# terms

id: PBO:0047585
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroblast growth factor receptor 3 pseudogene 5","termid":"PBO:0047585"}


id: GO:0000989
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to a specific transcription factor, which may be a single protein or a complex, in order to modulate transcription. A protein binding transcription factor may or may not also interact with the template nucleic acid (either DNA or RNA) as well.","definition_xrefs":["GOC:txnOH"],"gene_count":0,"genotype_count":0,"name":"obsolete transcription factor activity, transcription factor binding (obsolete GO:0000989)","synonyms":[{"name":"transcription factor binding transcription factor activity","type":"exact"}],"termid":"GO:0000989"}


id: PBO:0087116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosome biogenesis factor; nucleolar protein associated with pre-rRNA components of the 90S preribosome, required for cleavage of pre-rRNA at A0, A1 and A2 sites; interacts with RNA helicase Dhr2p and RNA helicase-like protein Utp25p; required for incorporation of Utp25p into preribosomes","termid":"PBO:0087116"}


id: PBO:0113251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"One of two type I myosin motors; involved in clathrin-mediated endocytosis; activation by TEDS site phosphorylation increases actin gliding, motor activity and ligand-induced endocytosis; contains proline-rich tail homology 2 (TH2) and SH3 domains; MYO5 deletion has little effect on growth, but myo3 myo5 double deletion causes severe defects in growth and actin cytoskeleton organization; MYO5 has a paralog, MYO3, that arose from the whole genome duplication","termid":"PBO:0113251"}


id: PR:Q09700
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gep3 gene.","definition_xrefs":["UniProtKB:Q09700","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 C2F7.09c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2F7.09c","synonyms":[{"name":"Spom972h-gep3","type":"exact"}],"termid":"PR:Q09700"}


id: MONDO:0012082
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"Asperger syndrome","termid":"MONDO:0005259"},{"relation_name":"is_a","term_name":"Asperger syndrome, susceptibility to","termid":"MONDO:0100440"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"asperger syndrome, susceptibility to, 1","secondary_identifiers":["MEDGEN:325218","OMIM:608638","UMLS:C1837646"],"synonyms":[{"name":"ASPERGER syndrome, susceptibility to, 1","type":"related"},{"name":"ASPG1","type":"exact"},{"name":"Asperger syndrome susceptibility 1, Isolated cases","type":"exact"}],"termid":"MONDO:0012082","xrefs":{"Monarch":{"xref_id":"0012082"}}}


id: MONDO:0003589
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant adipose tissue neoplasm of the ovary.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian sarcoma","termid":"MONDO:0002225"},{"relation_name":"is_a","term_name":"liposarcoma","termid":"MONDO:0005060"}],"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":"liposarcoma of the ovary","secondary_identifiers":["DOID:5697","NCIT:C6419","UMLS:C1335165","MEDGEN:233808"],"synonyms":[{"name":"liposarcoma of ovary","type":"exact"},{"name":"ovarian liposarcoma","type":"exact"},{"name":"ovary liposarcoma","type":"exact"}],"termid":"MONDO:0003589","xrefs":{"Monarch":{"xref_id":"0003589"}}}


id: PBO:0028248
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_actin_cable","termid":"PBO:0028248"}


id: PBO:0027744
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_nucleus_during_glucose_starvation","termid":"PBO:0027744"}


id: PBO:0075626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPRING1 pseudogene 3","termid":"PBO:0075626"}


id: PBO:0066444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"REV1 DNA directed polymerase","termid":"PBO:0066444"}


id: PBO:0070377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"roundabout guidance receptor 3","termid":"PBO:0070377"}


id: MONDO:0013580
data:
  {"annotated_genes":["SJAG_03064"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86293],"is_not":false,"summary":null,"term":"MONDO:0013580"}]},"cv_name":"mondo","definition":"Pyruvate dehydrogenase E1-beta deficiency is an extremely rare form of pyruvate dehydrogenase deficiency (PDHD) characterized by severe lactic acidosis, developmental delay and hypotonia.","definition_xrefs":["Orphanet:255138"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate dehydrogenase deficiency","termid":"MONDO:0019169"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03064":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005244","MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"pyruvate dehydrogenase E1-beta deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C566729","OMIM:614111","GARD:17236","MEDGEN:481471","UMLS:C3279841"],"synonyms":[{"name":"PDHBD","type":"exact"},{"name":"pyruvate dehydrogenase E1-BETA deficiency","type":"related"},{"name":"pyruvate dehydrogenase E1-beta deficiency","type":"exact"},{"name":"pyruvate dehydrogenase complex E1 component subunit beta deficiency","type":"exact"}],"termid":"MONDO:0013580","terms_by_termid":{"MONDO:0013580":null},"xrefs":{"Monarch":{"xref_id":"0013580"}}}


id: PBO:0002755
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis protein Rrp12 (predicted)","termid":"PBO:0002755"}


id: PBO:0055904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 27","termid":"PBO:0055904"}


id: MONDO:0017596
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A diffuse large B-cell lymphoma arising from the central nervous system.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse large B-cell lymphoma","termid":"MONDO:0018905"},{"relation_name":"is_a","term_name":"central nervous system non-hodgkin lymphoma","termid":"MONDO:0044887"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"diffuse large B-cell lymphoma of the central nervous system","secondary_identifiers":["icd11.foundation:1029172881","UMLS:C2026186","SCTID:734066005","ICDO:9680/3","GARD:21246","Orphanet:300849","NCIT:C71720","DOID:0081313","MEDGEN:378339"],"synonyms":[{"name":"CNS DLBCL","type":"exact"},{"name":"DLBCL of the CNS","type":"exact"},{"name":"central nervous system diffuse large B-cell lymphoma","type":"exact"},{"name":"diffuse large B-cell lymphoma of central nervous system","type":"exact"},{"name":"primary DLBCL of the CNS","type":"exact"},{"name":"primary diffuse large B-cell lymphoma of the central nervous system","type":"exact"}],"termid":"MONDO:0017596","xrefs":{"Monarch":{"xref_id":"0017596"}}}


id: PBO:0111295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase chadoprop types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"goa_version","termid":"PBO:0111295"}


id: PBO:0075300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"suppressor of cytokine signaling 1","termid":"PBO:0075300"}


id: PBO:0090705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA(Ser) residue 32 (cytosine-3-)-methyltransferase Trm141","termid":"PBO:0090705"}


id: GO:0140678
data:
  {"annotated_genes":["SJAG_02380","SJAG_04398","SJAG_01867","SJAG_02485","SJAG_01515","SJAG_02470","SJAG_02594","SJAG_04699","SJAG_01330","SJAG_01210","SJAG_00452","SJAG_03272","SJAG_03931","SJAG_01245","SJAG_02786","SJAG_01072","SJAG_04203","SJAG_04627","SJAG_01348","SJAG_03974","SJAG_01150","SJAG_04422","SJAG_00460","SJAG_03309","SJAG_04633","SJAG_04505","SJAG_04999","SJAG_04546","SJAG_03717","SJAG_02874","SJAG_03629","SJAG_01821","SJAG_02194","SJAG_01118"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[92230,106696],"is_not":false,"summary":null,"term":"GO:0140678"},{"annotations":[118325,118387,100878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042030"},{"annotations":[71377],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004862"},{"annotations":[109275],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004861"},{"annotations":[103645,66586,117212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004866"},{"annotations":[89197],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060698"},{"annotations":[109619,117373],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004857"},{"annotations":[116689],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005095"},{"annotations":[92565,97585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990624"},{"annotations":[66074],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008073"},{"annotations":[100334],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030414"},{"annotations":[76289,107387],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004860"},{"annotations":[70619,89742],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004864"},{"annotations":[108786,118425],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030291"},{"annotations":[76364,88210,75010],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004865"},{"annotations":[95854,97439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990846"},{"annotations":[93550],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004867"},{"annotations":[77264],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010521"},{"annotations":[115943,99052],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990948"},{"annotations":[115013],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0055105"}]},"cv_name":"molecular_function","definition":"A molecular function regulator that inhibits or decreases the activity of its target via non-covalent binding that does not result in covalent modification to the target.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular function regulator activity","termid":"GO:0098772"}],"gene_count":34,"genes_by_uniquename":{"SJAG_00452":null,"SJAG_00460":null,"SJAG_01072":null,"SJAG_01118":null,"SJAG_01150":null,"SJAG_01210":null,"SJAG_01245":null,"SJAG_01330":null,"SJAG_01348":null,"SJAG_01515":null,"SJAG_01821":null,"SJAG_01867":null,"SJAG_02194":null,"SJAG_02380":null,"SJAG_02470":null,"SJAG_02485":null,"SJAG_02594":null,"SJAG_02786":null,"SJAG_02874":null,"SJAG_03272":null,"SJAG_03309":null,"SJAG_03629":null,"SJAG_03717":null,"SJAG_03931":null,"SJAG_03974":null,"SJAG_04203":null,"SJAG_04398":null,"SJAG_04422":null,"SJAG_04505":null,"SJAG_04546":null,"SJAG_04627":null,"SJAG_04633":null,"SJAG_04699":null,"SJAG_04999":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0003674","GO:0098772"],"is_obsolete":false,"name":"molecular function inhibitor activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0140678","terms_by_termid":{"GO:0004857":null,"GO:0004860":null,"GO:0004861":null,"GO:0004862":null,"GO:0004864":null,"GO:0004865":null,"GO:0004866":null,"GO:0004867":null,"GO:0005095":null,"GO:0008073":null,"GO:0010521":null,"GO:0030291":null,"GO:0030414":null,"GO:0042030":null,"GO:0055105":null,"GO:0060698":null,"GO:0140678":null,"GO:1990624":null,"GO:1990846":null,"GO:1990948":null}}


id: PBO:0065414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 20S subunit beta 3","termid":"PBO:0065414"}


id: GO:0015806
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of S-methylmethionine 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":"modified amino acid transport","termid":"GO:0072337"},{"relation_name":"is_a","term_name":"sulfur compound transport","termid":"GO:0072348"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"S-methylmethionine transport","termid":"GO:0015806"}


id: GO:0010484
data:
  {"annotated_genes":["SJAG_01204","SJAG_02773","SJAG_02165","SJAG_02990"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91120,91777],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036408"},{"annotations":[91778],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043993"},{"annotations":[99326],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044016"},{"annotations":[72971],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032931"},{"annotations":[91779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043992"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + histone H3 = CoA + acetyl-histone H3.","definition_xrefs":["PMID:19056256"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone acetyltransferase activity","termid":"GO:0004402"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01204":null,"SJAG_02165":null,"SJAG_02773":null,"SJAG_02990":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0034212"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140096","GO:0003824","GO:0003674","GO:0034212","GO:0016746","GO:0016740"],"is_obsolete":false,"name":"histone H3 acetyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"H3 histone acetylase activity","type":"exact"},{"name":"H3 histone acetyltransferase activity","type":"exact"}],"termid":"GO:0010484","terms_by_termid":{"GO:0032931":null,"GO:0036408":null,"GO:0043992":null,"GO:0043993":null,"GO:0044016":null}}


id: PBO:0003701
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HMG box protein","termid":"PBO:0003701"}


id: MONDO:0019162
data:
  {"annotated_genes":["SJAG_04335"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87042],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013782"}]},"cv_name":"mondo","definition":"A rare inherited form of hypertension characterized by hyperkalemia, hyperchloremic metabolic acidosis, normal or elevated aldosterone, low renin, and normal renal function.","definition_xrefs":["Orphanet:757"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited pseudohypoaldosteronism","termid":"MONDO:0100323"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04335":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"pseudohypoaldosteronism type 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:4553","OMIMPS:145260","UMLS:C1449844","MEDGEN:259599","ICD9:588.89","icd11.foundation:715347509","NCIT:C123252","NANDO:2200369","SCTID:15689008"],"synonyms":[{"name":"Gordon hyperkalemia-hypertension syndrome","type":"exact"},{"name":"Gordon syndrome","type":"related"},{"name":"PHA2","type":"exact"},{"name":"PHAII","type":"exact"},{"name":"Spitzer-Weinstein syndrome","type":"exact"},{"name":"chloride shunt syndrome","type":"exact"},{"name":"familial hyperkalemic hypertension","type":"exact"},{"name":"hyperkalemia-hypertension syndrome, Gordon type","type":"exact"},{"name":"hyperpotassemia and hypertension familial","type":"related"},{"name":"hypertensive hyperkalemia","type":"exact"},{"name":"mineralocorticoid resistant hyperkalemia","type":"exact"},{"name":"pseudohypoaldosteronism, type 2","type":"exact"},{"name":"pseudohypoaldosteronism, type II","type":"exact"}],"termid":"MONDO:0019162","terms_by_termid":{"MONDO:0013782":null},"xrefs":{"Monarch":{"xref_id":"0019162"}}}


id: GO:0002057
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to guanine.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleobase binding","termid":"GO:0002060"}],"gene_count":0,"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":"guanine binding","termid":"GO:0002057"}


id: MONDO:0859592
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An anaplastic oligodendroglioma that has material basis in IDH gene family mutation and combined whole-arm losses of 1p and 19q (1p/19q codeletion).","definition_xrefs":["DOID:0080882"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anaplastic oligodendroglioma","termid":"MONDO:0016696"}],"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":"IDH-mutant and 1p/19q-codeleted oligodendroglioma","secondary_identifiers":["NCIT:C129318","UMLS:C4288558","MEDGEN:926090"],"termid":"MONDO:0859592","xrefs":{"Monarch":{"xref_id":"0859592"}}}


id: GO:1901333
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of lateral root development.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of post-embryonic development","termid":"GO:0048582"},{"relation_name":"is_a","term_name":"regulation of lateral root development","termid":"GO:2000023"},{"relation_name":"positively_regulates","term_name":"lateral root development","termid":"GO:0048527"}],"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 lateral root development","synonyms":[{"name":"activation of lateral root development","type":"narrow"},{"name":"up regulation of lateral root development","type":"exact"},{"name":"up-regulation of lateral root development","type":"exact"},{"name":"upregulation of lateral root development","type":"exact"}],"termid":"GO:1901333"}


id: GO:0043802
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 L-glutamine + 2 ATP + 2 H2O + hydrogenobyrinate = 2 L-glutamate + 2 ADP + 4 H+ + hydrogenobyrinate a,c-diamide + 2 phosphate.","definition_xrefs":["RHEA:12544","EC:6.3.5.9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-nitrogen ligase activity, with glutamine as amido-N-donor","termid":"GO:0016884"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016874","GO:0003674"],"is_obsolete":false,"name":"hydrogenobyrinic acid a,c-diamide synthase (glutamine-hydrolysing) activity","secondary_identifiers":["KEGG_REACTION:R05224","MetaCyc:R341-RXN"],"synonyms":[{"name":"CobB","type":"related"},{"name":"hydrogenobyrinic acid a,c diamide synthase (glutamine-hydrolysing) activity","type":"exact"},{"name":"hydrogenobyrinic-acid:L-glutamine amido-ligase (AMP-forming)","type":"exact"}],"termid":"GO:0043802"}


id: PBO:0001919
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-oxoacyl-[acyl-carrier-protein] reductase Oar2 (predicted)","termid":"PBO:0001919"}


id: PBO:0045368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diphthamide biosynthesis 3 pseudogene 1","termid":"PBO:0045368"}


id: PBO:0072305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S25 pseudogene 2","termid":"PBO:0072305"}


id: PBO:0066203
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 17 pseudogene 4","termid":"PBO:0066203"}


id: MONDO:0700116
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A brain disorder caused by biallelic variants in NDE1 that is characterized by extreme microcephaly (typically head circumference of more than 10 standard deviations (SD) below the mean), profound motor and intellectual disability, spasticity, and incomplete cerebral formation. Radiologic studies demonstrate overt microcephaly with cortical dysgenesis ranging from simplification to pachygyria/lissencephaly to hydranencephaly. Agenesis of the corpus callosum as well as hypoplasia of the brainstem and cerebellum are typically present.","definition_xrefs":["PMID:21529751","PMID:22526350"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microcephaly","termid":"MONDO:0001149"},{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"microcephaly with lissencephaly and/or hydranencephaly","termid":"MONDO:0700116","xrefs":{"Monarch":{"xref_id":"0700116"}}}


id: GO:0033420
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a CUG codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003723","GO:0005488","GO:0003674","GO:0060090"],"is_obsolete":false,"name":"CUG codon-amino acid adaptor activity","synonyms":[{"name":"CTG codon-amino acid adaptor activity","type":"exact"},{"name":"leucine tRNA","type":"related"}],"termid":"GO:0033420"}


id: PBO:0057262
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 487b","termid":"PBO:0057262"}


id: PBO:0038891
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADD3 antisense RNA 1","termid":"PBO:0038891"}


id: GO:0033821
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a beta-D-glucosyl residue from UDP-glucose to a hydroxymethylcytosine residue in DNA.","definition_xrefs":["EC:2.4.1.27"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucosyltransferase activity","termid":"GO:0046527"},{"relation_name":"is_a","term_name":"catalytic activity, acting on DNA","termid":"GO:0140097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140097"},{"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:0016740","GO:0140097","GO:0003674","GO:0003824","GO:0016757"],"is_obsolete":false,"name":"DNA beta-glucosyltransferase activity","secondary_identifiers":["MetaCyc:2.4.1.27-RXN"],"synonyms":[{"name":"T4 phage beta-glucosyltransferase activity","type":"related"},{"name":"T4-HMC-beta-glucosyl transferase activity","type":"related"},{"name":"T4-beta-glucosyl transferase activity","type":"related"},{"name":"UDP glucose-DNA beta-glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:DNA beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:DNA beta-D-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-deoxyribonucleate beta-glucosyltransferase activity","type":"related"}],"termid":"GO:0033821"}


id: GO:0009539
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An integral membrane complex containing P680, the chlorophyll a molecule that functions as a primary electron donor. In the light, functioning as a water-plastoquinone oxidoreductase, it transfers electrons from water to plastoquinone.","definition_xrefs":["ISBN:0943088399","GOC:kd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"part_of","term_name":"photosystem II","termid":"GO:0009523"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"photosystem II reaction center","synonyms":[{"name":"photosystem II reaction centre","type":"exact"}],"termid":"GO:0009539"}


id: PBO:0067945
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 247","termid":"PBO:0067945"}


id: MONDO:0043797
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Penetrating and non-penetrating injuries to the spinal cord resulting from traumatic external forces (e.g., WOUNDS, GUNSHOT; WHIPLASH INJURIES; etc.).","definition_xrefs":["MESH:D013119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vertebral column disorder","termid":"MONDO:0000812"},{"relation_name":"is_a","term_name":"spinal cord disorder","termid":"MONDO:0002545"},{"relation_name":"is_a","term_name":"spinal injury","termid":"MONDO:0037747"},{"relation_name":"is_a","term_name":"nervous system injury","termid":"MONDO:0044745"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinal cord injury","secondary_identifiers":["SCTID:90584004","GARD:19109","Orphanet:90058"],"synonyms":[{"name":"Contusions, spinal cord","type":"related"},{"name":"Injuries, spinal cord","type":"related"},{"name":"Lacerations, spinal cord","type":"related"},{"name":"Myelopathies, post-traumatic","type":"related"},{"name":"Myelopathies, traumatic","type":"related"},{"name":"Transections, spinal cord","type":"related"},{"name":"Traumas, spinal cord","type":"related"},{"name":"contusion, spinal cord","type":"related"},{"name":"cord Contusions, spinal","type":"related"},{"name":"cord Injuries, spinal","type":"related"},{"name":"cord Lacerations, spinal","type":"related"},{"name":"cord Transections, spinal","type":"related"},{"name":"cord Traumas, spinal","type":"related"},{"name":"cord contusion, spinal","type":"related"},{"name":"cord injury, spinal","type":"related"},{"name":"cord laceration, spinal","type":"related"},{"name":"cord transection, spinal","type":"related"},{"name":"cord trauma, spinal","type":"related"},{"name":"injury of spinal cord","type":"exact"},{"name":"injury, spinal cord","type":"related"},{"name":"laceration, spinal cord","type":"related"},{"name":"myelopathy, post-traumatic","type":"related"},{"name":"myelopathy, traumatic","type":"related"},{"name":"post traumatic myelopathy","type":"related"},{"name":"post-traumatic Myelopathies","type":"related"},{"name":"post-traumatic myelopathy","type":"related"},{"name":"spinal cord Contusions","type":"related"},{"name":"spinal cord Lacerations","type":"related"},{"name":"spinal cord Transections","type":"related"},{"name":"spinal cord Traumas","type":"related"},{"name":"spinal cord contusion","type":"related"},{"name":"spinal cord injury","type":"exact"},{"name":"spinal cord laceration","type":"related"},{"name":"spinal cord transection","type":"related"},{"name":"spinal cord trauma","type":"related"},{"name":"transection, spinal cord","type":"related"},{"name":"trauma, spinal cord","type":"related"},{"name":"traumatic Myelopathies","type":"related"},{"name":"traumatic myelopathy","type":"related"}],"termid":"MONDO:0043797","xrefs":{"Monarch":{"xref_id":"0043797"}}}


id: GO:0102700
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: geranyl diphosphate(3-) = alpha-thujene + diphosphoric acid.","definition_xrefs":["MetaCyc:RXN-5105"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"alpha-thujene synthase activity","termid":"GO:0102700"}


id: MONDO:0056795
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cause of male infertility characterized by X-linked inheritance in which only Sertoli cells (cells that nurture the immature sperm) line the seminiferous tubules (tubes inside the testicles where sperm develop) and there are not any sperm cells present in the seminiferous tubules.","definition_xrefs":["GARD:0008406"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"X-linked spermatogenic failure 1","secondary_identifiers":["ICD9:752.89","NCIT:C168988","GARD:8406","MESH:D054331","OMIM:305700","SCTID:73465006","DOID:0070189"],"synonyms":[{"name":"Del Castillo syndrome","type":"exact"},{"name":"Germinal cell aplasia","type":"exact"},{"name":"SPGFX1","type":"exact"},{"name":"Sertoli cell-only syndrome","type":"exact"},{"name":"spermatogenic failure, X-linked, type 1","type":"exact"}],"termid":"MONDO:0056795","xrefs":{"Monarch":{"xref_id":"0056795"}}}


id: GO:2001003
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of pectin catabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of polysaccharide metabolic process","termid":"GO:0032881"},{"relation_name":"is_a","term_name":"regulation of carbohydrate catabolic process","termid":"GO:0043470"},{"relation_name":"regulates","term_name":"pectin catabolic process","termid":"GO:0045490"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"regulation of pectin catabolic process","synonyms":[{"name":"regulation of pectin breakdown","type":"exact"},{"name":"regulation of pectin catabolism","type":"exact"},{"name":"regulation of pectin degradation","type":"exact"}],"termid":"GO:2001003"}


id: PBO:0071453
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 59","termid":"PBO:0071453"}


id: PBO:0045396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"developmental pluripotency associated 2 pseudogene 3","termid":"PBO:0045396"}


id: MONDO:0006424
data:
  {"annotated_genes":["SJAG_00991","SJAG_00289","SJAG_04755","SJAG_00490","SJAG_03689","SJAG_01111","SJAG_05313","SJAG_04213","SJAG_05346"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011655"},{"annotations":[87298,87299,87300],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011705"},{"annotations":[85555,85556],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012252"},{"annotations":[87692,87691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013224"},{"annotations":[87305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859046"}]},"cv_name":"mondo","definition":"A benign, intermediate, or malignant neoplasm that arises from the soft tissue. The most common types are lipomatous (fatty), vascular, smooth muscle, fibrous, and fibrohistiocytic neoplasms.","definition_xrefs":["NCIT:C3377"],"direct_ancestors":[{"relation_name":"is_a","term_name":"connective and soft tissue neoplasm","termid":"MONDO:0044334"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00289":null,"SJAG_00490":null,"SJAG_00991":null,"SJAG_01111":null,"SJAG_03689":null,"SJAG_04213":null,"SJAG_04755":null,"SJAG_05313":null,"SJAG_05346":null},"genotype_count":0,"is_obsolete":false,"name":"soft tissue neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:387837005","EFO:1000541","ONCOTREE:SOFTTISSUE","UMLS:C0037579","MEDGEN:11495"],"synonyms":[{"name":"SOFTTISSUE","type":"related"},{"name":"neoplasm of soft tissue","type":"exact"},{"name":"neoplasm of the soft tissue","type":"exact"},{"name":"soft tissue neoplasm","type":"exact"},{"name":"soft tissue tumor","type":"exact"},{"name":"soft tissue tumors","type":"exact"},{"name":"soft tissue tumour","type":"exact"},{"name":"soft tissue tumours","type":"exact"},{"name":"tumor of soft tissue","type":"exact"},{"name":"tumor of the soft tissue","type":"exact"},{"name":"tumour of soft tissue","type":"exact"},{"name":"tumour of the soft tissue","type":"exact"}],"termid":"MONDO:0006424","terms_by_termid":{"MONDO:0011655":null,"MONDO:0011705":null,"MONDO:0012252":null,"MONDO:0013224":null,"MONDO:0859046":null},"xrefs":{"Monarch":{"xref_id":"0006424"}}}


id: PBO:0082699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the Mcm2-7 hexameric helicase complex; MCM2-7 primes origins of DNA replication in G1 and becomes an active ATP-dependent helicase that promotes DNA melting and elongation in S-phase; forms an Mcm4p-6p-7p subcomplex","termid":"PBO:0082699"}


id: GO:0141146
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism effects a change that impairs the structure or function of a host tissue. This can occur via the disruption of the extracellular matrix, or the detachment of cells from the extracellular matrix, or the dissociation of the cells composing that tissue. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:14651638","PMID:26355030","PMID:11982763"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated disruption of host anatomical structure","termid":"GO:0052111"}],"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 disruption of host tissue","synonyms":[{"name":"cytopathogenic effect","type":"related"}],"termid":"GO:0141146"}


id: FYPO:0001308
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of long-chain fatty acid-CoA ligase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal long-chain fatty acid-CoA ligase activity","termid":"FYPO:0001305"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000661","FYPO:0000654","FYPO:0005447","FYPO:0000707","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"increased long-chain fatty acid-CoA ligase activity","synonyms":[{"name":"increased lcfa-ligase activity","type":"exact"}],"termid":"FYPO:0001308"}


id: PR:O13982
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An angio-associated migratory cell protein that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01061","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 WD repeat-containing protein C25H1.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC25H1.08c","secondary_identifiers":["UniProtKB:O13982"],"synonyms":[{"name":"Spom972h-AAMP","type":"exact"}],"termid":"PR:O13982"}


id: MONDO:0014249
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mammary polyadenomatosis is characterized by the presence in both breasts of multiple voluminous fibroadenomas with heterogeneous echo patterns.","definition_xrefs":["Orphanet:50920"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast benign neoplasm","termid":"MONDO:0000620"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple fibroadenoma of the breast","secondary_identifiers":["MEDGEN:816248","OMIM:615554","UMLS:C3809918"],"synonyms":[{"name":"MFAB","type":"related"},{"name":"mammary polyadenomatosis","type":"exact"},{"name":"multiple fibroadenomas of the breast","type":"related"}],"termid":"MONDO:0014249","xrefs":{"Monarch":{"xref_id":"0014249"}}}


id: PBO:0012001
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"possible horizonal transfer","termid":"PBO:0012001"}


id: PBO:0034802
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"residue T239 is T275 in the updated structure","termid":"PBO:0034802"}


id: GO:0019573
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of D-arabinose to form D-xylulose 5-phosphate. D-arabinose is converted into D-ribulose, which is phosphorylated to D-ribulose-5-phosphate, which is isomerized to give D-xylulose-5-phosphate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-arabinose catabolic process","termid":"GO:0019571"},{"relation_name":"is_a","term_name":"D-xylulose 5-phosphate metabolic process","termid":"GO:0051167"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0005975","GO:0008150"],"is_obsolete":false,"name":"D-arabinose catabolic process to D-xylulose 5-phosphate","secondary_identifiers":["MetaCyc:DARABCAT-PWY"],"synonyms":[{"name":"D-arabinose breakdown to xylulose 5-phosphate","type":"exact"},{"name":"D-arabinose degradation to xylulose 5-phosphate","type":"exact"}],"termid":"GO:0019573"}


id: MONDO:0021508
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the epicardium.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm of epicardium","termid":"MONDO:0021379"},{"relation_name":"is_a","term_name":"benign neoplasm of heart","termid":"MONDO:0021450"},{"relation_name":"is_a","term_name":"benign neoplasm of pericardium","termid":"MONDO:0021514"}],"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":"benign neoplasm of epicardium","secondary_identifiers":["icd11.foundation:1295571347","MEDGEN:146342","NCIT:C8535","UMLS:C0685115","SCTID:92087008"],"synonyms":[{"name":"benign epicardial neoplasm","type":"exact"},{"name":"benign epicardial tumor","type":"exact"},{"name":"benign epicardial tumour","type":"exact"},{"name":"benign neoplasm of the epicardium","type":"exact"},{"name":"benign tumor of epicardium","type":"exact"},{"name":"benign tumor of the epicardium","type":"exact"},{"name":"benign tumour of epicardium","type":"exact"},{"name":"benign tumour of the epicardium","type":"exact"},{"name":"epicardium benign neoplasm","type":"exact"}],"termid":"MONDO:0021508","xrefs":{"Monarch":{"xref_id":"0021508"}}}


id: GO:1900215
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of apoptotic process involved in metanephric collecting duct development.","definition_xrefs":["GOC:TermGenie","GOC:mtg_kidney_jan10","GOC:yaf","PMID:17314325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of apoptotic process involved in metanephric collecting duct development","termid":"GO:1900214"},{"relation_name":"is_a","term_name":"negative regulation of apoptotic process involved in development","termid":"GO:1904746"},{"relation_name":"negatively_regulates","term_name":"apoptotic process involved in metanephric collecting duct development","termid":"GO:1900204"}],"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 apoptotic process involved in metanephric collecting duct development","synonyms":[{"name":"down regulation of apoptosis of metanephric collecting duct development","type":"narrow"},{"name":"down regulation of apoptotic cell death of metanephric collecting duct development","type":"exact"},{"name":"down regulation of apoptotic process involved in metanephric collecting duct development","type":"exact"},{"name":"down regulation of apoptotic process of metanephric collecting duct development","type":"exact"},{"name":"down regulation of apoptotic program of metanephric collecting duct development","type":"narrow"},{"name":"down regulation of apoptotic programmed cell death of metanephric collecting duct development","type":"exact"},{"name":"down regulation of programmed cell death by apoptosis of metanephric collecting duct development","type":"exact"},{"name":"down regulation of signaling (initiator) caspase activity of metanephric collecting duct development","type":"related"},{"name":"down regulation of type I programmed cell death of metanephric collecting duct development","type":"narrow"},{"name":"down-regulation of apoptosis of metanephric collecting duct development","type":"narrow"},{"name":"down-regulation of apoptotic cell death of metanephric collecting duct development","type":"exact"},{"name":"down-regulation of apoptotic process involved in metanephric collecting duct development","type":"exact"},{"name":"down-regulation of apoptotic process of metanephric collecting duct development","type":"exact"},{"name":"down-regulation of apoptotic program of metanephric collecting duct development","type":"narrow"},{"name":"down-regulation of apoptotic programmed cell death of metanephric collecting duct development","type":"exact"},{"name":"down-regulation of programmed cell death by apoptosis of metanephric collecting duct development","type":"exact"},{"name":"down-regulation of signaling (initiator) caspase activity of metanephric collecting duct development","type":"related"},{"name":"down-regulation of type I programmed cell death of metanephric collecting duct development","type":"narrow"},{"name":"downregulation of apoptosis of metanephric collecting duct development","type":"narrow"},{"name":"downregulation of apoptotic cell death of metanephric collecting duct development","type":"exact"},{"name":"downregulation of apoptotic process involved in metanephric collecting duct development","type":"exact"},{"name":"downregulation of apoptotic process of metanephric collecting duct development","type":"exact"},{"name":"downregulation of apoptotic program of metanephric collecting duct development","type":"narrow"},{"name":"downregulation of apoptotic programmed cell death of metanephric collecting duct development","type":"exact"},{"name":"downregulation of programmed cell death by apoptosis of metanephric collecting duct development","type":"exact"},{"name":"downregulation of signaling (initiator) caspase activity of metanephric collecting duct development","type":"related"},{"name":"downregulation of type I programmed cell death of metanephric collecting duct development","type":"narrow"},{"name":"inhibition of apoptosis of metanephric collecting duct development","type":"narrow"},{"name":"inhibition of apoptotic cell death of metanephric collecting duct development","type":"exact"},{"name":"inhibition of apoptotic process involved in metanephric collecting duct development","type":"narrow"},{"name":"inhibition of apoptotic process of metanephric collecting duct development","type":"exact"},{"name":"inhibition of apoptotic program of metanephric collecting duct development","type":"narrow"},{"name":"inhibition of apoptotic programmed cell death of metanephric collecting duct development","type":"exact"},{"name":"inhibition of programmed cell death by apoptosis of metanephric collecting duct development","type":"exact"},{"name":"inhibition of signaling (initiator) caspase activity of metanephric collecting duct development","type":"related"},{"name":"inhibition of type I programmed cell death of metanephric collecting duct development","type":"narrow"},{"name":"negative regulation of apoptosis of metanephric collecting duct development","type":"narrow"},{"name":"negative regulation of apoptotic cell death of metanephric collecting duct development","type":"exact"},{"name":"negative regulation of apoptotic process of metanephric collecting duct development","type":"exact"},{"name":"negative regulation of apoptotic program of metanephric collecting duct development","type":"narrow"},{"name":"negative regulation of apoptotic programmed cell death of metanephric collecting duct development","type":"exact"},{"name":"negative regulation of programmed cell death by apoptosis of metanephric collecting duct development","type":"exact"},{"name":"negative regulation of signaling (initiator) caspase activity of metanephric collecting duct development","type":"related"},{"name":"negative regulation of type I programmed cell death of metanephric collecting duct development","type":"narrow"}],"termid":"GO:1900215"}


id: MONDO:0014428
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 EPS8 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 102","secondary_identifiers":["DOID:0110463","GARD:22652","MEDGEN:856149","OMIM:615974","UMLS:C3892050"],"synonyms":[{"name":"DFNB102","type":"narrow"},{"name":"EPS8 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 102","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 102","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in EPS8","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 102","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 102","type":"exact"},{"name":"deafness, autosomal recessive 102","type":"narrow"},{"name":"deafness, autosomal recessive type 102","type":"narrow"}],"termid":"MONDO:0014428","xrefs":{"Monarch":{"xref_id":"0014428"}}}


id: PBO:0109969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CIA machinery iron sulphur cluster to apoprotein adaptor Mms19","termid":"PBO:0109969"}


id: MOD:01333
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-isoleucine residue to 6x(13)C labeled L-isoleucine.","definition_xrefs":["PubMed:12766232","PubMed:12716131","Unimod:188#I"],"direct_ancestors":[{"relation_name":"is_a","term_name":"6x(13)C labeled residue","termid":"MOD:00544"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6x(13)C labeled L-isoleucine","synonyms":[{"name":"13C(6) Silac label","type":"related"},{"name":"Label:13C(6)","type":"related"}],"termid":"MOD:01333"}


id: MONDO:0017366
data:
  {"annotated_genes":["SJAG_03920","SJAG_00260","SJAG_02398","SJAG_01671","SJAG_01895"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008192"},{"annotations":[87387],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011121"},{"annotations":[87297],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011544"},{"annotations":[86001],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007273"},{"annotations":[86209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013602"}]},"cv_name":"mondo","definition":"Hereditary paraganglioma-pheochromocytomas (PGL/PCC) are rare neuroendocrine tumors represented by paragangliomas (occurring in any paraganglia from the skull base to the pelvic floor) and pheochromocytomas (adrenal medullary paragangliomas).","definition_xrefs":["Orphanet:29072"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adrenal gland disorder","termid":"MONDO:0005495"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00260":null,"SJAG_01671":null,"SJAG_01895":null,"SJAG_02398":null,"SJAG_03920":null},"genotype_count":0,"is_obsolete":false,"name":"hereditary pheochromocytoma-paraganglioma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:11984","MEDGEN:313270","UMLS:C1708353"],"synonyms":[{"name":"SDHx-related paraganglioma-pheochromocytoma","type":"related"},{"name":"familial pheochromocytoma-paraganglioma","type":"exact"},{"name":"hereditary paraganglioma-pheochromocytoma","type":"related"},{"name":"hereditary pheochromocytoma-paraganglioma","type":"exact"}],"termid":"MONDO:0017366","terms_by_termid":{"MONDO:0007273":null,"MONDO:0008192":null,"MONDO:0011121":null,"MONDO:0011544":null,"MONDO:0013602":null},"xrefs":{"Monarch":{"xref_id":"0017366"}}}


id: MONDO:0006335
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An endometrioid adenocarcinoma arising from the ovary. It comprises 10% to 25% of all primary ovarian carcinomas. Grossly, endometrioid carcinoma may present as a cystic or solid mass. Microscopically, the tumor greatly resembles the appearance of the ordinary type of endometrial adenocarcinoma. As a group, endometrioid carcinoma has a prognosis twice as good as that of serous or mucinous carcinoma.","definition_xrefs":["NCIT:C7979"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian adenocarcinoma","termid":"MONDO:0002752"},{"relation_name":"is_a","term_name":"ovarian endometrial cancer","termid":"MONDO:0003812"},{"relation_name":"is_a","term_name":"endometrioid adenocarcinoma","termid":"MONDO:0005026"},{"relation_name":"is_a","term_name":"endometrium adenocarcinoma","termid":"MONDO:0005461"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"ovarian endometrioid adenocarcinoma","secondary_identifiers":["Orphanet:454723","MEDGEN:91087","EFO:1000416","DOID:5828","GARD:21893","ONCOTREE:EOV","UMLS:C0346163","SCTID:254852002"],"synonyms":[{"name":"endometrioid adenocarcinoma of ovary","type":"exact"},{"name":"endometrioid adenocarcinoma of the ovary","type":"exact"},{"name":"endometrioid cancer of ovary","type":"exact"},{"name":"endometrioid cancer of the ovary","type":"exact"},{"name":"endometrioid carcinoma of ovary","type":"exact"},{"name":"endometrioid carcinoma of the ovary","type":"exact"},{"name":"endometrioid carcinoma ovary","type":"exact"},{"name":"endometrioid ovarian cancer","type":"related"},{"name":"endometrioid ovary carcinoma","type":"exact"},{"name":"endometrium adenocarcinoma of ovary","type":"exact"},{"name":"ovarian endometrioid adenocarcinoma","type":"exact"},{"name":"ovarian endometrioid cancer","type":"exact"},{"name":"ovarian endometrioid carcinoma","type":"exact"},{"name":"ovary endometrium adenocarcinoma","type":"exact"}],"termid":"MONDO:0006335","xrefs":{"Monarch":{"xref_id":"0006335"}}}


id: PBO:0026833
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_poly(U)_RNA_binding","termid":"PBO:0026833"}


id: PBO:0047759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"folate receptor 1 pseudogene 1","termid":"PBO:0047759"}


id: GO:1901842
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of high voltage-gated calcium channel activity.","definition_xrefs":["GOC:BHF","PMID:12754254","GOC:rl","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of voltage-gated calcium channel activity","termid":"GO:1901386"},{"relation_name":"is_a","term_name":"regulation of high voltage-gated calcium channel activity","termid":"GO:1901841"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"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"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"negative regulation of high voltage-gated calcium channel activity","synonyms":[{"name":"down regulation of high voltage gated calcium channel activity","type":"exact"},{"name":"down regulation of high voltage-dependent calcium channel activity","type":"exact"},{"name":"down regulation of high voltage-gated calcium channel activity","type":"exact"},{"name":"down-regulation of high voltage gated calcium channel activity","type":"exact"},{"name":"down-regulation of high voltage-dependent calcium channel activity","type":"exact"},{"name":"down-regulation of high voltage-gated calcium channel activity","type":"exact"},{"name":"downregulation of high voltage gated calcium channel activity","type":"exact"},{"name":"downregulation of high voltage-dependent calcium channel activity","type":"exact"},{"name":"downregulation of high voltage-gated calcium channel activity","type":"exact"},{"name":"inhibition of high voltage gated calcium channel activity","type":"exact"},{"name":"inhibition of high voltage-dependent calcium channel activity","type":"exact"},{"name":"inhibition of high voltage-gated calcium channel activity","type":"narrow"},{"name":"negative regulation of high voltage gated calcium channel activity","type":"exact"},{"name":"negative regulation of high voltage-dependent calcium channel activity","type":"exact"}],"termid":"GO:1901842"}


id: GO:0009882
data:
  {"annotated_genes":["SJAG_02860"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[119598],"is_not":false,"summary":null,"term":"GO:0009882"}]},"cv_name":"molecular_function","definition":"The function of absorbing and responding to electromagnetic radiation with a wavelength of approximately 400-470nm. The response may involve a change in conformation.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"photoreceptor activity","termid":"GO:0009881"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02860":null},"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":"blue light photoreceptor activity","references_by_uniquename":{"PMID:23873862":null},"termid":"GO:0009882","terms_by_termid":{"GO:0009882":null}}


id: MOD:00676
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively adds oxygen atoms to a residue with or without the removal of hydrogen atoms.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidized residue","termid":"MOD:00675"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oxygenated residue","synonyms":[{"name":"OxyRes","type":"exact"}],"termid":"MOD:00676"}


id: PBO:0066715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 12","termid":"PBO:0066715"}


id: PBO:0079002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Thr (anticodon CGT) 2-1","termid":"PBO:0079002"}


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


id: PBO:0043519
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centrobin, centriole duplication and spindle assembly protein","termid":"PBO:0043519"}


id: GO:0046625
data:
  {"annotated_genes":["SJAG_01848","SJAG_03690"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[109022],"is_not":false,"summary":null,"term":"GO:0046625"},{"annotations":[117897],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097001"}]},"cv_name":"molecular_function","definition":"Binding to a sphingolipid, a class of lipids containing the long-chain amine diol sphingosine or a closely related base (a sphingoid).","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid binding","termid":"GO:0008289"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01848":null,"SJAG_03690":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0008289","GO:0005488"],"is_obsolete":false,"name":"sphingolipid binding","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0046625","terms_by_termid":{"GO:0046625":null,"GO:0097001":null}}


id: MONDO:0005780
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any infection caused by a virus of the genus Hantavirus, which is transmitted by aerosolized rodent excreta or rodent bites, that can result in a variety of clinical manifestations from hemorrhagic fever with renal syndrome to a pulmonary syndrome.","definition_xrefs":["NCIT:C3899"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Bunyaviridae infectious disease","termid":"MONDO:0021641"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hantavirus infectious disease","secondary_identifiers":["EFO:0007295","ICD9:079.81","MONDO:0042492","MEDGEN:67028","MESH:D018778","SCTID:359761005","UMLS:C0242994"],"synonyms":[{"name":"Hantavirus caused disease or disorder","type":"exact"},{"name":"Hantavirus disease or disorder","type":"exact"},{"name":"Hantavirus infection","type":"exact"},{"name":"Hantavirus infectious disease","type":"exact"},{"name":"disease caused by hantavirus","type":"related"},{"name":"disease due to hantavirus","type":"exact"},{"name":"infections, Hantavirus","type":"related"}],"termid":"MONDO:0005780","xrefs":{"Monarch":{"xref_id":"0005780"}}}


id: PBO:0078376
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"triggering receptor expressed on myeloid cells 2","termid":"PBO:0078376"}


id: GO:0033453
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a GCU codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0003674","GO:0003723","GO:0005488","GO:0060090"],"is_obsolete":false,"name":"GCU codon-amino acid adaptor activity","synonyms":[{"name":"GCT codon-amino acid adaptor activity","type":"exact"},{"name":"alanine tRNA","type":"related"}],"termid":"GO:0033453"}


id: PR:O14119
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A seipin that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR21212:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"seipin homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3A11.04","secondary_identifiers":["UniProtKB:O14119"],"synonyms":[{"name":"Spom972h-BSCL2","type":"exact"}],"termid":"PR:O14119"}


id: GO:0009644
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 high light intensity stimulus.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to light intensity","termid":"GO:0009642"}],"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 high light intensity","termid":"GO:0009644"}


id: MONDO:0012347
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":"hamartoma, Precalcaneal congenital fibrolipomatous","secondary_identifiers":["OMIM:609808","MESH:C565226","MEDGEN:342846","UMLS:C1853298"],"synonyms":[{"name":"Pcfh","type":"related"},{"name":"hamartoma, Precalcaneal congenital fibrolipomatous","type":"exact"}],"termid":"MONDO:0012347","xrefs":{"Monarch":{"xref_id":"0012347"}}}


id: GO:0044445
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Any constituent part of cytosol, that part of the cytoplasm that does not contain membranous or particulate subcellular components.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete cytosolic part (obsolete GO:0044445)","synonyms":[{"name":"cytosol component","type":"exact"}],"termid":"GO:0044445"}


id: GO:0039604
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont inhibits or disrupts the translation of host mRNA into protein, for example by cleavage of the host mRNAs. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:32703221","PMID:22046136","PMID:22174690"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host translation","termid":"GO:0019057"}],"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 translation","secondary_identifiers":["GO:0039599","GO:0039600","VZ:1579"],"synonyms":[{"name":"host mRNA cleavage by viral endoribonuclease","type":"narrow"},{"name":"host translation shutoff","type":"exact"},{"name":"host translation shutoff by virus","type":"narrow"},{"name":"suppression by virus of host translation","type":"narrow"},{"name":"viral host shutoff protein","type":"narrow"},{"name":"viral inhibition of cellular protein synthesis","type":"narrow"},{"name":"viral shutoff of host protein synthesis","type":"narrow"}],"termid":"GO:0039604"}


id: PR:O14173
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- csi2 gene.","definition_xrefs":["UniProtKB:O14173","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 C4D7.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.07c","synonyms":[{"name":"Spom972h-csi2","type":"exact"}],"termid":"PR:O14173"}


id: GO:0015935
data:
  {"annotated_genes":["SJAG_04663","SJAG_00465","SJAG_02020","SJAG_04168","SJAG_04814","SJAG_02870","SJAG_04324","SJAG_01734","SJAG_04998","SJAG_04342","SJAG_02749","SJAG_02253","SJAG_02803","SJAG_00468","SJAG_03262","SJAG_02335","SJAG_02046","SJAG_00544","SJAG_00069","SJAG_04746","SJAG_02224","SJAG_02585","SJAG_02359","SJAG_00523","SJAG_01132","SJAG_00503","SJAG_05320","SJAG_00105","SJAG_02682","SJAG_01520","SJAG_04188","SJAG_01287","SJAG_02477","SJAG_03859","SJAG_04672","SJAG_03424","SJAG_00782","SJAG_02894","SJAG_03584","SJAG_00860","SJAG_00944","SJAG_02280","SJAG_03034","SJAG_01632","SJAG_02340","SJAG_04788","SJAG_04174","SJAG_02452","SJAG_00628","SJAG_01226","SJAG_03762","SJAG_02201","SJAG_04204","SJAG_02643","SJAG_01366","SJAG_04476","SJAG_04695","SJAG_02861","SJAG_03053","SJAG_02479","SJAG_04753","SJAG_00733","SJAG_00148","SJAG_01512","SJAG_01609","SJAG_02777","SJAG_02324","SJAG_01548","SJAG_04029","SJAG_02904","SJAG_04494","SJAG_02067","SJAG_00060","SJAG_03422","SJAG_04475","SJAG_00889","SJAG_03065","SJAG_03254","SJAG_01767","SJAG_01296","SJAG_04256","SJAG_02184","SJAG_03568","SJAG_04918","SJAG_02522","SJAG_01387","SJAG_04164","SJAG_01468","SJAG_04281","SJAG_04378","SJAG_04173","SJAG_00513"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[74735,58986,75119,100407,74896,74047,75603,78008,78741,79467,71342,80259,77602,105797,74829,113810,75110,105771,76299,116676,74128,73812,105770,73644,105796,116675,100153,101913,77461,76283,95123,75599,71608,80606,74894,114579,78824,76959,71528,100152,72346,114578,70418,70250,77036,101914,75520,73673,69305,70825,73190,71590,107079,74432,80620,113811,74237,79010,74051,91963],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0022627"},{"annotations":[72777,94852,108964,110764,106407,98343,106769,90292,112745,118464,108458,108717,102670,98344,103443,74499,110512,96985,116394,78761,92441,96285,74609,72997,104365,94554,76229,73629,111044,98575,76878,115972],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005763"}]},"cv_name":"cellular_component","definition":"The smaller of the two subunits of a ribosome.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribosomal subunit","termid":"GO:0044391"}],"gene_count":92,"genes_by_uniquename":{"SJAG_00060":null,"SJAG_00069":null,"SJAG_00105":null,"SJAG_00148":null,"SJAG_00465":null,"SJAG_00468":null,"SJAG_00503":null,"SJAG_00513":null,"SJAG_00523":null,"SJAG_00544":null,"SJAG_00628":null,"SJAG_00733":null,"SJAG_00782":null,"SJAG_00860":null,"SJAG_00889":null,"SJAG_00944":null,"SJAG_01132":null,"SJAG_01226":null,"SJAG_01287":null,"SJAG_01296":null,"SJAG_01366":null,"SJAG_01387":null,"SJAG_01468":null,"SJAG_01512":null,"SJAG_01520":null,"SJAG_01548":null,"SJAG_01609":null,"SJAG_01632":null,"SJAG_01734":null,"SJAG_01767":null,"SJAG_02020":null,"SJAG_02046":null,"SJAG_02067":null,"SJAG_02184":null,"SJAG_02201":null,"SJAG_02224":null,"SJAG_02253":null,"SJAG_02280":null,"SJAG_02324":null,"SJAG_02335":null,"SJAG_02340":null,"SJAG_02359":null,"SJAG_02452":null,"SJAG_02477":null,"SJAG_02479":null,"SJAG_02522":null,"SJAG_02585":null,"SJAG_02643":null,"SJAG_02682":null,"SJAG_02749":null,"SJAG_02777":null,"SJAG_02803":null,"SJAG_02861":null,"SJAG_02870":null,"SJAG_02894":null,"SJAG_02904":null,"SJAG_03034":null,"SJAG_03053":null,"SJAG_03065":null,"SJAG_03254":null,"SJAG_03262":null,"SJAG_03422":null,"SJAG_03424":null,"SJAG_03568":null,"SJAG_03584":null,"SJAG_03762":null,"SJAG_03859":null,"SJAG_04029":null,"SJAG_04164":null,"SJAG_04168":null,"SJAG_04173":null,"SJAG_04174":null,"SJAG_04188":null,"SJAG_04204":null,"SJAG_04256":null,"SJAG_04281":null,"SJAG_04324":null,"SJAG_04342":null,"SJAG_04378":null,"SJAG_04475":null,"SJAG_04476":null,"SJAG_04494":null,"SJAG_04663":null,"SJAG_04672":null,"SJAG_04695":null,"SJAG_04746":null,"SJAG_04753":null,"SJAG_04788":null,"SJAG_04814":null,"SJAG_04918":null,"SJAG_04998":null,"SJAG_05320":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"small ribosomal subunit","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"ribosomal small subunit","type":"exact"}],"termid":"GO:0015935","terms_by_termid":{"GO:0005763":null,"GO:0022627":null}}


id: MONDO:0800490
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neonatal/infantile epilepsy syndrome characterized by the onset of non-self-limiting seizures and developmental regression or delay in infants/neonates. This condition is typically caused by genetic mutations that disrupt normal brain development, affecting both cognitive and motor development that is not responsive to typical seizure treatments.","direct_ancestors":[{"relation_name":"is_a","term_name":"neonatal/infantile epilepsy syndrome","termid":"MONDO:0100022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"neonatal/infantile-onset epilepsy syndrome with developmental and epileptic encephalopathy","synonyms":[{"name":"NIE-SDE","type":"exact"}],"termid":"MONDO:0800490","xrefs":{"Monarch":{"xref_id":"0800490"}}}


id: MONDO:0800448
data:
  {"annotated_genes":["SJAG_03678","SJAG_02307","SJAG_01576","SJAG_01659","SJAG_01797","SJAG_02471"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86699],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020507"},{"annotations":[86892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957870"},{"annotations":[86890],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957871"},{"annotations":[86891],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957872"},{"annotations":[86888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957873"},{"annotations":[86812],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014387"}]},"cv_name":"mondo","definition":"A new leukoencephalopathy, the CACH syndrome (Childhood Ataxia with Central nervous system Hypomyelination) or VWM (Vanishing White Matter) was identified on clinical and MRI criteria. Classically, this disease is characterized by (1) an onset between 2 and 5 years of age, with a cerebello-spastic syndrome exacerbated by episodes of fever or head trauma leading to death after 5 to 10 years of disease evolution, (2) a diffuse involvement of the white matter on cerebral MRI with a CSF-like signal intensity (cavitation), (3) a recessive autosomal mode of inheritance, (4) neuropathologic findings consistent with a cavitating orthochromatic leukodystrophy with increased number of oligodendrocytes with sometimes \\\"foamy'' aspect.","definition_xrefs":["Orphanet:135"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01576":null,"SJAG_01659":null,"SJAG_01797":null,"SJAG_02307":null,"SJAG_02471":null,"SJAG_03678":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"leukoencephalopathy with vanishing white matter","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C1858991","DOID:0060868","GARD:231","MEDGEN:347037","NCIT:C122664","OMIMPS:603896","SCTID:447351004"],"synonyms":[{"name":"CACH","type":"exact"},{"name":"CACH syndrome","type":"related"},{"name":"CACH/VWM","type":"related"},{"name":"CACH/VWM syndrome","type":"related"},{"name":"Cree leukoencephalopathy","type":"narrow"},{"name":"VWM","type":"related"},{"name":"childhood ataxia with central nervous system hypomyelination","type":"exact"},{"name":"childhood ataxia with central nervous system hypomyelination/vanishing white matter","type":"related"},{"name":"childhood ataxia with central nervous system hypomyelinization","type":"related"},{"name":"childhood ataxia with diffuse central nervous system hypomyelination","type":"exact"},{"name":"leukoencephalopathy with vanishing WHITE matter","type":"related"},{"name":"leukoencephalopathy with vanishing white matter","type":"exact"},{"name":"myelinosis centralis diffusa","type":"exact"},{"name":"ovarioleukodystrophy","type":"related"},{"name":"vanishing White matter leukodystrophy","type":"related"},{"name":"vanishing White matter leukodystrophy with ovarian failure","type":"related"},{"name":"vanishing white matter disease","type":"related"},{"name":"vanishing white matter leukodystrophy","type":"related"}],"termid":"MONDO:0800448","terms_by_termid":{"MONDO:0014387":null,"MONDO:0020507":null,"MONDO:0957870":null,"MONDO:0957871":null,"MONDO:0957872":null,"MONDO:0957873":null},"xrefs":{"Monarch":{"xref_id":"0800448"}}}


id: MONDO:0010067
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":"splenoportal vascular anomalies","secondary_identifiers":["MEDGEN:137945","OMIM:271500","MESH:C562761","SCTID:234131004","UMLS:C0340826"],"synonyms":[{"name":"splenoportal vascular anomalies","type":"exact"}],"termid":"MONDO:0010067","xrefs":{"Monarch":{"xref_id":"0010067"}}}


id: GO:0055076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process involved in the maintenance of an internal steady state of transition metal ions within an organism or cell. A transition metal is an element whose atom has an incomplete d-subshell of extranuclear electrons, or which gives rise to a cation or cations with an incomplete d-subshell. Transition metals often have more than one valency state. Biologically relevant transition metals include vanadium, manganese, iron, copper, cobalt, nickel, molybdenum and silver.","definition_xrefs":["ISBN:0198506732","GOC:mah","GOC:jid"],"gene_count":0,"genotype_count":0,"name":"obsolete transition metal ion homeostasis (obsolete GO:0055076)","termid":"GO:0055076"}


id: PBO:0062737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 52 subfamily E member 4","termid":"PBO:0062737"}


id: GO:2000892
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a cellobiose.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disaccharide catabolic process","termid":"GO:0046352"},{"relation_name":"is_a","term_name":"cellobiose metabolic process","termid":"GO:2000891"}],"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":"cellobiose catabolic process","synonyms":[{"name":"cellobiose catabolism","type":"exact"}],"termid":"GO:2000892"}


id: GO:0051610
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of serotonin into a cell, typically presynaptic neurons or glial cells. Serotonin (5-hydroxytryptamine) is a monoamine neurotransmitter occurring in the peripheral and central nervous systems.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serotonin transport","termid":"GO:0006837"},{"relation_name":"is_a","term_name":"neurotransmitter reuptake","termid":"GO:0098810"}],"gene_count":0,"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:0051179","GO:0006810"],"is_obsolete":false,"name":"serotonin uptake","synonyms":[{"name":"5-HT uptake","type":"exact"},{"name":"5-hydroxytryptamine uptake","type":"exact"},{"name":"5HT uptake","type":"exact"},{"name":"serotonin import","type":"exact"}],"termid":"GO:0051610"}


id: MONDO:0000621
data:
  {"annotated_genes":["SJAG_01013","SJAG_02527","SJAG_01748","SJAG_03453","SJAG_01349","SJAG_05979","SJAG_03905"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87574,87726,87573,87571,87572,87727],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018874"},{"annotations":[87693],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009693"}]},"cv_name":"mondo","definition":"A malignant neoplasm involving the immune system","direct_ancestors":[{"relation_name":"is_a","term_name":"cancer","termid":"MONDO:0004992"},{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"}],"gene_count":7,"genes_by_uniquename":{"SJAG_01013":null,"SJAG_01349":null,"SJAG_01748":null,"SJAG_02527":null,"SJAG_03453":null,"SJAG_03905":null,"SJAG_05979":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"immune system cancer","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0060083"],"synonyms":[{"name":"cancer of immune system","type":"exact"},{"name":"immune system cancer","type":"exact"},{"name":"malignant immune system neoplasm","type":"exact"},{"name":"malignant neoplasm of immune system","type":"exact"}],"termid":"MONDO:0000621","terms_by_termid":{"MONDO:0009693":null,"MONDO:0018874":null},"xrefs":{"Monarch":{"xref_id":"0000621"}}}


id: FYPO:0001893
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A sporulation phenotype in which azygotic asci that contain more or fewer than four spores form following conjugation, diploid growth, and subsequent azygotic sporulation. Azygotic ascus formation occurs when meiosis takes place within a diploid cell rather than in a zygote produced by sporulation. Zygotes can resume vegetative growth and form colonies of diploid cells if returned to rich media before commitment to meiosis; under nitrogen starvation, diploid cells heterozygous for mating type will undergo azygotic meiosis. Azygotic asci have a characteristic linear morphology resembling that of a single vegetatively growing cell.","definition_xrefs":["PMID:22558440","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal sporulation resulting in formation of ascus with more or fewer than four spores","termid":"FYPO:0001894"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000121"}],"interesting_parent_ids":["FYPO:0000121","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0000631"],"is_obsolete":false,"name":"abnormal sporulation resulting in formation of azygotic ascus with more or fewer than four spores","synonyms":[{"name":"abnormal sporulation resulting in formation of azygotic asci with more or fewer than four spores","type":"exact"},{"name":"sporulation defects, azygotic asci with more or fewer than four spores","type":"exact"}],"termid":"FYPO:0001893"}


id: PBO:0065794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"R3HDM2 divergent transcript","termid":"PBO:0065794"}


id: PBO:0027650
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_vegetative_cell_population_growth","termid":"PBO:0027650"}


id: MONDO:0023098
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":"extrasystoles short stature hyperpigmentation microcephaly","secondary_identifiers":["UMLS:C4749763","MEDGEN:1660843"],"synonyms":[{"name":"Char douglas Dungan syndrome","type":"related"}],"termid":"MONDO:0023098","xrefs":{"Monarch":{"xref_id":"0023098"}}}


id: GO:1990430
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a protein that is part of an extracellular matrix.","definition_xrefs":["PMID:22355679"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"extracellular matrix protein binding","termid":"GO:1990430"}


id: GO:0051468
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events by which a glucocorticoid hormone stimulus is received by a cell and converted into a molecular signal. Glucocorticoids are hormonal C21 corticosteroids synthesized from cholesterol with the ability to bind with the cortisol receptor and trigger similar effects. Glucocorticoids act primarily on carbohydrate and protein metabolism, and have anti-inflammatory effects.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to glucocorticoid","termid":"GO:0051384"},{"relation_name":"is_a","term_name":"detection of steroid hormone stimulus","termid":"GO:0051467"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of glucocorticoid hormone stimulus","termid":"GO:0051468"}


id: PBO:0047916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FRA10A associated CGG repeat 1","termid":"PBO:0047916"}


id: PBO:0074424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 23","termid":"PBO:0074424"}


id: PBO:0087235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sensor-transducer of the stress-activated PKC1-MPK1 signaling pathway; involved in maintenance of cell wall integrity; involved in response to heat shock and other stressors; regulates 1,3-beta-glucan synthesis; WSC3 has a paralog, WSC2, that arose from the whole genome duplication","termid":"PBO:0087235"}


id: GO:0033533
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving verbascose, the pentasaccharide beta-D-fructofuranosyl alpha-D-galactopyranosyl-(1->6)-alpha-D-galactopyranosyl-(1->6)-alpha-D-galactopyranosyl-(1->6)-alpha-D-glucopyranoside.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharide metabolic process","termid":"GO:0009311"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"verbascose metabolic process","synonyms":[{"name":"verbascose metabolism","type":"exact"}],"termid":"GO:0033533"}


id: PBO:0036216
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-incomplete_actomyosin_contractile_ring_contraction","termid":"PBO:0036216"}


id: GO:0002200
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The somatic process allowing for the production of immune receptors whose specificity is not encoded in the germline genomic sequences.","definition_xrefs":["ISBN:0781735149","GOC:add","PMID:16166509","PMID:16102575"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system process","termid":"GO:0002376"},{"relation_name":"part_of","term_name":"immune system development","termid":"GO:0002520"}],"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":"somatic diversification of immune receptors","termid":"GO:0002200"}


id: MONDO:0957575
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":"amegakaryocytic thrombocytopenia, congenital, 2","secondary_identifiers":["MEDGEN:1848998","OMIM:620481","UMLS:C5882679"],"termid":"MONDO:0957575","xrefs":{"Monarch":{"xref_id":"0957575"}}}


id: PBO:0088982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERMES complex subunit, membrane tether and lipid transfer protein Mdm34","termid":"PBO:0088982"}


id: GO:0015709
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of thiosulfate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inorganic anion transport","termid":"GO:0015698"},{"relation_name":"is_a","term_name":"sulfur compound transport","termid":"GO:0072348"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"thiosulfate transport","synonyms":[{"name":"thiosulphate transport","type":"exact"}],"termid":"GO:0015709"}


id: GO:0045777
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which the force of blood traveling through the circulatory system is increased.","definition_xrefs":["GOC:go_curators","GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of blood pressure","termid":"GO:0008217"}],"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 blood pressure","synonyms":[{"name":"activation of blood pressure","type":"narrow"},{"name":"stimulation of blood pressure","type":"narrow"},{"name":"up regulation of blood pressure","type":"exact"},{"name":"up-regulation of blood pressure","type":"exact"},{"name":"upregulation of blood pressure","type":"exact"}],"termid":"GO:0045777"}


id: PBO:0043093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carbohydrate sulfotransferase 5","termid":"PBO:0043093"}


id: PBO:0080406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar protein sorting 36 homolog","termid":"PBO:0080406"}


id: GO:0008481
data:
  {"annotated_genes":["SJAG_02429"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017050"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a sphingoid base + ATP = a sphingoid 1-phosphate + ADP + H+.","definition_xrefs":["RHEA:51496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid kinase activity","termid":"GO:0001727"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02429":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674","GO:0016301"],"is_obsolete":false,"name":"sphingosine kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["EC:2.7.1.91","GO:0001728","MetaCyc:SPHINGANINE-KINASE-RXN"],"synonyms":[{"name":"ATP:sphinganine 1-phosphotransferase activity","type":"related"},{"name":"dihydrosphingosine kinase (phosphorylating)","type":"related"},{"name":"dihydrosphingosine kinase activity","type":"related"},{"name":"sphinganine kinase activity","type":"related"},{"name":"sphingosine kinase (phosphorylating)","type":"related"}],"termid":"GO:0008481","terms_by_termid":{"GO:0017050":null}}


id: GO:0051681
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of 6-alpha-maltosylglucose, also known as isopanose.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharide catabolic process","termid":"GO:0009313"},{"relation_name":"is_a","term_name":"6-alpha-maltosylglucose metabolic process","termid":"GO:0051679"}],"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":"6-alpha-maltosylglucose catabolic process","synonyms":[{"name":"isopanose catabolic process","type":"exact"},{"name":"isopanose catabolism","type":"exact"}],"termid":"GO:0051681"}


id: PBO:0030986
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_metabolic_process_during_vegetative_growth","termid":"PBO:0030986"}


id: MONDO:0010680
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked form of Emery-Dreifuss muscular dystrophy.","definition_xrefs":["MONDO:patterns/x_linked"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked disease","termid":"MONDO:0000425"},{"relation_name":"is_a","term_name":"Emery-Dreifuss muscular dystrophy","termid":"MONDO:0016830"},{"relation_name":"is_a","term_name":"laminopathy","termid":"MONDO:0021106"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0005267"],"is_obsolete":false,"name":"X-linked Emery-Dreifuss muscular dystrophy","secondary_identifiers":["UMLS:C0751337","GARD:2102","MEDGEN:148284","MESH:D000083143","Orphanet:98863"],"synonyms":[{"name":"Emerinopathy","type":"exact"},{"name":"Emery-Dreifuss muscular dystrophy, X-linked","type":"exact"},{"name":"X-linked Emery-Dreifuss muscular dystrophy","type":"exact"},{"name":"muscular dystrophy, tardive Emery-Dreifuss type, with contractures","type":"related"},{"name":"muscular dystrophy, tardive, Dreifuss-Emery type, with contractures","type":"related"}],"termid":"MONDO:0010680","xrefs":{"Monarch":{"xref_id":"0010680"}}}


id: GO:0071278
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a cesium stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cesium ion","termid":"GO:0010164"},{"relation_name":"is_a","term_name":"cellular response to metal ion","termid":"GO:0071248"}],"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 cesium ion","synonyms":[{"name":"cellular response to cesium","type":"exact"}],"termid":"GO:0071278"}


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


id: FYPO:0004654
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 a cell forms a secondary septum that is thinner than normal and does not extend over the entire cell division site.","definition_xrefs":["PomBase:mah","PMID:25473118"],"direct_ancestors":[{"relation_name":"has_part","term_name":"decreased secondary cell septum thickness","termid":"FYPO:0004651"},{"relation_name":"is_a","term_name":"decreased secondary cell septum thickness","termid":"FYPO:0004651"},{"relation_name":"is_a","term_name":"incomplete septum","termid":"FYPO:0005870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000631","FYPO:0000002","FYPO:0001320","FYPO:0000032"],"is_obsolete":false,"name":"thin, incomplete secondary cell septum","synonyms":[{"name":"incomplete secondary cell septum with decreased thickness","type":"exact"},{"name":"incomplete secondary cell septum with reduced thickness","type":"exact"},{"name":"thin, discontinuous secondary septum","type":"exact"},{"name":"thin, incomplete secondary cell septum during mitotic cell cycle","type":"related"},{"name":"thin, incomplete secondary cell septum during vegetative growth","type":"exact"},{"name":"thin, incomplete secondary septum","type":"exact"}],"termid":"FYPO:0004654"}


id: FYPO:0008033
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetative cell is elongated, has no septum, and contains one nucleus, and is arrested in mototic S-phase","direct_ancestors":[{"relation_name":"is_a","term_name":"elongated mononucleate aseptate vegetative cell","termid":"FYPO:0005773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0000032"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0000631","FYPO:0000005","FYPO:0000032","FYPO:0001985"],"is_obsolete":false,"name":"elongated mononucleate aseptate cell with cell cycle arrest in mitotic S-phase","termid":"FYPO:0008033"}


id: PBO:0088093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UDP-N-acetylglucosamine pyrophosphorylase; catalyzes the formation of UDP-N-acetylglucosamine (UDP-GlcNAc), which is important in cell wall biosynthesis, protein N-glycosylation, and GPI anchor biosynthesis; protein abundance increases in response to DNA replication stress","termid":"PBO:0088093"}


id: PBO:0091446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit VIII","termid":"PBO:0091446"}


id: FYPO:0002617
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to sodium butyrate. Cells stop growing (and may die) at a concentration of sodium butyrate that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000139","FYPO:0002683","FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to sodium butyrate","synonyms":[{"name":"hypersensitive to sodium butyrate","type":"exact"},{"name":"sensitive to sodium butyrate during mitotic cell cycle","type":"related"},{"name":"sensitive to sodium butyrate during vegetative growth","type":"exact"}],"termid":"FYPO:0002617"}


id: GO:0090339
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of formin-nucleated actin cable assembly. Formin-nucleated actin cable assembly is the aggregation, arrangement and bonding together of a set of components to form a formin-nucleated actin cable. A formin-nucleated actin cable is an actin filament bundle that consists of short filaments organized into bundles of uniform polarity, and is nucleated by formins.","definition_xrefs":["PMID:12810699","GOC:tb","GOC:jh","PMID:15923184"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of actin filament bundle assembly","termid":"GO:0032232"},{"relation_name":"is_a","term_name":"regulation of formin-nucleated actin cable assembly","termid":"GO:0090337"},{"relation_name":"negatively_regulates","term_name":"formin-nucleated actin cable assembly","termid":"GO:0070649"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"negatively_regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0007010","GO:0030036"],"is_obsolete":false,"name":"negative regulation of formin-nucleated actin cable assembly","termid":"GO:0090339"}


id: PBO:0112851
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"asynchronous replication autosomal RNA 15-1","termid":"PBO:0112851"}


id: MONDO:1011534
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hyperadrenocorticism that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperadrenocorticism, non-human animal","termid":"MONDO:1011403"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperadrenocorticism, horse","secondary_identifiers":["OMIA:000494-9796"],"termid":"MONDO:1011534","xrefs":{"Monarch":{"xref_id":"1011534"}}}


id: PBO:0049723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HAUS augmin like complex subunit 6 pseudogene 1","termid":"PBO:0049723"}


id: GO:1903225
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of endodermal cell differentiation.","definition_xrefs":["PMID:23154389","GOC:als","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell differentiation","termid":"GO:0045596"},{"relation_name":"is_a","term_name":"regulation of endodermal cell differentiation","termid":"GO:1903224"},{"relation_name":"negatively_regulates","term_name":"endodermal cell differentiation","termid":"GO:0035987"}],"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 endodermal cell differentiation","synonyms":[{"name":"down regulation of endoderm cell differentiation","type":"exact"},{"name":"down regulation of endodermal cell differentiation","type":"exact"},{"name":"down-regulation of endoderm cell differentiation","type":"exact"},{"name":"down-regulation of endodermal cell differentiation","type":"exact"},{"name":"downregulation of endoderm cell differentiation","type":"exact"},{"name":"downregulation of endodermal cell differentiation","type":"exact"},{"name":"inhibition of endoderm cell differentiation","type":"narrow"},{"name":"inhibition of endodermal cell differentiation","type":"narrow"},{"name":"negative regulation of endoderm cell differentiation","type":"exact"}],"termid":"GO:1903225"}


id: PBO:0028870
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_poly(A)_tail_length","termid":"PBO:0028870"}


id: PBO:0062753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 52 subfamily L member 2 pseudogene","termid":"PBO:0062753"}


id: PBO:0088326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor, MADS-box Map1","termid":"PBO:0088326"}


id: FYPO:0006840
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which LinE complex assembly is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein-containing complex assembly","termid":"FYPO:0006839"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal LinE complex assembly","synonyms":[{"name":"normal linear element protein complex assembly","type":"exact"}],"termid":"FYPO:0006840"}


id: PBO:0051807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IQ motif and Sec7 domain 3 pseudogene 1","termid":"PBO:0051807"}


id: MONDO:0019676
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition characterized by incomplete development (hypoplasia) or absence of the outermost bones of the fingers and toes (distal phalanges) and nails. Additional features may include hypoplasia of the middle phalanges, fusion of the joints (symphalangism), broad thumbs, and webbed fingers (syndactyly). The feet are often less severely affected than the hands. There are 2 types of this condition, designated as type 1 and 2. BDB type 1 is caused by mutations in the ROR2 gene. BDB type 2 is caused by mutations in the NOG gene. Inheritance of both types is autosomal dominant. Treatment may include surgery if the condition affects hand function, or for cosmetic reasons.","definition_xrefs":["GARD:0000985"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brachydactyly","termid":"MONDO:0021004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brachydactyly type B","secondary_identifiers":["SCTID:389168002","GARD:985","icd11.foundation:1534264812","UMLS:C1300267","Orphanet:93383","MEDGEN:722046"],"termid":"MONDO:0019676","xrefs":{"Monarch":{"xref_id":"0019676"}}}


id: GO:0140561
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-alpha-D-glucose + [protein with EGF-like domain]-L-serine = UDP + [protein with EGF-like domain]-3-O-(beta-D-glucosyl)-L-serine.","definition_xrefs":["RHEA:58116"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016757","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"EGF-domain serine glucosyltransferase activity","secondary_identifiers":["EC:2.4.1.376"],"termid":"GO:0140561"}


id: MONDO:0018773
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"neuronopathy, distal hereditary motor, autosomal dominant","termid":"MONDO:0015362"},{"relation_name":"is_a","term_name":"myofibrillar myopathy","termid":"MONDO:0018943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0000426","MONDO:0005244","MONDO:0005336","MONDO:0005559"],"is_obsolete":false,"name":"autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome","secondary_identifiers":["GARD:21949","Orphanet:476093","UMLS:C5568137","MEDGEN:1799560"],"termid":"MONDO:0018773","xrefs":{"Monarch":{"xref_id":"0018773"}}}


id: MONDO:0009270
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Genitopalatocardiac syndrome is a rare, multiple congenital anomalies/dysmorphic syndrome characterized by male, 46,XY gonadal dysgenesis, cleft palate, micrognathia, conotruncal heart defects and unspecific skeletal, brain and kidney anomalies.","definition_xrefs":["Orphanet:2075"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"genito-palato-cardiac syndrome","secondary_identifiers":["icd11.foundation:2011995320","UMLS:C1856466","MEDGEN:341558","OMIM:231060","GARD:2460","MESH:C537683"],"synonyms":[{"name":"GENITOPALATOCARDIAC syndrome","type":"related"},{"name":"Gardner-Silengo-Wachtel syndrome","type":"exact"},{"name":"Male pseudohermaphroditism with micrognathia, cleft palate, and conotruncal Cardiac defect","type":"related"},{"name":"genito palato cardiac syndrome","type":"related"}],"termid":"MONDO:0009270","xrefs":{"Monarch":{"xref_id":"0009270"}}}


id: FYPO:0002130
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, does not occur during a cellular response to heat.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein phosphorylation during vegetative growth","termid":"FYPO:0002033"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0002494","FYPO:0002274","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abolished protein phosphorylation during cellular response to heat","synonyms":[{"name":"abolished protein phosphorylation during cellular response to heat during mitotic cell cycle","type":"related"},{"name":"abolished protein phosphorylation during cellular response to heat during vegetative growth","type":"exact"},{"name":"abolished protein phosphorylation during cellular response to heat shock","type":"narrow"},{"name":"protein phosphorylation abolished during cellular response to heat","type":"exact"}],"termid":"FYPO:0002130"}


id: MONDO:0006407
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A diffuse malignant mesothelioma arising from the pleura and less often the peritoneum. It is characterized by the presence of spindle cells. Anaplastic morphologic features and multinucleated malignant cells may also be seen.","definition_xrefs":["NCIT:C45655"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant mesothelioma","termid":"MONDO:0006292"}],"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":"sarcomatoid mesothelioma","secondary_identifiers":["EFO:1000521","UMLS:C0334513","DOID:4488","MEDGEN:137774"],"synonyms":[{"name":"malignant fibrous mesothelioma","type":"exact"},{"name":"malignant fibrous mesothelioma (morphologic abnormality)","type":"exact"},{"name":"sarcomatoid mesothelioma","type":"exact"},{"name":"sarcomatoid mesothelioma (morphologic abnormality)","type":"exact"},{"name":"spindled mesothelioma","type":"exact"}],"termid":"MONDO:0006407","xrefs":{"Monarch":{"xref_id":"0006407"}}}


id: FYPO:0003642
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of urease activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000654","FYPO:0000652","FYPO:0000661","FYPO:0000707"],"is_obsolete":false,"name":"abnormal urease activity","termid":"FYPO:0003642"}


id: PBO:0074530
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small NF90 (ILF3) associated RNA D","termid":"PBO:0074530"}


id: GO:0030450
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the classical pathway of complement activation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of humoral immune response mediated by circulating immunoglobulin","termid":"GO:0002923"},{"relation_name":"is_a","term_name":"regulation of complement activation","termid":"GO:0030449"},{"relation_name":"regulates","term_name":"complement activation, classical pathway","termid":"GO:0006958"}],"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 complement activation, classical pathway","synonyms":[{"name":"regulation of complement cascade, classical pathway","type":"exact"}],"termid":"GO:0030450"}


id: GO:0047631
data:
  {"annotated_genes":["SJAG_03977"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74365],"is_not":false,"summary":null,"term":"GO:0047631"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ADP-ribose + H2O = AMP + D-ribose 5-phosphate.","definition_xrefs":["EC:3.6.1.13"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03977":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"ADP-ribose diphosphatase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-5696049","MetaCyc:RXN0-1441","Reactome:R-HSA-2393954","Reactome:R-HSA-2393939","RHEA:10412"],"synonyms":[{"name":"ADP-ribose phosphohydrolase activity","type":"exact"},{"name":"ADP-ribose pyrophosphatase activity","type":"exact"},{"name":"ADP-ribose ribophosphohydrolase activity","type":"related"},{"name":"ADPR-PPase activity","type":"exact"},{"name":"ADPribose diphosphatase activity","type":"related"},{"name":"ADPribose pyrophosphatase activity","type":"related"},{"name":"adenosine diphosphoribose pyrophosphatase activity","type":"exact"}],"termid":"GO:0047631","terms_by_termid":{"GO:0047631":null}}


id: MONDO:0030680
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dilated cardiomyopathy that is characterized by refractory ventricular arrhythmias and severe heart failure and that has material basis in homozygous mutation in the BAG5 gene on chromosome 14q32.","definition_xrefs":["DOID:0081162"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial isolated dilated cardiomyopathy","termid":"MONDO:0700335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"cardiomyopathy, dilated, 2F","secondary_identifiers":["UMLS:C5676917","MEDGEN:1802616","OMIM:619747"],"synonyms":[{"name":"CMD2F","type":"exact"},{"name":"cardiomyopathy, dilated, 2F","type":"exact"}],"termid":"MONDO:0030680","xrefs":{"Monarch":{"xref_id":"0030680"}}}


id: MONDO:0001402
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm involving the vagina. Representative examples include carcinomas and sarcomas.","definition_xrefs":["NCIT:C7410"],"direct_ancestors":[{"relation_name":"is_a","term_name":"female reproductive organ cancer","termid":"MONDO:0001416"},{"relation_name":"is_a","term_name":"vaginal neoplasm","termid":"MONDO:0021050"}],"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":"vaginal cancer","secondary_identifiers":["MEDGEN:12040","ICD9:184.0","MESH:D014625","DOID:119","UMLS:C0042237","SCTID:363445000"],"synonyms":[{"name":"cancer of vagina","type":"exact"},{"name":"malignant neoplasm of the vagina","type":"exact"},{"name":"malignant neoplasm of vagina","type":"exact"},{"name":"malignant tumor of the vagina","type":"exact"},{"name":"malignant tumor of vagina","type":"exact"},{"name":"malignant tumour of the vagina","type":"exact"},{"name":"malignant tumour of vagina","type":"exact"},{"name":"malignant vagina neoplasm","type":"exact"},{"name":"malignant vagina tumor","type":"exact"},{"name":"malignant vagina tumour","type":"exact"},{"name":"malignant vaginal neoplasm","type":"exact"},{"name":"malignant vaginal tumor","type":"exact"},{"name":"malignant vaginal tumour","type":"exact"},{"name":"vagina cancer","type":"exact"},{"name":"vagina neoplasm","type":"broad"},{"name":"vaginal tumor","type":"broad"},{"name":"vaginal tumour","type":"broad"}],"termid":"MONDO:0001402","xrefs":{"Monarch":{"xref_id":"0001402"}}}


id: GO:0008872
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glucarate = 5-dehydro-4-deoxy-D-glucarate + H2O.","definition_xrefs":["EC:4.2.1.40"],"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:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"glucarate dehydratase activity","secondary_identifiers":["RHEA:14573","MetaCyc:GLUCARDEHYDRA-RXN"],"synonyms":[{"name":"D-glucarate dehydratase activity","type":"related"},{"name":"D-glucarate hydro-lyase (5-dehydro-4-deoxy-D-glucarate-forming)","type":"related"},{"name":"D-glucarate hydro-lyase activity","type":"related"}],"termid":"GO:0008872"}


id: PR:Q10990
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cdt2 gene.","definition_xrefs":["UniProtKB:Q10990","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":"cell division cycle protein cdt2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17H9.19c","synonyms":[{"name":"Spom972h-cdt2","type":"exact"}],"termid":"PR:Q10990"}


id: PBO:0058367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4739","termid":"PBO:0058367"}


id: PBO:0075393
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sp6 transcription factor","termid":"PBO:0075393"}


id: GO:0003716
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any activity that brings about termination of transcription by RNA polymerase I.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete RNA polymerase I transcription termination factor activity (obsolete GO:0003716)","synonyms":[{"name":"Pol I transcription termination factor activity","type":"exact"},{"name":"RNA polymerase I transcription termination factor activity","type":"exact"}],"termid":"GO:0003716"}


id: PBO:0073224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"semaphorin 7A (John Milton Hagen blood group)","termid":"PBO:0073224"}


id: MONDO:0014393
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary lymphedema in which the cause of the disease is a mutation in the VEGFC gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphatic malformation","termid":"MONDO:0019313"}],"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":"lymphatic malformation 4","secondary_identifiers":["GARD:16468","MEDGEN:1651756","OMIM:615907","UMLS:C4747769","DOID:0070209"],"synonyms":[{"name":"LMPH1D","type":"related"},{"name":"VEGFC hereditary lymphedema","type":"exact"},{"name":"hereditary lymphedema caused by mutation in VEGFC","type":"exact"},{"name":"lymphedema, hereditary, 1D","type":"exact"},{"name":"lymphedema, hereditary, type 1D","type":"exact"}],"termid":"MONDO:0014393","xrefs":{"Monarch":{"xref_id":"0014393"}}}


id: PBO:0111823
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein","termid":"PBO:0111823"}


id: GO:0102413
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 6-O-methyl-N-deacetylisoipecoside + H2O = 6-O-methyl-N-deacetylisoipecoside aglycon + D-glucose.","definition_xrefs":["RHEA:78891"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0016798","GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"6-O-methyl-deacetylisoipecoside beta-glucosidase activity","secondary_identifiers":["MetaCyc:RXN-13791"],"termid":"GO:0102413"}


id: MONDO:0002286
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the renal artery.","direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"},{"relation_name":"is_a","term_name":"aortic disorder","termid":"MONDO:0005561"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"renal artery disease","secondary_identifiers":["MEDGEN:768693","SCTID:16934004","NCIT:C101254","UMLS:C3640053","DOID:2388","ICD9:593.81"],"synonyms":[{"name":"renal vascular disease","type":"exact"},{"name":"vascular disorder of kidney","type":"exact"}],"termid":"MONDO:0002286","xrefs":{"Monarch":{"xref_id":"0002286"}}}


id: PBO:0090481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENP-A chaperone, CHD family Hrp1","termid":"PBO:0090481"}


id: PBO:0029008
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-protein_mislocalized_to_nucleoplasm","termid":"PBO:0029008"}


id: MONDO:0032801
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"erythrokeratodermia variabilis","termid":"MONDO:0017851"}],"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":"erythrokeratodermia variabilis et progressiva 6","secondary_identifiers":["UMLS:C5193144","MEDGEN:1681026","GARD:18672","DOID:0080766","OMIM:618531"],"synonyms":[{"name":"EKVP6","type":"related"},{"name":"ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 6","type":"related"}],"termid":"MONDO:0032801","xrefs":{"Monarch":{"xref_id":"0032801"}}}


id: MONDO:0700220
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Disease that occurs as a consequence of immunosuppression in a recipient of a solid organ or bone marrow transplant, or as a consequence of the transplantation.","direct_ancestors":[{"relation_name":"is_a","term_name":"human disease","termid":"MONDO:0700096"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disease related to transplantation","secondary_identifiers":["Orphanet:306644","MEDGEN:745174","UMLS:C1998172","GARD:21259"],"termid":"MONDO:0700220","xrefs":{"Monarch":{"xref_id":"0700220"}}}


id: GO:0006139
data:
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id: MONDO:0010053
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary spherocytosis in which the cause of the disease is a mutation in the SPTA1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spherocytosis","termid":"MONDO:0019350"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"hereditary spherocytosis type 3","secondary_identifiers":["DOID:0110918","GARD:15236","MESH:C567489","OMIM:270970","MEDGEN:394798","UMLS:C2678338"],"synonyms":[{"name":"HS3","type":"exact"},{"name":"SPH3","type":"exact"},{"name":"SPTA1 hereditary spherocytosis","type":"exact"},{"name":"hereditary spherocytosis 3","type":"exact"},{"name":"hereditary spherocytosis caused by mutation in SPTA1","type":"exact"},{"name":"spherocytosis, hereditary, 3","type":"related"},{"name":"spherocytosis, type 3","type":"related"}],"termid":"MONDO:0010053","xrefs":{"Monarch":{"xref_id":"0010053"}}}


id: GO:0141161
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cAMP/PKA signal transduction.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular signal transduction","termid":"GO:1902531"},{"relation_name":"regulates","term_name":"cAMP/PKA signal transduction","termid":"GO:0141156"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of cAMP/PKA signal transduction","synonyms":[{"name":"regulation of cAMP/PKA signaling","type":"exact"}],"termid":"GO:0141161"}


id: GO:1903691
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of wound healing, spreading of epidermal cells.","definition_xrefs":["GOC:TermGenie","GOC:als","GO_REF:0000058","PMID:18394891"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell migration","termid":"GO:0030335"},{"relation_name":"is_a","term_name":"positive regulation of wound healing","termid":"GO:0090303"},{"relation_name":"is_a","term_name":"regulation of wound healing, spreading of epidermal cells","termid":"GO:1903689"},{"relation_name":"positively_regulates","term_name":"wound healing, spreading of epidermal cells","termid":"GO:0035313"}],"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 wound healing, spreading of epidermal cells","synonyms":[{"name":"activation of wound healing, spreading of epidermal cells","type":"narrow"},{"name":"up regulation of wound healing, spreading of epidermal cells","type":"exact"},{"name":"up-regulation of wound healing, spreading of epidermal cells","type":"exact"},{"name":"upregulation of wound healing, spreading of epidermal cells","type":"exact"}],"termid":"GO:1903691"}


id: GO:1990835
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The appearance of an insulin-like growth factor due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["PMID:21993393"],"gene_count":0,"genotype_count":0,"name":"obsolete insulin-like growth factor production (obsolete GO:1990835)","synonyms":[{"name":"IGF production","type":"related"}],"termid":"GO:1990835"}


id: PBO:0068250
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 28S ribosomal N2","termid":"PBO:0068250"}


id: PBO:0062222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily AQ member 1 pseudogene","termid":"PBO:0062222"}


id: PATO:0002185
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  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Acyclic cyclicity inheres in a molecule when the atoms within the molecule do not contain at least one cycle in the atom-atom connection paths (through the bonds).","definition_xrefs":["PATOC:JH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclicity","termid":"PATO:0002183"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyclic cyclicity","termid":"PATO:0002185"}


id: PBO:0041766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calpain 6","termid":"PBO:0041766"}


id: GO:0010118
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of opening or closing of stomata, which is directly related to the stomatal conductance (measuring rate of passage of either water vapor or carbon dioxide (CO2) through stomata).","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process","termid":"GO:0009987"}],"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":"stomatal movement","termid":"GO:0010118"}


id: GO:0047497
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a mitochondrion along a microtubule, mediated by motor proteins.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of mitochondrion localization, microtubule-mediated","termid":"GO:0034643"},{"relation_name":"is_a","term_name":"organelle transport along microtubule","termid":"GO:0072384"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"mitochondrion transport along microtubule","synonyms":[{"name":"mitochondrial migration along microtubule","type":"exact"},{"name":"mitochondrial transport along microtubule","type":"exact"}],"termid":"GO:0047497"}


id: GO:0045116
data:
  {"annotated_genes":["SJAG_03950","SJAG_05297","SJAG_00615","SJAG_00878","SJAG_00033","SJAG_01018"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71786,73136,74611,75345,79953,89610],"is_not":false,"summary":null,"term":"GO:0045116"}]},"cv_name":"biological_process","definition":"Covalent attachment of the ubiquitin-like protein NEDD8 (RUB1) to another protein.","definition_xrefs":["PMID:11698580"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification by small protein conjugation","termid":"GO:0032446"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00033":null,"SJAG_00615":null,"SJAG_00878":null,"SJAG_01018":null,"SJAG_03950":null,"SJAG_05297":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"protein neddylation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0019943"],"synonyms":[{"name":"RUB1-protein conjugation","type":"exact"}],"termid":"GO:0045116","terms_by_termid":{"GO:0045116":null}}


id: GO:2000219
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of invasive growth in response to glucose limitation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of growth of unicellular organism as a thread of attached cells","termid":"GO:0070786"},{"relation_name":"is_a","term_name":"regulation of invasive growth in response to glucose limitation","termid":"GO:2000217"},{"relation_name":"positively_regulates","term_name":"invasive growth in response to glucose limitation","termid":"GO:0001403"}],"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 invasive growth in response to glucose limitation","synonyms":[{"name":"positive regulation of colony morphology","type":"related"}],"termid":"GO:2000219"}


id: GO:0086005
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An action potential that occurs in a ventricular cardiac muscle cell.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac muscle cell action potential involved in contraction","termid":"GO:0086002"}],"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":"ventricular cardiac muscle cell action potential","termid":"GO:0086005"}


id: GO:0010434
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to a bract. This process pertains to the initial formation of a structure from unspecified parts. A bract is a leaf, usually different in form from the foliage leaves, subtending a flower or inflorescence.","definition_xrefs":["PO:0009055","GOC:tb","PMID:16554366"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant organ formation","termid":"GO:1905393"},{"relation_name":"part_of","term_name":"bract morphogenesis","termid":"GO:0010433"}],"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":"bract formation","termid":"GO:0010434"}


id: PBO:0090267
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoglycerate kinase Pgk1","termid":"PBO:0090267"}


id: PBO:0090375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ergothioneine biosynthesis methyltransferase Egt2","termid":"PBO:0090375"}


id: PBO:0069841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1127, pseudogene","termid":"PBO:0069841"}


id: GO:0050564
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-2-aminoadipate + L-cysteine + L-valine + 3 ATP + H2O = N-[(5S)-5-amino-5-carboxypentanoyl]-L-cysteinyl-D-valine + 3 AMP + 3 diphosphate + 6 H+.","definition_xrefs":["EC:6.3.2.26","RHEA:23196"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-amino acid ligase activity","termid":"GO:0016881"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016874","GO:0003674"],"is_obsolete":false,"name":"N-(5-amino-5-carboxypentanoyl)-L-cysteinyl-D-valine synthase activity","secondary_identifiers":["KEGG_REACTION:R04870","MetaCyc:6.3.2.26-RXN"],"synonyms":[{"name":"ACV synthetase activity","type":"broad"},{"name":"L-2-aminohexanedioate:L-cysteine:L-valine ligase (AMP-forming, valine-inverting)","type":"related"},{"name":"L-alpha-aminoadipyl-cysteinyl-valine synthetase activity","type":"related"},{"name":"L-delta-(alpha-aminoadipoyl)-L-cysteinyl-D-valine synthetase activity","type":"related"},{"name":"delta-(L-alpha-aminoadipyl)-L-cysteinyl-D-valine synthetase activity","type":"exact"}],"termid":"GO:0050564"}


id: MONDO:0014350
data:
  {"annotated_genes":["SJAG_04183"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86771],"is_not":false,"summary":null,"term":"MONDO:0014350"}]},"cv_name":"mondo","definition":"Any Seckel syndrome in which the cause of the disease is a mutation in the DNA2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Seckel syndrome","termid":"MONDO:0019342"},{"relation_name":"is_a","term_name":"primordial dwarfism and slender bone disorder","termid":"MONDO:0800063"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04183":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Seckel syndrome 8","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070009","OMIM:615807","GARD:16013","MEDGEN:856014","UMLS:C3891452"],"synonyms":[{"name":"DNA2 Seckel syndrome","type":"exact"},{"name":"SCKL8","type":"exact"},{"name":"Seckel syndrome 8","type":"exact"},{"name":"Seckel syndrome caused by mutation in DNA2","type":"exact"},{"name":"Seckel syndrome type 8","type":"exact"}],"termid":"MONDO:0014350","terms_by_termid":{"MONDO:0014350":null},"xrefs":{"Monarch":{"xref_id":"0014350"}}}


id: GO:0010624
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency or rate of multiplication or reproduction of Schwann cells, resulting in the expansion of their population. Schwann cells are a type of glial cell in the peripheral nervous system.","definition_xrefs":["GOC:dph","GOC:tb","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glial cell proliferation","termid":"GO:0060251"},{"relation_name":"regulates","term_name":"Schwann cell proliferation","termid":"GO:0014010"}],"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 Schwann cell proliferation","termid":"GO:0010624"}


id: GO:0010143
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of cutin, a waxy substance, which combined with cellulose forms a substance nearly impervious to water and constituting the cuticle in plants.","definition_xrefs":["ISBN:0028623819"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule biosynthetic process","termid":"GO:0009059"},{"relation_name":"part_of","term_name":"cutin-based cuticle development","termid":"GO:0160062"}],"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":"cutin biosynthetic process","secondary_identifiers":["MetaCyc:PWY-321"],"synonyms":[{"name":"cutin anabolism","type":"exact"},{"name":"cutin biosynthesis","type":"exact"},{"name":"cutin formation","type":"exact"},{"name":"cutin synthesis","type":"exact"}],"termid":"GO:0010143"}


id: GO:0044272
data:
  {"annotated_genes":["SJAG_04007","SJAG_03731","SJAG_02689","SJAG_02972","SJAG_00381","SJAG_00827","SJAG_01271","SJAG_03313","SJAG_00866","SJAG_02158","SJAG_00881","SJAG_01970","SJAG_03152","SJAG_03290","SJAG_02290","SJAG_03881","SJAG_01139","SJAG_03659","SJAG_00832","SJAG_05277","SJAG_00582","SJAG_01351","SJAG_00427","SJAG_04282","SJAG_01880","SJAG_02293","SJAG_01466","SJAG_04425","SJAG_04627","SJAG_04288","SJAG_00309","SJAG_02406","SJAG_02769","SJAG_01935","SJAG_03494","SJAG_01402","SJAG_04042","SJAG_03064","SJAG_04866","SJAG_03614","SJAG_00673","SJAG_04067","SJAG_00988","SJAG_04459","SJAG_02421","SJAG_03362","SJAG_03712","SJAG_02599","SJAG_02006","SJAG_04305","SJAG_02420","SJAG_00395","SJAG_03553","SJAG_03538","SJAG_03310","SJAG_03198","SJAG_01404","SJAG_02741","SJAG_03856","SJAG_03671"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106366,111474,68800,65634],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071266"},{"annotations":[98731],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006085"},{"annotations":[68914,91802],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019427"},{"annotations":[117432],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990181"},{"annotations":[79714,76740],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009102"},{"annotations":[80323,72005,78955,89737,71529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015937"},{"annotations":[110887],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019344"},{"annotations":[76526,66482,60430],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006535"},{"annotations":[103990,111920],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052699"},{"annotations":[108810,79146,57802,77699],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006750"},{"annotations":[110888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071269"},{"annotations":[101035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019280"},{"annotations":[80476,78236,58783,77283,79596,78686],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019509"},{"annotations":[98882],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019284"},{"annotations":[97520,75513,98223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009107"},{"annotations":[107843],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035338"},{"annotations":[66304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001295"},{"annotations":[74923,112354,72270,71459,79412],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009086"},{"annotations":[89399,114065],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090180"},{"annotations":[73773,88213,87783,75005,79428,73143],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006086"},{"annotations":[75489],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0010510"},{"annotations":[75526],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006556"},{"annotations":[70567,77523,61750,74396,78790,74317],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009228"},{"annotations":[116402,67728,78597,113971,66040,113977],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009229"},{"annotations":[99888,110829,110828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036172"},{"annotations":[74130],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052837"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of compounds that contain sulfur, such as the amino acids methionine and cysteine or the tripeptide glutathione.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"relation_name":"is_a","term_name":"biosynthetic 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compound biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"sulfur biosynthesis","type":"narrow"},{"name":"sulfur biosynthetic process","type":"narrow"},{"name":"sulfur compound anabolism","type":"exact"},{"name":"sulfur compound biosynthesis","type":"exact"},{"name":"sulfur compound formation","type":"exact"},{"name":"sulfur compound synthesis","type":"exact"}],"termid":"GO:0044272","terms_by_termid":{"GO:0006085":null,"GO:0006086":null,"GO:0006535":null,"GO:0006556":null,"GO:0006750":null,"GO:0009086":null,"GO:0009102":null,"GO:0009107":null,"GO:0009228":null,"GO:0009229":null,"GO:0010510":null,"GO:0015937":null,"GO:0019280":null,"GO:0019284":null,"GO:0019344":null,"GO:0019427":null,"GO:0019509":null,"GO:0035338":null,"GO:0036172":null,"GO:0052699":null,"GO:0052837":null,"GO:0071266":null,"GO:0071269":null,"GO:0090180":null,"GO:1990181":null,"GO:2001295":null}}


id: MONDO:0031019
data:
  {"annotated_genes":["SJAG_02322","SJAG_03895"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87204,87205],"is_not":false,"summary":null,"term":"MONDO:0031019"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02322":null,"SJAG_03895":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"spastic paraplegia 87, autosomal recessive","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070456","OMIM:619966","Orphanet:631088","MEDGEN:1813069","UMLS:C5774182"],"synonyms":[{"name":"SPG87","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 87","type":"exact"},{"name":"spastic paraplegia 87, autosomal recessive","type":"exact"}],"termid":"MONDO:0031019","terms_by_termid":{"MONDO:0031019":null},"xrefs":{"Monarch":{"xref_id":"0031019"}}}


id: PBO:0048295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanidinoacetate N-methyltransferase pseudogene 2","termid":"PBO:0048295"}


id: GO:1902955
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of early endosome to recycling endosome transport.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","GOC:sjp","PMID:22621900"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of intracellular transport","termid":"GO:0032388"},{"relation_name":"is_a","term_name":"regulation of early endosome to recycling endosome transport","termid":"GO:1902954"},{"relation_name":"positively_regulates","term_name":"early endosome to recycling endosome transport","termid":"GO:0061502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0016192"],"is_obsolete":false,"name":"positive regulation of early endosome to recycling endosome transport","synonyms":[{"name":"activation of early endosome to recycling endosome transport","type":"narrow"},{"name":"up regulation of early endosome to recycling endosome transport","type":"exact"},{"name":"up-regulation of early endosome to recycling endosome transport","type":"exact"},{"name":"upregulation of early endosome to recycling endosome transport","type":"exact"}],"termid":"GO:1902955"}


id: MONDO:0016902
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of chromosome 3","termid":"MONDO:0016868"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of the long arm of chromosome 3","secondary_identifiers":["GARD:20823","UMLS:C5679675","icd11.foundation:1054533453","MEDGEN:1825968","Orphanet:262019"],"synonyms":[{"name":"partial deletion of chromosome 3q","type":"exact"},{"name":"partial deletion of the long arm of chromosome type 3","type":"exact"},{"name":"partial monosomy of chromosome 3q","type":"exact"},{"name":"partial monosomy of the long arm of chromosome 3","type":"exact"}],"termid":"MONDO:0016902","xrefs":{"Monarch":{"xref_id":"0016902"}}}


id: GO:0035987
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of an endoderm cell, a cell of the inner of the three germ layers of the embryo.","definition_xrefs":["PMID:17624332","CL:0000223","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"endoderm formation","termid":"GO:0001706"}],"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":"endodermal cell differentiation","synonyms":[{"name":"endoderm cell differentiation","type":"exact"}],"termid":"GO:0035987"}


id: GO:1905593
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of optical nerve axon regeneration.","definition_xrefs":["PMID:16699509","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of axon regeneration","termid":"GO:0048680"},{"relation_name":"is_a","term_name":"regulation of optical nerve axon regeneration","termid":"GO:1905591"},{"relation_name":"positively_regulates","term_name":"optical nerve axon regeneration","termid":"GO:0101027"}],"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 optical nerve axon regeneration","synonyms":[{"name":"activation of optical nerve axon regeneration","type":"narrow"},{"name":"up regulation of optical nerve axon regeneration","type":"exact"},{"name":"up-regulation of optical nerve axon regeneration","type":"exact"},{"name":"upregulation of optical nerve axon regeneration","type":"exact"}],"termid":"GO:1905593"}


id: MONDO:0014183
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myopia","termid":"MONDO:0001384"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"myopia 23, autosomal recessive","secondary_identifiers":["OMIM:615431","GARD:18198","MEDGEN:815812","UMLS:C3809482"],"synonyms":[{"name":"MYP23","type":"related"},{"name":"myopia 23, autosomal recessive","type":"exact"}],"termid":"MONDO:0014183","xrefs":{"Monarch":{"xref_id":"0014183"}}}


id: PBO:0062525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily T member 1 pseudogene","termid":"PBO:0062525"}


id: GO:0032208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of a recombinational process involved in the maintenance of proper telomeric length.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of telomere maintenance","termid":"GO:0032205"},{"relation_name":"is_a","term_name":"regulation of telomere maintenance via recombination","termid":"GO:0032207"},{"relation_name":"is_a","term_name":"negative regulation of mitotic recombination","termid":"GO:0045950"},{"relation_name":"is_a","term_name":"negative regulation of DNA recombination at telomere","termid":"GO:0048239"},{"relation_name":"negatively_regulates","term_name":"telomere maintenance via recombination","termid":"GO:0000722"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0032200"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"negatively_regulates","termid":"GO:0006310"},{"rel_name":"regulates","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0032200"}],"interesting_parent_ids":["GO:0032200","GO:0006310","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"negative regulation of telomere maintenance via recombination","synonyms":[{"name":"down regulation of telomere maintenance via recombination","type":"exact"},{"name":"down-regulation of telomere maintenance via recombination","type":"exact"},{"name":"downregulation of telomere maintenance via recombination","type":"exact"},{"name":"inhibition of telomere maintenance via recombination","type":"narrow"}],"termid":"GO:0032208"}


id: GO:0140949
data:
  {"annotated_genes":["SJAG_04574"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[63106],"is_not":false,"summary":null,"term":"GO:0140949"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-lysyl9-[histone H3] + 3 S-adenosyl-L-methionine = 3 H+ + N6,N6,N6-trimethyl-L-lysyl9-[histone H3] + 3 S-adenosyl-L-homocysteine. This reaction is the successive addition of three methyl groups to the unmethylated lysine residue at position 9 of histone H3, producing histone H3K9me3.","definition_xrefs":["RHEA:60276"],"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:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0140096","GO:0016741","GO:0003824","GO:0008276"],"is_obsolete":false,"name":"histone H3K9 trimethyltransferase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["EC:2.1.1.355"],"synonyms":[{"name":"histone H3-K9 trimethylation","type":"broad"},{"name":"histone H3K9 mono/di/trimethylase activity","type":"exact"},{"name":"histone H3K9 trimethylase activity","type":"exact"},{"name":"histone H3K9 trimethylation","type":"broad"},{"name":"histone lysine N-trimethyltransferase activity (H3-K9 specific)","type":"exact"}],"termid":"GO:0140949","terms_by_termid":{"GO:0140949":null}}


id: GO:1905473
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of histone H3-K79 dimethylation.","definition_xrefs":["PMID:27541139","GO_REF:0000058","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of histone H3-K79 dimethylation (obsolete GO:1905473)","synonyms":[{"name":"activation of histone H3 K79 dimethylation","type":"narrow"},{"name":"activation of histone H3-K79 dimethylation","type":"narrow"},{"name":"activation of histone lysine H3 K79 dimethylation","type":"narrow"},{"name":"positive regulation of histone H3 K79 dimethylation","type":"exact"},{"name":"positive regulation of histone lysine H3 K79 dimethylation","type":"exact"},{"name":"up regulation of histone H3 K79 dimethylation","type":"exact"},{"name":"up regulation of histone H3-K79 dimethylation","type":"exact"},{"name":"up regulation of histone lysine H3 K79 dimethylation","type":"exact"},{"name":"up-regulation of histone H3 K79 dimethylation","type":"exact"},{"name":"up-regulation of histone H3-K79 dimethylation","type":"exact"},{"name":"up-regulation of histone lysine H3 K79 dimethylation","type":"exact"},{"name":"upregulation of histone H3 K79 dimethylation","type":"exact"},{"name":"upregulation of histone H3-K79 dimethylation","type":"exact"},{"name":"upregulation of histone lysine H3 K79 dimethylation","type":"exact"}],"termid":"GO:1905473"}


id: PBO:0066601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ras homolog family member T1","termid":"PBO:0066601"}


id: MONDO:0002540
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An oligodendroglioma that arises from the central nervous system and occurs during childhood.","definition_xrefs":["NCIT:C4045"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood malignant neoplasm","termid":"MONDO:0006517"},{"relation_name":"is_a","term_name":"oligodendroglioma","termid":"MONDO:0016695"}],"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":"childhood oligodendroglioma","secondary_identifiers":["NANDO:2200089","UMLS:C0280475","DOID:3183","MEDGEN:76116"],"synonyms":[{"name":"oligodendroglioma","type":"broad"},{"name":"oligodendroglioma of childhood","type":"exact"},{"name":"paediatric oligodendroglioma","type":"exact"},{"name":"pediatric oligodendroglioma","type":"exact"}],"termid":"MONDO:0002540","xrefs":{"Monarch":{"xref_id":"0002540"}}}


id: GO:0034766
data:
  {"annotated_genes":["SJAG_00296","SJAG_03631"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91580,113745],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905949"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of ions from one side of a membrane to the other.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transmembrane transport","termid":"GO:0034763"},{"relation_name":"is_a","term_name":"regulation of monoatomic ion transmembrane transport","termid":"GO:0034765"},{"relation_name":"is_a","term_name":"negative regulation of monoatomic ion transport","termid":"GO:0043271"},{"relation_name":"negatively_regulates","term_name":"monoatomic ion transmembrane transport","termid":"GO:0034220"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00296":null,"SJAG_03631":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of monoatomic ion transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of transmembrane ion transport","type":"exact"},{"name":"down-regulation of transmembrane ion transport","type":"exact"},{"name":"downregulation of transmembrane ion transport","type":"exact"},{"name":"inhibition of transmembrane ion transport","type":"narrow"},{"name":"negative regulation of ion membrane transport","type":"exact"},{"name":"negative regulation of ion transmembrane transport","type":"broad"},{"name":"negative regulation of transmembrane ion transport","type":"exact"}],"termid":"GO:0034766","terms_by_termid":{"GO:1905949":null}}


id: MONDO:0002470
data:
  {"annotated_genes":["SJAG_03206","SJAG_01207","SJAG_00995"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011125"},{"annotations":[85663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014615"},{"annotations":[85664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014619"}]},"cv_name":"mondo","definition":"A trichothiodystrophy that is photosensitive, and caused by defects in the NER pathway","definition_xrefs":["Wikipedia:Trichothiodystrophy#Photosensitive_forms"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trichothiodystrophy","termid":"MONDO:0018053"},{"relation_name":"is_a","term_name":"DNA repair disease","termid":"MONDO:0021190"},{"relation_name":"is_a","term_name":"radiation-induced disorder","termid":"MONDO:0043459"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00995":null,"SJAG_01207":null,"SJAG_03206":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005093","MONDO:0021190"],"is_obsolete":false,"name":"photosensitive trichothiodystrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:453","MEDGEN:336339","DOID:2960","NANDO:1200626","NCIT:C4924","UMLS:C1848412"],"synonyms":[{"name":"IBIDS syndrome","type":"exact"},{"name":"Ichtyosis, brittle hair, intellectual impairment, decreased fertility, and short stature","type":"related"},{"name":"Tay syndrome","type":"exact"},{"name":"sulfur-deficient brittle hair syndrome","type":"exact"},{"name":"trichothiodystrophy","type":"broad"},{"name":"trichothiodystrophy with congenital ichthyosis","type":"broad"},{"name":"trichothiodystrophy with congenital ichtyosis","type":"related"}],"termid":"MONDO:0002470","terms_by_termid":{"MONDO:0011125":null,"MONDO:0014615":null,"MONDO:0014619":null},"xrefs":{"Monarch":{"xref_id":"0002470"}}}


id: MONDO:0017482
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"humeral agenesis/hypoplasia","termid":"MONDO:0017440"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"humeral agenesis/hypoplasia, unilateral","secondary_identifiers":["Orphanet:295061"],"synonyms":[{"name":"humeral intercalary meromelia, unilateral","type":"exact"}],"termid":"MONDO:0017482","xrefs":{"Monarch":{"xref_id":"0017482"}}}


id: FYPO:0007443
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 the protein is present in the cytosol instead.","definition_xrefs":["PMID:32320462","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to endoplasmic reticulum during vegetative growth","termid":"FYPO:0003777"}],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"abolished protein localization to endoplasmic reticulum membrane, with protein mislocalized to cytosol","synonyms":[{"name":"abolished protein localization to ER membrane, with protein mislocalized to cytosol","type":"exact"},{"name":"abolished protein localization to endoplasmic reticulum membrane, with protein mislocalized to cytosol during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to endoplasmic reticulum membrane, with protein mislocalized to cytosol during vegetative growth","type":"exact"}],"termid":"FYPO:0007443"}


id: PBO:0051603
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 26","termid":"PBO:0051603"}


id: PBO:0062069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 3 subfamily D member 1 pseudogene","termid":"PBO:0062069"}


id: PBO:0060742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase complex assembly factor 7","termid":"PBO:0060742"}


id: MONDO:0010140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypothyroidism due to dysfunction of the hypothalamus, assumed to result in reduced secretion of thyrotropin- releasing hormone.","definition_xrefs":["NCIT:C121741"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"central congenital hypothyroidism","termid":"MONDO:0016410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isolated thyrotropin-releasing hormone deficiency","secondary_identifiers":["Orphanet:238670","MEDGEN:113137","UMLS:C0220998","GARD:17179","ICD9:253.4","OMIM:275120","SCTID:10736002"],"synonyms":[{"name":"TRH deficiency","type":"related"},{"name":"hypothalamic hypothyroidism","type":"related"},{"name":"isolated TRF deficiency","type":"exact"},{"name":"isolated TRH deficiency","type":"exact"},{"name":"isolated TSH-releasing factor deficiency","type":"exact"},{"name":"isolated prothyroliberin deficiency","type":"exact"},{"name":"isolated protirelin deficiency","type":"exact"},{"name":"isolated thyroliberin deficiency","type":"exact"},{"name":"isolated thyrotropin-releasing factor deficiency","type":"exact"},{"name":"tertiary hypothyroidism","type":"exact"},{"name":"thyrotropin-releasing hormone deficiency","type":"related"}],"termid":"MONDO:0010140","xrefs":{"Monarch":{"xref_id":"0010140"}}}


id: GO:0097733
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A specialised 9+0 non-motile cilium found in photoreceptor cells. A ciliary transition zone called 'photoreceptor connecting cilium' links the photoreceptor outer segment to the inner segment.","definition_xrefs":["Wikipedia:Photoreceptor_cell#Histology","GOC:cilia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron projection","termid":"GO:0043005"},{"relation_name":"is_a","term_name":"9+0 non-motile cilium","termid":"GO:0097731"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"photoreceptor cell cilium","synonyms":[{"name":"photoreceptor cilium","type":"exact"}],"termid":"GO:0097733"}


id: PBO:0083282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; not conserved in closely related Saccharomyces species; partially overlaps the verified essential gene RRP14","termid":"PBO:0083282"}


id: GO:0072341
data:
  {"annotated_genes":["SJAG_04077","SJAG_05181","SJAG_00869","SJAG_04031","SJAG_01351","SJAG_00053","SJAG_02572","SJAG_03170"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70863,99634],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043295"},{"annotations":[88352,104745,90778,102787],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001786"},{"annotations":[65111,59351],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031177"}]},"cv_name":"molecular_function","definition":"Binding to a modified amino acid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding","termid":"GO:0005488"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_00869":null,"SJAG_01351":null,"SJAG_02572":null,"SJAG_03170":null,"SJAG_04031":null,"SJAG_04077":null,"SJAG_05181":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"modified amino acid binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"amino acid derivative binding","type":"exact"}],"termid":"GO:0072341","terms_by_termid":{"GO:0001786":null,"GO:0031177":null,"GO:0043295":null}}


id: GO:0002352
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process leading to negative selection in B cells. Mechanisms of negative selection include anergy and deletion.","definition_xrefs":["GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B cell selection","termid":"GO:0002339"}],"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":"B cell negative selection","synonyms":[{"name":"B lymphocyte negative selection","type":"exact"},{"name":"B-cell negative selection","type":"exact"},{"name":"B-lymphocyte negative selection","type":"exact"}],"termid":"GO:0002352"}


id: PBO:0016558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hikeshi protein, Opi10","termid":"PBO:0016558"}


id: FYPO:0006165
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is branched, has more than one nucleus, and has a larger volume and is longer, than normal. In a swollen cell, both length and diameter may be greater than normal, although the cell is only considered elongated if the length:diameter ratio is also greater than normal.","definition_xrefs":["PomBase:jh","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"elongated multinucleate vegetative cell","termid":"FYPO:0000133"},{"relation_name":"is_a","term_name":"swollen elongated cell","termid":"FYPO:0001429"},{"relation_name":"is_a","term_name":"branched, elongated cell","termid":"FYPO:0001512"},{"relation_name":"is_a","term_name":"swollen multinucleate vegetative cell","termid":"FYPO:0004257"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000631","FYPO:0000032","FYPO:0001985","FYPO:0000005","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"branched, swollen, elongated, multinucleate vegetative cell","synonyms":[{"name":"branched, elongated, swollen, multinucleate vegetative cell","type":"exact"},{"name":"branched, swollen, elongated, multinucleate cell during vegetative growth","type":"exact"},{"name":"branched, swollen, elongated, multinucleate vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0006165"}


id: GO:0033662
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The alternation by a symbiont of the levels of defense-related proteins in its host. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by symbiont of host defense-related protein level (obsolete GO:0033662)","termid":"GO:0033662"}


id: GO:0051425
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a phosphotyrosine-binding (PTB) Binding to a phosphotyrosine-bindin domain.","definition_xrefs":["PMID:15924411","Pfam:PF02174"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"PTB domain binding","synonyms":[{"name":"PID binding","type":"broad"},{"name":"phosphotyrosine-interacting domain binding","type":"exact"}],"termid":"GO:0051425"}


id: PBO:0077794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"torsin family 1 member A","termid":"PBO:0077794"}


id: MONDO:0957278
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited oocyte maturation defect","termid":"MONDO:0014769"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"oocyte/zygote/embryo maturation arrest 20","secondary_identifiers":["MEDGEN:1841175","OMIM:620383","UMLS:C5830539"],"termid":"MONDO:0957278","xrefs":{"Monarch":{"xref_id":"0957278"}}}


id: PBO:0016577
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by A. thaliana XCT","termid":"PBO:0016577"}


id: SO:0001639
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that encodes an RNase P RNA.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzymatic_RNA_gene","termid":"SO:0002180"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNase_P_RNA_gene","synonyms":[{"name":"RNase P RNA gene","type":"exact"}],"termid":"SO:0001639"}


id: PBO:0090000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribokinase Rbk1","termid":"PBO:0090000"}


id: GO:0072743
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 erythromycin stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to erythromycin","termid":"GO:1901323"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to erythromycin","termid":"GO:0072743"}


id: PBO:0014257
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Small Tyrosine Phosphatase","termid":"PBO:0014257"}


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


id: GO:0036224
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A special chromosome region located towards one end of a chromosome that contains dispersed copies of short, repetitive DNA sequences and functions as a cis-acting element essential for presynaptic homologous chromosome pairing and chromosome-nuclear envelope attachment.","definition_xrefs":["GOC:kmv","PMID:18597662"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"condensed nuclear chromosome","termid":"GO:0000794"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005694","GO:0005634"],"is_obsolete":false,"name":"pairing center","synonyms":[{"name":"homolog recognition region","type":"exact"}],"termid":"GO:0036224"}


id: PBO:0089281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell wall 1,3-beta-glucanosyltransferase Gas2","termid":"PBO:0089281"}


id: PBO:0040062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin related protein 2/3 complex inhibitor","termid":"PBO:0040062"}


id: PBO:0039094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenosylhomocysteinase","termid":"PBO:0039094"}


id: PBO:0072993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Scm polycomb group protein like 2","termid":"PBO:0072993"}


id: PBO:0074462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sphingomyelin phosphodiesterase 4 pseudogene 2","termid":"PBO:0074462"}


id: PBO:0068049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 354","termid":"PBO:0068049"}


id: PBO:0059798
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 24","termid":"PBO:0059798"}


id: GO:0099061
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the postsynaptic density membrane consisting of the gene products and protein complexes having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete integral component of postsynaptic density membrane (obsolete GO:0099061)","termid":"GO:0099061"}


id: GO:0052088
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont alters or subverts a jasmonic acid-mediated signal transduction pathway in its host. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06","PMID:35698792","PMID:29222513"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host signal transduction pathway","termid":"GO:0052027"},{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host innate immune response","termid":"GO:0052167"}],"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 perturbation of host jasmonic acid signaling","secondary_identifiers":["GO:0052082","GO:0052073","GO:0052266","GO:0052267","GO:0052068","GO:0052069","GO:0052271","GO:0052283","GO:0052443"],"synonyms":[{"name":"activation by organism of defense-related host SA-mediated signal transduction pathway","type":"narrow"},{"name":"activation by organism of defense-related host jasmonic acid-mediated signal transduction pathway","type":"narrow"},{"name":"activation by symbiont of defense-related host jasmonic acid-mediated signal transduction pathway","type":"narrow"},{"name":"down regulation by symbiont of host jasmonic acid-mediated defense response","type":"narrow"},{"name":"down-regulation by symbiont of host jasmonic acid-mediated defense response","type":"narrow"},{"name":"downregulation by symbiont of host jasmonic acid-mediated defense response","type":"narrow"},{"name":"induction by organism of defense-related host SA-mediated signal transduction pathway","type":"narrow"},{"name":"induction by organism of defense-related host jasmonic acid-mediated signal transduction pathway","type":"narrow"},{"name":"induction by symbiont of defense-related host jasmonic acid-mediated signal transduction pathway","type":"narrow"},{"name":"inhibition by symbiont of host jasmonic acid-mediated defense response","type":"narrow"},{"name":"modulation by organism of defense-related jasmonic acid-mediated signal transduction pathway in other organism involved in symbiotic interaction","type":"narrow"},{"name":"modulation by organism of host JA-mediated defense response","type":"narrow"},{"name":"modulation by organism of jasmonic acid-mediated defense response of other organism involved in symbiotic interaction","type":"narrow"},{"name":"modulation by symbiont of defense-related host jasmonic acid-mediated signal transduction pathway","type":"narrow"},{"name":"negative regulation by organism of defense-related jasmonic acid-mediated signal transduction pathway in other organism involved in symbiotic interaction","type":"narrow"},{"name":"negative regulation by organism of jasmonic acid-mediated defense response of other organism involved in symbiotic interaction","type":"narrow"},{"name":"negative regulation by symbiont of defense-related host jasmonic acid-mediated signal transduction pathway","type":"narrow"},{"name":"negative regulation by symbiont of host jasmonic acid-mediated defense response","type":"narrow"},{"name":"positive regulation by organism of defense-related host SA-mediated signal transduction pathway","type":"narrow"},{"name":"positive regulation by organism of defense-related jasmonic acid-mediated signal transduction pathway in other organism involved in symbiotic interaction","type":"narrow"},{"name":"positive regulation by symbiont of defense-related host jasmonic acid-mediated signal transduction pathway","type":"narrow"},{"name":"stimulation by symbiont of defense-related host jasmonic acid-mediated signal transduction pathway","type":"narrow"},{"name":"suppression by organism of host JA-mediated defense response","type":"exact"},{"name":"suppression by symbiont of host jasmonic acid-mediated defense response","type":"related"},{"name":"symbiont defense to host-produced jasmonic acid","type":"exact"},{"name":"up regulation by symbiont of defense-related host jasmonic acid-mediated signal transduction pathway","type":"narrow"},{"name":"up-regulation by symbiont of defense-related host jasmonic acid-mediated signal transduction pathway","type":"narrow"},{"name":"upregulation by organism of defense-related host SA-mediated signal transduction pathway","type":"narrow"},{"name":"upregulation by organism of defense-related host jasmonic acid-mediated signal transduction pathway","type":"narrow"},{"name":"upregulation by symbiont of defense-related host jasmonic acid-mediated signal transduction pathway","type":"narrow"}],"termid":"GO:0052088"}


id: GO:0045089
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the innate immune response, the organism's first line of defense against infection.","definition_xrefs":["GOC:ebc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of response to biotic stimulus","termid":"GO:0002833"},{"relation_name":"is_a","term_name":"positive regulation of defense response","termid":"GO:0031349"},{"relation_name":"is_a","term_name":"positive regulation of response to external stimulus","termid":"GO:0032103"},{"relation_name":"is_a","term_name":"regulation of innate immune response","termid":"GO:0045088"},{"relation_name":"is_a","term_name":"positive regulation of immune response","termid":"GO:0050778"},{"relation_name":"positively_regulates","term_name":"innate immune response","termid":"GO:0045087"}],"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 innate immune response","synonyms":[{"name":"stimulation of innate immune response","type":"narrow"},{"name":"up regulation of innate immune response","type":"exact"},{"name":"up-regulation of innate immune response","type":"exact"},{"name":"upregulation of innate immune response","type":"exact"}],"termid":"GO:0045089"}


id: MONDO:1012130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin A deficiency, non-human animal","termid":"MONDO:1011726"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin A deficiency, dog","secondary_identifiers":["OMIA:000552-9615"],"termid":"MONDO:1012130","xrefs":{"Monarch":{"xref_id":"1012130"}}}


id: PBO:0051100
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 1-3","termid":"PBO:0051100"}


id: PBO:0051503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IK cytokine","termid":"PBO:0051503"}


id: GO:1904630
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a diterpene stimulus.","definition_xrefs":["GO_REF:0000071","PMID:19765580","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to lipid","termid":"GO:0071396"},{"relation_name":"is_a","term_name":"response to diterpene","termid":"GO:1904629"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to diterpene","termid":"GO:1904630"}


id: GO:0003820
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete class I major histocompatibility complex antigen (obsolete GO:0003820)","synonyms":[{"name":"class I major histocompatibility complex antigen","type":"exact"}],"termid":"GO:0003820"}


id: PBO:0088521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S5","termid":"PBO:0088521"}


id: FYPO:0004219
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which methylation of lysine at position 20 of histone H4 is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone methylation during vegetative growth","termid":"FYPO:0000861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002","FYPO:0001312"],"is_obsolete":false,"name":"normal histone H4-K20 methylation during vegetative growth","synonyms":[{"name":"normal histone H4 K20 methylation during vegetative growth","type":"exact"},{"name":"normal histone H4-K20 methylation during mitotic cell cycle","type":"related"},{"name":"normal histone H4K20me during vegetative growth","type":"exact"},{"name":"normal histone lysine H4 K20 methylation during vegetative growth","type":"exact"}],"termid":"FYPO:0004219"}


id: MONDO:0012641
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"restless legs syndrome, susceptibility to","termid":"MONDO:0100170"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"restless legs syndrome, susceptibility to, 5","secondary_identifiers":["UMLS:C1970010","MEDGEN:370807","OMIM:611242"],"synonyms":[{"name":"RLS 5","type":"related"},{"name":"RLS5","type":"exact"},{"name":"restless legs syndrome 5","type":"exact"},{"name":"restless legs syndrome, susceptibility to, 5","type":"exact"}],"termid":"MONDO:0012641","xrefs":{"Monarch":{"xref_id":"0012641"}}}


id: PBO:0047155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 184 member A","termid":"PBO:0047155"}


id: PBO:0069789
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1075, pseudogene","termid":"PBO:0069789"}


id: PBO:0083371
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; overlaps verified ORF YCL005W-A; mutations in YCL007C were thought to confer sensitivity to calcofluor white, but this phenotype was later shown to be due to the defect in YCL005W-A","termid":"PBO:0083371"}


id: GO:1902961
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of aspartic-type endopeptidase activity involved in amyloid precursor protein catabolic process.","definition_xrefs":["GOC:TermGenie","GO_REF:0000059","GOC:sjp","PMID:24577224"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of aspartic-type endopeptidase activity involved in amyloid precursor protein catabolic process (obsolete GO:1902961)","synonyms":[{"name":"activation of aspartate protease activity involved in APP catabolic process","type":"narrow"},{"name":"activation of aspartate protease activity involved in APP catabolism","type":"narrow"},{"name":"activation of aspartate protease activity involved in amyloid precursor protein breakdown","type":"narrow"},{"name":"activation of aspartate protease activity involved in amyloid precursor protein catabolic process","type":"narrow"},{"name":"activation of aspartate protease activity involved in amyloid precursor protein catabolism","type":"narrow"},{"name":"activation of aspartate protease activity involved in amyloid precursor protein degradation","type":"narrow"},{"name":"activation of aspartic endopeptidase activity involved in APP catabolic process","type":"narrow"},{"name":"activation of aspartic endopeptidase activity involved in APP catabolism","type":"narrow"},{"name":"activation of aspartic endopeptidase activity involved in amyloid precursor protein breakdown","type":"narrow"},{"name":"activation of aspartic endopeptidase activity involved in amyloid precursor protein catabolic process","type":"narrow"},{"name":"activation of aspartic endopeptidase activity involved in amyloid precursor protein catabolism","type":"narrow"},{"name":"activation of aspartic endopeptidase activity involved in amyloid precursor protein degradation","type":"narrow"},{"name":"activation of aspartic protease activity involved in APP catabolic process","type":"narrow"},{"name":"activation of aspartic protease activity involved in APP catabolism","type":"narrow"},{"name":"activation of aspartic protease activity involved in amyloid precursor protein breakdown","type":"narrow"},{"name":"activation of aspartic protease activity involved in amyloid precursor protein catabolic process","type":"narrow"},{"name":"activation of aspartic protease activity involved in amyloid precursor protein catabolism","type":"narrow"},{"name":"activation of aspartic protease activity involved in amyloid precursor protein degradation","type":"narrow"},{"name":"activation of aspartic-type endopeptidase activity involved in APP catabolic process","type":"narrow"},{"name":"activation of aspartic-type endopeptidase activity involved in APP catabolism","type":"narrow"},{"name":"activation of aspartic-type endopeptidase activity involved in amyloid precursor protein breakdown","type":"narrow"},{"name":"activation of aspartic-type endopeptidase activity involved in amyloid precursor protein catabolic process","type":"narrow"},{"name":"activation of aspartic-type endopeptidase activity involved in amyloid precursor protein catabolism","type":"narrow"},{"name":"activation of aspartic-type endopeptidase activity involved in amyloid precursor protein degradation","type":"narrow"},{"name":"activation of aspartyl protease activity involved in APP catabolic process","type":"narrow"},{"name":"activation of aspartyl protease activity involved in APP catabolism","type":"narrow"},{"name":"activation of aspartyl protease activity involved in amyloid precursor protein breakdown","type":"narrow"},{"name":"activation of aspartyl protease activity involved in amyloid precursor protein catabolic process","type":"narrow"},{"name":"activation of aspartyl protease activity involved in amyloid precursor protein catabolism","type":"narrow"},{"name":"activation of aspartyl protease activity involved in amyloid precursor protein degradation","type":"narrow"},{"name":"activation of carboxyl protease activity involved in APP catabolic process","type":"narrow"},{"name":"activation of carboxyl protease activity involved in APP catabolism","type":"narrow"},{"name":"activation of carboxyl protease activity involved in amyloid precursor protein breakdown","type":"narrow"},{"name":"activation of carboxyl protease activity involved in amyloid precursor protein catabolic process","type":"narrow"},{"name":"activation of carboxyl protease activity involved in amyloid precursor protein catabolism","type":"narrow"},{"name":"activation of carboxyl protease activity involved in amyloid precursor protein degradation","type":"narrow"},{"name":"positive regulation of aspartate protease activity involved in APP catabolic process","type":"exact"},{"name":"positive regulation of aspartate protease activity involved in APP catabolism","type":"exact"},{"name":"positive regulation of aspartate protease activity involved in amyloid precursor protein breakdown","type":"exact"},{"name":"positive regulation of aspartate protease activity involved in amyloid precursor protein catabolic process","type":"exact"},{"name":"positive regulation of aspartate protease activity involved in amyloid precursor protein catabolism","type":"exact"},{"name":"positive regulation of aspartate protease activity involved in amyloid precursor protein degradation","type":"exact"},{"name":"positive regulation of aspartic endopeptidase activity involved in APP catabolic process","type":"exact"},{"name":"positive regulation of aspartic endopeptidase activity involved in APP catabolism","type":"exact"},{"name":"positive regulation of aspartic endopeptidase activity involved in amyloid precursor protein breakdown","type":"exact"},{"name":"positive regulation of aspartic endopeptidase activity involved in amyloid precursor protein catabolic process","type":"exact"},{"name":"positive regulation of aspartic endopeptidase activity involved in amyloid precursor protein catabolism","type":"exact"},{"name":"positive regulation of aspartic endopeptidase activity involved in amyloid precursor protein degradation","type":"exact"},{"name":"positive regulation of aspartic protease activity involved in APP catabolic process","type":"exact"},{"name":"positive regulation of aspartic protease activity involved in APP catabolism","type":"exact"},{"name":"positive regulation of aspartic protease activity involved in amyloid precursor protein breakdown","type":"exact"},{"name":"positive regulation of aspartic protease activity involved in amyloid precursor protein catabolic process","type":"exact"},{"name":"positive regulation of aspartic protease activity involved in amyloid precursor protein catabolism","type":"exact"},{"name":"positive regulation of aspartic protease activity involved in amyloid precursor protein degradation","type":"exact"},{"name":"positive regulation of aspartic-type endopeptidase activity involved in APP catabolic process","type":"exact"},{"name":"positive regulation of aspartic-type endopeptidase activity involved in APP catabolism","type":"exact"},{"name":"positive regulation of aspartic-type endopeptidase activity involved in amyloid precursor protein breakdown","type":"exact"},{"name":"positive regulation of aspartic-type endopeptidase activity involved in amyloid precursor protein catabolism","type":"exact"},{"name":"positive regulation of aspartic-type endopeptidase activity involved in amyloid precursor protein degradation","type":"exact"},{"name":"positive regulation of aspartyl protease activity involved in APP catabolic process","type":"exact"},{"name":"positive regulation of aspartyl protease activity involved in APP catabolism","type":"exact"},{"name":"positive regulation of aspartyl protease activity involved in amyloid precursor protein breakdown","type":"exact"},{"name":"positive regulation of aspartyl protease activity involved in amyloid precursor protein catabolic process","type":"exact"},{"name":"positive regulation of aspartyl protease activity involved in amyloid precursor protein catabolism","type":"exact"},{"name":"positive regulation of aspartyl protease activity involved in amyloid precursor protein degradation","type":"exact"},{"name":"positive regulation of carboxyl protease activity involved in APP catabolic process","type":"exact"},{"name":"positive regulation of carboxyl protease activity involved in APP catabolism","type":"exact"},{"name":"positive regulation of carboxyl protease activity involved in amyloid precursor protein breakdown","type":"exact"},{"name":"positive regulation of carboxyl protease activity involved in amyloid precursor protein catabolic process","type":"exact"},{"name":"positive regulation of carboxyl protease activity involved in amyloid precursor protein catabolism","type":"exact"},{"name":"positive regulation of carboxyl protease activity involved in amyloid precursor protein degradation","type":"exact"},{"name":"up regulation of aspartate protease activity involved in APP catabolic process","type":"exact"},{"name":"up regulation of aspartate protease activity involved in APP catabolism","type":"exact"},{"name":"up regulation of aspartate protease activity involved in amyloid precursor protein breakdown","type":"exact"},{"name":"up regulation of aspartate protease activity involved in amyloid precursor protein catabolic process","type":"exact"},{"name":"up regulation of aspartate protease activity involved in amyloid precursor protein catabolism","type":"exact"},{"name":"up regulation of aspartate protease activity involved in amyloid precursor protein degradation","type":"exact"},{"name":"up regulation of aspartic endopeptidase activity involved in APP catabolic process","type":"exact"},{"name":"up regulation of aspartic endopeptidase activity involved in APP catabolism","type":"exact"},{"name":"up regulation of aspartic endopeptidase activity involved in amyloid precursor protein breakdown","type":"exact"},{"name":"up regulation of aspartic endopeptidase 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protease activity involved in APP catabolic process","type":"exact"},{"name":"upregulation of carboxyl protease activity involved in APP catabolism","type":"exact"},{"name":"upregulation of carboxyl protease activity involved in amyloid precursor protein breakdown","type":"exact"},{"name":"upregulation of carboxyl protease activity involved in amyloid precursor protein catabolic process","type":"exact"},{"name":"upregulation of carboxyl protease activity involved in amyloid precursor protein catabolism","type":"exact"},{"name":"upregulation of carboxyl protease activity involved in amyloid precursor protein degradation","type":"exact"}],"termid":"GO:1902961"}


id: MONDO:1010107
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute intermittent porphyria that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute disease, non-human animal","termid":"MONDO:1011300"},{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"},{"relation_name":"is_a","term_name":"porphyria, non-human animal","termid":"MONDO:1011418"},{"relation_name":"is_a","term_name":"liver disorder, non-human animal","termid":"MONDO:1012967"},{"relation_name":"is_a","term_name":"inborn errors of metabolism, non-human animal","termid":"MONDO:1012979"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute intermittent porphyria, non-human animal","secondary_identifiers":["OMIA:001493"],"termid":"MONDO:1010107","xrefs":{"Monarch":{"xref_id":"1010107"}}}


id: PBO:0080480
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vault RNA 3-1, pseudogene","termid":"PBO:0080480"}


id: FYPO:0001409
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cells grow normally (i.e. indistinguishably from wild type) in a medium containing glycerol as the carbon source.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0000257","FYPO:0000139","FYPO:0002060","FYPO:0000003","FYPO:0002058"],"is_obsolete":false,"name":"normal growth on glycerol carbon source","synonyms":[{"name":"normal cell population growth on glycerol carbon source","type":"exact"},{"name":"normal vegetative cell population growth on glycerol carbon source","type":"exact"}],"termid":"FYPO:0001409"}


id: GO:0006033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which chitin is transported to, or maintained in, a specific location.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide localization","termid":"GO:0033037"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"chitin localization","synonyms":[{"name":"chitin localisation","type":"exact"},{"name":"establishment and maintenance of chitin localization","type":"exact"}],"termid":"GO:0006033"}


id: PBO:0070878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L15 pseudogene 9","termid":"PBO:0070878"}


id: MONDO:0021941
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infection with Trypanosoma brucei rhodesiense.","definition_xrefs":["NCIT:C35085"],"direct_ancestors":[{"relation_name":"is_a","term_name":"human African trypanosomiasis","termid":"MONDO:0005459"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infection by Trypanosoma rhodesiense","secondary_identifiers":["MEDGEN:11934","ICD9:086.4","SCTID:42872003","UMLS:C0041233"],"synonyms":[{"name":"acute sleeping sickness","type":"related"},{"name":"infection by trypanosoma rhodesiense","type":"exact"},{"name":"infection caused by trypanosoma rhodesiense","type":"related"},{"name":"rhodesian sleeping sickness","type":"related"},{"name":"rhodesian trypanosomiasis","type":"exact"}],"termid":"MONDO:0021941","xrefs":{"Monarch":{"xref_id":"0021941"}}}


id: GO:0018613
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 9-fluorenone + 2 NADPH + O2 = 2 NADP+ + 3,4-dihydroxy-3,4-dihydro-9-fluorenone.","definition_xrefs":["UM-BBD_reactionID:r0409"],"gene_count":0,"genotype_count":0,"name":"obsolete 9-fluorenone dioxygenase activity (obsolete GO:0018613)","termid":"GO:0018613"}


id: PATO:0002121
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial pattern inhering in a bearer by virtue of the bearer's structureresembling an irregular meshwork with cross-linking struts.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"irregular spatial pattern","termid":"PATO:0000330"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trabecular","termid":"PATO:0002121"}


id: MONDO:0012215
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, late adult-onset myofibrillar myopathy characterized by progressive distal muscle weakness associated with peripheral neuropathy and hyporeflexia. Ambulation may be lost within a few years.","definition_xrefs":["Orphanet:98911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"muscular dystrophy, limb-girdle, autosomal dominant","termid":"MONDO:0015151"},{"relation_name":"is_a","term_name":"autosomal dominant distal myopathy","termid":"MONDO:0016108"},{"relation_name":"is_a","term_name":"myofibrillar myopathy","termid":"MONDO:0018943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0000426","MONDO:0002320"],"is_obsolete":false,"name":"myofibrillar myopathy 3","secondary_identifiers":["SCTID:719985001","DOID:0080094","MESH:C563775","GARD:16871","Orphanet:266","SCTID:765196004","UMLS:C3714934","OMIM:159000","OMIM:182920","MESH:C000598645","MESH:C535906","Orphanet:268129","OMIM:609200","SCTID:765092004","MEDGEN:811509","DOID:0110300"],"synonyms":[{"name":"LGMD1","type":"related"},{"name":"LGMD1A","type":"exact"},{"name":"MFM3","type":"related"},{"name":"MYOT autosomal dominant distal myopathy","type":"exact"},{"name":"MYOT autosomal dominant limb-girdle muscular dystrophy","type":"exact"},{"name":"autosomal dominant distal myopathy caused by mutation in MYOT","type":"exact"},{"name":"autosomal dominant limb-girdle muscular dystrophy caused by mutation in MYOT","type":"exact"},{"name":"autosomal dominant limb-girdle muscular dystrophy type 1A","type":"exact"},{"name":"autosomal dominant spheroid body myopathy","type":"related"},{"name":"distal myotilinopathy","type":"exact"},{"name":"limb-girdle muscular dystrophy due to myotilin deficiency","type":"exact"},{"name":"limb-girdle muscular dystrophy type 1A","type":"related"},{"name":"muscular dystrophy limb-girdle type 1A","type":"exact"},{"name":"muscular dystrophy, limb-girdle, type 1A","type":"related"},{"name":"muscular dystrophy, proximal, type 1A","type":"related"},{"name":"myofibrillar myopathy type 3","type":"exact"},{"name":"myopathy, myofibrillar, 3","type":"related"},{"name":"myopathy, myofibrillar, myotilin-related","type":"related"},{"name":"myopathy, myofibrillar, type 3","type":"exact"},{"name":"myopathy, spheroid body","type":"related"},{"name":"myotilinopathy","type":"exact"},{"name":"proximal muscular dystrophy type 1A","type":"exact"},{"name":"spheroid body myopathy","type":"exact"}],"termid":"MONDO:0012215","xrefs":{"Monarch":{"xref_id":"0012215"}}}


id: MONDO:0012925
data:
  {"annotated_genes":["SJAG_00166","SJAG_04414"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87119,87120],"is_not":false,"summary":null,"term":"MONDO:0012925"}]},"cv_name":"mondo","definition":"Any Diamond-Blackfan anemia in which the cause of the disease is a mutation in the RPL35A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Diamond-Blackfan anemia","termid":"MONDO:0015253"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00166":null,"SJAG_04414":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"Diamond-Blackfan anemia 5","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C176914","DOID:0111883","MEDGEN:382705","GARD:15562","MESH:C567280","OMIM:612528","UMLS:C2675859"],"synonyms":[{"name":"DBA5","type":"related"},{"name":"Diamond-Blackfan Anaemia type 5","type":"exact"},{"name":"Diamond-Blackfan Anemia type 5","type":"exact"},{"name":"Diamond-Blackfan anaemia caused by mutation in RPL35A","type":"exact"},{"name":"Diamond-Blackfan anemia 5","type":"exact"},{"name":"Diamond-Blackfan anemia caused by mutation in RPL35A","type":"exact"},{"name":"RPL35A Diamond-Blackfan anaemia","type":"exact"},{"name":"RPL35A Diamond-Blackfan anemia","type":"exact"}],"termid":"MONDO:0012925","terms_by_termid":{"MONDO:0012925":null},"xrefs":{"Monarch":{"xref_id":"0012925"}}}


id: PBO:0003991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6-phosphofructokinase (predicted)","termid":"PBO:0003991"}


id: MONDO:0006045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant glandular epithelial neoplasm characterized by the presence of clear and hobnail cells. It is highly associated with ovarian endometriosis, pelvic endometriosis and paraendocrine hypercalcemia.","definition_xrefs":["NCIT:C40078"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian clear cell cancer","termid":"MONDO:0000548"},{"relation_name":"is_a","term_name":"ovarian adenocarcinoma","termid":"MONDO:0002752"},{"relation_name":"is_a","term_name":"clear cell adenocarcinoma","termid":"MONDO:0005004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"ovarian clear cell adenocarcinoma","secondary_identifiers":["DOID:5304","icd11.foundation:315825558","MEDGEN:276659","Orphanet:398971","UMLS:C1518693","SCTID:763131005","GARD:21652","EFO:1000042"],"synonyms":[{"name":"clear cell adenocarcinoma of ovary","type":"exact"},{"name":"clear cell adenocarcinoma of the ovary","type":"related"},{"name":"ovarian clear cell adenocarcinoma","type":"exact"},{"name":"ovary clear cell adenocarcinoma","type":"exact"}],"termid":"MONDO:0006045","xrefs":{"Monarch":{"xref_id":"0006045"}}}


id: PBO:0051537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 5","termid":"PBO:0051537"}


id: PBO:0078999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Thr (anticodon AGT) 6-1","termid":"PBO:0078999"}


id: GO:0150047
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"G protein-coupled neurotransmitter receptor activity, occurring in the presynaptic membrane, involved in regulation of presynaptic membrane potential.","definition_xrefs":["PMID:11498050","GOC:bc","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled neurotransmitter receptor activity","termid":"GO:0099528"}],"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":"G protein-coupled neurotransmitter receptor activity involved in regulation of presynaptic membrane potential","synonyms":[{"name":"G-protein coupled neurotransmitter receptor activity involved in regulation of presynaptic membrane potential","type":"exact"}],"termid":"GO:0150047"}


id: MONDO:0006289
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete malignant epitheloid mesothelioma (obsolete MONDO:0006289)","termid":"MONDO:0006289","xrefs":{"Monarch":{"xref_id":"0006289"}}}


id: MONDO:1010550
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Patent urachus that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"patent urachus, non-human animal","termid":"MONDO:1010046"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"patent urachus, dog","secondary_identifiers":["OMIA:000781-9615"],"termid":"MONDO:1010550","xrefs":{"Monarch":{"xref_id":"1010550"}}}


id: PBO:0082320
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase involved in protein folding and the response to stress; plays a role in SRP-dependent cotranslational protein-membrane targeting and translocation; member of the heat shock protein 70 (HSP70) family; localized to the cytoplasm; SSA3 has a paralog, SSA4, that arose from the whole genome duplication","termid":"PBO:0082320"}


id: GO:0102457
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1-O-(4-hydroxy-3-methoxybenzoyl)-beta-D-glucose + cyanidin 3-O-beta-D-glucoside = cyanidin 3,7-di-O-beta-D-glucoside + vanillate.","definition_xrefs":["RHEA:35431"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016757","GO:0016740"],"is_obsolete":false,"name":"cyanidin 3-O-glucoside 7-O-glucosyltransferase (acyl-glucose) activity","secondary_identifiers":["EC:2.4.1.300","MetaCyc:RXN-13969"],"synonyms":[{"name":"cyanidin 3-O-glucoside 7-O-glucosyltransferase (vanilloyl-glucose dependent) activity","type":"related"}],"termid":"GO:0102457"}


id: FYPO:0007942
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which chromatin  loop  formation  during meiotic prophase I results in  chromatin loops of increased length.","definition_xrefs":["PomBase:val"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin loop formation during meiotic prophase I","termid":"FYPO:0007944"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000631","FYPO:0000641","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased length of chromatin loops during meiotic prophase I","termid":"FYPO:0007942"}


id: MONDO:0015708
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn error of immunity","termid":"MONDO:0003778"}],"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":"immuno-osseous dysplasia","secondary_identifiers":["UMLS:C0432218","icd11.foundation:1948303413","GARD:20115","MEDGEN:609410","Orphanet:169349","SCTID:254067002"],"termid":"MONDO:0015708","xrefs":{"Monarch":{"xref_id":"0015708"}}}


id: PBO:0073097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate dehydrogenase complex subunit D pseudogene 1","termid":"PBO:0073097"}


id: PBO:0001546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA primase catalytic subunit Spp1","termid":"PBO:0001546"}


id: PR:Q10235
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A tubulin-folding cofactor B that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00930"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell polarity protein alp11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13D6.05","secondary_identifiers":["UniProtKB:Q10235"],"synonyms":[{"name":"Spom972h-TBCB","type":"exact"},{"name":"altered polarity protein 11 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10235"}


id: PATO:0000267
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000267 relative visual_acuity (obsolete PATO:0000267)","termid":"PATO:0000267"}


id: SO:0000147
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of the transcript sequence within a gene which is not removed from the primary RNA transcript by RNA splicing.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript_region","termid":"SO:0000833"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exon","secondary_identifiers":["http://en.wikipedia.org/wiki/Exon"],"synonyms":[{"name":"INSDC_feature:exon","type":"exact"}],"termid":"SO:0000147"}


id: PBO:0077436
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 170A","termid":"PBO:0077436"}


id: MONDO:0016993
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"generalized peeling skin syndrome","termid":"MONDO:0010033"}],"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":"generalized peeling skin syndrome type C","secondary_identifiers":["GARD:20904","Orphanet:263558"],"synonyms":[{"name":"generalised deciduous skin type C","type":"exact"},{"name":"generalized deciduous skin type C","type":"exact"},{"name":"peeling skin syndrome type C","type":"related"}],"termid":"MONDO:0016993","xrefs":{"Monarch":{"xref_id":"0016993"}}}


id: PATO:0001163
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A concentration which is lower relative to the normal or average.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"concentrated","termid":"PATO:0001159"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased concentration","synonyms":[{"name":"low concentration","type":"exact"}],"termid":"PATO:0001163"}


id: PBO:0047016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A19","termid":"PBO:0047016"}


id: FYPO:0008381
data:
  {"alleles_by_uniquename":{"SJAG_01834:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01834","name":"pom152delta","uniquename":"SJAG_01834:allele-1"},"SJAG_03449:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03449","name":"man1delta","uniquename":"SJAG_03449:allele-1"},"SJAG_03449:allele-2":{"allele_type":"partial_amino_acid_deletion","description":"man1DHEH","gene_uniquename":"SJAG_03449","name":"Man1DHEH","uniquename":"SJAG_03449:allele-2"},"SJAG_03449:allele-3":{"allele_type":"amino_acid_insertion_and_deletion","description":"man1-1-488","gene_uniquename":"SJAG_03449","name":"man1-1-488","uniquename":"SJAG_03449:allele-3"},"SJAG_03892:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03892","name":"vps4delta","uniquename":"SJAG_03892:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007770"},{"annotations":[119618,119622,119620,119619],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0004890"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype that affects the localization of a  specific region of a chromosome in a cell in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"localization phenotype during vegetative growth","termid":"FYPO:0001337"},{"relation_name":"is_a","term_name":"chromosome region localization phenotype","termid":"FYPO:0008383"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01834":null,"SJAG_03449":null,"SJAG_03892":null},"genotype_count":5,"genotypes_by_uniquename":{"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"Man1DHEH(man1DHEH)","display_uniquename":"Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-2","expression":"Not assayed or wild type"}]}]},"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type":{"display_name":"man1-1-488(aa)","display_uniquename":"man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-3","expression":"Not assayed or wild type"}]}]},"man1delta":{"display_name":"man1delta","display_uniquename":"man1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03449:allele-1","expression":"Null"}]}]},"pom152delta":{"display_name":"pom152delta","display_uniquename":"pom152delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01834:allele-1","expression":"Null"}]}]},"vps4delta":{"display_name":"vps4delta","display_uniquename":"vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0001320"],"is_obsolete":false,"name":"chromosome region localization phenotype during vegetative growth","references_by_uniquename":{"PMID:24184107":null,"PMID:32109380":null},"single_locus_annotated_genes":["SJAG_01834","SJAG_03892","SJAG_03449"],"single_locus_genotype_uniquenames":["man1delta","Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","pom152delta","man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","vps4delta"],"termid":"FYPO:0008381","terms_by_termid":{"FYPO:0004890":null,"FYPO:0007770":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: MONDO:0004422
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A meningioma that affects the falx cerebri.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anterior cranial fossa meningioma","termid":"MONDO:0002997"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral falx meningioma","secondary_identifiers":["MEDGEN:272627","UMLS:C1333597","DOID:7986","NCIT:C5267"],"synonyms":[{"name":"Falcine meningioma","type":"exact"},{"name":"falx cerebri meningioma","type":"exact"},{"name":"falx cerebri meningioma (disease)","type":"exact"},{"name":"meningioma (disease) of falx cerebri","type":"exact"},{"name":"meningioma of cerebral falx","type":"exact"},{"name":"meningioma of falx cerebri","type":"exact"},{"name":"meningioma of falx of cerebrum","type":"exact"},{"name":"meningioma of the cerebral falx","type":"exact"},{"name":"meningioma of the falx cerebri","type":"exact"},{"name":"meningioma of the falx of the cerebrum","type":"exact"}],"termid":"MONDO:0004422","xrefs":{"Monarch":{"xref_id":"0004422"}}}


id: PBO:0043819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copine family member 9","termid":"PBO:0043819"}


id: FYPO:0002407
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which all cells in the population are viable and curved along the long axis, and the cell diameter is larger than normal and the cell length is shorter than normal, in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete viable curved stubby vegetative cell population (obsolete FYPO:0002407)","synonyms":[{"name":"curved stubby viable vegetative cell population","type":"exact"}],"termid":"FYPO:0002407"}


id: MONDO:0013419
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare defect resulting in C1 deficiency and impaired activation of the complement classical pathway. C1 deficiency generally leads to severe immune complex disease with features of systemic lupus erythematosus and glomerulonephritis.","definition_xrefs":["PMID:11390518"],"direct_ancestors":[{"relation_name":"is_a","term_name":"classic complement early component deficiency","termid":"MONDO:0000015"},{"relation_name":"is_a","term_name":"immunodeficiency due to a classical component pathway complement deficiency","termid":"MONDO:0015699"}],"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":"complement component C1s deficiency","secondary_identifiers":["MEDGEN:462428","OMIM:613783","MESH:C565170","UMLS:C3151078","GARD:15707","NANDO:2200779"],"synonyms":[{"name":"C1SD","type":"related"},{"name":"C1s deficiency","type":"related"},{"name":"complement component C1s deficiency","type":"exact"}],"termid":"MONDO:0013419","xrefs":{"Monarch":{"xref_id":"0013419"}}}


id: GO:0010872
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of cholesterol esterification. Cholesterol esterification is the lipid modification process in which a sterol ester is formed by the combination of a carboxylic acid (often a fatty acid) and cholesterol. In the blood this process is associated with the conversion of free cholesterol into cholesteryl ester, which is then sequestered into the core of a lipoprotein particle.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cholesterol esterification (obsolete GO:0010872)","termid":"GO:0010872"}


id: PBO:0036248
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by A. thaliana COQ4","termid":"PBO:0036248"}


id: MONDO:0859588
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A keratosis pilaris atrophicans that is characterized by scar-like follicular depressions and loss of hair primarily in the eyebrow area.","definition_xrefs":["DOID:0080752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"keratosis pilaris atrophicans","termid":"MONDO:0018855"}],"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":"keratosis pilaris atrophicans faciei","termid":"MONDO:0859588","xrefs":{"Monarch":{"xref_id":"0859588"}}}


id: PBO:0088625
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial aspartate aminotransferase Maa1","termid":"PBO:0088625"}


id: GO:0070049
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A SNARE complex that contains endobrevin (VAMP8), SNAP-25, and syntaxin 2 (or orthologs thereof).","definition_xrefs":["PMID:10336434"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SNARE complex","termid":"GO:0031201"}],"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":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"endobrevin-SNAP-25-syntaxin-2 complex","synonyms":[{"name":"SNARE complex (Stx2, Snap25, Vamp8)","type":"narrow"},{"name":"Stx2-Snap25-Vamp8 complex","type":"narrow"}],"termid":"GO:0070049"}


id: PBO:0058346
data:
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id: GO:0008757
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id: PBO:0058156
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id: FYPO:0001120
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id: GO:0009619
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id: GO:0036157
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id: GO:1902161
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id: MONDO:1010299
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Osteochondrosis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"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":"osteochondrosis, non-human animal","secondary_identifiers":["OMIA:000750"],"termid":"MONDO:1010299","xrefs":{"Monarch":{"xref_id":"1010299"}}}


id: MONDO:0015250
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spinal atrophy-ophthalmoplegia-pyramidal syndrome is a rare, bulbospinal muscular atrophy characterized by generalized neonatal hypotonia, progressive pontobulbar and spinal palsy, pyramidal signs, and deafness. External ophthalmoplegia and bilateral mydriasis are typical signs. There have been no further descriptions in the literature since 1994.","definition_xrefs":["Orphanet:1217"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bulbospinal muscular atrophy","termid":"MONDO:0016113"}],"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":"spinal atrophy-ophthalmoplegia-pyramidal syndrome","secondary_identifiers":["GARD:4942","MEDGEN:419294","MESH:C535625","UMLS:C2930956"],"synonyms":[{"name":"Hamano Tsukamoto syndrome","type":"related"},{"name":"Hamano-Tsukamoto syndrome","type":"exact"},{"name":"infantile progressive spinal muscular atrophy with ophthalmoplegia and pyramidal symptoms","type":"related"},{"name":"spinal atrophy ophthalmoplegia pyramidal syndrome","type":"related"}],"termid":"MONDO:0015250","xrefs":{"Monarch":{"xref_id":"0015250"}}}


id: PBO:0067888
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id: PBO:0041841
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id: MONDO:0001519
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id: MONDO:0010868
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id: CHEBI:37903
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id: PBO:0065950
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id: PBO:0074086
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id: PBO:0004348
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id: GO:0034110
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id: PBO:0062313
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id: PBO:0051880
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id: GO:0007351
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id: GO:0004141
data:
  {"annotated_genes":["SJAG_00673"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[76741],"is_not":false,"summary":null,"term":"GO:0004141"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 7,8-diaminononanoate + ATP + CO2 = ADP + dethiobiotin + 4 H+ + phosphate.","definition_xrefs":["EC:6.3.3.3","RHEA:15805"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclo-ligase activity","termid":"GO:0016882"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00673":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016874","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"dethiobiotin synthase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:DETHIOBIOTIN-SYN-RXN","KEGG_REACTION:R03182"],"synonyms":[{"name":"7,8-diaminononanoate:carbon-dioxide cyclo-ligase (ADP-forming)","type":"related"},{"name":"DTB synthetase activity","type":"related"},{"name":"desthiobiotin synthase activity","type":"related"}],"termid":"GO:0004141","terms_by_termid":{"GO:0004141":null}}


id: PBO:0088166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD40 repeat-containing protein associated with the CCR4-NOT complex; interacts in a Ccr4p-dependent manner with Ssn2p; also interacts with Fis1p, Mdv1p and Dnm1p and plays a role in mitochondrial fission; CAF4 has a paralog, MDV1, that arose from the whole genome duplication","termid":"PBO:0088166"}


id: PBO:0116993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GREB1L antisense RNA 1","termid":"PBO:0116993"}


id: GO:0018169
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the posttranslational transfer of one or more glutamic acid residues to the C-terminus of ribosomal protein S6.","definition_xrefs":["GOC:mah","PMID:2570347"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-glutamic acid ligase activity","termid":"GO:0070739"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140096","GO:0003674","GO:0016874","GO:0003824"],"is_obsolete":false,"name":"ribosomal S6-glutamic acid ligase activity","termid":"GO:0018169"}


id: PBO:0055762
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lncRNA sorafenib resistance in renal cell carcinoma associated","termid":"PBO:0055762"}


id: PBO:0016928
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WIn Suppressing","termid":"PBO:0016928"}


id: PBO:0090706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase (CK1 family) Hhp1","termid":"PBO:0090706"}


id: PBO:0056389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAPK activated protein kinase 5","termid":"PBO:0056389"}


id: PBO:0058439
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5003","termid":"PBO:0058439"}


id: MONDO:0010660
data:
  {"annotated_genes":["SJAG_01269"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85416],"is_not":false,"summary":null,"term":"MONDO:0010660"}]},"cv_name":"mondo","definition":"Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the FTSJ1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic X-linked intellectual disability","termid":"MONDO:0019181"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01269":null},"genotype_count":0,"is_obsolete":false,"name":"intellectual disability, X-linked 9","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0112034","MESH:C563137","MEDGEN:167112","OMIM:309549","GARD:22700","UMLS:C0796215"],"synonyms":[{"name":"FTSJ1 non-syndromic X-linked intellectual disability","type":"exact"},{"name":"MRX9","type":"related"},{"name":"intellectual developmental disorder, X-linked 9, X-linked recessive","type":"exact"},{"name":"intellectual disability, X-linked 44","type":"related"},{"name":"intellectual disability, X-linked 9","type":"exact"},{"name":"intellectual disability, X-linked type 9","type":"exact"},{"name":"mental retardation, X-linked 44","type":"related"},{"name":"mental retardation, X-linked 9","type":"related"},{"name":"mental retardation, X-linked type 9","type":"exact"},{"name":"non-syndromic X-linked intellectual disability caused by mutation in FTSJ1","type":"exact"}],"termid":"MONDO:0010660","terms_by_termid":{"MONDO:0010660":null},"xrefs":{"Monarch":{"xref_id":"0010660"}}}


id: PBO:0087300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sirtuin, histone H3 deacetylase; involved along with Hst4p in telomeric silencing, cell cycle progression, radiation resistance, genomic stability and short-chain fatty acid metabolism; member of the Sir2 family of NAD(+)-dependent protein deacetylases","termid":"PBO:0087300"}


id: PBO:0091493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-coding RNA Meu16","termid":"PBO:0091493"}


id: SO:0001285
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"N4-acetylcytidine is a modified cytidine.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_cytidine","termid":"SO:0001275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N4_acetylcytidine","secondary_identifiers":["RNAMOD:024"],"synonyms":[{"name":"N4 acetylcytidine","type":"exact"},{"name":"N4-acetylcytidine","type":"exact"},{"name":"ac4C","type":"exact"}],"termid":"SO:0001285"}


