"},{"name":"androgen receptor activity","type":"narrow"},{"name":"calcitriol receptor activity","type":"narrow"},{"name":"ecdysteroid hormone receptor activity","type":"narrow"},{"name":"estrogen nuclear receptor activity","type":"narrow"},{"name":"glucocorticoid receptor activity","type":"narrow"},{"name":"juvenile hormone receptor activity","type":"narrow"},{"name":"ligand-activated sequence-specific DNA binding RNA polymerase II transcription factor activity","type":"exact"},{"name":"ligand-dependent nuclear receptor activity","type":"related"},{"name":"ligand-dependent transcription factor activity","type":"related"},{"name":"nuclear hormone receptor","type":"narrow"},{"name":"retinoic acid receptor activity","type":"narrow"},{"name":"retinoid-X receptor activity","type":"narrow"},{"name":"thyroid hormone receptor activity","type":"narrow"},{"name":"vitamin A receptor activity","type":"narrow"},{"name":"vitamin D receptor activity","type":"narrow"},{"name":"vitamin D3 receptor activity","type":"narrow"}],"termid":"GO:0004879"}


id: PBO:0069034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 279, pseudogene","termid":"PBO:0069034"}


id: GO:0098694
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of synaptic vesicle budding from presynaptic endocytic zone membrane.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of organelle organization","termid":"GO:0033043"},{"relation_name":"regulates","term_name":"synaptic vesicle budding from presynaptic endocytic zone membrane","termid":"GO:0016185"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0061024"],"is_obsolete":false,"name":"regulation of synaptic vesicle budding from presynaptic endocytic zone membrane","termid":"GO:0098694"}


id: GO:0038203
data:
  {"annotated_genes":["SJAG_04987","SJAG_03067","SJAG_05030","SJAG_01020","SJAG_04460","SJAG_01320","SJAG_00143","SJAG_06588","SJAG_00117","SJAG_04206"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74276,78788,79243,101162,108497,110393],"is_not":false,"summary":null,"term":"GO:0038203"},{"annotations":[118115],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1903940"},{"annotations":[92965,99529,108806],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1904515"}]},"cv_name":"biological_process","definition":"A series of intracellular molecular signals mediated by TORC2; TOR (rapamycin-insensitive companion of TOR) in complex with at least Rictor (regulatory-associated protein of TOR), or orthologs of, and other signaling components.","definition_xrefs":["GOC:lb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"TOR signaling","termid":"GO:0031929"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00117":null,"SJAG_00143":null,"SJAG_01020":null,"SJAG_01320":null,"SJAG_03067":null,"SJAG_04206":null,"SJAG_04460":null,"SJAG_04987":null,"SJAG_05030":null,"SJAG_06588":null},"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":"TORC2 signaling","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"TORC2 signal transduction","type":"exact"}],"termid":"GO:0038203","terms_by_termid":{"GO:0038203":null,"GO:1903940":null,"GO:1904515":null}}


id: GO:0042909
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of acridine (10-azaanthracene), a heterocyclic ring compound found in crude coal-tar anthracene, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["Wikipedia:Acridine","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete acridine transport (obsolete GO:0042909)","termid":"GO:0042909"}


id: MONDO:0017449
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Split hand is a rare, non-syndromic limb reduction defect, clinically and genetically heterogeneous, characterized by bilateral or unilateral underdevelopment or absence of the central rays of the autopod, with absence of all or just some of the central phalanges and at least part of the associated metacarpal bones, yielding a cleft appearance of the hand. It is frequently associated with syndactyly and aplasia/hypoplasia of remaining digits and metacarpal bones. No other dysmorphic features are observed and development is appropriate for age.","definition_xrefs":["Orphanet:294992"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"split hand","secondary_identifiers":["icd11.foundation:924222970","MEDGEN:397570","HP:0001171","UMLS:C2699510"],"synonyms":[{"name":"ectrodactyly of hand","type":"exact"},{"name":"split hand","type":"exact"},{"name":"split hand (disease)","type":"exact"}],"termid":"MONDO:0017449","xrefs":{"Monarch":{"xref_id":"0017449"}}}


id: MONDO:0021948
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"extrapulmonary tuberculosis","termid":"MONDO:0000368"},{"relation_name":"is_a","term_name":"skin disease caused by bacterial infection","termid":"MONDO:0024295"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"cutaneous tuberculosis","secondary_identifiers":["UMLS:C0041309","SCTID:66986005","MEDGEN:22515","icd11.foundation:625292625"],"synonyms":[{"name":"Cutaneous Tuberculoses","type":"related"},{"name":"Cutaneous Tuberculosis","type":"related"},{"name":"Cutaneous tuberculosis","type":"related"},{"name":"Skin Tuberculoses","type":"related"},{"name":"Skin Tuberculosis","type":"related"},{"name":"Tuberculoderma","type":"related"},{"name":"Tuberculoses, Cutaneous","type":"related"},{"name":"Tuberculoses, Skin","type":"related"},{"name":"Tuberculosis cutis","type":"related"},{"name":"Tuberculosis of skin","type":"related"},{"name":"Tuberculosis, Cutaneous","type":"related"},{"name":"Tuberculosis, Skin","type":"related"},{"name":"cutaneous tuberculosis","type":"exact"},{"name":"tuberculoderma","type":"related"},{"name":"tuberculosis cutis","type":"related"},{"name":"tuberculosis of skin","type":"exact"}],"termid":"MONDO:0021948","xrefs":{"Monarch":{"xref_id":"0021948"}}}


id: GO:0050401
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-xylonate = 2-dehydro-3-deoxy-D-arabinonate + H2O.","definition_xrefs":["RHEA:19157","EC:4.2.1.82"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"xylonate dehydratase activity","secondary_identifiers":["KEGG_REACTION:R02429","MetaCyc:XYLONATE-DEHYDRATASE-RXN"],"synonyms":[{"name":"D-xylo-aldonate dehydratase activity","type":"related"},{"name":"D-xylonate dehydratase activity","type":"related"},{"name":"D-xylonate hydro-lyase (2-dehydro-3-deoxy-D-xylonate-forming)","type":"related"},{"name":"D-xylonate hydro-lyase activity","type":"related"}],"termid":"GO:0050401"}


id: PBO:0049192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate ionotropic receptor AMPA type subunit 3","termid":"PBO:0049192"}


id: PBO:0030130
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_potassium_level","termid":"PBO:0030130"}


id: PBO:0080990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and BTB domain containing 21","termid":"PBO:0080990"}


id: PBO:0080687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WIZ pseudogene 1","termid":"PBO:0080687"}


id: MONDO:0005998
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infestation with mites of the genus Trombiculidae, whose larvae carry the rickettsial agent of scrub typhus.","definition_xrefs":["MESH:D014323-modified"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mite infestation","termid":"MONDO:0004389"}],"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":"trombiculiasis","secondary_identifiers":["UMLS:C0041170","MEDGEN:11928","DOID:8399","MESH:D014323"],"synonyms":[{"name":"Trombiculidae caused disease or disorder","type":"exact"},{"name":"Trombiculidae disease or disorder","type":"exact"},{"name":"Trombiculidae infectious disease","type":"exact"}],"termid":"MONDO:0005998","xrefs":{"Monarch":{"xref_id":"0005998"}}}


id: PBO:0080399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS29 retromer complex component","termid":"PBO:0080399"}


id: GO:0097565
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Set of two basal bodies found in Giardia species (trophozoite stage). It comprises the caudal and posteriolateral basal bodies located to the left of the right nucleus of the trophozoite when viewed dorsally.","definition_xrefs":["GOC:giardia","ISBN:9780124260207","PMID:16607022","PMID:5961344"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cell projection","termid":"GO:0042995"}],"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":"right middle basal body pair","termid":"GO:0097565"}


id: MONDO:0019493
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Adult heart tumor refers to neoplasms of the heart that manifest in adults and generally present with a variety of non-specific manifestations (depending on tumor site and infiltration) such as weight loss, exhaustion, hemorrhagic pericardial effusion, heart failure, arrhythmias, and embolisms, or that can also be asymptomatic. In adults 75% of heart tumors are benign, with myxoma being the most common benign tumor (accounting for 50-70% of all primary heart tumors) and rhabdomyosarcoma comprising 75% of malignant heart tumors. Other malignant tumors of the heart include fibrosarcoma and leiomyosarcoma (see these terms).","definition_xrefs":["Orphanet:874"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart neoplasm","termid":"MONDO:0021209"}],"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":"primary adult heart tumor","secondary_identifiers":["ICD10CM:D15.1","UMLS:C4275152","SCTID:715403006","GARD:18709","MEDGEN:900582"],"synonyms":[{"name":"adult cardiac tumor","type":"exact"},{"name":"adult cardiac tumour","type":"exact"},{"name":"adult heart tumor","type":"exact"},{"name":"adult heart tumour","type":"exact"}],"termid":"MONDO:0019493","xrefs":{"Monarch":{"xref_id":"0019493"}}}


id: PBO:0062018
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily L member 9 pseudogene","termid":"PBO:0062018"}


id: PBO:0116408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S. pombe specific DUF999 family protein 4","termid":"PBO:0116408"}


id: PBO:0001007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi phosphoprotein 3 family (predicted)","termid":"PBO:0001007"}


id: MONDO:0021251
data:
  {"annotated_genes":["SJAG_01419","SJAG_02748"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86763,89031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011962"}]},"cv_name":"mondo","definition":"A neoplasm (disease) that involves the endometrium.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endometrial disorder","termid":"MONDO:0000931"},{"relation_name":"is_a","term_name":"tumor of uterus","termid":"MONDO:0021353"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01419":null,"SJAG_02748":null},"genotype_count":0,"is_obsolete":false,"name":"endometrium neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:239.5","SCTID:123844007","UMLS:C0014170","MEDGEN:8619","MESH:D016889","NCIT:C3012"],"synonyms":[{"name":"endometrial neoplasm","type":"exact"},{"name":"endometrial tumor","type":"exact"},{"name":"endometrial tumour","type":"exact"},{"name":"endometrium neoplasm (disease)","type":"exact"},{"name":"endometrium tumor","type":"exact"},{"name":"endometrium tumour","type":"exact"},{"name":"neoplasm of endometrium","type":"exact"},{"name":"neoplasm of the endometrium","type":"exact"},{"name":"tumor of endometrium","type":"exact"},{"name":"tumor of the endometrium","type":"exact"},{"name":"tumour of endometrium","type":"exact"},{"name":"tumour of the endometrium","type":"exact"}],"termid":"MONDO:0021251","terms_by_termid":{"MONDO:0011962":null},"xrefs":{"Monarch":{"xref_id":"0021251"}}}


id: PBO:0029517
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_vegetative_cell_with_abnormal_cell_shape","termid":"PBO:0029517"}


id: GO:0061191
data:
  {"annotated_genes":["SJAG_02433","SJAG_03137"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99407,112091],"is_not":false,"summary":null,"term":"GO:0061191"}]},"cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of the fusion of two vacuole membranes to form a single vacuole.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vacuole fusion, non-autophagic","termid":"GO:0032889"},{"relation_name":"is_a","term_name":"positive regulation of vacuole organization","termid":"GO:0044090"},{"relation_name":"positively_regulates","term_name":"vacuole fusion, non-autophagic","termid":"GO:0042144"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02433":null,"SJAG_03137":null},"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 vacuole fusion, non-autophagic","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0061191","terms_by_termid":{"GO:0061191":null}}


id: PBO:0057785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3065","termid":"PBO:0057785"}


id: MONDO:1011950
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":"osteochondroma causing progressive posterior paresis, non-human animal","secondary_identifiers":["OMIA:000749"],"termid":"MONDO:1011950","xrefs":{"Monarch":{"xref_id":"1011950"}}}


id: GO:0047763
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + 3,4-dihydroxy-trans-cinnamate = S-adenosyl-L-homocysteine + 3-methoxy-4-hydroxy-trans-cinnamate.","definition_xrefs":["EC:2.1.1.68"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-methyltransferase activity","termid":"GO:0008171"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016741","GO:0016740"],"is_obsolete":false,"name":"caffeate O-methyltransferase activity","secondary_identifiers":["MetaCyc:RXN-1104","RHEA:20225"],"synonyms":[{"name":"S-adenosyl-L-methionine:3,4-dihydroxy-trans-cinnamate 3-O-methyltransferase activity","type":"related"},{"name":"S-adenosyl-L-methionine:caffeic acid-O-methyltransferase activity","type":"related"},{"name":"caffeate 3-O-methyltransferase activity","type":"related"},{"name":"caffeate methyltransferase activity","type":"related"}],"termid":"GO:0047763"}


id: MONDO:0019202
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant fibroblastic neoplasm arising from the soft tissue. It is characterized by the presence of spindle-shaped cells, cellular pleomorphism, thin-walled blood vessels, fibrous septa, and myxoid stroma.","definition_xrefs":["NCIT:C6496"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete muscular tumor (obsolete MONDO:0016123)","termid":"MONDO:0016123"},{"relation_name":"is_a","term_name":"soft tissue sarcoma","termid":"MONDO:0018078"}],"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":"myxofibrosarcoma","secondary_identifiers":["DOID:0080534","GARD:18941","ONCOTREE:MFS","icd11.foundation:405689402","MEDGEN:811359","SCTID:253042009","Orphanet:79105","MedDRA:10066948","UMLS:C3714524","ICDO:8811/3"],"synonyms":[{"name":"MFS","type":"related"},{"name":"fibromyxosarcoma","type":"exact"},{"name":"myxofibrosarcoma","type":"exact"},{"name":"myxoid MFH","type":"exact"},{"name":"myxoid fibrous histiocytoma","type":"exact"},{"name":"myxoid malignant fibrous histiocytoma","type":"exact"}],"termid":"MONDO:0019202","xrefs":{"Monarch":{"xref_id":"0019202"}}}


id: PBO:0076217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sad1 and UNC84 domain containing 5","termid":"PBO:0076217"}


id: PBO:0018142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein carboxyl methyltransferase, implicated in DNA damage response","termid":"PBO:0018142"}


id: PBO:0038530
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abhydrolase domain containing 4, N-acyl phospholipase B","termid":"PBO:0038530"}


id: MONDO:0011804
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autoimmune lymphoproliferative syndrome (ALPS) with recurrent viral infections is a rare genetic disorder characterized by lymphadenopathy and/or splenomegaly and recurrent infections due to herpes viruses.","definition_xrefs":["Orphanet:275517"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune lymphoproliferative syndrome","termid":"MONDO:0017979"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune lymphoproliferative syndrome type 2B","secondary_identifiers":["OMIM:607271","UMLS:C1846545","GARD:9796","DOID:0110116","MEDGEN:339548","SCTID:722290008","NANDO:2200740"],"synonyms":[{"name":"ALPS with recurrent viral infections","type":"exact"},{"name":"ALPS2B","type":"exact"},{"name":"CASP8 autoimmune lymphoproliferative syndrome","type":"exact"},{"name":"CEDS","type":"exact"},{"name":"Ceds","type":"related"},{"name":"autoimmune lymphoproliferative syndrome caused by mutation in CASP8","type":"exact"},{"name":"autoimmune lymphoproliferative syndrome type IIB","type":"exact"},{"name":"autoimmune lymphoproliferative syndrome with recurrent viral infections","type":"exact"},{"name":"autoimmune lymphoproliferative syndrome, type 2B","type":"related"},{"name":"autoimmune lymphoproliferative syndrome, type IIB","type":"exact"},{"name":"caspase 8 deficiency","type":"exact"},{"name":"caspase 8 deficiency syndrome","type":"exact"},{"name":"caspase eight deficiency state","type":"exact"},{"name":"caspase-8 deficiency","type":"related"}],"termid":"MONDO:0011804","xrefs":{"Monarch":{"xref_id":"0011804"}}}


id: PBO:0085135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleolar protein required for 60S ribosome subunit biogenesis; constituent of 66S pre-ribosomal particles; physically interacts with Nop8p and the exosome subunit Rrp43p","termid":"PBO:0085135"}


id: GO:0004484
data:
  {"annotated_genes":["SJAG_01724"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77173],"is_not":false,"summary":null,"term":"GO:0004484"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: GTP + (5')pp-Pur-mRNA = diphosphate + G(5')ppp-Pur-mRNA; G(5')ppp-Pur-mRNA is mRNA containing a guanosine residue linked 5' through three phosphates to the 5' position of the terminal residue.","definition_xrefs":["EC:2.7.7.50"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA guanylyltransferase activity","termid":"GO:0008192"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01724":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016779","GO:0140098"],"is_obsolete":false,"name":"mRNA guanylyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:MRNA-GUANYLYLTRANSFERASE-RXN","Reactome:R-HSA-77083","Reactome:R-HSA-77081","Reactome:R-HSA-9815529","RHEA:54592"],"synonyms":[{"name":"GTP--RNA guanylyltransferase activity","type":"related"},{"name":"GTP:mRNA guanylyltransferase activity","type":"exact"},{"name":"mRNA capping enzyme activity","type":"related"},{"name":"messenger RNA guanylyltransferase activity","type":"related"},{"name":"protein lambda2","type":"related"}],"termid":"GO:0004484","terms_by_termid":{"GO:0004484":null}}


id: GO:1900595
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of (+)-kotanin.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary metabolite catabolic process","termid":"GO:0090487"},{"relation_name":"is_a","term_name":"(+)-kotanin metabolic process","termid":"GO:1900594"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"(+)-kotanin catabolic process","synonyms":[{"name":"(+)-kotanin breakdown","type":"exact"},{"name":"(+)-kotanin catabolism","type":"exact"},{"name":"(+)-kotanin degradation","type":"exact"}],"termid":"GO:1900595"}


id: MONDO:0013317
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Torsade-de-pointes (TdP) syndrome with short coupling interval is a very rare variant of Torsade de pointes, a polymorphic ventricular tachycardia, which is characterized by a short coupling interval of the first TdP beat on electrocardiogram in the absence of any structural heart disease. It manifests in early adulthood with syncope, often results in ventricular fibrillation and shows a high risk of sudden cardiac death.","definition_xrefs":["Orphanet:51084"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac rhythm disease","termid":"MONDO:0007263"}],"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":"torsade-de-pointes syndrome with short coupling interval","secondary_identifiers":["GARD:16651","OMIM:613600","SCTID:718104007","MEDGEN:462201","UMLS:C3150851"],"synonyms":[{"name":"torsade DE pointes, short-coupled variant","type":"related"}],"termid":"MONDO:0013317","xrefs":{"Monarch":{"xref_id":"0013317"}}}


id: GO:1903326
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of tRNA metabolic process.","definition_xrefs":["GOC:vw","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of RNA metabolic process","termid":"GO:0051252"},{"relation_name":"regulates","term_name":"tRNA metabolic process","termid":"GO:0006399"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006399","GO:0008150"],"is_obsolete":false,"name":"regulation of tRNA metabolic process","synonyms":[{"name":"regulation of tRNA metabolism","type":"exact"}],"termid":"GO:1903326"}


id: PBO:0078496
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ile (anticodon GAT) 1-3","termid":"PBO:0078496"}


id: PBO:0001487
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Telomere-associated in Yarrowia lipolytica","termid":"PBO:0001487"}


id: MONDO:0016430
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tumefactive multiple sclerosis is characterized by a tumor-like lesion larger than two centimeters and signs and symptoms similar to those of a brain tumor. It is a rare form of multiple sclerosis (MS). Symptoms of tumefactive MS often differ from other MS cases and may include, headaches, changes in thinking, confusion, speech problems, seizures, and weakness. The cause of tumefactive MS is not known. It often develops into the relapsing-remitting form of MS. In other cases there is only one occurrence of the condition. In still others the disease process remains less clear. While there is no cure for tumefactive MS, treatments such as corticosteroids are available to decrease disease activity.","definition_xrefs":["GARD:0005885"],"direct_ancestors":[{"relation_name":"is_a","term_name":"demyelinating disease","termid":"MONDO:0002562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"Balo concentric sclerosis","secondary_identifiers":["Orphanet:228165","NCIT:C35257","DOID:0060215","SCTID:49692006","GARD:5885","MEDGEN:498","MedDRA:10010252","NORD:835","SCTID:20415001","SCTID:230380005","NANDO:1200028","UMLS:C0004712","ICD9:341.1"],"synonyms":[{"name":"Balo Disease","type":"exact"},{"name":"Balo concentric sclerosis","type":"exact"},{"name":"Balo disease","type":"related"},{"name":"Balo's concentric sclerosis","type":"exact"},{"name":"Balo's disease","type":"related"},{"name":"Baló concentric sclerosis","type":"related"},{"name":"Marburg variant","type":"related"},{"name":"Tumefactive multiple sclerosis","type":"related"},{"name":"concentric demyelination","type":"exact"},{"name":"diffuse cerebral sclerosis of Schilder","type":"related"},{"name":"encephalitis periaxialis concentrica","type":"related"}],"termid":"MONDO:0016430","xrefs":{"Monarch":{"xref_id":"0016430"}}}


id: GO:1901901
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any regulation of protein localization to cell division site that is involved in cytokinesis.","definition_xrefs":["GOC:TermGenie","GOC:dph","PMID:22573892"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to cell division site","termid":"GO:1901900"},{"relation_name":"part_of","term_name":"cytokinesis","termid":"GO:0000910"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of protein localization to cell division site involved in cytokinesis","synonyms":[{"name":"regulation of protein localisation to cell division site involved in cytokinesis","type":"exact"}],"termid":"GO:1901901"}


id: GO:0048809
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of analia are generated and organized. The analia is the posterior-most vertral appendage that develops from the genital disc. An example of this process is analia morphogenesis in Drosophila melanogaster.","definition_xrefs":["GOC:ai","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"genital disc morphogenesis","termid":"GO:0007483"},{"relation_name":"part_of","term_name":"analia development","termid":"GO:0007487"}],"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":"analia morphogenesis","termid":"GO:0048809"}


id: GO:0032688
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of interferon-beta production.","definition_xrefs":["PMID:15546383","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of type I interferon production","termid":"GO:0032480"},{"relation_name":"is_a","term_name":"regulation of interferon-beta production","termid":"GO:0032648"},{"relation_name":"negatively_regulates","term_name":"interferon-beta production","termid":"GO:0032608"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of interferon-beta production","secondary_identifiers":["GO:0035548","GO:0045358"],"synonyms":[{"name":"down regulation of interferon-beta production","type":"exact"},{"name":"down-regulation of interferon-beta production","type":"exact"},{"name":"downregulation of interferon-beta production","type":"exact"},{"name":"inhibition of interferon-beta production","type":"narrow"},{"name":"negative regulation of IFN-beta production","type":"exact"},{"name":"negative regulation of interferon-beta biosynthetic process","type":"narrow"},{"name":"negative regulation of interferon-beta secretion","type":"narrow"}],"termid":"GO:0032688"}


id: GO:0009402
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete toxin resistance (obsolete GO:0009402)","synonyms":[{"name":"toxin resistance","type":"exact"}],"termid":"GO:0009402"}


id: PBO:0047686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FLRT2 antisense RNA 1","termid":"PBO:0047686"}


id: GO:0097079
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: selenite(out) + H+(out) = selenite(in) + H+(in).","definition_xrefs":["GOC:mcc","PMID:20861301"],"direct_ancestors":[{"relation_name":"is_a","term_name":"solute:proton symporter activity","termid":"GO:0015295"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"selenite:proton symporter activity","synonyms":[{"name":"selenite:H+ symporter activity","type":"exact"},{"name":"selenite:hydrogen symporter activity","type":"exact"}],"termid":"GO:0097079"}


id: PBO:0066227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBM33 divergent transcript","termid":"PBO:0066227"}


id: PR:P36586
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ypt5 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P36586"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"},{"relation_name":"is_a","term_name":"GTP-binding protein ypt5 (Schizosaccharomyces pombe)","termid":"PR:000030005"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP-binding protein ypt5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6F6.15","synonyms":[{"name":"SPAC6F6.15","type":"related"},{"name":"Spom972h-ypt5","type":"exact"}],"termid":"PR:P36586"}


id: GO:0031594
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The junction between the axon of a motor neuron and a muscle fiber. In response to the arrival of action potentials, the presynaptic button releases molecules of neurotransmitters into the synaptic cleft. These diffuse across the cleft and transmit the signal to the postsynaptic membrane of the muscle fiber, leading to a change in post-synaptic potential.","definition_xrefs":["GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synapse","termid":"GO:0045202"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"neuromuscular junction","secondary_identifiers":["NIF_Subcellular:sao1124888485","Wikipedia:Neuromuscular_junction"],"synonyms":[{"name":"NMJ","type":"related"},{"name":"motor endplate","type":"related"}],"termid":"GO:0031594"}


id: PBO:0046523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endoplasmic reticulum metallopeptidase 1","termid":"PBO:0046523"}


id: PBO:0075686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRC proto-oncogene, non-receptor tyrosine kinase","termid":"PBO:0075686"}


id: PBO:0038546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"abhydrolase domain containing 17A, depalmitoylase","termid":"PBO:0038546"}


id: GO:1900641
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of austinol biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biosynthetic process","termid":"GO:0009890"},{"relation_name":"is_a","term_name":"regulation of austinol biosynthetic process","termid":"GO:1900640"},{"relation_name":"negatively_regulates","term_name":"austinol biosynthetic process","termid":"GO:1900560"}],"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 austinol biosynthetic process","synonyms":[{"name":"down regulation of austinol anabolism","type":"exact"},{"name":"down regulation of austinol biosynthesis","type":"exact"},{"name":"down regulation of austinol biosynthetic process","type":"exact"},{"name":"down regulation of austinol formation","type":"exact"},{"name":"down regulation of austinol synthesis","type":"exact"},{"name":"down-regulation of austinol anabolism","type":"exact"},{"name":"down-regulation of austinol biosynthesis","type":"exact"},{"name":"down-regulation of austinol biosynthetic process","type":"exact"},{"name":"down-regulation of austinol formation","type":"exact"},{"name":"down-regulation of austinol synthesis","type":"exact"},{"name":"downregulation of austinol anabolism","type":"exact"},{"name":"downregulation of austinol biosynthesis","type":"exact"},{"name":"downregulation of austinol biosynthetic process","type":"exact"},{"name":"downregulation of austinol formation","type":"exact"},{"name":"downregulation of austinol synthesis","type":"exact"},{"name":"inhibition of austinol anabolism","type":"exact"},{"name":"inhibition of austinol biosynthesis","type":"exact"},{"name":"inhibition of austinol biosynthetic process","type":"narrow"},{"name":"inhibition of austinol formation","type":"exact"},{"name":"inhibition of austinol synthesis","type":"exact"},{"name":"negative regulation of austinol anabolism","type":"exact"},{"name":"negative regulation of austinol biosynthesis","type":"exact"},{"name":"negative regulation of austinol formation","type":"exact"},{"name":"negative regulation of austinol synthesis","type":"exact"}],"termid":"GO:1900641"}


id: MONDO:0700021
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosomal disorder in which chromosome 14 is affected.","definition_xrefs":["MONDO:patterns/chromosome_type"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal anomaly","termid":"MONDO:0020049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 14 disorder","termid":"MONDO:0700021","xrefs":{"Monarch":{"xref_id":"0700021"}}}


id: MONDO:0016567
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Locked-in syndrome (LIS) is a neurological condition characterized by the presence of sustained eye opening, quadriplegia or quadriparesis, anarthria, preserved cognitive functioning and a primary code of communication that uses vertical eye movements or blinking.","definition_xrefs":["Orphanet:2406"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"locked-in syndrome","secondary_identifiers":["MedDRA:10024792","GARD:6919","icd11.foundation:17562655","MEDGEN:7378","DOID:12697","MESH:D011782","NORD:1376","SCTID:38023001","UMLS:C0023944","ICD10CM:G83.5","ICD9:344.81","MESH:D000080422"],"synonyms":[{"name":"Cerebromedullospinal disconnection","type":"exact"},{"name":"Locked In Syndrome","type":"exact"},{"name":"locked in syndrome","type":"exact"},{"name":"locked-in state","type":"exact"}],"termid":"MONDO:0016567","xrefs":{"Monarch":{"xref_id":"0016567"}}}


id: PBO:0049330
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIF subunit 2","termid":"PBO:0049330"}


id: MONDO:0009711
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare genetic disorder caused by mutations in the TPM3, ACTA1, RYR1 or SEPN1 genes. It is inherited in an autosomal dominant or recessive pattern and rarely in an X-linked pattern. It manifests with myopathy throughout the body, particularly in the muscles of the shoulders, upper arms, hips, and thighs. Affected individuals may have contractures, lordosis, or scoliosis. In a minority of cases mild to severe breathing problems may occur.","definition_xrefs":["NCIT:C120046","PMID:31578728"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"qualitative or quantitative defects of alpha-actin","termid":"MONDO:0016193"},{"relation_name":"excluded_subClassOf","term_name":"qualitative or quantitative defects of selenoprotein N1","termid":"MONDO:0016197"},{"relation_name":"excluded_subClassOf","term_name":"qualitative or quantitative defects of tropomyosin","termid":"MONDO:0017303"},{"relation_name":"excluded_subClassOf","term_name":"alpha-actinopathy","termid":"MONDO:0100084"},{"relation_name":"excluded_subClassOf","term_name":"TPM3-related myopathy","termid":"MONDO:0100108"},{"relation_name":"excluded_subClassOf","term_name":"RYR1-related myopathy","termid":"MONDO:0100150"},{"relation_name":"excluded_subClassOf","term_name":"TPM2-related myopathy","termid":"MONDO:0100196"},{"relation_name":"is_a","term_name":"congenital structural myopathy","termid":"MONDO:0002921"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"congenital fiber-type disproportion myopathy","secondary_identifiers":["UMLS:C0546264","MEDGEN:108177","GARD:6161","NANDO:1200483","NANDO:2200868","Orphanet:2020","DOID:0080102"],"synonyms":[{"name":"CFTDM","type":"exact"},{"name":"congenital fiber type disproportion","type":"related"},{"name":"congenital fiber-type disproportion","type":"exact"},{"name":"congenital fibre type disproportion","type":"related"},{"name":"congenital myopathy with fiber type disproportion","type":"exact"},{"name":"congenital myopathy with fibre type disproportion","type":"exact"},{"name":"myopathy, congenital with fiber-type disproportion","type":"related"}],"termid":"MONDO:0009711","xrefs":{"Monarch":{"xref_id":"0009711"}}}


id: FYPO:0001794
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to purvalanol A is normal (i.e. indistinguishable from wild type). Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA level during vegetative growth","termid":"FYPO:0001317"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000257","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal RNA level during cellular response to purvalanol A","synonyms":[{"name":"normal RNA accumulation during cellular response to purvalanol A","type":"related"},{"name":"normal RNA level during cellular response to purvalanol A during mitotic cell cycle","type":"related"},{"name":"normal RNA level during cellular response to purvalanol A during vegetative growth","type":"exact"},{"name":"normal mRNA level during cellular response to purvalanol A","type":"narrow"},{"name":"normal transcript level during cellular response to purvalanol A","type":"exact"}],"termid":"FYPO:0001794"}


id: GO:0048891
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a lateral line ganglion neuron.","definition_xrefs":["PMID:15018940"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peripheral nervous system neuron differentiation","termid":"GO:0048934"},{"relation_name":"part_of","term_name":"lateral line ganglion development","termid":"GO:0048890"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lateral line ganglion neuron differentiation","synonyms":[{"name":"gLL neuron differentiation","type":"exact"}],"termid":"GO:0048891"}


id: PBO:0003902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translation initiation factor (predicted)","termid":"PBO:0003902"}


id: GO:1903183
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of SUMO ligase activity.","definition_xrefs":["GO_REF:0000059","PMID:16731528","GOC:PARL","GOC:bf","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of SUMO transferase activity (obsolete GO:1903183)","synonyms":[{"name":"down regulation of SMT3 conjugating enzyme","type":"exact"},{"name":"down regulation of SUMO conjugating enzyme activity","type":"exact"},{"name":"down regulation of SUMO ligase activity","type":"exact"},{"name":"down-regulation of SMT3 conjugating enzyme","type":"exact"},{"name":"down-regulation of SUMO conjugating enzyme activity","type":"exact"},{"name":"down-regulation of SUMO ligase activity","type":"exact"},{"name":"downregulation of SMT3 conjugating enzyme","type":"exact"},{"name":"downregulation of SUMO conjugating enzyme activity","type":"exact"},{"name":"downregulation of SUMO ligase activity","type":"exact"},{"name":"inhibition of SMT3 conjugating enzyme","type":"narrow"},{"name":"inhibition of SUMO conjugating enzyme activity","type":"narrow"},{"name":"inhibition of SUMO ligase activity","type":"narrow"},{"name":"negative regulation of SMT3 conjugating enzyme","type":"exact"},{"name":"negative regulation of SUMO conjugating enzyme activity","type":"exact"}],"termid":"GO:1903183"}


id: MONDO:0000895
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A bronchiolo-alveolar adenocarcinoma that is characterized by cells with cuboidal or columnar morphology with eosinophilic or clear cytoplasm and shows Clara cell or type 2 pneumocyte differentiation.","definition_xrefs":["DOID:0080186","PMID:17616987"],"direct_ancestors":[{"relation_name":"is_a","term_name":"minimally invasive lung adenocarcinoma","termid":"MONDO:0004991"}],"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":"nonmucinous bronchioloalveolar adenocarcinoma","secondary_identifiers":["UMLS:C1266034","NCIT:C7269","MEDGEN:266089"],"termid":"MONDO:0000895","xrefs":{"Monarch":{"xref_id":"0000895"}}}


id: GO:0006106
data:
  {"annotated_genes":["SJAG_00203","SJAG_04843"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80984,91941],"is_not":false,"summary":null,"term":"GO:0006106"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving fumarate, the anion of trans-1,2-ethenedicarboxylic acid, the diastereoisomer of maleate. It is a key intermediate in metabolism and is formed in the TCA cycle from succinate and converted into malate.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid metabolic process","termid":"GO:0043648"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00203":null,"SJAG_04843":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"fumarate metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"fumarate metabolism","type":"exact"}],"termid":"GO:0006106","terms_by_termid":{"GO:0006106":null}}


id: GO:0008104
data:
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id: FYPO:0000686
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal catalytic activity","termid":"FYPO:0000660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000654","FYPO:0000652"],"is_obsolete":false,"name":"normal peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase activity","termid":"FYPO:0000686"}


id: GO:0098616
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + H2SeO4 => diphosphate + adenylylselenate.","definition_xrefs":["PMID:2537056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylyltransferase activity","termid":"GO:0070566"}],"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:0016779"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016779","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"selenate adenylyltransferase (ATP) activity","secondary_identifiers":["Reactome:R-HSA-2408525"],"termid":"GO:0098616"}


id: GO:0006900
data:
  {"annotated_genes":["SJAG_05207","SJAG_02539","SJAG_00072","SJAG_05344","SJAG_03558","SJAG_04643","SJAG_03153","SJAG_04391","SJAG_03268","SJAG_05345","SJAG_03907","SJAG_00284","SJAG_01516","SJAG_01748","SJAG_01242","SJAG_02349","SJAG_00416"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71816,72387,75315,77915,80940],"is_not":false,"summary":null,"term":"GO:0006900"},{"annotations":[119591,72943],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0048205"},{"annotations":[74694],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090114"},{"annotations":[76523,77322,76877,78787,80151,78212,73028],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090110"},{"annotations":[79281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048194"},{"annotations":[97300],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006901"}]},"cv_name":"biological_process","definition":"The evagination of a membrane, resulting in formation of a vesicle.","definition_xrefs":["GOC:jid","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle organization","termid":"GO:0016050"},{"relation_name":"is_a","term_name":"membrane organization","termid":"GO:0061024"},{"relation_name":"part_of","term_name":"vesicle-mediated transport","termid":"GO:0016192"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00072":null,"SJAG_00284":null,"SJAG_00416":null,"SJAG_01242":null,"SJAG_01516":null,"SJAG_01748":null,"SJAG_02349":null,"SJAG_02539":null,"SJAG_03153":null,"SJAG_03268":null,"SJAG_03558":null,"SJAG_03907":null,"SJAG_04391":null,"SJAG_04643":null,"SJAG_05207":null,"SJAG_05344":null,"SJAG_05345":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0061024","GO:0016192"],"is_obsolete":false,"name":"vesicle budding from membrane","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:1902591","GO:0006902"],"synonyms":[{"name":"membrane evagination","type":"exact"},{"name":"nonselective vesicle assembly","type":"related"},{"name":"single organism membrane budding","type":"related"},{"name":"single-organism membrane budding","type":"related"},{"name":"vesicle biosynthesis","type":"exact"},{"name":"vesicle budding","type":"related"},{"name":"vesicle formation","type":"exact"}],"termid":"GO:0006900","terms_by_termid":{"GO:0006900":null,"GO:0006901":null,"GO:0048194":null,"GO:0048205":null,"GO:0090110":null,"GO:0090114":null}}


id: PBO:0054109
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 1474","termid":"PBO:0054109"}


id: PBO:0057191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 363","termid":"PBO:0057191"}


id: PBO:0065328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine protease 52, pseudogene","termid":"PBO:0065328"}


id: MONDO:1011801
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":"type 2 polysaccharide storage myopathy, non-human animal","secondary_identifiers":["OMIA:001537"],"termid":"MONDO:1011801","xrefs":{"Monarch":{"xref_id":"1011801"}}}


id: PATO:0001315
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A temperature which is increased by a low degree.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased temperature","termid":"PATO:0001305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mild increased temperature","termid":"PATO:0001315"}


id: GO:0050128
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-feruloylglycine + H2O = ferulate + glycine.","definition_xrefs":["RHEA:10484","EC:3.5.1.71"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787","GO:0016810"],"is_obsolete":false,"name":"N-feruloylglycine deacylase activity","secondary_identifiers":["MetaCyc:N-FERULOYLGLYCINE-DEACYLASE-RXN","KEGG_REACTION:R03579"],"synonyms":[{"name":"N-feruloylglycine amidohydrolase activity","type":"related"},{"name":"N-feruloylglycine hydrolase activity","type":"related"}],"termid":"GO:0050128"}


id: MONDO:0001099
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Single or multiple, milk-containing nodules in the breast. It is caused by obstruction of the breast ducts during lactation. Needle aspiration of the milk is the treatment of choice.","definition_xrefs":["NCIT:C3515"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast cyst","termid":"MONDO:0001011"},{"relation_name":"is_a","term_name":"lactation disease","termid":"MONDO:0045019"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lactocele","secondary_identifiers":["MESH:C535998","MEDGEN:101829","SCTID:42385006","UMLS:C0152243","icd11.foundation:1987155556","DOID:10686","ICD9:611.5"],"synonyms":[{"name":"Galactocoele","type":"related"},{"name":"galactocele","type":"exact"},{"name":"lacteal cyst","type":"related"}],"termid":"MONDO:0001099","xrefs":{"Monarch":{"xref_id":"0001099"}}}


id: PBO:0039685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amyloid beta precursor protein binding family B member 2","termid":"PBO:0039685"}


id: GO:0047885
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,6-trans-farnesol = 2-cis,6-trans-farnesol.","definition_xrefs":["EC:5.2.1.9","RHEA:13401"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cis-trans isomerase activity","termid":"GO:0016859"}],"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:0016853"}],"interesting_parent_ids":["GO:0003674","GO:0016853","GO:0003824"],"is_obsolete":false,"name":"farnesol 2-isomerase activity","secondary_identifiers":["MetaCyc:FARNESOL-2-ISOMERASE-RXN","KEGG_REACTION:R03265"],"synonyms":[{"name":"2-trans,6-trans-farnesol 2-cis-trans-isomerase activity","type":"related"},{"name":"farnesol isomerase activity","type":"related"}],"termid":"GO:0047885"}


id: PBO:0077450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 183A","termid":"PBO:0077450"}


id: PBO:0051258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable (III)-44 (pseudogene)","termid":"PBO:0051258"}


id: PBO:0040978
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 interacting protein like","termid":"PBO:0040978"}


id: FYPO:0002915
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which RNA splicing is abnormal. All RNA splicing may be abnormal, or one splicing of or more specific RNA molecules may be selectively affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal RNA metabolic process","termid":"FYPO:0004851"},{"relation_name":"is_a","term_name":"abnormal gene expression","termid":"FYPO:0006551"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0000002","FYPO:0006551","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal RNA splicing, via spliceosome","synonyms":[{"name":"abnormal RNA splicing during mitotic cell cycle","type":"related"},{"name":"abnormal RNA splicing during vegetative growth","type":"exact"},{"name":"abnormal RNA splicing, via transesterification reactions with bulged adenosine as nucleophile","type":"exact"}],"termid":"FYPO:0002915"}


id: MONDO:0003512
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant soft tissue neoplasm of the mediastinum. Representative examples of benign mediastinal soft tissue neoplasms include chondroma, leiomyoma, lipoma, and rhabdomyoma. Representative examples of malignant mediastinal soft tissue neoplasms include angiosarcoma, leiomyosarcoma, liposarcoma, osteosarcoma, rhabdomyosarcoma, and synovial sarcoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"mediastinal cancer","termid":"MONDO:0005843"},{"relation_name":"is_a","term_name":"soft tissue neoplasm","termid":"MONDO:0006424"},{"relation_name":"is_a","term_name":"neoplasm of mediastinum","termid":"MONDO:0021386"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediastinal mesenchymal tumor","secondary_identifiers":["MEDGEN:233171","DOID:5560","NCIT:C6637","UMLS:C1334669"],"synonyms":[{"name":"mediastinal soft tissue neoplasm","type":"exact"},{"name":"mediastinal soft tissue tumor","type":"exact"},{"name":"mediastinal soft tissue tumour","type":"exact"},{"name":"soft tissue neoplasm of mediastinum","type":"exact"},{"name":"soft tissue neoplasm of the mediastinum","type":"exact"},{"name":"soft tissue tumor of mediastinum","type":"exact"},{"name":"soft tissue tumor of the mediastinum","type":"exact"},{"name":"soft tissue tumour of mediastinum","type":"exact"},{"name":"soft tissue tumour of the mediastinum","type":"exact"}],"termid":"MONDO:0003512","xrefs":{"Monarch":{"xref_id":"0003512"}}}


id: MONDO:0005377
data:
  {"annotated_genes":["SJAG_04000","SJAG_04621","SJAG_03182","SJAG_03986","SJAG_04013","SJAG_04148","SJAG_00471","SJAG_01185","SJAG_04017","SJAG_00864","SJAG_01374","SJAG_03361","SJAG_00933","SJAG_00093"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88037],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013836"},{"annotations":[86830],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011303"},{"annotations":[87638],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014752"},{"annotations":[87561,87562],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014817"},{"annotations":[87560],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014818"},{"annotations":[88128],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032580"},{"annotations":[88129,88130],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032581"},{"annotations":[88126],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032582"},{"annotations":[87647,87648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0026726"},{"annotations":[86732],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014099"},{"annotations":[87566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014257"}]},"cv_name":"mondo","definition":"A collection of symptoms that include severe edema, proteinuria, and hypoalbuminemia; it is indicative of renal dysfunction.","definition_xrefs":["NCIT:C34845"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"nephrosis","termid":"MONDO:0002331"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00093":null,"SJAG_00471":null,"SJAG_00864":null,"SJAG_00933":null,"SJAG_01185":null,"SJAG_01374":null,"SJAG_03182":null,"SJAG_03361":null,"SJAG_03986":null,"SJAG_04000":null,"SJAG_04013":null,"SJAG_04017":null,"SJAG_04148":null,"SJAG_04621":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"nephrotic syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:1184","ICD9:581.9","NANDO:2100009","ICD10CM:N04","UMLS:C0027726","MEDGEN:10308","icd11.foundation:1184209951","MESH:D009404","EFO:0004255","ICD9:581","SCTID:52254009"],"synonyms":[{"name":"nephrosis","type":"related"},{"name":"nephrotic syndrome","type":"exact"},{"name":"nephrotic syndromes","type":"exact"},{"name":"syndrome, nephrotic","type":"exact"},{"name":"syndromes, nephrotic","type":"exact"}],"termid":"MONDO:0005377","terms_by_termid":{"MONDO:0011303":null,"MONDO:0013836":null,"MONDO:0014099":null,"MONDO:0014257":null,"MONDO:0014752":null,"MONDO:0014817":null,"MONDO:0014818":null,"MONDO:0026726":null,"MONDO:0032580":null,"MONDO:0032581":null,"MONDO:0032582":null},"xrefs":{"Monarch":{"xref_id":"0005377"}}}


id: PATO:0001441
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A cellular adhesivity quality inhering in a molecule in one cell by virtue of the bearer's attachment to an nonidentical molecule in an adjacent cell.","definition_xrefs":["GO:GO"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular adhesivity","termid":"PATO:0001531"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterophilic","termid":"PATO:0001441"}


id: MONDO:0000833
data:
  {"annotated_genes":["SJAG_00516","SJAG_01181","SJAG_00993","SJAG_02342","SJAG_01183"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88136],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009815"},{"annotations":[87223,87221,87222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007970"},{"annotations":[88305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957262"}]},"cv_name":"mondo","definition":"A bone disease that results in formation or resorption abnormalities located in bone.","definition_xrefs":["DOID:0080005"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone disorder","termid":"MONDO:0005381"}],"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":"bone remodeling disease","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0000833","terms_by_termid":{"MONDO:0007970":null,"MONDO:0009815":null,"MONDO:0957262":null},"xrefs":{"Monarch":{"xref_id":"0000833"}}}


id: PBO:0067938
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 240","termid":"PBO:0067938"}


id: PBO:0048048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"formimidoyltransferase cyclodeaminase","termid":"PBO:0048048"}


id: GO:0090093
data:
  {"annotated_genes":["SJAG_04771","SJAG_04666"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89279,94193],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140748"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of fungal-type cell wall beta-glucan biosynthesis, the chemical reactions and pathways resulting in the formation of beta-glucans, compounds composed of glucose residues linked by beta-D-glucosidic bonds, found in the walls of fungal cells.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell wall macromolecule metabolic process","termid":"GO:0010981"},{"relation_name":"is_a","term_name":"regulation of beta-glucan biosynthetic process","termid":"GO:0032951"},{"relation_name":"is_a","term_name":"regulation of fungal-type cell wall biogenesis","termid":"GO:0032995"},{"relation_name":"regulates","term_name":"fungal-type cell wall beta-glucan biosynthetic process","termid":"GO:0070880"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04666":null,"SJAG_04771":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0005975","GO:0071554"],"is_obsolete":false,"name":"regulation of fungal-type cell wall beta-glucan biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0090093","terms_by_termid":{"GO:0140748":null}}


id: PBO:0088438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific protein Tam13/Mug147, tandem fusion","termid":"PBO:0088438"}


id: PBO:0084811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial protein of unknown function; mCherry fusion protein localizes to the vacuole","termid":"PBO:0084811"}


id: GO:0050304
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + 2 cytochrome c + nitrogen = 2 reduced cytochrome c + nitrous oxide.","definition_xrefs":["EC:1.7.2.4","MetaCyc:RXN-12130"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on other nitrogenous compounds as donors, cytochrome as acceptor","termid":"GO:0016662"}],"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":"nitrous-oxide reductase activity","secondary_identifiers":["KEGG_REACTION:R02804","RHEA:43108"],"synonyms":[{"name":"N2O reductase activity","type":"related"},{"name":"nitrogen:(acceptor) oxidoreductase (N2O-forming)","type":"related"},{"name":"nitrogen:acceptor oxidoreductase (N2O-forming)","type":"related"},{"name":"nitrous oxide reductase activity","type":"related"}],"termid":"GO:0050304"}


id: PBO:0071054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 56","termid":"PBO:0071054"}


id: GO:0110162
data:
  {"annotated_genes":["SJAG_00244"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116891],"is_not":false,"summary":null,"term":"GO:0110162"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the cell cycle process in which the distance is lengthened between poles of the mitotic spindle during mitotic anaphase B (spindle phase three).","definition_xrefs":["GOC:vw","PMID:27697865"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic spindle elongation","termid":"GO:0032888"},{"relation_name":"is_a","term_name":"regulation of mitotic spindle organization","termid":"GO:0060236"},{"relation_name":"regulates","term_name":"mitotic spindle elongation (spindle phase three)","termid":"GO:0061805"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00244":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0000226"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007010","GO:0000226","GO:0007049"],"is_obsolete":false,"name":"regulation of mitotic spindle elongation (spindle phase three)","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0110162","terms_by_termid":{"GO:0110162":null}}


id: PR:O60096
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- bot1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O60096"],"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":"37S ribosomal protein S35, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC14C8.16c","synonyms":[{"name":"Spom972h-bot1","type":"exact"}],"termid":"PR:O60096"}


id: GO:2000388
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of antral ovarian follicle growth.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental growth","termid":"GO:0048639"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"is_a","term_name":"regulation of antral ovarian follicle growth","termid":"GO:2000387"},{"relation_name":"positively_regulates","term_name":"antral ovarian follicle growth","termid":"GO:0001547"}],"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 antral ovarian follicle growth","termid":"GO:2000388"}


id: GO:0051390
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that terminates the activity of the active enzyme MAP kinase kinase kinase (MAPKKK).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete inactivation of MAPKKK activity (obsolete GO:0051390)","synonyms":[{"name":"inactivation of MAP kinase kinase kinase activity","type":"exact"},{"name":"termination of MAP kinase kinase kinase activity","type":"exact"},{"name":"termination of MAPKKK activity","type":"exact"}],"termid":"GO:0051390"}


id: MONDO:0018554
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare subgroup of pulmonary arterial hypertension (PAH) characterized by obliterative fibrosis of the small pulmonary veins and venules and/or capillary infiltration of the pulmonary interstitium leading to increased pulmonary vascular resistance and right ventricular dysfunction.","definition_xrefs":["Orphanet:431353"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"},{"relation_name":"is_a","term_name":"pulmonary arterial hypertension","termid":"MONDO:0015924"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis","secondary_identifiers":["NANDO:1200426","NANDO:1200428","UMLS:C3698354","MEDGEN:785618","EFO:0009199","GARD:21801"],"synonyms":[{"name":"PVOD and/or PCH","type":"exact"}],"termid":"MONDO:0018554","xrefs":{"Monarch":{"xref_id":"0018554"}}}


id: PBO:0071128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 130","termid":"PBO:0071128"}


id: MONDO:0019812
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tricuspid valve prolapse (obsolete MONDO:0019812)","termid":"MONDO:0019812","xrefs":{"Monarch":{"xref_id":"0019812"}}}


id: PBO:0059941
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND2 pseudogene 27","termid":"PBO:0059941"}


id: PBO:0052134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KCNH1 intronic transcript 1","termid":"PBO:0052134"}


id: PBO:0059251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L20","termid":"PBO:0059251"}


id: MONDO:1010973
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hepatic encephalopathy that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hepatic encephalopathy, non-human animal","termid":"MONDO:1010230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hepatic encephalopathy, dog","secondary_identifiers":["OMIA:000453-9615"],"termid":"MONDO:1010973","xrefs":{"Monarch":{"xref_id":"1010973"}}}


id: GO:0043654
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell interprets signals (in the form of specific proteins and lipids) on the surface of a dying cell which it will engulf and remove by phagocytosis.","definition_xrefs":["GOC:rk","PMID:15536015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phagocytosis, recognition","termid":"GO:0006910"},{"relation_name":"part_of","term_name":"apoptotic cell clearance","termid":"GO:0043277"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0008150","GO:0016192","GO:0006810"],"is_obsolete":false,"name":"recognition of apoptotic cell","synonyms":[{"name":"detection of apoptotic cell","type":"exact"},{"name":"detection of apoptotic cell corpse","type":"exact"},{"name":"detection of cell corpse","type":"exact"},{"name":"recognition of apoptotic cell corpse","type":"exact"},{"name":"recognition of cell corpse","type":"exact"}],"termid":"GO:0043654"}


id: GO:0140865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by interleukin-22 binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:34755534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"interleukin-22-mediated signaling pathway","synonyms":[{"name":"IL-22-mediated signaling pathway","type":"exact"},{"name":"interleukin-22-mediated signalling pathway","type":"exact"}],"termid":"GO:0140865"}


id: PBO:0061607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear casein kinase and cyclin dependent kinase substrate 1","termid":"PBO:0061607"}


id: MONDO:0022855
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital vagal hyperreflexivity","termid":"MONDO:0022855","xrefs":{"Monarch":{"xref_id":"0022855"}}}


id: MONDO:0044937
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant epithelial neoplasm that arises from the rectum and invades through the muscularis mucosa into the submucosa. The vast majority are adenocarcinomas.","definition_xrefs":["NCIT:C9382"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rectal cancer","termid":"MONDO:0006519"},{"relation_name":"is_a","term_name":"colorectal carcinoma","termid":"MONDO:0024331"},{"relation_name":"is_a","term_name":"epithelial neoplasm of rectum","termid":"MONDO:0024476"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"rectal carcinoma","secondary_identifiers":["UMLS:C0007113","MEDGEN:40100"],"synonyms":[{"name":"cancer of rectum","type":"broad"},{"name":"cancer of the rectum","type":"broad"},{"name":"carcinoma of rectum","type":"exact"},{"name":"carcinoma of the rectum","type":"exact"},{"name":"rectal cancer","type":"broad"},{"name":"rectal carcinoma","type":"exact"},{"name":"rectum carcinoma","type":"exact"}],"termid":"MONDO:0044937","xrefs":{"Monarch":{"xref_id":"0044937"}}}


id: MONDO:0004180
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-metastasizing neoplasm that arises from the organs that comprise the urinary system. Representative examples include renal oncocytoma, bladder inverted papilloma, and urothelial papilloma.","definition_xrefs":["NCIT:C4893"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign neoplasm","termid":"MONDO:0005165"},{"relation_name":"is_a","term_name":"urinary system neoplasm","termid":"MONDO:0021066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign urinary system neoplasm","secondary_identifiers":["ICD9:223.89","ICD9:223.9","MESH:D014571","DOID:731","SCTID:92468007","NCIT:C192667","MEDGEN:146348","UMLS:C0686167"],"synonyms":[{"name":"benign neoplasm of the urinary tract","type":"exact"},{"name":"benign neoplasm of urinary tract","type":"exact"},{"name":"benign tumor of the urinary tract","type":"exact"},{"name":"benign tumor of urinary tract","type":"exact"},{"name":"benign tumour of the urinary tract","type":"exact"},{"name":"benign tumour of urinary tract","type":"exact"},{"name":"benign urinary system neoplasm","type":"exact"},{"name":"benign urinary tract neoplasm","type":"exact"},{"name":"benign urinary tract tumor","type":"exact"},{"name":"benign urinary tract tumour","type":"exact"},{"name":"neoplasm of urinary system","type":"broad"},{"name":"renal system benign neoplasm","type":"exact"},{"name":"tumor of the urinary system","type":"broad"},{"name":"tumor of urinary tract","type":"broad"},{"name":"tumour of the urinary system","type":"broad"},{"name":"tumour of urinary tract","type":"broad"},{"name":"urinary system benign neoplasm","type":"related"},{"name":"urinary tract neoplasm","type":"broad"}],"termid":"MONDO:0004180","xrefs":{"Monarch":{"xref_id":"0004180"}}}


id: MONDO:0009115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital lactase deficiency is a rare severe gastrointestinal disorder in newborns primarily reported in Finland and characterized clinically by watery diarrhea on feeding with breast-milk or lactose-containing formula.","definition_xrefs":["Orphanet:53690"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of carbohydrate transmembrane transport and absorption","termid":"MONDO:0017706"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"congenital lactase deficiency","secondary_identifiers":["ICD10CM:E73.0","DOID:0111646","MESH:C562600","UMLS:C0268179","MEDGEN:120617","OMIM:223000","GARD:12311","ICD9:271.3","icd11.foundation:2109252471","SCTID:5388008"],"synonyms":[{"name":"Alactasia, congenital","type":"related"},{"name":"congenital lactase deficiency","type":"exact"},{"name":"disaccharide intolerance 2","type":"related"},{"name":"lactase deficiency, congenital","type":"related"}],"termid":"MONDO:0009115","xrefs":{"Monarch":{"xref_id":"0009115"}}}


id: PBO:0038693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ACTB pseudogene 4","termid":"PBO:0038693"}


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: GO:0099611
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that regulates the potential at which an axon potential is triggered.","definition_xrefs":["ISBN:978-0071390118"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of action potential","termid":"GO:0098900"}],"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 action potential firing threshold","termid":"GO:0099611"}


id: GO:0000204
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Upregulation of a MAP kinase kinase in the context of sporulation. As in, but not restricted to, the taxon Saccharomyces (Saccharomyces, ncbi_taxonomy_id:4930).","definition_xrefs":["PMID:9561267"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of MAPKK during sporulation (sensu Saccharomyces) (obsolete GO:0000204)","synonyms":[{"name":"activation of MAPKK during sporulation (sensu Saccharomyces)","type":"exact"}],"termid":"GO:0000204"}


id: PBO:0066217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 22 pseudogene 13","termid":"PBO:0066217"}


id: PR:O13934
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- atg15 gene.","definition_xrefs":["UniProtKB:O13934","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":"lipase atg15 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23C4.16c","synonyms":[{"name":"Spom972h-atg15","type":"exact"},{"name":"autophagy-related protein 15 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13934"}


id: FYPO:0006097
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 actin cables is increased.","definition_xrefs":["PomBase:mah","PMID:20705471"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to actin cable","termid":"FYPO:0006096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000138"],"is_obsolete":false,"name":"increased protein localization to actin cable","synonyms":[{"name":"increased protein localisation to actin cable during vegetative growth","type":"exact"},{"name":"increased protein localization to actin cable during mitotic cell cycle","type":"related"},{"name":"increased protein localization to actin cable during vegetative growth","type":"exact"},{"name":"increased protein localization to formin-nucleated actin cable","type":"exact"}],"termid":"FYPO:0006097"}


id: PBO:0117261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIM23 translocase complex subunit Pam17","termid":"PBO:0117261"}


id: MONDO:0018672
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin G4-related sclerosing disease","termid":"MONDO:0017287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"IgG4-related aortitis","secondary_identifiers":["MEDGEN:1800431","UMLS:C5569008","GARD:21883","Orphanet:449400","icd11.foundation:593151236"],"synonyms":[{"name":"IgG4-related periaortitis","type":"exact"}],"termid":"MONDO:0018672","xrefs":{"Monarch":{"xref_id":"0018672"}}}


id: PBO:0078523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 14","termid":"PBO:0078523"}


id: MONDO:0033481
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia type I","termid":"MONDO:0019792"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0000426","MONDO:0005559"],"is_obsolete":false,"name":"spinocerebellar ataxia 46","secondary_identifiers":["UMLS:C4540404","OMIM:617770","GARD:22352","DOID:0080288","MEDGEN:1624251","Orphanet:589522"],"synonyms":[{"name":"SCA46","type":"related"},{"name":"spinocerebellar ataxia 46","type":"exact"},{"name":"spinocerebellar ataxia, 46, autosomal dominant, with sensory axonal neuropathy","type":"related"}],"termid":"MONDO:0033481","xrefs":{"Monarch":{"xref_id":"0033481"}}}


id: GO:0042998
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the transport of proteins from the Golgi to the plasma membrane.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of Golgi to plasma membrane protein transport","termid":"GO:0042996"},{"relation_name":"is_a","term_name":"positive regulation of protein transport","termid":"GO:0051222"},{"relation_name":"is_a","term_name":"positive regulation of protein localization to plasma membrane","termid":"GO:1903078"},{"relation_name":"positively_regulates","term_name":"Golgi to plasma membrane protein transport","termid":"GO:0043001"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0016192"],"is_obsolete":false,"name":"positive regulation of Golgi to plasma membrane protein transport","synonyms":[{"name":"activation of Golgi to plasma membrane protein transport","type":"narrow"},{"name":"stimulation of Golgi to plasma membrane protein transport","type":"narrow"},{"name":"up regulation of Golgi to plasma membrane protein transport","type":"exact"},{"name":"up-regulation of Golgi to plasma membrane protein transport","type":"exact"},{"name":"upregulation of Golgi to plasma membrane protein transport","type":"exact"}],"termid":"GO:0042998"}


id: MONDO:0016106
data:
  {"annotated_genes":["SJAG_02431","SJAG_02396","SJAG_04601","SJAG_04053","SJAG_04316","SJAG_03145","SJAG_03703","SJAG_03470","SJAG_03715","SJAG_03188","SJAG_01939","SJAG_04228","SJAG_01491","SJAG_04003","SJAG_02043"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87416],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0021018"},{"annotations":[87524],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012034"},{"annotations":[86931],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012248"},{"annotations":[88413,88412],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013162"},{"annotations":[87682],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014142"},{"annotations":[87617,87618],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008409"},{"annotations":[87893],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008030"},{"annotations":[88514],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010912"},{"annotations":[88311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957270"},{"annotations":[87985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011266"},{"annotations":[87356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958176"},{"annotations":[87532],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014800"},{"annotations":[87176],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010684"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy","termid":"MONDO:0020121"}],"gene_count":15,"genes_by_uniquename":{"SJAG_01491":null,"SJAG_01939":null,"SJAG_02043":null,"SJAG_02396":null,"SJAG_02431":null,"SJAG_03145":null,"SJAG_03188":null,"SJAG_03470":null,"SJAG_03703":null,"SJAG_03715":null,"SJAG_04003":null,"SJAG_04053":null,"SJAG_04228":null,"SJAG_04316":null,"SJAG_04601":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"progressive muscular dystrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4551827","MEDGEN:1633060","Orphanet:206644","GARD:20360"],"synonyms":[{"name":"progressive muscular dystrophy","type":"exact"}],"termid":"MONDO:0016106","terms_by_termid":{"MONDO:0008030":null,"MONDO:0008409":null,"MONDO:0010684":null,"MONDO:0010912":null,"MONDO:0011266":null,"MONDO:0012034":null,"MONDO:0012248":null,"MONDO:0013162":null,"MONDO:0014142":null,"MONDO:0014800":null,"MONDO:0021018":null,"MONDO:0957270":null,"MONDO:0958176":null},"xrefs":{"Monarch":{"xref_id":"0016106"}}}


id: PBO:0065179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prolyl-tRNA synthetase associated domain containing 1, pseudogene","termid":"PBO:0065179"}


id: FYPO:0001129
data:
  {"alleles_by_uniquename":{"SJAG_01050:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01050","name":"nur1delta","uniquename":"SJAG_01050:allele-1"},"SJAG_01745:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01745","name":"lem2delta","uniquename":"SJAG_01745:allele-1"},"SJAG_03783:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03783","name":"vps24delta","uniquename":"SJAG_03783:allele-1"},"SJAG_03892:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03892","name":"vps4delta","uniquename":"SJAG_03892:allele-1"},"SJAG_03892:allele-2":{"allele_type":"amino_acid_mutation","description":"E233Q","gene_uniquename":"SJAG_03892","name":"Vps4-EQ","uniquename":"SJAG_03892:allele-2"},"SJAG_03892:allele-3":{"allele_type":"amino_acid_mutation","description":"I307T L327S","gene_uniquename":"SJAG_03892","name":"vps4-ts","uniquename":"SJAG_03892:allele-3"},"SJAG_04489:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04489","name":"did4delta","uniquename":"SJAG_04489:allele-1"},"SJAG_05207:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_05207","name":"cmp7delta","uniquename":"SJAG_05207:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121384],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007771"}],"single_locus_phenotype":[{"annotations":[121383,121360,121388,121385,121389,121370,121359,121366,121386,121387,121369,121390,121367],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007771"},{"annotations":[121363],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007073"},{"annotations":[121362],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0003657"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the nucleus is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during vegetative growth","termid":"FYPO:0000443"},{"relation_name":"is_a","term_name":"abnormal protein localization to nucleus","termid":"FYPO:0002956"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01050":null,"SJAG_01745":null,"SJAG_03783":null,"SJAG_03892":null,"SJAG_04489":null,"SJAG_05207":null},"genotype_count":9,"genotypes_by_uniquename":{"Vps4-EQ-E233Q-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"Vps4-EQ(E233Q aa)","display_uniquename":"Vps4-EQ-E233Q-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-2","expression":"Not assayed or wild type"}]}]},"cmp7delta":{"display_name":"cmp7delta","display_uniquename":"cmp7delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_05207:allele-1","expression":"Null"}]}]},"cmp7delta__vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cmp7delta vps4-ts(I307T L327S aa)","display_uniquename":"cmp7delta__vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_05207:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-3","expression":"Not assayed or wild type"}]}]},"did4delta":{"display_name":"did4delta","display_uniquename":"did4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04489:allele-1","expression":"Null"}]}]},"lem2delta":{"display_name":"lem2delta","display_uniquename":"lem2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01745:allele-1","expression":"Null"}]}]},"nur1delta":{"display_name":"nur1delta","display_uniquename":"nur1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01050:allele-1","expression":"Null"}]}]},"vps24delta":{"display_name":"vps24delta","display_uniquename":"vps24delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03783:allele-1","expression":"Null"}]}]},"vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"vps4-ts(I307T L327S aa)","display_uniquename":"vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-3","expression":"Not assayed or wild type"}]}]},"vps4delta":{"display_name":"vps4delta","display_uniquename":"vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_03892","SJAG_05207"],"name":"abnormal protein localization to nucleus during vegetative growth","references_by_uniquename":{"PMID:32109380":null},"single_locus_annotated_genes":["SJAG_05207","SJAG_04489","SJAG_03892","SJAG_01050","SJAG_01745","SJAG_03783"],"single_locus_genotype_uniquenames":["Vps4-EQ-E233Q-amino_acid_mutation-expression-not_assayed_or_wild_type","nur1delta","vps4delta","cmp7delta","vps4-ts-I307T_L327S-amino_acid_mutation-expression-not_assayed_or_wild_type","did4delta","lem2delta","vps24delta"],"synonyms":[{"name":"abnormal protein localisation to nucleus during vegetative growth","type":"exact"},{"name":"abnormal protein localization to nucleus during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001129","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000137":null,"FYPO:0003657":null,"FYPO:0007073":null,"FYPO:0007771":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: PBO:0090803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAPP complex subunit 2-like Tca17","termid":"PBO:0090803"}


id: PBO:0042556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase 19","termid":"PBO:0042556"}


id: PBO:0091631
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-lactate dehydrogenase","termid":"PBO:0091631"}


id: PBO:0049763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex group 4B","termid":"PBO:0049763"}


id: PBO:0058313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4686","termid":"PBO:0058313"}


id: PBO:0055767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucyl and cystinyl aminopeptidase","termid":"PBO:0055767"}


id: SO:0002130
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript that contains a CDS but has no stop codon before the polyA site is reached.","definition_xrefs":["GENCODE:http://www.gencodegenes.org/gencode_biotypes.html"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA","termid":"SO:0000234"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NSD_transcript","synonyms":[{"name":"non_stop_decay_transcript","type":"exact"}],"termid":"SO:0002130"}


id: PBO:0088507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribulose phosphate 3-epimerase Rpe1","termid":"PBO:0088507"}


id: MOD:01006
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively substitutes two hydrogen atoms of an L-tyrosine residue with two bromine atoms.","definition_xrefs":["Unimod:534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brominated tyrosine","termid":"MOD:00988"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dibrominated tyrosine","synonyms":[{"name":"Br2Tyr","type":"exact"},{"name":"Dibromo","type":"related"}],"termid":"MOD:01006"}


id: PBO:0052840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 2-5, pseudogene","termid":"PBO:0052840"}


id: MONDO:1010909
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Muscular dystrophy that occurs in chicken.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy, non-human animal","termid":"MONDO:0024965"},{"relation_name":"is_a","term_name":"myopathy, chicken","termid":"MONDO:1010916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"muscular dystrophy, chicken","secondary_identifiers":["OMIA:000679-9031"],"termid":"MONDO:1010909","xrefs":{"Monarch":{"xref_id":"1010909"}}}


id: MONDO:0018074
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete American trypanosomiasis (obsolete MONDO:0018074)","termid":"MONDO:0018074","xrefs":{"Monarch":{"xref_id":"0018074"}}}


id: PBO:0060959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NFKB inhibitor like 1","termid":"PBO:0060959"}


id: GO:0043314
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the rate of neutrophil degranulation.","definition_xrefs":["ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of myeloid leukocyte mediated immunity","termid":"GO:0002887"},{"relation_name":"is_a","term_name":"negative regulation of leukocyte degranulation","termid":"GO:0043301"},{"relation_name":"is_a","term_name":"regulation of neutrophil degranulation","termid":"GO:0043313"},{"relation_name":"is_a","term_name":"negative regulation of immune response","termid":"GO:0050777"},{"relation_name":"negatively_regulates","term_name":"neutrophil degranulation","termid":"GO:0043312"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0016192"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"negative regulation of neutrophil degranulation","synonyms":[{"name":"down regulation of neutrophil degranulation","type":"exact"},{"name":"down-regulation of neutrophil degranulation","type":"exact"},{"name":"downregulation of neutrophil degranulation","type":"exact"},{"name":"inhibition of neutrophil degranulation","type":"narrow"},{"name":"negative regulation of neutrophil granule exocytosis","type":"exact"}],"termid":"GO:0043314"}


id: GO:0043040
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The synthesis of aminoacyl tRNA by the formation of an ester bond between the 3'-hydroxyl group of the most 3' adenosine of the tRNA, to be used in nonribosomal peptide synthesis.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA aminoacylation","termid":"GO:0043039"},{"relation_name":"is_a","term_name":"amino acid activation for nonribosomal peptide biosynthetic process","termid":"GO:0043041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0006399","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"tRNA aminoacylation for nonribosomal peptide biosynthetic process","synonyms":[{"name":"tRNA aminoacylation for nonribosomal peptide anabolism","type":"exact"},{"name":"tRNA aminoacylation for nonribosomal peptide biosynthesis","type":"exact"},{"name":"tRNA aminoacylation for nonribosomal peptide formation","type":"exact"},{"name":"tRNA aminoacylation for nonribosomal peptide synthesis","type":"exact"}],"termid":"GO:0043040"}


id: GO:0009998
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that restricts, stops or prevents a cell from specifying into a retinal cone cell.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell fate specification","termid":"GO:0009996"},{"relation_name":"is_a","term_name":"regulation of retinal cone cell fate specification","termid":"GO:0042673"},{"relation_name":"is_a","term_name":"negative regulation of retinal cone cell fate commitment","termid":"GO:0060226"},{"relation_name":"negatively_regulates","term_name":"retinal cone cell fate specification","termid":"GO:0042672"}],"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 retinal cone cell fate specification","synonyms":[{"name":"down regulation of retinal cone cell fate specification","type":"exact"},{"name":"down-regulation of retinal cone cell fate specification","type":"exact"},{"name":"downregulation of retinal cone cell fate specification","type":"exact"},{"name":"inhibition of retinal cone cell fate specification","type":"narrow"},{"name":"negative regulation of retina cone cell fate specification","type":"exact"},{"name":"suppression of retina cone cell fate","type":"exact"},{"name":"suppression of retinal cone cell fate","type":"exact"}],"termid":"GO:0009998"}


id: GO:0007091
data:
  {"annotated_genes":["SJAG_02498","SJAG_00666","SJAG_03575","SJAG_03048","SJAG_04126","SJAG_01837","SJAG_01330","SJAG_04259","SJAG_03126","SJAG_03681","SJAG_01679","SJAG_05329","SJAG_04699","SJAG_01956","SJAG_01297","SJAG_04884","SJAG_01082","SJAG_03353","SJAG_02451","SJAG_04999","SJAG_02169","SJAG_04573","SJAG_01805","SJAG_04968","SJAG_02336","SJAG_02380","SJAG_00883"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72541,74723,80075],"is_not":false,"summary":null,"term":"GO:0007091"},{"annotations":[117741,105688,110070,92492,101373,116110,113792,115622,109043],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[101215,117399,103593,111730,116340,108127],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0007094"},{"annotations":[95972],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[118519],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090267"},{"annotations":[99480,103902,101930,95580,113207,104178,116607],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045842"}]},"cv_name":"biological_process","definition":"The cell cycle process in which a cell progresses from metaphase to anaphase during mitosis, triggered by the activation of the anaphase promoting complex by Cdc20/Sleepy homolog which results in the degradation of Securin.","definition_xrefs":["GOC:mtg_cell_cycle","PMID:10465783"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic cell cycle phase transition","termid":"GO:0044772"},{"relation_name":"is_a","term_name":"metaphase/anaphase transition of cell cycle","termid":"GO:0044784"}],"gene_count":27,"genes_by_uniquename":{"SJAG_00666":null,"SJAG_00883":null,"SJAG_01082":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01679":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_01956":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02380":null,"SJAG_02451":null,"SJAG_02498":null,"SJAG_03048":null,"SJAG_03126":null,"SJAG_03353":null,"SJAG_03575":null,"SJAG_03681":null,"SJAG_04126":null,"SJAG_04259":null,"SJAG_04573":null,"SJAG_04699":null,"SJAG_04884":null,"SJAG_04968":null,"SJAG_04999":null,"SJAG_05329":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044772"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0044772","GO:0008150"],"is_obsolete":false,"name":"metaphase/anaphase transition of mitotic cell cycle","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-68881"],"synonyms":[{"name":"metaphase/anaphase transition by anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process","type":"exact"},{"name":"mitotic metaphase/anaphase transition","type":"exact"}],"termid":"GO:0007091","terms_by_termid":{"GO:0007091":null,"GO:0007094":null,"GO:0045842":null,"GO:0090267":null,"GO:0140499":null,"GO:1902426":null}}


id: GO:0047485
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to a protein N-terminus, the end of any peptide chain at which the 2-amino (or 2-imino) function of a constituent amino acid is not attached in peptide linkage to another amino-acid residue.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete protein N-terminus binding (obsolete GO:0047485)","synonyms":[{"name":"N-terminal binding","type":"exact"},{"name":"N-terminal end binding","type":"exact"},{"name":"NH2-terminal binding","type":"narrow"},{"name":"NH2-terminus binding","type":"narrow"},{"name":"amino-terminal binding","type":"related"},{"name":"amino-terminus binding","type":"related"}],"termid":"GO:0047485"}


id: PBO:0028490
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-separate_mitotic_half_spindles_present","termid":"PBO:0028490"}


id: MONDO:0006724
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete desmoplastic small round cell tumor (obsolete MONDO:0006724)","termid":"MONDO:0006724","xrefs":{"Monarch":{"xref_id":"0006724"}}}


id: GO:0005986
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of sucrose, the disaccharide fructofuranosyl-glucopyranoside.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sucrose metabolic process","termid":"GO:0005985"},{"relation_name":"is_a","term_name":"disaccharide biosynthetic process","termid":"GO:0046351"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"sucrose biosynthetic process","secondary_identifiers":["MetaCyc:SUCSYN-PWY"],"synonyms":[{"name":"sucrose anabolism","type":"exact"},{"name":"sucrose biosynthesis","type":"exact"},{"name":"sucrose formation","type":"exact"},{"name":"sucrose synthesis","type":"exact"}],"termid":"GO:0005986"}


id: GO:0043988
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by the addition of an phosphate group to a serine residue at position 28 of the histone.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-S28 phosphorylation (obsolete GO:0043988)","synonyms":[{"name":"histone H3 phosphorylation at S28","type":"exact"},{"name":"histone H3S28 phosphorylation","type":"exact"}],"termid":"GO:0043988"}


id: PBO:0034810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human MYH1 and MYH2 and MYH3 and MYH4and MYH6 and MYH7 and MYH7B and MYH8 and MYH9 and MYH10 and MYH11 and MYH13 MYH14 and MYH15 ortholog","termid":"PBO:0034810"}


id: PBO:0064175
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase A2 group XB, pseudogene","termid":"PBO:0064175"}


id: PR:P14965
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ura4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P14965"],"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":"orotidine 5'-phosphate decarboxylase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC330.05c","synonyms":[{"name":"OMP decarboxylase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"OMPDCase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"OMPdecase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ura4","type":"exact"},{"name":"UMP synthase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"uridine 5'-monophosphate synthase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P14965"}


id: PBO:0055208
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 2633","termid":"PBO:0055208"}


id: MONDO:0003821
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A germ cell tumor that arises from the ovary and is composed of tissues that originate from two or three of the following germ layers, endoderm, ectoderm, or mesoderm.","definition_xrefs":["NCIT:C39992"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian teratoma","termid":"MONDO:0005602"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian biphasic or triphasic teratoma","secondary_identifiers":["MEDGEN:274086","UMLS:C1518691","DOID:6232"],"synonyms":[{"name":"ovarian biphasic or triphasic teratoma","type":"exact"}],"termid":"MONDO:0003821","xrefs":{"Monarch":{"xref_id":"0003821"}}}


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


id: GO:0048774
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a cyanophore cell. Cyanophores are pigment cells derived from the neural crest. They contain a blue pigment of unknown chemical composition. The pigment is stored in fibrous organelles termed cyanosomes.","definition_xrefs":["GOC:mh","GOC:jid"],"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":"cyanophore differentiation","synonyms":[{"name":"cyanophore cell differentiation","type":"exact"}],"termid":"GO:0048774"}


id: PBO:0059285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L42","termid":"PBO:0059285"}


id: GO:1902495
data:
  {"annotated_genes":["SJAG_MIT20","SJAG_07007","SJAG_03962","SJAG_05294","SJAG_01471","SJAG_05204","SJAG_00976","SJAG_01817","SJAG_01447","SJAG_01397","SJAG_00836","SJAG_05229","SJAG_MIT13","SJAG_03114","SJAG_01077","SJAG_02564","SJAG_MIT03","SJAG_03406","SJAG_MIT04","SJAG_01913","SJAG_00601","SJAG_MIT37","SJAG_02782","SJAG_04015","SJAG_00755","SJAG_04122","SJAG_01190","SJAG_00438","SJAG_00915","SJAG_03925","SJAG_03490","SJAG_00516","SJAG_01763","SJAG_MIT09","SJAG_00080","SJAG_00212","SJAG_01490","SJAG_04955","SJAG_01355","SJAG_05629","SJAG_00136","SJAG_00542","SJAG_00985","SJAG_02023","SJAG_03337","SJAG_04677","SJAG_02646","SJAG_07003","SJAG_MIT15","SJAG_00133","SJAG_04675","SJAG_02598","SJAG_02105","SJAG_07006","SJAG_02504"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[79409,79625],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033573"},{"annotations":[65100,79507,105473,58027,96623,120935,71860,68536,109714,68320,117685,120940,120929,65412,74421,66145,60316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045259"},{"annotations":[77367,115238,119532,62437,105871,77449,73858,120924,75444],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045275"},{"annotations":[90995,120897,73521,62471,69367,117299,120919,120948,110101,75934,116067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045277"},{"annotations":[97611,105703,101732,93826,91930,62649,97430],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000220"},{"annotations":[89801,61008,72896,98393,100698,120593,104467,111694],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000221"},{"annotations":[76135],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005891"}]},"cv_name":"cellular_component","definition":"A transmembrane protein complex which enables the transfer of a substance from one side of a membrane to the other.","definition_xrefs":["PMID:18024586","GOC:TermGenie","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"is_a","term_name":"transporter complex","termid":"GO:1990351"}],"gene_count":55,"genes_by_uniquename":{"SJAG_00080":null,"SJAG_00133":null,"SJAG_00136":null,"SJAG_00212":null,"SJAG_00438":null,"SJAG_00516":null,"SJAG_00542":null,"SJAG_00601":null,"SJAG_00755":null,"SJAG_00836":null,"SJAG_00915":null,"SJAG_00976":null,"SJAG_00985":null,"SJAG_01077":null,"SJAG_01190":null,"SJAG_01355":null,"SJAG_01397":null,"SJAG_01447":null,"SJAG_01471":null,"SJAG_01490":null,"SJAG_01763":null,"SJAG_01817":null,"SJAG_01913":null,"SJAG_02023":null,"SJAG_02105":null,"SJAG_02504":null,"SJAG_02564":null,"SJAG_02598":null,"SJAG_02646":null,"SJAG_02782":null,"SJAG_03114":null,"SJAG_03337":null,"SJAG_03406":null,"SJAG_03490":null,"SJAG_03925":null,"SJAG_03962":null,"SJAG_04015":null,"SJAG_04122":null,"SJAG_04675":null,"SJAG_04677":null,"SJAG_04955":null,"SJAG_05204":null,"SJAG_05229":null,"SJAG_05294":null,"SJAG_05629":null,"SJAG_07003":null,"SJAG_07006":null,"SJAG_07007":null,"SJAG_MIT03":null,"SJAG_MIT04":null,"SJAG_MIT09":null,"SJAG_MIT13":null,"SJAG_MIT15":null,"SJAG_MIT20":null,"SJAG_MIT37":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":"transmembrane transporter complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:1902495","terms_by_termid":{"GO:0000220":null,"GO:0000221":null,"GO:0005891":null,"GO:0033573":null,"GO:0045259":null,"GO:0045275":null,"GO:0045277":null}}


id: PBO:0030401
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_SAGA_complex_assembly","termid":"PBO:0030401"}


id: MONDO:0005180
data:
  {"annotated_genes":["SJAG_04545","SJAG_00078","SJAG_00421","SJAG_01317","SJAG_01039","SJAG_04404","SJAG_01270","SJAG_04757","SJAG_02106","SJAG_01229","SJAG_16459","SJAG_00063","SJAG_03866"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87528,87529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014796"},{"annotations":[87929,87930],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011658"},{"annotations":[87538,87537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014233"},{"annotations":[88691,88690],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011706"},{"annotations":[89103,89104],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008199"},{"annotations":[89067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013625"},{"annotations":[88124,88125],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957576"}]},"cv_name":"mondo","definition":"A progressive degenerative disorder of the central nervous system characterized by loss of dopamine producing neurons in the substantia nigra and the presence of Lewy bodies in the substantia nigra and locus coeruleus. Signs and symptoms include tremor which is most pronounced during rest, muscle rigidity, slowing of the voluntary movements, a tendency to fall back, and a mask-like facial expression.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"synucleinopathy","termid":"MONDO:0000510"},{"relation_name":"is_a","term_name":"parkinsonian disorder","termid":"MONDO:0021095"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00063":null,"SJAG_00078":null,"SJAG_00421":null,"SJAG_01039":null,"SJAG_01229":null,"SJAG_01270":null,"SJAG_01317":null,"SJAG_02106":null,"SJAG_03866":null,"SJAG_04404":null,"SJAG_04545":null,"SJAG_04757":null,"SJAG_16459":null},"genotype_count":0,"is_obsolete":false,"name":"Parkinson disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:332","UMLS:C0030567","birnlex:2098","NCIT:C26845","NANDO:1200010","SCTID:49049000","ICD9:332.0","MEDGEN:10590","Orphanet:319705","ICD10CM:G20","OMIMPS:168600","MESH:D010300","DOID:14330","icd11.foundation:296066191"],"synonyms":[{"name":"PD","type":"exact"},{"name":"Parkinson disease","type":"exact"},{"name":"Parkinson's disease","type":"exact"},{"name":"paralysis agitans","type":"exact"}],"termid":"MONDO:0005180","terms_by_termid":{"MONDO:0008199":null,"MONDO:0011658":null,"MONDO:0011706":null,"MONDO:0013625":null,"MONDO:0014233":null,"MONDO:0014796":null,"MONDO:0957576":null},"xrefs":{"Monarch":{"xref_id":"0005180"}}}


id: PR:Q8TFG8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAPB15E9.02c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q8TFG8"],"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 PB15E9.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB15E9.02c","synonyms":[{"name":"Spom972h-SPAPB15E9.02c","type":"exact"}],"termid":"PR:Q8TFG8"}


id: GO:0043700
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A tissue-specific, membrane-bounded cytoplasmic organelle within which pteridine pigments are synthesized and stored. Pterinosomes are synthesized in xanthophores and erythrophore cells and are yellow, orange or red in appearance.","definition_xrefs":["GOC:mh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pigment granule","termid":"GO:0048770"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0005575","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"pterinosome","termid":"GO:0043700"}


id: FYPO:0003337
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 cell septum is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to septum","termid":"FYPO:0002718"},{"relation_name":"is_a","term_name":"increased protein localization to cell division site","termid":"FYPO:0004655"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased protein localization to septum","synonyms":[{"name":"increased protein localisation to septum","type":"exact"},{"name":"increased protein localization to cell septum","type":"exact"},{"name":"increased protein localization to division septum","type":"exact"},{"name":"increased protein localization to septum during mitotic cell cycle","type":"related"},{"name":"increased protein localization to septum during vegetative growth","type":"exact"}],"termid":"FYPO:0003337"}


id: GO:0061935
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The binding and fusion of a sperm, with the plasma membrane of the oocyte as part of the process of double fertilization forming two zygotes.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process involved in reproduction in multicellular organism","termid":"GO:0022412"},{"relation_name":"is_a","term_name":"plasma membrane fusion","termid":"GO:0045026"},{"relation_name":"part_of","term_name":"double fertilization forming two zygotes","termid":"GO:0009677"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0061024"],"is_obsolete":false,"name":"fusion of sperm to egg plasma membrane involved in double fertilization forming two zygotes","termid":"GO:0061935"}


id: PBO:0005703
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-NF-X1 zinc finger","termid":"PBO:0005703"}


id: PBO:0055992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeats and WD repeat domain containing 1","termid":"PBO:0055992"}


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: GO:0004124
data:
  {"annotated_genes":["SJAG_02972","SJAG_00582"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[111283,112335],"is_not":false,"summary":null,"term":"GO:0004124"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: O3-acetyl-L-serine + hydrogen sulfide = L-cysteine + acetate.","definition_xrefs":["EC:2.5.1.47"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00582":null,"SJAG_02972":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016765","GO:0003674"],"is_obsolete":false,"name":"cysteine synthase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:14829","MetaCyc:ACSERLY-RXN"],"synonyms":[{"name":"3-O-acetyl-L-serine:hydrogen-sulfide 2-amino-2-carboxyethyltransferase activity","type":"related"},{"name":"O(3)-acetyl-L-serine acetate-lyase (adding hydrogen-sulfide) activity","type":"related"},{"name":"O-acetyl-L-serine sulfhydrylase activity","type":"related"},{"name":"O-acetyl-L-serine sulfohydrolase activity","type":"related"},{"name":"O-acetylserine (thiol)-lyase A activity","type":"narrow"},{"name":"O-acetylserine (thiol)-lyase activity","type":"related"},{"name":"O-acetylserine sulfhydrylase activity","type":"related"},{"name":"O3-acetyl-L-serine acetate-lyase (adding hydrogen-sulfide)","type":"related"},{"name":"O3-acetyl-L-serine:hydrogen-sulfide 2-amino-2-carboxyethyltransferase activity","type":"related"},{"name":"OAS sulfhydrylase activity","type":"related"},{"name":"acetylserine sulfhydrylase activity","type":"related"},{"name":"cysteine synthase activity, acting on O-acetyl-L-serine","type":"exact"},{"name":"cysteine synthetase activity","type":"related"}],"termid":"GO:0004124","terms_by_termid":{"GO:0004124":null}}


id: PBO:0087759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the ubiqunol-cytochrome c oxidoreductase complex; this complex comprises part of the mitochondrial respiratory chain; members include Cobp, Rip1p, Cyt1p, Cor1p, Qcr2p, Qcr6p, Qcr7p, Qcr8p, Qcr9p, and Qcr10p and comprises part of the mitochondrial respiratory chain","termid":"PBO:0087759"}


id: MONDO:0030484
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"immunodeficiency 89 and autoimmunity","secondary_identifiers":["UMLS:C5562027","MEDGEN:1794237","OMIM:619632"],"synonyms":[{"name":"IMD89","type":"exact"}],"termid":"MONDO:0030484","xrefs":{"Monarch":{"xref_id":"0030484"}}}


id: PBO:0054150
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 1517","termid":"PBO:0054150"}


id: PBO:0013457
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ForMaldehyde Dehydrogenase","termid":"PBO:0013457"}


id: MONDO:0003105
data:
  {"annotated_genes":["SJAG_03131","SJAG_00997","SJAG_04885","SJAG_04884","SJAG_04287"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88376,88377,88378],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0700275"},{"annotations":[89082,89083],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013872"}]},"cv_name":"mondo","definition":"A disease involving the prostate gland.","direct_ancestors":[{"relation_name":"is_a","term_name":"male reproductive system disorder","termid":"MONDO:0003150"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00997":null,"SJAG_03131":null,"SJAG_04287":null,"SJAG_04884":null,"SJAG_04885":null},"genotype_count":0,"is_obsolete":false,"name":"prostate disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:10964","SCTID:30281009","EFO:0009602","NCIT:C26865","ICD9:602.9","UMLS:C0033575","MESH:D011469","ICD9:602.8","DOID:47"],"synonyms":[{"name":"disease of prostate gland","type":"exact"},{"name":"disease or disorder of prostate gland","type":"exact"},{"name":"disorder of prostate gland","type":"exact"},{"name":"prostate disease","type":"exact"},{"name":"prostate disorder","type":"exact"},{"name":"prostate gland disease","type":"exact"},{"name":"prostate gland disease or disorder","type":"exact"}],"termid":"MONDO:0003105","terms_by_termid":{"MONDO:0013872":null,"MONDO:0700275":null},"xrefs":{"Monarch":{"xref_id":"0003105"}}}


id: PBO:0045487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA replication and sister chromatid cohesion 1","termid":"PBO:0045487"}


id: PBO:0080568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat and FYVE domain containing 3","termid":"PBO:0080568"}


id: MOD:00330
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-histidine residue to a (phospho-5'-guanosine)-L-histidine.","definition_xrefs":["PubMed:7559521","RESID:AA0325","PubMed:10869342","Unimod:413#H","PubMed:10529169"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"},{"relation_name":"is_a","term_name":"guanylated residue","termid":"MOD:01163"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(phospho-5'-guanosine)-L-histidine","synonyms":[{"name":"(2S)-2-amino-3-(1-(5'-adenosine phosphono)imidazol-4-yl)propanoic acid","type":"exact"},{"name":"1'-(phospho-5'-guanosine)-L-histidine","type":"exact"},{"name":"ACT_SITE GMP-histidine intermediate","type":"exact"},{"name":"L-histidine 5'-guanosine phosphoramidester","type":"exact"},{"name":"L-histidine monoanhydride with 5'-guanylic acid","type":"exact"},{"name":"N(tau)-5'-guanylic-L-histidine","type":"exact"},{"name":"N1'-guanylylated histidine","type":"exact"},{"name":"Phosphoguanosine","type":"related"},{"name":"phospho-guanosine","type":"related"},{"name":"tele-5'-guanylic-L-histidine","type":"exact"}],"termid":"MOD:00330"}


id: PBO:0002704
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"checkpoint clamp complex protein Hus1","termid":"PBO:0002704"}


id: PBO:0057522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 640","termid":"PBO:0057522"}


id: PBO:0003864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II transcription elongation factor SpELL","termid":"PBO:0003864"}


id: GO:0047161
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: hydroxymalonate + sinapoyl-CoA = CoA + sinapoyltartronate.","definition_xrefs":["RHEA:10952","EC:2.3.1.106"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-hydroxycinnamoyltransferase activity","termid":"GO:0050737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824","GO:0016746"],"is_obsolete":false,"name":"tartronate O-hydroxycinnamoyltransferase activity","secondary_identifiers":["KEGG_REACTION:R03965","MetaCyc:2.3.1.106-RXN"],"synonyms":[{"name":"hydroxycinnamoyl-coenzyme-A:tartronate hydroxycinnamoyltransferase activity","type":"related"},{"name":"sinapoyl-CoA:2-hydroxymalonate O-(hydroxycinnamoyl)transferase activity","type":"related"},{"name":"tartronate sinapoyltransferase activity","type":"related"}],"termid":"GO:0047161"}


id: PBO:0043478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canopy FGF signaling regulator 1","termid":"PBO:0043478"}


id: GO:0005999
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of xylulose, the ketopentose threo-2-pentulose.","definition_xrefs":["ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xylulose metabolic process","termid":"GO:0005997"},{"relation_name":"is_a","term_name":"pentose biosynthetic process","termid":"GO:0019322"}],"gene_count":0,"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":"xylulose biosynthetic process","secondary_identifiers":["Reactome:R-HSA-163754"],"synonyms":[{"name":"xylulose anabolism","type":"exact"},{"name":"xylulose biosynthesis","type":"exact"},{"name":"xylulose formation","type":"exact"},{"name":"xylulose synthesis","type":"exact"}],"termid":"GO:0005999"}


id: PBO:0063353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PCOLCE antisense RNA 1","termid":"PBO:0063353"}


id: MONDO:0044083
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Opportunistic fungal infection by a member of Alternaria genus.","definition_xrefs":["MESH:D060487"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fungal infectious disease","termid":"MONDO:0002041"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alternariosis","secondary_identifiers":["SCTID:238436005","UMLS:C3178962","MEDGEN:465430"],"synonyms":[{"name":"Alternarioses","type":"related"},{"name":"Alternarioses, cutaneous","type":"related"},{"name":"Alternarioses, dermal","type":"related"},{"name":"Alternarioses, subcutaneous","type":"related"},{"name":"Alternariosis, cutaneous","type":"related"},{"name":"Alternariosis, dermal","type":"related"},{"name":"Alternariosis, subcutaneous","type":"related"},{"name":"cutaneous Alternarioses","type":"related"},{"name":"cutaneous Alternariosis","type":"related"},{"name":"cutaneous alternariosis","type":"exact"},{"name":"dermal Alternarioses","type":"related"},{"name":"dermal Alternariosis","type":"related"},{"name":"subcutaneous Alternarioses","type":"related"},{"name":"subcutaneous Alternariosis","type":"related"}],"termid":"MONDO:0044083","xrefs":{"Monarch":{"xref_id":"0044083"}}}


id: MONDO:0000253
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Either of two diseases resulting from fungal infection of the hair shafts. Black piedra occurs mainly in and on the hairs of the scalp and is caused by Piedraia hortae; white piedra occurs in and on the hairs of the scalp, beard, mustache and genital areas and is caused by Trichosporon species.","definition_xrefs":["MESH:D010854"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of pilosebaceous unit","termid":"MONDO:0002917"},{"relation_name":"is_a","term_name":"superficial mycosis","termid":"MONDO:0024268"},{"relation_name":"is_a","term_name":"skin appendage disorder","termid":"MONDO:0024481"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piedra","secondary_identifiers":["SCTID:402135006","UMLS:C0031898","MEDGEN:45923"],"synonyms":[{"name":"Piedras","type":"related"},{"name":"Piedras, White","type":"narrow"},{"name":"Piedras, black","type":"narrow"},{"name":"White Piedras","type":"narrow"},{"name":"White piedra","type":"narrow"},{"name":"black Piedras","type":"narrow"},{"name":"black piedra","type":"narrow"},{"name":"hair shaft fungal infectious disease","type":"exact"},{"name":"piedra, White","type":"narrow"},{"name":"piedra, black","type":"narrow"},{"name":"steroid-modified tinea infection","type":"narrow"}],"termid":"MONDO:0000253","xrefs":{"Monarch":{"xref_id":"0000253"}}}


id: GO:0034311
data:
  {"annotated_genes":["SJAG_02429","SJAG_02706","SJAG_02305","SJAG_00880","SJAG_03098","SJAG_01057","SJAG_03275","SJAG_04178"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78540,75381,98682,111539,80611,107797],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046512"},{"annotations":[110339,71563],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006729"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving a diol, a compound that contains two hydroxy groups, generally assumed to be, but not necessarily, alcoholic.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyol metabolic process","termid":"GO:0019751"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00880":null,"SJAG_01057":null,"SJAG_02305":null,"SJAG_02429":null,"SJAG_02706":null,"SJAG_03098":null,"SJAG_03275":null,"SJAG_04178":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"diol metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"dihydric alcohol metabolic process","type":"related"},{"name":"diol metabolism","type":"exact"}],"termid":"GO:0034311","terms_by_termid":{"GO:0006729":null,"GO:0046512":null}}


id: MONDO:0015892
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Growth hormone insensitivity syndrome (GHIS) is a group of diseases characterized by marked short stature associated with normal or elevated growth hormone (GH) concentrations, which fail to respond to exogenous GH administration. GHIS comprises growth delay due to IGF-1 deficiency, growth delay due to IGF-1 resistance, Laron syndrome, short stature due to STAT5b deficiency and primary acid-labile subunit (ALS) deficiency.","definition_xrefs":["Orphanet:181393"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary endocrine growth disease","termid":"MONDO:0015514"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growth hormone insensitivity syndrome","secondary_identifiers":["NANDO:2100114","MEDGEN:1384226","NANDO:2200321","NCIT:C129867","UMLS:C4318479","GARD:3924"],"synonyms":[{"name":"GHIS","type":"exact"},{"name":"Growth hormone insensitivity syndromes","type":"exact"},{"name":"short stature due to a defect in growth hormone receptor or post-receptor pathway","type":"exact"}],"termid":"MONDO:0015892","xrefs":{"Monarch":{"xref_id":"0015892"}}}


id: GO:1902312
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of copper ion transmembrane transport.","definition_xrefs":["GOC:di","PMID:21489137","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of copper ion transmembrane transport","termid":"GO:1902311"},{"relation_name":"is_a","term_name":"negative regulation of cation transmembrane transport","termid":"GO:1904063"},{"relation_name":"negatively_regulates","term_name":"copper ion transmembrane transport","termid":"GO:0035434"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"negative regulation of copper ion transmembrane transport","synonyms":[{"name":"down regulation of copper cation transmembrane transport","type":"exact"},{"name":"down regulation of copper ion membrane transport","type":"exact"},{"name":"down regulation of copper ion transmembrane transport","type":"exact"},{"name":"down-regulation of copper cation transmembrane transport","type":"exact"},{"name":"down-regulation of copper ion membrane transport","type":"exact"},{"name":"down-regulation of copper ion transmembrane transport","type":"exact"},{"name":"downregulation of copper cation transmembrane transport","type":"exact"},{"name":"downregulation of copper ion membrane transport","type":"exact"},{"name":"downregulation of copper ion transmembrane transport","type":"exact"},{"name":"inhibition of copper cation transmembrane transport","type":"narrow"},{"name":"inhibition of copper ion membrane transport","type":"narrow"},{"name":"inhibition of copper ion transmembrane transport","type":"narrow"},{"name":"negative regulation of copper cation transmembrane transport","type":"exact"},{"name":"negative regulation of copper ion membrane transport","type":"exact"}],"termid":"GO:1902312"}


id: PBO:0054443
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 1840","termid":"PBO:0054443"}


id: GO:1901247
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of lung ciliated cell differentiation.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of epithelial cell differentiation","termid":"GO:0030857"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of lung ciliated cell differentiation","termid":"GO:1901246"},{"relation_name":"negatively_regulates","term_name":"lung ciliated cell differentiation","termid":"GO:0061141"}],"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 lung ciliated cell differentiation","synonyms":[{"name":"down regulation of lung ciliated cell differentiation","type":"exact"},{"name":"down-regulation of lung ciliated cell differentiation","type":"exact"},{"name":"downregulation of lung ciliated cell differentiation","type":"exact"},{"name":"inhibition of lung ciliated cell differentiation","type":"narrow"}],"termid":"GO:1901247"}


id: FYPO:0006852
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of progression through S phase of the meiotic cell cycle (preceding meiosis I) is shorter than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased duration of meiotic cell cycle phase","termid":"FYPO:0006851"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased duration of meiotic S phase","synonyms":[{"name":"decreased duration of S phase during meiotic cell cycle","type":"exact"},{"name":"decreased duration of premeiotic DNA replication","type":"related"},{"name":"reduced duration of meiotic S phase","type":"exact"}],"termid":"FYPO:0006852"}


id: PR:O14183
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug114 gene.","definition_xrefs":["UniProtKB:O14183","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":"meiotically up-regulated gene 114 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4F8.08","synonyms":[{"name":"Spom972h-mug114","type":"exact"}],"termid":"PR:O14183"}


id: PBO:0017623
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial inner membrane protein Mdm31","termid":"PBO:0017623"}


id: FYPO:0007448
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which autophagic degradation of the endoplasmic reticulum is normal (i.e. indistinguishable from wild type) when the cell is subject to nitrogen starvation.","definition_xrefs":["PMID:32735772","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process","termid":"FYPO:0000627"},{"relation_name":"is_a","term_name":"abnormal macroautophagy during nitrogen starvation","termid":"FYPO:0004670"},{"relation_name":"is_a","term_name":"abnormal reticulophagy","termid":"FYPO:0008083"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0000257"],"is_obsolete":false,"name":"normal reticulophagy during nitrogen starvation","synonyms":[{"name":"normal ER autophagy during nitrogen starvation","type":"exact"},{"name":"normal ER degradation during nitrogen starvation","type":"related"},{"name":"normal ER-phagy during nitrogen starvation","type":"exact"},{"name":"normal endoplasmic reticulum autophagy during nitrogen starvation","type":"exact"},{"name":"normal reticulophagy during nitrogen depletion","type":"exact"},{"name":"normal reticulophagy during nitrogen deprivation","type":"exact"}],"termid":"FYPO:0007448"}


id: GO:0047433
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-3-methyl-2-oxopentanoate + H+ = 2-methylbutanal + CO2.","definition_xrefs":["RHEA:21108","EC:4.1.1.72"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"branched-chain-2-oxoacid decarboxylase activity","secondary_identifiers":["MetaCyc:4.1.1.72-RXN","KEGG_REACTION:R03894"],"synonyms":[{"name":"(3S)-3-methyl-2-oxopentanoate carboxy-lyase (2-methylbutanal-forming)","type":"related"},{"name":"(3S)-3-methyl-2-oxopentanoate carboxy-lyase activity","type":"related"},{"name":"BCKA","type":"related"},{"name":"branched-chain alpha-keto acid decarboxylase activity","type":"related"},{"name":"branched-chain keto acid decarboxylase activity","type":"related"},{"name":"branched-chain oxo acid decarboxylase activity","type":"related"}],"termid":"GO:0047433"}


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


id: PBO:0076651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBX5 antisense RNA 1","termid":"PBO:0076651"}


id: PR:O14077
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An insulin-degrading enzyme that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11851:SF64","OMA:SCHPO01213","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":"zinc protease mug138 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPACUNK4.12c","secondary_identifiers":["UniProtKB:O14077"],"synonyms":[{"name":"Spom972h-IDE","type":"exact"},{"name":"meiotically up-regulated gene 138 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14077"}


id: GO:0006911
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The internalization of bacteria, immune complexes and other particulate matter or of an apoptotic cell by phagocytosis, including the membrane and cytoskeletal processes required, which involves one of three mechanisms: zippering of pseudopods around a target via repeated receptor-ligand interactions, sinking of the target directly into plasma membrane of the phagocytosing cell, or induced uptake via an enhanced membrane ruffling of the phagocytosing cell similar to macropinocytosis.","definition_xrefs":["GOC:curators","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane invagination","termid":"GO:0099024"},{"relation_name":"part_of","term_name":"phagocytosis","termid":"GO:0006909"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0061024","GO:0006810","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"phagocytosis, engulfment","synonyms":[{"name":"phagosome biosynthesis","type":"related"},{"name":"phagosome formation","type":"related"}],"termid":"GO:0006911"}


id: PBO:0083251
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; identified by homology to a hemiascomycetous yeast protein","termid":"PBO:0083251"}


id: PBO:0083220
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 verified gene PRO3; identified by gene-trapping, microarray expression analysis, and genome-wide homology searching","termid":"PBO:0083220"}


id: MONDO:0008643
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":"veins, pattern of, on anterior thorax","secondary_identifiers":["MEDGEN:348117","OMIM:192400","UMLS:C1860490"],"synonyms":[{"name":"veins, pattern of, on anterior thorax","type":"exact"}],"termid":"MONDO:0008643","xrefs":{"Monarch":{"xref_id":"0008643"}}}


id: GO:1901426
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a furfural stimulus.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"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 furfural","termid":"GO:1901426"}


id: GO:0044674
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A hexameric complex consisting of three polypeptides in an alpha2beta2gamma2 arrangement. Involved in the reduction of the coenzyme M-bound methyl group to methane, which is the final step in methanogenesis.","definition_xrefs":["PMID:9367957","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"methyl coenzyme M reductase complex","termid":"GO:0044674"}


id: MONDO:0015089
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Autosomal recessive form of complex hereditary spastic paraplegia.","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"gene_count":0,"genotype_count":0,"name":"obsolete autosomal recessive complex spastic paraplegia (obsolete MONDO:0015089)","secondary_identifiers":["Orphanet:100981"],"synonyms":[{"name":"autosomal recessive complex HSP","type":"exact"},{"name":"autosomal recessive complex SPG","type":"exact"},{"name":"autosomal recessive complex hereditary spastic paraplegia","type":"exact"},{"name":"autosomal recessive complicated HSP","type":"exact"},{"name":"autosomal recessive complicated SPG","type":"exact"},{"name":"autosomal recessive complicated spastic paraplegia","type":"exact"},{"name":"complex hereditary spastic paraplegia, autosomal recessive","type":"exact"}],"termid":"MONDO:0015089","xrefs":{"Monarch":{"xref_id":"0015089"}}}


id: PBO:0057860
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3171","termid":"PBO:0057860"}


id: PBO:0108699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ArfGEF","termid":"PBO:0108699"}


id: PBO:0048774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GDP-mannose pyrophosphorylase A","termid":"PBO:0048774"}


id: PBO:0039886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGAP42 pseudogene 3","termid":"PBO:0039886"}


id: PBO:0070400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RP1 axonemal microtubule associated","termid":"PBO:0070400"}


id: PBO:0043561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collagen type V alpha 3 chain","termid":"PBO:0043561"}


id: FYPO:0002504
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the palmitoylation of one or more specific proteins, or of specific protein sites, does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein modification","termid":"FYPO:0002497"},{"relation_name":"is_a","term_name":"abnormal protein palmitoylation","termid":"FYPO:0002503"},{"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:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0002494","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein palmitoylation","synonyms":[{"name":"protein palmitoylation abolished","type":"exact"},{"name":"protein palmitoylation absent","type":"exact"}],"termid":"FYPO:0002504"}


id: PR:Q9USL5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein pelota that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04428","PANTHER:PTHR10853: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 dom34 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC18B5.06","secondary_identifiers":["UniProtKB:Q9USL5"],"synonyms":[{"name":"Spom972h-PELO","type":"exact"}],"termid":"PR:Q9USL5"}


id: GO:0106115
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of mitotic cohesin dsDNA (leading strand) loading.","definition_xrefs":["PMID:29358048"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of mitotic cohesin dsDNA (leading strand) loading (obsolete GO:0106115)","termid":"GO:0106115"}


id: MONDO:0018524
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete intraductal papillary mucinous carcinoma of pancreas (obsolete MONDO:0018524)","termid":"MONDO:0018524","xrefs":{"Monarch":{"xref_id":"0018524"}}}


id: GO:0043490
data:
  {"annotated_genes":["SJAG_03306","SJAG_00714","SJAG_00522","SJAG_01753"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89611,98343,113643,118400],"is_not":false,"summary":null,"term":"GO:0043490"}]},"cv_name":"biological_process","definition":"The process of transferring reducing equivalents from NADH in the cytosol to the mitochondria via malate. Cytosolic aspartate aminotransferase converts aspartate to oxaloacetate, and cytosolic malate dehydrogenase uses NADH to convert oxaloacetate to malate in the cytosol; the malate-alpha-ketoglutarate carrier then transports the malate into the mitochondria where mitochondrial malate dehydrogenase uses NAD to convert malate back to oxaloacetate; the electrons on the reduced NADH are then available for use in the electron transport chain; mitochondrial aspartate aminotransferase converts oxaloacetate to aspartate, and the glutamate-aspartate carrier transports the aspartate back to the cytosol to complete the cycle.","definition_xrefs":["GOC:sjm","PMID:16368075"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NAD+ metabolic process","termid":"GO:0019674"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00522":null,"SJAG_00714":null,"SJAG_01753":null,"SJAG_03306":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"malate-aspartate shuttle","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:MALATE-ASPARTATE-SHUTTLE-PWY","Wikipedia:Malate-aspartate_shuttle","Reactome:R-HSA-9856872"],"synonyms":[{"name":"malate aspartate shuttle","type":"exact"},{"name":"malate/aspartate shuttle","type":"exact"},{"name":"malate:aspartate shuttle","type":"exact"}],"termid":"GO:0043490","terms_by_termid":{"GO:0043490":null}}


id: PBO:0050966
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon production regulator","termid":"PBO:0050966"}


id: PBO:0042780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centrosomal protein 104","termid":"PBO:0042780"}


id: GO:2000359
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of binding of sperm to the zona pellucida.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular process","termid":"GO:0050794"},{"relation_name":"regulates","term_name":"binding of sperm to zona pellucida","termid":"GO:0007339"}],"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 binding of sperm to zona pellucida","synonyms":[{"name":"regulation of ZPG binding","type":"related"}],"termid":"GO:2000359"}


id: MONDO:0002108
data:
  {"annotated_genes":["SJAG_03453","SJAG_04067","SJAG_01970"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87591,89068,89069],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008566"}]},"cv_name":"mondo","definition":"A malignant neoplasm involving the thyroid gland","direct_ancestors":[{"relation_name":"is_a","term_name":"thyroid tumor","termid":"MONDO:0015074"},{"relation_name":"is_a","term_name":"malignant endocrine neoplasm","termid":"MONDO:0021069"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01970":null,"SJAG_03453":null,"SJAG_04067":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"thyroid cancer","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:193","MEDGEN:2869","UMLS:C0007115","NANDO:2200074","SCTID:363478007","NCIT:C7510","ICD10CM:C73","DOID:1781"],"synonyms":[{"name":"cancer of thyroid gland","type":"exact"},{"name":"malignant neoplasm of the thyroid","type":"exact"},{"name":"malignant neoplasm of the thyroid gland","type":"exact"},{"name":"malignant neoplasm of thyroid","type":"exact"},{"name":"malignant neoplasm of thyroid gland","type":"exact"},{"name":"malignant thyroid gland neoplasm","type":"exact"},{"name":"malignant thyroid gland tumor","type":"exact"},{"name":"malignant thyroid gland tumour","type":"exact"},{"name":"malignant thyroid neoplasm","type":"exact"},{"name":"malignant thyroid tumor","type":"exact"},{"name":"malignant thyroid tumour","type":"exact"},{"name":"malignant tumor of the thyroid","type":"exact"},{"name":"malignant tumor of the thyroid gland","type":"exact"},{"name":"malignant tumor of thyroid","type":"exact"},{"name":"malignant tumor of thyroid gland","type":"exact"},{"name":"malignant tumour of the thyroid","type":"exact"},{"name":"malignant tumour of the thyroid gland","type":"exact"},{"name":"malignant tumour of thyroid","type":"exact"},{"name":"malignant tumour of thyroid gland","type":"exact"},{"name":"neoplasm of thyroid gland","type":"broad"},{"name":"thyroid gland cancer","type":"exact"},{"name":"thyroid gland neoplasm","type":"broad"}],"termid":"MONDO:0002108","terms_by_termid":{"MONDO:0008566":null},"xrefs":{"Monarch":{"xref_id":"0002108"}}}


id: PBO:0076705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TCF4 antisense RNA 2","termid":"PBO:0076705"}


id: GO:0051192
data:
  {"annotated_genes":["SJAG_01238"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77464],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000036"}]},"cv_name":"molecular_function","definition":"Binding to a prosthetic group, the non-amino acid portion of certain protein molecules. Prosthetic groups may be inorganic or organic and are usually required for the biological activity of the protein.","definition_xrefs":["GOC:ai","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding","termid":"GO:0005488"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01238":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"prosthetic group binding","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0051192","terms_by_termid":{"GO:0000036":null}}


id: PBO:0083136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dual-specificity protein phosphatase; maintains low levels of both basal and induced cell integrity pathway signaling by dephosphorylation of the Slt2p MAPK; reciprocally regulated by Slt2p through phosphorylation; minor role with Ptp2p in the adaptive response to pheromone through the dephosphorylation of the Fus3p MAPK with major contribution by Ptp3p; inhibits the nuclear accumulation of Fus3p; two isoforms exist as the result of alternative translation initiation starts","termid":"PBO:0083136"}


id: GO:0031385
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of the end of mating projection formation by unicellular fungi.","definition_xrefs":["PMID:14734532"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mating projection assembly","termid":"GO:0031383"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of termination of mating projection growth","termid":"GO:0031385"}


id: GO:0071341
data:
  {"annotated_genes":["SJAG_00773","SJAG_00807","SJAG_01456","SJAG_01889","SJAG_00279","SJAG_02169","SJAG_02368","SJAG_04498","SJAG_05290","SJAG_01143","SJAG_01665","SJAG_03596","SJAG_00228","SJAG_03602","SJAG_03703","SJAG_04486","SJAG_03564","SJAG_04280"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[90037,90722,92486,94092,94356,95634,98103,99806,102484,103051,106981,108007,118876,119719],"is_not":false,"summary":null,"term":"GO:0071341"},{"annotations":[117840,100204,105277,100778],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0110115"}]},"cv_name":"cellular_component","definition":"A component of the cell division site that contains the mid1, cdr2, wee1, klp8, and blt1 proteins, and is involved in contractile ring localization. Medial cortical node complexes appear as cortical dots in the middle of the cell during interphase, and function to recruit other ring components in early mitosis.","definition_xrefs":["PMID:19474789","GOC:mah","GOC:vw","PMID:19959363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"medial cortex","termid":"GO:0031097"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00228":null,"SJAG_00279":null,"SJAG_00773":null,"SJAG_00807":null,"SJAG_01143":null,"SJAG_01456":null,"SJAG_01665":null,"SJAG_01889":null,"SJAG_02169":null,"SJAG_02368":null,"SJAG_03564":null,"SJAG_03596":null,"SJAG_03602":null,"SJAG_03703":null,"SJAG_04280":null,"SJAG_04486":null,"SJAG_04498":null,"SJAG_05290":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005938"}],"interesting_parent_ids":["GO:0005575","GO:0005938","GO:0005737"],"is_obsolete":false,"name":"medial cortical node","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"mid1p medial cortical dot","type":"exact"},{"name":"midsome","type":"exact"}],"termid":"GO:0071341","terms_by_termid":{"GO:0071341":null,"GO:0110115":null}}


id: PBO:0036086
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_spatial_extent_of_heterochromatin_assembly","termid":"PBO:0036086"}


id: PBO:0052556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"killer cell lectin like receptor G1","termid":"PBO:0052556"}


id: GO:0101023
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of blood vessel endothelial cells, resulting in the expansion of a cell population.","definition_xrefs":["PMID:23201774","GOC:BHF_telomere","GOC:nc","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endothelial cell proliferation","termid":"GO:0001935"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"vascular endothelial cell proliferation","termid":"GO:0101023"}


id: MOD:00211
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-cysteine residue and a glycine residue by a thioester bond to form S-glycyl-L-cysteine.","definition_xrefs":["RESID:AA0206","ChEBI:22050","PubMed:3306404"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thioester crosslinked residues","termid":"MOD:00395"},{"relation_name":"is_a","term_name":"crosslinked residues with loss of water","termid":"MOD:00954"},{"relation_name":"is_a","term_name":"crosslinked glycine residue","termid":"MOD:02047"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-(glycyl)-L-cysteine (Cys-Gly)","synonyms":[{"name":"(2R)-2-amino-3-[(aminoacetyl)sulfanyl]propanoic acid","type":"exact"},{"name":"1-(cystein-S-yl)-glycinate","type":"exact"},{"name":"ACT_SITE Glycyl thioester intermediate","type":"exact"},{"name":"S-(2-amino-1-oxoethyl)cysteine","type":"exact"},{"name":"S-(glycyl)-L-cysteine","type":"exact"},{"name":"XLNK-SCys-1Gly","type":"exact"},{"name":"glycine cysteine thioester","type":"exact"}],"termid":"MOD:00211"}


id: GO:2001166
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of histone H2B ubiquitination.","definition_xrefs":["PMID:12876293"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone H2B ubiquitination (obsolete GO:2001166)","termid":"GO:2001166"}


id: MONDO:0014705
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any craniosynostosis in which the cause of the disease is a mutation in the ZIC1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated oxycephaly","termid":"MONDO:0018971"}],"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":"craniosynostosis 6","secondary_identifiers":["MEDGEN:904675","GARD:18048","OMIM:616602","Orphanet:672985","UMLS:C4225269"],"synonyms":[{"name":"CRS6","type":"related"},{"name":"ZIC1 craniosynostosis","type":"exact"},{"name":"craniosynostosis 6","type":"exact"},{"name":"craniosynostosis caused by mutation in ZIC1","type":"exact"},{"name":"craniosynostosis type 6","type":"exact"}],"termid":"MONDO:0014705","xrefs":{"Monarch":{"xref_id":"0014705"}}}


id: PBO:0087193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA splicing factor; required for ATP-independent portion of 2nd catalytic step of spliceosomal RNA splicing; interacts with Prp18p; contains zinc knuckle domain","termid":"PBO:0087193"}


id: GO:0090613
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5'deoxyadenosine + H2O = 5'deoxyinosine + NH3.","definition_xrefs":["RHEA:42892","PMID:23968233"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines","termid":"GO:0016814"},{"relation_name":"is_a","term_name":"deaminase activity","termid":"GO:0019239"}],"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:0016810"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674","GO:0016810"],"is_obsolete":false,"name":"5'-deoxyadenosine deaminase activity","secondary_identifiers":["EC:3.5.4.41"],"termid":"GO:0090613"}


id: GO:1902894
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of microRNA (miRNA) gene transcription.","definition_xrefs":["GOC:kmv","GO_REF:0000058","GOC:dph","GOC:TermGenie","PMID:24699545"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of DNA-templated transcription","termid":"GO:0045892"},{"relation_name":"is_a","term_name":"regulation of miRNA transcription","termid":"GO:1902893"},{"relation_name":"is_a","term_name":"negative regulation of miRNA metabolic process","termid":"GO:2000629"},{"relation_name":"negatively_regulates","term_name":"miRNA transcription","termid":"GO:0061614"}],"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"},{"rel_name":"negatively_regulates","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006355","GO:0006351"],"is_obsolete":false,"name":"negative regulation of miRNA transcription","synonyms":[{"name":"down regulation of pri-miRNA transcription from RNA polymerase II promoter","type":"exact"},{"name":"down-regulation of pri-miRNA transcription from RNA polymerase II promoter","type":"exact"},{"name":"downregulation of pri-miRNA transcription from RNA polymerase II promoter","type":"exact"},{"name":"inhibition of pri-miRNA transcription from RNA polymerase II promoter","type":"narrow"},{"name":"negative regulation of miRNA gene transcription","type":"exact"},{"name":"negative regulation of microRNA gene transcription","type":"exact"},{"name":"negative regulation of pri-miRNA transcription by RNA polymerase II","type":"exact"},{"name":"negative regulation of pri-miRNA transcription from RNA polymerase II promoter","type":"exact"},{"name":"negative regulation of primary miRNA gene transcription","type":"exact"}],"termid":"GO:1902894"}


id: GO:0046657
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of folic acid, pteroylglutamic acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"folic acid-containing compound catabolic process","termid":"GO:0009397"},{"relation_name":"is_a","term_name":"water-soluble vitamin catabolic process","termid":"GO:0042365"},{"relation_name":"is_a","term_name":"dicarboxylic acid catabolic process","termid":"GO:0043649"},{"relation_name":"is_a","term_name":"folic acid metabolic process","termid":"GO:0046655"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006766"}],"interesting_parent_ids":["GO:0008150","GO:0006766","GO:0044281"],"is_obsolete":false,"name":"folic acid catabolic process","synonyms":[{"name":"folate catabolic process","type":"exact"},{"name":"folate catabolism","type":"exact"},{"name":"folic acid breakdown","type":"exact"},{"name":"folic acid catabolism","type":"exact"},{"name":"folic acid degradation","type":"exact"},{"name":"vitamin B9 catabolic process","type":"exact"},{"name":"vitamin B9 catabolism","type":"exact"},{"name":"vitamin M catabolic process","type":"exact"},{"name":"vitamin M catabolism","type":"exact"}],"termid":"GO:0046657"}


id: PBO:0065394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 20S subunit alpha 2","termid":"PBO:0065394"}


id: PBO:0052388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin family member 26B","termid":"PBO:0052388"}


id: GO:0046425
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of receptor signaling via JAK-STAT.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of receptor signaling pathway via STAT","termid":"GO:1904892"},{"relation_name":"regulates","term_name":"cell surface receptor signaling pathway via JAK-STAT","termid":"GO:0007259"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of receptor signaling pathway via JAK-STAT","secondary_identifiers":["GO:2000364","GO:0007262"],"synonyms":[{"name":"STAT protein import into nucleus","type":"narrow"},{"name":"regulation of STAT protein import into nucleus","type":"narrow"},{"name":"regulation of STAT protein nuclear translocation","type":"narrow"}],"termid":"GO:0046425"}


id: MONDO:1010112
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease characterized by the height of an individual two standard deviations below the corresponding mean height for a given age, sex and population group with no known cause.","definition_xrefs":["PMID:8805048"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isolated short stature","synonyms":[{"name":"idiopathic short stature","type":"related"}],"termid":"MONDO:1010112","xrefs":{"Monarch":{"xref_id":"1010112"}}}


id: GO:0034836
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 6-hydroxy-2-mercaptobenzothiazole + 1/2 O2 = 6,7-dihydroxy-2-mercaptobenzothiazole.","definition_xrefs":["UM-BBD_reactionID:r1181"],"gene_count":0,"genotype_count":0,"name":"obsolete 6-hydroxy-2-mercaptobenzothiazole monooxygenase activity (obsolete GO:0034836)","termid":"GO:0034836"}


id: GO:0021978
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regionalization process that creates areas within the forebrain that will direct the behavior of cell migration in differentiation as the telencephalon develops.","definition_xrefs":["GOC:cls","GOC:dgh","GOC:mgi_curators","GO_REF:0000021","GOC:jid","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"},{"relation_name":"part_of","term_name":"telencephalon development","termid":"GO:0021537"},{"relation_name":"part_of","term_name":"forebrain regionalization","termid":"GO:0021871"}],"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":"telencephalon regionalization","termid":"GO:0021978"}


id: MONDO:0957531
data:
  {"annotated_genes":["SJAG_03267"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88096],"is_not":false,"summary":null,"term":"MONDO:0957531"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03267":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 microcephaly and movement abnormalities","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620445","MEDGEN:1841260","UMLS:C5830624"],"termid":"MONDO:0957531","terms_by_termid":{"MONDO:0957531":null},"xrefs":{"Monarch":{"xref_id":"0957531"}}}


id: PBO:0070908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 16","termid":"PBO:0070908"}


id: PBO:0026713
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_regulation_of_translation_in_response_to_UV","termid":"PBO:0026713"}


id: PBO:0004805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centractin family actin-like protein Arp1 (predicted)","termid":"PBO:0004805"}


id: PBO:0070259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U11 small nuclear 4, pseudogene","termid":"PBO:0070259"}


id: MONDO:0014739
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MET gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 97","secondary_identifiers":["OMIM:616705","DOID:0110539","GARD:22655","UMLS:C4084709","MEDGEN:899875"],"synonyms":[{"name":"DFNB97","type":"narrow"},{"name":"MET autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 97","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 97","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in MET","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 97","type":"narrow"},{"name":"deafness, autosomal recessive 97","type":"narrow"},{"name":"deafness, autosomal recessive type 97","type":"narrow"}],"termid":"MONDO:0014739","xrefs":{"Monarch":{"xref_id":"0014739"}}}


id: PR:O14239
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rax2 gene.","definition_xrefs":["UniProtKB:O14239","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":"polarized growth protein rax2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6F6.06c","synonyms":[{"name":"Spom972h-rax2","type":"exact"},{"name":"revert to axial protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14239"}


id: GO:1990762
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of coupling alanine to alanyl-tRNA, catalyzed by alanyl-tRNA synthetase involved in cytoplasmic translation.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alanyl-tRNA aminoacylation","termid":"GO:0006419"},{"relation_name":"part_of","term_name":"cytoplasmic translation","termid":"GO:0002181"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0002181"}],"interesting_parent_ids":["GO:0010467","GO:0006399","GO:0006520","GO:0008150","GO:0002181"],"is_obsolete":false,"name":"cytoplasmic alanyl-tRNA aminoacylation","termid":"GO:1990762"}


id: PBO:0070001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1297, pseudogene","termid":"PBO:0070001"}


id: PBO:0048525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gem nuclear organelle associated protein 2","termid":"PBO:0048525"}


id: PBO:0074821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 19","termid":"PBO:0074821"}


id: PBO:0070075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6atac small nuclear 32, pseudogene","termid":"PBO:0070075"}


id: PBO:0059775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 1","termid":"PBO:0059775"}


id: GO:0046140
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of corrin, C19H22N4, the fundamental heterocyclic skeleton of the corrinoids. It consists of four reduced pyrrole rings joined into a macrocyclic ring. Corrin is the core of the vitamin B12 molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"corrin metabolic process","termid":"GO:0015009"},{"relation_name":"is_a","term_name":"tetrapyrrole biosynthetic process","termid":"GO:0033014"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0033013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0033013","GO:0008150"],"is_obsolete":false,"name":"corrin biosynthetic process","synonyms":[{"name":"corrin anabolism","type":"exact"},{"name":"corrin biosynthesis","type":"exact"},{"name":"corrin formation","type":"exact"},{"name":"corrin synthesis","type":"exact"}],"termid":"GO:0046140"}


id: _global:input_of
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"inverse of has input","direct_ancestors":[{"relation_name":"is_a","term_name":"functionally_related_to","termid":"_global:functionally_related_to"},{"relation_name":"is_a","term_name":"participates_in","termid":"_global:participates_in"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"input_of","secondary_identifiers":["RO:0002352"],"termid":"_global:input_of"}


id: PBO:0069783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1068, pseudogene","termid":"PBO:0069783"}


id: GO:0102463
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: quercetin-3-gentiobioside + UDP-L-rhamnose = quercetin 3-O-gentiobioside-7-O-rhamnoside + UDP + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete quercetin 3-gentiobioside 7-O-rhamnosyltransferase activity (obsolete GO:0102463)","termid":"GO:0102463"}


id: GO:0003025
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The neural regulation of blood pressure in which baroreceptors sense the amount of stretch occurring in vessels and respond to the input via central nervous system control.","definition_xrefs":["GOC:dph","GOC:mtg_cardio","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system process involved in regulation of systemic arterial blood pressure","termid":"GO:0001976"}],"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 systemic arterial blood pressure by baroreceptor feedback","synonyms":[{"name":"baroreceptor regulation of systemic arterial blood pressure","type":"exact"}],"termid":"GO:0003025"}


id: PBO:0002200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retromer complex subunit Vps29","termid":"PBO:0002200"}


id: PR:Q9US22
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl1502 gene.","definition_xrefs":["UniProtKB:Q9US22","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":"60S ribosomal protein L15-B (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1783.08c","synonyms":[{"name":"Spom972h-rpl1502","type":"exact"}],"termid":"PR:Q9US22"}


id: PBO:0082392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Beta' regulatory subunit of casein kinase 2 (CK2); a Ser/Thr protein kinase with roles in cell growth and proliferation; CK2, comprised of CKA1, CKA2, CKB1 and CKB2, has many substrates including transcription factors and all RNA polymerase","termid":"PBO:0082392"}


id: MONDO:1011210
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"GAPO syndrome that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"GAPO syndrome, non-human animal","termid":"MONDO:1010318"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GAPO syndrome, pig","secondary_identifiers":["OMIA:002544-9823"],"termid":"MONDO:1011210","xrefs":{"Monarch":{"xref_id":"1011210"}}}


id: MONDO:1011112
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cryptorchidism that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cryptorchidism, non-human animal","termid":"MONDO:1010275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cryptorchidism, pig","secondary_identifiers":["OMIA:000243-9823"],"termid":"MONDO:1011112","xrefs":{"Monarch":{"xref_id":"1011112"}}}


id: MOD:00258
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively cross-links an L-cysteine residue and an L-threonine residue by a thioether bond to form S-(2-aminovinyl)-3-methyl-D-cysteine.","definition_xrefs":["PubMed:9119018","RESID:AA0253"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thioether crosslinked residues","termid":"MOD:00687"},{"relation_name":"is_a","term_name":"crosslinked L-threonine residue","termid":"MOD:02056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-(2-aminovinyl)-3-methyl-D-cysteine","synonyms":[{"name":"(2S,3S)-2-amino-3-[((Z)-2-aminoethenyl)sulfanyl]butanoic acid","type":"exact"},{"name":"2-amino-3-[(2-aminovinyl)sulfanyl]butanoic acid","type":"exact"},{"name":"CROSSLNK S-(2-aminovinyl)-3-methyl-D-cysteine (Thr-Cys)","type":"exact"},{"name":"S-(2-aminovinyl)-3-methyl-D-cysteine","type":"exact"},{"name":"decarboxylated methyllanthionine","type":"exact"}],"termid":"MOD:00258"}


id: MOD:01286
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-isoleucine residue to 6x(13)C,1x(15)N isotope labeled L-isoleucine.","definition_xrefs":["Unimod:695#I","PubMed:11999733","PubMed:12175151","PubMed:11857757"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-isoleucine residue","termid":"MOD:00910"},{"relation_name":"is_a","term_name":"6x(13)C,1x(15)N labeled residue","termid":"MOD:01370"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6x(13)C,1x(15)N labeled L-isoleucine","synonyms":[{"name":"13C(6) 15N(1) Silac label","type":"related"},{"name":"Label:13C(6)15N(1)","type":"related"}],"termid":"MOD:01286"}


id: PBO:0045190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJB6 pseudogene 3","termid":"PBO:0045190"}


id: FYPO:0008213
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population phenotype in which cell growth is increased relative to normal in a medium containing lactate as the carbon source.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased vegetative cell population growth","termid":"FYPO:0004557"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002058"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0000139","FYPO:0002057","FYPO:0005447","FYPO:0001985","FYPO:0002058"],"is_obsolete":false,"name":"increased vegetative cell population growth on lactate carbon source","termid":"FYPO:0008213"}


id: GO:1902743
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of lamellipodium organization.","definition_xrefs":["GOC:als","PMID:16054028","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of plasma membrane bounded cell projection organization","termid":"GO:0120035"},{"relation_name":"regulates","term_name":"lamellipodium organization","termid":"GO:0097581"}],"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 lamellipodium organization","termid":"GO:1902743"}


id: PBO:0017001
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Eighteen Interacting Centromere protein","termid":"PBO:0017001"}


id: PBO:0060131
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND6 pseudogene 32","termid":"PBO:0060131"}


id: GO:0006410
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The cellular synthesis of DNA on a template of RNA.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete transcription, RNA-dependent (obsolete GO:0006410)","synonyms":[{"name":"transcription, RNA-dependent","type":"exact"}],"termid":"GO:0006410"}


id: PR:Q96TL7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rap1 gene.","definition_xrefs":["UniProtKB:Q96TL7","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-binding protein rap1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1778.02","synonyms":[{"name":"Spom972h-rap1","type":"exact"}],"termid":"PR:Q96TL7"}


id: GO:0032927
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the activity of any activin receptor signaling pathway.","definition_xrefs":["GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of activin receptor signaling pathway","termid":"GO:0032925"},{"relation_name":"is_a","term_name":"positive regulation of transmembrane receptor protein serine/threonine kinase signaling pathway","termid":"GO:0090100"},{"relation_name":"positively_regulates","term_name":"activin receptor signaling pathway","termid":"GO:0032924"}],"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 activin receptor signaling pathway","synonyms":[{"name":"activation of activin receptor signaling pathway","type":"narrow"},{"name":"positive regulation of activin receptor signalling pathway","type":"exact"},{"name":"positive regulation of activin signaling pathway","type":"related"},{"name":"positive regulation of activin signalling pathway","type":"related"},{"name":"stimulation of activin receptor signaling pathway","type":"narrow"},{"name":"up regulation of activin receptor signaling pathway","type":"exact"},{"name":"up-regulation of activin receptor signaling pathway","type":"exact"},{"name":"upregulation of activin receptor signaling pathway","type":"exact"}],"termid":"GO:0032927"}


id: MOD:00008
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"Entry from Unimod representing one or more entries in RESID. OBSOLETE because organizational use is no longer required.","definition_xrefs":["PubMed:18688235"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:00008 common (obsolete MOD:00008)","termid":"MOD:00008"}


id: GO:0004080
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: ATP + biotin + apo-(propanoyl-CoA:carbon-dioxide ligase (ADP-forming)) = AMP + diphosphate + (propanoyl-CoA:carbon-dioxide ligase (ADP-forming)).","definition_xrefs":["GOC:rynl"],"gene_count":0,"genotype_count":0,"name":"obsolete biotin-[propionyl-CoA-carboxylase (ATP-hydrolyzing)] ligase activity (obsolete GO:0004080)","termid":"GO:0004080"}


id: MONDO:0030042
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":"proteinuria, chronic benign","secondary_identifiers":["UMLS:C5394384","MEDGEN:1714078","OMIM:618884"],"synonyms":[{"name":"PROCHOB","type":"exact"},{"name":"PROTEINURIA, CHRONIC BENIGN","type":"exact"},{"name":"proteinuria, chronic benign","type":"exact"}],"termid":"MONDO:0030042","xrefs":{"Monarch":{"xref_id":"0030042"}}}


id: GO:0005667
data:
  {"annotated_genes":["SJAG_02311","SJAG_04977","SJAG_00901","SJAG_00934","SJAG_00692","SJAG_00584","SJAG_02541","SJAG_03143","SJAG_04009","SJAG_02174","SJAG_03007","SJAG_00512","SJAG_00861","SJAG_03982","SJAG_02458","SJAG_01475","SJAG_00958","SJAG_02494","SJAG_04274","SJAG_00987","SJAG_03120","SJAG_04420","SJAG_04368","SJAG_01062","SJAG_01808","SJAG_04921","SJAG_00421","SJAG_02813","SJAG_04654","SJAG_03622","SJAG_02472","SJAG_05153","SJAG_00758","SJAG_00872","SJAG_03095","SJAG_04766","SJAG_03546","SJAG_00297","SJAG_00290","SJAG_04607","SJAG_00150","SJAG_01771","SJAG_02747","SJAG_04036","SJAG_01710","SJAG_00266","SJAG_05331","SJAG_02849","SJAG_00995","SJAG_04813","SJAG_02778","SJAG_00159","SJAG_02815","SJAG_04917","SJAG_02810","SJAG_00735","SJAG_01207","SJAG_04083","SJAG_03285","SJAG_03618","SJAG_04705","SJAG_00095","SJAG_03573","SJAG_00202","SJAG_00116","SJAG_03900","SJAG_02255","SJAG_05247","SJAG_04381","SJAG_03354","SJAG_00698","SJAG_03107","SJAG_04614","SJAG_04852","SJAG_00693","SJAG_01728","SJAG_00904","SJAG_03206","SJAG_03844","SJAG_01827","SJAG_05339","SJAG_00585","SJAG_04647","SJAG_00741","SJAG_02218","SJAG_01157"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[78437,91482],"is_not":false,"summary":null,"term":"GO:0005667"},{"annotations":[109780,94520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990243"},{"annotations":[113707,77415,71725,106050],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016602"},{"annotations":[79993,71488,75913,77644,76260,79287,79111,103748],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070847"},{"annotations":[100666,108810,93024],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160051"},{"annotations":[107920,106236,112548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097221"},{"annotations":[79132,77492,105749,110047,79090,108539],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030907"},{"annotations":[72170,73022],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017054"},{"annotations":[80936,81567,77409],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070860"},{"annotations":[97356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000120"},{"annotations":[80874,107078,94946,73770],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000500"},{"annotations":[81831,102286,110622,108860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090575"},{"annotations":[109973,113936,73342,115126],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070824"},{"annotations":[73728,80345],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005672"},{"annotations":[71575,78527,76124,58100,72319,105410,78398,77257,97357,82034,75331,76642,73049,69565,59938,119412],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005669"},{"annotations":[71835,77844],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005673"},{"annotations":[82149,71576,80896],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005674"},{"annotations":[77847,57408,71817,63095,80412,92026,93942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000439"},{"annotations":[77848,72044,93943,110799,116666,76069,71818,80413],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005675"},{"annotations":[73487,97358,79250],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000126"},{"annotations":[71483,78168,72796,75426,89952,73512],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000127"},{"annotations":[61393,67297,77904],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0070985"}]},"cv_name":"cellular_component","definition":"A protein complex that is capable of associating with DNA by direct binding, or via other DNA-binding proteins or complexes, and regulating transcription.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":86,"genes_by_uniquename":{"SJAG_00095":null,"SJAG_00116":null,"SJAG_00150":null,"SJAG_00159":null,"SJAG_00202":null,"SJAG_00266":null,"SJAG_00290":null,"SJAG_00297":null,"SJAG_00421":null,"SJAG_00512":null,"SJAG_00584":null,"SJAG_00585":null,"SJAG_00692":null,"SJAG_00693":null,"SJAG_00698":null,"SJAG_00735":null,"SJAG_00741":null,"SJAG_00758":null,"SJAG_00861":null,"SJAG_00872":null,"SJAG_00901":null,"SJAG_00904":null,"SJAG_00934":null,"SJAG_00958":null,"SJAG_00987":null,"SJAG_00995":null,"SJAG_01062":null,"SJAG_01157":null,"SJAG_01207":null,"SJAG_01475":null,"SJAG_01710":null,"SJAG_01728":null,"SJAG_01771":null,"SJAG_01808":null,"SJAG_01827":null,"SJAG_02174":null,"SJAG_02218":null,"SJAG_02255":null,"SJAG_02311":null,"SJAG_02458":null,"SJAG_02472":null,"SJAG_02494":null,"SJAG_02541":null,"SJAG_02747":null,"SJAG_02778":null,"SJAG_02810":null,"SJAG_02813":null,"SJAG_02815":null,"SJAG_02849":null,"SJAG_03007":null,"SJAG_03095":null,"SJAG_03107":null,"SJAG_03120":null,"SJAG_03143":null,"SJAG_03206":null,"SJAG_03285":null,"SJAG_03354":null,"SJAG_03546":null,"SJAG_03573":null,"SJAG_03618":null,"SJAG_03622":null,"SJAG_03844":null,"SJAG_03900":null,"SJAG_03982":null,"SJAG_04009":null,"SJAG_04036":null,"SJAG_04083":null,"SJAG_04274":null,"SJAG_04368":null,"SJAG_04381":null,"SJAG_04420":null,"SJAG_04607":null,"SJAG_04614":null,"SJAG_04647":null,"SJAG_04654":null,"SJAG_04705":null,"SJAG_04766":null,"SJAG_04813":null,"SJAG_04852":null,"SJAG_04917":null,"SJAG_04921":null,"SJAG_04977":null,"SJAG_05153":null,"SJAG_05247":null,"SJAG_05331":null,"SJAG_05339":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":"transcription regulator complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0044798","GO:0044797"],"synonyms":[{"name":"cytoplasmic transcription factor complex","type":"related"},{"name":"nuclear transcription factor complex","type":"related"},{"name":"transcription factor complex","type":"related"}],"termid":"GO:0005667","terms_by_termid":{"GO:0000120":null,"GO:0000126":null,"GO:0000127":null,"GO:0000439":null,"GO:0000500":null,"GO:0005667":null,"GO:0005669":null,"GO:0005672":null,"GO:0005673":null,"GO:0005674":null,"GO:0005675":null,"GO:0016602":null,"GO:0017054":null,"GO:0030907":null,"GO:0070824":null,"GO:0070847":null,"GO:0070860":null,"GO:0070985":null,"GO:0090575":null,"GO:0097221":null,"GO:0160051":null,"GO:1990243":null}}


id: PBO:0004276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi transport protein Tvp23 (predicted)","termid":"PBO:0004276"}


id: GO:0001314
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Replication of circular DNA following excision from the chromosome of dividing cells as they age; replication of extrachromosomal circular DNA generally occurs independently of chromosomal replication.","definition_xrefs":["GOC:jh"],"gene_count":0,"genotype_count":0,"name":"obsolete replication of extrachromosomal circular DNA involved in replicative cell aging (obsolete GO:0001314)","synonyms":[{"name":"replication of extrachromosomal circular DNA during replicative cell ageing","type":"exact"},{"name":"replication of extrachromosomal circular DNA during replicative cell aging","type":"related"}],"termid":"GO:0001314"}


id: GO:0043678
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The innermost of the major layers of the pollen grain wall which underlies the exine and borders the cytoplasm.","definition_xrefs":["PMID:33706055"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"pollen wall","termid":"GO:0043667"}],"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":"intine","termid":"GO:0043678"}


id: GO:0019428
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of allantoin, (2,5-dioxo-4-imidazolidinyl)urea.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"allantoin metabolic process","termid":"GO:0000255"},{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"}],"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":"allantoin biosynthetic process","secondary_identifiers":["MetaCyc:URSIN-PWY"],"synonyms":[{"name":"allantoin anabolism","type":"exact"},{"name":"allantoin biosynthesis","type":"exact"},{"name":"allantoin formation","type":"exact"},{"name":"allantoin synthesis","type":"exact"}],"termid":"GO:0019428"}


id: PBO:0034742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA replication ATPase Mgs1 (predicted)","termid":"PBO:0034742"}


id: PBO:0086379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative ATPase of the CDC48/PAS1/SEC18 (AAA) family; localized to the cortex of mother cells but not to daughter cells; relocalizes from cytoplasm to plasma membrane foci upon DNA replication stress","termid":"PBO:0086379"}


id: GO:0002597
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of antigen processing and presentation of peptide antigen via MHC class Ib.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of antigen processing and presentation of peptide antigen","termid":"GO:0002585"},{"relation_name":"is_a","term_name":"positive regulation of antigen processing and presentation via MHC class Ib","termid":"GO:0002594"},{"relation_name":"is_a","term_name":"regulation of antigen processing and presentation of peptide antigen via MHC class Ib","termid":"GO:0002595"},{"relation_name":"positively_regulates","term_name":"antigen processing and presentation of peptide antigen via MHC class Ib","termid":"GO:0002428"}],"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 antigen processing and presentation of peptide antigen via MHC class Ib","synonyms":[{"name":"activation of antigen processing and presentation of peptide antigen via MHC class Ib","type":"narrow"},{"name":"positive regulation of peptide antigen processing and presentation via MHC class Ib","type":"exact"},{"name":"stimulation of antigen processing and presentation of peptide antigen via MHC class Ib","type":"narrow"},{"name":"up regulation of antigen processing and presentation of peptide antigen via MHC class Ib","type":"exact"},{"name":"up-regulation of antigen processing and presentation of peptide antigen via MHC class Ib","type":"exact"},{"name":"upregulation of antigen processing and presentation of peptide antigen via MHC class Ib","type":"exact"}],"termid":"GO:0002597"}


id: PBO:0085714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein Involved in spore wall assembly; localizes to lipid droplets found on or outside of the prospore membrane; shares similarity with Lds2p and Rrt8p, and a strain mutant for all 3 genes exhibits reduced dityrosine fluorescence relative to the single mutants","termid":"PBO:0085714"}


id: PBO:0008392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FKBP12 peptidyl-prolyl cis-trans isomerase Fkh1","termid":"PBO:0008392"}


id: PBO:0086264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that regulates ubiquitination of Rsp5p; has a WW domain consensus motif of PPPSY (residues 131-135) that mediates binding of Rsp5p to Ubp2p; contains an UBA domain; relative distribution to the nucleus increases upon DNA replication stress","termid":"PBO:0086264"}


id: PBO:0054803
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 2216","termid":"PBO:0054803"}


id: PBO:0070149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 63 pseudogene","termid":"PBO:0070149"}


id: MONDO:0002872
data:
  {"annotated_genes":["SJAG_01156"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88889],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032747"}]},"cv_name":"mondo","definition":"A gestational or non-gestational neoplasm composed of neoplastic trophoblastic cells. Representative examples include hydatidiform mole and choriocarcinoma.","definition_xrefs":["NCIT:C3422"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete germ cell and embryonal cancer (obsolete MONDO:0002510)","termid":"MONDO:0002510"},{"relation_name":"is_a","term_name":"neoplasm","termid":"MONDO:0005070"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01156":null},"genotype_count":0,"is_obsolete":false,"name":"trophoblastic neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0041182","MESH:D014328","DOID:4085","MEDGEN:21708"],"synonyms":[{"name":"neoplasm of trophoblast","type":"exact"},{"name":"trophoblast neoplasm","type":"exact"},{"name":"trophoblast neoplasm (disease)","type":"exact"},{"name":"trophoblast tumor","type":"exact"},{"name":"trophoblast tumour","type":"exact"},{"name":"trophoblastic neoplasm","type":"exact"},{"name":"trophoblastic neoplasm (morphologic abnormality)","type":"exact"},{"name":"trophoblastic neoplasm NOS (morphologic abnormality)","type":"exact"},{"name":"trophoblastic neoplasms","type":"exact"},{"name":"trophoblastic tumor","type":"exact"},{"name":"trophoblastic tumor (qualifier value)","type":"exact"},{"name":"trophoblastic tumour","type":"exact"},{"name":"trophoblastic tumour (qualifier value)","type":"exact"},{"name":"tumor of trophoblast","type":"exact"},{"name":"tumour of trophoblast","type":"exact"}],"termid":"MONDO:0002872","terms_by_termid":{"MONDO:0032747":null},"xrefs":{"Monarch":{"xref_id":"0002872"}}}


id: PBO:0082564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chaperone protein; required for the assembly of box H/ACA snoRNPs and thus for pre-rRNA processing; functions as an RNA mimic; forms a complex with Naf1p and interacts with H/ACA snoRNP components Nhp2p and Cbf5p; homology with known Hsp90p cochaperones; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0082564"}


id: PBO:0073041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SCUBE3 antisense RNA 1","termid":"PBO:0073041"}


id: PBO:0069395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 655, pseudogene","termid":"PBO:0069395"}


id: PBO:0054143
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 1509","termid":"PBO:0054143"}


id: PBO:0085116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleolar peptidyl-prolyl cis-trans isomerase (PPIase); FK506 binding protein; affects expression of multiple genes via its role in nucleosome assembly; phosphorylated by casein kinase II (Cka1p-Cka2p-Ckb1p-Ckb2p) and dephosphorylated by Ptp1p; PPIase domain acts as a transcriptional repressor when tethered to DNA by lexA, and repressor activity is dependent on PPIase activity; FPR3 has a paralog, FPR4, that arose from the whole genome duplication","termid":"PBO:0085116"}


id: GO:0010121
data:
  {"annotated_genes":["SJAG_00495","SJAG_03398"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80095,115041],"is_not":false,"summary":null,"term":"GO:0010121"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of arginine into other compounds, including proline, via ornithine.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-arginine catabolic process","termid":"GO:0006527"},{"relation_name":"is_a","term_name":"proline metabolic process","termid":"GO:0006560"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00495":null,"SJAG_03398":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:0006520"}],"interesting_parent_ids":["GO:0008150","GO:0006520","GO:0044281"],"is_obsolete":false,"name":"L-arginine catabolic process to proline via ornithine","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"arginine breakdown to proline via ornithine","type":"exact"},{"name":"arginine degradation to proline via ornithine","type":"exact"}],"termid":"GO:0010121","terms_by_termid":{"GO:0010121":null}}


id: MONDO:0035293
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"infection-related hemolytic uremic syndrome","termid":"MONDO:0034103"}],"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":"streptococcus pneumoniae-associated hemolytic uremic syndrome","secondary_identifiers":["UMLS:C5680164","MEDGEN:1842720","GARD:22235","ICD10CM:D58.8","Orphanet:544493"],"synonyms":[{"name":"S. pneumoniae-associated HUS","type":"exact"},{"name":"SP-HUS","type":"exact"}],"termid":"MONDO:0035293","xrefs":{"Monarch":{"xref_id":"0035293"}}}


id: GO:0009687
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving abscisic acid, 5-(1-hydroxy-2,6,6,trimethyl-4-oxocyclohex-2-en-1-y1)-3-methylpenta-2,4-dienoic acid.","definition_xrefs":["ISBN:0387969845"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sesquiterpenoid metabolic process","termid":"GO:0006714"},{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"apocarotenoid metabolic process","termid":"GO:0043288"},{"relation_name":"is_a","term_name":"olefinic compound metabolic process","termid":"GO:0120254"},{"relation_name":"is_a","term_name":"tertiary alcohol metabolic process","termid":"GO:1902644"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"abscisic acid metabolic process","synonyms":[{"name":"abscisic acid metabolism","type":"exact"}],"termid":"GO:0009687"}


id: MONDO:0017819
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dentin dysplasia type I","termid":"MONDO:0007436"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atypical dentin dysplasia due to SMOC2 deficiency","secondary_identifiers":["UMLS:C5190802","MEDGEN:1673452","GARD:17433","Orphanet:314721"],"synonyms":[{"name":"dentin dysplasia type 1 with microdontia and shape anomalies","type":"exact"}],"termid":"MONDO:0017819","xrefs":{"Monarch":{"xref_id":"0017819"}}}


id: PBO:0000085
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"possible horizontal transfer","termid":"PBO:0000085"}


id: PBO:0050295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A0","termid":"PBO:0050295"}


id: MONDO:0009476
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atresia of small intestine is a special form of intestinal atresia with absence of mesentery, which is most likely due to an intrauterine intestinal vascular accident. Newborns are usually preterm infants with low birth-weights, that encounter feeding difficulties (including vomiting with initial feeds, which may later worsened and the abdomen becomes progressively distended) as well as failure to thrive. Affected children present disrupted bowel loops assuming a spiral configuration resembling an 'apple peel' and may have less than half of the normal length of the small bowel and a physiologically short bowel. Atresia of small intestine is characterized by jejunal atresia near the ligament of Treitz, foreshortened bowel, and a large mesenteric gap. The bowel distal to the atresia is precariously supplied. Atresia of small intestine may be a manifestation of cystic fibrosis. The most important cause of mortality is short bowel syndrome, encountered in 65% of cases.","definition_xrefs":["Orphanet:1201"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"},{"relation_name":"is_a","term_name":"small intestine disorder","termid":"MONDO:0024635"}],"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":"atresia of small intestine","secondary_identifiers":["icd11.foundation:1949256262","MedDRA:10010626","MESH:C538260","OMIM:243600","NCIT:C98828","MEDGEN:78590","NORD:1309","UMLS:C0266172","GARD:140"],"synonyms":[{"name":"APSB","type":"related"},{"name":"Jejunal Atresia","type":"exact"},{"name":"Jejunoileal atresia","type":"exact"},{"name":"apple peel small bowel syndrome","type":"related"},{"name":"apple peel syndrome","type":"exact"},{"name":"apple-peel intestinal atresia","type":"related"},{"name":"atresia of the small intestine","type":"exact"},{"name":"congenital atresia of the small intestine","type":"related"},{"name":"congenital small intestine atresia","type":"exact"},{"name":"familial apple peel jejunal atresia","type":"related"},{"name":"intestinal atresia type IIIb","type":"exact"},{"name":"jejunal atresia","type":"exact"},{"name":"small intestinal atresia","type":"exact"},{"name":"small intestine atresia","type":"exact"}],"termid":"MONDO:0009476","xrefs":{"Monarch":{"xref_id":"0009476"}}}


id: MOD:00447
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively results from forming an adduct with a glucuronic acid either through a carboxyl group amide or ester bond, or through C1-glycosylation.","definition_xrefs":["PubMed:7398618","Unimod:54#N-term","DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycoconjugated residue","termid":"MOD:00764"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"N-glucuronylated residue","synonyms":[{"name":"Glucuronyl","type":"related"},{"name":"N-Glucuronyl (N terminus)","type":"exact"},{"name":"N-glucuronylation","type":"related"}],"termid":"MOD:00447"}


id: GO:0003196
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process pertaining to the initial formation of the ventriculo bulbo valve from unspecified parts. This process begins with the specific processes that contribute to the appearance of the discrete structure and ends when the structural rudiment is recognizable.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart valve formation","termid":"GO:0003188"},{"relation_name":"part_of","term_name":"ventriculo bulbo valve morphogenesis","termid":"GO:0003187"}],"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":"ventriculo bulbo valve formation","termid":"GO:0003196"}


id: FYPO:0002576
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 abnormal. The affected gene product may be encoded by the mutated gene, or by a different gene, and may normally bind DNA, protein, or both in chromatin.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal molecular function","termid":"FYPO:0000707"},{"relation_name":"is_a","term_name":"binding phenotype","termid":"FYPO:0001092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000707","FYPO:0001985"],"is_obsolete":false,"name":"abnormal chromatin binding","termid":"FYPO:0002576"}


id: MONDO:0957427
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"B-cell acute lymphoblastic leukemia","termid":"MONDO:0004947"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2)","secondary_identifiers":["Orphanet:641372","UMLS:C5816790","MEDGEN:1843410"],"termid":"MONDO:0957427","xrefs":{"Monarch":{"xref_id":"0957427"}}}


id: MONDO:0010501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Macrocephaly-intellectual disability-left ventricular non compaction syndrome is a rare, genetic, syndromic intellectual disability characterized by motor and cognitive developmental delay with language impairment, macrocephaly, hypotonia, dysmorphic facial features (including long face, slanting palpebral fissures and prominent, flattened nose) and left ventricular noncompaction cardiomyopathy. Patients also present skeletal abnormalities (e.g. scoliosis, finger clinodactyly, pes planus), slender build and shy behavior. Strabismus and various neurological signs (including ataxia, tremor and hyperreflexia) may be associated, as well as epilepsy, autism and MRI findings showing a small cerebellum and abnormalities of the corpus callosum. A phenotypic variant with no cardiac involvement has been reported.","definition_xrefs":["Orphanet:466791"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"syndromic X-linked intellectual disability 34","secondary_identifiers":["GARD:17832","OMIM:300967","MEDGEN:902184","DOID:0060817","UMLS:C4225417"],"synonyms":[{"name":"MRXS34","type":"exact"},{"name":"MRXSML","type":"exact"},{"name":"NONO X-linked syndromic intellectual disability","type":"exact"},{"name":"X-linked syndromic intellectual disability caused by mutation in NONO","type":"exact"},{"name":"intellectual developmental disorder, X-linked syndromic 34","type":"exact"},{"name":"intellectual disability, X-linked, syndromic 34","type":"exact"},{"name":"intellectual disability, X-linked, syndromic type 34","type":"exact"},{"name":"intellectual disability, X-linked, syndromic, Mircsof-Langouet type","type":"related"},{"name":"macrocephaly-intellectual disability-left ventricular non compaction syndrome","type":"exact"},{"name":"mental retardation, X-linked, syndromic 34","type":"exact"},{"name":"mental retardation, X-linked, syndromic type 34","type":"exact"},{"name":"mental retardation, X-linked, syndromic, Mircsof-Langouet type","type":"related"},{"name":"syndromic X-linked intellectual disability Mircsof-Langouet type","type":"exact"},{"name":"syndromic X-linked intellectual disability type 34","type":"exact"},{"name":"syndromic X-linked mental retardation Mircsof-Langouet type","type":"exact"}],"termid":"MONDO:0010501","xrefs":{"Monarch":{"xref_id":"0010501"}}}


id: GO:1902371
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of tRNA catabolic process.","definition_xrefs":["PMID:22919049","GOC:bf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of RNA catabolic process","termid":"GO:1902369"},{"relation_name":"is_a","term_name":"regulation of tRNA catabolic process","termid":"GO:1902370"},{"relation_name":"is_a","term_name":"negative regulation of tRNA metabolic process","termid":"GO:1903327"},{"relation_name":"negatively_regulates","term_name":"tRNA decay","termid":"GO:0016078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0008150","GO:0006399"],"is_obsolete":false,"name":"negative regulation of tRNA catabolic process","synonyms":[{"name":"down regulation of tRNA breakdown","type":"exact"},{"name":"down regulation of tRNA catabolic process","type":"exact"},{"name":"down regulation of tRNA catabolism","type":"exact"},{"name":"down regulation of tRNA degradation","type":"exact"},{"name":"down-regulation of tRNA breakdown","type":"exact"},{"name":"down-regulation of tRNA catabolic process","type":"exact"},{"name":"down-regulation of tRNA catabolism","type":"exact"},{"name":"down-regulation of tRNA degradation","type":"exact"},{"name":"downregulation of tRNA breakdown","type":"exact"},{"name":"downregulation of tRNA catabolic process","type":"exact"},{"name":"downregulation of tRNA catabolism","type":"exact"},{"name":"downregulation of tRNA degradation","type":"exact"},{"name":"inhibition of tRNA breakdown","type":"narrow"},{"name":"inhibition of tRNA catabolic process","type":"narrow"},{"name":"inhibition of tRNA catabolism","type":"narrow"},{"name":"inhibition of tRNA degradation","type":"narrow"},{"name":"negative regulation of tRNA breakdown","type":"exact"},{"name":"negative regulation of tRNA catabolism","type":"exact"},{"name":"negative regulation of tRNA degradation","type":"exact"}],"termid":"GO:1902371"}


id: PBO:0084802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial protein of unknown function; conserved among S. cerevisiae strains; extensively overlaps a Ty1 LTR; YER181C is not an essential gene","termid":"PBO:0084802"}


id: GO:1904753
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of vascular associated smooth muscle cell migration.","definition_xrefs":["GOC:BHF_miRNA","GOC:BHF","GOC:TermGenie","GOC:rph","GO_REF:0000058","PMID:20693317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of smooth muscle cell migration","termid":"GO:0014912"},{"relation_name":"is_a","term_name":"regulation of vascular associated smooth muscle cell migration","termid":"GO:1904752"},{"relation_name":"negatively_regulates","term_name":"vascular associated smooth muscle cell migration","termid":"GO:1904738"}],"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 vascular associated smooth muscle cell migration","synonyms":[{"name":"down regulation of vascular associated smooth muscle cell migration","type":"exact"},{"name":"down regulation of vascular smooth muscle cell migration","type":"exact"},{"name":"down-regulation of vascular associated smooth muscle cell migration","type":"exact"},{"name":"down-regulation of vascular smooth muscle cell migration","type":"exact"},{"name":"downregulation of vascular associated smooth muscle cell migration","type":"exact"},{"name":"downregulation of vascular smooth muscle cell migration","type":"exact"},{"name":"inhibition of vascular associated smooth muscle cell migration","type":"narrow"},{"name":"inhibition of vascular smooth muscle cell migration","type":"narrow"},{"name":"negative regulation of vascular smooth muscle cell migration","type":"exact"}],"termid":"GO:1904753"}


id: MONDO:0100192
data:
  {"annotated_genes":["SJAG_01166","SJAG_02015","SJAG_04956","SJAG_00358"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87267],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013111"},{"annotations":[87659],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024568"},{"annotations":[86863],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014659"},{"annotations":[88598],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032844"}]},"cv_name":"mondo","definition":"A liver disease characterized by the liver losing or has lost all of its function.","direct_ancestors":[{"relation_name":"is_a","term_name":"liver disorder","termid":"MONDO:0005154"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00358":null,"SJAG_01166":null,"SJAG_02015":null,"SJAG_04956":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"liver failure","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C26922","MESH:D017093","MEDGEN:88444","UMLS:C0085605"],"synonyms":[{"name":"hepatic failure","type":"exact"}],"termid":"MONDO:0100192","terms_by_termid":{"MONDO:0013111":null,"MONDO:0014659":null,"MONDO:0024568":null,"MONDO:0032844":null},"xrefs":{"Monarch":{"xref_id":"0100192"}}}


id: GO:0019380
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 3-phenylpropionate, the anion of phenylpropanoic acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"3-phenylpropionate metabolic process","termid":"GO:0018962"},{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"},{"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":"3-phenylpropionate catabolic process","secondary_identifiers":["MetaCyc:P281-PWY"],"synonyms":[{"name":"3-phenylpropionate breakdown","type":"exact"},{"name":"3-phenylpropionate catabolism","type":"exact"},{"name":"3-phenylpropionate degradation","type":"exact"}],"termid":"GO:0019380"}


id: PBO:0052278
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine demethylase 5D pseudogene 1","termid":"PBO:0052278"}


id: MONDO:0044983
data:
  {"annotated_genes":["SJAG_00031"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88432],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007908"}]},"cv_name":"mondo","definition":"A benign mesenchymal neoplasm composed of adipose (fatty) tissue. The most common representative of this category is the lipoma.","definition_xrefs":["NCIT:C4502"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign connective and soft tissue neoplasm","termid":"MONDO:0000654"},{"relation_name":"is_a","term_name":"tumor of adipose tissue","termid":"MONDO:0021354"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00031":null},"genotype_count":0,"is_obsolete":false,"name":"benign lipomatous neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD10CM:D17","MEDGEN:91084","icd11.foundation:226447034","UMLS:C0346118"],"synonyms":[{"name":"adipose tissue benign connective and soft tissue neoplasm","type":"exact"},{"name":"benign adipose tissue neoplasm","type":"exact"},{"name":"benign adipose tissue tumor","type":"exact"},{"name":"benign adipose tissue tumour","type":"exact"},{"name":"benign connective and soft tissue neoplasm of adipose tissue","type":"exact"},{"name":"benign lipomatous neoplasm","type":"exact"},{"name":"benign lipomatous tumor","type":"exact"},{"name":"benign lipomatous tumour","type":"exact"},{"name":"benign neoplasm of adipose tissue","type":"exact"},{"name":"benign neoplasm of the adipose tissue","type":"exact"},{"name":"benign tumor of adipose tissue","type":"related"},{"name":"benign tumor of the adipose tissue","type":"exact"},{"name":"benign tumour of adipose tissue","type":"related"},{"name":"benign tumour of the adipose tissue","type":"exact"}],"termid":"MONDO:0044983","terms_by_termid":{"MONDO:0007908":null},"xrefs":{"Monarch":{"xref_id":"0044983"}}}


id: GO:0140533
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which a symbiont inhibits or disrupts the host's RNAi-mediated antiviral immune response. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:17693253"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host innate immune response","termid":"GO:0052170"}],"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 RNAi-mediated antiviral immune response","synonyms":[{"name":"suppression of host RNAi-mediated antiviral immune response","type":"exact"},{"name":"suppression of host RNAi-mediated antiviral immunity","type":"exact"},{"name":"suppression of host RNAi-mediated gene silencing","type":"exact"}],"termid":"GO:0140533"}


id: GO:1990060
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Protein complex facilitating ATP-dependent maltose transport through inner cell membrane (periplasm to cytoplasm) in Gram-negative bacteria. In E. coli the system is composed of a periplasmic maltose-binding protein (MBP), two integral membrane proteins, MalF and MalG, and two copies of the cytoplasmic ATP-binding cassette MalK.","definition_xrefs":["PMID:18033289"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATP-binding cassette (ABC) transporter complex","termid":"GO:0043190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"maltose transport complex","synonyms":[{"name":"maltose ABC transporter complex","type":"exact"},{"name":"maltose ATP-binding cassette transporter complex","type":"exact"}],"termid":"GO:1990060"}


id: PBO:0057348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 543","termid":"PBO:0057348"}


id: GO:0098911
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of action potential creation, propagation or termination in a ventricular cardiac muscle cell contributing to the regulation of its contraction. This typically occurs via modulation of the activity or expression of voltage-gated ion channels.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardiac muscle cell contraction","termid":"GO:0086004"},{"relation_name":"is_a","term_name":"regulation of cardiac muscle cell action potential","termid":"GO:0098901"},{"relation_name":"regulates","term_name":"ventricular cardiac muscle cell action potential","termid":"GO:0086005"}],"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 ventricular cardiac muscle cell action potential","termid":"GO:0098911"}


id: PBO:0055193
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 2617","termid":"PBO:0055193"}


id: GO:0045937
data:
  {"annotated_genes":["SJAG_00685","SJAG_02613"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[119380],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902648"},{"annotations":[91466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905857"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways involving phosphates.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of phosphorus metabolic process","termid":"GO:0010562"},{"relation_name":"is_a","term_name":"regulation of phosphate metabolic process","termid":"GO:0019220"},{"relation_name":"positively_regulates","term_name":"phosphate-containing compound metabolic process","termid":"GO:0006796"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00685":null,"SJAG_02613":null},"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 phosphate metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of phosphate metabolic process","type":"narrow"},{"name":"positive regulation of phosphate metabolism","type":"exact"},{"name":"stimulation of phosphate metabolic process","type":"narrow"},{"name":"up regulation of phosphate metabolic process","type":"exact"},{"name":"up-regulation of phosphate metabolic process","type":"exact"},{"name":"upregulation of phosphate metabolic process","type":"exact"}],"termid":"GO:0045937","terms_by_termid":{"GO:1902648":null,"GO:1905857":null}}


id: PBO:0049684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HOXD antisense growth-associated long non-coding RNA","termid":"PBO:0049684"}


id: MONDO:1010344
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Peters anomaly 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":"disorder of orbital region, non-human animal","termid":"MONDO:1011315"},{"relation_name":"is_a","term_name":"disorder of visual system, non-human animal","termid":"MONDO:1011316"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peters anomaly, non-human animal","secondary_identifiers":["OMIA:001914"],"termid":"MONDO:1010344","xrefs":{"Monarch":{"xref_id":"1010344"}}}


id: GO:0030992
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The larger subcomplex of the intraciliary transport particle; characterized complexes have molecular weights around 550 kDa.","definition_xrefs":["GOC:cilia","GOC:kmv","PMID:14570576","PMID:19253336"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"intraciliary transport particle","termid":"GO:0030990"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"intraciliary transport particle B","synonyms":[{"name":"IFT B complex","type":"related"},{"name":"IFT complex B","type":"related"},{"name":"intraflagellar transport complex B","type":"exact"},{"name":"intraflagellar transport particle B","type":"exact"}],"termid":"GO:0030992"}


id: PBO:0027198
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cytoplasmic_microtubule_formation_from_nuclear_microtubules","termid":"PBO:0027198"}


id: MONDO:0002509
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Granulomatous inflammation of the testis. It is characterized by the formation of granulomas around the seminiferous tubules. History of trauma may be present. It is assumed to be a reactive process due to autoimmune phenomena.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orchitis","termid":"MONDO:0006882"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-specific granulomatous orchitis","secondary_identifiers":["MEDGEN:98504","DOID:3089","UMLS:C0436545","SCTID:50390006","NCIT:C27162"],"synonyms":[{"name":"granulomatous orchitis","type":"broad"}],"termid":"MONDO:0002509","xrefs":{"Monarch":{"xref_id":"0002509"}}}


id: GO:0141115
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which a symbiont disrupts or prematurely activates host complement so that its microbial-destroying activities fail.","definition_xrefs":["PMID:34305859","PMID:24312361"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host complement activation","termid":"GO:0042784"}],"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 complement activation by inactivation of complement proteins","synonyms":[{"name":"suppression of complement activation by another organism by inactivation of complement proteins","type":"broad"}],"termid":"GO:0141115"}


id: PBO:0049764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex group 4 pseudogene 1","termid":"PBO:0049764"}


id: PBO:0045496
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"desmoglein 1","termid":"PBO:0045496"}


id: PBO:0058670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6798","termid":"PBO:0058670"}


id: MOD:01469
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to L-selenocysteinyl tungsten bis(molybdopterin guanine dinucleotide) (not known as a natural, post-translational modification process).","definition_xrefs":["RESID:AA0376#CYS","PubMed:11372198","PubMed:12220497"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tungsten containing modified residue","termid":"MOD:00746"},{"relation_name":"is_a","term_name":"pterin modified residue","termid":"MOD:00748"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-selenocysteine residue","termid":"MOD:02073"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-selenocysteinyl tungsten bis(molybdopterin guanine dinucleotide) (Cys)","termid":"MOD:01469"}


id: PBO:0001605
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expressed in response to nitrogen starvation","termid":"PBO:0001605"}


id: GO:0055022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of cardiac muscle growth.","definition_xrefs":["GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardiac muscle tissue growth","termid":"GO:0055021"},{"relation_name":"is_a","term_name":"negative regulation of heart growth","termid":"GO:0061117"},{"relation_name":"negatively_regulates","term_name":"cardiac muscle tissue growth","termid":"GO:0055017"}],"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 muscle tissue growth","synonyms":[{"name":"down regulation of cardiac muscle growth","type":"exact"},{"name":"down-regulation of cardiac muscle growth","type":"exact"},{"name":"downregulation of cardiac muscle growth","type":"exact"},{"name":"inhibition of cardiac muscle growth","type":"narrow"},{"name":"negative regulation of heart muscle growth","type":"related"}],"termid":"GO:0055022"}


id: GO:0005503
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to all-trans retinal, a compound that plays an important role in the visual process in most vertebrates. All-trans retinal (trans r., visual yellow) results from the bleaching of rhodopsin by light, in which the 11-cis form is converted to the all-trans form. Retinal is one of the forms of vitamin A.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal binding","termid":"GO:0016918"}],"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:0008289","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"all-trans retinal binding","synonyms":[{"name":"all-trans retinaldehyde binding","type":"exact"},{"name":"trans retinal binding","type":"exact"},{"name":"visual yellow binding","type":"exact"},{"name":"vitamin A binding","type":"broad"},{"name":"xanthopsin","type":"related"}],"termid":"GO:0005503"}


id: GO:0009556
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the microsporocyte undergoes meiosis, giving rise to four haploid microspores.","definition_xrefs":["GOC:tb","GOC:mtg_plant"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant-type sporogenesis","termid":"GO:0048236"},{"relation_name":"part_of","term_name":"pollen development","termid":"GO:0009555"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"microsporogenesis","synonyms":[{"name":"microspore development","type":"exact"}],"termid":"GO:0009556"}


id: PBO:0057402
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548h-4","termid":"PBO:0057402"}


id: PBO:0034293
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-attached_to","termid":"PBO:0034293"}


id: PBO:0085606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in control of DNA replication; binds Rap1p C-terminus, telomeres, centromeres, replication origins; contributes to resection of DNA double strand breaks (DSBs); acts synergistically with Rif2p to help control telomere length and establish telomeric silencing; in addition to controlling DNA replication initiation, plays ongoing role after initiation and controls events at blocked replication forks","termid":"PBO:0085606"}


id: PBO:0030236
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_cellular_calcium_level","termid":"PBO:0030236"}


id: PBO:0044388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 2 subfamily AC member 1, pseudogene","termid":"PBO:0044388"}


id: PBO:0063705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidoglycan recognition protein 4","termid":"PBO:0063705"}


id: SO:0001996
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Region of intronic sequence within 10 bases of an exon.","definition_xrefs":["SANGER:am"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intron_domain","termid":"SO:0001014"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"extended_intronic_splice_region","synonyms":[{"name":"extended intronic splice region ","type":"exact"}],"termid":"SO:0001996"}


id: PBO:0028479
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_growing_cell_tip","termid":"PBO:0028479"}


id: FYPO:0000511
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which karyogamy involved in conjugation with cellular fusion does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear fusion during mating","termid":"FYPO:0000510"},{"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:0000301"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000301"],"is_obsolete":false,"name":"abolished nuclear fusion during mating","synonyms":[{"name":"abolished nuclear fusion during conjugation","type":"exact"},{"name":"absent nuclear fusion during mating","type":"exact"},{"name":"karyogamy abolished","type":"exact"},{"name":"karyogamy involved in conjugation with cellular fusion abolished","type":"exact"},{"name":"nuclear fusion during mating abolished","type":"exact"},{"name":"nuclear fusion during mating: absent","type":"related"}],"termid":"FYPO:0000511"}


id: PBO:0059711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO2 pseudogene 19","termid":"PBO:0059711"}


id: PBO:0015244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NatC N-acetyltransferase non-catalytic Sm-like domain subunit Naa38 (predicted)","termid":"PBO:0015244"}


id: PBO:0047338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibulin 7","termid":"PBO:0047338"}


id: MONDO:0014694
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive spondylocostal dysostosis in which the cause of the disease is a mutation in the RIPPLY2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive spondylocostal dysostosis","termid":"MONDO:0010180"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0024322","MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"spondylocostal dysostosis 6, autosomal recessive","secondary_identifiers":["OMIM:616566","GARD:12807","DOID:0112360","MEDGEN:899713","UMLS:C4225279"],"synonyms":[{"name":"RIPPLY2 autosomal recessive spondylocostal dysostosis","type":"exact"},{"name":"SCDO6","type":"related"},{"name":"autosomal recessive spondylocostal dysostosis caused by mutation in RIPPLY2","type":"exact"},{"name":"spondylocostal dysostosis 6","type":"related"},{"name":"spondylocostal dysostosis 6, autosomal recessive","type":"exact"}],"termid":"MONDO:0014694","xrefs":{"Monarch":{"xref_id":"0014694"}}}


id: FYPO:0002844
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which a cell undergoes one or a few rounds of cell division before cells die, resulting in the formation a colony that contains only a few inviable cells which are septated, elongated, and have a larger than normal cell volume. Up to 6 rounds of cell division (generating 64 cells) may be observed, but 3 divisions or fewer is more typical.","definition_xrefs":["PomBase:vw","PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable microcolony, swollen elongated septated cells (obsolete FYPO:0002844)","synonyms":[{"name":"inviable microcolony, enlarged long septated vegetative cells","type":"related"},{"name":"inviable microcolony, large elongated septated vegetative cells","type":"related"},{"name":"inviable microcolony, swollen elongated septated vegetative cells","type":"exact"}],"termid":"FYPO:0002844"}


id: GO:0003312
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells acquire specialized structural and functional features of a pancreatic polypeptide-producing cell. A pancreatic polypeptide-producing cell is a cell in the pancreas that produces pancreatic polypeptide.","definition_xrefs":["GOC:dph","PMID:11076772"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enteroendocrine cell differentiation","termid":"GO:0035883"},{"relation_name":"part_of","term_name":"endocrine pancreas development","termid":"GO:0031018"}],"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":"pancreatic PP cell differentiation","synonyms":[{"name":"pancreatic polypeptide-producing cell differentiation","type":"exact"}],"termid":"GO:0003312"}


id: GO:1902875
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of embryonic pattern specification.","definition_xrefs":["GO_REF:0000058","GOC:mr","GOC:TermGenie","PMID:16872597"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"regulates","term_name":"embryonic pattern specification","termid":"GO:0009880"}],"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 embryonic pattern specification","synonyms":[{"name":"regulation of embryonic pattern biosynthesis","type":"broad"},{"name":"regulation of embryonic pattern formation","type":"broad"},{"name":"regulation of ventral/lateral system","type":"related"}],"termid":"GO:1902875"}


id: MONDO:0012106
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the ASPM gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive primary microcephaly","termid":"MONDO:0016660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0700092"],"is_obsolete":false,"name":"microcephaly 5, primary, autosomal recessive","secondary_identifiers":["GARD:15441","MEDGEN:373344","MESH:C563871","OMIM:608716","UMLS:C1837501","DOID:0070280"],"synonyms":[{"name":"ASPM autosomal recessive primary microcephaly","type":"exact"},{"name":"MCPH5","type":"related"},{"name":"autosomal recessive primary microcephaly caused by mutation in ASPM","type":"exact"},{"name":"microcephaly 5, primary, autosomal recessive","type":"exact"}],"termid":"MONDO:0012106","xrefs":{"Monarch":{"xref_id":"0012106"}}}


id: MOD:02037
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod N-linked glycosylation, Hex(7) HexNAc(2)","definition_xrefs":["PubMed:33135055","Unimod:1480"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N4-glycosyl-L-asparagine","termid":"MOD:00160"},{"relation_name":"is_a","term_name":"complex glycosylation","termid":"MOD:00725"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"Hex7HexNAc2 N4-glycosylated asparagine","synonyms":[{"name":"M7/Man7","type":"related"}],"termid":"MOD:02037"}


id: GO:0140178
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The membrane leaflet of the cis-Golgi network directly contacts the Golgi lumen and may be involved in glycosylation, cargo sorting, or interactions with resident Golgi proteins.","definition_xrefs":["PMID:1747103","PMID:29802621","PMID:34080016"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lumenal side of membrane","termid":"GO:0098576"},{"relation_name":"part_of","term_name":"cis-Golgi network membrane","termid":"GO:0033106"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005794"}],"interesting_parent_ids":["GO:0005794","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"lumenal side of cis-Golgi network membrane","termid":"GO:0140178"}


id: PBO:0051889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ITFG2 antisense RNA 1","termid":"PBO:0051889"}


id: FYPO:0002531
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 nucleoplasm is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to nucleus during vegetative growth","termid":"FYPO:0001424"},{"relation_name":"is_a","term_name":"abnormal protein localization to nucleoplasm","termid":"FYPO:0002529"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abolished protein localization to nucleoplasm","synonyms":[{"name":"abolished protein localisation to nucleoplasm","type":"exact"},{"name":"abolished protein localization to nucleoplasm during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to nucleoplasm during vegetative growth","type":"exact"},{"name":"protein localization to nucleoplasm abolished","type":"exact"}],"termid":"FYPO:0002531"}


id: FYPO:0000388
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of biofilm formation is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal biofilm formation","termid":"FYPO:0000630"}],"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"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased biofilm formation","synonyms":[{"name":"biofilm formation: increased","type":"related"}],"termid":"FYPO:0000388"}


id: GO:0015805
data:
  {"annotated_genes":["SJAG_01890","SJAG_01589"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104404,90034],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990543"}]},"cv_name":"biological_process","definition":"The directed movement of S-adenosylmethionine, S-(5'-adenosyl)-L-methionine, an important intermediate in one-carbon metabolism, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"},{"relation_name":"is_a","term_name":"sulfur compound transport","termid":"GO:0072348"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01589":null,"SJAG_01890":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"S-adenosyl-L-methionine transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"S-adenosyl methionine transport","type":"exact"},{"name":"S-adenosylmethionine transport","type":"exact"},{"name":"SAM transport","type":"exact"}],"termid":"GO:0015805","terms_by_termid":{"GO:1990543":null}}


