# terms

id: GO:0003077
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that reduces the rate of diuresis. Diuresis is the process of renal water excretion.","definition_xrefs":["GOC:mtg_cardio"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of diuresis (obsolete GO:0003077)","synonyms":[{"name":"negative regulation of diuresis","type":"exact"}],"termid":"GO:0003077"}


id: MONDO:0956990
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A suptratentorial ependymoma that is characterized by the presence of a fusion gene involving ZFTA gene.","definition_xrefs":["DOID:0081252"],"direct_ancestors":[{"relation_name":"is_a","term_name":"supratentorial ependymoma","termid":"MONDO:0850340"}],"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":"supratentorial ependymoma, ZFTA fusion–positive","secondary_identifiers":["NCIT:C186350"],"termid":"MONDO:0956990","xrefs":{"Monarch":{"xref_id":"0956990"}}}


id: PR:Q9UU76
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- puf6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UU76"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pumilio homology domain family member 6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCP1E11.11","synonyms":[{"name":"Spom972h-puf6","type":"exact"}],"termid":"PR:Q9UU76"}


id: PBO:0027837
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_cortical_microtubule_cytoskeleton","termid":"PBO:0027837"}


id: PBO:0051872
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin superfamily containing leucine rich repeat 2","termid":"PBO:0051872"}


id: GO:0001608
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a nucleotide and transmitting the signal across the membrane by activating an associated G-protein; promotes the exchange of GDP for GTP on the alpha subunit of a heterotrimeric G-protein complex.","definition_xrefs":["IUPHAR_GPCR:1294","GOC:bf","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"}],"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 nucleotide receptor activity","synonyms":[{"name":"G protein coupled nucleotide receptor activity","type":"exact"},{"name":"G-protein coupled nucleotide receptor activity","type":"exact"},{"name":"nucleotide receptor activity, G protein coupled","type":"exact"},{"name":"nucleotide receptor activity, G-protein coupled","type":"exact"}],"termid":"GO:0001608"}


id: PBO:0058431
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4801","termid":"PBO:0058431"}


id: PBO:0004231
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bouquet formation protein Bqt4","termid":"PBO:0004231"}


id: GO:0009376
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that possesses ATP-dependent protease activity; consists of an ATPase large subunit with homology to other ClpX family ATPases and a peptidase small subunit related to the proteasomal beta-subunits of eukaryotes. In the E. coli complex, a double ring-shaped homohexamer of HslV is capped on each side by a ring-shaped HslU homohexamer.","definition_xrefs":["GOC:bhm","UniProt:P0A6H5","PMID:12670962"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytosolic proteasome complex","termid":"GO:0031597"}],"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"},{"rel_name":"part_of","termid":"GO:0005829"}],"interesting_parent_ids":["GO:0032991","GO:0005737","GO:0005575","GO:0005829"],"is_obsolete":false,"name":"HslUV protease complex","synonyms":[{"name":"ClpYQ protease complex","type":"exact"}],"termid":"GO:0009376"}


id: MONDO:0013791
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary thrombophilia due to congenital protein S deficiency","termid":"MONDO:0019144"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"thrombophilia due to protein S deficiency, autosomal recessive","secondary_identifiers":["GARD:18569","MEDGEN:482722","OMIM:614514","UMLS:C3281092"],"synonyms":[{"name":"THPH6","type":"related"},{"name":"thrombophilia 5 due to protein S deficiency, autosomal recessive","type":"exact"},{"name":"thrombophilia due to PROTEIN S deficiency, autosomal recessive","type":"related"},{"name":"thrombophilia due to protein S deficiency, autosomal recessive","type":"exact"}],"termid":"MONDO:0013791","xrefs":{"Monarch":{"xref_id":"0013791"}}}


id: GO:0103113
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: glucosyl-oleandomycin + ATP + H2O = glucosyl-oleandomycin + ADP + hydrogenphosphate + H+.","definition_xrefs":["EC:3.6.3.-","GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete glucosyl-oleandomycin-exporting ATPase activity (obsolete GO:0103113)","termid":"GO:0103113"}


id: PBO:0063432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDE4DIP pseudogene 6","termid":"PBO:0063432"}


id: MONDO:0008707
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acro-renal-mandibular syndrome is a very rare multiple congenital anomalies syndrome characterized by limb deficiencies and renal anomalies that include split hand-split foot malformation, renal agenesis, polycystic kidneys, uterine anomalies and severe mandibular hypoplasia. An autosomal recessive mode of inheritance has been suggested.","definition_xrefs":["Orphanet:958"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acro-renal-mandibular syndrome","secondary_identifiers":["SCTID:720414005","MEDGEN:395425","UMLS:C1860166","icd11.foundation:879242648","MESH:C535665","GARD:480","OMIM:200980"],"synonyms":[{"name":"acro-renal-uterine-mandibular syndrome","type":"related"},{"name":"acrorenal mandibular syndrome","type":"related"},{"name":"acrorenal-mandibular syndrome","type":"related"},{"name":"acrorenal-uterine-mandibular syndrome","type":"related"},{"name":"split hand split foot mandibular hypoplasia","type":"related"},{"name":"split hand/split foot-mandibular hypoplasia syndrome","type":"exact"},{"name":"split-hand and split-foot with mandibular hypoplasia","type":"related"}],"termid":"MONDO:0008707","xrefs":{"Monarch":{"xref_id":"0008707"}}}


id: GO:0062037
data:
  {"annotated_genes":["SJAG_04671"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[99693],"is_not":false,"summary":null,"term":"GO:0062037"}]},"cv_name":"molecular_function","definition":"Binding to a DNA D-loop. A D-loop is a three-stranded DNA structure formed by the invasion of a single DNA strand that base pairs with one strand of duplex DNA, while the rest of the double-stranded DNA does not unwind.","definition_xrefs":["PMID:20924116"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA secondary structure binding","termid":"GO:0000217"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04671":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003677","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"D-loop DNA binding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DNA displacement loop binding","type":"exact"}],"termid":"GO:0062037","terms_by_termid":{"GO:0062037":null}}


id: PBO:0053983
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 1299","termid":"PBO:0053983"}


id: PBO:0072413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27 pseudogene 18","termid":"PBO:0072413"}


id: GO:0015130
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of mevalonate from one side of a membrane to the other. Mevalonate is the anion of mevalonic acid; its (R)-enantiomer is a strategic intermediate derived from hydroxymethylglutaryl-CoA in the biosynthesis of polyprenyl compounds.","definition_xrefs":["ISBN:0198506732","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"mevalonate transmembrane transporter activity","synonyms":[{"name":"monocarboxylate (lactate, pyruvate, mevalonate) uptake/efflux porter activity","type":"related"}],"termid":"GO:0015130"}


id: PBO:0083464
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; partially overlaps the verified gene MET4/YNL104C","termid":"PBO:0083464"}


id: GO:0005008
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with hepatocyte growth factor receptor ligand and transmitting the signal across the plasma membrane to initiate a change in cell activity.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane receptor protein tyrosine kinase activity","termid":"GO:0004714"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0003674","GO:0016301","GO:0003824","GO:0038023","GO:0016740","GO:0004672","GO:0140096"],"is_obsolete":false,"name":"hepatocyte growth factor receptor activity","synonyms":[{"name":"HGF receptor activity","type":"exact"},{"name":"HGF-activated receptor activity","type":"exact"},{"name":"hepatocyte growth factor-activated receptor activity","type":"exact"}],"termid":"GO:0005008"}


id: MOD:01654
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that is produced by reaction with 5-dimethylaminonaphthalene-1-sulfonyl chloride, dansyl chloride, to form N6-Dansyl-lysine.","definition_xrefs":["Unimod:139#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"},{"relation_name":"is_a","term_name":"dansyl chloride derivatized residue","termid":"MOD:01653"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N6-Dansyl derivatized lysine","synonyms":[{"name":"5-dimethylaminonaphthalene-1-sulfonyl","type":"related"},{"name":"Dansyl","type":"related"},{"name":"N6DansylLys","type":"exact"}],"termid":"MOD:01654"}


id: PBO:0065808
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB3B, member RAS oncogene family","termid":"PBO:0065808"}


id: GO:1905864
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of Atg1/ULK1 kinase complex assembly.","definition_xrefs":["GO_REF:0000058","GOC:mf","GOC:TermGenie","GOC:autophagy","PMID:26567215"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein-containing complex assembly","termid":"GO:0043254"},{"relation_name":"regulates","term_name":"Atg1/ULK1 kinase complex assembly","termid":"GO:1904745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0065003"],"is_obsolete":false,"name":"regulation of Atg1/ULK1 kinase complex assembly","synonyms":[{"name":"regulation of ATG1 kinase complex assembly","type":"exact"},{"name":"regulation of ATG1 kinase complex formation","type":"exact"},{"name":"regulation of ATG1-ATG13 complex assembly","type":"exact"},{"name":"regulation of ATG1-ATG13 complex formation","type":"exact"},{"name":"regulation of ATG1/ULK1 kinase complex formation","type":"exact"},{"name":"regulation of ATG1/ULK1 signaling complex assembly","type":"exact"},{"name":"regulation of ATG1/ULK1 signaling complex formation","type":"exact"},{"name":"regulation of Atg1p signalling complex assembly","type":"exact"},{"name":"regulation of Atg1p signalling complex formation","type":"exact"},{"name":"regulation of ULK1 signaling complex assembly","type":"exact"},{"name":"regulation of ULK1 signaling complex formation","type":"exact"},{"name":"regulation of ULK1-ATG13-FIP200 complex assembly","type":"exact"},{"name":"regulation of ULK1-ATG13-FIP200 complex formation","type":"exact"},{"name":"regulation of ULK1-ATG13-RB1CC1 complex assembly","type":"exact"},{"name":"regulation of ULK1-ATG13-RB1CC1 complex formation","type":"exact"}],"termid":"GO:1905864"}


id: MONDO:0018307
data:
  {"annotated_genes":["SJAG_03866","SJAG_04757","SJAG_00115","SJAG_05277"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87287,87286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011706"},{"annotations":[87272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010476"},{"annotations":[85989],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014290"}]},"cv_name":"mondo","definition":"Neurodegeneration with brain iron accumulation (NBIA, formerly Hallervorden-Spatz syndrome) encompasses a group of rare neurodegenerative disorders characterized by progressive extrapyramidal dysfunction (dystonia, rigidity, choreoathetosis), iron accumulation in the brain and the presence of axonal spheroids, usually limited to the central nervous system.","definition_xrefs":["Orphanet:385"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iron metabolism disease","termid":"MONDO:0002279"},{"relation_name":"is_a","term_name":"neuroaxonal dystrophy","termid":"MONDO:0002283"},{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"},{"relation_name":"is_a","term_name":"hereditary dementia","termid":"MONDO:0015547"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"},{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00115":null,"SJAG_03866":null,"SJAG_04757":null,"SJAG_05277":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0005066","MONDO:0005559"],"is_obsolete":false,"name":"neurodegeneration with brain iron accumulation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:2100241","DOID:0110734","OMIMPS:234200","MEDGEN:444156","MESH:C538421","GARD:11899","UMLS:C2931845","icd11.foundation:440483530"],"synonyms":[{"name":"NBIA","type":"exact"},{"name":"neurodegeneration with brain iron accumulation","type":"exact"}],"termid":"MONDO:0018307","terms_by_termid":{"MONDO:0010476":null,"MONDO:0011706":null,"MONDO:0014290":null},"xrefs":{"Monarch":{"xref_id":"0018307"}}}


id: PATO:0001171
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An elasticity quality inhering in a bearer by virtue of the bearer's ability to recover its size and shape after deformation in any way.","definition_xrefs":["merriam-webster:merriam-webster"],"direct_ancestors":[{"relation_name":"is_a","term_name":"elasticity","termid":"PATO:0001031"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elastic","termid":"PATO:0001171"}


id: GO:0048376
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of lateral mesoderm cell fate determination.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of mesodermal cell fate determination","termid":"GO:0048336"},{"relation_name":"is_a","term_name":"regulation of lateral mesodermal cell fate determination","termid":"GO:0048374"},{"relation_name":"positively_regulates","term_name":"lateral mesodermal cell fate determination","termid":"GO:0048373"}],"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 mesodermal cell fate determination","synonyms":[{"name":"activation of lateral mesodermal cell fate determination","type":"narrow"},{"name":"positive regulation of lateral plate mesodermal cell fate determination","type":"exact"},{"name":"stimulation of lateral mesodermal cell fate determination","type":"narrow"},{"name":"up regulation of lateral mesodermal cell fate determination","type":"exact"},{"name":"up-regulation of lateral mesodermal cell fate determination","type":"exact"},{"name":"upregulation of lateral mesodermal cell fate determination","type":"exact"}],"termid":"GO:0048376"}


id: PBO:0038815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 20 pseudogene 2","termid":"PBO:0038815"}


id: PBO:0046506
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate rich 2","termid":"PBO:0046506"}


id: FYPO:0002397
data:
  {"alleles_by_uniquename":{"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_04280:allele-2":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-2"},"SJAG_04522:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04522","name":"rga4delta","uniquename":"SJAG_04522:allele-1"},"SJAG_04703:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04703","name":"for3delta","uniquename":"SJAG_04703:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[119800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001369"}],"single_locus_phenotype":[{"annotations":[119732],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0003315"},{"annotations":[119603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002026"},{"annotations":[119801],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001369"}]},"cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the amount, distribution, or morphology of all or part of the cytoskeleton is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component","termid":"FYPO:0000287"},{"relation_name":"output_of","term_name":"abnormal cytoskeleton organization","termid":"FYPO:0000802"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02392":null,"SJAG_04280":null,"SJAG_04522":null,"SJAG_04703":null},"genotype_count":4,"genotypes_by_uniquename":{"for3delta":{"display_name":"for3delta","display_uniquename":"for3delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04703:allele-1","expression":"Null"}]}]},"pom1delta":{"display_name":"pom1delta","display_uniquename":"pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"rga4delta":{"display_name":"rga4delta","display_uniquename":"rga4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]}]},"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"rga4delta wee1-as8(T582G aa)","display_uniquename":"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-2","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_04280","SJAG_04522"],"name":"abnormal cytoskeleton","references_by_uniquename":{"PMID:25866389":null,"PMID:30664646":null,"PMID:30726171":null},"single_locus_annotated_genes":["SJAG_02392","SJAG_04522","SJAG_04703"],"single_locus_genotype_uniquenames":["for3delta","rga4delta","pom1delta"],"synonyms":[{"name":"abnormal cytoskeleton physical object quality","type":"exact"}],"termid":"FYPO:0002397","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYECO:0000338":null,"FYPO:0001369":null,"FYPO:0002026":null,"FYPO:0003315":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: PBO:0060224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"matrix remodeling associated 5 Y-linked (pseudogene)","termid":"PBO:0060224"}


id: PBO:0091094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic and meiotic spindle pole body protein, gamma tubulin complex linker-related Spo15","termid":"PBO:0091094"}


id: FYPO:0006706
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which a calcium-transporting ATPase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished transporter activity","termid":"FYPO:0002117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0002114"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000707","FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0000652","FYPO:0002114"],"is_obsolete":false,"name":"abolished calcium-transporting ATPase activity","synonyms":[{"name":"calcium-transporting ATPase activity abolished","type":"exact"}],"termid":"FYPO:0006706"}


id: GO:0102628
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (+)-costunolide (12,6alpha) + reduced [NADPH-hemoprotein reductase] + dioxygen = 3beta-hydroxycostunolide + oxidized [NADPH-hemoprotein reductase] + H2O.","definition_xrefs":["MetaCyc:RXN-15533"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"costunolide 3beta-hydroxylase activity","termid":"GO:0102628"}


id: GO:0032362
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of FAD, the oxidized form of flavin-adenine dinucleotide.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete FAD catabolic process (obsolete GO:0032362)","synonyms":[{"name":"FAD breakdown","type":"exact"},{"name":"FAD catabolism","type":"exact"},{"name":"FAD degradation","type":"exact"},{"name":"oxidized flavin adenine dinucleotide catabolic process","type":"exact"}],"termid":"GO:0032362"}


id: SO:0001375
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"3_2prime_O_dimethyluridine is a modified uridine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_uridine","termid":"SO:0001277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_two_prime_O_dimethyluridine","secondary_identifiers":["RNAMOD:092"],"synonyms":[{"name":"3,2'-O-dimethyluridine","type":"exact"},{"name":"m3Um","type":"exact"},{"name":"three two prime O dimethyluridine","type":"exact"}],"termid":"SO:0001375"}


id: GO:1904547
data:
  {"annotated_genes":["SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102704],"is_not":false,"summary":null,"term":"GO:1904547"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cellular response to glucose starvation.","definition_xrefs":["GO_REF:0000058","PMID:21118717","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to nutrient levels","termid":"GO:0032107"},{"relation_name":"is_a","term_name":"regulation of cellular response to stress","termid":"GO:0080135"},{"relation_name":"regulates","term_name":"cellular response to glucose starvation","termid":"GO:0042149"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03048":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cellular response to glucose starvation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1904547","terms_by_termid":{"GO:1904547":null}}


id: GO:0031911
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Stable, specialized structure for extrusion of waste by the cell into the surrounding medium.","definition_xrefs":["PMID:10503189","PMID:27889663","PMID:23317460"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"plasma membrane","termid":"GO:0005886"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"cytoproct","termid":"GO:0031911"}


id: GO:0090536
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An ISWI complex that contains an ATPase subunit of the ISWI family (specifically SNF2H in mammals, which contain two ISWI homologs) and a Tip5 homolog. In mammals, NoRC is involved in regulation of transcription from RNAP I and RNA polymerase III promoters.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ISWI-type complex","termid":"GO:0031010"}],"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":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634","GO:0005694"],"is_obsolete":false,"name":"NoRC complex","termid":"GO:0090536"}


id: MONDO:0023660
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary angioedema","termid":"MONDO:0019623"}],"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":"angioedema, hereditary, 6","secondary_identifiers":["UMLS:C5543516","MEDGEN:1785484","OMIM:619363"],"synonyms":[{"name":"HAE6","type":"exact"}],"termid":"MONDO:0023660","xrefs":{"Monarch":{"xref_id":"0023660"}}}


id: PBO:0041194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BUB3 mitotic checkpoint protein","termid":"PBO:0041194"}


id: MONDO:0003639
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that arises from the hilar region of the lung.","definition_xrefs":["NCIT:C5671"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung neoplasm","termid":"MONDO:0021117"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lung hilum neoplasm","secondary_identifiers":["UMLS:C1290358","SCTID:126707007","MEDGEN:224849","DOID:5767"],"synonyms":[{"name":"hilar lung neoplasm","type":"exact"},{"name":"hilar lung tumor","type":"exact"},{"name":"hilar lung tumour","type":"exact"},{"name":"lung hilum neoplasm","type":"exact"},{"name":"lung hilum tumor","type":"exact"},{"name":"lung hilum tumour","type":"exact"},{"name":"lung hilus neoplasm","type":"exact"},{"name":"lung hilus neoplasm (disease)","type":"exact"},{"name":"lung hilus tumor","type":"exact"},{"name":"lung hilus tumour","type":"exact"},{"name":"neoplasm of hilus of lung","type":"exact"},{"name":"neoplasm of lung hilus","type":"exact"},{"name":"tumor of lung hilus","type":"exact"},{"name":"tumour of lung hilus","type":"exact"}],"termid":"MONDO:0003639","xrefs":{"Monarch":{"xref_id":"0003639"}}}


id: GO:1900289
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of coenzyme F420-dependent bicyclic nitroimidazole catabolic process.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of catabolic process","termid":"GO:0009895"},{"relation_name":"is_a","term_name":"regulation of coenzyme F420-dependent bicyclic nitroimidazole catabolic process","termid":"GO:1900288"},{"relation_name":"negatively_regulates","term_name":"coenzyme F420-dependent bicyclic nitroimidazole catabolic process","termid":"GO:0052799"}],"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 coenzyme F420-dependent bicyclic nitroimidazole catabolic process","synonyms":[{"name":"down regulation of coenzyme F420-dependent bicyclic nitroimidazole catabolic process","type":"exact"},{"name":"down regulation of coenzyme F420-dependent nitroimidazole breakdown","type":"exact"},{"name":"down regulation of coenzyme F420-dependent nitroimidazole catabolism","type":"exact"},{"name":"down regulation of coenzyme F420-dependent nitroimidazole reduction","type":"exact"},{"name":"down regulation of coenzyme F420-dependent nitroreductase activity","type":"related"},{"name":"down-regulation of coenzyme F420-dependent bicyclic nitroimidazole catabolic process","type":"exact"},{"name":"down-regulation of coenzyme F420-dependent nitroimidazole breakdown","type":"exact"},{"name":"down-regulation of coenzyme F420-dependent nitroimidazole catabolism","type":"exact"},{"name":"down-regulation of coenzyme F420-dependent nitroimidazole reduction","type":"exact"},{"name":"down-regulation of coenzyme F420-dependent nitroreductase activity","type":"related"},{"name":"downregulation of coenzyme F420-dependent bicyclic nitroimidazole catabolic process","type":"exact"},{"name":"downregulation of coenzyme F420-dependent nitroimidazole breakdown","type":"exact"},{"name":"downregulation of coenzyme F420-dependent nitroimidazole catabolism","type":"exact"},{"name":"downregulation of coenzyme F420-dependent nitroimidazole reduction","type":"exact"},{"name":"downregulation of coenzyme F420-dependent nitroreductase activity","type":"related"},{"name":"inhibition of coenzyme F420-dependent bicyclic nitroimidazole catabolic process","type":"narrow"},{"name":"inhibition of coenzyme F420-dependent nitroimidazole breakdown","type":"narrow"},{"name":"inhibition of coenzyme F420-dependent nitroimidazole catabolism","type":"narrow"},{"name":"inhibition of coenzyme F420-dependent nitroimidazole reduction","type":"narrow"},{"name":"inhibition of coenzyme F420-dependent nitroreductase activity","type":"related"},{"name":"negative regulation of coenzyme F420-dependent nitroimidazole breakdown","type":"exact"},{"name":"negative regulation of coenzyme F420-dependent nitroimidazole catabolism","type":"exact"},{"name":"negative regulation of coenzyme F420-dependent nitroimidazole reduction","type":"exact"},{"name":"negative regulation of coenzyme F420-dependent nitroreductase activity","type":"related"}],"termid":"GO:1900289"}


id: PBO:0034703
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Clr6 histone deacetylase associated PHD protein Cph2","termid":"PBO:0034703"}


id: FYPO:0006834
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 rate, or speed, of primary cell septum biogenesis is increased.","definition_xrefs":["PomBase:al","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal primary cell septum biogenesis","termid":"FYPO:0003890"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0000631","FYPO:0000032"],"is_obsolete":false,"name":"increased rate of primary cell septum biogenesis","synonyms":[{"name":"decreased duration of primary cell septum biogenesis","type":"related"},{"name":"increased rate of primary cell septum biogenesis during mitotic cell cycle","type":"related"},{"name":"increased rate of primary cell septum biogenesis during vegetative growth","type":"exact"},{"name":"increased rate of primary septum biogenesis","type":"exact"},{"name":"increased rate of primary septum synthesis","type":"related"}],"termid":"FYPO:0006834"}


id: PBO:0066045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAP1B pseudogene 1","termid":"PBO:0066045"}


id: MONDO:0007943
data:
  {"annotated_genes":["SJAG_00504"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85533],"is_not":false,"summary":null,"term":"MONDO:0007943"}]},"cv_name":"mondo","definition":"Nager syndrome, also called Nager acrofacial dysostosis (NAFD) is a congenital malformation syndrome characterized by mandibulofacial dystosis (malar hypoplasia, micrognathia, external ear malformations) and variable preaxial limb defects.","definition_xrefs":["Orphanet:245"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"SF3B4-related acrofacial dysostosis","termid":"MONDO:0800483"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00504":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"Nager acrofacial dysostosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0265245","DOID:5768","GARD:498","MESH:C538184","NORD:1487","MEDGEN:120519","SCTID:35520007","OMIM:154400"],"synonyms":[{"name":"AFD","type":"related"},{"name":"AFD, Nager type","type":"related"},{"name":"AFD1","type":"related"},{"name":"NAFD","type":"exact"},{"name":"Nager Syndrome","type":"exact"},{"name":"Nager acrofacial dysostosis","type":"exact"},{"name":"Nager acrofacial dysostosis syndrome","type":"exact"},{"name":"Nager syndrome","type":"exact"},{"name":"acrofacial dysostosis 1, Nager type","type":"exact"},{"name":"mandibulofacial dysostosis with preaxial limb anomalies","type":"exact"},{"name":"mandibulofacial dysostosis, Treacher Collins type, with limb anomalies","type":"related"},{"name":"preaxial acrodysostosis","type":"exact"},{"name":"preaxial acrofacial dysostosis","type":"related"},{"name":"preaxial manibulofacial dysostosis","type":"related"},{"name":"split hand deformity-mandibulofacial dysostosis","type":"related"}],"termid":"MONDO:0007943","terms_by_termid":{"MONDO:0007943":null},"xrefs":{"Monarch":{"xref_id":"0007943"}}}


id: PATO:0001544
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality inhering in a bearer by virtue of the bearer's ability of being turned, bowed, or twisted without breaking.","definition_xrefs":["merriam-webster:merriam-webster"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flexibility","termid":"PATO:0001543"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"flexible","synonyms":[{"name":"bendy","type":"exact"}],"termid":"PATO:0001544"}


id: PBO:0014295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cdc48-Ufd1-Npl4 complex subunit Ufd1 involved in ubiquitin-dependent protein catabolism (predicted)","termid":"PBO:0014295"}


id: GO:0019802
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cyclization of glutamine to yield an L-glutamimide residue at the C-terminus of an excised intein during protein splicing.","definition_xrefs":["GOC:dph","RESID:AA0303","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glutamine metabolic process","termid":"GO:0006541"},{"relation_name":"part_of","term_name":"intein-mediated protein splicing","termid":"GO:0016539"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0051604"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0008150","GO:0051604","GO:0010467"],"is_obsolete":false,"name":"cyclization of glutamine involved in intein-mediated protein splicing","synonyms":[{"name":"cyclization of glutamine, during protein splicing","type":"related"}],"termid":"GO:0019802"}


id: GO:1901398
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transforming growth factor beta3 activation.","definition_xrefs":["GOC:sl","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transforming growth factor beta3 activation (obsolete GO:1901398)","synonyms":[{"name":"regulation of TGF-beta 3 activation","type":"exact"},{"name":"regulation of TGFB3 activation","type":"exact"},{"name":"regulation of TGFbeta 3 activation","type":"exact"}],"termid":"GO:1901398"}


id: GO:0098780
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.) in response to the depolarization of one or more mitochondria.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to stress","termid":"GO:0033554"}],"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 mitochondrial depolarisation","secondary_identifiers":["Reactome:R-HSA-9840373"],"termid":"GO:0098780"}


id: GO:1905819
data:
  {"annotated_genes":["SJAG_04126","SJAG_01330","SJAG_02169","SJAG_04699","SJAG_02336","SJAG_03681","SJAG_03126","SJAG_01082","SJAG_04884","SJAG_02451","SJAG_01679","SJAG_00883","SJAG_03353","SJAG_03327","SJAG_00460","SJAG_01297","SJAG_01837","SJAG_04259","SJAG_04999","SJAG_01515"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104210,112267,114085,107546,108567,91062,99914,116200,114572],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[106636,114799],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905318"},{"annotations":[116966,75747],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033316"},{"annotations":[99758,114802,115857,102116,106638,110216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007094"},{"annotations":[99019],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902103"},{"annotations":[103595],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000816"},{"annotations":[94537],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0140499"},{"annotations":[114090],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905326"},{"annotations":[116973],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090267"},{"annotations":[101658],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905325"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of chromosome separation.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","GOC:bhm","PMID:21795393"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of chromosome segregation","termid":"GO:0051985"},{"relation_name":"is_a","term_name":"regulation of chromosome separation","termid":"GO:1905818"},{"relation_name":"negatively_regulates","term_name":"chromosome separation","termid":"GO:0051304"}],"gene_count":20,"genes_by_uniquename":{"SJAG_00460":null,"SJAG_00883":null,"SJAG_01082":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01515":null,"SJAG_01679":null,"SJAG_01837":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02451":null,"SJAG_03126":null,"SJAG_03327":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04126":null,"SJAG_04259":null,"SJAG_04699":null,"SJAG_04884":null,"SJAG_04999":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"negative regulation of chromosome separation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of chromatid release","type":"related"},{"name":"down regulation of chromosome separation","type":"exact"},{"name":"down regulation of rDNA separation","type":"narrow"},{"name":"down-regulation of chromatid release","type":"related"},{"name":"down-regulation of chromosome separation","type":"exact"},{"name":"down-regulation of rDNA separation","type":"narrow"},{"name":"downregulation of chromatid release","type":"related"},{"name":"downregulation of chromosome separation","type":"exact"},{"name":"downregulation of rDNA separation","type":"narrow"},{"name":"inhibition of chromatid release","type":"related"},{"name":"inhibition of chromosome separation","type":"narrow"},{"name":"inhibition of rDNA separation","type":"narrow"},{"name":"negative regulation of chromatid release","type":"related"},{"name":"negative regulation of rDNA separation","type":"narrow"}],"termid":"GO:1905819","terms_by_termid":{"GO:0007094":null,"GO:0033316":null,"GO:0090267":null,"GO:0140499":null,"GO:1902103":null,"GO:1902426":null,"GO:1905318":null,"GO:1905325":null,"GO:1905326":null,"GO:2000816":null}}


id: PBO:0075679
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SQLE divergent transcript","termid":"PBO:0075679"}


id: MONDO:0013141
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete autosomal dominant macrothrombocytopenia TUBB1-related (obsolete MONDO:0013141)","secondary_identifiers":["NANDO:2200667"],"termid":"MONDO:0013141","xrefs":{"Monarch":{"xref_id":"0013141"}}}


id: GO:0070823
data:
  {"annotated_genes":["SJAG_03685"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[64679],"is_not":false,"summary":null,"term":"GO:0070823"}]},"cv_name":"cellular_component","definition":"A tetrameric histone deacetylase complex that contains a Class II deacetylase catalytic subunit. In S. cerevisiae it is composed of two Hda1p subunits along with Hda2p and Hda3p.","definition_xrefs":["GOC:mah","PMID:11287668","PMID:8663039","GOC:dgf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone deacetylase complex","termid":"GO:0000118"},{"relation_name":"part_of","term_name":"chromatin","termid":"GO:0000785"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03685":null},"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"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005654"}],"interesting_parent_ids":["GO:0032991","GO:0005654","GO:0005694","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"HDA1 complex","references_by_uniquename":{"GO_REF:0000002":null},"termid":"GO:0070823","terms_by_termid":{"GO:0070823":null}}


id: GO:0060604
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Creation of the central hole of the mammary gland duct by the hollowing out of a solid rod.","definition_xrefs":["GOC:dph","PMID:17120154"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tube lumen cavitation","termid":"GO:0060605"},{"relation_name":"part_of","term_name":"mammary gland duct morphogenesis","termid":"GO:0060603"}],"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":"mammary gland duct cavitation","synonyms":[{"name":"milk duct cavitation","type":"related"}],"termid":"GO:0060604"}


id: PBO:0027257
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_phosphorylation_during_mitosis","termid":"PBO:0027257"}


id: GO:1901286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving iron-sulfur-molybdenum cofactor.","definition_xrefs":["GOC:TermGenie","GOC:yaf","UniPathway:UPA00782"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"}],"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":"iron-sulfur-molybdenum cofactor metabolic process","synonyms":[{"name":"FeMo-co metabolic process","type":"exact"},{"name":"FeMo-co metabolism","type":"exact"},{"name":"iron-molybdenum cofactor metabolic process","type":"exact"},{"name":"iron-molybdenum cofactor metabolism","type":"exact"},{"name":"iron-sulfur-molybdenum cofactor metabolism","type":"exact"}],"termid":"GO:1901286"}


id: GO:0034948
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2,6-dihydroxypseudooxynicotine + H2O = 2,6-dihydroxypyridine + 4-methylaminobutyrate.","definition_xrefs":["UM-BBD_reactionID:r0482"],"gene_count":0,"genotype_count":0,"name":"obsolete 2,6-dihydroxypseudooxynicotine hydrolase activity (obsolete GO:0034948)","termid":"GO:0034948"}


id: PBO:0064635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoribosyl pyrophosphate amidotransferase pseudogene 1","termid":"PBO:0064635"}


id: PBO:0081318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 101 pseudogene 1","termid":"PBO:0081318"}


id: MONDO:0006611
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Formation of non-necrotizing granulomas in the skin. It may be a manifestation of systemic sarcoidosis or may also arise in isolation.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"},{"relation_name":"is_a","term_name":"sarcoidosis","termid":"MONDO:0019338"}],"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":"skin sarcoidosis","secondary_identifiers":["ICD10CM:D86.3","EFO:1000767","Wikipedia:Cutaneous_manifestations_of_sarcoidosis","SCTID:55941000","UMLS:C0036203","NCIT:C34996","MEDGEN:19872","DOID:13402"],"synonyms":[{"name":"cutaneous sarcoid","type":"exact"},{"name":"cutaneous sarcoidosis","type":"exact"},{"name":"sarcoidosis of zone of skin","type":"exact"},{"name":"zone of skin sarcoidosis","type":"exact"}],"termid":"MONDO:0006611","xrefs":{"Monarch":{"xref_id":"0006611"}}}


id: PBO:0048550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP dependent ribosome recycling factor mitochondrial 2","termid":"PBO:0048550"}


id: MONDO:0012276
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Generalized epilepsy-paroxysmal dyskinesia syndrome is characterized by the association of paroxysmal dyskinesia and generalized epilepsy (usually absence or generalized tonic-clonic seizures) in the same individual or family. The prevalence is unknown. Analysis in one of the reported families led to the identification of a causative mutation in the KCNMA1 gene (chromosome 10q22), encoding the alpha subunit of the BK channel. Transmission is autosomal dominant.","definition_xrefs":["Orphanet:79137"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial partial epilepsy","termid":"MONDO:0017704"}],"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":"generalized epilepsy-paroxysmal dyskinesia syndrome","secondary_identifiers":["UMLS:C5574945","GARD:16704","MEDGEN:1801137","DOID:0070442","MESH:C563719","OMIM:609446"],"synonyms":[{"name":"GEPD","type":"exact"},{"name":"PNKD3","type":"related"},{"name":"epilepsy, generalized, with paroxysmal dyskinesia","type":"related"},{"name":"generalised epilepsy and paroxysmal dyskinesia","type":"related"},{"name":"generalized epilepsy and paroxysmal dyskinesia","type":"related"},{"name":"paroxysmal nonkinesigenic dyskinesia, 3, with or without generalised epilepsy","type":"related"},{"name":"paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy","type":"related"}],"termid":"MONDO:0012276","xrefs":{"Monarch":{"xref_id":"0012276"}}}


id: PR:O13698
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A malonyl-CoA-acyl carrier protein transacylase, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10982:SF4","OMA:SCHPO01650","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":"malonyl CoA-acyl carrier protein transacylase, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11G7.05c","secondary_identifiers":["UniProtKB:O13698"],"synonyms":[{"name":"MCT (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-MCAT","type":"exact"},{"name":"malonyl-CoA:ACP transferase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13698"}


id: SO:0000157
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A plasmid which carries within its sequence a bacteriophage replication origin. When the host bacterium is infected with \\\"helper\\\" phage, a phagemid is replicated along with the phage DNA and packaged into phage capsids.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vector_replicon","termid":"SO:0000440"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phagemid","secondary_identifiers":["http://en.wikipedia.org/wiki/Phagemid"],"synonyms":[{"name":"phagemid vector","type":"related"}],"termid":"SO:0000157"}


id: MONDO:0019139
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acquired hemophilia is a bleeding disorder that interferes with the body's blood clotting process. Signs and symptoms include prolonged bleeding, frequent nosebleeds, bruising throughout the body, solid swellings of congealed blood (hematomas), hematuria, and gastrointestinal or urologic bleeding. Acquired hemophilia occurs when the body's immune system attacks and disables a certain protein that helps the blood clot. About half of the cases are associated with other conditions, such as pregnancy, autoimmune disease, cancer, skin diseases, or allergic reactions to medications.","definition_xrefs":["GARD:0010350"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemorrhagic disease","termid":"MONDO:0002243"},{"relation_name":"is_a","term_name":"hemophilia","termid":"MONDO:0018660"},{"relation_name":"is_a","term_name":"acquired coagulation factor deficiency","termid":"MONDO:0020599"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"acquired hemophilia","secondary_identifiers":["NANDO:1200898","ICD10CM:D68.311","GARD:10350","Orphanet:73274","MEDGEN:204253","UMLS:C1096116","MESH:C536392","MedDRA:10053745"],"synonyms":[{"name":"acquired hemophilia","type":"exact"},{"name":"hemophilia, acquired","type":"exact"}],"termid":"MONDO:0019139","xrefs":{"Monarch":{"xref_id":"0019139"}}}


id: PBO:0060718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit A7","termid":"PBO:0060718"}


id: MONDO:0014378
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the CCNO gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary ciliary dyskinesia","termid":"MONDO:0016575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary ciliary dyskinesia 29","secondary_identifiers":["OMIM:615872","DOID:0110600","GARD:16025","MEDGEN:862971","UMLS:C4014534","NCIT:C172393"],"synonyms":[{"name":"CCNO primary ciliary dyskinesia","type":"exact"},{"name":"CILD29","type":"exact"},{"name":"ciliary dyskinesia, primary, 29","type":"related"},{"name":"ciliary dyskinesia, primary, 29, without situs inversus","type":"related"},{"name":"ciliary dyskinesia, primary, type 29","type":"exact"},{"name":"primary ciliary dyskinesia 29 without situs inversus","type":"exact"},{"name":"primary ciliary dyskinesia caused by mutation in CCNO","type":"exact"},{"name":"primary ciliary dyskinesia type 29","type":"exact"}],"termid":"MONDO:0014378","xrefs":{"Monarch":{"xref_id":"0014378"}}}


id: PBO:0041911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CBLL1 pseudogene 1","termid":"PBO:0041911"}


id: FYPO:0005098
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of poly(A) polymerase activity (EC name polynucleotide adenylyltransferase 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:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000661","FYPO:0000707","FYPO:0001985","FYPO:0000654"],"is_obsolete":false,"name":"abnormal poly(A) polymerase activity","synonyms":[{"name":"abnormal PAP activity","type":"exact"},{"name":"abnormal polynucleotide adenylyltransferase activity","type":"exact"}],"termid":"FYPO:0005098"}


id: PBO:0061601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NUBP iron-sulfur cluster assembly factor 2, cytosolic","termid":"PBO:0061601"}


id: MONDO:0001289
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete endometriosis of ovary (obsolete MONDO:0001289)","termid":"MONDO:0001289","xrefs":{"Monarch":{"xref_id":"0001289"}}}


id: PBO:0068302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 7","termid":"PBO:0068302"}


id: MONDO:0011130
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":"sebaceous gland hyperplasia, familial presenile","secondary_identifiers":["MESH:C537530","MEDGEN:356529","UMLS:C1866428","OMIM:601700"],"synonyms":[{"name":"sebaceous gland hyperplasia, familial presenile","type":"exact"}],"termid":"MONDO:0011130","xrefs":{"Monarch":{"xref_id":"0011130"}}}


id: PBO:0050899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon gamma inducible protein 16","termid":"PBO:0050899"}


id: PBO:0077988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ala (TGC) 10-1","termid":"PBO:0077988"}


id: FYPO:0002123
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of 4,6-pyruvylated D-galactose (4,6-O-[(1R)-1-carboxyethylidene]-D-galactose) measured in a cell is too low to detect.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"substance absent from cell during vegetative growth","termid":"FYPO:0001208"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"pyruvylated galactose absent from cell","synonyms":[{"name":"4,6-O-[(1R)-1-carboxyethylidene]-D-galactose absent from cell","type":"exact"},{"name":"4,6-pyruvylated D-galactose absent from cell","type":"exact"},{"name":"PvGal absent from cell","type":"exact"},{"name":"pyruvylated galactose absent from cell during mitotic cell cycle","type":"related"},{"name":"pyruvylated galactose absent from cell during vegetative growth","type":"exact"}],"termid":"FYPO:0002123"}


id: MONDO:1010628
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chediak-Higashi syndrome that occurs in Arctic fox.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Chediak-Higashi syndrome, non-human animal","termid":"MONDO:1010070"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chediak-Higashi syndrome, Arctic fox","secondary_identifiers":["OMIA:000185-494514"],"termid":"MONDO:1010628","xrefs":{"Monarch":{"xref_id":"1010628"}}}


id: PBO:0073276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"septin 10 pseudogene 1","termid":"PBO:0073276"}


id: GO:0043213
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a bacteriocin into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Bacteriocins are a group of antibiotics produced by bacteria and are encoded by a group of naturally occurring plasmids, e.g. Col E1. Bacteriocins are toxic to bacteria closely related to the bacteriocin producing strain.","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide transport","termid":"GO:0042886"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"bacteriocin transport","termid":"GO:0043213"}


id: GO:1905386
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein localization to presynapse.","definition_xrefs":["PMID:24449494","GO_REF:0000058","GOC:TermGenie","GOC:bf","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein localization to synapse","termid":"GO:1902474"},{"relation_name":"is_a","term_name":"regulation of protein localization to presynapse","termid":"GO:1905384"},{"relation_name":"positively_regulates","term_name":"protein localization to presynapse","termid":"GO:1905383"}],"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 protein localization to presynapse","synonyms":[{"name":"activation of protein localisation in presynapse","type":"narrow"},{"name":"activation of protein localisation to presynapse","type":"narrow"},{"name":"activation of protein localization in presynapse","type":"narrow"},{"name":"activation of protein localization to presynapse","type":"narrow"},{"name":"activation of recruitment of presynaptic proteins","type":"narrow"},{"name":"positive regulation of protein localisation in presynapse","type":"exact"},{"name":"positive regulation of protein localisation to presynapse","type":"exact"},{"name":"positive regulation of protein localization in presynapse","type":"exact"},{"name":"positive regulation of recruitment of presynaptic proteins","type":"exact"},{"name":"up regulation of protein localisation in presynapse","type":"exact"},{"name":"up regulation of protein localisation to presynapse","type":"exact"},{"name":"up regulation of protein localization in presynapse","type":"exact"},{"name":"up regulation of protein localization to presynapse","type":"exact"},{"name":"up regulation of recruitment of presynaptic proteins","type":"exact"},{"name":"up-regulation of protein localisation in presynapse","type":"exact"},{"name":"up-regulation of protein localisation to presynapse","type":"exact"},{"name":"up-regulation of protein localization in presynapse","type":"exact"},{"name":"up-regulation of protein localization to presynapse","type":"exact"},{"name":"up-regulation of recruitment of presynaptic proteins","type":"exact"},{"name":"upregulation of protein localisation in presynapse","type":"exact"},{"name":"upregulation of protein localisation to presynapse","type":"exact"},{"name":"upregulation of protein localization in presynapse","type":"exact"},{"name":"upregulation of protein localization to presynapse","type":"exact"},{"name":"upregulation of recruitment of presynaptic proteins","type":"exact"}],"termid":"GO:1905386"}


id: MONDO:0850162
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A B-lymphoblastic leukemia/lymphoma that is characterized by amplification of a portion of chromosome 21.","definition_xrefs":["DOID:0080651"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B-cell acute lymphoblastic leukemia","termid":"MONDO:0004947"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"B-lymphoblastic leukemia/lymphoma with IAMP21","secondary_identifiers":["NCIT:C130039"],"termid":"MONDO:0850162","xrefs":{"Monarch":{"xref_id":"0850162"}}}


id: GO:0038041
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Inhibition of one protomer of a G protein-coupled receptor (GPCR) heterodimer by the associated subunit. For example, agonist activation of one cytokine receptor can prevent activation of its associated cytokine receptor subunit.","definition_xrefs":["GOC:al","PMID:15979374","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of G protein-coupled receptor signaling pathway","termid":"GO:0008277"},{"relation_name":"is_a","term_name":"negative regulation of signaling receptor activity","termid":"GO:2000272"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"cross-receptor inhibition within G protein-coupled receptor heterodimer","synonyms":[{"name":"cross-receptor inhibition within G-protein coupled receptor heterodimer","type":"exact"}],"termid":"GO:0038041"}


id: PBO:0013093
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Replication Uncoupled from Mitosis","termid":"PBO:0013093"}


id: GO:0035944
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of a perforin protein due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:rv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"production of molecular mediator of immune response","termid":"GO:0002440"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"perforin production","termid":"GO:0035944"}


id: GO:2000712
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of maintenance of meiotic sister chromatid cohesion along the chromosome arms.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of maintenance of meiotic sister chromatid cohesion, arms (obsolete GO:2000712)","synonyms":[{"name":"regulation of maintenance of meiotic sister chromatin cohesion along arms","type":"exact"},{"name":"regulation of maintenance of sister chromatin cohesion along arms at meiosis I","type":"exact"}],"termid":"GO:2000712"}


id: PBO:0034796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin family plus-end microtubule motor Tea2","termid":"PBO:0034796"}


id: PBO:0116311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoribosylanthranilate isomerase/indole-3-glycerol-phosphate synthase/unknown aminotransferase, multifunctional enzyme Trp1","termid":"PBO:0116311"}


id: PBO:0076829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TEPSIN adaptor related protein complex 4 accessory protein","termid":"PBO:0076829"}


id: PBO:0001698
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.6.3.8","termid":"PBO:0001698"}


id: GO:0015859
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a nucleoside, a nucleobase linked to either beta-D-ribofuranose (ribonucleoside) or 2-deoxy-beta-D-ribofuranose, (a deoxyribonucleotide), within a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside transport","termid":"GO:0015858"},{"relation_name":"is_a","term_name":"intracellular transport","termid":"GO:0046907"}],"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:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"intracellular nucleoside transport","termid":"GO:0015859"}


id: PBO:0062932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prolyl 3-hydroxylase family member 4 (inactive)","termid":"PBO:0062932"}


id: MONDO:0032759
data:
  {"annotated_genes":["SJAG_04963","SJAG_01783"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87491,87492],"is_not":false,"summary":null,"term":"MONDO:0032759"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01783":null,"SJAG_04963":null},"genotype_count":0,"is_obsolete":false,"name":"intellectual developmental disorder with short stature and variable skeletal anomalies","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5193105","MEDGEN:1680968","OMIM:618453"],"synonyms":[{"name":"IDDSSA","type":"related"},{"name":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES","type":"related"}],"termid":"MONDO:0032759","terms_by_termid":{"MONDO:0032759":null},"xrefs":{"Monarch":{"xref_id":"0032759"}}}


id: MONDO:0000800
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A allergic disease involving a brown shrimp.","definition_xrefs":["MONDO:patterns/allergy"],"gene_count":0,"genotype_count":0,"name":"obsolete brown shrimp allergy (obsolete MONDO:0000800)","secondary_identifiers":["DOID:0060525"],"synonyms":[{"name":"Farfantepenaeus aztecus allergy","type":"exact"},{"name":"allergy of brown shrimp","type":"exact"},{"name":"brown shrimp allergic disease","type":"exact"}],"termid":"MONDO:0000800","xrefs":{"Monarch":{"xref_id":"0000800"}}}


id: PBO:0036099
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_nucleus_during_cellular_response_to_heat","termid":"PBO:0036099"}


id: PBO:0074194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 39 member 4","termid":"PBO:0074194"}


id: GO:0071615
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of removing one or more ethyl groups from a molecule, involving the oxidation (i.e. electron loss) of one or more atoms in the substrate.","definition_xrefs":["GOC:BHF","GOC:mah","GOC:rl"],"gene_count":0,"genotype_count":0,"name":"obsolete oxidative deethylation (obsolete GO:0071615)","termid":"GO:0071615"}


id: SO:1001279
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A recoding stimulatory region, the stem-loop secondary structural element is downstream of the redefined region.","definition_xrefs":["SO:ke","PMID:12519954"],"direct_ancestors":[{"relation_name":"is_a","term_name":"three_prime_recoding_site","termid":"SO:1001277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_prime_stem_loop_structure","synonyms":[{"name":"three prime stem loop structure","type":"exact"}],"termid":"SO:1001279"}


id: PBO:0016109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome b5 reductase Cbr1 (predicted)","termid":"PBO:0016109"}


id: GO:0004379
data:
  {"annotated_genes":["SJAG_00102"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78498],"is_not":false,"summary":null,"term":"GO:0004379"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: tetradecanoyl-CoA + glycyl-peptide = CoA + N-tetradecanoylglycyl-peptide.","definition_xrefs":["EC:2.3.1.97"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acyltransferase activity","termid":"GO:0016410"},{"relation_name":"is_a","term_name":"myristoyltransferase activity","termid":"GO:0019107"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00102":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016746","GO:0003674"],"is_obsolete":false,"name":"glycylpeptide N-tetradecanoyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-184392","MetaCyc:2.3.1.97-RXN","GO:0019106","Reactome:R-HSA-203611","Reactome:R-HSA-2534087","RHEA:15521"],"synonyms":[{"name":"N-myristoyltransferase activity","type":"exact"},{"name":"myristoyl-CoA-protein N-myristoyltransferase activity","type":"related"},{"name":"myristoyl-coenzyme A:protein N-myristoyl transferase activity","type":"related"},{"name":"myristoylating enzymes","type":"related"},{"name":"peptide N-myristoyltransferase activity","type":"related"},{"name":"peptide N-tetradecanoyltransferase activity","type":"related"},{"name":"protein N-myristoyltransferase activity","type":"related"},{"name":"tetradecanoyl-CoA:glycylpeptide N-tetradecanoyltransferase activity","type":"related"}],"termid":"GO:0004379","terms_by_termid":{"GO:0004379":null}}


id: MONDO:0023910
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"RAB18 deficiency","termid":"MONDO:0700247"}],"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":"Martsolf syndrome","secondary_identifiers":["MEDGEN:208658","UMLS:C0796037","OMIMPS:212720"],"termid":"MONDO:0023910","xrefs":{"Monarch":{"xref_id":"0023910"}}}


id: GO:0043917
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: alpha-D-ribose 1,5-bisphosphate = D-ribulose 1,5-bisphosphate.","definition_xrefs":["RHEA:32243"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, interconverting aldoses and ketoses","termid":"GO:0016861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016853","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"ribose 1,5-bisphosphate isomerase activity","secondary_identifiers":["EC:5.3.1.29","MetaCyc:RXN-8801"],"synonyms":[{"name":"ribose-1,5-bisphosphate isomerase activity","type":"exact"}],"termid":"GO:0043917"}


id: PBO:0018270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis protein Rrs1","termid":"PBO:0018270"}


id: PBO:0070337
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY4 pseudogene 9","termid":"PBO:0070337"}


id: PBO:0044868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DENND2B antisense RNA 1","termid":"PBO:0044868"}


id: PATO:0000179
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000179 body position (obsolete PATO:0000179)","termid":"PATO:0000179"}


id: PBO:0079857
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unc-93 homolog B6 (pseudogene)","termid":"PBO:0079857"}


id: PBO:0110350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CMPK1 pseudogene 2","termid":"PBO:0110350"}


id: FYPO:0005069
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic sister chromatid segregation fails to separate chromosomes into two equal masses after the cell has undergone a normal mitotic nuclear division and passed through the subsequent mitotic interphase. Unequal mitotic sister chromatid separation may be complete, with two distinct unequal DNA masses located at or near the ends of an elongated mitotic spindle, or incomplete.","definition_xrefs":["PomBase:mah","PMID:18180284"],"direct_ancestors":[{"relation_name":"is_a","term_name":"unequal mitotic sister chromatid segregation","termid":"FYPO:0003241"},{"relation_name":"is_a","term_name":"abnormal mitosis following normal mitosis","termid":"FYPO:0004588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0005447","FYPO:0000337","FYPO:0000641","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"unequal mitotic sister chromatid segregation following normal mitosis","synonyms":[{"name":"mitotic chromosome nondisjunction following normal mitosis","type":"exact"},{"name":"unequal mitotic chromosome segregation following normal mitosis","type":"exact"},{"name":"unequal mitotic sister chromatid segregation during vegetative growth following normal mitosis","type":"exact"},{"name":"unequal mitotic sister chromatid separation following normal mitosis","type":"related"},{"name":"unequal sister chromatid segregation following normal mitosis during mitotic cell cycle","type":"related"}],"termid":"FYPO:0005069"}


id: GO:0051680
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of 6-alpha-maltosylglucose, also known as isopanose.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharide biosynthetic process","termid":"GO:0009312"},{"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:0008150","GO:0005975"],"is_obsolete":false,"name":"6-alpha-maltosylglucose biosynthetic process","synonyms":[{"name":"isopanose biosynthesis","type":"exact"},{"name":"isopanose biosynthetic process","type":"exact"}],"termid":"GO:0051680"}


id: PBO:0046160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"E74 like ETS transcription factor 2","termid":"PBO:0046160"}


id: FYPO:0000683
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype in which the basal activity of an enzyme is increased relative to normal. Basal enzyme activity is the activity observed in the absence of a regulator. Abnormally elevated basal activity may or may not reach the levels observed in the normal activated state.","definition_xrefs":["PomBase:mah","PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity phenotype","termid":"FYPO:0000654"},{"relation_name":"output_of","term_name":"abnormal regulation of catalytic activity","termid":"FYPO:0004916"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000652","FYPO:0001320","FYPO:0000654"],"is_obsolete":false,"name":"constitutive catalytic activity","synonyms":[{"name":"constitutive catalytic activity during mitotic cell cycle","type":"related"},{"name":"constitutive catalytic activity during vegetative growth","type":"exact"},{"name":"constitutive enzymatic activity","type":"exact"},{"name":"constitutively active enzyme","type":"related"}],"termid":"FYPO:0000683"}


id: PBO:0084414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Magnesium-dependent acid phosphatase; member of the haloacid dehalogenase superfamily; non-essential gene","termid":"PBO:0084414"}


id: PBO:0085950
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; null mutant exhibits a respiratory growth defect and synthetic interactions with prohibitin (phb1) and gem1; authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies","termid":"PBO:0085950"}


id: MONDO:0005492
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A vascular reaction of the skin characterized by erythema and wheal formation due to localized increase of vascular permeability. The causative mechanism may be allergy, infection, or stress.","definition_xrefs":["MESH:D014581"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatitis","termid":"MONDO:0002406"}],"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":"urticaria","secondary_identifiers":["EFO:0005531","SCTID:126485001","ICD9:708.9","ICD9:708.8","DOID:1555","HP:0001025","UMLS:C0042109","NCIT:C3432","MEDGEN:22587","ICD9:708","ICD10CM:L50"],"synonyms":[{"name":"Urticarias","type":"related"},{"name":"hives","type":"exact"},{"name":"urticaria","type":"exact"},{"name":"urticaria (disease)","type":"exact"}],"termid":"MONDO:0005492","xrefs":{"Monarch":{"xref_id":"0005492"}}}


id: MONDO:0100103
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the DOK7 gene.","definition_xrefs":["OMIM:618389"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fetal akinesia deformation sequence","termid":"MONDO:0008824"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fetal akinesia deformation sequence 3","secondary_identifiers":["UMLS:C4760599","DOID:0111376","GARD:16496","MEDGEN:1680087"],"synonyms":[{"name":"FADS3","type":"exact"}],"termid":"MONDO:0100103","xrefs":{"Monarch":{"xref_id":"0100103"}}}


id: PBO:0076201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO2 pseudogene 11","termid":"PBO:0076201"}


id: PBO:0060299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin light chain 9","termid":"PBO:0060299"}


id: GO:0072679
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The movement of a thymocyte through distinct intrathymic niches (e.g. medulla, cortex), where it receives a unique set of developmental cues required for T-cell development.","definition_xrefs":["GOC:mah","CL:0000893","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell migration","termid":"GO:0072678"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"thymocyte migration","synonyms":[{"name":"immature T cell migration","type":"related"},{"name":"immature T lymphocyte migration","type":"related"},{"name":"immature T-cell migration","type":"related"},{"name":"immature T-lymphocyte migration","type":"related"},{"name":"thymic lymphocyte migration","type":"exact"}],"termid":"GO:0072679"}


id: PBO:0070808
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 38","termid":"PBO:0070808"}


id: PBO:0116190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-oxoprolinase (ATP-hydrolizing), Oxp2","termid":"PBO:0116190"}


id: PBO:0040004
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARL14EP divergent transcript","termid":"PBO:0040004"}


id: PBO:0089634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stress-responsive DNA-binding transcription factor Prr1","termid":"PBO:0089634"}


id: PBO:0089781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CIA machinery involved in ribosome biogenesis protein Lto1","termid":"PBO:0089781"}


id: FYPO:0003114
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of nitric oxide measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cellular reactive oxygen species level during vegetative growth","termid":"FYPO:0003004"},{"relation_name":"is_a","term_name":"altered cellular nitric oxide level","termid":"FYPO:0006408"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular nitric oxide level during vegetative growth","synonyms":[{"name":"increased cellular NO level during vegetative growth","type":"exact"},{"name":"increased cellular nitric oxide level during mitotic cell cycle","type":"related"},{"name":"increased nitric oxide accumulation during vegetative growth","type":"related"}],"termid":"FYPO:0003114"}


id: GO:0048937
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process aimed at the progression of a lateral line glial cell over time, from initial commitment of the cell to a specific fate, to the fully functional differentiated cell.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glial cell development","termid":"GO:0021782"},{"relation_name":"part_of","term_name":"lateral line nerve glial cell differentiation","termid":"GO:0048895"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lateral line nerve glial cell development","termid":"GO:0048937"}


id: MONDO:0006517
data:
  {"annotated_genes":["SJAG_03689"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011014"}]},"cv_name":"mondo","definition":"A malignant tumor that occurs in children. Representative examples include soft tissue and bone sarcomas (e.g. osteosarcoma) and embryonal neoplasms (e.g. hepatoblastoma and rhabdoid tumor).","definition_xrefs":["NCIT:C4005"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cancer","termid":"MONDO:0004992"},{"relation_name":"is_a","term_name":"childhood neoplasm","termid":"MONDO:0021079"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03689":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"childhood malignant neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:82962","UMLS:C0278704","EFO:1000654"],"synonyms":[{"name":"childhood cancer","type":"exact"},{"name":"childhood malignant neoplasm","type":"exact"},{"name":"childhood neoplasm, malignant","type":"exact"},{"name":"malignant childhood neoplasm","type":"exact"},{"name":"malignant childhood tumor","type":"exact"},{"name":"malignant childhood tumour","type":"exact"},{"name":"malignant neoplasm","type":"narrow"},{"name":"malignant paediatric neoplasm","type":"exact"},{"name":"malignant paediatric tumour","type":"exact"},{"name":"malignant pediatric neoplasm","type":"exact"},{"name":"malignant pediatric tumor","type":"exact"},{"name":"paediatric cancer","type":"exact"},{"name":"pediatric cancer","type":"exact"}],"termid":"MONDO:0006517","terms_by_termid":{"MONDO:0011014":null},"xrefs":{"Monarch":{"xref_id":"0006517"}}}


id: GO:0021885
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a cell from one site to another at least one of which is located in the forebrain.","definition_xrefs":["GOC:dph","GOC:dgh","GO_REF:0000021","GOC:jid","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell migration","termid":"GO:0016477"},{"relation_name":"part_of","term_name":"forebrain development","termid":"GO:0030900"}],"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":"forebrain cell migration","termid":"GO:0021885"}


id: MONDO:0000319
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete infant botulism (obsolete MONDO:0000319)","termid":"MONDO:0000319","xrefs":{"Monarch":{"xref_id":"0000319"}}}


id: MONDO:0013789
data:
  {"annotated_genes":["SJAG_01069"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86778],"is_not":false,"summary":null,"term":"MONDO:0013789"}]},"cv_name":"mondo","definition":"DDOST-CDG is a form of congenital disorders of N-linked glycosylation characterized by failure to thrive, developmental delay, hypotonia, strabismus and hepatic dysfunction. The disease is caused by mutations in the gene DDOST (1p36.1).","definition_xrefs":["Orphanet:300536"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type I","termid":"MONDO:0005500"},{"relation_name":"is_a","term_name":"disorder of protein N-glycosylation","termid":"MONDO:0017740"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01069":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322"],"is_obsolete":false,"name":"DDOST-congenital disorder of glycosylation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:482714","GARD:12398","OMIM:614507","SCTID:733083006","DOID:0080569","UMLS:C3281084"],"synonyms":[{"name":"CDG syndrome type Ir","type":"exact"},{"name":"CDG-Ir","type":"exact"},{"name":"CDG1R","type":"exact"},{"name":"DDOST-CDG","type":"exact"},{"name":"DDOST-CDG (CDG-Ir)","type":"related"},{"name":"DDOST-congenital disorder of glycosylation","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type","type":"related"},{"name":"carbohydrate deficient glycoprotein syndrome type Ir","type":"exact"},{"name":"congenital disorder of glycosylation type 1r","type":"exact"},{"name":"congenital disorder of glycosylation type Ir","type":"exact"},{"name":"congenital disorder of glycosylation, type Ir","type":"related"}],"termid":"MONDO:0013789","terms_by_termid":{"MONDO:0013789":null},"xrefs":{"Monarch":{"xref_id":"0013789"}}}


id: PBO:0081387
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 226","termid":"PBO:0081387"}


id: MONDO:0032768
data:
  {"annotated_genes":["SJAG_02869","SJAG_03579","SJAG_01016"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87507,87508,87509],"is_not":false,"summary":null,"term":"MONDO:0032768"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01016":null,"SJAG_02869":null,"SJAG_03579":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 76","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:618468","UMLS:C5193113","MEDGEN:1673011","DOID:0112212","GARD:16355"],"synonyms":[{"name":"DEE76","type":"exact"},{"name":"Developmental Delay, Epileptic Encephalopathy, Cerebral Atrophy, and Abnormal Myelination","type":"related"},{"name":"EIEE76","type":"exact"},{"name":"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 76","type":"exact"},{"name":"developmental and epileptic encephalopathy 76","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 76","type":"exact"}],"termid":"MONDO:0032768","terms_by_termid":{"MONDO:0032768":null},"xrefs":{"Monarch":{"xref_id":"0032768"}}}


id: GO:0033585
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of L-phenylalanine from other compounds, including chorismate, via the intermediate phenylpyruvate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-phenylalanine biosynthetic process","termid":"GO:0009094"},{"relation_name":"is_a","term_name":"chorismate metabolic process","termid":"GO:0046417"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"L-phenylalanine biosynthetic process from chorismate via phenylpyruvate","secondary_identifiers":["MetaCyc:PHESYN"],"synonyms":[{"name":"L-phenylalanine anabolism from chorismate via phenylpyruvate","type":"exact"},{"name":"L-phenylalanine biosynthesis from chorismate via phenylpyruvate","type":"exact"},{"name":"L-phenylalanine formation from chorismate via phenylpyruvate","type":"exact"},{"name":"L-phenylalanine synthesis from chorismate via phenylpyruvate","type":"exact"}],"termid":"GO:0033585"}


id: GO:0006681
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving galactosylceramides, any compound formed by the replacement of the glycosidic hydroxyl group of a cyclic form of galactose by a ceramide group.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosylceramide metabolic process","termid":"GO:0006677"},{"relation_name":"is_a","term_name":"galactolipid metabolic process","termid":"GO:0019374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"galactosylceramide metabolic process","synonyms":[{"name":"galactosylceramide metabolism","type":"exact"}],"termid":"GO:0006681"}


id: MONDO:0002167
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant melanocytic neoplasm that arises from the rectum.","definition_xrefs":["NCIT:C4640"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rectal cancer","termid":"MONDO:0006519"},{"relation_name":"is_a","term_name":"digestive system melanoma","termid":"MONDO:0045070"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"rectum malignant melanoma","secondary_identifiers":["MEDGEN:87605","UMLS:C0349539","DOID:1992","SCTID:276822007"],"synonyms":[{"name":"malignant melanoma of rectum","type":"exact"},{"name":"malignant melanoma of the rectum","type":"exact"},{"name":"melanoma (disease) of rectum","type":"exact"},{"name":"melanoma of rectum","type":"exact"},{"name":"melanoma of the rectum","type":"exact"},{"name":"rectal malignant melanoma","type":"exact"},{"name":"rectal melanoma","type":"exact"},{"name":"rectum melanoma","type":"exact"},{"name":"rectum melanoma (disease)","type":"exact"}],"termid":"MONDO:0002167","xrefs":{"Monarch":{"xref_id":"0002167"}}}


id: PBO:0000143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nifs homolog, possible cysteine desulfurase","termid":"PBO:0000143"}


id: PBO:0070646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 pseudogene 17","termid":"PBO:0070646"}


id: GO:0006011
data:
  {"annotated_genes":["SJAG_01089","SJAG_02178","SJAG_01209"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72907,80400,109215],"is_not":false,"summary":null,"term":"GO:0006011"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving UDP-alpha-D-glucose, a substance composed of alpha-D-glucose in glycosidic linkage with uridine diphosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-sugar metabolic process","termid":"GO:0009225"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01089":null,"SJAG_01209":null,"SJAG_02178":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"UDP-alpha-D-glucose metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"UDP-glucose metabolism","type":"exact"}],"termid":"GO:0006011","terms_by_termid":{"GO:0006011":null}}


id: PBO:0079523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane immune signaling adaptor TYROBP","termid":"PBO:0079523"}


id: GO:0007213
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway initiated by a ligand binding to an acetylcholine receptor on the surface of a target cell, and ends with regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:mah","ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway","termid":"GO:0007186"},{"relation_name":"is_a","term_name":"acetylcholine receptor signaling pathway","termid":"GO:0095500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"G protein-coupled acetylcholine receptor signaling pathway","synonyms":[{"name":"G-protein coupled acetylcholine receptor signaling pathway","type":"exact"},{"name":"acetylcholine receptor signalling, muscarinic pathway","type":"exact"},{"name":"muscarinic acetylcholine receptor signaling pathway","type":"exact"}],"termid":"GO:0007213"}


id: MONDO:0000759
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete acrorenal syndrome (obsolete MONDO:0000759)","termid":"MONDO:0000759","xrefs":{"Monarch":{"xref_id":"0000759"}}}


id: MONDO:0016533
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial visceral amyloidosis","termid":"MONDO:0007099"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0021179"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0021179","MONDO:0005066"],"is_obsolete":false,"name":"apolipoprotein A-II amyloidosis","secondary_identifiers":["GARD:20631","UMLS:C5679845","MEDGEN:1842484","Orphanet:238269"],"synonyms":[{"name":"AApoAII amyloidosis","type":"exact"},{"name":"familial amyloid nephropathy due to apolipoprotein A-II variant","type":"exact"},{"name":"familial renal amyloidosis due to apolipoprotein A-II variant","type":"exact"},{"name":"hereditary amyloid nephropathy due to apolipoprotein A-II variant","type":"exact"},{"name":"hereditary renal amyloidosis due to apolipoprotein A-II variant","type":"exact"}],"termid":"MONDO:0016533","xrefs":{"Monarch":{"xref_id":"0016533"}}}


id: PR:P05734
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl1901 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P05734"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L19-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC56F2.02","synonyms":[{"name":"Spom972h-rpl1901","type":"exact"},{"name":"YL15 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P05734"}


id: MONDO:0017568
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acrodysplasia scoliosis is a rare, genetic dysostosis disorder characterized by brachydactyly and other finger/toe anomalies (short and/or wide metacarpals, abnormal or absent metatarsals, broad halluces), carpal synostosis, fused cervical vertebrae, scoliosis and spina bifida occulta. There have been no further descriptions in the literature since 1984.","definition_xrefs":["Orphanet:2956"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"Prata-Liberal-Goncalves syndrome","secondary_identifiers":["MEDGEN:419156","GARD:491","UMLS:C2931761"],"synonyms":[{"name":"acrodysplasia scoliosis","type":"exact"},{"name":"brachydactyly-scoliosis-carpal fusion syndrome","type":"exact"}],"termid":"MONDO:0017568","xrefs":{"Monarch":{"xref_id":"0017568"}}}


id: PBO:0061500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuropilin 2","termid":"PBO:0061500"}


id: PBO:0004978
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"18S ribosomal RNA","termid":"PBO:0004978"}


id: GO:0005111
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 2 fibroblast growth factor receptor (FGFR2).","definition_xrefs":["GOC:fb_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibroblast growth factor receptor binding","termid":"GO:0005104"}],"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:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"type 2 fibroblast growth factor receptor binding","synonyms":[{"name":"FGFR2 binding","type":"exact"},{"name":"FGFR2 ligand","type":"narrow"},{"name":"heartless binding","type":"exact"},{"name":"heartless ligand","type":"narrow"},{"name":"type 2 fibroblast growth factor receptor ligand","type":"narrow"}],"termid":"GO:0005111"}


id: GO:0098880
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process which maintains the organization and the arrangement of proteins in the presynaptic specialization.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"postsynaptic density organization","termid":"GO:0097106"},{"relation_name":"is_a","term_name":"maintenance of synapse structure","termid":"GO:0099558"}],"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":"maintenance of postsynaptic specialization structure","termid":"GO:0098880"}


id: PATO:0000035
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000035 carbohydrate concentration (obsolete PATO:0000035)","termid":"PATO:0000035"}


id: PBO:0108980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm associated microtubule inner protein 4","termid":"PBO:0108980"}


id: MONDO:0020124
data:
  {"annotated_genes":["SJAG_04821","SJAG_01872","SJAG_03056","SJAG_00826","SJAG_04728","SJAG_00924"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86328],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012518"},{"annotations":[86520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013883"},{"annotations":[85764],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014543"},{"annotations":[85761],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014542"},{"annotations":[85604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014590"},{"annotations":[86388],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012157"},{"annotations":[86629],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032596"}]},"cv_name":"mondo","definition":"Conditions characterized by impaired transmission of impulses at the neuromuscular junction. This may result from disorders that affect receptor function, pre- or postsynaptic membrane function, or acetylcholinesterase activity. The majority of diseases in this category are associated with autoimmune, toxic, or inherited conditions.","definition_xrefs":["MESH:D020511"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuromuscular disease","termid":"MONDO:0019056"},{"relation_name":"is_a","term_name":"synaptopathy","termid":"MONDO:0021017"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00826":null,"SJAG_00924":null,"SJAG_01872":null,"SJAG_03056":null,"SJAG_04728":null,"SJAG_04821":null},"genotype_count":0,"is_obsolete":false,"name":"neuromuscular junction disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:439","GARD:19473","UMLS:C0751950","MEDGEN:155665","Orphanet:98491","SCTID:128213006"],"termid":"MONDO:0020124","terms_by_termid":{"MONDO:0012157":null,"MONDO:0012518":null,"MONDO:0013883":null,"MONDO:0014542":null,"MONDO:0014543":null,"MONDO:0014590":null,"MONDO:0032596":null},"xrefs":{"Monarch":{"xref_id":"0020124"}}}


id: GO:1903679
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cap-independent translational initiation.","definition_xrefs":["PMID:11959995","GO_REF:0000058","GOC:TermGenie","GOC:PARL","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cap-independent translational initiation","termid":"GO:1903677"},{"relation_name":"is_a","term_name":"positive regulation of cytoplasmic translational initiation","termid":"GO:1904690"},{"relation_name":"positively_regulates","term_name":"cap-independent translational initiation","termid":"GO:0002190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0002181"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0002181","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of cap-independent translational initiation","synonyms":[{"name":"activation of cap-independent translational initiation","type":"narrow"},{"name":"up regulation of cap-independent translational initiation","type":"exact"},{"name":"up-regulation of cap-independent translational initiation","type":"exact"},{"name":"upregulation of cap-independent translational initiation","type":"exact"}],"termid":"GO:1903679"}


id: GO:0043413
data:
  {"annotated_genes":["SJAG_00183","SJAG_00924","SJAG_02648","SJAG_01276","SJAG_04095","SJAG_03150","SJAG_01021","SJAG_03774","SJAG_01950","SJAG_03082","SJAG_03656","SJAG_00554","SJAG_02056","SJAG_04401","SJAG_02519","SJAG_02903","SJAG_03056","SJAG_00394","SJAG_03032","SJAG_00598","SJAG_04728","SJAG_02996","SJAG_03871","SJAG_05219","SJAG_03790","SJAG_04053","SJAG_01264","SJAG_05348","SJAG_03149","SJAG_00816","SJAG_02783","SJAG_01595","SJAG_04127","SJAG_00437","SJAG_02163","SJAG_04363","SJAG_00747","SJAG_03676","SJAG_03330","SJAG_04231","SJAG_02102","SJAG_03764","SJAG_03188","SJAG_01972","SJAG_03333","SJAG_04906","SJAG_04571","SJAG_04090","SJAG_00831","SJAG_04821","SJAG_03311","SJAG_03555","SJAG_01006","SJAG_04954","SJAG_04770","SJAG_04952","SJAG_01491","SJAG_01069","SJAG_04316","SJAG_01389","SJAG_00334"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105327,61695,63586,75334,77076,77573,100317,73446,69411,111397,94239,64577,65806,91467,100109,80365],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006488"},{"annotations":[63296,118123,68926,67036,58726,63658,96040,100353,114261,75824,108704,72313,74829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006486"},{"annotations":[78687,79706,74921,70299,78384,80276,111016,76031,77425,111022,75712,75149,77976,79502,74006],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006487"},{"annotations":[98214,100652,79103,99103,99104,99105,99106,118350,79546,79918,105273,74647,87848,76576],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0018279"},{"annotations":[63015,111023,118351,79707,75150,77977,111017],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006493"},{"annotations":[93378,106287,101861],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035269"}]},"cv_name":"biological_process","definition":"The covalent attachment of a glycosyl residue to one or more monomeric units in a polypeptide, polynucleotide, polysaccharide, or other biological macromolecule.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule modification","termid":"GO:0043412"},{"relation_name":"is_a","term_name":"glycosylation","termid":"GO:0070085"}],"gene_count":61,"genes_by_uniquename":{"SJAG_00183":null,"SJAG_00334":null,"SJAG_00394":null,"SJAG_00437":null,"SJAG_00554":null,"SJAG_00598":null,"SJAG_00747":null,"SJAG_00816":null,"SJAG_00831":null,"SJAG_00924":null,"SJAG_01006":null,"SJAG_01021":null,"SJAG_01069":null,"SJAG_01264":null,"SJAG_01276":null,"SJAG_01389":null,"SJAG_01491":null,"SJAG_01595":null,"SJAG_01950":null,"SJAG_01972":null,"SJAG_02056":null,"SJAG_02102":null,"SJAG_02163":null,"SJAG_02519":null,"SJAG_02648":null,"SJAG_02783":null,"SJAG_02903":null,"SJAG_02996":null,"SJAG_03032":null,"SJAG_03056":null,"SJAG_03082":null,"SJAG_03149":null,"SJAG_03150":null,"SJAG_03188":null,"SJAG_03311":null,"SJAG_03330":null,"SJAG_03333":null,"SJAG_03555":null,"SJAG_03656":null,"SJAG_03676":null,"SJAG_03764":null,"SJAG_03774":null,"SJAG_03790":null,"SJAG_03871":null,"SJAG_04053":null,"SJAG_04090":null,"SJAG_04095":null,"SJAG_04127":null,"SJAG_04231":null,"SJAG_04316":null,"SJAG_04363":null,"SJAG_04401":null,"SJAG_04571":null,"SJAG_04728":null,"SJAG_04770":null,"SJAG_04821":null,"SJAG_04906":null,"SJAG_04952":null,"SJAG_04954":null,"SJAG_05219":null,"SJAG_05348":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"macromolecule glycosylation","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"termid":"GO:0043413","terms_by_termid":{"GO:0006486":null,"GO:0006487":null,"GO:0006488":null,"GO:0006493":null,"GO:0018279":null,"GO:0035269":null}}


id: PBO:0079150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetraspanin 11","termid":"PBO:0079150"}


id: PBO:0071045
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 47","termid":"PBO:0071045"}


id: PBO:0077145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thymidine kinase 2","termid":"PBO:0077145"}


id: GO:0052572
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 detecting the immune response of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated response to host defenses","termid":"GO:0052200"}],"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 host immune response","secondary_identifiers":["Reactome:R-HSA-1222499","GO:0052564"],"synonyms":[{"name":"response to immune response of other organism involved in symbiotic interaction","type":"broad"}],"termid":"GO:0052572"}


id: PBO:0038931
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adhesion G protein-coupled receptor L4","termid":"PBO:0038931"}


id: PBO:0052854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 4-11","termid":"PBO:0052854"}


id: PBO:0062421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 66 pseudogene","termid":"PBO:0062421"}


id: MONDO:0800039
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any MELAS syndromein which the cause of the disease is a mutation in the MTND5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"MELAS syndrome","termid":"MONDO:0010789"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"MELAS syndrome caused by mutation in MTND5","synonyms":[{"name":"MTND5 MELAS syndrome","type":"exact"}],"termid":"MONDO:0800039","xrefs":{"Monarch":{"xref_id":"0800039"}}}


id: GO:0046671
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of programmed cell death that occurs in the retina.","definition_xrefs":["GOC:ai","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of programmed cell death","termid":"GO:0043069"},{"relation_name":"is_a","term_name":"regulation of retinal cell programmed cell death","termid":"GO:0046668"},{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"negatively_regulates","term_name":"retinal cell programmed cell death","termid":"GO:0046666"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of retinal cell programmed cell death","synonyms":[{"name":"down regulation of retinal programmed cell death","type":"exact"},{"name":"down-regulation of retinal programmed cell death","type":"exact"},{"name":"downregulation of retinal programmed cell death","type":"exact"},{"name":"inhibition of retinal programmed cell death","type":"narrow"},{"name":"negative regulation of retinal programmed cell death","type":"exact"}],"termid":"GO:0046671"}


id: PBO:0083558
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; partially overlaps verified gene PKH2/YOL100W; may interact with ribosomes","termid":"PBO:0083558"}


id: PBO:0044958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DHRS4 antisense RNA 1","termid":"PBO:0044958"}


id: PBO:0090451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP-ribose diphosphatase, NudF subfamily Ysa1","termid":"PBO:0090451"}


id: GO:0039571
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus stops, prevents, or reduces the frequency, rate or extent of host STAT1 (signal transducer and activator of transcription-1) activity by stopping, preventing, or reducing the frequency, rate or extent of the introduction of a phosphate group to a tyrosine residue of a STAT1 protein. For example, the measles virus V protein inhibits tyrosine phosphorylation of STAT1, thereby preventing STAT1 activation.","definition_xrefs":["PMID:12804771"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host STAT1 activity by negative regulation of STAT1 tyrosine phosphorylation (obsolete GO:0039571)","synonyms":[{"name":"inhibition by virus of tyrosine phosphorylation of STAT1","type":"related"}],"termid":"GO:0039571"}


id: PBO:0069171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 424, pseudogene","termid":"PBO:0069171"}


id: GO:0061770
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a translation elongation factor, any polypeptide factor involved in the peptide elongation in ribosome-mediated translation.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"translation elongation factor binding","termid":"GO:0061770"}


id: GO:0032939
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of translation as a result of oxidative stress, a state often resulting from exposure to high levels of reactive oxygen species, e.g. superoxide anions, hydrogen peroxide (H2O2), and hydroxyl radicals.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of translation in response to stress","termid":"GO:0032056"},{"relation_name":"part_of","term_name":"cellular response to oxidative stress","termid":"GO:0034599"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of translation in response to oxidative stress","synonyms":[{"name":"activation of translation in response to oxidative stress","type":"narrow"},{"name":"stimulation of translation in response to oxidative stress","type":"narrow"},{"name":"up regulation of translation in response to oxidative stress","type":"exact"},{"name":"up-regulation of translation in response to oxidative stress","type":"exact"},{"name":"upregulation of translation in response to oxidative stress","type":"exact"}],"termid":"GO:0032939"}


id: PBO:0013014
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fe Repressor of Activation","termid":"PBO:0013014"}


id: MONDO:1040030
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A susceptibility or predisposition to Parkinsons disease in which the cause of the disease is the presence of a monoallelic pathogenic variant or risk allele in the GBA1 gene.","definition_xrefs":["PMID:19846850","PMID:19433656","PMID:19858467"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GBA1-related Parkinson disease, susceptibility","termid":"MONDO:1040030","xrefs":{"Monarch":{"xref_id":"1040030"}}}


id: GO:0099044
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The initial, indirect interaction between a transport vesicle membrane and the membrane of the endoplasmic reticulum. This interaction is mediated by tethering factors (or complexes), which interact with both membranes. Interaction can occur via direct binding to membrane phospholipids or membrane proteins, or via binding to vesicle coat proteins. This process is distinct from and prior fusion.","definition_xrefs":["PMID:27243008"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle tethering","termid":"GO:0099022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"vesicle tethering to endoplasmic reticulum","termid":"GO:0099044"}


id: MONDO:0004720
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A orthopoxvirus that causes a milder clinical syndrome than smallpox.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"smallpox","termid":"MONDO:0004651"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"variola minor infection","secondary_identifiers":["UMLS:C0001906","ICD9:050.1","MEDGEN:1393","DOID:9153","SCTID:72294005","NCIT:C34365"],"synonyms":[{"name":"Variola minor","type":"exact"},{"name":"alastrim","type":"exact"},{"name":"cottonpox","type":"exact"},{"name":"milkpox","type":"exact"},{"name":"whitepox","type":"exact"}],"termid":"MONDO:0004720","xrefs":{"Monarch":{"xref_id":"0004720"}}}


id: GO:0007180
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete transforming growth factor beta ligand binding to type II receptor (obsolete GO:0007180)","synonyms":[{"name":"TGF-beta ligand binding to type II receptor","type":"exact"},{"name":"TGFbeta ligand binding to type II receptor","type":"exact"},{"name":"transforming growth factor beta ligand binding to type II receptor","type":"exact"}],"termid":"GO:0007180"}


id: PBO:0059248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L17","termid":"PBO:0059248"}


id: GO:0051053
data:
  {"annotated_genes":["SJAG_00266","SJAG_03097","SJAG_00573","SJAG_01210","SJAG_03997","SJAG_03048","SJAG_01068","SJAG_02724","SJAG_02162","SJAG_04671","SJAG_04855","SJAG_00247"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102681],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001033"},{"annotations":[112068],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904332"},{"annotations":[117146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903464"},{"annotations":[109207,98100,102685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903467"},{"annotations":[108284],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045128"},{"annotations":[103543],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902681"},{"annotations":[99687,103544,108832,106952],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0011000"},{"annotations":[102595,115326,99688],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031582"},{"annotations":[99689],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090001"},{"annotations":[102596],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071807"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways involving DNA.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of macromolecule metabolic process","termid":"GO:0010605"},{"relation_name":"is_a","term_name":"negative regulation of nucleobase-containing compound metabolic process","termid":"GO:0045934"},{"relation_name":"is_a","term_name":"regulation of DNA metabolic process","termid":"GO:0051052"},{"relation_name":"negatively_regulates","term_name":"DNA metabolic process","termid":"GO:0006259"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00247":null,"SJAG_00266":null,"SJAG_00573":null,"SJAG_01068":null,"SJAG_01210":null,"SJAG_02162":null,"SJAG_02724":null,"SJAG_03048":null,"SJAG_03097":null,"SJAG_03997":null,"SJAG_04671":null,"SJAG_04855":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"negative regulation of DNA metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of DNA metabolic process","type":"exact"},{"name":"down-regulation of DNA metabolic process","type":"exact"},{"name":"downregulation of DNA metabolic process","type":"exact"},{"name":"inhibition of DNA metabolic process","type":"narrow"},{"name":"negative regulation of DNA metabolism","type":"exact"}],"termid":"GO:0051053","terms_by_termid":{"GO:0011000":null,"GO:0031582":null,"GO:0045128":null,"GO:0071807":null,"GO:0090001":null,"GO:1902681":null,"GO:1903464":null,"GO:1903467":null,"GO:1904332":null,"GO:2001033":null}}


id: GO:0007307
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Amplification by up to 60-fold of the loci containing the chorion gene clusters. Amplification is necessary for the rapid synthesis of chorion proteins by the follicle cells, and occurs by repeated firing of one or more origins located within each gene cluster.","definition_xrefs":["GOC:mtg_sensu","PMID:11157771"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA amplification","termid":"GO:0006277"},{"relation_name":"is_a","term_name":"cellular process involved in reproduction in multicellular organism","termid":"GO:0022412"},{"relation_name":"part_of","term_name":"egg chorion assembly","termid":"GO:0007306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006259","GO:0044085"],"is_obsolete":false,"name":"eggshell chorion gene amplification","termid":"GO:0007307"}


id: MONDO:0010873
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"subcortical band heterotopia","termid":"MONDO:0020491"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"band heterotopia of brain","secondary_identifiers":["MESH:C563950","OMIM:600348","UMLS:C4284594","GARD:2250","MEDGEN:924885"],"synonyms":[{"name":"BH","type":"related"},{"name":"band heterotopia","type":"related"},{"name":"band heterotopia of brain","type":"exact"}],"termid":"MONDO:0010873","xrefs":{"Monarch":{"xref_id":"0010873"}}}


id: GO:1903012
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of bone development.","definition_xrefs":["PMID:22510437","GOC:TermGenie","GOC:mr","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of bone development","termid":"GO:1903010"},{"relation_name":"positively_regulates","term_name":"bone development","termid":"GO:0060348"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of bone development","synonyms":[{"name":"activation of bone development","type":"narrow"},{"name":"up regulation of bone development","type":"exact"},{"name":"up-regulation of bone development","type":"exact"},{"name":"upregulation of bone development","type":"exact"}],"termid":"GO:1903012"}


id: PBO:0044235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cullin 4A pseudogene 1","termid":"PBO:0044235"}


id: GO:0070323
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of translation as a result of a stimulus indicating deprivation of nitrogen.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of translation in response to nitrogen starvation (obsolete GO:0070323)","synonyms":[{"name":"activation of translation in response to nitrogen starvation","type":"narrow"},{"name":"stimulation of translation in response to nitrogen starvation","type":"narrow"},{"name":"up regulation of translation in response to nitrogen starvation","type":"exact"},{"name":"up-regulation of translation in response to nitrogen starvation","type":"exact"},{"name":"upregulation of translation in response to nitrogen starvation","type":"exact"}],"termid":"GO:0070323"}


id: PBO:0087931
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transketolase; catalyzes conversion of xylulose-5-phosphate and ribose-5-phosphate to sedoheptulose-7-phosphate and glyceraldehyde-3-phosphate in the pentose phosphate pathway; needed for synthesis of aromatic amino acids; TKL1 has a paralog, TKL2, that arose from the whole genome duplication","termid":"PBO:0087931"}


id: PBO:0078976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ser (anticodon GCT) 4-1","termid":"PBO:0078976"}


id: GO:0102313
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: geranyl diphosphate(3-) + H2O = 1,8-cineole + diphosphoric acid.","definition_xrefs":["RHEA:32543","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"1,8-cineole synthase activity","secondary_identifiers":["EC:4.2.3.108","MetaCyc:RXN-12980"],"termid":"GO:0102313"}


id: PBO:0084326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Karyopherin responsible for the nuclear import of Rpf1p; Rpf1p is a ribosome maturation factor","termid":"PBO:0084326"}


id: GO:1901373
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a lipid hydroperoxide into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid transport","termid":"GO:0006869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"lipid hydroperoxide transport","termid":"GO:1901373"}


id: GO:0002810
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of antifungal peptide biosynthesis.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of antifungal peptide production","termid":"GO:0002788"},{"relation_name":"is_a","term_name":"regulation of antimicrobial peptide biosynthetic process","termid":"GO:0002805"},{"relation_name":"regulates","term_name":"antifungal peptide biosynthetic process","termid":"GO:0002783"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of antifungal peptide biosynthetic process","termid":"GO:0002810"}


id: GO:0017181
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of peptidyl-diphthine, a modified histidine residue.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-diphthine catabolic process (obsolete GO:0017181)","synonyms":[{"name":"peptidyl-diphthine breakdown","type":"exact"},{"name":"peptidyl-diphthine catabolism","type":"exact"},{"name":"peptidyl-diphthine degradation","type":"exact"}],"termid":"GO:0017181"}


id: MONDO:0011081
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dislocation of the hip-dysmorphism syndrome is a rare multiple congenital anomalies syndrome characterized by bilateral congenital dislocation of the hip, characteristic facial features (flat mid-face, hypertelorism, epicanthus, puffiness around the eyes, broad nasal bridge, carp-shaped mouth), and joint hyperextensibility. Congenital heart defects, congenital dislocation of the knee, congenital inguinal hernia, and vesicoureteric reflux have also been reported. There have been no further descriptions in the literature since 1995.","definition_xrefs":["Orphanet:2412"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dislocation of the hip-dysmorphism syndrome","secondary_identifiers":["SCTID:763755009","OMIM:601450","MESH:C563315","GARD:1428","UMLS:C1832353","MEDGEN:316970"],"synonyms":[{"name":"Collins Pope syndrome","type":"related"},{"name":"Collins-Pope syndrome","type":"exact"},{"name":"dislocation of hip, congenital, with hyperextensibility of fingers and facial dysmorphism","type":"related"},{"name":"dislocation of the hip dysmorphism","type":"related"},{"name":"hip, congenital dislocation of, with hyperextensibility of fingers and Facial Dysmorphism","type":"related"}],"termid":"MONDO:0011081","xrefs":{"Monarch":{"xref_id":"0011081"}}}


id: PBO:0062445
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 110 pseudogene","termid":"PBO:0062445"}


id: GO:0046942
data:
  {"annotated_genes":["SJAG_04920","SJAG_00543","SJAG_04725","SJAG_04637","SJAG_05175","SJAG_04295","SJAG_04588","SJAG_03591","SJAG_01872","SJAG_03400","SJAG_02780","SJAG_05325","SJAG_01505","SJAG_04718","SJAG_00991","SJAG_03970","SJAG_02779","SJAG_02716","SJAG_03256","SJAG_00232","SJAG_03899","SJAG_01406","SJAG_03503","SJAG_02011","SJAG_04984","SJAG_05346","SJAG_02029","SJAG_00626","SJAG_00276","SJAG_00671","SJAG_02605","SJAG_01960","SJAG_00522","SJAG_04905","SJAG_02140","SJAG_04593","SJAG_00275","SJAG_04706","SJAG_03644","SJAG_01924"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71884],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015742"},{"annotations":[110335,103115],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990591"},{"annotations":[72144,79599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905135"},{"annotations":[69630,87801,69322,58402],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905039"},{"annotations":[63673],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903712"},{"annotations":[92400],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905136"},{"annotations":[61892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015884"},{"annotations":[92831],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140270"},{"annotations":[63575],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006868"},{"annotations":[70289,98549],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904983"},{"annotations":[110336,103116],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903714"},{"annotations":[96357],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902475"},{"annotations":[100681],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097638"},{"annotations":[97684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990818"},{"annotations":[104147],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090518"},{"annotations":[99149,63576],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903826"},{"annotations":[96889],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070778"},{"annotations":[98550],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110141"},{"annotations":[104148],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901481"},{"annotations":[104149],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090515"},{"annotations":[96890],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015813"},{"annotations":[97685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0089708"},{"annotations":[104150],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090513"},{"annotations":[100682],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097639"},{"annotations":[103117,104151],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901482"},{"annotations":[97686],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0089707"},{"annotations":[110337],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090517"},{"annotations":[104153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090516"},{"annotations":[65874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015825"},{"annotations":[104154],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090514"},{"annotations":[101973],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098714"},{"annotations":[67747],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071423"},{"annotations":[63954],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015743"},{"annotations":[101974],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098715"},{"annotations":[65015],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901553"},{"annotations":[96892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990551"},{"annotations":[96893],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990550"},{"annotations":[71886,72893],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006843"},{"annotations":[88752],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990556"},{"annotations":[108219],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990575"},{"annotations":[88753],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990555"},{"annotations":[77109,63093],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006850"},{"annotations":[88431],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905533"},{"annotations":[72855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098717"},{"annotations":[76955,93684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990536"},{"annotations":[99024],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006847"},{"annotations":[90268],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0035432"},{"annotations":[92081,93675,99204,110850],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905589"},{"annotations":[92082,93676,99205],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905534"},{"annotations":[93677],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905626"},{"annotations":[101536,100675],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905647"},{"annotations":[90957],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140300"},{"annotations":[101975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098720"},{"annotations":[63574],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015828"}]},"cv_name":"biological_process","definition":"The directed movement of carboxylic acids into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Carboxylic acids are organic acids containing one or more carboxyl (COOH) groups or anions (COO-).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transport","termid":"GO:0015711"},{"relation_name":"is_a","term_name":"organic acid transport","termid":"GO:0015849"}],"gene_count":40,"genes_by_uniquename":{"SJAG_00232":null,"SJAG_00275":null,"SJAG_00276":null,"SJAG_00522":null,"SJAG_00543":null,"SJAG_00626":null,"SJAG_00671":null,"SJAG_00991":null,"SJAG_01406":null,"SJAG_01505":null,"SJAG_01872":null,"SJAG_01924":null,"SJAG_01960":null,"SJAG_02011":null,"SJAG_02029":null,"SJAG_02140":null,"SJAG_02605":null,"SJAG_02716":null,"SJAG_02779":null,"SJAG_02780":null,"SJAG_03256":null,"SJAG_03400":null,"SJAG_03503":null,"SJAG_03591":null,"SJAG_03644":null,"SJAG_03899":null,"SJAG_03970":null,"SJAG_04295":null,"SJAG_04588":null,"SJAG_04593":null,"SJAG_04637":null,"SJAG_04706":null,"SJAG_04718":null,"SJAG_04725":null,"SJAG_04905":null,"SJAG_04920":null,"SJAG_04984":null,"SJAG_05175":null,"SJAG_05325":null,"SJAG_05346":null},"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:0051179","GO:0006810"],"is_obsolete":false,"name":"carboxylic acid transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"termid":"GO:0046942","terms_by_termid":{"GO:0006843":null,"GO:0006847":null,"GO:0006850":null,"GO:0006868":null,"GO:0015742":null,"GO:0015743":null,"GO:0015813":null,"GO:0015825":null,"GO:0015828":null,"GO:0015884":null,"GO:0035432":null,"GO:0070778":null,"GO:0071423":null,"GO:0089707":null,"GO:0089708":null,"GO:0090513":null,"GO:0090514":null,"GO:0090515":null,"GO:0090516":null,"GO:0090517":null,"GO:0090518":null,"GO:0097638":null,"GO:0097639":null,"GO:0098714":null,"GO:0098715":null,"GO:0098717":null,"GO:0098720":null,"GO:0110141":null,"GO:0140270":null,"GO:0140300":null,"GO:1901481":null,"GO:1901482":null,"GO:1901553":null,"GO:1902475":null,"GO:1903712":null,"GO:1903714":null,"GO:1903826":null,"GO:1904983":null,"GO:1905039":null,"GO:1905135":null,"GO:1905136":null,"GO:1905533":null,"GO:1905534":null,"GO:1905589":null,"GO:1905626":null,"GO:1905647":null,"GO:1990536":null,"GO:1990550":null,"GO:1990551":null,"GO:1990555":null,"GO:1990556":null,"GO:1990575":null,"GO:1990591":null,"GO:1990818":null}}


id: MONDO:0019441
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare hereditary Transthyretin (TTR)-related systemic amyloidosis (ATTR) with predominant cardiac involvement resulting from myocardial infiltration of abnormal amyloid protein.","definition_xrefs":["Orphanet:85451"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial restrictive cardiomyopathy","termid":"MONDO:0016340"},{"relation_name":"is_a","term_name":"amyloidosis, hereditary systemic 1","termid":"MONDO:0971004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0021179"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005244","MONDO:0005267","MONDO:0021179"],"is_obsolete":false,"name":"ATTRV122I amyloidosis","secondary_identifiers":["icd11.foundation:1449168185","ICD10EXP:E85.4+","MEDGEN:907865","SCTID:715655000","GARD:16755","UMLS:C4275067","ICD10EXP:I43.1*"],"synonyms":[{"name":"ATTRV122I-related amyloidosis","type":"exact"}],"termid":"MONDO:0019441","xrefs":{"Monarch":{"xref_id":"0019441"}}}


id: GO:0102542
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: aclacinomycin A + H2O = 15-demethoxy-aclacinomycin A + methanol + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete aclacinomycin A methylesterase activity (obsolete GO:0102542)","termid":"GO:0102542"}


id: GO:2000428
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of neutrophil aggregation.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of leukocyte cell-cell adhesion","termid":"GO:1903037"},{"relation_name":"regulates","term_name":"neutrophil aggregation","termid":"GO:0070488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"regulation of neutrophil aggregation","synonyms":[{"name":"regulation of neutrocyte aggregation","type":"exact"},{"name":"regulation of neutrophil leucocyte aggregation","type":"exact"},{"name":"regulation of neutrophilic leukocyte aggregation","type":"exact"}],"termid":"GO:2000428"}


id: GO:1900162
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of phospholipid scramblase activity.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of phospholipid scramblase activity (obsolete GO:1900162)","synonyms":[{"name":"down regulation of phospholipid scramblase activity","type":"exact"},{"name":"down-regulation of phospholipid scramblase activity","type":"exact"},{"name":"downregulation of phospholipid scramblase activity","type":"exact"},{"name":"inhibition of phospholipid scramblase activity","type":"narrow"}],"termid":"GO:1900162"}


id: PBO:0052853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 4-9","termid":"PBO:0052853"}


id: MONDO:0041447
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The spread of a malignant neoplasm to the colon. This may be from a primary large intestine malignant neoplasm, or from a malignant neoplasm at a distant site.","definition_xrefs":["NCIT:C8411"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"malignant colon neoplasm","termid":"MONDO:0021063"},{"relation_name":"is_a","term_name":"metastatic malignant neoplasm","termid":"MONDO:0024880"}],"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":"metastatic malignant neoplasm in the colon","secondary_identifiers":["UMLS:C0346974","MEDGEN:83432"],"synonyms":[{"name":"metastatic malignant neoplasm in the colon","type":"exact"},{"name":"metastatic malignant neoplasm to the colon","type":"exact"},{"name":"metastatic neoplasm to the colon","type":"exact"},{"name":"metastatic tumor to the colon","type":"exact"},{"name":"metastatic tumour to the colon","type":"exact"}],"termid":"MONDO:0041447","xrefs":{"Monarch":{"xref_id":"0041447"}}}


id: GO:0042531
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the introduction of a phosphate group to a tyrosine residue of a STAT (Signal Transducer and Activator of Transcription) protein.","definition_xrefs":["PMID:11426647","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of tyrosine phosphorylation of STAT protein","termid":"GO:0042509"},{"relation_name":"is_a","term_name":"positive regulation of peptidyl-tyrosine phosphorylation","termid":"GO:0050731"},{"relation_name":"positively_regulates","term_name":"tyrosine phosphorylation of STAT protein","termid":"GO:0007260"}],"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 tyrosine phosphorylation of STAT protein","secondary_identifiers":["GO:0042515","GO:0042523","GO:0042526","GO:0042511","GO:0042517","GO:0042520","GO:0042529"],"synonyms":[{"name":"activation of tyrosine phosphorylation of STAT protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat1 protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat2 protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat3 protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat4 protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat5 protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat6 protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat7 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat1 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat2 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat3 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat4 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat5 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat6 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat7 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of STAT protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat1 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat2 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat3 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat4 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat5 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat6 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat7 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of STAT protein","type":"exact"},{"name":"up regulation of tyrosine phosphorylation of Stat1 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of Stat2 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of Stat3 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of Stat4 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of Stat5 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of Stat6 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of Stat7 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of STAT protein","type":"exact"},{"name":"up-regulation of tyrosine phosphorylation of Stat1 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of Stat2 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of Stat3 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of Stat4 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of Stat5 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of Stat6 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of Stat7 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of STAT protein","type":"exact"},{"name":"upregulation of tyrosine phosphorylation of Stat1 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of Stat2 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of Stat3 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of Stat4 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of Stat5 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of Stat6 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of Stat7 protein","type":"narrow"}],"termid":"GO:0042531"}


id: PR:Q9USP9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rmn1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9USP9"],"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 RNA-binding protein C902.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC902.04","synonyms":[{"name":"Spom972h-rmn1","type":"exact"}],"termid":"PR:Q9USP9"}


id: GO:0002604
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of dendritic cell antigen processing and presentation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of antigen processing and presentation","termid":"GO:0002577"},{"relation_name":"regulates","term_name":"dendritic cell antigen processing and presentation","termid":"GO:0002468"}],"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 dendritic cell antigen processing and presentation","termid":"GO:0002604"}


id: PBO:0066141
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RB associated KRAB zinc finger","termid":"PBO:0066141"}


id: GO:0160143
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: uridine(2819) in 21S rRNA = pseudouridine(2819) in 21S rRNA.","definition_xrefs":["RHEA:42556","EC:5.4.99.43"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA pseudouridine synthase activity","termid":"GO:0120159"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0003824","GO:0016853","GO:0003674","GO:0140098"],"is_obsolete":false,"name":"21S rRNA pseudouridine(2819) synthase activity","termid":"GO:0160143"}


id: MONDO:0006727
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Heart failure caused by abnormal myocardial relaxation during diastole leading to defective cardiac filling.","definition_xrefs":["MESH:D054144"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congestive heart failure","termid":"MONDO:0005009"}],"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":"diastolic heart failure","secondary_identifiers":["EFO:1000899","MedDRA:10069211","UMLS:C1135196","ICD9:428.30","MEDGEN:210051","DOID:9775","ICD9:428.3","SCTID:418304008"],"termid":"MONDO:0006727","xrefs":{"Monarch":{"xref_id":"0006727"}}}


id: PBO:0003180
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BRCT domain protein Brc1","termid":"PBO:0003180"}


id: GO:0001974
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The reorganization or renovation of existing blood vessels.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue remodeling","termid":"GO:0048771"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"blood vessel remodeling","synonyms":[{"name":"blood vessel remodelling","type":"exact"}],"termid":"GO:0001974"}


id: GO:0075312
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of sporangium development, a process that leads to the formation of sporangium, a single-celled or many-celled structure in which spores are produced, as in fungi, algae, mosses, and ferns, gymnosperms, angiosperms.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of spore-bearing organ development","termid":"GO:0075262"},{"relation_name":"is_a","term_name":"regulation of sporangium development","termid":"GO:0075310"},{"relation_name":"negatively_regulates","term_name":"sporangium development","termid":"GO:0043582"}],"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 sporangium development","termid":"GO:0075312"}


id: GO:0050221
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (5Z,13E)-(15S)-9-alpha,11-alpha,15-trihydroxyprosta-5,13-dienoate + NADP+ = (5Z,13E)-(15S)-11-alpha,15-dihydroxy-9-oxoprosta-5,13-dienoate + NADPH.","definition_xrefs":["EC:1.1.1.189","MetaCyc:PROSTAGLANDIN-E2-9-REDUCTASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"prostaglandin E2 9-reductase activity","secondary_identifiers":["Reactome:R-HSA-2161651","RHEA:24508"],"synonyms":[{"name":"(5Z,13E)-(15S)-9alpha,11alpha,15-trihydroxyprosta-5,13-dienoate:NADP+ 9-oxidoreductase activity","type":"related"},{"name":"9-keto-prostaglandin E(2) reductase activity","type":"related"},{"name":"9-keto-prostaglandin E2 reductase activity","type":"related"},{"name":"9-ketoprostaglandin reductase activity","type":"related"},{"name":"PGE(2) 9-ketoreductase activity","type":"related"},{"name":"PGE(2) 9-oxoreductase activity","type":"related"},{"name":"PGE-9-ketoreductase activity","type":"related"},{"name":"PGE2 9-ketoreductase activity","type":"related"},{"name":"PGE2 9-oxoreductase activity","type":"related"},{"name":"PGE2-9-OR","type":"related"},{"name":"PGE2-9-ketoreductase activity","type":"related"},{"name":"prostaglandin E 9-ketoreductase activity","type":"related"},{"name":"prostaglandin E2-9-oxoreductase activity","type":"related"},{"name":"prostaglandin-E(2) 9-oxoreductase activity","type":"related"},{"name":"prostaglandin-E2 9-oxoreductase activity","type":"related"},{"name":"reductase, 15-hydroxy-9-oxoprostaglandin","type":"related"}],"termid":"GO:0050221"}


id: PBO:0067674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 856, pseudogene","termid":"PBO:0067674"}


id: PBO:0029579
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_cellular_reactive_oxygen_species_level","termid":"PBO:0029579"}


id: MONDO:0007917
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lymphedema-cerebral arteriovenous anomaly syndrome is characterized by the variable association of a cerebrovascular malformation, foot lymphoedema and primary pulmonary hypertension. It has been described in a woman and four of her children.","definition_xrefs":["Orphanet:86914"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lymphedema-cerebral arteriovenous anomaly syndrome","secondary_identifiers":["MESH:C563612","MEDGEN:322617","UMLS:C1835272","GARD:9217","OMIM:152900"],"synonyms":[{"name":"lymphedema and cerebral arteriovenous anomaly","type":"related"},{"name":"primary pulmonary hypertension, cerebrovascular malformation and lymphedema feet","type":"related"}],"termid":"MONDO:0007917","xrefs":{"Monarch":{"xref_id":"0007917"}}}


id: PBO:0054621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 2026","termid":"PBO:0054621"}


id: PBO:0065304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine protease 21","termid":"PBO:0065304"}


id: MONDO:0015111
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete gastroesophageal disease (obsolete MONDO:0015111)","secondary_identifiers":["Orphanet:101936"],"termid":"MONDO:0015111","xrefs":{"Monarch":{"xref_id":"0015111"}}}


id: MONDO:0015820
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"primary cutaneous lymphoma","termid":"MONDO:0018898"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093","MONDO:0005570"],"is_obsolete":false,"name":"primary cutaneous B-cell lymphoma","secondary_identifiers":["SCTID:402881008","NCIT:C6858","GARD:20165","Orphanet:178563","MEDGEN:697651","UMLS:C1274310","ICD9:202.80"],"termid":"MONDO:0015820","xrefs":{"Monarch":{"xref_id":"0015820"}}}


id: GO:0090111
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of COPII vesicle uncoating, the process in which COPII vesicle coat proteins are disassembled, and released.","definition_xrefs":["GOC:tb","GOC:dph","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein depolymerization","termid":"GO:1901879"},{"relation_name":"regulates","term_name":"COPII vesicle uncoating","termid":"GO:0090112"}],"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 COPII vesicle uncoating","termid":"GO:0090111"}


id: PATO:0002308
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A triangular quality inhering in a bearer by virtue of the bearer's having all sides of unequal length.","definition_xrefs":["PATOC:JB"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triangular","termid":"PATO:0001875"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scalene triangular","termid":"PATO:0002308"}


id: GO:0102217
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: n ATP + n H2O + a 6-phosphogluco-maltodextrin = n AMP + n hydrogenphosphate + a poly-6-phosphogluco-maltodextrin.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 6-phosphoglucan, water dikinase activity (obsolete GO:0102217)","termid":"GO:0102217"}


id: MONDO:0001934
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete primary hypertrophic osteoarthropathy (obsolete MONDO:0001934)","termid":"MONDO:0001934","xrefs":{"Monarch":{"xref_id":"0001934"}}}


id: GO:0034571
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4'-(2-hydroxyisopropyl)phenylurea + H2O = 4'-(2-hydroxyisopropyl)phenylaniline + carbamic acid.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 4'-(2-hydroxyisopropyl)phenylurea amidohydrolase activity (obsolete GO:0034571)","termid":"GO:0034571"}


id: MONDO:0007007
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with bacteria of the genus ureaplasma.","definition_xrefs":["MESH:D016869"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urethritis","termid":"MONDO:0005297"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ureaplasma urethritis","secondary_identifiers":["EFO:1001225","UMLS:C0854510","MEDGEN:1843394","SCTID:51105006"],"synonyms":[{"name":"Ureaplasma caused disease or disorder","type":"exact"},{"name":"Ureaplasma disease or disorder","type":"exact"},{"name":"Ureaplasma infection","type":"related"},{"name":"Ureaplasma infectious disease","type":"exact"},{"name":"infection, Ureaplasma","type":"related"},{"name":"infections, Ureaplasma","type":"related"}],"termid":"MONDO:0007007","xrefs":{"Monarch":{"xref_id":"0007007"}}}


id: SO:0000473
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The gene product is involved in its own transcriptional regulation where it decreases transcription.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcriptionally_repressed","termid":"SO:0000126"},{"relation_name":"is_a","term_name":"autoregulated","termid":"SO:0000471"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"negatively_autoregulated","synonyms":[{"name":"negatively autoregulated","type":"exact"}],"termid":"SO:0000473"}


id: PBO:0040111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ASAP1 intronic transcript 2","termid":"PBO:0040111"}


id: GO:2000386
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ovarian follicle development.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"regulation of ovarian follicle development","termid":"GO:2000354"},{"relation_name":"positively_regulates","term_name":"ovarian follicle development","termid":"GO:0001541"}],"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 ovarian follicle development","synonyms":[{"name":"positive regulation of follicular phase","type":"related"}],"termid":"GO:2000386"}


id: FYPO:0004725
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the nuclear envelope has one or more extensions that protrude into the cytoplasm during interphase of the mitotic cell cycle.","definition_xrefs":["PMID:15772152","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear envelope morphology during vegetative growth","termid":"FYPO:0000769"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002403","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"nuclear envelope protrusion present during mitotic interphase","synonyms":[{"name":"nuclear envelope deformation during mitotic interphase","type":"related"},{"name":"nuclear envelope protrusion present during interphase","type":"exact"},{"name":"nuclear envelope protrusion present during interphase during mitotic cell cycle","type":"related"},{"name":"nuclear envelope protrusion present during interphase during vegetative growth","type":"exact"},{"name":"protruding nuclear envelope during mitotic interphase","type":"exact"}],"termid":"FYPO:0004725"}


id: PBO:0015263
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RDRC and RITS complexes associate together, and with noncoding centromeric RNA in a Dcr1 (hence siRNA) and Clr4 dependent manner","termid":"PBO:0015263"}


id: GO:1904328
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of myofibroblast contraction.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:19239477"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin filament-based movement","termid":"GO:1903115"},{"relation_name":"regulates","term_name":"myofibroblast contraction","termid":"GO:1990764"}],"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 myofibroblast contraction","synonyms":[{"name":"regulation of MF contraction","type":"exact"},{"name":"regulation of MFB contraction","type":"exact"}],"termid":"GO:1904328"}


id: GO:0001720
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification process that results in the conversion of lysine, carried by a specialized lysine-accepting tRNA (possessing a CUA anticodon), to pyrrolysine (a lysine with an amide linkage to a (4R,5R)-4-substituted pyrroline-5-carboxylate).","definition_xrefs":["PMID:12029131","PMID:12029132","PMID:12121639"],"direct_ancestors":[{"relation_name":"is_a","term_name":"charged-tRNA amino acid modification","termid":"GO:0019988"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0010467","GO:0006399","GO:0008150"],"is_obsolete":false,"name":"conversion of lysyl-tRNA to pyrrolysyl-tRNA","termid":"GO:0001720"}


id: PBO:0088804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell wall and ascospore endo-1,3-beta-glucanase Eng2","termid":"PBO:0088804"}


id: MONDO:0016831
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"melanocytic nevus","termid":"MONDO:0005073"}],"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":"linear verrucous nevus syndrome","secondary_identifiers":["UMLS:C5679838","Orphanet:2611","GARD:3259","MEDGEN:1806291"],"synonyms":[{"name":"linear hamartoma syndrome","type":"exact"}],"termid":"MONDO:0016831","xrefs":{"Monarch":{"xref_id":"0016831"}}}


id: PBO:0110326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALDOC antisense RNA 1","termid":"PBO:0110326"}


id: GO:0033347
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a tetrose, any monosaccharide with a chain of four carbon atoms in the molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monosaccharide metabolic process","termid":"GO:0005996"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0005975","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"tetrose metabolic process","synonyms":[{"name":"tetrose metabolism","type":"exact"}],"termid":"GO:0033347"}


id: MONDO:0009201
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":"facial abnormalities, kyphoscoliosis, and intellectual disability","secondary_identifiers":["OMIM:227250","UMLS:C1856893","MEDGEN:347325","MESH:C565580"],"synonyms":[{"name":"facial abnormalities, kyphoscoliosis, and intellectual disability","type":"exact"},{"name":"facial abnormalities, kyphoscoliosis, and mental retardation","type":"exact"}],"termid":"MONDO:0009201","xrefs":{"Monarch":{"xref_id":"0009201"}}}


id: GO:0061978
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of mandibular joint condyle articular cartilage over time, from its formation to the mature structure.","definition_xrefs":["PMID:20679519"],"direct_ancestors":[{"relation_name":"is_a","term_name":"temporomandibular joint articular cartilage development","termid":"GO:0061976"}],"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":"mandibular condyle articular cartilage development","termid":"GO:0061978"}


id: GO:0097094
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which any suture between cranial and/or facial bones is generated and organized.","definition_xrefs":["Wikipedia:Cranial_sutures","GOC:pr","Wikipedia:Head_and_neck_anatomy#Musculoskeletal_system","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"bone morphogenesis","termid":"GO:0060349"},{"relation_name":"part_of","term_name":"cranial skeletal system development","termid":"GO:1904888"}],"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":"craniofacial suture morphogenesis","termid":"GO:0097094"}


id: PBO:0112692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome-b5 reductase activity/ NAD(P)H-dependent reductase for Dph3, Cbr1","termid":"PBO:0112692"}


id: GO:0080034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in the state or activity of a host cell or organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of the formation of an abnormal mass of cells in the host organism, induced by a symbiont. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:18836040"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to symbiont","termid":"GO:0009608"}],"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":"host response to induction by symbiont of tumor, nodule or growth in host","termid":"GO:0080034"}


id: PBO:0082567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chaperone that facilitates the assembly of cytochrome c oxidase; integral to the mitochondrial inner membrane; interacts with a subcomplex of subunits VII, VIIa, and VIII (Cox7p, Cox9p, and Cox8p) but not with the holoenzyme","termid":"PBO:0082567"}


id: PBO:0114671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial dihydrolipoamide S-acetyltransferase (e3 component), Lat1","termid":"PBO:0114671"}


id: GO:0047338
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: alpha-D-xylose 1-phosphate + UTP = UDP-D-xylose + diphosphate.","definition_xrefs":["EC:2.7.7.11","MetaCyc:2.7.7.11-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UTP-monosaccharide-1-phosphate uridylyltransferase activity","termid":"GO:0051748"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016779"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016779","GO:0016740"],"is_obsolete":false,"name":"UTP:xylose-1-phosphate uridylyltransferase activity","secondary_identifiers":["RHEA:18389"],"synonyms":[{"name":"UDP-xylose pyrophosphorylase activity","type":"related"},{"name":"UTP-xylose-1-phosphate uridylyltransferase activity","type":"related"},{"name":"UTP:alpha-D-xylose-1-phosphate uridylyltransferase activity","type":"related"},{"name":"uridine diphosphoxylose pyrophosphorylase activity","type":"related"},{"name":"uridylyltransferase, xylose 1-phosphate","type":"related"},{"name":"xylose 1-phosphate uridylyltransferase activity","type":"related"},{"name":"xylose-1-phosphate uridylyltransferase activity","type":"related"}],"termid":"GO:0047338"}


id: GO:0051186
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving a cofactor, a substance that is required for the activity of an enzyme or other protein. Cofactors may be inorganic, such as the metal atoms zinc, iron, and copper in certain forms, or organic, in which case they are referred to as coenzymes. Cofactors may either be bound tightly to active sites or bind loosely with the substrate.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete cofactor metabolic process (obsolete GO:0051186)","synonyms":[{"name":"cofactor metabolism","type":"exact"}],"termid":"GO:0051186"}


id: PBO:0047809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box L3","termid":"PBO:0047809"}


id: FYPO:0006943
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of an 3'-5' RNA helicase activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal catalytic activity","termid":"FYPO:0000660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000654","FYPO:0000257"],"is_obsolete":false,"name":"normal 3'-5' RNA helicase activity","termid":"FYPO:0006943"}


id: GO:0010402
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving pectic arabinan, a polymer with an alpha-(1->5)-linked L-arabinofuranose (Araf) backbone that can be substituted with Araf-alpha-(1->2)-, Araf-alpha-(1->3)-, and/or Araf-alpha-(1->3)-Araf-alpha-(1->3)-side chains. Arabinan can be found as a side chain of the pectin rhamnogalacturonan I.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhamnogalacturonan I side chain metabolic process","termid":"GO:0010400"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0071554","GO:0008150","GO:0005975"],"is_obsolete":false,"name":"pectic arabinan metabolic process","synonyms":[{"name":"pectic arabinan metabolism","type":"exact"}],"termid":"GO:0010402"}


id: GO:1904299
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of transcytosis.","definition_xrefs":["GOC:TermGenie","PMID:9664076","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"negative regulation of transport","termid":"GO:0051051"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of transcytosis","termid":"GO:1904298"},{"relation_name":"negatively_regulates","term_name":"transcytosis","termid":"GO:0045056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"negatively_regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"negative regulation of transcytosis","synonyms":[{"name":"down regulation of transcytosis","type":"exact"},{"name":"down-regulation of transcytosis","type":"exact"},{"name":"downregulation of transcytosis","type":"exact"},{"name":"inhibition of transcytosis","type":"narrow"}],"termid":"GO:1904299"}


id: MONDO:0008481
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":"spondylosis, cervical","secondary_identifiers":["OMIM:184300","SCTID:387800004","MEDGEN:235174","UMLS:C1384641","EFO:0009610"],"synonyms":[{"name":"spondylosis, cervical","type":"exact"}],"termid":"MONDO:0008481","xrefs":{"Monarch":{"xref_id":"0008481"}}}


id: GO:0098616
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + H2SeO4 => diphosphate + adenylylselenate.","definition_xrefs":["PMID:2537056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylyltransferase activity","termid":"GO:0070566"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824","GO:0016779"],"is_obsolete":false,"name":"selenate adenylyltransferase (ATP) activity","secondary_identifiers":["Reactome:R-HSA-2408525"],"termid":"GO:0098616"}


id: PBO:0052024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"junctophilin 2","termid":"PBO:0052024"}


id: FYPO:0001764
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 posttranscriptional addition of methyl groups to the C48, C49, C60, C61 and C62 residues in a tRNA-Asp molecule, is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal tRNA methylation","termid":"FYPO:0001763"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001320","FYPO:0001312"],"is_obsolete":false,"name":"normal tRNA-Asp C48, C49, C60, C61 and C62 methylation","synonyms":[{"name":"normal tRNA-Asp C48, C49, C60, C61 and C62 methylation during mitotic cell cycle","type":"related"},{"name":"normal tRNA-Asp C48, C49, C60, C61 and C62 methylation during vegetative growth","type":"exact"},{"name":"normal tRNA-Asp methylation on C48, C49, C60, C61 and C62","type":"exact"}],"termid":"FYPO:0001764"}


id: PBO:0051304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 1/OR-2 (pseudogene)","termid":"PBO:0051304"}


id: PBO:0031051
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_metabolic_process_during_vegetative_growth","termid":"PBO:0031051"}


id: PBO:0030333
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_phosphoinositide_level","termid":"PBO:0030333"}


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


id: MONDO:0003215
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the apocrine sweat gland.","direct_ancestors":[{"relation_name":"is_a","term_name":"sweat gland cancer","termid":"MONDO:0002206"},{"relation_name":"is_a","term_name":"apocrine sweat gland neoplasm","termid":"MONDO:0003686"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"apocrine sweat gland cancer","secondary_identifiers":["NCIT:C6800","UMLS:C1334561","MEDGEN:277327","DOID:4934"],"synonyms":[{"name":"apocrine sweat gland cancer","type":"exact"},{"name":"cancer of apocrine sweat gland","type":"exact"},{"name":"malignant apocrine neoplasm","type":"exact"},{"name":"malignant apocrine neoplasm of skin","type":"exact"},{"name":"malignant apocrine neoplasm of the skin","type":"exact"},{"name":"malignant apocrine skin neoplasm","type":"exact"},{"name":"malignant apocrine skin tumor","type":"exact"},{"name":"malignant apocrine skin tumour","type":"exact"},{"name":"malignant apocrine sweat gland neoplasm","type":"exact"},{"name":"malignant apocrine tumor","type":"exact"},{"name":"malignant apocrine tumor of skin","type":"exact"},{"name":"malignant apocrine tumor of the skin","type":"exact"},{"name":"malignant apocrine tumour","type":"exact"},{"name":"malignant apocrine tumour of skin","type":"exact"},{"name":"malignant apocrine tumour of the skin","type":"exact"},{"name":"malignant neoplasm of apocrine sweat gland","type":"exact"}],"termid":"MONDO:0003215","xrefs":{"Monarch":{"xref_id":"0003215"}}}


id: MONDO:0013053
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type is a rare syndrome with cardiac malformations, characterized by prenatal-onset growth retardation (low birth weight and short stature), hypotonia, developmental delay and intellectual disability associated with microcephaly and craniofacial (low anterior hairline, hypotelorism, thick lips with carp-shaped mouth, high-arched palate, low-set ears), cardiac (conotruncal heart malformations such as tetralogy of Fallot) and skeletal (hypoplastic thumbs and first metacarpals) abnormalities.","definition_xrefs":["Orphanet:217026"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart disorder","termid":"MONDO:0005267"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type","secondary_identifiers":["MESH:C567850","OMIM:612946","SCTID:719395001","MEDGEN:414129","UMLS:C2751878","GARD:17116"],"synonyms":[{"name":"Hadziselimovic syndrome","type":"exact"},{"name":"microcephaly-faciocardioskeletal syndrome","type":"exact"}],"termid":"MONDO:0013053","xrefs":{"Monarch":{"xref_id":"0013053"}}}


id: MONDO:0016835
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"14q11.2 microduplication syndrome is a rare chromosomal anomaly characterized by developmental delay, mild to severe intellectual disability with speech impairment and epilepsy. Additionally, it may include dysmorphic features (such as hypo- or hypertelorism, dysplastic ears, short palpebral fissures), microcephaly or macrocephaly, behavioral abnormalities, stereotyped hand movements, ataxia, hypotonia, cleft palate.","definition_xrefs":["Orphanet:261229"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of the long arm of chromosome 14","termid":"MONDO:0016964"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"14q11.2 microduplication syndrome","secondary_identifiers":["GARD:20773","UMLS:C4749855","MEDGEN:1657429"],"synonyms":[{"name":"dup(14)(q11.2)","type":"exact"},{"name":"trisomy 14q11.2","type":"exact"}],"termid":"MONDO:0016835","xrefs":{"Monarch":{"xref_id":"0016835"}}}


id: GO:0106146
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of sideretin.","definition_xrefs":["PMID:29581584","GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coumarin biosynthetic process","termid":"GO:0009805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"sideretin biosynthesis","termid":"GO:0106146"}


id: MONDO:0002996
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A meningioma that affects the cavernous sinus.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skull base meningioma","termid":"MONDO:0002998"},{"relation_name":"is_a","term_name":"vein disorder","termid":"MONDO:0004634"},{"relation_name":"is_a","term_name":"blood vessel neoplasm","termid":"MONDO:0021080"},{"relation_name":"is_a","term_name":"vascular bone neoplasm","termid":"MONDO:0024499"},{"relation_name":"is_a","term_name":"neurovascular disorder","termid":"MONDO:0043218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cavernous sinus meningioma","secondary_identifiers":["DOID:4435","MEDGEN:232034","NCIT:C5268","UMLS:C1332865"],"synonyms":[{"name":"cavernous sinus meningioma (disease)","type":"exact"},{"name":"meningioma (disease) of cavernous sinus","type":"exact"},{"name":"meningioma of cavernous sinus","type":"exact"},{"name":"meningioma of the cavernous sinus","type":"exact"}],"termid":"MONDO:0002996","xrefs":{"Monarch":{"xref_id":"0002996"}}}


id: GO:0009968
data:
  {"annotated_genes":["SJAG_00424","SJAG_04455","SJAG_01114","SJAG_01386","SJAG_02000","SJAG_02765","SJAG_04551","SJAG_04522","SJAG_02336","SJAG_03893","SJAG_03974","SJAG_02426","SJAG_04910","SJAG_03501","SJAG_06270","SJAG_02379","SJAG_03355","SJAG_01464","SJAG_04206","SJAG_00610","SJAG_03508","SJAG_01253","SJAG_03089","SJAG_00526","SJAG_02392","SJAG_02514","SJAG_00289","SJAG_00991","SJAG_03072","SJAG_01142","SJAG_03799","SJAG_02481","SJAG_03678","SJAG_02451","SJAG_02233","SJAG_00457","SJAG_04259","SJAG_04825","SJAG_00293","SJAG_00824","SJAG_03185","SJAG_00990","SJAG_04249","SJAG_02858","SJAG_00229","SJAG_00266","SJAG_03681","SJAG_03592","SJAG_02169","SJAG_03263","SJAG_03486","SJAG_05000","SJAG_03353","SJAG_04462","SJAG_00883","SJAG_00642","SJAG_00209","SJAG_02311","SJAG_02013","SJAG_00975","SJAG_01679","SJAG_01245","SJAG_01184","SJAG_01297","SJAG_03126","SJAG_05346","SJAG_02231","SJAG_01790","SJAG_01983","SJAG_00875","SJAG_04943","SJAG_00169"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99914,108567,104210,112267,114572,114085,107546,116200,91062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902426"},{"annotations":[108282,116680,93092,92427,100762],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110034"},{"annotations":[101315,116428],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106057"},{"annotations":[104118,107363,107924,99765,118614,96184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903138"},{"annotations":[102461,103158,89777],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902660"},{"annotations":[88547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043409"},{"annotations":[94537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140499"},{"annotations":[92002,99767,117376,118615,95370,96304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903753"},{"annotations":[107452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180040"},{"annotations":[93668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090029"},{"annotations":[72514],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046580"},{"annotations":[71915],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035024"},{"annotations":[93185,99916,116203,93269,107413,93803,73126,107854,107548,95972,91066,105363,101595,110479,92071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031030"},{"annotations":[112021,106219,91578],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000639"},{"annotations":[73524],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032007"},{"annotations":[73936,103327,109983,80292,99202,99898,105454,109580,107464,114881,101772,118337,114280,88363,73957,116429,96430,93674,117340,116781,118529,113463],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904262"},{"annotations":[116574],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903940"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of signal transduction.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"is_a","term_name":"negative regulation of cell communication","termid":"GO:0010648"},{"relation_name":"is_a","term_name":"negative regulation of signaling","termid":"GO:0023057"},{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"negatively_regulates","term_name":"signal 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regulation of signal transduction","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0035467","Reactome:R-HSA-8849472"],"synonyms":[{"name":"down regulation of signal transduction","type":"exact"},{"name":"down-regulation of signal transduction","type":"exact"},{"name":"downregulation of signal transduction","type":"exact"},{"name":"inhibition of signal transduction","type":"narrow"},{"name":"negative regulation of signaling pathway","type":"related"},{"name":"negative regulation of signalling pathway","type":"related"}],"termid":"GO:0009968","terms_by_termid":{"GO:0031030":null,"GO:0032007":null,"GO:0035024":null,"GO:0043409":null,"GO:0046580":null,"GO:0090029":null,"GO:0106057":null,"GO:0110034":null,"GO:0140499":null,"GO:0180040":null,"GO:1902426":null,"GO:1902660":null,"GO:1903138":null,"GO:1903753":null,"GO:1903940":null,"GO:1904262":null,"GO:2000639":null}}


id: MONDO:0971011
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"MHC class I deficiency","termid":"MONDO:0011476"}],"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":"MHC class I deficiency 2","secondary_identifiers":["MEDGEN:1862135","UMLS:C5935617","OMIM:620813"],"termid":"MONDO:0971011","xrefs":{"Monarch":{"xref_id":"0971011"}}}


id: PBO:0058192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4485","termid":"PBO:0058192"}


id: PBO:0039089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angiotensin II receptor associated protein","termid":"PBO:0039089"}


id: PBO:0063578
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PERP pseudogene 1","termid":"PBO:0063578"}


id: PBO:0083705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER localized heme oxygenase; involved in heme degradation during iron starvation and in the oxidative stress response; expression is regulated by AFT1 and oxidative stress; relocates to the perinuclear region in the presence of oxidants","termid":"PBO:0083705"}


id: GO:1903314
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of nitrogen cycle metabolic process.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of metabolic process","termid":"GO:0019222"},{"relation_name":"regulates","term_name":"nitrogen cycle metabolic process","termid":"GO:0071941"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0071941"}],"interesting_parent_ids":["GO:0008150","GO:0071941"],"is_obsolete":false,"name":"regulation of nitrogen cycle metabolic process","termid":"GO:1903314"}


id: GO:2000990
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of hemicellulose catabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell wall polysaccharide catabolic process","termid":"GO:2000968"},{"relation_name":"is_a","term_name":"regulation of hemicellulose catabolic process","termid":"GO:2000988"},{"relation_name":"positively_regulates","term_name":"hemicellulose catabolic process","termid":"GO:2000895"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"positive regulation of hemicellulose catabolic process","synonyms":[{"name":"positive regulation of hemicellulose catabolism","type":"exact"}],"termid":"GO:2000990"}


id: GO:0007352
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specification of the dorsal/ventral axis of the embryo, through the products of genes expressed in the zygote.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic axis specification","termid":"GO:0000578"},{"relation_name":"is_a","term_name":"dorsal/ventral axis specification","termid":"GO:0009950"}],"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":"zygotic specification of dorsal/ventral axis","synonyms":[{"name":"zygotic determination of dorsal-ventral axis","type":"related"},{"name":"zygotic determination of dorsal/ventral axis","type":"related"},{"name":"zygotic determination of dorsoventral axis","type":"related"}],"termid":"GO:0007352"}


id: SO:1000110
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A mutation that reverts the sequence of a previous frameshift mutation back to the initial frame.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000110 frame_restoring_sequence_variant (obsolete SO:1000110)","synonyms":[{"name":"frame restoring mutation","type":"exact"},{"name":"frame restoring sequence variant","type":"exact"}],"termid":"SO:1000110"}


id: FYPO:0004857
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of glucan endo-1,6-beta-glucosidase 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 endo-1,6-beta-glucosidase activity","termid":"FYPO:0004856"}],"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:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000652","FYPO:0000661","FYPO:0000654","FYPO:0000707"],"is_obsolete":false,"name":"increased endo-1,6-beta-glucosidase activity","synonyms":[{"name":"increased glucan endo-1,6-beta-glucosidase activity","type":"exact"}],"termid":"FYPO:0004857"}


id: MONDO:0007046
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A keratosis of the hands and feet characterized by persistent, asymptomatic, yellowish to white papules and plaques associated with fine-textured scalp hair and an atopic diathesis.","definition_xrefs":["EFO:1000708"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"cholesteatoma","termid":"MONDO:0006530"},{"relation_name":"is_a","term_name":"keratosis","termid":"MONDO:0006566"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"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":"hereditary papulotranslucent acrokeratoderma","secondary_identifiers":["UMLS:C1863343","OMIM:101840","DOID:0060360","MEDGEN:350144","MESH:C566323"],"synonyms":[{"name":"acrokeratoderma, hereditary papulotranslucent","type":"related"}],"termid":"MONDO:0007046","xrefs":{"Monarch":{"xref_id":"0007046"}}}


id: GO:0039711
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The assembly of a helical viral capsid in the cytoplasm. Occurs by assembling around the viral genome.","definition_xrefs":["VZ:1950"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic capsid assembly","termid":"GO:0039709"}],"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":"cytoplasmic helical capsid assembly","termid":"GO:0039711"}


id: MONDO:0022740
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":"Christian Johnson angenieta syndrome","termid":"MONDO:0022740","xrefs":{"Monarch":{"xref_id":"0022740"}}}


id: GO:1901871
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of ecgonone methyl ester.","definition_xrefs":["GOC:TermGenie","PMID:22665766"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkaloid catabolic process","termid":"GO:0009822"},{"relation_name":"is_a","term_name":"ketone catabolic process","termid":"GO:0042182"},{"relation_name":"is_a","term_name":"ecgonone methyl ester metabolic process","termid":"GO:1901870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"ecgonone methyl ester catabolic process","synonyms":[{"name":"ecgonone methyl ester breakdown","type":"exact"},{"name":"ecgonone methyl ester catabolism","type":"exact"},{"name":"ecgonone methyl ester degradation","type":"exact"}],"termid":"GO:1901871"}


id: PBO:0085455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Potassium transporter that mediates K+ influx; activates high-affinity Ca2+ influx system (HACS) during mating pheromone response; expression up-regulated in response to alpha factor; localized to sites of polarized growth; member of a fungal-specific gene family; potential Cdc28p substrate; KCH1 has a paralog, PRM6, that arose from the whole genome duplication","termid":"PBO:0085455"}


id: GO:0034283
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 9-alpha-copalyl diphosphate = stemod-13(17)-ene + diphosphate.","definition_xrefs":["RHEA:25556"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"syn-stemod-13(17)-ene synthase activity","secondary_identifiers":["EC:4.2.3.34","KEGG_REACTION:R09116","MetaCyc:RXN-9291"],"synonyms":[{"name":"9alpha-copalyl-diphosphate diphosphate-lyase [stemod-13(17)-ene-forming] activity","type":"exact"},{"name":"exo-stemodene synthase activity","type":"exact"},{"name":"stemod-13(17)-ene synthase activity","type":"exact"},{"name":"stemodene synthase activity","type":"exact"},{"name":"syn-stemodene synthase activity","type":"exact"}],"termid":"GO:0034283"}


id: PBO:0055981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat neuronal 4","termid":"PBO:0055981"}


id: GO:0046209
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving nitric oxide, nitrogen monoxide (NO), a colorless gas only slightly soluble in water.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reactive nitrogen species metabolic process","termid":"GO:2001057"}],"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":"nitric oxide metabolic process","secondary_identifiers":["Reactome:R-HSA-202131"],"synonyms":[{"name":"nitric oxide metabolism","type":"exact"}],"termid":"GO:0046209"}


id: PBO:0078948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon TCG) 6-1","termid":"PBO:0078948"}


id: PBO:0049341
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIi","termid":"PBO:0049341"}


id: GO:0018052
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The formation of a C-terminal peptidyl-tyrosine amide by hydrolysis and oxidation of an interior Tyr-Gly peptide in a secreted protein.","definition_xrefs":["RESID:AA0099"],"gene_count":0,"genotype_count":0,"name":"obsolete C-terminal peptidyl-tyrosine amidation (obsolete GO:0018052)","termid":"GO:0018052"}


id: PBO:0067428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 547, pseudogene","termid":"PBO:0067428"}


id: GO:0048249
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of phosphate from one side of a membrane to the other. In high-affinity transport the transporter is able to bind the solute even if it is only present at very low concentrations.","definition_xrefs":["PMID:8709965","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphate transmembrane transporter activity","termid":"GO:0005315"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"high-affinity phosphate transmembrane transporter activity","synonyms":[{"name":"high affinity phosphate transmembrane transporter activity","type":"exact"}],"termid":"GO:0048249"}


id: GO:0007031
data:
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id: GO:0030003
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id: GO:2000306
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id: PBO:0013006
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id: GO:0061952
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id: GO:0019240
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id: PBO:0090385
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id: MONDO:0021259
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id: PBO:0036299
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id: PBO:0001828
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id: MONDO:0975754
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id: PBO:0047251
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 239 member B","termid":"PBO:0047251"}


id: GO:1901772
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id: PBO:0058237
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id: MONDO:0005564
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id: PBO:0074617
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id: MONDO:0015498
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id: PBO:0074676
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id: PBO:0031425
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id: PBO:0092018
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Leucine (uaa), mitochondrial","termid":"PBO:0092018"}


id: MONDO:0018234
data:
  {"annotated_genes":["SJAG_02165","SJAG_02431","SJAG_00197","SJAG_00322","SJAG_03144","SJAG_04270","SJAG_00539","SJAG_00414","SJAG_04825","SJAG_01852","SJAG_02200","SJAG_04092","SJAG_03703","SJAG_04995","SJAG_03249","SJAG_00504","SJAG_03484"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85476],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014651"},{"annotations":[86493,86494],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013895"},{"annotations":[85964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008726"},{"annotations":[85439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020667"},{"annotations":[85370],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014700"},{"annotations":[85787],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014558"},{"annotations":[85893,85894],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009039"},{"annotations":[86668,86669],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012137"},{"annotations":[86079,86080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958175"},{"annotations":[86760],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011640"},{"annotations":[86965],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013740"},{"annotations":[86327],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012516"},{"annotations":[85533],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007943"},{"annotations":[85756],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009903"},{"annotations":[85916,85917],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009955"},{"annotations":[87436],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010121"}]},"cv_name":"mondo","definition":"A group of disorders in which the skeletal involvement is predominantly manifested as abnormalities of individual bones or in a group of bones.","direct_ancestors":[{"relation_name":"is_a","term_name":"bone development disease","termid":"MONDO:0005497"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00197":null,"SJAG_00322":null,"SJAG_00414":null,"SJAG_00504":null,"SJAG_00539":null,"SJAG_01852":null,"SJAG_02165":null,"SJAG_02200":null,"SJAG_02431":null,"SJAG_03144":null,"SJAG_03249":null,"SJAG_03484":null,"SJAG_03703":null,"SJAG_04092":null,"SJAG_04270":null,"SJAG_04825":null,"SJAG_04995":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"dysostosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:21571","MEDGEN:4430","DOID:1934","MESH:D004413","NCIT:C34560","SCTID:109420003","Orphanet:364559","ICD9:756.9","UMLS:C0013393"],"synonyms":[{"name":"dysostosis","type":"exact"}],"termid":"MONDO:0018234","terms_by_termid":{"MONDO:0007943":null,"MONDO:0008726":null,"MONDO:0009039":null,"MONDO:0009903":null,"MONDO:0009955":null,"MONDO:0010121":null,"MONDO:0011640":null,"MONDO:0012137":null,"MONDO:0012516":null,"MONDO:0013740":null,"MONDO:0013895":null,"MONDO:0014558":null,"MONDO:0014651":null,"MONDO:0014700":null,"MONDO:0020667":null,"MONDO:0958175":null},"xrefs":{"Monarch":{"xref_id":"0018234"}}}


id: GO:1902346
data:
  {"annotated_genes":["SJAG_02294"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[100968],"is_not":false,"summary":null,"term":"GO:1902346"}]},"cv_name":"biological_process","definition":"Any meiotic strand displacement that is involved in double-strand break repair via synthesis-dependent strand annealing (SDSA).","definition_xrefs":["GOC:TermGenie","PMID:22723423","GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic strand displacement","termid":"GO:0000714"},{"relation_name":"part_of","term_name":"double-strand break repair via synthesis-dependent strand annealing","termid":"GO:0045003"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02294":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006310"}],"interesting_parent_ids":["GO:0007049","GO:0006281","GO:0008150","GO:0006310","GO:0006259"],"is_obsolete":false,"name":"meiotic strand displacement involved in double-strand break repair via SDSA","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"meiotic D-loop dissociation involved in double-strand break repair via synthesis-dependent strand annealing","type":"related"},{"name":"meiotic D-loop dissociation involved in mitotic gene conversion","type":"related"},{"name":"meiotic D-loop processing involved in double-strand break repair via synthesis-dependent strand annealing","type":"related"},{"name":"meiotic D-loop processing involved in mitotic gene conversion","type":"related"},{"name":"meiotic displacement loop dissociation involved in double-strand break repair via synthesis-dependent strand annealing","type":"related"},{"name":"meiotic displacement loop dissociation involved in mitotic gene conversion","type":"related"},{"name":"meiotic displacement loop processing involved in double-strand break repair via synthesis-dependent strand annealing","type":"related"},{"name":"meiotic displacement loop processing involved in mitotic gene conversion","type":"related"},{"name":"meiotic strand displacement involved in SDSA","type":"broad"},{"name":"meiotic strand displacement involved in double-strand break repair via synthesis-dependent strand annealing","type":"exact"},{"name":"meiotic strand displacement involved in mitotic gene conversion","type":"related"}],"termid":"GO:1902346","terms_by_termid":{"GO:1902346":null}}


id: PBO:0053558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 566","termid":"PBO:0053558"}


id: PBO:0061352
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleophosmin 1 pseudogene 10","termid":"PBO:0061352"}


id: PR:O74442
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ubp16 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74442"],"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":"ubiquitin carboxyl-terminal hydrolase 16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1682.12c","synonyms":[{"name":"Spom972h-ubp16","type":"exact"},{"name":"deubiquitinating enzyme 16 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin thioesterase 16 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin-specific-processing protease 16 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74442"}


id: PBO:0061118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NLR family pyrin domain containing 8","termid":"PBO:0061118"}


id: PBO:0064401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pancreatic lipase","termid":"PBO:0064401"}


id: GO:0043172
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of ferredoxin, any simple, nonenzymatic iron-sulfur protein that is characterized by having equal numbers of atoms of iron and labile sulfur. Iron and sulfur atoms are present in one or two clusters of two or four atoms of each.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete ferredoxin biosynthetic process (obsolete GO:0043172)","synonyms":[{"name":"ferredoxin anabolism","type":"exact"},{"name":"ferredoxin biosynthesis","type":"exact"},{"name":"ferredoxin formation","type":"exact"},{"name":"ferredoxin synthesis","type":"exact"}],"termid":"GO:0043172"}


id: MONDO:1010646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hemophilia B that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemophilia B, non-human animal","termid":"MONDO:1010075"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemophilia B, pig","secondary_identifiers":["OMIA:000438-9823"],"termid":"MONDO:1010646","xrefs":{"Monarch":{"xref_id":"1010646"}}}


id: MONDO:0005367
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Physical and psychological dependence on the drug heroin.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"opiate dependence","termid":"MONDO:0005530"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heroin dependence","secondary_identifiers":["UMLS:C0019337","EFO:0004240","DOID:9976","icd11.foundation:443161089","MEDGEN:5532","SCTID:231477003","NCIT:C34694","MESH:D006556"],"synonyms":[{"name":"Heroin addiction","type":"exact"}],"termid":"MONDO:0005367","xrefs":{"Monarch":{"xref_id":"0005367"}}}


id: MONDO:0016559
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Glaucoma secondary to spherophakia/ectopia lentis and megalocornea is a rare, genetic, non-syndromic developmental defect of the eye disorder characterized by congenital megalocornea associated with spherophakia and/or ectopia lentis leading to pupillary block and secondary glaucoma. Additional features may include flat irides, iridodonesis, axial myopia, very deep anterior chambers, miotic, oval pupils without well-defined borders, ocular pain and irritability manifesting as conjunctival injection, corneal edema and central scarring, as well as a high arched palate.","definition_xrefs":["Orphanet:238763"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma","termid":"MONDO:0009633"},{"relation_name":"is_a","term_name":"hereditary glaucoma","termid":"MONDO:0018174"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"glaucoma secondary to spherophakia/ectopia lentis and megalocornea","secondary_identifiers":["UMLS:C5190883","MEDGEN:1674483","GARD:10942"],"synonyms":[{"name":"megalocornea-spherophakia-secondary glaucoma syndrome","type":"exact"}],"termid":"MONDO:0016559","xrefs":{"Monarch":{"xref_id":"0016559"}}}


id: PBO:0089412
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amino acid transmembrane transporter","termid":"PBO:0089412"}


id: FYPO:0007825
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of protein measured in a cell during a cellular response to amino acid starvation is lower than normal. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah","PMID:33534698"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein level during vegetative growth","termid":"FYPO:0001324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0006551","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"decreased protein level during cellular response to amino acid starvation","synonyms":[{"name":"decreased protein accumulation during cellular response to amino acid starvation","type":"related"},{"name":"decreased protein level during cellular response to amino acid starvation during mitotic cell cycle","type":"related"},{"name":"decreased protein level during cellular response to amino acid starvation during vegetative growth","type":"exact"},{"name":"reduced protein level during cellular response to amino acid starvation","type":"exact"}],"termid":"FYPO:0007825"}


id: PBO:0066365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinol dehydrogenase 8","termid":"PBO:0066365"}


id: PBO:0055276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 2703","termid":"PBO:0055276"}


id: PBO:0049526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2AZ1 divergent transcript","termid":"PBO:0049526"}


id: PBO:0078700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Leu (anticodon CAA) 2-1","termid":"PBO:0078700"}


id: SO:0000041
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An operation that can be applied to a sequence, that results in a change.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000041 sequence_operation (obsolete SO:0000041)","synonyms":[{"name":"sequence operation","type":"exact"}],"termid":"SO:0000041"}


id: PBO:0080857
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YES1 pseudogene 1","termid":"PBO:0080857"}


id: GO:0033856
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1-deoxy-D-xylulose 5-phosphate + 3-amino-2-oxopropyl phosphate = 2 H2O + H+ + phosphate + pyridoxine 5'-phosphate.","definition_xrefs":["RHEA:15265"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring nitrogenous groups","termid":"GO:0016769"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016769"],"is_obsolete":false,"name":"pyridoxine 5'-phosphate synthase activity","secondary_identifiers":["EC:2.6.99.2","MetaCyc:PDXJ-RXN","KEGG_REACTION:R05838"],"synonyms":[{"name":"1-deoxy-D-xylulose-5-phosphate:3-amino-2-oxopropyl phosphate 3-amino-2-oxopropyltransferase (phosphate-hydrolysing; cyclizing) activity","type":"related"},{"name":"PNP synthase activity","type":"related"},{"name":"pyridoxine 5-phosphate phospho lyase activity","type":"related"}],"termid":"GO:0033856"}


id: PBO:0041133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BTB domain containing 16","termid":"PBO:0041133"}


id: MOD:00555
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because Unimod entry 202 was merged with entry 195, remap to MOD:00548. modification from Unimod Chemical derivative","definition_xrefs":["Unimod:203"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:00555 APTA-d0 with quaternary amine loss (obsolete MOD:00555)","termid":"MOD:00555"}


id: MONDO:0020097
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Autosomal recessive form of disease with focal palmoplantar keratoderma as a major feature.","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"gene_count":0,"genotype_count":0,"name":"obsolete autosomal recessive disease with focal palmoplantar keratoderma as a major feature (obsolete MONDO:0020097)","secondary_identifiers":["Orphanet:98357"],"synonyms":[{"name":"autosomal recessive disease with focal palmoplantar hyperkeratosis as a major feature","type":"exact"},{"name":"disease with focal palmoplantar keratoderma as a major feature, autosomal recessive","type":"exact"}],"termid":"MONDO:0020097","xrefs":{"Monarch":{"xref_id":"0020097"}}}


id: PBO:0053105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"late cornified envelope pseudogene 4","termid":"PBO:0053105"}


id: PBO:0004196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial single stranded DNA specific 5'-3' exodeoxyribonuclease Exo5 (predicted)","termid":"PBO:0004196"}


id: PR:P40385
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rec6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P40385"],"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":"meiotic recombination protein rec6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC21B10.12","synonyms":[{"name":"Spom972h-rec6","type":"exact"}],"termid":"PR:P40385"}


id: PBO:0056523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane bound transcription factor peptidase, site 2","termid":"PBO:0056523"}


id: PBO:0050495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox B5","termid":"PBO:0050495"}


id: GO:2000350
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of signaling via the CD40 signaling pathway.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of signal transduction","termid":"GO:0009967"},{"relation_name":"is_a","term_name":"regulation of CD40 signaling pathway","termid":"GO:2000348"},{"relation_name":"positively_regulates","term_name":"CD40 signaling pathway","termid":"GO:0023035"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of CD40 signaling pathway","synonyms":[{"name":"positive regulation of CD40 signalling pathway","type":"exact"}],"termid":"GO:2000350"}


id: PBO:0038756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ACTR3B pseudogene 1","termid":"PBO:0038756"}


id: MONDO:0007610
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Gingival fibromatosis - hypertrichosis syndrome is a rare autosomal dominant disorder characterized by a generalized enlargement of the gingiva occurring at birth or during childhood that is associated with generalized hypertrichosis developing at birth, during the first years of life, or at puberty and predominantly affecting the face, upper limbs, and midback.","definition_xrefs":["Orphanet:2026"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertrichosis","termid":"MONDO:0019280"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"gingival fibromatosis-hypertrichosis syndrome","secondary_identifiers":["MEDGEN:342675","MESH:C565016","GARD:2324","SCTID:716008002","OMIM:135400","UMLS:C1851120"],"synonyms":[{"name":"CGHT","type":"exact"},{"name":"HTC3","type":"related"},{"name":"chromosome 17Q24.2-q24.3 Duplication syndrome","type":"related"},{"name":"chromosome 17Q24.2-q24.3 deletion syndrome","type":"related"},{"name":"congenital generalised hypertrichosis terminalis","type":"exact"},{"name":"congenital generalized hypertrichosis terminalis","type":"exact"},{"name":"extreme hirsutism with gingival fibromatosis","type":"related"},{"name":"fibromatosis, gingival, with hypertrichosis","type":"related"},{"name":"gingival fibromatosis with hypertrichosis","type":"related"},{"name":"hereditary gingival fibromatosis with hypertrichosis","type":"related"},{"name":"hirsutism-congenital gingival hyperplasia syndrome","type":"exact"},{"name":"hypertrichosis terminalis, generalized, with gingival hyperplasia","type":"related"},{"name":"hypertrichosis terminalis, generalized, with or without gingival hyperplasia","type":"related"},{"name":"hypertrichosis with or without gingival hyperplasia","type":"exact"},{"name":"hypertrichosis, congenital generalized, with gingival hyperplasia","type":"exact"},{"name":"hypertrichosis, congenital generalized, with or without gingival hyperplasia","type":"related"},{"name":"microdeletion 17Q24.2-q24.3 syndrome","type":"related"},{"name":"microduplication 17Q24.2-q24.3 syndrome","type":"related"}],"termid":"MONDO:0007610","xrefs":{"Monarch":{"xref_id":"0007610"}}}


id: PR:Q09895
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC24B11.08c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09895"],"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 C24B11.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC24B11.08c","synonyms":[{"name":"Spom972h-SPAC24B11.08c","type":"exact"}],"termid":"PR:Q09895"}


id: FYPO:0001076
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of a specific substance measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular physical quality phenotype","termid":"FYPO:0007723"}],"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:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal level of substance in cell","termid":"FYPO:0001076"}


id: GO:0060319
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Erythrocyte differentiation which occurs as part of the process of primitive hemopoiesis.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"erythrocyte differentiation","termid":"GO:0030218"},{"relation_name":"part_of","term_name":"primitive hemopoiesis","termid":"GO:0060215"}],"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":"primitive erythrocyte differentiation","synonyms":[{"name":"primitive RBC differentiation","type":"exact"},{"name":"primitive erythropoiesis","type":"exact"},{"name":"primitive red blood cell differentiation","type":"exact"}],"termid":"GO:0060319"}


id: SO:0000366
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The junction where an insertion occurred.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"junction","termid":"SO:0000699"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insertion_site","synonyms":[{"name":"insertion site","type":"exact"}],"termid":"SO:0000366"}


id: PBO:0059489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MSRB3 antisense RNA 1","termid":"PBO:0059489"}


id: GO:0075215
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of spore encystment on host. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell development","termid":"GO:0060284"},{"relation_name":"regulates","term_name":"spore encystment","termid":"GO:0075214"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"modulation of spore encystment on host","termid":"GO:0075215"}


id: GO:1901508
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of acylglycerol transport.","definition_xrefs":["GOC:sart","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of lipid transport","termid":"GO:0032370"},{"relation_name":"is_a","term_name":"regulation of acylglycerol transport","termid":"GO:1901506"},{"relation_name":"positively_regulates","term_name":"acylglycerol transport","termid":"GO:0034196"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of acylglycerol transport","synonyms":[{"name":"activation of acylglycerol transport","type":"narrow"},{"name":"activation of glyceride transport","type":"narrow"},{"name":"positive regulation of glyceride transport","type":"exact"},{"name":"up regulation of acylglycerol transport","type":"exact"},{"name":"up regulation of glyceride transport","type":"exact"},{"name":"up-regulation of acylglycerol transport","type":"exact"},{"name":"up-regulation of glyceride transport","type":"exact"},{"name":"upregulation of acylglycerol transport","type":"exact"},{"name":"upregulation of glyceride transport","type":"exact"}],"termid":"GO:1901508"}


id: GO:0009014
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-succinyl-LL-2,6-diaminopimelate + H2O = LL-2,6-diaminopimelate + succinate.","definition_xrefs":["RHEA:22608","EC:3.5.1.18"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016810"},{"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:0016810","GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"succinyl-diaminopimelate desuccinylase activity","secondary_identifiers":["KEGG_REACTION:R02734","MetaCyc:SUCCDIAMINOPIMDESUCC-RXN"],"synonyms":[{"name":"N-succinyl-L-alpha,epsilon-diaminopimelic acid deacylase activity","type":"related"},{"name":"N-succinyl-LL-2,6-diaminoheptanedioate amidohydrolase activity","type":"related"}],"termid":"GO:0009014"}


id: PBO:0038587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetyl-CoA carboxylase alpha","termid":"PBO:0038587"}


id: GO:0042363
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of any of a diverse group of vitamins that are soluble in organic solvents and relatively insoluble in water.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fat-soluble vitamin metabolic process","termid":"GO:0006775"},{"relation_name":"is_a","term_name":"vitamin catabolic process","termid":"GO:0009111"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006766"}],"interesting_parent_ids":["GO:0008150","GO:0006766","GO:0044281"],"is_obsolete":false,"name":"fat-soluble vitamin catabolic process","synonyms":[{"name":"fat-soluble vitamin breakdown","type":"exact"},{"name":"fat-soluble vitamin catabolism","type":"exact"},{"name":"fat-soluble vitamin degradation","type":"exact"}],"termid":"GO:0042363"}


id: PBO:0028638
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-meiotic_spindle_absent_from_cell_during_meiosis_II","termid":"PBO:0028638"}


id: MONDO:0017759
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of neurotransmitter metabolism and transport","termid":"MONDO:0019219"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"disorder of catecholamine synthesis","secondary_identifiers":["SCTID:237921002","UMLS:C0342685","Orphanet:309830","icd11.foundation:1382276026","GARD:21351","MEDGEN:575179","ICD9:270.8"],"termid":"MONDO:0017759","xrefs":{"Monarch":{"xref_id":"0017759"}}}


id: PBO:0031651
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_re-entry_into_mitotic_cell_cycle_after_pheromone_arrest","termid":"PBO:0031651"}


id: GO:1903103
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of potassium:proton antiporter activity.","definition_xrefs":["GOC:bhm","GOC:TermGenie","PMID:21041667","GO_REF:0000088"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter complex","termid":"GO:1902495"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"potassium:proton antiporter complex","termid":"GO:1903103"}


id: PBO:0015255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sir antagonist, ubiquitin-protein ligase E3","termid":"PBO:0015255"}


id: PBO:0064367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphomannomutase 1","termid":"PBO:0064367"}


id: PBO:0082158
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Adenine deaminase (adenine aminohydrolase); converts adenine to hypoxanthine; involved in purine salvage; transcriptionally regulated by nutrient levels and growth phase; Aah1p degraded upon entry into quiescence via SCF and the proteasome","termid":"PBO:0082158"}


id: GO:2000384
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of ectoderm development.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"regulation of ectoderm development","termid":"GO:2000383"},{"relation_name":"negatively_regulates","term_name":"ectoderm development","termid":"GO:0007398"}],"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 ectoderm development","termid":"GO:2000384"}


id: PBO:0036551
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secondary septum 1,6 branched 1,3-beta-glucan synthase catalytic subunit Bgs4","termid":"PBO:0036551"}


id: PBO:0083953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Gamma-tubulin; involved in nucleating microtubules from both the cytoplasmic and nuclear faces of the spindle pole body; protein abundance increases in response to DNA replication stress; null mutation is complemented by human TUBG1","termid":"PBO:0083953"}


id: MONDO:0001446
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"urinary bladder disorder","termid":"MONDO:0006026"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"low compliance bladder","secondary_identifiers":["MEDGEN:635444","SCTID:9009001","DOID:12144","UMLS:C0489967","ICD9:596.52"],"synonyms":[{"name":"hyperactivity of bladder","type":"exact"},{"name":"hypertonic bladder","type":"exact"},{"name":"hypertonicity of bladder","type":"exact"},{"name":"low bladder compliance","type":"exact"}],"termid":"MONDO:0001446","xrefs":{"Monarch":{"xref_id":"0001446"}}}


id: GO:1901491
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of lymphangiogenesis.","definition_xrefs":["GOC:dph","PMID:20133819","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"regulation of lymphangiogenesis","termid":"GO:1901490"},{"relation_name":"negatively_regulates","term_name":"lymphangiogenesis","termid":"GO:0001946"}],"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 lymphangiogenesis","synonyms":[{"name":"down regulation of lymph vessel formation","type":"exact"},{"name":"down regulation of lymphangiogenesis","type":"exact"},{"name":"down-regulation of lymph vessel formation","type":"exact"},{"name":"down-regulation of lymphangiogenesis","type":"exact"},{"name":"downregulation of lymph vessel formation","type":"exact"},{"name":"downregulation of lymphangiogenesis","type":"exact"},{"name":"inhibition of lymph vessel formation","type":"narrow"},{"name":"inhibition of lymphangiogenesis","type":"narrow"},{"name":"negative regulation of lymph vessel formation","type":"exact"}],"termid":"GO:1901491"}


id: MONDO:0001479
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually mild form of diphtheria characterized by infection of the skin by corynebacterium diphtheria and the resulting formation of a chronic, shallow ulcer that is sometimes bordered or followed by a bulla.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyoderma","termid":"MONDO:0002922"},{"relation_name":"is_a","term_name":"diphtheria","termid":"MONDO:0005504"},{"relation_name":"is_a","term_name":"skin infection","termid":"MONDO:0021201"},{"relation_name":"is_a","term_name":"skin disease caused by bacterial infection","termid":"MONDO:0024295"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"cutaneous diphtheria","secondary_identifiers":["icd11.foundation:618920860","MEDGEN:41599","DOID:12275","UMLS:C0012555","ICD10CM:A36.3","NCIT:C34544","ICD9:032.85","SCTID:18901009"],"synonyms":[{"name":"cutaneous diphtheria","type":"exact"}],"termid":"MONDO:0001479","xrefs":{"Monarch":{"xref_id":"0001479"}}}


id: PBO:0056334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAP3K14 antisense RNA 1","termid":"PBO:0056334"}


id: GO:0046179
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of keto-D-gluconate, the anion of keto-D-gluconic acid, an aldonic acid derived from glucose.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"keto-D-gluconate metabolic process","termid":"GO:0019525"},{"relation_name":"is_a","term_name":"ketogluconate biosynthetic process","termid":"GO:0046180"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0005975","GO:0008150"],"is_obsolete":false,"name":"keto-D-gluconate biosynthetic process","synonyms":[{"name":"keto-D-gluconate anabolism","type":"exact"},{"name":"keto-D-gluconate biosynthesis","type":"exact"},{"name":"keto-D-gluconate formation","type":"exact"},{"name":"keto-D-gluconate synthesis","type":"exact"}],"termid":"GO:0046179"}


id: GO:0060823
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell, followed by propagation of the signal via beta-catenin, and ending with a change in transcription of target genes that contributes to the formation of the neural plate anterior/posterior pattern.","definition_xrefs":["GOC:sdb_2009","GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete canonical Wnt signaling pathway involved in neural plate anterior/posterior pattern formation (obsolete GO:0060823)","synonyms":[{"name":"Wnt receptor signaling pathway through beta-catenin involved in neural plate anterior/posterior pattern formation","type":"exact"},{"name":"canonical Wnt receptor signaling pathway involved in neural plate anterior/posterior pattern formation","type":"exact"},{"name":"canonical Wnt receptor signalling pathway involved in neural plate anterior/posterior pattern formation","type":"exact"},{"name":"canonical Wnt-activated signaling pathway involved in neural plate anterior/posterior pattern formation","type":"exact"}],"termid":"GO:0060823"}


id: GO:0045219
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of FasL.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of FasL production (obsolete GO:0045219)","synonyms":[{"name":"regulation of FasL anabolism","type":"exact"},{"name":"regulation of FasL biosynthesis","type":"exact"},{"name":"regulation of FasL formation","type":"exact"},{"name":"regulation of FasL synthesis","type":"exact"}],"termid":"GO:0045219"}


id: GO:0047267
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: GDP-mannose + undecaprenyl phosphate = GDP + D-mannosyl-1-phosphoundecaprenol.","definition_xrefs":["EC:2.4.1.54"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mannosyltransferase activity","termid":"GO:0000030"}],"gene_count":0,"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:0003824"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0016757","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"undecaprenyl-phosphate mannosyltransferase activity","synonyms":[{"name":"GDP mannose-undecaprenyl phosphate mannosyltransferase activity","type":"related"},{"name":"GDP-D-mannose:lipid phosphate transmannosylase activity","type":"related"},{"name":"GDP-mannose:undecaprenyl-phosphate D-mannosyltransferase activity","type":"related"},{"name":"guanosine diphosphomannose-undecaprenyl phosphate mannosyltransferase activity","type":"related"}],"termid":"GO:0047267"}


id: GO:0003092
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which renal water excretion is decreased.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of urine volume","termid":"GO:0035811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"renal water retention","synonyms":[{"name":"negative regulation of renal water excretion","type":"exact"}],"termid":"GO:0003092"}


id: PBO:0117420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zDHHC palmitoyltransferase 15","termid":"PBO:0117420"}


id: PBO:0045247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member C27","termid":"PBO:0045247"}


id: PBO:0026632
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H3-K4_methylation","termid":"PBO:0026632"}


id: PBO:0087321
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Snf1p-related nutrient-responsive protein kinase; overexpression increases sodium and lithium tolerance, whereas gene disruption increases cation and low pH sensitivity and impairs potassium uptake, suggesting a role in regulation of Trk1p and/or Trk2p transporters; HAL5 has a paralog, KKQ8, that arose from the whole genome duplication","termid":"PBO:0087321"}


id: PBO:0063744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHB1 pseudogene 9","termid":"PBO:0063744"}


id: MONDO:0013154
data:
  {"annotated_genes":["SJAG_04053","SJAG_04316"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87011,87012],"is_not":false,"summary":null,"term":"MONDO:0013154"}]},"cv_name":"mondo","definition":"An autosomal recessive muscular dystrophy caused by mutations in the POMT2 gene. It is associated with characteristic brain and eye malformations and profound mental retardation.","definition_xrefs":["NCIT:C126742"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy, type A","termid":"MONDO:0000171"},{"relation_name":"is_a","term_name":"muscle-eye-brain disease","termid":"MONDO:0018939"},{"relation_name":"is_a","term_name":"myopathy caused by variation in POMT2","termid":"MONDO:0700071"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04053":null,"SJAG_04316":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0005066","MONDO:0024322","MONDO:0002320"],"is_obsolete":false,"name":"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:15624","MEDGEN:461761","DOID:0111240","OMIM:613150","UMLS:C3150411"],"synonyms":[{"name":"MDDGA2","type":"exact"},{"name":"Walker-Warburg syndrome or muscle-eye-brain disease, Pomt2-related","type":"exact"},{"name":"muscle-eye-brain-POMT2 related","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 2","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2","type":"exact"}],"termid":"MONDO:0013154","terms_by_termid":{"MONDO:0013154":null},"xrefs":{"Monarch":{"xref_id":"0013154"}}}


id: PR:O74834
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A uracil-DNA glycosylase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04380","PANTHER:PTHR11264: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":"uracil-DNA glycosylase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1183.06","secondary_identifiers":["UniProtKB:O74834"],"synonyms":[{"name":"Spom972h-UNG","type":"exact"},{"name":"UDG (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74834"}


id: PBO:0003621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar membrane palmitoyltransferase Pfa5 (predicted)","termid":"PBO:0003621"}


id: PBO:0058133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4433b","termid":"PBO:0058133"}


id: FYPO:0002118
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a specified transporter activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transmembrane transporter activity","termid":"FYPO:0002116"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002114"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000652","FYPO:0000707","FYPO:0002114","FYPO:0001985","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"decreased transporter activity","synonyms":[{"name":"reduced transporter activity","type":"exact"}],"termid":"FYPO:0002118"}


id: GO:1904904
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of endothelial cell-matrix adhesion via fibronectin.","definition_xrefs":["GOC:bc","GOC:BHF","GOC:TermGenie","GO_REF:0000058","GOC:BHF_miRNA","PMID:19460962"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell-matrix adhesion","termid":"GO:0001952"},{"relation_name":"regulates","term_name":"endothelial cell-matrix adhesion via fibronectin","termid":"GO:0090674"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"regulation of endothelial cell-matrix adhesion via fibronectin","termid":"GO:1904904"}


id: GO:1990656
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The clustering process in which t-SNARES are localized to distinct domains in the cell membrane. t-SNAREs are cell surface proteins which are part of secretory microdomain assemblies.","definition_xrefs":["PMID:22528485"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to membrane","termid":"GO:0072657"}],"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":"t-SNARE clustering","termid":"GO:1990656"}


id: FYPO:0002549
data:
  {"alleles_by_uniquename":{"SJAG_00266:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00266","name":"atf1delta","uniquename":"SJAG_00266:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_04312:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04312","name":"pka1delta","uniquename":"SJAG_04312:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000087"},{"annotations":[119648,119660],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000726"},{"annotations":[119647,119659],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000271"}]},"cv_name":"fission_yeast_phenotype","definition":"A phenotype in which cells in a population show increased sensitivity to a stress. Typically, a cell population is deemed sensitive to a stress if cells in the population stop growing (and may die) when exposed to the stress at an intensity that allows a population of wild type cells to grow and divide.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell population growth","termid":"FYPO:0000045"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00266":null,"SJAG_02592":null,"SJAG_04312":null},"genotype_count":3,"genotypes_by_uniquename":{"atf1delta":{"display_name":"atf1delta","display_uniquename":"atf1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00266:allele-1","expression":"Null"}]}]},"pka1delta":{"display_name":"pka1delta","display_uniquename":"pka1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04312:allele-1","expression":"Null"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000139","FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to stress","references_by_uniquename":{"PMID:27678009":null,"PMID:31150379":null},"single_locus_annotated_genes":["SJAG_00266","SJAG_04312","SJAG_02592"],"single_locus_genotype_uniquenames":["sty1delta","pka1delta","atf1delta"],"synonyms":[{"name":"decreased growth during cellular response to stress","type":"exact"},{"name":"decreased vegetative cell population growth during cellular response to stress","type":"exact"},{"name":"hypersensitive to stress","type":"exact"},{"name":"stress resistance: decreased","type":"related"}],"termid":"FYPO:0002549","terms_by_termid":{"FYECO:0000078":null,"FYECO:0000207":null,"FYPO:0000087":null,"FYPO:0000271":null,"FYPO:0000726":null,"FYPO_EXT:0000001":null}}


id: PBO:0080904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 4","termid":"PBO:0080904"}


id: FYPO:0004179
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 small aggregates of misfolded protein fuse into larger aggregates to a lower extent than normal.","definition_xrefs":["PomBase:mah","PMID:24936793"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased protein aggregate fusion","synonyms":[{"name":"decreased protein aggregate fusion during mitotic cell cycle","type":"related"},{"name":"decreased protein aggregate fusion during vegetative growth","type":"exact"},{"name":"reduced protein aggregate fusion","type":"exact"}],"termid":"FYPO:0004179"}


id: GO:0150034
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"That part of an axon close to and including the growth cone or the axon terminus.","definition_xrefs":["PMID:17202468","GOC:aruk","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"axon","termid":"GO:0030424"}],"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":"distal axon","synonyms":[{"name":"distal part of axon","type":"exact"},{"name":"distal part of the axon","type":"exact"}],"termid":"GO:0150034"}


id: GO:0090315
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of the process of directing proteins towards a membrane, usually using signals contained within the protein.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein targeting to membrane","termid":"GO:0090313"},{"relation_name":"is_a","term_name":"negative regulation of establishment of protein localization","termid":"GO:1904950"},{"relation_name":"is_a","term_name":"negative regulation of protein localization to membrane","termid":"GO:1905476"},{"relation_name":"negatively_regulates","term_name":"protein targeting to membrane","termid":"GO:0006612"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006605"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006605"}],"interesting_parent_ids":["GO:0008150","GO:0006605"],"is_obsolete":false,"name":"negative regulation of protein targeting to membrane","termid":"GO:0090315"}


id: MONDO:0002686
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete mast-cell sarcoma (obsolete MONDO:0002686)","termid":"MONDO:0002686","xrefs":{"Monarch":{"xref_id":"0002686"}}}


id: MONDO:0015428
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Choroidal atrophy - alopecia is a very rare ectodermal dysplasia syndrome, characterized by the association of choroidal atrophy (sometimes regional), together with other ectodermal dysplasia features including fine and sparse hair, absent or decreased lashes and eyebrows, and possibly mild visual loss and dysplastic/thick/grooved nails.","definition_xrefs":["Orphanet:1433"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"choroidal atrophy-alopecia syndrome","secondary_identifiers":["SCTID:720850008","MESH:C535810","UMLS:C2931026","GARD:3704","MEDGEN:419316"],"synonyms":[{"name":"Moloney syndrome","type":"exact"},{"name":"choroidal atrophy alopecia","type":"related"},{"name":"fine hair, absent/decreased lashes, absent/decreased eyebrows, visual loss-mild/suspected, dysplastic/thick/grooved toenails and fingernails","type":"related"},{"name":"regional choroidal atrophy and alopecia","type":"exact"}],"termid":"MONDO:0015428","xrefs":{"Monarch":{"xref_id":"0015428"}}}


id: PBO:0028355
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_phosphatase_activity","termid":"PBO:0028355"}


id: GO:0061787
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A peptidoglycan endopeptidase activity that acts on a peptidoglycan cross-bridge.","definition_xrefs":["GOC:jh","PMID:22748813","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidoglycan endopeptidase activity","termid":"GO:0061785"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0140096","GO:0003674","GO:0008233","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"peptidoglycan cross-bridge peptide endopeptidase activity","synonyms":[{"name":"lysostaphin activity","type":"narrow"}],"termid":"GO:0061787"}


id: PBO:0081714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 639","termid":"PBO:0081714"}


id: PATO:0000690
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality of a single process inhering in a bearer by virtue of the bearer's being marked by breaks or interruptions.","definition_xrefs":["thefreedictionary.com:thefreedictionary.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"occurrence","termid":"PATO:0000057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"discontinuous","secondary_identifiers":["PATO:0000426"],"synonyms":[{"name":"intermittent","type":"related"},{"name":"interrupted","type":"exact"}],"termid":"PATO:0000690"}


id: PBO:0085089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear envelope protein that acts as a recycling factor; mediates the nuclear export of Srp1p (importin alpha) back to the cytoplasm after its import substrates have been released into the nucleoplasm, thereby allowing the participation of Srp1p in multiple rounds of nuclear import; required for accurate chromosome segregation; homolog of metazoan CAS and human CSE1L, overexpression of which is implicated in cancer progression","termid":"PBO:0085089"}


id: MONDO:0012979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the RSPH9 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary ciliary dyskinesia","termid":"MONDO:0016575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary ciliary dyskinesia 12","secondary_identifiers":["MEDGEN:436379","UMLS:C2675228","GARD:15575","OMIM:612650","DOID:0110601","MESH:C567211"],"synonyms":[{"name":"CILD12","type":"exact"},{"name":"RSPH9 primary ciliary dyskinesia","type":"exact"},{"name":"ciliary dyskinesia, primary, 12","type":"related"},{"name":"ciliary dyskinesia, primary, 12, without situs inversus","type":"related"},{"name":"ciliary dyskinesia, primary, type 12","type":"exact"},{"name":"primary ciliary dyskinesia 12 without situs inversus","type":"exact"},{"name":"primary ciliary dyskinesia caused by mutation in RSPH9","type":"exact"},{"name":"primary ciliary dyskinesia type 12","type":"exact"}],"termid":"MONDO:0012979","xrefs":{"Monarch":{"xref_id":"0012979"}}}


id: GO:0106413
data:
  {"annotated_genes":["SJAG_00174","SJAG_01041","SJAG_03240","SJAG_03236"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[89799,105012,109943,118719],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106414"},{"annotations":[109944],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102262"},{"annotations":[109945],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102263"},{"annotations":[105013],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102264"},{"annotations":[118720],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102266"},{"annotations":[118721],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102267"},{"annotations":[66145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102265"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: RNA-uracil + NAD(P)+ = RNA-dihydrouridine + NAD(P)H + H+.","definition_xrefs":["PMID:12581659","PMID:25073379"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00174":null,"SJAG_01041":null,"SJAG_03236":null,"SJAG_03240":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"RNA dihydrouridine synthase activity","references_by_uniquename":{"GO_REF:0000003":null,"GO_REF:0000107":null},"termid":"GO:0106413","terms_by_termid":{"GO:0102262":null,"GO:0102263":null,"GO:0102264":null,"GO:0102265":null,"GO:0102266":null,"GO:0102267":null,"GO:0106414":null}}


id: GO:0090663
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of the peptide neurotransmitter galanin binding to a cell surface receptor.","definition_xrefs":["GOC:lb","PMID:25691535"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuropeptide signaling pathway","termid":"GO:0007218"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"galanin-activated signaling pathway","synonyms":[{"name":"galanin signaling pathway","type":"related"},{"name":"galanin signalling pathway","type":"related"},{"name":"galanin-activated signalling pathway","type":"exact"}],"termid":"GO:0090663"}


id: MONDO:0002812
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the anatomical structures of the inner ear secondary to an infectious process. Symptoms include severe vertigo, nausea, vomiting, anxiety, and pain. Viral etiology is most common, and recent history of an upper respiratory infection is common. In rare cases an infection of the middle ear can spread to the inner ear, resulting in a bacterial or fungal etiology.","definition_xrefs":["NCIT:C27339"],"direct_ancestors":[{"relation_name":"is_a","term_name":"labyrinthitis","termid":"MONDO:0002008"},{"relation_name":"is_a","term_name":"ear infection","termid":"MONDO:0021666"},{"relation_name":"is_a","term_name":"post-infectious disorder","termid":"MONDO:0021669"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infectious otitis interna","secondary_identifiers":["UMLS:C1168225","MEDGEN:217000"],"synonyms":[{"name":"infectious labyrinthitis","type":"exact"},{"name":"infectious otitis interna","type":"exact"},{"name":"inner Ear infection","type":"exact"},{"name":"inner ear infection","type":"exact"},{"name":"internal Ear infection","type":"exact"}],"termid":"MONDO:0002812","xrefs":{"Monarch":{"xref_id":"0002812"}}}


id: PBO:0051923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ITGB5 antisense RNA 1","termid":"PBO:0051923"}


id: GO:0009081
data:
  {"annotated_genes":["SJAG_00944","SJAG_00107","SJAG_04149","SJAG_00830","SJAG_03562","SJAG_02841","SJAG_00396","SJAG_06635","SJAG_03243","SJAG_04098","SJAG_03985"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110745,111407,113559,108631,91024,103610,104094],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901705"},{"annotations":[59354,75181,77296,80294,91025,103611,113560],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009098"},{"annotations":[111408],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006551"},{"annotations":[76454,80295,64047,77346,58687],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009099"},{"annotations":[73441],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006574"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving amino acids containing a branched carbon skeleton, comprising isoleucine, leucine and valine.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid metabolic process","termid":"GO:0006520"},{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00107":null,"SJAG_00396":null,"SJAG_00830":null,"SJAG_00944":null,"SJAG_02841":null,"SJAG_03243":null,"SJAG_03562":null,"SJAG_03985":null,"SJAG_04098":null,"SJAG_04149":null,"SJAG_06635":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"branched-chain amino acid metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"synonyms":[{"name":"branched chain family amino acid metabolism","type":"exact"}],"termid":"GO:0009081","terms_by_termid":{"GO:0006551":null,"GO:0006574":null,"GO:0009098":null,"GO:0009099":null,"GO:1901705":null}}


id: GO:1901897
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of relaxation of cardiac muscle.","definition_xrefs":["GOC:rl","GOC:TermGenie","PMID:19708671","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of relaxation of muscle","termid":"GO:1901077"},{"relation_name":"regulates","term_name":"relaxation of cardiac muscle","termid":"GO:0055119"}],"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 relaxation of cardiac muscle","termid":"GO:1901897"}


id: PBO:0045392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DPP10 antisense RNA 3","termid":"PBO:0045392"}


id: PBO:0048613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase, IMAP family member 5","termid":"PBO:0048613"}


id: MONDO:0019962
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lymphoma primarily involving the thyroid gland.","definition_xrefs":["NCIT:C5265"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thyroid cancer","termid":"MONDO:0002108"},{"relation_name":"is_a","term_name":"primary organ-specific lymphoma","termid":"MONDO:0017207"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570"],"is_obsolete":false,"name":"thyroid lymphoma","secondary_identifiers":["GARD:19359","Orphanet:97285","UMLS:C1336753","DOID:10011","MEDGEN:234947","icd11.foundation:571063415"],"synonyms":[{"name":"lymphoma of the thyroid","type":"exact"},{"name":"lymphoma of the thyroid gland","type":"exact"},{"name":"lymphoma of thyroid","type":"exact"},{"name":"lymphoma of thyroid gland","type":"exact"},{"name":"primary thyroid gland lymphoma","type":"exact"},{"name":"thyroid gland lymphoma","type":"exact"},{"name":"thyroid lymphoma","type":"exact"}],"termid":"MONDO:0019962","xrefs":{"Monarch":{"xref_id":"0019962"}}}


id: PBO:0043116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CIAO2A pseudogene 1","termid":"PBO:0043116"}


id: MONDO:0009696
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The most common hereditary idiopathic generalized epilepsy syndrome and is characterized by myoclonic jerks of the upper limbs on awakening, generalized tonic-clonic seizures manifesting during adolescence and triggered by sleep deprivation, alcohol intake, and cognitive activities, and typical absence seizures (30% of cases).","definition_xrefs":["Orphanet:307"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"adolescence-adult electroclinical syndrome","termid":"MONDO:0000415"},{"relation_name":"excluded_subClassOf","term_name":"movement disorder","termid":"MONDO:0005395"},{"relation_name":"excluded_subClassOf","term_name":"familial partial epilepsy","termid":"MONDO:0017704"},{"relation_name":"excluded_subClassOf","term_name":"obsolete adolescent/adult-onset epilepsy syndrome (obsolete MONDO:0100030)","termid":"MONDO:0100030"},{"relation_name":"is_a","term_name":"myoclonic epilepsy","termid":"MONDO:0100577"},{"relation_name":"is_a","term_name":"variable-age onset idiopathic generalized epilepsy syndrome","termid":"MONDO:0800487"}],"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":"juvenile myoclonic epilepsy","secondary_identifiers":["NCIT:C84796","ICD9:345.10","MedDRA:10071082","MEDGEN:78738","OMIM:254770","DOID:4890","MESH:D020190","UMLS:C0270853","OMIM:606904","OMIMPS:254770","icd11.foundation:1014397110","SCTID:6204001","GARD:6808"],"synonyms":[{"name":"EJM","type":"exact"},{"name":"JME","type":"exact"},{"name":"Janz syndrome","type":"narrow"},{"name":"epilepsy, myoclonic juvenile","type":"exact"},{"name":"juvenile myoclonus epilepsy","type":"exact"},{"name":"myoclonic epilepsy, juvenile","type":"exact"},{"name":"myoclonic epilepsy, juvenile, 1","type":"exact"},{"name":"myoclonic epilepsy, juvenile, susceptibility to, 1","type":"narrow"},{"name":"petit mal, impulsive","type":"narrow"}],"termid":"MONDO:0009696","xrefs":{"Monarch":{"xref_id":"0009696"}}}


id: FYPO:0001585
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the cell tip is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization during vegetative growth","termid":"FYPO:0001179"},{"relation_name":"is_a","term_name":"abnormal protein localization to cell tip during vegetative growth","termid":"FYPO:0001584"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000138","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abolished protein localization to cell tip during vegetative growth","synonyms":[{"name":"abolished protein localisation to cell tip during vegetative growth","type":"exact"},{"name":"abolished protein localization to cell end during vegetative growth","type":"exact"},{"name":"abolished protein localization to cell tip during mitotic cell cycle","type":"related"},{"name":"protein localization to cell tip abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0001585"}


id: GO:0070941
data:
  {"annotated_genes":["SJAG_02626","SJAG_02338","SJAG_02707","SJAG_04227"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70151,71725,104191,118143],"is_not":false,"summary":null,"term":"GO:0070941"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form an eisosome, a cell part that is composed of the eisosome membrane and eisosome filaments. The eisosome membrane, also called the MCC domain, is a furrow-like plasma membrane sub-domain with associated integral transmembrane proteins. The eisosome filaments form a scaffolding lattice on the cytoplasmic face of the membrane.","definition_xrefs":["PMID:19564405","GOC:al","GOC:jp","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02338":null,"SJAG_02626":null,"SJAG_02707":null,"SJAG_04227":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"eisosome assembly","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0070941","terms_by_termid":{"GO:0070941":null}}


id: _global:is_kinase_activity
data:
  {"annotation_feature_type":"gene","cv_name":"external","direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_interaction_relation_helper_property","termid":"_global:molecular_interaction_relation_helper_property"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is_kinase_activity","secondary_identifiers":["RO:0002481"],"termid":"_global:is_kinase_activity"}


id: PATO:0001247
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of cyan hue and high brightness.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyan","termid":"PATO:0000319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"light cyan","termid":"PATO:0001247"}


id: PBO:0039256
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldehyde dehydrogenase 5 family member A1","termid":"PBO:0039256"}


id: PBO:0085104
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear protein that negatively regulates pseudohyphal differentiation; plays a regulatory role in the cyclic AMP (cAMP)-dependent protein kinase (PKA) signal transduction pathway; relocalizes to the cytosol in response to hypoxia; SOK2 has a paralog, PHD1, that arose from the whole genome duplication","termid":"PBO:0085104"}


id: PBO:0046367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ENTPD3 antisense RNA 1","termid":"PBO:0046367"}


id: MOD:01828
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue sulfhydryl hydrogen with a Thermo Scientific cysTMT6plex-131 reporter+balance group.","definition_xrefs":["PubMed:18688235","URL:http://www.piercenet.com/files/2162220.pdf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysTMT6plex reporter+balance reagent cysteine disulfide","termid":"MOD:01821"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"cysTMT6plex-131 reporter+balance reagent cysteine disulfide","synonyms":[{"name":"S-(2-{3-[2-(2,6-dimethylpiperidin-1-yl)acetamido]propanamido}ethyl)sulfanyl","type":"exact"},{"name":"cysTMT6plex","type":"related"},{"name":"cysteine-reactive Sixplex Tandem Mass Tag(TM)","type":"related"}],"termid":"MOD:01828"}


id: GO:1905815
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of dorsal/ventral axon guidance.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:18434533"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of axon guidance","termid":"GO:1902667"},{"relation_name":"regulates","term_name":"dorsal/ventral axon guidance","termid":"GO:0033563"}],"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 dorsal/ventral axon guidance","synonyms":[{"name":"regulation of dorsal-ventral axon guidance","type":"exact"},{"name":"regulation of dorsal/ventral axon pathfinding","type":"exact"},{"name":"regulation of dorsoventral axon guidance","type":"exact"}],"termid":"GO:1905815"}


id: PBO:0088914
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L37","termid":"PBO:0088914"}


id: FYPO:0004526
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A transcription regulation phenotype in which any process of regulation of transcription is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription regulation phenotype","termid":"FYPO:0000143"},{"relation_name":"is_a","term_name":"abnormal gene expression","termid":"FYPO:0006551"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0006551","FYPO:0005447"],"is_obsolete":false,"name":"abnormal regulation of transcription","synonyms":[{"name":"abnormal regulation of cellular transcription, DNA-dependent","type":"exact"},{"name":"abnormal regulation of gene-specific transcription","type":"related"},{"name":"abnormal regulation of transcription, DNA-dependent","type":"exact"}],"termid":"FYPO:0004526"}


id: PBO:0066378
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RDM1 pseudogene 5","termid":"PBO:0066378"}


id: SO:0100009
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A peptide that acts as a signal for both membrane translocation and lipid attachment in prokaryotes.","definition_xrefs":["EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cleaved_peptide_region","termid":"SO:0100011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"lipoprotein_signal_peptide","synonyms":[{"name":"lipoprotein signal peptide","type":"exact"},{"name":"prokaryotic membrane lipoprotein lipid attachment site","type":"exact"}],"termid":"SO:0100009"}


id: GO:0045620
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of lymphocyte differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lymphocyte differentiation","termid":"GO:0045619"},{"relation_name":"is_a","term_name":"negative regulation of lymphocyte activation","termid":"GO:0051250"},{"relation_name":"is_a","term_name":"negative regulation of leukocyte differentiation","termid":"GO:1902106"},{"relation_name":"negatively_regulates","term_name":"lymphocyte differentiation","termid":"GO:0030098"}],"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 lymphocyte differentiation","synonyms":[{"name":"down regulation of lymphocyte differentiation","type":"exact"},{"name":"down-regulation of lymphocyte differentiation","type":"exact"},{"name":"downregulation of lymphocyte differentiation","type":"exact"},{"name":"inhibition of lymphocyte differentiation","type":"narrow"},{"name":"negative regulation of lymphocyte development","type":"related"}],"termid":"GO:0045620"}


id: PBO:0088235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ornithine decarboxylase Spe1","termid":"PBO:0088235"}


id: GO:0047671
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: anthranilate + 2 ATP + L-phenylalanine + S-adenosyl-L-methionine = 2 AMP + cyclopeptine + 2 diphosphate + 2 H+ + S-adenosyl-L-homocysteine.","definition_xrefs":["EC:6.3.2.40","PMID:2995633","RHEA:35091"],"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:0016874","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"cyclopeptine synthase activity","secondary_identifiers":["MetaCyc:RXN-13989","KEGG_REACTION:R00979"],"synonyms":[{"name":"ATP:anthranilate adenylyltransferase activity","type":"exact"},{"name":"anthranilate adenylyltransferase activity","type":"related"}],"termid":"GO:0047671"}


id: GO:0061252
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into a mesonephric glomerular epithelial cell. Mesonephric glomerular epithelial cells are specialized epithelial cells that form part of the mesonephric glomerulus; there are two types, mesonephric glomerular parietal epithelial cells and mesonephric glomerular visceral epithelial cells.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerular epithelial cell fate commitment","termid":"GO:0072314"},{"relation_name":"part_of","term_name":"mesonephric glomerular epithelial cell differentiation","termid":"GO:0061250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mesonephric glomerular epithelial cell fate commitment","termid":"GO:0061252"}


id: GO:0102863
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 1-18:3-2-18:1-phosphatidylcholine + O2 + a reduced electron acceptor = 1-18:3-2-18:2-phosphatidylcholine + 2 H2O + an oxidized electron acceptor.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 1-18:3-2-18:1-phosphatidylcholine desaturase activity (obsolete GO:0102863)","termid":"GO:0102863"}


id: PBO:0049073
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 89B","termid":"PBO:0049073"}


id: MONDO:0013543
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":"trypsinogen deficiency","secondary_identifiers":["ICD9:277.89","SCTID:190953007","MEDGEN:450540","OMIM:614044","UMLS:C0268417"],"synonyms":[{"name":"trypsinogen deficiency","type":"exact"}],"termid":"MONDO:0013543","xrefs":{"Monarch":{"xref_id":"0013543"}}}


id: GO:0042067
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specification of polarized ommatidia. Ommatidia occur in two chiral forms. The trapezoidal arrangement of photoreceptors in the dorsal part of the eye is the mirror image of that in the ventral part.","definition_xrefs":["PMID:3076112","PMID:3937883","GOC:dph","GOC:ascb_2009","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of planar polarity","termid":"GO:0001736"},{"relation_name":"is_a","term_name":"establishment or maintenance of cell polarity","termid":"GO:0007163"},{"relation_name":"part_of","term_name":"compound eye morphogenesis","termid":"GO:0001745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0008150","GO:0007163"],"is_obsolete":false,"name":"establishment of ommatidial planar polarity","synonyms":[{"name":"establishment of ommatidial polarity","type":"exact"}],"termid":"GO:0042067"}


id: MONDO:0012639
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, complex type of hereditary spastic paraplegia characterized by progressive spastic paraplegia (presenting in early childhood) associated with delayed motor development, severe intellectual disability and joint contractures. A thin corpus callosum is equally noted on brain magnetic resonance imaging. SPG18 is caused by a mutation in the ERLIN2 gene (8p11.2) encoding the protein, Erlin-2.","definition_xrefs":["Orphanet:209951"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"hereditary spastic paraplegia 18","secondary_identifiers":["MESH:C567628","MEDGEN:442343","GARD:4922","SCTID:732932004","OMIM:611225","DOID:0110771","UMLS:C2749936"],"synonyms":[{"name":"ERLIN2 autosomal recessive complex spastic paraplegia","type":"exact"},{"name":"SPG18","type":"exact"},{"name":"autosomal recessive complex spastic paraplegia caused by mutation in ERLIN2","type":"exact"},{"name":"autosomal recessive spastic paraplegia 18","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 18","type":"exact"},{"name":"hereditary spastic paraplegia type 18","type":"exact"},{"name":"intellectual disability, motor dysfunction and joint contractures","type":"exact"},{"name":"intellectual disability, motor dysfunction, and Joint contractures","type":"related"},{"name":"spastic paraplegia 18","type":"related"},{"name":"spastic paraplegia 18, autosomal recessive","type":"related"}],"termid":"MONDO:0012639","xrefs":{"Monarch":{"xref_id":"0012639"}}}


id: PBO:0086194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein subunit of mitochondrial RNase P; has roles in nuclear transcription, cytoplasmic and mitochondrial RNA processing, and mitochondrial translation; distributed to mitochondria, cytoplasmic processing bodies, and the nucleus","termid":"PBO:0086194"}


id: MOD:01975
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-(poly-3-hydroxybutyrate)-L-cysteine.","definition_xrefs":["RESID:AA0617","PubMed:19711985","PubMed:9888824"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-acylated residue","termid":"MOD:00672"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-poly(3-hydroxybutyrate)-L-cysteine","synonyms":[{"name":"(alpha)-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-(omega)-[(3R)-3-hydroxybutanoyl]-poly([(3R)-3-methyl-1-oxopropane-1,3-diyl]oxy)","type":"exact"},{"name":"MOD_RES S-poly(beta-hydroxybutyryl)lysine","type":"exact"},{"name":"S-poly(3-hydroxybutanoate)cysteine","type":"exact"},{"name":"S-poly(3-hydroxybutanoic acid)cysteine","type":"exact"},{"name":"S-poly(3-hydroxybutyrate)-L-cysteine","type":"exact"},{"name":"S-poly(3-hydroxybutyrate)cysteine","type":"exact"},{"name":"S-poly(3-hydroxybutyric acid)cysteine","type":"exact"},{"name":"S-poly(beta-hydroxybutyrate)cysteine","type":"exact"},{"name":"S-poly[(R)-3-hydroxybutyrate]cysteine","type":"exact"}],"termid":"MOD:01975"}


id: GO:0010310
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving hydrogen peroxide.","definition_xrefs":["PMID:14765119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of reactive oxygen species metabolic process","termid":"GO:2000377"},{"relation_name":"regulates","term_name":"hydrogen peroxide metabolic process","termid":"GO:0042743"}],"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 hydrogen peroxide metabolic process","synonyms":[{"name":"regulation of hydrogen peroxide metabolism","type":"exact"}],"termid":"GO:0010310"}


id: PBO:0084060
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase-activating protein (GAP) for yeast Rab family members; involved in ER to Golgi trafficking; exhibits GAP activity toward Ypt1p that is stimulated by Gyl1p, also acts on Sec4p; interacts with Gyl1p, Rvs161p and Rvs167p; involved in recruiting Rvs167p to the bud tip during polarized growth; relocalizes from bud neck to cytoplasm upon DNA replication stress; GYP5 has a paralog, GYL1, that arose from the whole genome duplication","termid":"PBO:0084060"}


id: MONDO:0032644
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":"epidermodysplasia verruciformis, susceptibility to","termid":"MONDO:0100043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epidermodysplasia verruciformis, susceptibility to, 3","secondary_identifiers":["MEDGEN:1648390","OMIM:618267","UMLS:C4748876"],"synonyms":[{"name":"EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 3","type":"related"},{"name":"EV3","type":"related"},{"name":"epidermodysplasia verruciformis 3","type":"exact"}],"termid":"MONDO:0032644","xrefs":{"Monarch":{"xref_id":"0032644"}}}


id: GO:1903388
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of synaptic vesicle uncoating.","definition_xrefs":["PMID:21563316","GOC:PARL","GOC:TermGenie","GOC:pad","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein depolymerization","termid":"GO:1901879"},{"relation_name":"regulates","term_name":"synaptic vesicle uncoating","termid":"GO:0016191"}],"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 synaptic vesicle uncoating","synonyms":[{"name":"regulation of synaptic vesicle coat depolymerization","type":"exact"},{"name":"regulation of synaptic vesicle coat protein depolymerization","type":"exact"}],"termid":"GO:1903388"}


id: GO:0075340
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of the increase in size or mass of an organism, or the progression of an organism from an initial condition to a later condition, occurring in, on or near the exterior of its host organism.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of growth or development of symbiont during interaction with host (obsolete GO:0075340)","synonyms":[{"name":"negative regulation of growth or development of symbiont during interaction with host","type":"exact"}],"termid":"GO:0075340"}


id: GO:1904178
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of adipose tissue development.","definition_xrefs":["GOC:TermGenie","PMID:23081848","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of adipose tissue development","termid":"GO:1904177"},{"relation_name":"negatively_regulates","term_name":"adipose tissue development","termid":"GO:0060612"}],"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 adipose tissue development","synonyms":[{"name":"down regulation of adipogenesis","type":"related"},{"name":"down regulation of adipose tissue development","type":"exact"},{"name":"down-regulation of adipogenesis","type":"related"},{"name":"down-regulation of adipose tissue development","type":"exact"},{"name":"downregulation of adipogenesis","type":"related"},{"name":"downregulation of adipose tissue development","type":"exact"},{"name":"inhibition of adipogenesis","type":"related"},{"name":"inhibition of adipose tissue development","type":"narrow"},{"name":"negative regulation of adipogenesis","type":"related"}],"termid":"GO:1904178"}


id: MONDO:0020350
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Miller-Fisher syndrome (obsolete MONDO:0020350)","termid":"MONDO:0020350","xrefs":{"Monarch":{"xref_id":"0020350"}}}


id: PR:Q9C0X0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC29A3.21 gene.","definition_xrefs":["UniProtKB:Q9C0X0","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 C29A3.21 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC29A3.21","synonyms":[{"name":"Spom972h-SPBC29A3.21","type":"exact"}],"termid":"PR:Q9C0X0"}


id: GO:1904290
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of mitotic DNA damage checkpoint.","definition_xrefs":["GOC:kmv","PMID:16549501","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell cycle process","termid":"GO:0010948"},{"relation_name":"is_a","term_name":"positive regulation of mitotic cell cycle","termid":"GO:0045931"},{"relation_name":"is_a","term_name":"regulation of mitotic DNA damage checkpoint","termid":"GO:1904289"},{"relation_name":"is_a","term_name":"negative regulation of DNA damage checkpoint","termid":"GO:2000002"},{"relation_name":"negatively_regulates","term_name":"mitotic DNA damage checkpoint signaling","termid":"GO:0044773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of mitotic DNA damage checkpoint","synonyms":[{"name":"down regulation of mitotic DNA damage checkpoint","type":"exact"},{"name":"down-regulation of mitotic DNA damage checkpoint","type":"exact"},{"name":"downregulation of mitotic DNA damage checkpoint","type":"exact"},{"name":"inhibition of mitotic DNA damage checkpoint","type":"narrow"}],"termid":"GO:1904290"}


id: PBO:0058843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 8072","termid":"PBO:0058843"}


id: PBO:0084118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Heme A:farnesyltransferase; catalyzes first step in conversion of protoheme to heme A prosthetic group required for cytochrome c oxidase activity; human ortholog COX10 can complement yeast cox10 null mutant; human ortholog COX10 is associated with mitochondrial disorders","termid":"PBO:0084118"}


id: PBO:0045832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 alpha 1 pseudogene 22","termid":"PBO:0045832"}


id: PBO:0087370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Spt4p/5p (DSIF) transcription elongation factor complex subunit; the Spt4/5 complex binds to ssRNA in a sequence-specific manner, and along with RNAP I and II has multiple roles regulating transcriptional elongation, RNA processing, quality control, and transcription-coupled repair; localizes to kinetochores and heterochromatin, influencing chromosomal dynamics and silencing; required for transcription through long trinucleotide repeats in ORFs and non-protein coding regions","termid":"PBO:0087370"}


id: PBO:0089878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pig-P subunit","termid":"PBO:0089878"}


id: PBO:0035883
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-ophthalmic_acid_absent_from_cell","termid":"PBO:0035883"}


id: MONDO:1040006
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neurodevelopmental disorder in which the cause of the disease is a variation in the CTR9 gene. This disorder is characterised by varying degrees of intellectual disability, neurodevelopmental delay, hypotonia, fatigability, behavioral abnormalities including autism spectrum disorder, anxiety and aggressive behavior, cardiac anomalies, and mild facial dysmorphism.","definition_xrefs":["PMID:35717577","PMID:35468861","PMID:35499524"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"CTR9-related neurodevelopmental disorder","termid":"MONDO:1040006","xrefs":{"Monarch":{"xref_id":"1040006"}}}


id: PR:000028936
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A peroxiredoxin tpx1 hyperoxidized form in Schizosaccharomyces pombe. The oxidation occurs in under oxidative stress.","definition_xrefs":["PMID:22245228","PRO:CNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxiredoxin tpx1","termid":"PR:000028932"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tpx1/HyperOx(C48)","pombase_gene_id":"SPCC576.03c","synonyms":[{"name":"PomBase_original_PRO_term_name: peroxiredoxin tpx1 hyperoxidized form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-tpx1/HyperOx+","type":"exact"},{"name":"tpx1/HyperOx(C48)","type":"exact"}],"termid":"PR:000028936"}


id: MONDO:0859226
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"craniotubular dysplasia, Ikegawa type","secondary_identifiers":["UMLS:C5575335","DOID:0112340","MEDGEN:1806238","OMIM:619727"],"termid":"MONDO:0859226","xrefs":{"Monarch":{"xref_id":"0859226"}}}


id: GO:1900657
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of diorcinol biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of small molecule metabolic process","termid":"GO:0062013"},{"relation_name":"is_a","term_name":"positive regulation of secondary metabolite biosynthetic process","termid":"GO:1900378"},{"relation_name":"is_a","term_name":"regulation of diorcinol biosynthetic process","termid":"GO:1900655"},{"relation_name":"positively_regulates","term_name":"diorcinol biosynthetic process","termid":"GO:1900572"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"positively_regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0019748","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"positive regulation of diorcinol biosynthetic process","synonyms":[{"name":"activation of diorcinol anabolism","type":"exact"},{"name":"activation of diorcinol biosynthesis","type":"exact"},{"name":"activation of diorcinol biosynthetic process","type":"narrow"},{"name":"activation of diorcinol formation","type":"exact"},{"name":"activation of diorcinol synthesis","type":"exact"},{"name":"positive regulation of diorcinol anabolism","type":"exact"},{"name":"positive regulation of diorcinol biosynthesis","type":"exact"},{"name":"positive regulation of diorcinol formation","type":"exact"},{"name":"positive regulation of diorcinol synthesis","type":"exact"},{"name":"up regulation of diorcinol anabolism","type":"exact"},{"name":"up regulation of diorcinol biosynthesis","type":"exact"},{"name":"up regulation of diorcinol biosynthetic process","type":"exact"},{"name":"up regulation of diorcinol formation","type":"exact"},{"name":"up regulation of diorcinol synthesis","type":"exact"},{"name":"up-regulation of diorcinol anabolism","type":"exact"},{"name":"up-regulation of diorcinol biosynthesis","type":"exact"},{"name":"up-regulation of diorcinol biosynthetic process","type":"exact"},{"name":"up-regulation of diorcinol formation","type":"exact"},{"name":"up-regulation of diorcinol synthesis","type":"exact"},{"name":"upregulation of diorcinol anabolism","type":"exact"},{"name":"upregulation of diorcinol biosynthesis","type":"exact"},{"name":"upregulation of diorcinol biosynthetic process","type":"exact"},{"name":"upregulation of diorcinol formation","type":"exact"},{"name":"upregulation of diorcinol synthesis","type":"exact"}],"termid":"GO:1900657"}


id: MOD:00885
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that crosslinks two residues by formation of an ester bond.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"crosslinked residues","termid":"MOD:00033"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ester crosslinked residues","termid":"MOD:00885"}


id: PBO:0005643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MVB sorting pathway protein (predicted)","termid":"PBO:0005643"}


id: GO:0014020
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of the neural tube from an epithelial cell sheet (the neuroepithelium or neural plate). In primary neurulation, the cells surrounding the neural plate direct the neural plate cells to proliferate, invaginate, and pinch off from the surface to form a hollow epithelial tube. Primary neurulation is the typical mechanism of formation of the anterior neural tube.","definition_xrefs":["GOC:ef","ISBN:0878932585","PMID:15327780"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic epithelial tube formation","termid":"GO:0001838"},{"relation_name":"part_of","term_name":"neural tube formation","termid":"GO:0001841"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"primary neural tube formation","secondary_identifiers":["GO:0014024"],"synonyms":[{"name":"neural rod cavitation","type":"related"},{"name":"primary neural tube morphogenesis","type":"exact"},{"name":"primary neurulation","type":"exact"}],"termid":"GO:0014020"}


id: MONDO:0001078
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare disorder of the digestive tract characterized by malabsorption and anemia. It is likely caused by infection leading to small intestinal mucosal injury, bacterial overgrowth and inflammatory changes. It is most prevalent in residents and visitors to tropical and subtropical climates. Clinical signs include anorexia, abdominal bloating, diarrhea and weight loss. Clinical course may progress to deficiencies of folate, vitamin B12 and iron. Prognosis is favorable with nutrient replacement and antibiotic therapy, however relapses are common.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malabsorption syndrome","termid":"MONDO:0020598"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"tropical sprue","secondary_identifiers":["DOID:10607","MEDGEN:21300","icd11.foundation:316377284","MESH:D013182","UMLS:C0038054","NCIT:C45428","ICD10CM:K90.1","ICD9:579.1","SCTID:47384003"],"synonyms":[{"name":"idiopathic tropical malabsorption syndrome","type":"related"},{"name":"post-infective tropical malabsorption","type":"exact"},{"name":"sprue - tropical","type":"exact"},{"name":"tropical enteropathy","type":"related"},{"name":"tropical steatorrhea","type":"exact"}],"termid":"MONDO:0001078","xrefs":{"Monarch":{"xref_id":"0001078"}}}


id: GO:0000112
data:
  {"annotated_genes":["SJAG_00512","SJAG_03206","SJAG_00995","SJAG_00901","SJAG_03618"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[70669,90226,92509,103466,112387],"is_not":false,"summary":null,"term":"GO:0000112"}]},"cv_name":"cellular_component","definition":"One of several protein complexes involved in nucleotide-excision repair; possesses endodeoxynuclease and DNA helicase activities. In S. cerevisiae, it is composed of Rad2p and the core TFIIH-Ssl2p complex (core TFIIH is composed of Rad3p, Tfb1p, Tfb2p, Ssl1p, Tfb4p and Tfb5p. Note that Ssl2p is also called Rad25p).","definition_xrefs":["PMID:7813015","GOC:ew","PMID:10915862","PMID:14500720"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-excision repair complex","termid":"GO:0000109"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00512":null,"SJAG_00901":null,"SJAG_00995":null,"SJAG_03206":null,"SJAG_03618":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"nucleotide-excision repair factor 3 complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"NEF3 complex","type":"exact"}],"termid":"GO:0000112","terms_by_termid":{"GO:0000112":null}}


id: MONDO:1010290
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pulmonary agenesis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder, non-human animal","termid":"MONDO:0700104"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis, non-human animal","termid":"MONDO:1011313"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary agenesis, non-human animal","secondary_identifiers":["OMIA:002520"],"termid":"MONDO:1010290","xrefs":{"Monarch":{"xref_id":"1010290"}}}


id: GO:0070494
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of a thrombin-activated receptor signaling pathway activity. A thrombin receptor signaling pathway is the series of molecular signals generated as a consequence of a thrombin-activated receptor binding to one of its physiological ligands.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of G protein-coupled receptor signaling pathway","termid":"GO:0008277"},{"relation_name":"regulates","term_name":"thrombin-activated receptor signaling pathway","termid":"GO:0070493"}],"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:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of thrombin-activated receptor signaling pathway","synonyms":[{"name":"regulation of thrombin receptor signaling pathway","type":"exact"},{"name":"regulation of thrombin receptor signalling pathway","type":"exact"}],"termid":"GO:0070494"}


id: GO:0070393
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of teichoic acid, which is a major component of the cell wall of Gram-positive bacteria and typically consists of a polymer of glycerol-phosphate or ribitol-phosphate to which are attached glycosyl and D-alanyl ester residues.","definition_xrefs":["GOC:add","PMID:14665680"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule catabolic process","termid":"GO:0009057"},{"relation_name":"is_a","term_name":"teichoic acid metabolic process","termid":"GO:0046374"},{"relation_name":"is_a","term_name":"carbohydrate derivative catabolic process","termid":"GO:1901136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"teichoic acid catabolic process","synonyms":[{"name":"teichoic acid breakdown","type":"exact"},{"name":"teichoic acid catabolism","type":"exact"},{"name":"teichoic acid degradation","type":"exact"}],"termid":"GO:0070393"}


id: MONDO:0032915
data:
  {"annotated_genes":["SJAG_04781","SJAG_04901"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87057,87058],"is_not":false,"summary":null,"term":"MONDO:0032915"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"catecholaminergic polymorphic ventricular tachycardia","termid":"MONDO:0017990"},{"relation_name":"is_a","term_name":"familial long QT syndrome","termid":"MONDO:0019171"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04781":null,"SJAG_04901":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"long QT syndrome 16","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5394068","DOID:0070533","MEDGEN:1713991","OMIM:618782"],"synonyms":[{"name":"LQT16","type":"related"},{"name":"Ventricular Tachycardia, Catecholaminergic Polymorphic 6","type":"related"},{"name":"long QT syndrome 16","type":"exact"}],"termid":"MONDO:0032915","terms_by_termid":{"MONDO:0032915":null},"xrefs":{"Monarch":{"xref_id":"0032915"}}}


id: MONDO:0017781
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 12p deletion","termid":"MONDO:0022174"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"12p12.1 microdeletion syndrome","secondary_identifiers":["UMLS:C4755260","MEDGEN:1652598","Orphanet:313884","GARD:17414"],"synonyms":[{"name":"Del(12)(p12.1)","type":"exact"},{"name":"monosomy 12p12.1","type":"exact"}],"termid":"MONDO:0017781","xrefs":{"Monarch":{"xref_id":"0017781"}}}


id: PBO:0052660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 28","termid":"PBO:0052660"}


id: GO:0045141
data:
  {"annotated_genes":["SJAG_03685","SJAG_03287","SJAG_01263","SJAG_05260","SJAG_05196","SJAG_05226","SJAG_01777","SJAG_00756","SJAG_03092","SJAG_03680","SJAG_01538"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97048,116244,117859,117995],"is_not":false,"summary":null,"term":"GO:0045141"},{"annotations":[90103,64705],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070197"},{"annotations":[87742,100247,105426,90104,103134],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032121"},{"annotations":[114291],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044821"}]},"cv_name":"biological_process","definition":"The cell cycle process in which the dynamic reorganization of telomeres occurs in early meiotic prophase, during which meiotic chromosome ends are gathered in a bouquet arrangement at the inner surface of the nuclear envelope proximal to the spindle pole body. This plays an important role in progression through meiosis and precedes synapsis.","definition_xrefs":["PMID:10690419","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telomere localization","termid":"GO:0034397"},{"relation_name":"is_a","term_name":"chromosome organization involved in meiotic cell cycle","termid":"GO:0070192"},{"relation_name":"is_a","term_name":"chromosome localization to nuclear envelope involved in homologous chromosome segregation","termid":"GO:0090220"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00756":null,"SJAG_01263":null,"SJAG_01538":null,"SJAG_01777":null,"SJAG_03092":null,"SJAG_03287":null,"SJAG_03680":null,"SJAG_03685":null,"SJAG_05196":null,"SJAG_05226":null,"SJAG_05260":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0140013","GO:0051179","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"meiotic telomere clustering","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"synonyms":[{"name":"bouquet biosynthesis","type":"narrow"},{"name":"bouquet formation","type":"narrow"}],"termid":"GO:0045141","terms_by_termid":{"GO:0032121":null,"GO:0044821":null,"GO:0045141":null,"GO:0070197":null}}


id: PBO:0075307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"suppressor of cytokine signaling 4","termid":"PBO:0075307"}


id: PBO:0065463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit, non-ATPase 7","termid":"PBO:0065463"}


id: PBO:0076079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"striatin interacting protein 1","termid":"PBO:0076079"}


id: PBO:0046333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ecto-NOX disulfide-thiol exchanger 2","termid":"PBO:0046333"}


id: PR:O43087
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- kms2 gene.","definition_xrefs":["UniProtKB:O43087","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":"karyogamy meiotic segregation protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC947.12","synonyms":[{"name":"Spom972h-kms2","type":"exact"}],"termid":"PR:O43087"}


id: PBO:0081630
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF559-ZNF177 readthrough","termid":"PBO:0081630"}


id: FYPO:0002377
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is viable and has a larger volume than normal. In a swollen cell, both length and diameter may be greater than normal, although the cell is only considered elongated if the length:diameter ratio is also greater than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"swollen vegetative cell","termid":"FYPO:0000646"},{"relation_name":"has_part","term_name":"viable vegetative cell","termid":"FYPO:0001491"},{"relation_name":"is_a","term_name":"swollen vegetative cell","termid":"FYPO:0000646"},{"relation_name":"is_a","term_name":"viable vegetative cell","termid":"FYPO:0001491"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0000004"],"is_obsolete":false,"name":"viable swollen vegetative cell","synonyms":[{"name":"viable enlarged vegetative cell","type":"related"},{"name":"viable large vegetative cell","type":"related"},{"name":"viable swollen cell during vegetative growth","type":"exact"},{"name":"viable swollen vegetative cell during mitotic cell cycle","type":"related"},{"name":"viable vegetative cell with increased cell size","type":"related"},{"name":"viable vegetative cell with increased cell volume","type":"exact"}],"termid":"FYPO:0002377"}


id: GO:1901702
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of salt from one side of a membrane to the other.","definition_xrefs":["GOC:pr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"salt transmembrane transporter activity","termid":"GO:1901702"}


id: PR:O94416
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A general transcription factor IIF subunit 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR13011:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription initiation factor IIF subunit alpha (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1620.09c","secondary_identifiers":["UniProtKB:O94416"],"synonyms":[{"name":"SPCC1620.09c","type":"related"},{"name":"Spom972h-GTF2F1","type":"exact"},{"name":"TFIIF large subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"TFIIF-alpha (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94416"}


id: PBO:0088974
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 Gas1","termid":"PBO:0088974"}


id: GO:0033211
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by adiponectin binding to its receptor on the surface of a cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:signaling","PMID:20536390","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone-mediated signaling pathway","termid":"GO:0009755"},{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"adiponectin-activated signaling pathway","synonyms":[{"name":"adipocytokine signaling pathway","type":"related"},{"name":"adiponectin-mediated signaling pathway","type":"related"},{"name":"adiponectin-mediated signalling pathway","type":"exact"}],"termid":"GO:0033211"}


id: PBO:0086482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative neutral trehalase, required for thermotolerance; may mediate resistance to other cellular stresses; NTH2 has a paralog, NTH1, that arose from the whole genome duplication","termid":"PBO:0086482"}


id: MOD:01303
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-asparagine residue to an N4-hexosaminyl-L-asparagine.","definition_xrefs":["Unimod:454#N","PubMed:11467524"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N4-glycosyl-L-asparagine","termid":"MOD:00160"},{"relation_name":"is_a","term_name":"hexosaminylated residue","termid":"MOD:00876"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"N4-hexosaminylated asparagine","synonyms":[{"name":"HexN","type":"related"},{"name":"Hexosamine","type":"related"}],"termid":"MOD:01303"}


id: MONDO:0020743
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute leukemia of ambiguous lineage. It is characterized by the presence of either separate populations of blasts of more than one lineage, or one population of blasts co-expressing markers of more than one lineage.","definition_xrefs":["NCIT:C82179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute leukemia of ambiguous lineage","termid":"MONDO:0019460"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0004992"],"is_obsolete":false,"name":"mixed phenotype acute leukemia","secondary_identifiers":["MEDGEN:417342","NANDO:2200018","MedDRA:10067399","UMLS:C2826025","Orphanet:530995","GARD:17972"],"synonyms":[{"name":"MPAL","type":"exact"},{"name":"mixed phenotype acute leukemia","type":"exact"}],"termid":"MONDO:0020743","xrefs":{"Monarch":{"xref_id":"0020743"}}}


id: FYPO:0001117
data:
  {"alleles_by_uniquename":{"SJAG_03689:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03689","name":"dcr1delta","uniquename":"SJAG_03689:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[119546],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004205"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell is lower than normal. Total RNA or a specific RNA, such as the mRNA transcribed from a gene of interest, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level","termid":"FYPO:0000826"},{"relation_name":"is_a","term_name":"altered RNA level during vegetative growth","termid":"FYPO:0001326"},{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03689":null},"genotype_count":1,"genotypes_by_uniquename":{"dcr1delta":{"display_name":"dcr1delta","display_uniquename":"dcr1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03689:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0006551"],"is_obsolete":false,"name":"decreased RNA level during vegetative growth","references_by_uniquename":{"PMID:35226668":null},"secondary_identifiers":["FYPO:0002935"],"single_locus_annotated_genes":["SJAG_03689"],"single_locus_genotype_uniquenames":["dcr1delta"],"synonyms":[{"name":"decreased RNA accumulation during vegetative growth","type":"related"},{"name":"decreased RNA level during mitotic cell cycle","type":"related"},{"name":"decreased cellular RNA level during vegetative growth","type":"exact"},{"name":"decreased cellular mRNA level during vegetative growth","type":"narrow"},{"name":"decreased mRNA accumulation during vegetative growth","type":"related"},{"name":"decreased mRNA level during mitotic cell cycle","type":"related"},{"name":"decreased mRNA level during vegetative growth","type":"narrow"},{"name":"decreased mRNA transcript level during vegetative growth","type":"narrow"},{"name":"decreased messenger RNA level during vegetative growth","type":"narrow"},{"name":"decreased transcript level during vegetative growth","type":"exact"},{"name":"reduced RNA level during vegetative growth","type":"exact"},{"name":"reduced mRNA level during vegetative growth","type":"narrow"}],"termid":"FYPO:0001117","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000162":null,"FYPO:0004205":null,"FYPO_EXT:0000001":null}}


id: PBO:0072797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spalt like transcription factor 4 pseudogene 3","termid":"PBO:0072797"}


id: GO:0140981
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an omega-methyl-medium-chain fatty acid + O2 + reduced [NADPH--hemoprotein reductase] = an omega-hydroxy-medium-chain fatty acid + H+ + H2O + oxidized [NADPH--hemoprotein reductase]. A medium-chain fatty acid has an aliphatic tail containing 6 to 12 carbons.","definition_xrefs":["RHEA:75279"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid omega-hydroxylase activity","termid":"GO:0120250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"medium-chain fatty acid omega-hydroxylase activity","secondary_identifiers":["MetaCyc:RXN-19719"],"termid":"GO:0140981"}


id: MONDO:0003070
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infection of the lymph nodes in the axilla.","definition_xrefs":["NCIT:C27333"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphadenitis","termid":"MONDO:0002052"}],"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":"axillary lymphadenitis","secondary_identifiers":["DOID:4640","MEDGEN:182522","UMLS:C0919797"],"synonyms":[{"name":"axilla lymphadenitis (disease)","type":"exact"},{"name":"axillary adenitis","type":"related"},{"name":"axillary lymphadenitis","type":"exact"},{"name":"lymphadenitis (disease) of axilla","type":"exact"}],"termid":"MONDO:0003070","xrefs":{"Monarch":{"xref_id":"0003070"}}}


id: PBO:0048306
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde-3-phosphate dehydrogenase pseudogene 16","termid":"PBO:0048306"}


id: GO:0006403
data:
  {"annotated_genes":["SJAG_01467","SJAG_03156","SJAG_04536","SJAG_00375","SJAG_04310","SJAG_03470","SJAG_03986","SJAG_01013","SJAG_02661","SJAG_01529","SJAG_03847","SJAG_04360","SJAG_03300","SJAG_01083","SJAG_02704","SJAG_01584","SJAG_04347","SJAG_00093","SJAG_04083","SJAG_04622","SJAG_00298","SJAG_02757","SJAG_02520","SJAG_04645","SJAG_04656","SJAG_02209","SJAG_04721","SJAG_00992","SJAG_00471","SJAG_03593","SJAG_03693","SJAG_04379","SJAG_01185","SJAG_05328","SJAG_01065","SJAG_03729","SJAG_04115","SJAG_01715","SJAG_03696","SJAG_04202","SJAG_04017","SJAG_04480","SJAG_04472","SJAG_02425","SJAG_02274","SJAG_04589","SJAG_04148","SJAG_00178","SJAG_03299","SJAG_00641","SJAG_03283","SJAG_01374","SJAG_03358","SJAG_01449","SJAG_02534","SJAG_01652","SJAG_03002"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[117583],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008298"},{"annotations":[101473,73188,77027,62621,117560,73115,89825,61233,74471,77859,80518],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006406"},{"annotations":[73543],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031990"},{"annotations":[58249,59770,64720],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051028"},{"annotations":[74308,92534,110168,73538,80768,118321,104260,114761,110738,73376,119224,76058,75071,74846,96863,71766,73992,102967,107947,116101,116354,97279,70157,74578,102182,111432,112058,101714,116613,77666],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016973"},{"annotations":[80380,75510,75818,105384,96458,94329],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006405"},{"annotations":[102873],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006404"},{"annotations":[106073,105599,78914,72364],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006409"},{"annotations":[79484],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016031"},{"annotations":[79931],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071528"}]},"cv_name":"biological_process","definition":"A process in which RNA is transported to, or maintained in, a specific location.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule localization","termid":"GO:0033036"}],"gene_count":57,"genes_by_uniquename":{"SJAG_00093":null,"SJAG_00178":null,"SJAG_00298":null,"SJAG_00375":null,"SJAG_00471":null,"SJAG_00641":null,"SJAG_00992":null,"SJAG_01013":null,"SJAG_01065":null,"SJAG_01083":null,"SJAG_01185":null,"SJAG_01374":null,"SJAG_01449":null,"SJAG_01467":null,"SJAG_01529":null,"SJAG_01584":null,"SJAG_01652":null,"SJAG_01715":null,"SJAG_02209":null,"SJAG_02274":null,"SJAG_02425":null,"SJAG_02520":null,"SJAG_02534":null,"SJAG_02661":null,"SJAG_02704":null,"SJAG_02757":null,"SJAG_03002":null,"SJAG_03156":null,"SJAG_03283":null,"SJAG_03299":null,"SJAG_03300":null,"SJAG_03358":null,"SJAG_03470":null,"SJAG_03593":null,"SJAG_03693":null,"SJAG_03696":null,"SJAG_03729":null,"SJAG_03847":null,"SJAG_03986":null,"SJAG_04017":null,"SJAG_04083":null,"SJAG_04115":null,"SJAG_04148":null,"SJAG_04202":null,"SJAG_04310":null,"SJAG_04347":null,"SJAG_04360":null,"SJAG_04379":null,"SJAG_04472":null,"SJAG_04480":null,"SJAG_04536":null,"SJAG_04589":null,"SJAG_04622":null,"SJAG_04645":null,"SJAG_04656":null,"SJAG_04721":null,"SJAG_05328":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"RNA localization","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"RNA localisation","type":"exact"},{"name":"establishment and maintenance of RNA localization","type":"exact"}],"termid":"GO:0006403","terms_by_termid":{"GO:0006404":null,"GO:0006405":null,"GO:0006406":null,"GO:0006409":null,"GO:0008298":null,"GO:0016031":null,"GO:0016973":null,"GO:0031990":null,"GO:0051028":null,"GO:0071528":null}}


id: PBO:0069743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1024, pseudogene","termid":"PBO:0069743"}


id: MONDO:0005517
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm that affects the pharynx.","definition_xrefs":["NCIT:C7545"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system cancer","termid":"MONDO:0000376"},{"relation_name":"is_a","term_name":"digestive system cancer","termid":"MONDO:0002516"},{"relation_name":"is_a","term_name":"disorder of pharynx","termid":"MONDO:0020592"},{"relation_name":"is_a","term_name":"pharynx neoplasm","termid":"MONDO:0021246"},{"relation_name":"is_a","term_name":"malignant tumor of neck","termid":"MONDO:0021310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"pharynx cancer","secondary_identifiers":["EFO:0005577","MESH:D010610","MEDGEN:57554","UMLS:C0153405","DOID:0060119"],"synonyms":[{"name":"cancer of chordate pharynx","type":"exact"},{"name":"cancer of pharynx","type":"exact"},{"name":"chordate pharynx cancer","type":"exact"},{"name":"malignant chordate pharynx neoplasm","type":"exact"},{"name":"malignant neoplasm of chordate pharynx","type":"exact"},{"name":"malignant neoplasm of pharynx","type":"exact"},{"name":"malignant pharyngeal neoplasm","type":"exact"},{"name":"malignant pharyngeal tumor","type":"exact"},{"name":"malignant pharyngeal tumour","type":"exact"},{"name":"malignant pharynx neoplasm","type":"exact"},{"name":"malignant pharynx tumor","type":"exact"},{"name":"malignant pharynx tumour","type":"exact"},{"name":"malignant tumor of pharynx","type":"exact"},{"name":"malignant tumor of the pharynx","type":"exact"},{"name":"malignant tumour of pharynx","type":"exact"},{"name":"malignant tumour of the pharynx","type":"exact"},{"name":"pharyngeal cancer","type":"related"},{"name":"pharyngeal neoplasm","type":"exact"},{"name":"pharynx cancer","type":"exact"},{"name":"pharynx neoplasm","type":"broad"}],"termid":"MONDO:0005517","xrefs":{"Monarch":{"xref_id":"0005517"}}}


id: PBO:0043609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COMM domain containing 2","termid":"PBO:0043609"}


id: FYPO:0007741
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 distribution of a protein localized to chromatin along the length of genes that can be transcribed by RNA polymerase II is abnormal during metaphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah","PMID:33771877"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein distribution along RNA polymerase II-transcribed genes","termid":"FYPO:0006020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"abnormal protein distribution along RNA polymerase II-transcribed genes during mitotic metaphase","synonyms":[{"name":"abnormal protein distribution across RNA polymerase II-transcribed genes during mitotic metaphase","type":"exact"},{"name":"abnormal protein distribution along RNA polymerase II-regulated genes during mitotic metaphase","type":"exact"},{"name":"abnormal protein distribution along RNA polymerase II-transcribed genes during metaphase during vegetative growth","type":"exact"},{"name":"abnormal protein distribution along RNA polymerase II-transcribed genes during metaphase of mitotic cell cycle","type":"exact"},{"name":"abnormal protein distribution in chromatin along RNA polymerase II-transcribed genes during mitotic metaphase","type":"exact"},{"name":"abnormal protein localization to chromatin along RNA polymerase II-transcribed genes during mitotic metaphase","type":"exact"}],"termid":"FYPO:0007741"}


id: PBO:0080420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS51 pseudogene 4","termid":"PBO:0080420"}


id: GO:0009917
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the removal of a C-5 double bond in the B ring of a sterol.","definition_xrefs":["ISBN:0943088399"],"gene_count":0,"genotype_count":0,"name":"obsolete sterol 5-alpha reductase activity (obsolete GO:0009917)","termid":"GO:0009917"}


id: MONDO:1012914
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any amyotrophic lateral sclerosis that occurs in crab-eating macaque due to a mutation in the TARDBP gene created by genetic engineering or gene editing.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iatrogenic disease, non-human animal","termid":"MONDO:1011322"},{"relation_name":"is_a","term_name":"amyotrophic lateral sclerosis, non-human animal","termid":"MONDO:1012954"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amyotrophic lateral sclerosis, TARDBP-related, crab-eating macaque","secondary_identifiers":["OMIA:002492-9541"],"termid":"MONDO:1012914","xrefs":{"Monarch":{"xref_id":"1012914"}}}


id: GO:1902783
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 decane stimulus.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators","GO_REF:0000071","PMID:23826995"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to alkane","termid":"GO:1902779"},{"relation_name":"is_a","term_name":"response to decane","termid":"GO:1902782"}],"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 decane","termid":"GO:1902783"}


id: GO:0044507
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. OBSOLETE. A process that activates or increases the frequency, rate or extent of the activity of a receptor in a second organism.","definition_xrefs":["GOC:fj","PMID:8405712","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete obsolete positive regulation of receptor activity in another organism (obsolete GO:0044507)","synonyms":[{"name":"positive regulation of receptor activity in other organism","type":"exact"}],"termid":"GO:0044507"}


id: PBO:0061166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear-encoded mitochondrial tRNA-Leu (TAA) 4-1","termid":"PBO:0061166"}


id: GO:0002476
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an antigen-presenting cell expresses a peptide antigen of endogenous origin on its cell surface in association with an MHC class Ib protein complex. The peptide is typically a fragment of a larger endogenous protein which has been degraded within the cell. Class Ib here refers to non-classical class I molecules, such as those of the HLA-E gene family.","definition_xrefs":["GOC:add","PMID:15928678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antigen processing and presentation of peptide antigen via MHC class Ib","termid":"GO:0002428"},{"relation_name":"is_a","term_name":"antigen processing and presentation of endogenous peptide antigen","termid":"GO:0002483"}],"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":"antigen processing and presentation of endogenous peptide antigen via MHC class Ib","synonyms":[{"name":"endogenous peptide antigen processing and presentation via MHC class Ib","type":"exact"}],"termid":"GO:0002476"}


id: GO:0072396
data:
  {"annotated_genes":["SJAG_01805","SJAG_04332","SJAG_03048","SJAG_00082","SJAG_04140","SJAG_04183","SJAG_01837"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90341,111511,102698,94146,116976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140429"},{"annotations":[104474],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072429"},{"annotations":[102709],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072441"},{"annotations":[102710],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990820"},{"annotations":[94882,102711],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072435"}]},"cv_name":"biological_process","definition":"A process that occurs in response to signals generated as a result of cell cycle checkpoint signaling.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to biotic stimulus","termid":"GO:0071216"},{"relation_name":"is_a","term_name":"cellular response to endogenous stimulus","termid":"GO:0071495"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_03048":null,"SJAG_04140":null,"SJAG_04183":null,"SJAG_04332":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to cell cycle checkpoint signaling","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0072405","GO:0072408"],"synonyms":[{"name":"G1/S transition checkpoint effector process","type":"related"},{"name":"G2/M transition checkpoint effector process","type":"related"},{"name":"cell cycle checkpoint effector process","type":"exact"},{"name":"response to G1/S transition checkpoint signaling","type":"related"},{"name":"response to G2/M transition checkpoint signaling","type":"related"},{"name":"response to signal involved in G1/S transition checkpoint","type":"related"},{"name":"response to signal involved in G2/M transition checkpoint","type":"related"},{"name":"response to signal involved in cell cycle checkpoint","type":"exact"}],"termid":"GO:0072396","terms_by_termid":{"GO:0072429":null,"GO:0072435":null,"GO:0072441":null,"GO:0140429":null,"GO:1990820":null}}


id: PBO:0078970
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ser (anticodon CGA) 2-1","termid":"PBO:0078970"}


id: MONDO:0968951
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary renal hypouricemia","termid":"MONDO:0009071"}],"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":"hypouricemia, renal","secondary_identifiers":["OMIMPS:220150"],"termid":"MONDO:0968951","xrefs":{"Monarch":{"xref_id":"0968951"}}}


id: PBO:0068374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 167","termid":"PBO:0068374"}


id: GO:0051622
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of norepinephrine into a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transport","termid":"GO:0051051"},{"relation_name":"is_a","term_name":"regulation of norepinephrine uptake","termid":"GO:0051621"},{"relation_name":"negatively_regulates","term_name":"norepinephrine uptake","termid":"GO:0051620"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of norepinephrine uptake","synonyms":[{"name":"down regulation of norepinephrine uptake","type":"exact"},{"name":"down-regulation of norepinephrine uptake","type":"exact"},{"name":"downregulation of norepinephrine uptake","type":"exact"},{"name":"negative regulation of levarterenol uptake","type":"exact"},{"name":"negative regulation of noradrenaline uptake","type":"exact"},{"name":"negative regulation of norepinephrine import","type":"exact"}],"termid":"GO:0051622"}


id: FYPO:0002735
data:
  {"alleles_by_uniquename":{"SJAG_00871:allele-1":{"allele_type":"amino_acid_mutation","description":"cut3-T19E","gene_uniquename":"SJAG_00871","name":"cut3-T19E","uniquename":"SJAG_00871:allele-1"},"SJAG_01956:allele-1":{"allele_type":"amino_acid_mutation","description":"E405K ts","gene_uniquename":"SJAG_01956","name":"nuc2-1051","uniquename":"SJAG_01956:allele-1"},"SJAG_03351:allele-1":{"allele_type":"amino_acid_mutation","description":"A186T ts","gene_uniquename":"SJAG_03351","name":"cut23-415","uniquename":"SJAG_03351:allele-1"},"SJAG_03575:allele-1":{"allele_type":"amino_acid_mutation","description":"E548K ts","gene_uniquename":"SJAG_03575","name":"apc2-361","uniquename":"SJAG_03575:allele-1"},"SJAG_04284:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04284","name":"nup61delta","uniquename":"SJAG_04284:allele-1"},"SJAG_04464:allele-1":{"allele_type":"amino_acid_mutation","description":"R152C","gene_uniquename":"SJAG_04464","name":"pim1-R152C","synonyms":[{"name":"Inferred CDK-phospho-mimic mutation","reference":"PMID:28954740","type":"exact"}],"uniquename":"SJAG_04464:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[119462],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000619"}],"single_locus_phenotype":[{"annotations":[119463],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000619"},{"annotations":[119774,119776,119775],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000618"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which a cell does not proceed normally through a specific cell cycle phase. A cell cycle phase is any of the distinct periods or stages into which the cell cycle is divided. Each phase is characterized by the occurrence of specific biochemical and morphological events.","definition_xrefs":["PomBase:mah","GO:0022403"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell cycle","termid":"FYPO:0000011"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00871":null,"SJAG_01956":null,"SJAG_03351":null,"SJAG_03575":null,"SJAG_04284":null,"SJAG_04464":null},"genotype_count":5,"genotypes_by_uniquename":{"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"apc2-361(E548K ts)","display_uniquename":"apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03575:allele-1","expression":"Not assayed or wild type"}]}]},"cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cut23-415(A186T ts)","display_uniquename":"cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03351:allele-1","expression":"Not assayed or wild type"}]}]},"cut3-T19E-cut3-T19E-amino_acid_mutation-expression-not_assayed_or_wild_type__pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cut3-T19E(aa) pim1-R152C(aa)","display_uniquename":"cut3-T19E-cut3-T19E-amino_acid_mutation-expression-not_assayed_or_wild_type__pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00871:allele-1","expression":"Not assayed or wild type"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04464:allele-1","expression":"Not assayed or wild type"}]}]},"nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"nuc2-1051(E405K ts)","display_uniquename":"nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01956:allele-1","expression":"Not assayed or wild type"}]}]},"nup61delta":{"display_name":"nup61delta","display_uniquename":"nup61delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04284:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000631","FYPO:0005447"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_00871","SJAG_04464"],"name":"abnormal cell cycle phase","references_by_uniquename":{"PMID:23786411":null,"PMID:28954740":null},"single_locus_annotated_genes":["SJAG_03575","SJAG_03351","SJAG_04284","SJAG_01956"],"single_locus_genotype_uniquenames":["nuc2-1051-E405K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","nup61delta","apc2-361-E548K_ts-amino_acid_mutation-expression-not_assayed_or_wild_type","cut23-415-A186T_ts-amino_acid_mutation-expression-not_assayed_or_wild_type"],"termid":"FYPO:0002735","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0000618":null,"FYPO:0000619":null,"FYPO_EXT:0000001":null}}


id: CHEBI:52646
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","definition":"A leptomycin having a (2E,10E,12E,16Z,18E)-double bond configuration as well as an ethyl substituent at position 17.","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leptomycin B","termid":"CHEBI:52646"}


id: MONDO:0019870
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal trisomy 1p36 is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the short arm of chromosome 1, characterized by borderline to mild intellectual disability, mild developmental delay, metopic craniosynostosis and mild craniofacial dysmorphism (incl. slopping forehead, bitemporal narrowing, blepharophimosis). Other associated abnormalities may include growth retardation, microcephaly, large hands, syndactyly, supernumerary ribs, rectal stenosis and/or anterior displacement of anus. Congenital heart malformations (e.g. atrial septal defect, patent ductus arteriosus) have also been reported.","definition_xrefs":["Orphanet:96069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of the short arm of chromosome 1","termid":"MONDO:0017012"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal trisomy 1p36","secondary_identifiers":["GARD:19303","SCTID:766053003","UMLS:C4707665","MEDGEN:1646544"],"synonyms":[{"name":"distal duplication 1p36","type":"exact"},{"name":"distal trisomy type 1p36","type":"exact"},{"name":"telomeric duplication 1p36","type":"exact"},{"name":"trisomy 1pter","type":"exact"}],"termid":"MONDO:0019870","xrefs":{"Monarch":{"xref_id":"0019870"}}}


id: PBO:0073873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 10 member 1","termid":"PBO:0073873"}


id: FYPO:0001404
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A colony morphology phenotype in which the outline of a colony growing on a solid surface is not symmetrical.","definition_xrefs":["PomBase:mah","PomBase:mp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal colony morphology","termid":"FYPO:0000150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"irregular colony morphology","synonyms":[{"name":"wavy-edged colony","type":"related"}],"termid":"FYPO:0001404"}


id: MONDO:0010071
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete spondyloenchondrodysplasia (obsolete MONDO:0010071)","termid":"MONDO:0010071","xrefs":{"Monarch":{"xref_id":"0010071"}}}


id: MONDO:0000092
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pyloric stenosis, infantile (obsolete MONDO:0000092)","termid":"MONDO:0000092","xrefs":{"Monarch":{"xref_id":"0000092"}}}


id: GO:1903228
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of xanthosine.","definition_xrefs":["GO_REF:0000068","GOC:TermGenie","PMID:7559336","PMID:7007809"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleoside catabolic process","termid":"GO:0046130"},{"relation_name":"is_a","term_name":"xanthosine metabolic process","termid":"GO:1903227"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"xanthosine catabolic process","synonyms":[{"name":"xanthosine breakdown","type":"exact"},{"name":"xanthosine catabolism","type":"exact"},{"name":"xanthosine degradation","type":"exact"}],"termid":"GO:1903228"}


