# terms

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":["PMID:20133819","GOC:dph","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:0009381
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hyperbilirubinemia","termid":"MONDO:0002408"}],"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":"hyperbilirubinemia, conjugated, type 3","secondary_identifiers":["MEDGEN:98323","UMLS:C0400964","MESH:C562885","SCTID:235906009","OMIM:237550"],"synonyms":[{"name":"hyperbilirubinemia, conjugated, type III","type":"related"}],"termid":"MONDO:0009381","xrefs":{"Monarch":{"xref_id":"0009381"}}}


id: PBO:0004154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJ protein Caj1/Djp1-type (predicted)","termid":"PBO:0004154"}


id: PBO:0080849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YBX2 pseudogene 2","termid":"PBO:0080849"}


id: GO:0030137
data:
  {"annotated_genes":["SJAG_01025","SJAG_03368","SJAG_02482","SJAG_02234","SJAG_01927","SJAG_01285","SJAG_04070","SJAG_02160","SJAG_01508","SJAG_04002","SJAG_04402","SJAG_04569","SJAG_04474","SJAG_04391","SJAG_00192"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[93560,95088,101469,116134],"is_not":false,"summary":null,"term":"GO:0030137"},{"annotations":[72758,80213,75527,79903,65472,81770,95174,109094,100400],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030126"},{"annotations":[58408,64465],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030663"}]},"cv_name":"cellular_component","definition":"A vesicle with a coat formed of the COPI coat complex proteins. COPI-coated vesicles are found associated with Golgi membranes at steady state, are involved in Golgi to endoplasmic reticulum (retrograde) vesicle transport, and possibly also in intra-Golgi transport.","definition_xrefs":["PMID:11252894","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Golgi-associated vesicle","termid":"GO:0005798"},{"relation_name":"is_a","term_name":"coated vesicle","termid":"GO:0030135"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00192":null,"SJAG_01025":null,"SJAG_01285":null,"SJAG_01508":null,"SJAG_01927":null,"SJAG_02160":null,"SJAG_02234":null,"SJAG_02482":null,"SJAG_03368":null,"SJAG_04002":null,"SJAG_04070":null,"SJAG_04391":null,"SJAG_04402":null,"SJAG_04474":null,"SJAG_04569":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0031410"],"is_obsolete":false,"name":"COPI-coated vesicle","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000044":null,"GO_REF:0000107":null},"synonyms":[{"name":"coatomer","type":"related"}],"termid":"GO:0030137","terms_by_termid":{"GO:0030126":null,"GO:0030137":null,"GO:0030663":null}}


id: MONDO:0020681
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome, musculocontractural type","termid":"MONDO:0011142"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066","MONDO:0005267"],"is_obsolete":false,"name":"Ehlers-Danlos syndrome, musculocontractural type 1","secondary_identifiers":["NCIT:C168975","DOID:0080736","OMIM:601776"],"synonyms":[{"name":"Arthrogryposis, Distal, with peculiar facies and hydronephrosis","type":"related"},{"name":"Dundar syndrome","type":"related"},{"name":"EDSMC","type":"related"},{"name":"EDSMC1","type":"related"},{"name":"Ehlers-Danlos syndrome, musculocontractural type, 1","type":"related"},{"name":"Ehlers-Danlos syndrome, type Vib","type":"related"},{"name":"Ehlers-Danlos syndrome, type Vib, formerly","type":"related"},{"name":"adducted thumb, clubfoot, and Progressive Joint and skin laxity syndrome","type":"related"},{"name":"adducted thumb-clubfoot syndrome","type":"related"}],"termid":"MONDO:0020681","xrefs":{"Monarch":{"xref_id":"0020681"}}}


id: PBO:0042764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centrosomal protein 57 like 1","termid":"PBO:0042764"}


id: PBO:0050675
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family A (Hsp70) member 8 pseudogene 2","termid":"PBO:0050675"}


id: MONDO:0033169
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"curariform drugs toxicity","secondary_identifiers":["Orphanet:413693"],"termid":"MONDO:0033169","xrefs":{"Monarch":{"xref_id":"0033169"}}}


id: PBO:0003128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ran GTPase binding protein Sbp1","termid":"PBO:0003128"}


id: PBO:0079737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBX domain protein 2B","termid":"PBO:0079737"}


id: PBO:0081713
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 638","termid":"PBO:0081713"}


id: GO:0009953
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regionalization process in which the areas along the dorsal/ventral axis are established that will lead to differences in cell differentiation. The dorsal/ventral axis is defined by a line that runs orthogonal to both the anterior/posterior and left/right axes. The dorsal end is defined by the upper or back side of an organism. The ventral end is defined by the lower or front side of an organism.","definition_xrefs":["GOC:go_curators","GOC:dph","GOC:isa_complete","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"dorsal/ventral pattern formation","synonyms":[{"name":"dorsal-ventral pattern formation","type":"exact"},{"name":"dorsal/ventral pattern specification","type":"narrow"},{"name":"dorsoventral pattern formation","type":"exact"}],"termid":"GO:0009953"}


id: GO:0010489
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-4-keto-6-deoxyglucose = UDP-4-keto-rhamnose.","definition_xrefs":["PMID:17190829","GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"racemase and epimerase activity, acting on carbohydrates and derivatives","termid":"GO:0016857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0003824","GO:0016853","GO:0003674"],"is_obsolete":false,"name":"UDP-4-keto-6-deoxy-glucose-3,5-epimerase activity","termid":"GO:0010489"}


id: PBO:0078054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 44","termid":"PBO:0078054"}


id: PR:O14003
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A replication factor C subunit 5 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01671"],"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":"replication factor C subunit 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC27E2.10c","secondary_identifiers":["UniProtKB:O14003"],"synonyms":[{"name":"Spom972h-RFC5","type":"exact"},{"name":"replication factor C3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14003"}


id: PBO:0004533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial dynamin family GTPase Msp1","termid":"PBO:0004533"}


id: PBO:0071167
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 6","termid":"PBO:0071167"}


id: PBO:0092003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"silenced P-specific trancription factor Pi","termid":"PBO:0092003"}


id: GO:1905555
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of blood vessel branching.","definition_xrefs":["GOC:BHF_telomere","GOC:nc","GO_REF:0000058","GOC:BHF","GOC:TermGenie","PMID:23201774"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of angiogenesis","termid":"GO:0045766"},{"relation_name":"is_a","term_name":"positive regulation of morphogenesis of an epithelium","termid":"GO:1905332"},{"relation_name":"is_a","term_name":"regulation of blood vessel branching","termid":"GO:1905553"},{"relation_name":"positively_regulates","term_name":"branching involved in blood vessel morphogenesis","termid":"GO:0001569"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of blood vessel branching","synonyms":[{"name":"activation of branching involved in blood vessel morphogenesis","type":"narrow"},{"name":"activation of patterning of blood vessels","type":"narrow"},{"name":"positive regulation of branching involved in blood vessel morphogenesis","type":"exact"},{"name":"up regulation of branching involved in blood vessel morphogenesis","type":"exact"},{"name":"up regulation of patterning of blood vessels","type":"exact"},{"name":"up-regulation of branching involved in blood vessel morphogenesis","type":"exact"},{"name":"up-regulation of patterning of blood vessels","type":"exact"},{"name":"upregulation of branching involved in blood vessel morphogenesis","type":"exact"},{"name":"upregulation of patterning of blood vessels","type":"exact"}],"termid":"GO:1905555"}


id: GO:0031424
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the cytoplasm of the outermost cells of the vertebrate epidermis is replaced by keratin. Keratinization occurs in the stratum corneum, feathers, hair, claws, nails, hooves, and horns.","definition_xrefs":["GOC:tb","GOC:sdb_2009","GOC:dph","GOC:ebc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"part_of","term_name":"keratinocyte differentiation","termid":"GO:0030216"}],"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":"keratinization","secondary_identifiers":["Reactome:R-HSA-6805567"],"termid":"GO:0031424"}


id: MONDO:0019889
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal trisomy 22q is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the long arm of chromosome 22, with variable phenotype principally characterized by varying degrees of intellectual disability and developmental delay, pre- and postnatal growth deficiency, hypotonia, and craniofacial dysmorphism (incl. microcephaly, hypertelorism, narrow and upslanted palpebral fissures, epicanthic folds, low-set dysplastic ears, broad and depressed nasal bridge, cleft lip an/or palate, long philtrum, retro/micrognathia). Congenital heart defects, as well as cerebral, skeletal, renal and genital anomalies, have also been reported.","definition_xrefs":["Orphanet:96109"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of the long arm of chromosome 22","termid":"MONDO:0016972"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal trisomy 22q","secondary_identifiers":["GARD:19322","MEDGEN:1642344","SCTID:764512003","UMLS:C4706936"],"synonyms":[{"name":"distal duplication 22q","type":"exact"},{"name":"distal trisomy type 22q","type":"exact"},{"name":"telomeric duplication 22q","type":"exact"},{"name":"trisomy 22qter","type":"exact"}],"termid":"MONDO:0019889","xrefs":{"Monarch":{"xref_id":"0019889"}}}


id: PBO:0027617
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_gamma-tubulin_complex_localization_to_mitotic_spindle_pole_body_following_normal_mitosis","termid":"PBO:0027617"}


id: PBO:0087079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L41A; comprises only 25 amino acids; rpl41a rpl41b double null mutant is viable; homologous to mammalian ribosomal protein L41, no bacterial homolog; RPL41A has a paralog, RPL41B, that arose from the whole genome duplication","termid":"PBO:0087079"}


id: GO:0010280
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-D-glucose + NADPH + H+ = UDP-L-rhamnose + NADP+ + H2O.","definition_xrefs":["MetaCyc:RXN-5482","PMID:14701918"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity","termid":"GO:0016740"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"UDP-L-rhamnose synthase activity","synonyms":[{"name":"UDP-4-keto-6-deoxy-D-glucose 3,5-epimerase-4-reductase activity","type":"narrow"}],"termid":"GO:0010280"}


id: PBO:0043265
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"claudin 24","termid":"PBO:0043265"}


id: GO:1900943
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of (Z)-nonadeca-1,14-diene biosynthetic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of olefin biosynthetic process","termid":"GO:1900913"},{"relation_name":"is_a","term_name":"positive regulation of (Z)-nonadeca-1,14-diene metabolic process","termid":"GO:1900940"},{"relation_name":"is_a","term_name":"regulation of (Z)-nonadeca-1,14-diene biosynthetic process","termid":"GO:1900941"},{"relation_name":"positively_regulates","term_name":"(Z)-nonadeca-1,14-diene biosynthetic process","termid":"GO:1900879"}],"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 (Z)-nonadeca-1,14-diene biosynthetic process","synonyms":[{"name":"activation of (Z)-nonadeca-1,14-diene anabolism","type":"narrow"},{"name":"activation of (Z)-nonadeca-1,14-diene biosynthesis","type":"narrow"},{"name":"activation of (Z)-nonadeca-1,14-diene biosynthetic process","type":"narrow"},{"name":"activation of (Z)-nonadeca-1,14-diene formation","type":"narrow"},{"name":"activation of (Z)-nonadeca-1,14-diene synthesis","type":"narrow"},{"name":"positive regulation of (Z)-nonadeca-1,14-diene anabolism","type":"exact"},{"name":"positive regulation of (Z)-nonadeca-1,14-diene biosynthesis","type":"exact"},{"name":"positive regulation of (Z)-nonadeca-1,14-diene formation","type":"exact"},{"name":"positive regulation of (Z)-nonadeca-1,14-diene synthesis","type":"exact"},{"name":"up regulation of (Z)-nonadeca-1,14-diene anabolism","type":"exact"},{"name":"up regulation of (Z)-nonadeca-1,14-diene biosynthesis","type":"exact"},{"name":"up regulation of (Z)-nonadeca-1,14-diene biosynthetic process","type":"exact"},{"name":"up regulation of (Z)-nonadeca-1,14-diene formation","type":"exact"},{"name":"up regulation of (Z)-nonadeca-1,14-diene synthesis","type":"exact"},{"name":"up-regulation of (Z)-nonadeca-1,14-diene anabolism","type":"exact"},{"name":"up-regulation of (Z)-nonadeca-1,14-diene biosynthesis","type":"exact"},{"name":"up-regulation of (Z)-nonadeca-1,14-diene biosynthetic process","type":"exact"},{"name":"up-regulation of (Z)-nonadeca-1,14-diene formation","type":"exact"},{"name":"up-regulation of (Z)-nonadeca-1,14-diene synthesis","type":"exact"},{"name":"upregulation of (Z)-nonadeca-1,14-diene anabolism","type":"exact"},{"name":"upregulation of (Z)-nonadeca-1,14-diene biosynthesis","type":"exact"},{"name":"upregulation of (Z)-nonadeca-1,14-diene biosynthetic process","type":"exact"},{"name":"upregulation of (Z)-nonadeca-1,14-diene formation","type":"exact"},{"name":"upregulation of (Z)-nonadeca-1,14-diene synthesis","type":"exact"}],"termid":"GO:1900943"}


id: PBO:0002544
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.1.30.-","termid":"PBO:0002544"}


id: PBO:0031633
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_gene_silencing","termid":"PBO:0031633"}


id: PBO:0074561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA host gene 15","termid":"PBO:0074561"}


id: PBO:0068217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 524","termid":"PBO:0068217"}


id: PBO:0075892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5","termid":"PBO:0075892"}


id: MONDO:0975809
data:
  {"annotated_genes":["SJAG_04199"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88778],"is_not":false,"summary":null,"term":"MONDO:0975809"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"microphthalmia, isolated, with coloboma","termid":"MONDO:0000170"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04199":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"microphthalmia/coloboma 13","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620968"],"termid":"MONDO:0975809","terms_by_termid":{"MONDO:0975809":null},"xrefs":{"Monarch":{"xref_id":"0975809"}}}


id: GO:1990636
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A life cycle stage during which the reproductive capacity and fitness of an organism declines.","definition_xrefs":["PMID:27353257","PMID:24914937","PMID:25523082"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological phase","termid":"GO:0044848"}],"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":"reproductive senescence","synonyms":[{"name":"ovarian senescence","type":"narrow"}],"termid":"GO:1990636"}


id: MONDO:0016276
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"High-grade neuroendocrine carcinoma of the cervix uteri is a rare, aggressive, primary cervical neoplasm, originating from neuroendocrine cells present in the lining epithelium of the cervix, characterized, macroscopically, by usually large lesions, sometimes with a barrel-shaped appearance. Patients often present with abnormal vaginal bleeding or discharge, pelvic/abdominal pain, post-coital spotting and/or dysuria, while symptoms related to carcinoid syndrome are not frequent.","definition_xrefs":["Orphanet:213777"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervical cancer","termid":"MONDO:0002974"}],"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":"high-grade neuroendocrine carcinoma of the cervix uteri","secondary_identifiers":["ICD10CM:C53.0","MEDGEN:1668378","UMLS:C4751235","NCIT:C128045","GARD:20489"],"synonyms":[{"name":"high-grade neuroendocrine carcinoma of the uterine cervix","type":"exact"},{"name":"poorly differentiated neuroendocrine carcinoma of the cervix uteri","type":"exact"},{"name":"poorly differentiated neuroendocrine cervical carcinoma","type":"exact"}],"termid":"MONDO:0016276","xrefs":{"Monarch":{"xref_id":"0016276"}}}


id: PBO:0068935
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 178, pseudogene","termid":"PBO:0068935"}


id: GO:0047973
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + guanidinoacetate = ADP + 2 H+ + phosphoguanidinoacetate.","definition_xrefs":["EC:2.7.3.1","RHEA:14145"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, nitrogenous group as acceptor","termid":"GO:0016775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016301"],"is_obsolete":false,"name":"guanidinoacetate kinase activity","secondary_identifiers":["MetaCyc:GUANIDOACETATE-KINASE-RXN","KEGG_REACTION:R02575"],"synonyms":[{"name":"ATP:guanidinoacetate N-phosphotransferase activity","type":"related"},{"name":"glycocyamine kinase activity","type":"related"},{"name":"guanidoacetate kinase activity","type":"exact"}],"termid":"GO:0047973"}


id: GO:0021849
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The division of neuroblasts in the subventricular zone of the forebrain. The interneuron precursors that these cells give rise to include adult olfactory bulb interneurons and migrate tangentially.","definition_xrefs":["GOC:jid","PMID:12626695","GO_REF:0000021","GOC:cls","GOC:dgh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroblast division","termid":"GO:0055057"},{"relation_name":"part_of","term_name":"cell proliferation in forebrain","termid":"GO:0021846"}],"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":"neuroblast division in subventricular zone","termid":"GO:0021849"}


id: GO:0044328
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 involved in the positive regulation of endothelial cell migration.","definition_xrefs":["GOC:jl","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete canonical Wnt signaling pathway involved in positive regulation of endothelial cell migration (obsolete GO:0044328)","synonyms":[{"name":"canonical Wnt receptor signaling pathway involved in positive regulation of endothelial cell migration","type":"exact"},{"name":"canonical Wnt receptor signalling pathway involved in positive regulation of endothelial cell migration","type":"exact"}],"termid":"GO:0044328"}


id: MOD:00323
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to L-lysine methyl ester.","definition_xrefs":["PubMed:10973948","PubMed:11875433","RESID:AA0318","Unimod:34#C-term"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monomethylated L-lysine","termid":"MOD:01683"},{"relation_name":"is_a","term_name":"alpha-carboxyl methylated residue","termid":"MOD:01689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"L-lysine methyl ester","synonyms":[{"name":"2,6-diaminohexanoic methyl ester","type":"exact"},{"name":"L-lysine methyl ester","type":"exact"},{"name":"MOD_RES Lysine methyl ester","type":"exact"},{"name":"Methyl","type":"related"},{"name":"Methylation","type":"related"},{"name":"OMeLys","type":"exact"},{"name":"alpha,epsilon-diaminocaproic methyl ester","type":"exact"},{"name":"methyl (S)-2,6-diaminohexanoate","type":"exact"},{"name":"methyl L-lysinate","type":"exact"},{"name":"methyl esterified L-lysine","type":"exact"}],"termid":"MOD:00323"}


id: PBO:0005629
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic recombination protein (predicted)","termid":"PBO:0005629"}


id: PBO:0034623
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_cleavage_furrow","termid":"PBO:0034623"}


id: MONDO:0008725
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital lipoid adrenal hyperplasia (CLAH) is one of the most severe forms of congenital adrenal hyperplasia (CAH) characterized by severe adrenal insufficiency and sex reversal in males.","definition_xrefs":["Orphanet:90790"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital adrenal hyperplasia","termid":"MONDO:0018479"},{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005047","MONDO:0002525"],"is_obsolete":false,"name":"congenital lipoid adrenal hyperplasia due to STAR deficency","secondary_identifiers":["OMIM:201710","SCTID:44231009","GARD:1465","MEDGEN:83341","UMLS:C0342474"],"synonyms":[{"name":"CLAH","type":"exact"},{"name":"LCAH","type":"related"},{"name":"adrenal hyperplasia 1","type":"related"},{"name":"congenital adrenal hyperplasia lipoid","type":"related"},{"name":"lipoid adrenal hyperplasia","type":"exact"},{"name":"lipoid congenital adrenal hyperplasia","type":"related"},{"name":"lipoid hyperplasia, congenital, of adrenal cortex with Male pseudohermaphroditism","type":"related"}],"termid":"MONDO:0008725","xrefs":{"Monarch":{"xref_id":"0008725"}}}


id: GO:0034351
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of glial cell apoptotic process.","definition_xrefs":["GOC:mah","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glial cell apoptotic process","termid":"GO:0034350"},{"relation_name":"is_a","term_name":"negative regulation of apoptotic process","termid":"GO:0043066"},{"relation_name":"negatively_regulates","term_name":"glial cell apoptotic process","termid":"GO:0034349"}],"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 glial cell apoptotic process","synonyms":[{"name":"down regulation of glial cell apoptosis","type":"exact"},{"name":"down-regulation of glial cell apoptosis","type":"exact"},{"name":"downregulation of glial cell apoptosis","type":"exact"},{"name":"inhibition of glial cell apoptosis","type":"narrow"},{"name":"negative regulation of glial cell apoptosis","type":"narrow"}],"termid":"GO:0034351"}


id: PBO:0055629
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 3068","termid":"PBO:0055629"}


id: MONDO:0010930
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Anophthalmia plus syndrome is a very rare multiple congenital anomaly syndrome characterized by the presence of anophthalmia or severe microphthalmia, cleft lip/palate, facial cleft and sacral neural tube defects, along with various additional anomalies including congenital glaucoma, iris coloboma, primary hyperplastic vitreous, hypertelorism, low-set ears, clinodactyly, choanal atresia/stenosis, dysgenesis of sacrum, tethering of spinal cord, syringomyelia, hypoplasia of corpus callosum, cerebral ventriculomegaly and endocrine abnormalities. An autosomal recessive inheritance has been suggested.","definition_xrefs":["Orphanet:1104"],"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"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anophthalmia plus syndrome","secondary_identifiers":["OMIM:600776","SCTID:720496006","UMLS:C1833339","MESH:C537767","MEDGEN:322166","GARD:719"],"synonyms":[{"name":"Fryns anophthalmia syndrome","type":"related"},{"name":"Fryns microphthalmia syndrome","type":"exact"},{"name":"Leichtman Wood Rohn syndrome","type":"related"},{"name":"anophthalmia, cleft lip/palate, facial anomalies, and CNS anomalies and hypothalamic disorder","type":"related"},{"name":"anophthalmia-plus syndrome","type":"related"},{"name":"microphthalmia with facial clefting","type":"exact"}],"termid":"MONDO:0010930","xrefs":{"Monarch":{"xref_id":"0010930"}}}


id: MONDO:0013617
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete overgrowth-macrocephaly-facial dysmorphism syndrome (obsolete MONDO:0013617)","secondary_identifiers":["OMIM:614192"],"termid":"MONDO:0013617","xrefs":{"Monarch":{"xref_id":"0013617"}}}


id: PBO:0082296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Arginyl-tRNA synthetase; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies; YDR341C has a paralog, MSR1, that arose from the whole genome duplication","termid":"PBO:0082296"}


id: PBO:0013811
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by G. gallus cdc2","termid":"PBO:0013811"}


id: PBO:0068568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 19, pseudogene","termid":"PBO:0068568"}


id: FYPO:0007933
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to 2,2′-dipyridyl. Cells stop growing (and may die) at a concentration of 2,2′-dipyridyl that allows wild type cells to grow.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000003","FYPO:0000139","FYPO:0001985","FYPO:0002683"],"is_obsolete":false,"name":"sensitive to 2,2′-dipyridyl","termid":"FYPO:0007933"}


id: GO:0047281
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: pyrophosphate + a 2,4-dioxotetrahydropyrimidine D-ribonucleotide = PRPP + a 2,4-dioxotetrahydropyrimidine.","definition_xrefs":["EC:2.4.2.20","MetaCyc:2.4.2.20-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentosyltransferase activity","termid":"GO:0016763"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016757","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"dioxotetrahydropyrimidine phosphoribosyltransferase activity","secondary_identifiers":["RHEA:10232"],"synonyms":[{"name":"2,4-dioxotetrahydropyrimidine-nucleotide:diphosphate phospho-alpha-D-ribosyltransferase activity","type":"related"},{"name":"dioxotetrahydropyrimidine phosphoribosyl transferase activity","type":"related"},{"name":"dioxotetrahydropyrimidine ribonucleotide pyrophosphorylase activity","type":"related"},{"name":"dioxotetrahydropyrimidine-ribonucleotide diphosphorylase activity","type":"related"},{"name":"dioxotetrahydropyrimidine-ribonucleotide pyrophosphorylase activity","type":"related"}],"termid":"GO:0047281"}


id: GO:1904476
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of small GTPase binding.","definition_xrefs":["PMID:15798216","GO_REF:0000059","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of small GTPase binding (obsolete GO:1904476)","synonyms":[{"name":"down regulation of small GTPase binding","type":"exact"},{"name":"down-regulation of Ras GTPase binding","type":"exact"},{"name":"downregulation of small GTPase binding","type":"exact"},{"name":"inhibition of small GTPase binding","type":"exact"},{"name":"negative regulation of Ras GTPase binding","type":"narrow"}],"termid":"GO:1904476"}


id: PBO:0048466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GCLC antisense RNA 1","termid":"PBO:0048466"}


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: PBO:0114343
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptional coactivator for ribosomal proteins via TOR signaling pathway Crf1/Ifh1","termid":"PBO:0114343"}


id: MONDO:0019419
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked intellectual disability-macrocephaly-macroorchidism syndrome is characterized by intellectual deficit affecting both sexes, macrocephaly, and macroorchidism in the majority of affected males. It has been described in 12 individuals from two generations of one family. Other males from this family did not display intellectual deficit but did present macroorchidism and macrocephaly. Transmission is X-linked and the causative gene has been localized to the q12-q21 region of the X chromosome.","definition_xrefs":["Orphanet:85320"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked intellectual disability-macrocephaly-macroorchidism syndrome","secondary_identifiers":["MEDGEN:930075","GARD:19055","UMLS:C4304406","SCTID:719825000"],"synonyms":[{"name":"Johnson syndrome","type":"exact"}],"termid":"MONDO:0019419","xrefs":{"Monarch":{"xref_id":"0019419"}}}


id: PBO:0040242
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy related 2B","termid":"PBO:0040242"}


id: GO:0098731
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process by which the number of skeletal muscle satellite stem cells in a skeletal muscle is maintained during skeletal muscle regeneration. There are at least two mechanisms by which this is achieved. Skeletal muscle satellite stem cell asymmetric division ensures satellite stem cell numbers are kept constant. Symmetric division of these cells amplifies the number of skeletal muscle satellite stem cells.","definition_xrefs":["PMID:23303905"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal muscle satellite cell maintenance involved in skeletal muscle regeneration","termid":"GO:0014834"},{"relation_name":"is_a","term_name":"somatic stem cell population maintenance","termid":"GO:0035019"}],"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":"skeletal muscle satellite stem cell maintenance involved in skeletal muscle regeneration","termid":"GO:0098731"}


id: PBO:0059465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mutS homolog 4","termid":"PBO:0059465"}


id: GO:0009346
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Citrate lyase is a multienzyme complex with three constituents: the alpha subunit, citrate-ACP transferase; the beta subunit, citryl-ACP lyase; and the gamma subunit, an acyl-carrier protein which also carries the prosthetic group components. All three subunits are required for citrate lyase enzyme activity. This enzyme has only been found in bacteria.","definition_xrefs":["PMID:32302313"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"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":"ATP-independent citrate lyase complex","secondary_identifiers":["MetaCyc:ACECITLY-CPLX"],"synonyms":[{"name":"citrate lyase complex","type":"broad"},{"name":"citrate synthase complex","type":"broad"}],"termid":"GO:0009346"}


id: GO:1901527
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any abscisic acid mediated signaling pathway that is involved in stomatal movement.","definition_xrefs":["PMID:22730405","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abscisic acid-activated signaling pathway","termid":"GO:0009738"},{"relation_name":"part_of","term_name":"stomatal movement","termid":"GO:0010118"}],"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":"abscisic acid-activated signaling pathway involved in stomatal movement","synonyms":[{"name":"abscisic acid mediated signaling pathway involved in stomatal movement","type":"related"},{"name":"abscisic acid mediated signalling involved in stomatal movement","type":"exact"}],"termid":"GO:1901527"}


id: PBO:0027927
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_RNA_level_during_cellular_response_to_pheromone_and_nitrogen_starvation","termid":"PBO:0027927"}


id: PBO:0045244
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 C24","termid":"PBO:0045244"}


id: PBO:0056885
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial contact site and cristae organizing system subunit 13","termid":"PBO:0056885"}


id: GO:0006466
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 protein disulfide-isomerase reaction (obsolete GO:0006466)","synonyms":[{"name":"protein disulfide-isomerase reaction","type":"exact"},{"name":"protein disulphide-isomerase reaction","type":"exact"}],"termid":"GO:0006466"}


id: PBO:0086382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative ATP-dependent RNA helicase of the DEAD-box family; involved in ribosomal biogenesis; required at post-transcriptional step for efficient retrotransposition; essential for growth under anaerobic conditions","termid":"PBO:0086382"}


id: FYPO:0003171
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a cell has two nuclei and the mitotic cell cycle is arrested after the septum has formed, but before cells have separated.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"binucleate vegetative cell","termid":"FYPO:0001222"},{"relation_name":"has_part","term_name":"monoseptate","termid":"FYPO:0001225"},{"relation_name":"has_part","term_name":"mitotic cell cycle arrest before cell separation","termid":"FYPO:0002888"},{"relation_name":"is_a","term_name":"binucleate vegetative cell","termid":"FYPO:0001222"},{"relation_name":"is_a","term_name":"septated vegetative cell","termid":"FYPO:0002342"},{"relation_name":"is_a","term_name":"mitotic cell cycle arrest before cell separation","termid":"FYPO:0002888"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000631","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"binucleate monoseptate cell with mitotic cell cycle arrest before cell separation","synonyms":[{"name":"binucleate monoseptate cell with cell cycle arrest before cell separation during mitotic cell cycle","type":"related"},{"name":"binucleate monoseptate cell with mitotic cell cycle arrest before cell separation after cytokinesis","type":"exact"},{"name":"binucleate monoseptate cell with mitotic cell cycle arrest before cell separation after cytokinesis during vegetative growth","type":"exact"},{"name":"binucleate monoseptate cell with mitotic cell cycle arrest before cytokinetic cell separation","type":"exact"},{"name":"mitotic cell cycle arrest before cell separation with binucleate monoseptate cell","type":"exact"},{"name":"nuclear division arrest with septation (normal cell length)","type":"exact"}],"termid":"FYPO:0003171"}


id: GO:0030816
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways involving the nucleotide cAMP (cyclic AMP, adenosine 3',5'-cyclophosphate).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of cAMP metabolic process (obsolete GO:0030816)","synonyms":[{"name":"activation of cAMP metabolic process","type":"narrow"},{"name":"positive regulation of 3',5' cAMP metabolic process","type":"exact"},{"name":"positive regulation of 3',5' cAMP metabolism","type":"exact"},{"name":"positive regulation of 3',5'-cAMP metabolic process","type":"exact"},{"name":"positive regulation of 3',5'-cAMP metabolism","type":"exact"},{"name":"positive regulation of adenosine 3',5'-cyclophosphate metabolic process","type":"exact"},{"name":"positive regulation of adenosine 3',5'-cyclophosphate metabolism","type":"exact"},{"name":"positive regulation of cAMP metabolism","type":"exact"},{"name":"positive regulation of cyclic AMP metabolic process","type":"exact"},{"name":"positive regulation of cyclic AMP metabolism","type":"exact"},{"name":"stimulation of cAMP metabolic process","type":"narrow"},{"name":"up regulation of cAMP metabolic process","type":"exact"},{"name":"up-regulation of cAMP metabolic process","type":"exact"},{"name":"upregulation of cAMP metabolic process","type":"exact"}],"termid":"GO:0030816"}


id: MONDO:0020132
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete non-syndromic central nervous system malformation (obsolete MONDO:0015219)","termid":"MONDO:0015219"}],"gene_count":0,"genotype_count":0,"name":"obsolete cranial nerve and nuclear aplasia (obsolete MONDO:0020132)","secondary_identifiers":["Orphanet:98518"],"termid":"MONDO:0020132","xrefs":{"Monarch":{"xref_id":"0020132"}}}


id: SO:0000331
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Short (typically a few hundred base pairs) DNA sequence that has a single occurrence in a genome and whose location and base sequence are known.","direct_ancestors":[{"relation_name":"is_a","term_name":"tag","termid":"SO:0000324"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STS","synonyms":[{"name":"INSDC_feature:STS","type":"exact"},{"name":"sequence tag site","type":"exact"}],"termid":"SO:0000331"}


id: FYPO:0003407
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of glyoxal than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0005447","FYPO:0001985","FYPO:0002682","FYPO:0000139"],"is_obsolete":false,"name":"resistance to glyoxal","synonyms":[{"name":"resistance to GO","type":"broad"},{"name":"resistance to glyoxal during mitotic cell cycle","type":"related"},{"name":"resistance to glyoxal during vegetative growth","type":"exact"},{"name":"resistant to glyoxal","type":"exact"}],"termid":"FYPO:0003407"}


id: PATO:0001378
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A polyploidy quality inhering in a bearer by virtue of the bearer's containing chromosomes derived from a single species.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Autopolyploid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyploid","termid":"PATO:0001377"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autopolyploid","termid":"PATO:0001378"}


id: PBO:0059501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded 7S DNA","termid":"PBO:0059501"}


id: PBO:0065952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAD18 E3 ubiquitin protein ligase","termid":"PBO:0065952"}


id: GO:0070380
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with high mobility group box 1 (HMBGB1) and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:add","GOC:signaling","PMID:18431461"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor activity","termid":"GO:0004896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"high mobility group box 1 receptor activity","synonyms":[{"name":"HMGB1 receptor activity","type":"exact"}],"termid":"GO:0070380"}


id: PBO:0059365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S18B","termid":"PBO:0059365"}


id: PBO:0053409
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 345","termid":"PBO:0053409"}


id: GO:0010362
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which blue light stops, prevents, or reduces the frequency, rate, or extent of the anion channel activity.","definition_xrefs":["PMID:17319842"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of anion channel activity by blue light (obsolete GO:0010362)","synonyms":[{"name":"inhibition by blue light of anion channel activity","type":"narrow"},{"name":"negative regulation by blue light of anion channel activity","type":"exact"}],"termid":"GO:0010362"}


id: MONDO:0012986
data:
  {"annotated_genes":["SJAG_02289"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87397],"is_not":false,"summary":null,"term":"MONDO:0012986"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bilateral polymicrogyria","termid":"MONDO:0017091"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02289":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"bilateral parasagittal parieto-occipital polymicrogyria","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:862085","DOID:0080923","MESH:C567201","UMLS:C4013648","icd11.foundation:293410499","Orphanet:208441","OMIM:612691","GARD:10785"],"synonyms":[{"name":"BTOP","type":"related"},{"name":"polymicrogyria, bilateral temporooccipital","type":"related"}],"termid":"MONDO:0012986","terms_by_termid":{"MONDO:0012986":null},"xrefs":{"Monarch":{"xref_id":"0012986"}}}


id: PBO:0111907
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DIPSY domain","termid":"PBO:0111907"}


id: GO:0061784
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of (1->4)-beta linkages of N-acetyl-D-glucosamine (GlcNAc) from peptidoglycan.","definition_xrefs":["PMID:22748813","GOC:dph","GOC:jh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosaminidase activity","termid":"GO:0015929"},{"relation_name":"is_a","term_name":"peptidoglycan muralytic activity","termid":"GO:0061783"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0016798","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"peptidoglycan N-acetylglucosaminidase activity","termid":"GO:0061784"}


id: PBO:0089954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UPF0642 conserved fungal protein","termid":"PBO:0089954"}


id: GO:0070326
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a very-low-density lipoprotein receptor.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoprotein particle receptor binding","termid":"GO:0070325"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"very-low-density lipoprotein particle receptor binding","synonyms":[{"name":"VLDL receptor binding","type":"exact"},{"name":"VLDLR binding","type":"exact"},{"name":"apolipoprotein E receptor binding","type":"related"},{"name":"very-low-density lipoprotein receptor binding","type":"exact"}],"termid":"GO:0070326"}


id: GO:0045329
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of carnitine (hydroxy-trimethyl aminobutyric acid), a compound that participates in the transfer of acyl groups across the inner mitochondrial membrane.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino-acid betaine biosynthetic process","termid":"GO:0006578"},{"relation_name":"is_a","term_name":"carnitine metabolic process","termid":"GO:0009437"}],"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":"carnitine biosynthetic process","secondary_identifiers":["Reactome:R-HSA-71262"],"synonyms":[{"name":"carnitine anabolism","type":"exact"},{"name":"carnitine biosynthesis","type":"exact"},{"name":"carnitine formation","type":"exact"},{"name":"carnitine synthesis","type":"exact"},{"name":"vitamin Bt biosynthesis","type":"exact"},{"name":"vitamin Bt biosynthetic process","type":"exact"}],"termid":"GO:0045329"}


id: MONDO:1011038
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any oculocutaneous albinism that occurs in western gorillas due to a mutation in the SLC45A2 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oculocutaneous albinism, non-human animal","termid":"MONDO:1012579"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oculocutaneous albinism, SLC45A2-related, western gorilla","secondary_identifiers":["OMIA:001821-9593"],"synonyms":[{"name":"coat color albinism, oculocutaneous type IV, western gorilla","type":"related"}],"termid":"MONDO:1011038","xrefs":{"Monarch":{"xref_id":"1011038"}}}


id: PBO:0015253
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNARE Tlg1 (predicted)","termid":"PBO:0015253"}


id: GO:0060888
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The pattern specification process that results in the subdivision of the epidermis of the limb in space to define a volume in which specific patterns of basal cell, spinous cell and granular cells will differentiate giving rise to the layers of the limb epidermis.","definition_xrefs":["GOC:dph","GOC:tb","GOC:sdb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"},{"relation_name":"is_a","term_name":"limb epidermis development","termid":"GO:0060887"}],"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":"limb epidermis stratification","termid":"GO:0060888"}


id: PBO:0062352
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily M member 3 pseudogene","termid":"PBO:0062352"}


id: GO:0004626
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: phosphatidylcholine + H2O = 1-acylglycerophosphocholine + a fatty acid anion.","definition_xrefs":["EC:3.1.1.4"],"gene_count":0,"genotype_count":0,"name":"obsolete cytosolic phospholipase A2 activity (obsolete GO:0004626)","synonyms":[{"name":"cytosolic phospholipase A2 activity","type":"exact"}],"termid":"GO:0004626"}


id: MONDO:0000874
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A T lymphoblastic lymphoma that occurs during childhood.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoblastic lymphoma","termid":"MONDO:0000873"},{"relation_name":"is_a","term_name":"pediatric lymphoma","termid":"MONDO:0003659"},{"relation_name":"is_a","term_name":"childhood precursor T-lymphoblastic lymphoma/leukemia","termid":"MONDO:0004403"}],"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:0005570","MONDO:0004992"],"is_obsolete":false,"name":"T-cell childhood lymphoblastic lymphoma","secondary_identifiers":["UMLS:C1332998","NCIT:C7210","DOID:0080148","MEDGEN:232068"],"synonyms":[{"name":"T lymphoblastic lymphoma","type":"exact"},{"name":"childhood T lymphoblastic lymphoma","type":"exact"},{"name":"childhood precursor T-lymphoblastic lymphoma","type":"exact"}],"termid":"MONDO:0000874","xrefs":{"Monarch":{"xref_id":"0000874"}}}


id: GO:1903896
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the IRE1-mediated unfolded protein response.","definition_xrefs":["PMID:22013210","GOC:bf","GO_REF:0000058","GOC:PARL","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of endoplasmic reticulum unfolded protein response","termid":"GO:1900103"},{"relation_name":"is_a","term_name":"regulation of IRE1-mediated unfolded protein response","termid":"GO:1903894"},{"relation_name":"positively_regulates","term_name":"IRE1-mediated unfolded protein response","termid":"GO:0036498"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of IRE1-mediated unfolded protein response","synonyms":[{"name":"activation of IRE1 branch of UPR","type":"narrow"},{"name":"activation of IRE1 signaling in response to endoplasmic reticulum stress","type":"related"},{"name":"activation of IRE1-mediated unfolded protein response","type":"narrow"},{"name":"activation of IRE1alpha unfolded protein response","type":"narrow"},{"name":"activation of IRE1p unfolded protein response","type":"narrow"},{"name":"activation of UPR signaling by IRE1 stress sensor","type":"narrow"},{"name":"activation of endoplasmic reticulum unfolded protein response; IRE1 signaling","type":"narrow"},{"name":"activation of inositol-requiring transmembrane kinase/endonuclease signal transduction","type":"related"},{"name":"positive regulation of ERN1-mediated unfolded protein response","type":"related"},{"name":"positive regulation of IRE1 branch of UPR","type":"exact"},{"name":"positive regulation of IRE1 signaling in response to endoplasmic reticulum stress","type":"related"},{"name":"positive regulation of IRE1alpha unfolded protein response","type":"narrow"},{"name":"positive regulation of IRE1p unfolded protein response","type":"narrow"},{"name":"positive regulation of UPR signaling by IRE1 stress sensor","type":"exact"},{"name":"positive regulation of endoplasmic reticulum unfolded protein response; IRE1 signaling","type":"exact"},{"name":"positive regulation of inositol-requiring transmembrane kinase/endonuclease signal transduction","type":"related"},{"name":"up regulation of IRE1 branch of UPR","type":"exact"},{"name":"up regulation of IRE1 signaling in response to endoplasmic reticulum stress","type":"related"},{"name":"up regulation of IRE1-mediated unfolded protein response","type":"exact"},{"name":"up regulation of IRE1alpha unfolded protein response","type":"narrow"},{"name":"up regulation of IRE1p unfolded protein response","type":"narrow"},{"name":"up regulation of UPR signaling by IRE1 stress sensor","type":"exact"},{"name":"up regulation of endoplasmic reticulum unfolded protein response; IRE1 signaling","type":"exact"},{"name":"up regulation of inositol-requiring transmembrane kinase/endonuclease signal transduction","type":"related"},{"name":"up-regulation of IRE1 branch of UPR","type":"exact"},{"name":"up-regulation of IRE1 signaling in response to endoplasmic reticulum stress","type":"related"},{"name":"up-regulation of IRE1-mediated unfolded protein response","type":"exact"},{"name":"up-regulation of IRE1alpha unfolded protein response","type":"narrow"},{"name":"up-regulation of IRE1p unfolded protein response","type":"narrow"},{"name":"up-regulation of UPR signaling by IRE1 stress sensor","type":"exact"},{"name":"up-regulation of endoplasmic reticulum unfolded protein response; IRE1 signaling","type":"exact"},{"name":"up-regulation of inositol-requiring transmembrane kinase/endonuclease signal transduction","type":"related"},{"name":"upregulation of IRE1 branch of UPR","type":"exact"},{"name":"upregulation of IRE1 signaling in response to endoplasmic reticulum stress","type":"related"},{"name":"upregulation of IRE1-mediated unfolded protein response","type":"exact"},{"name":"upregulation of IRE1alpha unfolded protein response","type":"narrow"},{"name":"upregulation of IRE1p unfolded protein response","type":"narrow"},{"name":"upregulation of UPR signaling by IRE1 stress sensor","type":"exact"},{"name":"upregulation of endoplasmic reticulum unfolded protein response; IRE1 signaling","type":"exact"},{"name":"upregulation of inositol-requiring transmembrane kinase/endonuclease signal transduction","type":"related"}],"termid":"GO:1903896"}


id: FYPO:0007850
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which microtubules self-assemble into a spindle without the participation of the spindle pole body (SPB) during the second meiotic nuclear division.","definition_xrefs":["PomBase:mah","PMID:34346498"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle assembly during meiosis II","termid":"FYPO:0004510"},{"relation_name":"is_a","term_name":"meiotic spindle self-assembly","termid":"FYPO:0007848"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000054","FYPO:0000631"],"is_obsolete":false,"name":"spindle self-assembly during meiosis II","synonyms":[{"name":"SPB-independent meiosis II spindle assembly","type":"exact"},{"name":"SPB-independent spindle assembly during meiosis II","type":"exact"},{"name":"acentrosomal meiotic spindle assembly","type":"related"},{"name":"acentrosomal spindle assembly during meiosis II","type":"related"},{"name":"meiosis II spindle self-assembly","type":"exact"},{"name":"meiotic SPB-independent spindle in meiosis II","type":"related"},{"name":"spindle pole body-independent meiosis II spindle assembly","type":"exact"},{"name":"spindle pole body-independent spindle assembly during meiosis II","type":"exact"},{"name":"spindle self-assembly during second meiotic nuclear division","type":"exact"}],"termid":"FYPO:0007850"}


id: FYPO:0000771
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A localization phenotype observed in the vegetative growth phase of the life cycle in which nuclear pore localization is normal (i.e. indistinguishable from wild type), resulting in a normal spatial arrangement of nuclear pores within the nuclear envelope.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization during vegetative growth","termid":"FYPO:0000644"},{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0000138"],"is_obsolete":false,"name":"normal nuclear pore localization","synonyms":[{"name":"normal NPC localization","type":"exact"},{"name":"normal nuclear pore complex localization","type":"exact"},{"name":"normal nuclear pore distribution","type":"exact"},{"name":"normal nuclear pore localisation","type":"exact"},{"name":"normal nuclear pore localization during mitotic cell cycle","type":"related"},{"name":"normal nuclear pore localization during vegetative growth","type":"exact"}],"termid":"FYPO:0000771"}


id: GO:0032325
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of the molybdopterin cofactor (Moco), essential for the catalytic activity of some enzymes, e.g. sulfite oxidase, xanthine dehydrogenase, and aldehyde oxidase. The cofactor consists of a mononuclear molybdenum (Mo-molybdopterin) or tungsten ion (W-molybdopterin) coordinated by one or two molybdopterin ligands.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molybdopterin cofactor metabolic process","termid":"GO:0043545"},{"relation_name":"is_a","term_name":"organophosphate catabolic process","termid":"GO:0046434"}],"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":"molybdopterin cofactor catabolic process","termid":"GO:0032325"}


id: GO:0030635
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving derivatives of acetic acid.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete acetate derivative metabolic process (obsolete GO:0030635)","synonyms":[{"name":"acetate derivative metabolic process","type":"exact"},{"name":"acetate derivative metabolism","type":"exact"}],"termid":"GO:0030635"}


id: SO:0001433
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A three prime RACE (Rapid Amplification of cDNA Ends) clone is a cDNA clone copied from the 3' end of an mRNA (using a poly-dT primer to capture the polyA tail and a gene-specific or randomly primed 5' primer), and spliced into a vector for propagation in a suitable host.","definition_xrefs":["modENCODE:nlw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cDNA_clone","termid":"SO:0000317"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_prime_RACE_clone","synonyms":[{"name":"3' RACE clone","type":"related"}],"termid":"SO:0001433"}


id: GO:2000619
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of histone H4-K16 acetylation.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of histone H4-K16 acetylation (obsolete GO:2000619)","synonyms":[{"name":"negative regulation of histone H4 acetylation at K16","type":"exact"}],"termid":"GO:2000619"}


id: MONDO:0020642
data:
  {"annotated_genes":["SJAG_03280","SJAG_00394"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87378],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010916"},{"annotations":[87672],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031062"}]},"cv_name":"mondo","definition":"A usually autosomal dominant and less frequently autosomal recessive genetic disorder characterized by the presence of numerous cysts in the kidneys leading to end-stage renal failure. The autosomal dominant trait is associated with abnormalities on the short arm of chromosome 16. Symptoms in patients with the autosomal dominant trait usually appear at middle age and include abdominal pain, hematuria, and high blood pressure. Patients may develop brain aneurysms and liver cysts. Patients with the autosomal recessive trait present with progressive renal failure early in life and symptoms resulting from hepatic fibrosis. The autosomal recessive trait is associated with abnormalities of chromosome 6. Polycystic kidney disease may also result as a side effect in patients on renal dialysis.","definition_xrefs":["NCIT:C75464"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial cystic renal disease","termid":"MONDO:0019741"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00394":null,"SJAG_03280":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"polycystic kidney disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0022680","MEDGEN:9639","NANDO:1200367","OMIMPS:173900","GARD:7419","EFO:0008620","SCTID:82525005","MESH:D007690","DOID:0080322","NANDO:2200152"],"synonyms":[{"name":"PKD - polycystic kidney disease","type":"exact"},{"name":"fibrocystic renal disease","type":"exact"},{"name":"polycystic kidney disease","type":"exact"}],"termid":"MONDO:0020642","terms_by_termid":{"MONDO:0010916":null,"MONDO:0031062":null},"xrefs":{"Monarch":{"xref_id":"0020642"}}}


id: PBO:0041819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cardiac mesoderm enhancer-associated non-coding RNA","termid":"PBO:0041819"}


id: PBO:0059903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND1 pseudogene 26","termid":"PBO:0059903"}


id: SO:0000432
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The U5 segment of the three-prime long terminal repeat.","direct_ancestors":[{"relation_name":"is_a","term_name":"three_prime_LTR_component","termid":"SO:0000849"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U5_three_prime_LTR_region","synonyms":[{"name":"U5 3' long terminal repeat region","type":"exact"},{"name":"U5 three prime LTR region","type":"exact"}],"termid":"SO:0000432"}


id: FYPO:0004377
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 heterochromatin at the silenced mating-type cassettes is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to heterochromatin during vegetative growth","termid":"FYPO:0001131"},{"relation_name":"is_a","term_name":"increased protein localization to chromatin during vegetative growth","termid":"FYPO:0003011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"increased protein localization to heterochromatin at silent mating-type cassette","synonyms":[{"name":"increased protein localisation to heterochromatin at silent mating-type cassette","type":"exact"},{"name":"increased protein localization to heterochromatin at mating-type region","type":"exact"},{"name":"increased protein localization to heterochromatin at mating-type region during vegetative growth","type":"exact"},{"name":"increased protein localization to heterochromatin at silent mating-type cassette during mitotic cell cycle","type":"related"},{"name":"increased protein localization to heterochromatin at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"increased protein localization to mating-type region heterochromatin","type":"exact"},{"name":"increased protein localization to silent mating type heterochromatin","type":"exact"}],"termid":"FYPO:0004377"}


id: MONDO:0015924
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease).","definition_xrefs":["PMID:30545973","Orphanet:182090"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary hypertension","termid":"MONDO:0005149"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary arterial hypertension","secondary_identifiers":["NANDO:2100103","GARD:7501","NANDO:2200298","MESH:D000081029","UMLS:C2973725","NANDO:1200425","MedDRA:10064911","NORD:1634","icd11.foundation:1931148955","SCTID:11399002","MEDGEN:425404","EFO:0001361"],"synonyms":[{"name":"PAH","type":"exact"},{"name":"PAH with overt features of venous/capillaries involvement","type":"narrow"},{"name":"PPH","type":"related"},{"name":"PVOD/PCH","type":"narrow"},{"name":"idiopathic pulmonary hypertension","type":"related"},{"name":"pulmonary arterial hypertension","type":"exact"}],"termid":"MONDO:0015924","xrefs":{"Monarch":{"xref_id":"0015924"}}}


id: GO:0160282
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The membrane leaflet of the trans-Golgi network membrane that faces the Golgi lumen.","definition_xrefs":["PMID:38307322","PMID:23913272","PMID:34597626"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lumenal side of membrane","termid":"GO:0098576"},{"relation_name":"part_of","term_name":"trans-Golgi network membrane","termid":"GO:0032588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005794"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005794"],"is_obsolete":false,"name":"lumenal side of trans-Golgi network membrane","synonyms":[{"name":"lumenal face of trans-Golgi network membrane","type":"exact"},{"name":"lumenal leaflet of trans-Golgi network membrane","type":"exact"},{"name":"lumenal side of trans-Golgi network","type":"exact"}],"termid":"GO:0160282"}


id: GO:0014009
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of glial cells by cell division, resulting in the expansion of their population. Glial cells exist throughout the nervous system, and include Schwann cells, astrocytes, and oligodendrocytes among others.","definition_xrefs":["GOC:ef","ISBN:0878932585"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population proliferation","termid":"GO:0008283"},{"relation_name":"part_of","term_name":"gliogenesis","termid":"GO:0042063"}],"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":"glial cell proliferation","synonyms":[{"name":"glia proliferation","type":"exact"}],"termid":"GO:0014009"}


id: MONDO:0013745
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Joubert syndrome in which the cause of the disease is a mutation in the TMEM237 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome with oculorenal defect","termid":"MONDO:0009480"},{"relation_name":"is_a","term_name":"Joubert syndrome with ocular defect","termid":"MONDO:0016364"},{"relation_name":"is_a","term_name":"Joubert syndrome","termid":"MONDO:0018772"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0020022","MONDO:0006025"],"is_obsolete":false,"name":"Joubert syndrome 14","secondary_identifiers":["DOID:0110983","GARD:15801","UMLS:C3280766","OMIM:614424","MEDGEN:482396"],"synonyms":[{"name":"JBTS14","type":"exact"},{"name":"Joubert syndrome 14","type":"exact"},{"name":"Joubert syndrome caused by mutation in TMEM237","type":"exact"},{"name":"Joubert syndrome type 14","type":"exact"},{"name":"TMEM237 Joubert syndrome","type":"exact"}],"termid":"MONDO:0013745","xrefs":{"Monarch":{"xref_id":"0013745"}}}


id: PBO:0087141
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein that may be involved in translational regulation; binds specific categories of mRNAs, including those that contain upstream open reading frames (uORFs) and internal ribosome entry sites (IRES); interacts genetically with chromatin remodelers and splicing factors, linking chromatin state, splicing and as a result mRNA maturation","termid":"PBO:0087141"}


id: PBO:0072232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S20 pseudogene 7","termid":"PBO:0072232"}


id: PATO:0001064
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001064 absolute flux (obsolete PATO:0001064)","termid":"PATO:0001064"}


id: PBO:0075886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 1","termid":"PBO:0075886"}


id: MONDO:0009402
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A very rare syndrome associating an acro-fronto-facio-nasal dysostosis with genitourinary anomalies.","definition_xrefs":["Orphanet:2211"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"acrofrontofacionasal dysostosis","termid":"MONDO:0008715"},{"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:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"acrofrontofacionasal dysostosis 2","secondary_identifiers":["SCTID:721835008","GARD:287","MEDGEN:383797","MESH:C538332","OMIM:239710","UMLS:C1855904"],"synonyms":[{"name":"AFFN dysostosis 2","type":"related"},{"name":"Naguib syndrome","type":"related"},{"name":"Naguib-Richieri-Costa syndrome","type":"exact"},{"name":"acrofrontofacionasal dysostosis 2","type":"exact"},{"name":"acrofrontofacionasal dysostosis type 2","type":"exact"},{"name":"acrofrontofacionasal dysostosis with genitourinary anomalies","type":"related"},{"name":"acrofrontofacionasal dysostosis, severe","type":"related"},{"name":"acrofrontofacionasal syndrome type 2","type":"exact"},{"name":"hypertelorism hypospadias polysyndactyly syndrome","type":"related"},{"name":"hypertelorism, hypospadias, and polysyndactyly syndrome","type":"related"},{"name":"hypertelorism-hypospadias-polysyndactyly syndrome","type":"exact"}],"termid":"MONDO:0009402","xrefs":{"Monarch":{"xref_id":"0009402"}}}


id: GO:0099581
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Any ATPase coupled ion transmembrane transporter activity, occurring in the postsynaptic membrane, that is involved in regulation of postsynaptic membrane potential.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATPase-coupled ion transmembrane transporter activity","termid":"GO:0042625"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"ATPase coupled ion transmembrane transporter activity involved in regulation of postsynaptic membrane potential","synonyms":[{"name":"ATPase coupled ion transmembrane transporter activity involved in regulation of post-synaptic membrane potential","type":"exact"},{"name":"ATPase-coupled ion transmembrane transporter activity involved in regulation of postsynaptic membrane potential","type":"exact"}],"termid":"GO:0099581"}


id: MONDO:0016365
data:
  {"annotated_genes":["SJAG_01151"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87582],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007767"},{"annotations":[87583],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007768"}]},"cv_name":"mondo","definition":"An instance of primary hyperparathyroidism (disease) that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary hyperparathyroidism","termid":"MONDO:0010837"},{"relation_name":"is_a","term_name":"hereditary hyperparathyroidism","termid":"MONDO:0016166"},{"relation_name":"is_a","term_name":"tumor of parathyroid gland","termid":"MONDO:0021360"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01151":null},"genotype_count":0,"is_obsolete":false,"name":"familial primary hyperparathyroidism","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0271846","icd11.foundation:1186866066","Orphanet:2207","MEDGEN:543605","GARD:2837"],"synonyms":[{"name":"hereditary primary hyperparathyroidism (disease)","type":"exact"}],"termid":"MONDO:0016365","terms_by_termid":{"MONDO:0007767":null,"MONDO:0007768":null},"xrefs":{"Monarch":{"xref_id":"0016365"}}}


id: PBO:0066490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ret finger protein like 4A pseudogene 1","termid":"PBO:0066490"}


id: MONDO:0006676
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Beriberi is a condition that occurs in people who are deficient in thiamine (vitamin B1). There are two major types of beriberi: wet beriberi which affects the cardiovascular system and dry beriberi which affects the nervous system. People with wet beriberi may experience increased heart rate, shortness of breath, and swelling of the lower legs. Signs and symptoms of dry beriberi include difficulty walking; loss of feeling in the hands and/or feet; paralysis of the lower legs; mental confusion; speech difficulty; pain; and/or vomiting. Beriberi is rare in the United States since many foods are now vitamin enriched; however, alcohol abuse, dialysis and taking high doses of diuretics increases the risk of developing the condition. In most cases,beriberi occurs sporadically in people with no family history of the condition. A rare condition known as genetic beriberi is inherited (passed down through families) and is associated with an inability to absorb thiamine from foods. Treatment generally includes thiamine supplementation, given by injection or taken by mouth.","direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin B deficiency","termid":"MONDO:0042976"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beriberi","secondary_identifiers":["MedDRA:10004482","DOID:0070313","MESH:D001602","SCTID:36656008","DOID:13725","ICD10CM:E51.1","UMLS:C0005122","MEDGEN:543","ICD9:265.0","NCIT:C34418","EFO:1000837","icd11.foundation:632832064"],"synonyms":[{"name":"Beri Beri","type":"exact"},{"name":"thiamine deficiency","type":"exact"},{"name":"vitamin B1 deficiency","type":"exact"}],"termid":"MONDO:0006676","xrefs":{"Monarch":{"xref_id":"0006676"}}}


id: GO:0016229
data:
  {"annotated_genes":["SJAG_03235","SJAG_02855","SJAG_01326","SJAG_02291","SJAG_04124"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[103768,119543],"is_not":false,"summary":null,"term":"GO:0016229"},{"annotations":[72815],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000253"},{"annotations":[112071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000252"},{"annotations":[63419],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003865"}]},"cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which one substrate is a sterol derivative.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity","termid":"GO:0016491"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01326":null,"SJAG_02291":null,"SJAG_02855":null,"SJAG_03235":null,"SJAG_04124":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"steroid dehydrogenase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0016229","terms_by_termid":{"GO:0000252":null,"GO:0000253":null,"GO:0003865":null,"GO:0016229":null}}


id: FYPO:0006624
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 phosphatidylinositol-3,4,5-trisphosphate measured in the plasma membrane is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal plasma membrane during vegetative growth","termid":"FYPO:0003278"},{"relation_name":"is_a","term_name":"increased cellular phosphatidylinositol-3,4,5-trisphosphate level","termid":"FYPO:0006488"},{"relation_name":"is_a","term_name":"altered level of substance in plasma membrane","termid":"FYPO:0008331"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased phosphatidylinositol-3,4,5-trisphosphate level in plasma membrane","synonyms":[{"name":"increased 1-phosphatidyl-1D-myo-inositol 3,4,5-trisphosphate level in plasma membrane","type":"exact"},{"name":"increased phosphatidylinositol-3,4,5-trisphosphate level in cell membrane","type":"exact"},{"name":"increased phosphatidylinositol-3,4,5-trisphosphate level in plasma membrane during mitotic cell cycle","type":"related"},{"name":"increased phosphatidylinositol-3,4,5-trisphosphate level in plasma membrane during vegetative growth","type":"exact"},{"name":"increased plasma membrane PI(3,4,5)P3 level","type":"exact"},{"name":"increased plasma membrane phosphatidylinositol-3,4,5-trisphosphate level","type":"exact"}],"termid":"FYPO:0006624"}


id: PBO:0034512
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_maintenance_of_protein_location_at_cell_tip","termid":"PBO:0034512"}


id: PBO:0002619
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6.3.4.4","termid":"PBO:0002619"}


id: MONDO:0013176
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Weill-Marchesani syndrome","termid":"MONDO:0018096"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Weill-Marchesani 4 syndrome, recessive","secondary_identifiers":["OMIM:613195","Orphanet:363992","UMLS:C2750787","MEDGEN:416383","GARD:17579","MESH:C567710"],"synonyms":[{"name":"15q26.3 microdeletion syndrome","type":"exact"},{"name":"WMS4","type":"exact"},{"name":"Weill-Marchesani syndrome 4","type":"exact"},{"name":"Weill-Marchesani-like syndrome","type":"exact"},{"name":"ichthyosis-short stature-brachydactyly-microspherophakia syndrome","type":"exact"}],"termid":"MONDO:0013176","xrefs":{"Monarch":{"xref_id":"0013176"}}}


id: PBO:0079834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uridine monophosphate synthetase","termid":"PBO:0079834"}


id: PBO:0068917
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 160, pseudogene","termid":"PBO:0068917"}


id: PBO:0057809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3130-2","termid":"PBO:0057809"}


id: PBO:0087530
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of NuA4 histone H4 acetyltransferase and SWR1 complexes; may function to antagonize silencing near telomeres; interacts directly with Swc4p; has homology to human leukemogenic protein AF9; contains a YEATS domain","termid":"PBO:0087530"}


id: PBO:0113177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Karyopherin beta; bidirectional nuclear transport receptor (biportin) that shuttles distinct sets of cargoes in opposite directions; responsible for import of Toa1p-Toa2p complex into nucleus; depletes eIF5A and eEF2 from cell nuclei; binds to nucleoporins Nup1p and Nup2p; may play a role in regulation of pleiotropic drug resistance","termid":"PBO:0113177"}


id: MONDO:1011990
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vision disorder, non-human animal","termid":"MONDO:1011367"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinal dysplasia and persistent primary vitreous, non-human animal","secondary_identifiers":["OMIA:001420"],"termid":"MONDO:1011990","xrefs":{"Monarch":{"xref_id":"1011990"}}}


id: PBO:0086013
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; SWAT-GFP and seamless-GFP fusion proteins localize to the endoplasmic reticulum; identified by gene-trapping, microarray-based expression analysis, and genome-wide homology searching","termid":"PBO:0086013"}


id: PBO:0072444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S29 pseudogene 8","termid":"PBO:0072444"}


id: PBO:0045282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynamin 1 pseudogene 33","termid":"PBO:0045282"}


id: GO:0042564
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A dimer consisting of an alpha and a beta-subunit that imports proteins with an NLS into the nucleus through a nuclear pore.","definition_xrefs":["GOC:jl","Wikipedia:Importin","PMID:9323134","PMID:9323123"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleocytoplasmic transport complex","termid":"GO:0031074"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"NLS-dependent protein nuclear import complex","termid":"GO:0042564"}


id: PBO:0044058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystatin S","termid":"PBO:0044058"}


id: PBO:0088605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin binding WD repeat protein, coronin Crn1","termid":"PBO:0088605"}


id: PBO:0051302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 1D-42 (non-functional)","termid":"PBO:0051302"}


id: PBO:0058197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4490","termid":"PBO:0058197"}


id: PBO:0053671
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 852","termid":"PBO:0053671"}


id: PBO:0116754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SWI/SNF related BAF chromatin remodeling complex subunit E1","termid":"PBO:0116754"}


id: PBO:0050123
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 33","termid":"PBO:0050123"}


id: MONDO:0019252
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete other metabolic disease with skin involvement (obsolete MONDO:0019252)","secondary_identifiers":["Orphanet:79217"],"termid":"MONDO:0019252","xrefs":{"Monarch":{"xref_id":"0019252"}}}


id: MONDO:0002940
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A basal cell carcinoma arising from the perianal skin. Local excision is the treatment of choice. Metastases are extremely rare.","definition_xrefs":["NCIT:C7473"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anal margin squamous cell carcinoma","termid":"MONDO:0001470"},{"relation_name":"is_a","term_name":"skin basal cell carcinoma","termid":"MONDO:0005341"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"anal margin basal cell carcinoma","secondary_identifiers":["UMLS:C1332269","ICD10CM:C44.510","DOID:4283","MEDGEN:231371"],"synonyms":[{"name":"anal margin basal cell carcinoma","type":"exact"},{"name":"basal cell carcinoma of anal margin","type":"exact"},{"name":"basal cell carcinoma of perianal skin","type":"exact"},{"name":"basal cell carcinoma of the anal margin","type":"exact"},{"name":"basal cell carcinoma of the perianal skin","type":"exact"},{"name":"perianal skin basal cell carcinoma","type":"exact"},{"name":"perianal skin skin basal cell carcinoma","type":"exact"},{"name":"skin basal cell carcinoma of perianal skin","type":"exact"}],"termid":"MONDO:0002940","xrefs":{"Monarch":{"xref_id":"0002940"}}}


id: PBO:0027048
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_number_of_Crb2_foci_during_cellular_response_to_ionizing_radiation","termid":"PBO:0027048"}


id: PBO:0048200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gamma-aminobutyric acid type A receptor subunit alpha4","termid":"PBO:0048200"}


id: PBO:0073706
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SKI8 subunit of superkiller complex","termid":"PBO:0073706"}


id: MONDO:0032578
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"complex cortical dysplasia with other brain malformations","termid":"MONDO:0000904"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cortical dysplasia, complex, with other brain malformations 9","secondary_identifiers":["UMLS:C4748540","MEDGEN:1648399","OMIM:618174"],"synonyms":[{"name":"CDCBM9","type":"related"},{"name":"CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9","type":"related"}],"termid":"MONDO:0032578","xrefs":{"Monarch":{"xref_id":"0032578"}}}


id: PBO:0066044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAP1B like (pseudogene)","termid":"PBO:0066044"}


id: PBO:0031110
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_regulation_of_translation_in_response_to_stress","termid":"PBO:0031110"}


id: PBO:0077028
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thymocyte selection associated family member 3, pseudogene","termid":"PBO:0077028"}


id: MONDO:0010236
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic X-linked intellectual disability","termid":"MONDO:0019181"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability, X-linked 14","secondary_identifiers":["UMLS:C0796220","DOID:0112027","MEDGEN:163231","OMIM:300062","GARD:8557","MESH:C537454"],"synonyms":[{"name":"MRX14","type":"exact"},{"name":"intellectual disability, X-linked 14","type":"exact"},{"name":"intellectual disability, X-linked nonspecific, type 14","type":"related"},{"name":"mental retardation, X-linked 14","type":"related"},{"name":"mental retardation, X-linked nonspecific, type 14","type":"related"}],"termid":"MONDO:0010236","xrefs":{"Monarch":{"xref_id":"0010236"}}}


id: MONDO:1010094
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Analphalipoproteinaemia that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn errors of metabolism, non-human animal","termid":"MONDO:1012979"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"analphalipoproteinaemia, non-human animal","secondary_identifiers":["OMIA:000042"],"termid":"MONDO:1010094","xrefs":{"Monarch":{"xref_id":"1010094"}}}


id: PBO:0031695
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_nuclear_import","termid":"PBO:0031695"}


id: FYPO:0002711
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the haploid nuclei formed by meiotic nuclear division do not separate normally. Nuclei may be closer together than normal, or remain attached by an incompletely separated outer nuclear membrane, or both.","definition_xrefs":["PMID:1417417","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal sporulation","termid":"FYPO:0000121"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000121"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000121"],"is_obsolete":false,"name":"abnormal nuclear separation after meiosis","synonyms":[{"name":"abnormal nuclear distribution after meiosis","type":"exact"},{"name":"abnormal nuclear separation after meiotic nuclear division","type":"exact"},{"name":"abnormal nuclear separation during sporulation","type":"related"},{"name":"abnormal nuclear separation in ascus","type":"exact"},{"name":"abnormal separation of nuclei in ascus","type":"exact"}],"termid":"FYPO:0002711"}


id: GO:0002812
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of an antibacterial peptide with activity against Gram-negative bacteria.","definition_xrefs":["GOC:add","PMID:11807545"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antibacterial peptide biosynthetic process","termid":"GO:0002780"},{"relation_name":"part_of","term_name":"defense response to Gram-negative bacterium","termid":"GO:0050829"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"biosynthetic process of antibacterial peptides active against Gram-negative bacteria","termid":"GO:0002812"}


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


id: FYPO:0000901
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A  microtubule cytoskeleton organization phenotype observed in the vegetative growth phase of the life cycle in which microtubule growth (polymerization), catastrophe (the transition from growth to shrinkage), shrinkage (depolymerization), or rescue (the transition from shrinkage to growth) is abnormal.","definition_xrefs":["PomBase:val","GO:0031109"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule cytoskeleton organization during vegetative growth","termid":"FYPO:0001350"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000054","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal microtubule dynamics during vegetative growth","synonyms":[{"name":"abnormal microtubule growth or shrinkage during vegetative growth","type":"narrow"},{"name":"abnormal microtubule polymerisation or depolymerisation during vegetative growth","type":"narrow"},{"name":"abnormal microtubule polymerization or depolymerization during vegetative growth","type":"narrow"}],"termid":"FYPO:0000901"}


id: SO:0001482
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An enhancer that drives the pattern of transcription and binds to the same TF as the primary enhancer, but is located in the intron of or on the far side of a neighboring gene.","definition_xrefs":["PMID:22083793"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enhancer","termid":"SO:0000165"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"shadow_enhancer","synonyms":[{"name":"shadow enhancer","type":"exact"}],"termid":"SO:0001482"}


id: MONDO:0007210
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":"Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay","secondary_identifiers":["OMIM:112370","UMLS:C1862171","MEDGEN:396307","MESH:C566206"],"synonyms":[{"name":"Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay","type":"exact"}],"termid":"MONDO:0007210","xrefs":{"Monarch":{"xref_id":"0007210"}}}


id: GO:0150020
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a dendritic tree are generated on the basal neuron side and organized into dendritic branches.","definition_xrefs":["PMID:22683681","GOC:aruk","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dendrite arborization","termid":"GO:0140059"},{"relation_name":"is_a","term_name":"basal dendrite morphogenesis","termid":"GO:0150019"}],"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":"basal dendrite arborization","termid":"GO:0150020"}


id: PATO:0001470
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's magnitude in respect to a related entity.","definition_xrefs":["PATOC:nw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality","termid":"PATO:0001018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proportionality to","synonyms":[{"name":"proportion","type":"exact"},{"name":"proportionality","type":"exact"},{"name":"quotient","type":"exact"},{"name":"rate","type":"related"},{"name":"ratio","type":"exact"}],"termid":"PATO:0001470"}


id: PBO:0049189
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyoxylate and hydroxypyruvate reductase","termid":"PBO:0049189"}


id: PBO:0060328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin IF","termid":"PBO:0060328"}


id: PBO:0076951
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transforming growth factor beta 1 induced transcript 1","termid":"PBO:0076951"}


id: GO:0018423
data:
  {"annotated_genes":["SJAG_02660"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78034],"is_not":false,"summary":null,"term":"GO:0018423"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + [protein]-L-leucine = S-adenosyl-L-homocysteine + [protein]-L-leucine methyl ester. This modification occurs only at the oxygen atoms of the free alpha carboxyl group of a leucine residue at the C-terminus of the protein.","definition_xrefs":["PMID:8514774"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein C-terminal carboxyl O-methyltransferase activity","termid":"GO:0003880"},{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02660":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0008276"}],"interesting_parent_ids":["GO:0016740","GO:0008276","GO:0016741","GO:0003674","GO:0140096","GO:0003824"],"is_obsolete":false,"name":"protein C-terminal leucine carboxyl O-methyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-8856945"],"synonyms":[{"name":"protein phosphatase methyltransferase activity","type":"narrow"},{"name":"protein-leucine O-methyltransferase activity","type":"exact"}],"termid":"GO:0018423","terms_by_termid":{"GO:0018423":null}}


id: PBO:0070559
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 25","termid":"PBO:0070559"}


id: GO:0072560
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A developmental process, independent of morphogenetic (shape) change, that is required for a type B pancreatic cell to attain its fully functional state. A type B pancreatic cell is a cell located towards center of the islets of Langerhans that secretes insulin.","definition_xrefs":["GOC:BHF","CL:0000169"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell maturation","termid":"GO:0002070"},{"relation_name":"part_of","term_name":"type B pancreatic cell development","termid":"GO:0003323"}],"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":"type B pancreatic cell maturation","synonyms":[{"name":"pancreatic B cell maturation","type":"exact"},{"name":"pancreatic beta cell maturation","type":"exact"}],"termid":"GO:0072560"}


id: PBO:0045572
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 22","termid":"PBO:0045572"}


id: GO:0019529
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of taurine (2-aminoethanesulfonic acid), a sulphur-containing amino acid derivative important in the metabolism of fats.","definition_xrefs":["ISBN:0198600461","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"taurine metabolic process","termid":"GO:0019530"},{"relation_name":"is_a","term_name":"alkanesulfonate catabolic process","termid":"GO:0046306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006790","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"taurine catabolic process","secondary_identifiers":["MetaCyc:TAURINEDEG-PWY"],"synonyms":[{"name":"taurine breakdown","type":"exact"},{"name":"taurine catabolism","type":"exact"},{"name":"taurine degradation","type":"exact"}],"termid":"GO:0019529"}


id: PBO:0054812
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 2225","termid":"PBO:0054812"}


id: GO:0005809
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete Golgi-vacuole transport vesicle (obsolete GO:0005809)","synonyms":[{"name":"Golgi-vacuole transport vesicle","type":"exact"}],"termid":"GO:0005809"}


id: PBO:0061395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nephronectin","termid":"PBO:0061395"}


id: PBO:0081874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 816","termid":"PBO:0081874"}


id: GO:0005657
data:
  {"annotated_genes":["SJAG_00874","SJAG_03128","SJAG_00198","SJAG_03927","SJAG_03780","SJAG_04150","SJAG_02439","SJAG_04671","SJAG_01010","SJAG_00729","SJAG_00327","SJAG_01823","SJAG_02172","SJAG_00153","SJAG_00814","SJAG_00272","SJAG_02610","SJAG_03722","SJAG_05197","SJAG_00696","SJAG_02198","SJAG_02182","SJAG_03097","SJAG_02818","SJAG_02394","SJAG_01267","SJAG_04791","SJAG_02348","SJAG_02908","SJAG_00863","SJAG_00536","SJAG_00958","SJAG_04877","SJAG_03495","SJAG_02800","SJAG_05301","SJAG_00857","SJAG_03451","SJAG_05239","SJAG_02074","SJAG_04210","SJAG_00884","SJAG_01698","SJAG_02627","SJAG_02724","SJAG_01354","SJAG_04879","SJAG_04272","SJAG_04190","SJAG_04994","SJAG_00399","SJAG_04995","SJAG_00611","SJAG_00618","SJAG_03855","SJAG_04183","SJAG_02667","SJAG_01762","SJAG_05232","SJAG_03898"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[76749,77136,72284,74837],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005658"},{"annotations":[76972,78764,104778,72886],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043625"},{"annotations":[79088,82162,118245],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005662"},{"annotations":[78360,78990,114821,74539,79675,70651],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043599"},{"annotations":[109698,111923,58806,94935,92607,104829,63808,97955,101251,79393,75754,114733,97017,106172,102566,109315,113634,67495,120194,99267,115169,115148,94504,105936,92386,96777,61965,115560,57438,62023,106103,110024,113259,113377,113892,105273,101368,109806,117401],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043596"},{"annotations":[114503],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043601"},{"annotations":[82251,101306,80133],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031298"}]},"cv_name":"cellular_component","definition":"The Y-shaped region of a replicating DNA molecule, resulting from the separation of the DNA strands and in which the synthesis of new strands takes place. Also includes associated protein complexes.","definition_xrefs":["GOC:mah","ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"chromosome","termid":"GO:0005694"}],"gene_count":60,"genes_by_uniquename":{"SJAG_00153":null,"SJAG_00198":null,"SJAG_00272":null,"SJAG_00327":null,"SJAG_00399":null,"SJAG_00536":null,"SJAG_00611":null,"SJAG_00618":null,"SJAG_00696":null,"SJAG_00729":null,"SJAG_00814":null,"SJAG_00857":null,"SJAG_00863":null,"SJAG_00874":null,"SJAG_00884":null,"SJAG_00958":null,"SJAG_01010":null,"SJAG_01267":null,"SJAG_01354":null,"SJAG_01698":null,"SJAG_01762":null,"SJAG_01823":null,"SJAG_02074":null,"SJAG_02172":null,"SJAG_02182":null,"SJAG_02198":null,"SJAG_02348":null,"SJAG_02394":null,"SJAG_02439":null,"SJAG_02610":null,"SJAG_02627":null,"SJAG_02667":null,"SJAG_02724":null,"SJAG_02800":null,"SJAG_02818":null,"SJAG_02908":null,"SJAG_03097":null,"SJAG_03128":null,"SJAG_03451":null,"SJAG_03495":null,"SJAG_03722":null,"SJAG_03780":null,"SJAG_03855":null,"SJAG_03898":null,"SJAG_03927":null,"SJAG_04150":null,"SJAG_04183":null,"SJAG_04190":null,"SJAG_04210":null,"SJAG_04272":null,"SJAG_04671":null,"SJAG_04791":null,"SJAG_04877":null,"SJAG_04879":null,"SJAG_04994":null,"SJAG_04995":null,"SJAG_05197":null,"SJAG_05232":null,"SJAG_05239":null,"SJAG_05301":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005694","GO:0005575"],"is_obsolete":false,"name":"replication fork","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Wikipedia:Replication_fork"],"synonyms":[{"name":"replication focus","type":"related"}],"termid":"GO:0005657","terms_by_termid":{"GO:0005658":null,"GO:0005662":null,"GO:0031298":null,"GO:0043596":null,"GO:0043599":null,"GO:0043601":null,"GO:0043625":null}}


id: GO:0000339
data:
  {"annotated_genes":["SJAG_01830","SJAG_00507","SJAG_05010","SJAG_01625","SJAG_01064","SJAG_04360","SJAG_03223"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72330],"is_not":false,"summary":null,"term":"GO:0000339"},{"annotations":[93508],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098808"},{"annotations":[101728,66816,76694,76106,81497],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000340"}]},"cv_name":"molecular_function","definition":"Binding to a 7-methylguanosine (m7G) group or derivative located at the 5' end of an RNA molecule.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA binding","termid":"GO:0003723"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00507":null,"SJAG_01064":null,"SJAG_01625":null,"SJAG_01830":null,"SJAG_03223":null,"SJAG_04360":null,"SJAG_05010":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003723"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0003723"],"is_obsolete":false,"name":"RNA cap binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"binding to mRNA cap","type":"narrow"},{"name":"mRNA cap binding","type":"narrow"},{"name":"snRNA cap binding","type":"narrow"}],"termid":"GO:0000339","terms_by_termid":{"GO:0000339":null,"GO:0000340":null,"GO:0098808":null}}


id: FYPO:0008208
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 neddylation of one or more specific proteins, or of specific protein sites, is abolished.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein neddylation during vegetative growth","termid":"FYPO:0005819"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0002274","FYPO:0002494","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein neddylation during vegetative growth","termid":"FYPO:0008208"}


id: PBO:0050893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immediate early response 5","termid":"PBO:0050893"}


id: PBO:0046232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongin C pseudogene 26","termid":"PBO:0046232"}


id: MONDO:0014942
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the GABRB1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"undetermined early-onset epileptic encephalopathy","termid":"MONDO:0018614"},{"relation_name":"is_a","term_name":"neonatal-onset developmental and epileptic encephalopathy","termid":"MONDO:0100455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005027","MONDO:0700092","MONDO:0004736"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 45","secondary_identifiers":["OMIM:617153","GARD:16203","DOID:0080428","MEDGEN:934658","UMLS:C4310691"],"synonyms":[{"name":"DEE45","type":"exact"},{"name":"EIEE45","type":"exact"},{"name":"GABRB1 early infantile epileptic encephalopathy","type":"exact"},{"name":"developmental and epileptic encephalopathy 45","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in GABRB1","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 45","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 45; EIEE45","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 45","type":"exact"}],"termid":"MONDO:0014942","xrefs":{"Monarch":{"xref_id":"0014942"}}}


id: GO:1905163
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of phagosome maturation.","definition_xrefs":["GOC:PARL","GOC:bf","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of organelle organization","termid":"GO:0010639"},{"relation_name":"is_a","term_name":"regulation of phagosome maturation","termid":"GO:1905162"},{"relation_name":"negatively_regulates","term_name":"phagosome maturation","termid":"GO:0090382"}],"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 phagosome maturation","synonyms":[{"name":"down regulation of phagosome maturation","type":"exact"},{"name":"down-regulation of phagosome maturation","type":"exact"},{"name":"downregulation of phagosome maturation","type":"exact"},{"name":"inhibition of phagosome maturation","type":"narrow"}],"termid":"GO:1905163"}


id: PBO:0082317
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase component of heat shock protein Hsp90 chaperone complex; serves as nucleotide exchange factor to load ATP onto the SSA class of cytosolic Hsp70s; plays a role in prion propagation and determining prion variants; binds unfolded proteins; member of Hsp110 subclass of HSP70 proteins; deletion results in spindle elongation in S phase; SSE1 has a paralog, SSE2, that arose from the whole genome duplication","termid":"PBO:0082317"}


id: PBO:0016878
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces pombe specific","termid":"PBO:0016878"}


id: MONDO:0004902
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"connective tissue disorder","termid":"MONDO:0003900"},{"relation_name":"is_a","term_name":"deep keratitis","termid":"MONDO:0004903"}],"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":"interstitial keratitis","secondary_identifiers":["MEDGEN:509779","ICD9:370.50","UMLS:C0155088","DOID:9857"],"termid":"MONDO:0004902","xrefs":{"Monarch":{"xref_id":"0004902"}}}


id: PBO:0088595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translation factor (GTPase) Mtg1","termid":"PBO:0088595"}


id: MONDO:0019981
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Unilateral multicystic dysplastic kidney is the form of multicystic dysplastic kidney (MCDK), a congenital anomaly of the kidney and urinary tract (CAKUT), in which one kidney is large, distended by multiple cysts, and non-functional.","definition_xrefs":["Orphanet:97363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicystic dysplastic kidney","termid":"MONDO:0015988"}],"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":"unilateral multicystic dysplastic kidney","secondary_identifiers":["MEDGEN:292613","UMLS:C1567426","GARD:19375"],"synonyms":[{"name":"unilateral MCDK","type":"exact"},{"name":"unilateral multicystic renal dysplasia","type":"exact"}],"termid":"MONDO:0019981","xrefs":{"Monarch":{"xref_id":"0019981"}}}


id: PR:C6Y4C9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spo13 gene.","definition_xrefs":["PRO:DNx","UniProtKB:C6Y4C9"],"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":"sporulation-specific protein 13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1183.12","synonyms":[{"name":"Spom972h-spo13","type":"exact"}],"termid":"PR:C6Y4C9"}


id: GO:0032501
data:
  {"annotated_genes":["SJAG_00845"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[59693],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0009791"}]},"cv_name":"biological_process","definition":"Any biological process, occurring at the level of a multicellular organism, pertinent to its function.","definition_xrefs":["GOC:dph","GOC:tb","GOC:curators","GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological_process","termid":"GO:0008150"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00845":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"multicellular organismal process","references_by_uniquename":{"GO_REF:0000117":null},"secondary_identifiers":["GO:0044707","GO:0050874"],"synonyms":[{"name":"organismal physiological process","type":"exact"},{"name":"single-multicellular organism process","type":"related"}],"termid":"GO:0032501","terms_by_termid":{"GO:0009791":null}}


id: MONDO:0016130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"fungal infectious disease","termid":"MONDO:0002041"},{"relation_name":"is_a","term_name":"myositis disease","termid":"MONDO:0021167"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"fungal myositis","secondary_identifiers":["Orphanet:207000","UMLS:C0410251","GARD:20380","icd11.foundation:1054267564","MEDGEN:592951","SCTID:240111007"],"termid":"MONDO:0016130","xrefs":{"Monarch":{"xref_id":"0016130"}}}


id: SO:0000011
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene which can be transcribed, but will not be translated into a protein.","direct_ancestors":[{"relation_name":"is_a","term_name":"gene_attribute","termid":"SO:0000401"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non_protein_coding","synonyms":[{"name":"non protein-coding","type":"exact"}],"termid":"SO:0000011"}


id: GO:0071693
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of proteins in the extracellular region, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein transport","termid":"GO:0015031"},{"relation_name":"is_a","term_name":"establishment of protein localization to extracellular region","termid":"GO:0035592"},{"relation_name":"is_a","term_name":"protein localization to extracellular region","termid":"GO:0071692"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"protein transport within extracellular region","termid":"GO:0071693"}


id: MONDO:0016598
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital secondary polycythemia","termid":"MONDO:0016540"}],"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":"autosomal recessive secondary polycythemia not associated with VHL gene","secondary_identifiers":["GARD:20658","Orphanet:247378"],"synonyms":[{"name":"autosomal recessive secondary erythrocytosis not associated with VHL gene","type":"exact"},{"name":"autosomal recessive secondary erythrocytosis, non-Chuvash type","type":"exact"},{"name":"autosomal recessive secondary polycythemia, non-Chuvash type","type":"exact"}],"termid":"MONDO:0016598","xrefs":{"Monarch":{"xref_id":"0016598"}}}


id: PBO:0050414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HNRNPDL pseudogene 3","termid":"PBO:0050414"}


id: PBO:0028975
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_nitrite","termid":"PBO:0028975"}


id: MONDO:0006759
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neuropathy of the femoral nerve.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mononeuropathy","termid":"MONDO:0001397"},{"relation_name":"is_a","term_name":"peripheral nerve lesion","termid":"MONDO:0024334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"femoral neuropathy","secondary_identifiers":["MESH:D020428","ICD9:355.2","NCIT:C27595","MEDGEN:148421","SCTID:25690000","UMLS:C0751931","DOID:4196"],"synonyms":[{"name":"femoral nerve dysfunction","type":"exact"},{"name":"femoral nerve lesions","type":"exact"},{"name":"femoral nerve peripheral nerve lesion","type":"exact"},{"name":"peripheral nerve lesion of femoral nerve","type":"exact"}],"termid":"MONDO:0006759","xrefs":{"Monarch":{"xref_id":"0006759"}}}


id: PBO:0086248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that mediates sphingolipid homeostasis; evolutionarily conserved, required for resistance to agents that induce unfolded protein response; Orm1p and Orm2p together control membrane biogenesis by coordinating lipid homeostasis with protein quality control; ORM1 has a paralog, ORM2, that arose from the whole genome duplication","termid":"PBO:0086248"}


id: GO:0032372
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 sterols into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lipid transport","termid":"GO:0032369"},{"relation_name":"is_a","term_name":"regulation of sterol transport","termid":"GO:0032371"},{"relation_name":"negatively_regulates","term_name":"sterol transport","termid":"GO:0015918"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of sterol transport","synonyms":[{"name":"down regulation of sterol transport","type":"exact"},{"name":"down-regulation of sterol transport","type":"exact"},{"name":"downregulation of sterol transport","type":"exact"},{"name":"inhibition of sterol transport","type":"narrow"}],"termid":"GO:0032372"}


id: PBO:0091246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADPH dehydrogenase, (Old yellow enzyme) involved in small alpha,beta-unsaturated carbonyl compounds","termid":"PBO:0091246"}


id: PBO:0057271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 495","termid":"PBO:0057271"}


id: GO:0021637
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to the act of creating the structural organization of the oculomotor nerve. This process pertains to the physical shaping of a rudimentary structure. The trigeminal nerve is composed of three large branches. They are the ophthalmic (V1, sensory), maxillary (V2, sensory) and mandibular (V3, motor and sensory) branches. The sensory ophthalmic branch travels through the superior orbital fissure and passes through the orbit to reach the skin of the forehead and top of the head. The maxillary nerve contains sensory branches that reach the pterygopalatine fossa via the inferior orbital fissure (face, cheek and upper teeth) and pterygopalatine canal (soft and hard palate, nasal cavity and pharynx). The motor part of the mandibular branch is distributed to the muscles of mastication, the mylohyoid muscle and the anterior belly of the digastric. The mandibular nerve also innervates the tensor veli palatini and tensor tympani muscles. The sensory part of the mandibular nerve is composed of branches that carry general sensory information from the mucous membranes of the mouth and cheek, anterior two-thirds of the tongue, lower teeth, skin of the lower jaw, side of the head and scalp and meninges of the anterior and middle cranial fossae.","definition_xrefs":["GOC:dph","GOC:jid","GOC:cls","GO_REF:0000021","GOC:dgh","ISBN:0838580343"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve structural organization","termid":"GO:0021604"},{"relation_name":"part_of","term_name":"trigeminal nerve morphogenesis","termid":"GO:0021636"}],"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":"trigeminal nerve structural organization","synonyms":[{"name":"CN V structural organization","type":"related"},{"name":"trigeminal nerve structural organisation","type":"exact"}],"termid":"GO:0021637"}


id: PBO:0001252
data:
  {"annotation_feature_type":"gene","cv_name":"ex_tools","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deletion solves arginine-conversion problem","termid":"PBO:0001252"}


id: PBO:0036133
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K4_dimethylation_during_vegetative_growth","termid":"PBO:0036133"}


id: PBO:0047921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, aphidicolin type, common, fra(10)(q26.1)","termid":"PBO:0047921"}


id: PR:Q9P329
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of any of the following genes in Schizosaccharomyces pombe 972h-: pfl6/SPBC1348.08c.","definition_xrefs":["UniProtKB:Q9P329","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell agglutination protein C1348.08c/C977.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1348.08c","synonyms":[{"name":"Spom972h-SPBC1348.08c","type":"exact"}],"termid":"PR:Q9P329"}


id: PBO:0027168
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_negative_regulation_of_DNA_replication_initiation","termid":"PBO:0027168"}


id: MONDO:0017619
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital sucrase-isomaltase deficiency","termid":"MONDO:0009114"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004335","MONDO:0037792"],"is_obsolete":false,"name":"congenital sucrase-isomaltase deficiency with minimal starch tolerance","secondary_identifiers":["Orphanet:306446"],"synonyms":[{"name":"CSID with minimal starch tolerance","type":"exact"},{"name":"congenital sucrase-isomaltose malabsorption with minimal starch tolerance","type":"exact"},{"name":"congenital sucrose intolerance with minimal starch tolerance","type":"exact"},{"name":"disaccharide intolerance with minimal starch tolerance","type":"exact"}],"termid":"MONDO:0017619","xrefs":{"Monarch":{"xref_id":"0017619"}}}


id: PBO:0027158
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_vacuolar_alanine_level","termid":"PBO:0027158"}


id: GO:0106433
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction O6-methyl-dGTP + H2O = O6-methyl-dGMP + diphosphate + H+.","definition_xrefs":["RHEA:67600","PMID:30304478"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides","termid":"GO:0016818"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"O6-methyl-dGTP hydrolase activity","termid":"GO:0106433"}


id: GO:0043331
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a double-stranded RNA stimulus.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to dsRNA","synonyms":[{"name":"response to double-stranded RNA","type":"exact"}],"termid":"GO:0043331"}


id: GO:0050625
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-hydroxy-1,4-benzoquinone + 2 H+ + NADH = benzene-1,2,4-triol + NAD+.","definition_xrefs":["RHEA:12428"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor","termid":"GO:0016655"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"2-hydroxy-1,4-benzoquinone reductase (NADH) activity","secondary_identifiers":["KEGG_REACTION:R05399","EC:1.6.5.7","MetaCyc:1.6.5.7-RXN","UM-BBD_reactionID:r0667","GO:0018540"],"synonyms":[{"name":"1,2,4-trihydroxybenzene:NAD oxidoreductase activity","type":"related"},{"name":"1,2,4-trihydroxybenzene:NAD+ oxidoreductase activity","type":"related"},{"name":"2-hydroxy-1,4-benzoquinone reductase activity","type":"exact"},{"name":"2-hydroxy-1,4-benzoquinone:NADH oxidoreductase activity","type":"related"},{"name":"NADH:2-hydroxy-1,4-benzoquinone oxidoreductase activity","type":"related"},{"name":"hydroxybenzoquinone reductase activity","type":"related"}],"termid":"GO:0050625"}


id: GO:0014029
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of the specialized region of ectoderm between the neural ectoderm (neural plate) and non-neural ectoderm. The neural crest gives rise to the neural crest cells that migrate away from this region as neural tube formation proceeds.","definition_xrefs":["GOC:ef","GOC:dh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial to mesenchymal transition","termid":"GO:0001837"},{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"chordate embryonic development","termid":"GO:0043009"}],"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":"neural crest formation","termid":"GO:0014029"}


id: PBO:0055179
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 2603","termid":"PBO:0055179"}


id: PR:Q9P6P2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rrp36 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P6P2"],"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":"rRNA biogenesis protein rrp36 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC823.04","synonyms":[{"name":"Spom972h-rrp36","type":"exact"},{"name":"ribosomal RNA-processing protein 36 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P6P2"}


id: GO:1903233
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of calcium ion-dependent exocytosis of neurotransmitter.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:16782817"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of calcium ion-dependent exocytosis","termid":"GO:0017158"},{"relation_name":"is_a","term_name":"regulation of synaptic vesicle exocytosis","termid":"GO:2000300"},{"relation_name":"regulates","term_name":"calcium ion-regulated exocytosis of neurotransmitter","termid":"GO:0048791"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0016192","GO:0023052","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of calcium ion-dependent exocytosis of neurotransmitter","termid":"GO:1903233"}


id: PBO:0073667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal induced proliferation associated 1 like 2","termid":"PBO:0073667"}


id: PBO:0055059
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 2475","termid":"PBO:0055059"}


id: PBO:0040253
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy related 9B","termid":"PBO:0040253"}


id: PBO:0032723
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H4-K12_acetylation_at_subtelomere","termid":"PBO:0032723"}


id: MONDO:0003579
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease that involves the nerve fiber layer of retina.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"visual pathway disorder","termid":"MONDO:0001834"},{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"}],"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":"retinal nerve fiber layer disorder","secondary_identifiers":["SCTID:193428001","MEDGEN:784046","DOID:5678","ICD9:362.85","UMLS:C3665426"],"synonyms":[{"name":"disease of nerve fiber layer of retina","type":"exact"},{"name":"disease of nerve fibre layer of retina","type":"exact"},{"name":"disease or disorder of nerve fiber layer of retina","type":"exact"},{"name":"disease or disorder of nerve fibre layer of retina","type":"exact"},{"name":"disorder of nerve fiber layer of retina","type":"exact"},{"name":"disorder of nerve fibre layer of retina","type":"exact"},{"name":"nerve fiber bundle defect","type":"related"},{"name":"nerve fiber layer of retina disease","type":"exact"},{"name":"nerve fiber layer of retina disease or disorder","type":"exact"},{"name":"nerve fibre bundle defect","type":"related"},{"name":"nerve fibre layer of retina disease","type":"exact"},{"name":"nerve fibre layer of retina disease or disorder","type":"exact"},{"name":"retinal nerve fiber bundle defects","type":"exact"},{"name":"retinal nerve fiber bundle deficiency","type":"exact"},{"name":"retinal nerve fibre bundle defects","type":"exact"},{"name":"retinal nerve fibre bundle deficiency","type":"exact"}],"termid":"MONDO:0003579","xrefs":{"Monarch":{"xref_id":"0003579"}}}


id: GO:0080011
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-2,3-epoxysqualene = baruol. Baruol is also known as D:B-Friedo-Baccharan-5,21-dien-3-ol.","definition_xrefs":["RHEA:31987","PMID:17705488"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidosqualene cyclase activity","termid":"GO:0031559"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"baruol synthase activity","secondary_identifiers":["EC:5.4.99.57","MetaCyc:RXN-9685"],"termid":"GO:0080011"}


id: PBO:0048754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerate kinase","termid":"PBO:0048754"}


id: GO:0001692
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving histamine, a physiologically active amine, found in plant and animal tissue and released from mast cells as part of an allergic reaction in humans.","definition_xrefs":["GOC:jl","ISBN:0395825172"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biogenic amine metabolic process","termid":"GO:0006576"},{"relation_name":"is_a","term_name":"imidazole-containing compound metabolic process","termid":"GO:0052803"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"histamine metabolic process","synonyms":[{"name":"histamine metabolism","type":"exact"}],"termid":"GO:0001692"}


id: PBO:0085891
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; involved in regulation of dNTP production; null mutant suppresses the lethality of lcd1 and rad53 mutations; expression is induced by Kar4p","termid":"PBO:0085891"}


id: MONDO:0010023
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Combined immunodeficiency due to ZAP70 deficiency is a very rare, severe, genetic, combined immunodeficiency disorder characterized by lymphocytosis, decreased peripheral CD8+ T-cells, and presence of normal circulating CD4+ T-cells, leading to immune dysfunction.","definition_xrefs":["Orphanet:911"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"non-SCID combined immunodeficiency","termid":"MONDO:0018814"},{"relation_name":"is_a","term_name":"combined immunodeficiency","termid":"MONDO:0015131"}],"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":"combined immunodeficiency due to ZAP70 deficiency","secondary_identifiers":["MESH:C536722","SCTID:716378008","OMIM:269840","GARD:387","DOID:0111943","NANDO:1200327","NANDO:2200700","icd11.foundation:1718367094","UMLS:C5575025","MEDGEN:1809040"],"synonyms":[{"name":"IMD48","type":"related"},{"name":"STCD","type":"related"},{"name":"ZAP-70 deficiency","type":"related"},{"name":"immunodeficiency 48","type":"related"},{"name":"selective T-cell defect","type":"related"},{"name":"severe combined immunodeficiency due to ZAP70 deficiency","type":"related"},{"name":"zeta-associated-protein 70 deficiency","type":"exact"}],"termid":"MONDO:0010023","xrefs":{"Monarch":{"xref_id":"0010023"}}}


id: PBO:0035723
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_glycosylation_during_vegetative_growth","termid":"PBO:0035723"}


id: PBO:0067011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 19, pseudogene","termid":"PBO:0067011"}


id: PBO:0086827
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; YOL131W has a paralog, STB1, that arose from the whole genome duplication","termid":"PBO:0086827"}


id: MOD:00050
data:
  {"annotated_genes":["SJAG_00733","SJAG_02522"],"annotation_feature_type":"gene","cv_annotations":{"PSI-MOD":[{"annotations":[82370,82544],"is_not":false,"summary":null,"term":"MOD:00050"}]},"cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-alanine residue to N-acetyl-L-alanine.","definition_xrefs":["RESID:AA0041","PubMed:363452","PubMed:4700463"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-alanine residue","termid":"MOD:00901"},{"relation_name":"is_a","term_name":"alpha-amino acetylated residue","termid":"MOD:01458"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00733":null,"SJAG_02522":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00408"}],"interesting_parent_ids":["MOD:00408"],"is_obsolete":false,"name":"N-acetyl-L-alanine","references_by_uniquename":{"PMID:36408920":null},"synonyms":[{"name":"(2S)-2-(acetamido)propanoic acid","type":"exact"},{"name":"2-(acetylamino)propanoic acid","type":"exact"},{"name":"2-(acetylazanyl)propanoic acid","type":"exact"},{"name":"AcAla","type":"exact"},{"name":"MOD_RES N-acetylalanine","type":"exact"},{"name":"N-acetyl-L-alanine","type":"exact"},{"name":"N-acetylated L-alanine","type":"exact"},{"name":"acetylalanine","type":"exact"}],"termid":"MOD:00050","terms_by_termid":{"MOD:00050":null}}


id: GO:1902447
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of shade avoidance.","definition_xrefs":["GOC:TermGenie","PMID:23763263"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of shade avoidance","termid":"GO:1902446"},{"relation_name":"negatively_regulates","term_name":"shade avoidance","termid":"GO:0009641"}],"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 shade avoidance","synonyms":[{"name":"down regulation of shade avoidance","type":"exact"},{"name":"down-regulation of shade avoidance","type":"exact"},{"name":"downregulation of shade avoidance","type":"exact"},{"name":"inhibition of shade avoidance","type":"narrow"}],"termid":"GO:1902447"}


id: GO:1903036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of response to wounding.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","GOC:kmv","PMID:19164535"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of response to stimulus","termid":"GO:0048584"},{"relation_name":"is_a","term_name":"regulation of response to wounding","termid":"GO:1903034"},{"relation_name":"positively_regulates","term_name":"response to wounding","termid":"GO:0009611"}],"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 response to wounding","synonyms":[{"name":"activation of physiological response to wounding","type":"narrow"},{"name":"activation of response to wounding","type":"narrow"},{"name":"positive regulation of physiological response to wounding","type":"exact"},{"name":"up regulation of physiological response to wounding","type":"exact"},{"name":"up regulation of response to wounding","type":"exact"},{"name":"up-regulation of physiological response to wounding","type":"exact"},{"name":"up-regulation of response to wounding","type":"exact"},{"name":"upregulation of physiological response to wounding","type":"exact"},{"name":"upregulation of response to wounding","type":"exact"}],"termid":"GO:1903036"}


id: PBO:0057854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3165","termid":"PBO:0057854"}


id: MONDO:0022757
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosome 20 trisomy, (also called trisomy 20) is a condition in which a fetus or individual has an extra full or partial copy of chromosome 20 in some or allof of his/her cells. An extra full copy of chromosome 20 in all of a person's cells is rare, and almost all fetuses with this do not survive past the first trimester ofpregnancy. The presence of an extra copyof only part of chromosome 20 is called partial trisomy 20; and an extra copy of chromosome 20 in only some of a person's cells is called mosaic trisomy 20. Mosaic trisomy 20 is the most common type of chromosome 20 trisomy and is one of the more common chromosomal abnormalities found during prenatal diagnostic testing. Studies have shown that the child is normal in the vast majority of prenatally diagnosed individuals. However, features that have been reported include spinal abnormalities (including spinal stenosis, vertebral fusion, and kyphosis), hypotonia (decreased muscle tone), life long constipation, sloped shoulders, and significant learning disabilities despite normal intelligence. Trisomy 20 usually results from an error that occurs when an egg or sperm cell develops (before fertilization); mosaic trisomy 20 usually results from errors in cell division soon after fertilization.","definition_xrefs":["GARD:0005332"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 20 disorder","termid":"MONDO:0700025"},{"relation_name":"is_a","term_name":"trisomy","termid":"MONDO:0700065"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 20 trisomy","secondary_identifiers":["NCIT:C36397","MEDGEN:120542","MESH:C535372","GARD:5332","UMLS:C0265479"],"synonyms":[{"name":"mosaic trisomy 20","type":"related"},{"name":"trisomy 20","type":"related"},{"name":"trisomy 20 mosaicism","type":"related"},{"name":"trisomy chromosome 20","type":"related"}],"termid":"MONDO:0022757","xrefs":{"Monarch":{"xref_id":"0022757"}}}


id: MONDO:0005162
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete influenza infection (obsolete MONDO:0005162)","termid":"MONDO:0005162","xrefs":{"Monarch":{"xref_id":"0005162"}}}


id: PBO:0081014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZBTB46 antisense RNA 2","termid":"PBO:0081014"}


id: PR:Q9Y7R3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A condensin complex subunit 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04301"],"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":"condensin complex subunit 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC306.03c","secondary_identifiers":["UniProtKB:Q9Y7R3"],"synonyms":[{"name":"CAPH homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-NCAPH","type":"exact"},{"name":"barren homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"p105 (Schizosaccharomyces pombe 972h-)","type":"broad"}],"termid":"PR:Q9Y7R3"}


id: FYECO:0000230
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed in glucose-based medium containing much less nitrogen than standard minimal medium (such as EMM). Note that for mating assays sporulation medium may be more appropriate.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping defined medium","termid":"FYECO:0000013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"low nitrogen glucose MM","synonyms":[{"name":"low nitrogen glucose minimal medium","type":"exact"}],"termid":"FYECO:0000230"}


id: GO:0003174
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the mitral valve over time, from its formation to the mature structure.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrioventricular valve development","termid":"GO:0003171"}],"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":"mitral valve development","termid":"GO:0003174"}


id: MONDO:0012797
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"otosclerosis","termid":"MONDO:0005349"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"otosclerosis 8","secondary_identifiers":["DOID:0060926","MESH:C567421","OMIM:612096","MEDGEN:436965","UMLS:C2677515"],"synonyms":[{"name":"OTSC8","type":"exact"},{"name":"otosclerosis 8","type":"exact"}],"termid":"MONDO:0012797","xrefs":{"Monarch":{"xref_id":"0012797"}}}


id: GO:0061248
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the mesonephric glomerulus vasculature are generated and organized. The mesonephric glomerulus vasculature is composed of the tubule structures that carry blood or lymph in the mesonephric glomerulus.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerulus vasculature morphogenesis","termid":"GO:0072103"},{"relation_name":"part_of","term_name":"mesonephric glomerulus vasculature development","termid":"GO:0061231"},{"relation_name":"part_of","term_name":"mesonephric glomerulus morphogenesis","termid":"GO:0061234"}],"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 glomerulus vasculature morphogenesis","termid":"GO:0061248"}


id: GO:7770003
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an L-alpha-amino acid + cholate = an N-choloyl-L-alpha-amino acid + H2O.","definition_xrefs":["PMID:38326609","PMID:40446798","RHEA:79087","PMID:38326608"],"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:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016810","GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"amino acid conjugated cholate hydrolase activity","termid":"GO:7770003"}


id: PBO:0039151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AK3 pseudogene 6","termid":"PBO:0039151"}


id: PBO:0027981
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cut_during_cellular_response_to_thiabendazole","termid":"PBO:0027981"}


id: GO:0097567
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Set of four basal bodies found in Giardia species (trophozoite stage). It comprises the right lateral basal body pair and the right middle basal body pair (i.e. the anterior, ventral, caudal and posteriolateral basal bodies located to the left of the right nucleus of the trophozoite when viewed dorsally).","definition_xrefs":["GOC:giardia","ISBN:9780124260207","PMID:16607022","PMID:5961344"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cell projection","termid":"GO:0042995"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"right tetrad","termid":"GO:0097567"}


id: PR:Q9Y7T2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A WD repeat-containing protein 89 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04472"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized WD repeat-containing protein C63.06 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC63.06","secondary_identifiers":["UniProtKB:Q9Y7T2"],"synonyms":[{"name":"Spom972h-WDR89","type":"exact"}],"termid":"PR:Q9Y7T2"}


id: PBO:0079190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis specific protein Y-linked 19, pseudogene","termid":"PBO:0079190"}


id: GO:0102656
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 1-18:2-2-trans-16:1-phosphatidylglycerol + O2 + a reduced electron acceptor = 1-18:3-2-trans-16:1-phosphatidylglycerol + 2 H2O + an oxidized electron acceptor.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 1-18:2-2-trans-16:1-phosphatidylglycerol desaturase activity (obsolete GO:0102656)","termid":"GO:0102656"}


id: PBO:0031101
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_septum_formation","termid":"PBO:0031101"}


id: MONDO:0043003
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of acanthosis nigricans (disease) that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acanthosis nigricans","termid":"MONDO:0007035"},{"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":"familial acanthosis nigricans","secondary_identifiers":["OMIM:100600","UMLS:C2930792","MEDGEN:419638","MESH:C531598"],"synonyms":[{"name":"acanthosis nigricans","type":"related"},{"name":"hereditary acanthosis nigricans (disease)","type":"exact"}],"termid":"MONDO:0043003","xrefs":{"Monarch":{"xref_id":"0043003"}}}


id: MOD:01366
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative -","definition_xrefs":["Unimod:478#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fluorescein-5-thiosemicarbazide","termid":"MOD:00626"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fluorescein-5-thiosemicarbazide - site K","synonyms":[{"name":"FTC","type":"related"},{"name":"fluorescein-5-thiosemicarbazide","type":"related"}],"termid":"MOD:01366"}


id: PR:O74945
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An elongation factor Tu GTP-binding domain-containing protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04255"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome assembly protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC553.08c","secondary_identifiers":["UniProtKB:O74945"],"synonyms":[{"name":"EF-2 like GTPase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-EFTUD1","type":"exact"},{"name":"elongation factor-like 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74945"}


id: GO:0098671
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process by which a virion attaches to a host cell by binding to a receptor on the host cell surface that does not mediate or trigger entry into the host cell. This binding is typically reversible and enhances significantly infectivity by concentrating the virus in the vicinity of its entry receptors, or bringing it to an organ in which its target cells are located.","definition_xrefs":["VZ:3943","PMID:18351291"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor-mediated virion attachment to host cell","termid":"GO:0046813"}],"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":"adhesion receptor-mediated virion attachment to host cell","synonyms":[{"name":"viral attachment to host adhesion receptor","type":"exact"}],"termid":"GO:0098671"}


id: MONDO:0006498
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polypoid adenoma that arises from and protrudes into the lumen of the colon. Epithelial dysplasia is always present. According to the architectural pattern it is classified as tubular, tubulovillous, or villous.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colon adenoma","termid":"MONDO:0000527"},{"relation_name":"is_a","term_name":"polyp of colon","termid":"MONDO:0021400"}],"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":"adenomatous colon polyp","secondary_identifiers":["HP:0005227","SCTID:428054006","MEDGEN:163407","NCIT:C96479","UMLS:C0850572","EFO:1000633"],"synonyms":[{"name":"adenomatous polyp of colon","type":"exact"},{"name":"adenomatous polyp of the colon","type":"exact"},{"name":"colon adenomatous polyp","type":"exact"},{"name":"colonic adenomatous polyp","type":"exact"}],"termid":"MONDO:0006498","xrefs":{"Monarch":{"xref_id":"0006498"}}}


id: MONDO:0006017
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete western equine encephalitis (obsolete MONDO:0006017)","termid":"MONDO:0006017","xrefs":{"Monarch":{"xref_id":"0006017"}}}


id: GO:1903553
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of extracellular vesicular exosome assembly.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:24105262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organelle assembly","termid":"GO:1902117"},{"relation_name":"is_a","term_name":"regulation of extracellular exosome assembly","termid":"GO:1903551"},{"relation_name":"positively_regulates","term_name":"extracellular exosome assembly","termid":"GO:0071971"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"positive regulation of extracellular exosome assembly","synonyms":[{"name":"activation of extracellular vesicular exosome assembly","type":"narrow"},{"name":"positive regulation of extracellular vesicular exosome assembly","type":"related"},{"name":"up regulation of extracellular vesicular exosome assembly","type":"exact"},{"name":"up-regulation of extracellular vesicular exosome assembly","type":"exact"},{"name":"upregulation of extracellular vesicular exosome assembly","type":"exact"}],"termid":"GO:1903553"}


id: MONDO:0005146
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An anxiety disorder precipitated by an experience of intense fear or horror while exposed to a traumatic (especially life-threatening) event. The disorder is characterized by intrusive recurring thoughts or images of the traumatic event; avoidance of anything associated with the event; a state of hyperarousal and diminished emotional responsiveness. These symptoms are present for at least one month and the disorder is usually long-term.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurotic disorder","termid":"MONDO:0005379"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"post-traumatic stress disorder","secondary_identifiers":["EFO:0001358","DOID:2055","MEDGEN:21345","ICD10CM:F43.1","birnlex:12679","UMLS:C0038436","ICD9:309.81","NCIT:C3389","SCTID:47505003","MESH:D013313"],"synonyms":[{"name":"PTSD","type":"exact"},{"name":"combat neurosis","type":"narrow"},{"name":"post-traumatic stress disorder","type":"exact"},{"name":"traumatic neurosis","type":"exact"}],"termid":"MONDO:0005146","xrefs":{"Monarch":{"xref_id":"0005146"}}}


id: PBO:0080331
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 95 pseudogene","termid":"PBO:0080331"}


id: MONDO:0018743
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete immune-mediated acquired neuromuscular junction disease (obsolete MONDO:0018743)","secondary_identifiers":["Orphanet:464764"],"termid":"MONDO:0018743","xrefs":{"Monarch":{"xref_id":"0018743"}}}


id: GO:0045237
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a CXCR1 chemokine receptor.","definition_xrefs":["PMID:11910892","GOC:ceb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interleukin-8 receptor binding","termid":"GO:0005153"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"CXCR1 chemokine receptor binding","synonyms":[{"name":"CXCR1 chemokine receptor ligand","type":"narrow"}],"termid":"GO:0045237"}


id: PBO:0052782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 19 pseudogene 6","termid":"PBO:0052782"}


id: PBO:0060179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metaxin 3","termid":"PBO:0060179"}


id: MONDO:0800405
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited retinopathy caused by bi-allelic variants in the CNGA1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"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":"CNGA1-related retinopathy","termid":"MONDO:0800405","xrefs":{"Monarch":{"xref_id":"0800405"}}}


id: MONDO:0004905
data:
  {"annotated_genes":["SJAG_03824","SJAG_02131"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88938,88939],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009114"}]},"cv_name":"mondo","definition":"Inherited or acquired disorders of sugar metabolism. Deficiencies of lactase, maltase or sucrase-isomaltase usually occur irreversibly and independent of one another. Congenital deficiencies are rare whereas acquired deficiencies are more common and may be seen following intestinal mucosal brush-border injury. Clinical signs include abdominal cramping, bloating, flatulence and diarrhea following dietary intake of lactose, maltose or sucrose. The clinical course leads to malabsorption of disaccharides which has implications for normal growth and development if manifested at an early age.","definition_xrefs":["EFO:1000060"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"inborn carbohydrate metabolic disorder","termid":"MONDO:0019214"},{"relation_name":"is_a","term_name":"malabsorption syndrome","termid":"MONDO:0020598"},{"relation_name":"is_a","term_name":"carbohydrate metabolism disease","termid":"MONDO:0037792"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02131":null,"SJAG_03824":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0004335","MONDO:0005066"],"is_obsolete":false,"name":"intestinal disaccharidase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:9868","SCTID:22169002","MEDGEN:675093","MONDO:0006062","ICD9:271.3","NCIT:C34731","UMLS:C0699848"],"synonyms":[{"name":"intestinal disaccharidase deficiency and disaccharide malabsorption","type":"exact"},{"name":"intestinal disaccharide deficiency and disaccharide malabsorption","type":"related"}],"termid":"MONDO:0004905","terms_by_termid":{"MONDO:0009114":null},"xrefs":{"Monarch":{"xref_id":"0004905"}}}


id: MONDO:0010914
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The severe infantile form of carnitine palmitoyltransferase II (CPT II) deficiency, an inherited disorder that affects mitochondrial oxidation of long chain fatty acids (LCFA), is the early-onset form of the disease.","definition_xrefs":["Orphanet:228305"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carnitine palmitoyltransferase II deficiency","termid":"MONDO:0015515"}],"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":"carnitine palmitoyl transferase II deficiency, severe infantile form","secondary_identifiers":["GARD:17150","OMIM:600649","MESH:C563462","UMLS:C1833511","MEDGEN:322211"],"synonyms":[{"name":"CARNITINE PALMITOYLTRANSFERASE II deficiency, infantile","type":"related"},{"name":"CPT 2 deficiency, hepatic","type":"related"},{"name":"CPT II deficiency, infantile","type":"exact"},{"name":"CPT2, hepatocardiomuscular form","type":"exact"},{"name":"CPT2, severe infantile form","type":"exact"},{"name":"CPTII, hepatocardiomuscular form","type":"exact"},{"name":"CPTII, severe infantile form","type":"exact"},{"name":"Carnitine Palmitoyltransferase 2 deficiency with hypoketotic hypoglycemia","type":"related"},{"name":"Carnitine Palmitoyltransferase 2 deficiency, hepatocardiomuscular","type":"related"},{"name":"Carnitine Palmitoyltransferase 2 deficiency, infantile","type":"related"},{"name":"Carnitine palmitoyl transferase II deficiency, hepatocardiomuscular form","type":"exact"},{"name":"Carnitine palmitoyl transferase deficiency type 2, hepatocardiomuscular form","type":"exact"},{"name":"Carnitine palmitoyl transferase deficiency type 2, severe infantile form","type":"exact"},{"name":"Cpt2 deficiency, infantile","type":"related"},{"name":"carnitine palmitoyl transferase II deficiency, severe infantile form","type":"exact"}],"termid":"MONDO:0010914","xrefs":{"Monarch":{"xref_id":"0010914"}}}


id: MONDO:0014233
data:
  {"annotated_genes":["SJAG_04545","SJAG_00063"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87715,87716],"is_not":false,"summary":null,"term":"MONDO:0014233"}]},"cv_name":"mondo","definition":"Any Parkinson disease in which the cause of the disease is a mutation in the SYNJ1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"young-onset Parkinson disease","termid":"MONDO:0017279"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00063":null,"SJAG_04545":null},"genotype_count":0,"is_obsolete":false,"name":"early-onset Parkinson disease 20","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:18462","MEDGEN:816154","OMIM:615530","DOID:0060898","UMLS:C3809824"],"synonyms":[{"name":"PARK20","type":"related"},{"name":"Parkinson disease 20, early-onset","type":"related"},{"name":"Parkinson disease caused by mutation in SYNJ1","type":"exact"},{"name":"SYNJ1 Parkinson disease","type":"exact"},{"name":"early-onset Parkinson disease type 20","type":"exact"},{"name":"early-onset Parkinson's disease 20","type":"related"}],"termid":"MONDO:0014233","terms_by_termid":{"MONDO:0014233":null},"xrefs":{"Monarch":{"xref_id":"0014233"}}}


id: PBO:0042617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"corneodesmosin","termid":"PBO:0042617"}


id: PBO:0000565
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carbamoyl-phosphate synthase (glutamine hydrolyzing), aspartate carbamoyltransferase Ura1","termid":"PBO:0000565"}


id: GO:0004295
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the preferential cleavage of Arg-Xaa, Lys-Xaa.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete trypsin activity (obsolete GO:0004295)","synonyms":[{"name":"alpha-trypsin activity","type":"narrow"},{"name":"beta-trypsin activity","type":"narrow"},{"name":"cocoonase activity","type":"related"},{"name":"parenzyme","type":"related"},{"name":"parenzymol","type":"related"},{"name":"pseudotrypsin","type":"related"},{"name":"sperm receptor hydrolase activity","type":"related"},{"name":"tripcellim","type":"related"},{"name":"trypsin activity","type":"exact"},{"name":"tryptar","type":"related"},{"name":"trypure","type":"related"}],"termid":"GO:0004295"}


id: GO:0004083
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2,3-bisphospho-D-glycerate + H2O = 3-phospho-D-glycerate + phosphate.","definition_xrefs":["PMID:9452443","PMID:8567632"],"gene_count":0,"genotype_count":0,"name":"obsolete bisphosphoglycerate 2-phosphatase activity (obsolete GO:0004083)","termid":"GO:0004083"}


id: GO:0004331
data:
  {"annotated_genes":["SJAG_00039","SJAG_05314","SJAG_00685","SJAG_02713"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74972,76904,78027,80694],"is_not":false,"summary":null,"term":"GO:0004331"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-fructose 2,6-bisphosphate + H2O = D-fructose-6-phosphate + phosphate.","definition_xrefs":["EC:3.1.3.46"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sugar-phosphatase activity","termid":"GO:0050308"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00039":null,"SJAG_00685":null,"SJAG_02713":null,"SJAG_05314":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0016788","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"fructose-2,6-bisphosphate 2-phosphatase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["RHEA:17289","MetaCyc:3.1.3.46-RXN","GO:0004330","Reactome:R-HSA-5628905","Reactome:R-HSA-70262"],"synonyms":[{"name":"D-fructose-2,6-bisphosphate 2-phosphohydrolase activity","type":"related"},{"name":"beta-D-fructose-2,6-bisphosphate 2-phosphohydrolase activity","type":"related"},{"name":"fructose-2,6-bisphosphatase activity","type":"related"}],"termid":"GO:0004331","terms_by_termid":{"GO:0004331":null}}


id: PBO:0071715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L39 pseudogene 13","termid":"PBO:0071715"}


id: PBO:0014291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sequence orphan, predicted GPI anchor","termid":"PBO:0014291"}


id: MONDO:0014834
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete dyskinesia, limb and orofacial, infantile-onset (obsolete MONDO:0014834)","termid":"MONDO:0014834","xrefs":{"Monarch":{"xref_id":"0014834"}}}


id: MONDO:1012478
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"upper airway syndrome, non-human animal","termid":"MONDO:1011931"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"upper airway syndrome, dog","secondary_identifiers":["OMIA:001893-9615"],"termid":"MONDO:1012478","xrefs":{"Monarch":{"xref_id":"1012478"}}}


id: PBO:0064216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase C beta 2","termid":"PBO:0064216"}


id: PBO:0072301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S24 pseudogene 19","termid":"PBO:0072301"}


id: PBO:0068463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 40, pseudogene","termid":"PBO:0068463"}


id: PBO:0086329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein with ubiquitin-like N terminus; subunit of Nuclear Excision Repair Factor 2 (NEF2) with Rad4p that binds damaged DNA; enhances protein deglycosylation activity of Png1p; also involved, with Rad4p, in ubiquitylated protein turnover; Rad4p-Rad23p heterodimer binds to promoters of DNA damage response genes to repress their transcription in the absence of DNA damage","termid":"PBO:0086329"}


id: FYPO:0008020
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population phenotype in which cell growth is decreased relative to normal in a medium containing leucine as the nitrogen source.","definition_xrefs":["PomBase:mlr","PMID:7903653"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased vegetative cell population growth","termid":"FYPO:0001355"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0000003","FYPO:0000139","FYPO:0005447","FYPO:0002060","FYPO:0002058","FYPO:0001985"],"is_obsolete":false,"name":"decreased cell population growth on leucine nitrogen source","synonyms":[{"name":"decreased growth on leucine nitrogen source","type":"broad"},{"name":"decreased vegetative cell growth on leucine nitrogen source","type":"exact"},{"name":"growth defect, slow growth with leucine nitrogen source","type":"narrow"},{"name":"reduced cell population growth on leucine nitrogen source","type":"exact"},{"name":"slow cell growth on leucine nitrogen source","type":"narrow"}],"termid":"FYPO:0008020"}


id: PBO:0072052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S10 pseudogene 22","termid":"PBO:0072052"}


id: PBO:0082733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the Rpd3L histone deacetylase complex; relieves transcriptional repression by binding to the Cyc8p-Tup1p corepressor and recruiting the SAGA complex to the repressed promoter; contains a PHD finger domain","termid":"PBO:0082733"}


id: PBO:0065786
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"quiescin sulfhydryl oxidase 2","termid":"PBO:0065786"}


id: MONDO:1010701
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pyruvate kinase deficiency of erythrocyte that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate kinase deficiency of erythrocyte, non-human animal","termid":"MONDO:1010099"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate kinase deficiency of erythrocyte, dog","secondary_identifiers":["OMIA:000844-9615"],"termid":"MONDO:1010701","xrefs":{"Monarch":{"xref_id":"1010701"}}}


id: PBO:0031495
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_oxidative_stress","termid":"PBO:0031495"}


id: GO:0099645
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a neurotransmitter is transported to, or maintained in, a location within the membrane adjacent to a postsynaptic specialization (e.g. postsynaptic density).","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex localization","termid":"GO:0031503"},{"relation_name":"is_a","term_name":"receptor localization to synapse","termid":"GO:0097120"},{"relation_name":"is_a","term_name":"regulation of postsynaptic membrane neurotransmitter receptor levels","termid":"GO:0099072"},{"relation_name":"is_a","term_name":"protein localization to postsynaptic specialization membrane","termid":"GO:0099633"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"neurotransmitter receptor localization to postsynaptic specialization membrane","synonyms":[{"name":"neurotransmitter receptor localisation in postsynaptic specialization membrane","type":"exact"}],"termid":"GO:0099645"}


id: GO:1901493
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a decalin stimulus.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to decalin","termid":"GO:1901493"}


id: GO:0048455
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to the act of giving rise to the stamen. This process pertains to the initial formation of a structure from unspecified parts.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"floral organ formation","termid":"GO:0048449"},{"relation_name":"part_of","term_name":"stamen morphogenesis","termid":"GO:0048448"}],"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":"stamen formation","secondary_identifiers":["GO:0048427"],"termid":"GO:0048455"}


id: PBO:0066612
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rhox homeobox family member 1 pseudogene 3","termid":"PBO:0066612"}


id: PBO:0045039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DIX domain containing 1","termid":"PBO:0045039"}


id: SO:0000362
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A cDNA clone constructed from more than one mRNA. Usually an experimental artifact.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"invalidated","termid":"SO:0000790"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"invalidated_by_chimeric_cDNA","synonyms":[{"name":"invalidated by chimeric cDNA","type":"exact"}],"termid":"SO:0000362"}


id: GO:0090320
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of chylomicron remnant clearance. Chylomicron clearance is the process in which a chylomicron remnant is removed from the blood via receptor-mediated endocytosis into liver cells and its constituent parts degraded.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of lipoprotein particle clearance","termid":"GO:0010984"},{"relation_name":"regulates","term_name":"chylomicron remnant clearance","termid":"GO:0034382"}],"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 chylomicron remnant clearance","termid":"GO:0090320"}


id: GO:0060844
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of a cell to an arterial endothelial cell fate and its capacity to differentiate into an arterial endothelial cell.","definition_xrefs":["GOC:sdb_2009","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood vessel endothelial cell fate commitment","termid":"GO:0060846"},{"relation_name":"part_of","term_name":"arterial endothelial cell differentiation","termid":"GO:0060842"}],"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":"arterial endothelial cell fate commitment","termid":"GO:0060844"}


id: PBO:0044090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer/testis antigen family 45 member A10","termid":"PBO:0044090"}


id: MONDO:0000214
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"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":"hypermanganesemia with dystonia","secondary_identifiers":["DOID:0080535","SCTID:768553002","UMLS:C4708509","MEDGEN:1632594","OMIMPS:613280"],"termid":"MONDO:0000214","xrefs":{"Monarch":{"xref_id":"0000214"}}}


id: GO:0097688
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The neurotransmitter-gated ion channel clustering process in which glutamate receptors are localized to distinct domains in the cell membrane.","definition_xrefs":["PMID:19723286","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurotransmitter-gated ion channel clustering","termid":"GO:0072578"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"glutamate receptor clustering","synonyms":[{"name":"glutamatergic receptor clustering","type":"exact"}],"termid":"GO:0097688"}


id: GO:0018288
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The incorporation of iron into a 4Fe-4S iron-sulfur cluster via tetrakis-L-cysteinyl tetrairon tetrasulfide.","definition_xrefs":["RESID:AA0140"],"gene_count":0,"genotype_count":0,"name":"obsolete iron incorporation into iron-sulfur cluster via tetrakis-L-cysteinyl tetrairon tetrasulfide (obsolete GO:0018288)","synonyms":[{"name":"iron incorporation into iron-sulphur cluster via tetrakis-L-cysteinyl tetrairon tetrasulphide","type":"exact"}],"termid":"GO:0018288"}


id: PATO:0002108
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's resembling small nipple like projection.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exserted","termid":"PATO:0000623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"papillary","termid":"PATO:0002108"}


id: PBO:0077493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMEM212 intronic transcript 1","termid":"PBO:0077493"}


id: GO:0034350
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of glial cell apoptotic process.","definition_xrefs":["GOC:mah","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of apoptotic process","termid":"GO:0042981"},{"relation_name":"regulates","term_name":"glial cell apoptotic process","termid":"GO:0034349"}],"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 glial cell apoptotic process","synonyms":[{"name":"regulation of glial cell apoptosis","type":"related"}],"termid":"GO:0034350"}


id: PBO:0055334
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 2762","termid":"PBO:0055334"}


id: PR:O74988
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cox5 gene.","definition_xrefs":["UniProtKB:O74988","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase polypeptide 5, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC338.10c","synonyms":[{"name":"Spom972h-cox5","type":"exact"},{"name":"cytochrome c oxidase polypeptide V (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74988"}


id: PBO:0120032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial glutathione reductase Pgr1 OR mitochondrial glutathione reductase Pgr1","termid":"PBO:0120032"}


id: GO:0102046
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3,4-dichlorobenzoate + O2 + a reduced electron acceptor = 3,4-dichlorobenzoate-cis-4,5-diol + an oxidized electron acceptor.","definition_xrefs":["PMID:9322760","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of two atoms of oxygen into one donor","termid":"GO:0016708"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"3,4-dichlorobenzoate-4,5-oxygenase activity","secondary_identifiers":["MetaCyc:RXN-10427"],"termid":"GO:0102046"}


id: GO:0060961
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of phospholipase D.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipase inhibitor activity","termid":"GO:0004859"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0098772","GO:0003674","GO:0030234","GO:0004857","GO:0140678"],"is_obsolete":false,"name":"phospholipase D inhibitor activity","termid":"GO:0060961"}


id: PBO:0030057
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_minichromosome_loss_during_vegetative_growth","termid":"PBO:0030057"}


id: GO:0071253
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a connexin, any of a group of related proteins that assemble to form gap junctions.","definition_xrefs":["GOC:mah","PMID:19864490"],"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:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"connexin binding","termid":"GO:0071253"}


id: FYPO:0002280
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a cell that undergoes a single round of cell division, and then dies.","definition_xrefs":["PomBase:vw","PomBase:jh","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination","termid":"FYPO:0000316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000004"],"is_obsolete":false,"name":"inviable after spore germination, single cell division","synonyms":[{"name":"inviable following spore germination, single cell division","type":"exact"},{"name":"inviable germinated spore, single cell division","type":"exact"},{"name":"lethal after spore germination, single cell division","type":"exact"}],"termid":"FYPO:0002280"}


id: GO:0047224
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-O-N-acetyl-D-galactosalaminyl-[protein] + UDP-N-acetyl-D-glucosamine = 3-O-N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl-[protein] + UDP. Linkage of the glycan to the protein occurs via the oxygen atom in the side chain of an L-serine or L-threonine residue.","definition_xrefs":["EC:2.4.1.147"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylglucosaminyltransferase activity","termid":"GO:0008375"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a glycoprotein","termid":"GO:0140103"}],"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"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0003824","GO:0016757","GO:0140096","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"acetylgalactosaminyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase activity","secondary_identifiers":["MetaCyc:2.4.1.147-RXN","Reactome:R-HSA-914010"],"synonyms":[{"name":"O-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase III activity","type":"related"},{"name":"UDP-N-acetyl-D-glucosamine:O-glycosyl-glycoprotein (N-acetyl-D-glucosamine to N-acetyl-D-galactosaminyl-R) beta-1,3-N-acetyl-D-glucosaminyltransferase activity","type":"related"},{"name":"core 3-beta-GlcNAc-transferase activity","type":"related"},{"name":"core 3beta-GlcNAc-transferase activity","type":"related"},{"name":"mucin core 3 beta3-GlcNAc-transferase activity","type":"related"},{"name":"uridine diphosphoacetylglucosamine-mucin beta(1->3)-acetylglucosaminyltransferase activity","type":"related"}],"termid":"GO:0047224"}


id: MONDO:0000500
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma that arises from the tongue. It usually presents as a painful ulcerated or nodular lesion. The size of the tumor and the status of the lymph nodes are the most important factors that determine prognosis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tongue cancer","termid":"MONDO:0004631"},{"relation_name":"is_a","term_name":"oral cavity squamous cell carcinoma","termid":"MONDO:0004958"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"tongue squamous cell carcinoma","secondary_identifiers":["UMLS:C0349566","MEDGEN:91153","NCIT:C4648","SCTID:276952000","DOID:0050865"],"synonyms":[{"name":"scc of the tongue","type":"exact"},{"name":"scc of tongue","type":"exact"},{"name":"squamous cell carcinoma of the tongue","type":"exact"},{"name":"squamous cell carcinoma of tongue","type":"exact"},{"name":"tongue scc","type":"exact"},{"name":"tongue squamous cell carcinoma","type":"exact"}],"termid":"MONDO:0000500","xrefs":{"Monarch":{"xref_id":"0000500"}}}


id: PBO:0089494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pumilio family RNA-binding protein Puf4","termid":"PBO:0089494"}


id: MONDO:0009150
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome is characterized by alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction (primary hypothyroidism), hypohidrosis, ephelides, enteropathy, and respiratory tract infections due to ciliary dyskinesia, leading to suggestion of the acronym ANother syndrome as alternative name for this condition. It has been described in three patients (two brothers and an unrelated girl). Transmission is autosomal recessive.","definition_xrefs":["Orphanet:1882"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"},{"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":"hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome","secondary_identifiers":["OMIM:225050","MESH:C565604","SCTID:239050000","UMLS:C1857052","MEDGEN:384046","GARD:2049"],"synonyms":[{"name":"HEDH syndrome","type":"exact"},{"name":"another syndrome","type":"exact"},{"name":"ectodermal dysplasia hypohidrotic with hypothyroidism and ciliary dyskinesia","type":"related"},{"name":"ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia","type":"related"},{"name":"hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia","type":"related"},{"name":"hypohidrotic ectodermal dysplasia with hypothyroidism","type":"related"},{"name":"hypohidrotic ectodermal dysplasia with hypothyroidism and ciliary dyskinesia","type":"related"}],"termid":"MONDO:0009150","xrefs":{"Monarch":{"xref_id":"0009150"}}}


id: PBO:0018127
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Coffin-Lowry Syndrome","termid":"PBO:0018127"}


id: MONDO:0004802
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition characterized by infiltration of the lung with eosinophils due to inflammation or other disease processes. Major eosinophilic lung diseases are the eosinophilic pneumonias caused by infections, allergens, or toxic agents.","definition_xrefs":["MESH:D011657"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypereosinophilic syndrome","termid":"MONDO:0015691"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"pulmonary eosinophilia","secondary_identifiers":["icd11.foundation:544479555","SCTID:367542003","DOID:9498","UMLS:C0034068","ICD9:518.3","MEDGEN:46208"],"termid":"MONDO:0004802","xrefs":{"Monarch":{"xref_id":"0004802"}}}


id: GO:1901832
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of all-trans-neoxanthin.","definition_xrefs":["MetaCyc:PWY-6809","GOC:yaf","UniPathway:UPA00388","PMID:11029576","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xanthophyll catabolic process","termid":"GO:0016124"},{"relation_name":"is_a","term_name":"olefinic compound catabolic process","termid":"GO:0120256"},{"relation_name":"is_a","term_name":"ether catabolic process","termid":"GO:1901502"},{"relation_name":"is_a","term_name":"all-trans-neoxanthin metabolic process","termid":"GO:1901831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"all-trans-neoxanthin catabolic process","synonyms":[{"name":"all-trans-neoxanthin breakdown","type":"exact"},{"name":"all-trans-neoxanthin catabolism","type":"exact"},{"name":"all-trans-neoxanthin degradation","type":"exact"},{"name":"neoxanthin breakdown","type":"exact"},{"name":"neoxanthin catabolic process","type":"exact"},{"name":"neoxanthin catabolism","type":"exact"},{"name":"neoxanthin degradation","type":"exact"}],"termid":"GO:1901832"}


id: PBO:0054193
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 1568","termid":"PBO:0054193"}


id: MONDO:0024772
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual developmental disorder, X-linked, syndromic, Pilorge type","secondary_identifiers":["DOID:0070422","UMLS:C5676881","OMIM:301076","MEDGEN:1803486"],"synonyms":[{"name":"MRXSP","type":"exact"},{"name":"intellectual developmental disorder, X-linked, syndromic, Pilorge type","type":"exact"}],"termid":"MONDO:0024772","xrefs":{"Monarch":{"xref_id":"0024772"}}}


id: PBO:0017842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione transmembrane transporter Pgt1","termid":"PBO:0017842"}


id: MONDO:0007493
data:
  {"annotated_genes":["SJAG_04003"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87126],"is_not":false,"summary":null,"term":"MONDO:0007493"}]},"cv_name":"mondo","definition":"DYT4 type primary dystonia is characterized by predominantly laryngeal dystonia (manifesting as whispering dysphonia) and cervical dystonia (manifesting as torticollis).","definition_xrefs":["Orphanet:98805"],"direct_ancestors":[{"relation_name":"is_a","term_name":"focal, segmental or multifocal dystonia","termid":"MONDO:0015990"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04003":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0003441"}],"interesting_parent_ids":["MONDO:0003441"],"is_obsolete":false,"name":"torsion dystonia 4","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0090041","NANDO:1200515","OMIM:128101","SCTID:719276005","UMLS:C1851943","GARD:10138","MEDGEN:342124"],"synonyms":[{"name":"DYT4","type":"exact"},{"name":"autosomal dominant torsion dystonia-4","type":"related"},{"name":"dystonia 4, torsion, autosomal dominant","type":"related"},{"name":"dystonia musculorum deformans 4","type":"related"},{"name":"hereditary whispering dysphonia","type":"exact"},{"name":"primary dystonia, DYT4 type","type":"related"},{"name":"torsion dystonia type 4","type":"exact"},{"name":"whispering dysphonia","type":"exact"},{"name":"whispering dysphonia, hereditary","type":"related"}],"termid":"MONDO:0007493","terms_by_termid":{"MONDO:0007493":null},"xrefs":{"Monarch":{"xref_id":"0007493"}}}


id: GO:0140434
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of protein localization to a meiotic spindle pole body.","definition_xrefs":["PMID:22438582"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to meiotic spindle pole body","termid":"GO:0140433"},{"relation_name":"is_a","term_name":"positive regulation of protein localization to spindle pole body","termid":"GO:1902365"},{"relation_name":"positively_regulates","term_name":"protein localization to meiotic spindle pole body","termid":"GO:1902441"}],"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 meiotic spindle pole body","termid":"GO:0140434"}


id: PBO:0075731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal recognition particle 14","termid":"PBO:0075731"}


id: PBO:0058259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4637","termid":"PBO:0058259"}


id: PBO:0087186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase subunit ABC10-alpha, found in RNA pol I, II, and III; relocalizes from nucleolus to cytoplasm upon DNA replication stress","termid":"PBO:0087186"}


id: GO:0061682
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a seminal vesicle are generated and organized.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gland morphogenesis","termid":"GO:0022612"},{"relation_name":"part_of","term_name":"seminal vesicle development","termid":"GO:0061107"}],"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":"seminal vesicle morphogenesis","termid":"GO:0061682"}


id: PBO:0025513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinetochore protein, INCENP ortholog Pic1","termid":"PBO:0025513"}


id: GO:0071409
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 cycloheximide stimulus. Cycloheximide (actidione) is an antibiotic produced by some Streptomyces species which interferes with protein synthesis in eukaryotes.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cycloheximide","termid":"GO:0046898"},{"relation_name":"is_a","term_name":"cellular response to alcohol","termid":"GO:0097306"},{"relation_name":"is_a","term_name":"cellular response to ketone","termid":"GO:1901655"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to cycloheximide","synonyms":[{"name":"cellular response to actidione","type":"exact"}],"termid":"GO:0071409"}


id: PBO:0049599
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 2","termid":"PBO:0049599"}


id: PBO:0031102
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_salt_stress","termid":"PBO:0031102"}


id: PBO:0074952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 113-3","termid":"PBO:0074952"}


id: PBO:0062659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 13 subfamily C member 9","termid":"PBO:0062659"}


id: MONDO:0006209
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, intermediate, or malignant mesenchymal neoplasm characterized by the presence of neoplastic fibroblasts.","definition_xrefs":["NCIT:C7075"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesenchymal cell neoplasm","termid":"MONDO:0002616"},{"relation_name":"is_a","term_name":"connective tissue neoplasm","termid":"MONDO:0021581"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroblastic neoplasm","secondary_identifiers":["EFO:1000255","MEDGEN:60198","UMLS:C0206643"],"synonyms":[{"name":"fibroblastic neoplasm","type":"exact"},{"name":"fibroblastic tumor","type":"exact"},{"name":"fibroblastic tumour","type":"exact"},{"name":"fibrocytic neoplasm","type":"exact"},{"name":"fibrocytic tumor","type":"exact"},{"name":"fibrocytic tumour","type":"exact"},{"name":"fibrogenic neoplasm","type":"exact"},{"name":"fibrogenicTumor","type":"exact"},{"name":"fibrous neoplasm","type":"exact"},{"name":"fibrous tumor","type":"exact"},{"name":"fibrous tumour","type":"exact"}],"termid":"MONDO:0006209","xrefs":{"Monarch":{"xref_id":"0006209"}}}


id: PBO:0002323
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6.1.1.10","termid":"PBO:0002323"}


id: PBO:0049923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homogentisate 1,2-dioxygenase","termid":"PBO:0049923"}


id: PBO:0055953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 63","termid":"PBO:0055953"}


id: GO:1990794
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The region of a cell situated by the cell sides which interface adjacent cells and near the base. Often used in reference to animal polarized epithelial cells.","definition_xrefs":["PMID:18495799"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"basal part of cell","termid":"GO:0045178"},{"relation_name":"part_of","term_name":"lateral part of cell","termid":"GO:0097574"}],"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":"basolateral part of cell","termid":"GO:1990794"}


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


id: PBO:0048777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanosine monophosphate reductase 2","termid":"PBO:0048777"}


id: PBO:0053076
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ladybird homeobox 2","termid":"PBO:0053076"}


id: PBO:0075665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine palmitoyltransferase long chain base subunit 1","termid":"PBO:0075665"}


id: PBO:0035860
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_rate_of_protein_movement_within_plasma_membrane_at_cell_tip","termid":"PBO:0035860"}


id: PBO:0059053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"motor neuron and pancreas homeobox 1","termid":"PBO:0059053"}


id: PBO:0040913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMS1 pseudogene 17","termid":"PBO:0040913"}


id: PBO:0061589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-coding transcript regulating alternative splicing","termid":"PBO:0061589"}


id: PBO:0059263
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L30","termid":"PBO:0059263"}


id: PBO:0071161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a","termid":"PBO:0071161"}


id: PBO:0060389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MZF1 antisense RNA 1","termid":"PBO:0060389"}


id: PBO:0080497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"von Willebrand factor","termid":"PBO:0080497"}


id: PBO:0046720
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EVA1C pseudogene 6","termid":"PBO:0046720"}


id: GO:0032009
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A membrane-bounded intracellular vesicle as initially formed upon the ingestion of particulate material by phagocytosis.","definition_xrefs":["GOC:mah","PMID:12388753"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phagocytic vesicle","termid":"GO:0045335"}],"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:0031410"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0031410"],"is_obsolete":false,"name":"early phagosome","synonyms":[{"name":"early phagocytic vesicle","type":"exact"}],"termid":"GO:0032009"}


id: SO:0002053
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant whereby new or enhanced function is conferred on the gene product.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"functionally_abnormal","termid":"SO:0002218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gain_of_function_variant","synonyms":[{"name":"gain of function variant","type":"exact"}],"termid":"SO:0002053"}


id: GO:0010875
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of cholesterol efflux. Cholesterol efflux is the directed movement of cholesterol, cholest-5-en-3-beta-ol, out of a cell or organelle.","definition_xrefs":["GOC:BHF","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cholesterol efflux","termid":"GO:0010874"},{"relation_name":"is_a","term_name":"positive regulation of cholesterol transport","termid":"GO:0032376"},{"relation_name":"positively_regulates","term_name":"cholesterol efflux","termid":"GO:0033344"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of cholesterol efflux","termid":"GO:0010875"}


id: PR:Q9Y7L8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rps001 gene.","definition_xrefs":["UniProtKB:Q9Y7L8","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":"40S ribosomal protein S0-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC685.06","synonyms":[{"name":"Spom972h-rps001","type":"exact"}],"termid":"PR:Q9Y7L8"}


id: PBO:0072024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S9","termid":"PBO:0072024"}


id: PBO:0050307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 9","termid":"PBO:0050307"}


id: GO:0102426
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: myricetin 3-O-beta-D-glucopyranoside + UDP-alpha-D-glucose = myricetin 3-O-gentiobioside + UDP + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete myricetin-3-O-glucoside 1,6-glucosyltransferase activity (obsolete GO:0102426)","termid":"GO:0102426"}


id: PATO:0002338
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's being shaped like a lance-head, considerably longer than wide, tapering towards the tip from below the middle together forming three angles; attached at the broad end.","definition_xrefs":["PATOC:DD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lanceolate","termid":"PATO:0001877"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lanceolate-triangular","termid":"PATO:0002338"}


id: PBO:0003502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"telomere cap complex subunit Stn1","termid":"PBO:0003502"}


id: GO:0003257
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of transcription from an RNA polymerase II promoter that contributes to the differentiation of a myocardial precursor cell.","definition_xrefs":["GOC:mtg_heart"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter involved in myocardial precursor cell differentiation (obsolete GO:0003257)","termid":"GO:0003257"}


id: PBO:0056373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase 8 interacting protein 1 pseudogene 1","termid":"PBO:0056373"}


id: FYPO:0002167
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to ethyl methanesulfonate. Cells stop growing (and may die) at a concentration of ethyl methanesulfonate that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensitive to DNA damaging agents","termid":"FYPO:0000266"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000003","FYPO:0000139","FYPO:0002683"],"is_obsolete":false,"name":"sensitive to ethyl methanesulfonate","synonyms":[{"name":"hypersensitive to ethyl methanesulfonate","type":"exact"},{"name":"sensitive to EMS","type":"exact"},{"name":"sensitive to ethyl methanesulfonate during mitotic cell cycle","type":"related"},{"name":"sensitive to ethyl methanesulfonate during vegetative growth","type":"exact"},{"name":"sensitive to ethyl methanesulphonate","type":"exact"}],"termid":"FYPO:0002167"}


id: FYPO:0002452
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 contains one or more septa, has abnormal morphology (i.e. size, shape, or structure) and is inviable.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"inviable vegetative cell","termid":"FYPO:0001489"},{"relation_name":"has_part","term_name":"septated vegetative cell","termid":"FYPO:0002342"},{"relation_name":"is_a","term_name":"inviable vegetative cell","termid":"FYPO:0001489"},{"relation_name":"is_a","term_name":"inviable vegetative cell with abnormal cell morphology","termid":"FYPO:0002273"},{"relation_name":"is_a","term_name":"septated vegetative cell","termid":"FYPO:0002342"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000005","FYPO:0000004","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"inviable septated vegetative cell with abnormal cell morphology","synonyms":[{"name":"lethal; septated vegetative cell with abnormal cell morphology","type":"exact"}],"termid":"FYPO:0002452"}


id: PBO:0005859
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Puf family RNA-binding protein Puf6 (predicted)","termid":"PBO:0005859"}


id: GO:0009607
data:
  {"annotated_genes":["SJAG_04332","SJAG_04183","SJAG_00082","SJAG_01837","SJAG_01805","SJAG_04140","SJAG_03048"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[113194,95755,118678,91948,104336],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140429"},{"annotations":[106112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072429"},{"annotations":[104345],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072441"},{"annotations":[104346],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990820"},{"annotations":[96495,104347],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072435"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a biotic stimulus, a stimulus caused or produced by a living organism.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stimulus","termid":"GO:0050896"}],"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 biotic stimulus","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"response to biotic stress","type":"narrow"}],"termid":"GO:0009607","terms_by_termid":{"GO:0072429":null,"GO:0072435":null,"GO:0072441":null,"GO:0140429":null,"GO:1990820":null}}


id: PBO:0075429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm adhesion molecule 1","termid":"PBO:0075429"}


id: PBO:0031674
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_secretion","termid":"PBO:0031674"}


id: GO:0001317
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Accumulation of proteins that have undergone reactions with reactive oxygen species in aging dividing cells and exhibit modifications such as increased protein carbonyl content, oxidized methionine, protein hydrophobicity, and cross-linking.","definition_xrefs":["GOC:jh"],"gene_count":0,"genotype_count":0,"name":"obsolete accumulation of oxidatively modified proteins involved in replicative cell aging (obsolete GO:0001317)","synonyms":[{"name":"accumulation of oxidatively modified proteins during replicative cell ageing","type":"related"},{"name":"accumulation of oxidatively modified proteins during replicative cell aging","type":"related"}],"termid":"GO:0001317"}


id: PBO:0012553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HP1/CBX family","termid":"PBO:0012553"}


id: PBO:0063454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphodiesterase 11A","termid":"PBO:0063454"}


id: GO:0048528
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the post-embryonic root over time, from its formation to the mature structure.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"root development","termid":"GO:0048364"},{"relation_name":"is_a","term_name":"post-embryonic plant organ development","termid":"GO:0090696"}],"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":"post-embryonic root development","termid":"GO:0048528"}


id: MONDO:0019335
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mild hyperphenylalaninemia (HPA) is a rare form of phenylketonuria, an inborn error of amino acid metabolism, characterized by mild symptoms of HPA.","definition_xrefs":["Orphanet:79651"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenylketonuria","termid":"MONDO:0009861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0006025","MONDO:0004736"],"is_obsolete":false,"name":"mild hyperphenylalaninemia","secondary_identifiers":["UMLS:C5680207","MEDGEN:1843033","GARD:19027"],"synonyms":[{"name":"mHPA","type":"exact"},{"name":"mild HPA","type":"exact"},{"name":"non-PKU HPA","type":"exact"}],"termid":"MONDO:0019335","xrefs":{"Monarch":{"xref_id":"0019335"}}}


id: PBO:0111908
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human SLC5A family","termid":"PBO:0111908"}


id: PBO:0075350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sosondowah ankyrin repeat domain family member A","termid":"PBO:0075350"}


id: GO:0102342
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (R)-3-hydroxycerotoyl-CoA + NADP = 3-oxohexacosanoyl-CoA + NADPH + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-oxo-cerotoyl-CoA reductase activity (obsolete GO:0102342)","termid":"GO:0102342"}


id: GO:1990683
data:
  {"annotated_genes":["SJAG_04142","SJAG_02837","SJAG_01538"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77837,81202,98664],"is_not":false,"summary":null,"term":"GO:1990683"}]},"cv_name":"biological_process","definition":"A process in which the DNA double-strand breaks are attached to the inner surface of the nuclear envelope proximal to the spindle pole body, or iMTOCs.","definition_xrefs":["PMID:24943839"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome attachment to the nuclear envelope","termid":"GO:0097240"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01538":null,"SJAG_02837":null,"SJAG_04142":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0007049"],"is_obsolete":false,"name":"DNA double-strand break attachment to nuclear envelope","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:1990683","terms_by_termid":{"GO:1990683":null}}


id: GO:0060077
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A synapse in which an action potential in the presynaptic cell reduces the probability of an action potential occurring in the postsynaptic cell.","definition_xrefs":["GOC:ef","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synapse","termid":"GO:0045202"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"inhibitory synapse","secondary_identifiers":["Wikipedia:Inhibitory_postsynaptic_potential"],"termid":"GO:0060077"}


id: FYPO:0004605
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the total distance travelled by the SPB during horsetail movement is decreased. Horsetail movement is the oscillatory movement of the nucleus that takes place during meiotic prophase I. PMID:24954111","definition_xrefs":["PomBase:mlr","GO:0030989"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal horsetail movement","termid":"FYPO:0000197"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000631","FYPO:0000138","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased distance travelled by the spindle pole body during horsetail movement","synonyms":[{"name":"decreased dynein-driven meiotic oscillatory nuclear movement","type":"related"},{"name":"decreased horsetail nuclear movement","type":"related"},{"name":"reduced horsetail movement","type":"related"}],"termid":"FYPO:0004605"}


id: GO:1900868
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of sarcinapterin.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tricarboxylic acid biosynthetic process","termid":"GO:0072351"},{"relation_name":"is_a","term_name":"sarcinapterin metabolic process","termid":"GO:1900867"},{"relation_name":"is_a","term_name":"methanopterin-containing compound biosynthetic process","termid":"GO:2001116"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0042559"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0042559","GO:0008150"],"is_obsolete":false,"name":"sarcinapterin biosynthetic process","synonyms":[{"name":"sarcinapterin anabolism","type":"exact"},{"name":"sarcinapterin biosynthesis","type":"exact"},{"name":"sarcinapterin formation","type":"exact"},{"name":"sarcinapterin synthesis","type":"exact"}],"termid":"GO:1900868"}


id: GO:0047298
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-3-amino-2-methylpropanoate + 2-oxoglutarate = 2-methyl-3-oxopropanoate + L-glutamate.","definition_xrefs":["RHEA:13993","EC:2.6.1.22"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"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:0016740"},{"rel_name":"is_a","termid":"GO:0016769"}],"interesting_parent_ids":["GO:0003674","GO:0016769","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"(S)-3-amino-2-methylpropionate transaminase activity","secondary_identifiers":["MetaCyc:2.6.1.22-RXN","KEGG_REACTION:R04188"],"synonyms":[{"name":"(S)-3-amino-2-methylpropanoate:2-oxoglutarate aminotransferase activity","type":"related"},{"name":"(S)-3-amino-2-methylpropionate aminotransferase activity","type":"exact"},{"name":"L-3-aminoisobutyrate aminotransferase activity","type":"related"},{"name":"L-3-aminoisobutyrate transaminase activity","type":"related"},{"name":"L-3-aminoisobutyric aminotransferase activity","type":"related"},{"name":"L-AIBAT activity","type":"related"},{"name":"beta-aminobutyric transaminase activity","type":"related"},{"name":"beta-aminoisobutyrate-alpha-ketoglutarate transaminase activity","type":"related"}],"termid":"GO:0047298"}


id: GO:0018178
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The adenylylation of peptidyl-threonine to form peptidyl-O-(phospho-5'-adenosine)-L-threonine.","definition_xrefs":["RESID:AA0267"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-threonine adenylylation (obsolete GO:0018178)","synonyms":[{"name":"peptidyl-threonine adenylation","type":"exact"}],"termid":"GO:0018178"}


id: MONDO:0032765
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited bleeding disorder, platelet-type","termid":"MONDO:0000009"}],"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":"bleeding disorder, platelet-type, 22","secondary_identifiers":["MEDGEN:1673822","OMIM:618462","UMLS:C5193111"],"synonyms":[{"name":"BDPLT22","type":"related"},{"name":"BLEEDING DISORDER, PLATELET-TYPE, 22","type":"related"}],"termid":"MONDO:0032765","xrefs":{"Monarch":{"xref_id":"0032765"}}}


id: FYECO:0000365
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Cells were blocked using carbendazim (MBC) and subsequently released from the block.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping condition combinations","termid":"FYECO:0000238"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MBC block and release","termid":"FYECO:0000365"}


id: PBO:0001339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF185 protein, mitochondrial","termid":"PBO:0001339"}


id: PBO:0085161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleotide excision repair (NER) protein; binds damaged DNA during NER; binds DNA in an ATP-dependent manner (with Rad7p) during NER; required for NER of non-transcribed chromatin; subunit of Nucleotide Excision Repair Factor 4 (NEF4) and the Elongin-Cullin-Socs (ECS) ligase complex","termid":"PBO:0085161"}


id: PBO:0047789
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box D4 like 6","termid":"PBO:0047789"}


id: PBO:0084857
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial ribosomal protein of the large subunit; protein abundance increases in response to DNA replication stress","termid":"PBO:0084857"}


id: PBO:0052638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 6","termid":"PBO:0052638"}


id: MONDO:0024744
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm that arises from the choroid plexus in the brain and occurs during childhood.","definition_xrefs":["NCIT:C42080"],"direct_ancestors":[{"relation_name":"is_a","term_name":"choroid plexus neoplasm","termid":"MONDO:0016717"},{"relation_name":"is_a","term_name":"childhood neoplasm","termid":"MONDO:0021079"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"childhood choroid plexus neoplasm","secondary_identifiers":["UMLS:C0280623","MEDGEN:76132"],"synonyms":[{"name":"childhood choroid plexus neoplasm","type":"exact"},{"name":"choroid plexus neoplasm","type":"broad"},{"name":"choroid plexus neoplasm of childhood","type":"exact"},{"name":"paediatric choroid plexus neoplasm","type":"exact"},{"name":"pediatric choroid plexus neoplasm","type":"exact"}],"termid":"MONDO:0024744","xrefs":{"Monarch":{"xref_id":"0024744"}}}


id: MONDO:0010566
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked cone-rod dystrophy","termid":"MONDO:0021155"},{"relation_name":"is_a","term_name":"RPGR-related retinopathy","termid":"MONDO:0100437"}],"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":"X-linked cone-rod dystrophy 1","secondary_identifiers":["DOID:0111008","MESH:C564438","UMLS:C1844776","MEDGEN:336777","GARD:10652","OMIM:304020"],"synonyms":[{"name":"COD1","type":"exact"},{"name":"CORDX1","type":"exact"},{"name":"X-linked cone dystrophy 1","type":"exact"},{"name":"X-linked cone-rod dystrophy type 1","type":"exact"},{"name":"cone dystrophy 1, X-linked","type":"related"},{"name":"cone dystrophy X-linked 1","type":"related"},{"name":"cone-rod dystrophy X-linked 1","type":"related"},{"name":"cone-rod dystrophy, X-linked, 1","type":"related"},{"name":"cone-rod dystrophy, X-linked, 1, X-linked recessive","type":"exact"},{"name":"cone-rod dystrophy, X-linked, type 1","type":"exact"}],"termid":"MONDO:0010566","xrefs":{"Monarch":{"xref_id":"0010566"}}}


id: GO:0106231
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction:H2O + N(6)-propanoyl-L-lysyl-[protein] + NAD+ = 3''-O-propanoyl-ADP-D-ribose + L-lysyl-[protein] + nicotinamide.","definition_xrefs":["RHEA:23500","GOC:sp","PMID:30026585"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NAD-dependent protein lysine deacylase activity","termid":"GO:0141218"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016746","GO:0140096","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"NAD-dependent protein-lysine depropionylase activity","termid":"GO:0106231"}


id: GO:0047175
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: sn-3-D-galactosyl-sn-2-acylglycerol + acyl-[acyl-carrier protein] = D-galactosyldiacylglycerol + [acyl-carrier protein].","definition_xrefs":["EC:2.3.1.141","MetaCyc:2.3.1.141-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acyltransferase activity","termid":"GO:0008374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016746","GO:0016740"],"is_obsolete":false,"name":"galactosylacylglycerol O-acyltransferase activity","secondary_identifiers":["RHEA:17057"],"synonyms":[{"name":"acyl-ACP:lyso-MGDG acyltransferase activity","type":"related"},{"name":"acyl-acyl-carrier protein: lysomonogalactosyldiacylglycerol acyltransferase activity","type":"related"},{"name":"acyl-acyl-carrier-protein:D-galactosylacylglycerol O-acyltransferase activity","type":"related"}],"termid":"GO:0047175"}


id: PBO:0083159
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; almost completely overlaps the dubious ORF YBR056W-A","termid":"PBO:0083159"}


id: FYPO:0004517
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 diameter larger than normal only near the middle of the cell, around the nucleus.","definition_xrefs":["PomBase:mah","PMID:25552606"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable vegetative cell with abnormal cell shape","termid":"FYPO:0002197"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0000005"],"is_obsolete":false,"name":"viable vegetative cell enlarged around nucleus","synonyms":[{"name":"viable cell enlarged around nucleus during vegetative growth","type":"exact"},{"name":"viable vegetative cell enlarged around nucleus during mitotic cell cycle","type":"related"}],"termid":"FYPO:0004517"}


id: MONDO:0020321
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare acute leukemia of ambiguous lineage in which the blasts do not express markers specific to myeloid or lymphoid lineage.","definition_xrefs":["NCIT:C9298"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"bilineal acute myeloid leukemia","termid":"MONDO:0011118"},{"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:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"acute undifferentiated leukemia","secondary_identifiers":["MedDRA:10045516","GARD:16863","SCTID:359631009","MEDGEN:79081","NANDO:2200017","ONCOTREE:AUL","Orphanet:98835","UMLS:C0280141"],"synonyms":[{"name":"AUL","type":"related"},{"name":"acute leukaemia not otherwise specified","type":"related"},{"name":"acute myeloid leukemia, minimal differentiation, FAB M0","type":"exact"},{"name":"acute undifferentiated leukemia","type":"exact"},{"name":"leukaemia stem cell","type":"exact"},{"name":"leukemia stem cell","type":"exact"},{"name":"stem cell acute leukaemia","type":"exact"},{"name":"stem cell acute leukemia","type":"exact"},{"name":"stem cell leukaemia","type":"exact"},{"name":"stem cell leukemia","type":"exact"},{"name":"undifferentiated acute leukaemia","type":"exact"},{"name":"undifferentiated acute leukemia","type":"exact"}],"termid":"MONDO:0020321","xrefs":{"Monarch":{"xref_id":"0020321"}}}


id: PBO:0065534
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"papillary thyroid carcinoma susceptibility candidate 1","termid":"PBO:0065534"}


id: PBO:0075677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermatogenic leucine zipper 1","termid":"PBO:0075677"}


id: FYPO:0001380
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the size, shape, or structure of the nucleus is normal (i.e. indistinguishable from wild type) in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component during vegetative growth","termid":"FYPO:0001313"},{"relation_name":"is_a","term_name":"normal nuclear morphology","termid":"FYPO:0001673"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"normal nuclear morphology during vegetative growth","synonyms":[{"name":"normal nuclear morphology during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001380"}


id: GO:0071808
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An axoneme part that is found in the flagella of mammalian sperm and is located in the middle piece between the outer dense fibers (on the concave side of outer dense fibers as seen in cross-section).","definition_xrefs":["GOC:mah","GOC:sl","PMID:20108326"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"axoneme","termid":"GO:0005930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"satellite fibril","termid":"GO:0071808"}


id: GO:0060471
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of secretion by a cell that results in the release of intracellular molecules contained within a cortical granule by fusion of the vesicle with the plasma membrane of a cell. A cortical granule is a specialized secretory vesicle that is released during egg activation that changes the surface of the egg to prevent polyspermy.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcium-ion regulated exocytosis","termid":"GO:0017156"},{"relation_name":"part_of","term_name":"prevention of polyspermy","termid":"GO:0060468"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016192"},{"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:0006810","GO:0016192","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"cortical granule exocytosis","synonyms":[{"name":"cortical granule release","type":"related"},{"name":"cortical reaction","type":"related"}],"termid":"GO:0060471"}


id: GO:0099113
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the concentration of calcium ions in the presynaptic cytosol.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytosolic calcium ion concentration","termid":"GO:0051481"}],"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 presynaptic cytosolic calcium concentration","termid":"GO:0099113"}


id: PBO:0083265
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; not conserved in closely related Saccharomyces species; 69% of ORF overlaps the uncharacterized ORF YKL075C","termid":"PBO:0083265"}


id: FYPO:0007326
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 mitochondrial tRNA 3'-end processing is decreased. In mitochondrial tRNA 3'-end processing, the 3' end of a mitochondrial pre-tRNA molecule is converted to that of a mature mitochondrial tRNA.","definition_xrefs":["GO:0006396","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitochondrial RNA 3'-end processing","termid":"FYPO:0004956"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000294","FYPO:0001320","FYPO:0001985","FYPO:0006551","FYPO:0000002"],"is_obsolete":false,"name":"decreased mitochondrial tRNA 3'-end processing","synonyms":[{"name":"decreased mitochondrial tRNA 3'-end processing during mitotic cell cycle","type":"related"},{"name":"decreased mitochondrial tRNA 3'-end processing during vegetative growth","type":"exact"},{"name":"decreased mitochondrial transfer RNA 3'-end processing","type":"exact"},{"name":"reduced mitochondrial tRNA 3'-end processing","type":"exact"}],"termid":"FYPO:0007326"}


id: GO:1901059
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of p-hydroxyphenyl lignin.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lignin catabolic process","termid":"GO:0046274"},{"relation_name":"is_a","term_name":"p-hydroxyphenyl lignin metabolic process","termid":"GO:1901058"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"p-hydroxyphenyl lignin catabolic process","synonyms":[{"name":"H-lignin catabolic process","type":"exact"},{"name":"p-hydroxyphenyl lignin breakdown","type":"exact"},{"name":"p-hydroxyphenyl lignin catabolism","type":"exact"},{"name":"p-hydroxyphenyl lignin degradation","type":"exact"}],"termid":"GO:1901059"}


id: GO:0042581
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Granule with a membranous, tubular internal structure, found primarily in mature neutrophil cells. Most are released into the extracellular fluid. Specific granules contain lactoferrin, lysozyme, vitamin B12 binding protein and elastase.","definition_xrefs":["ISBN:0721662544","PMID:7334549","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule","termid":"GO:0030141"}],"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:0031410"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0031410"],"is_obsolete":false,"name":"specific granule","secondary_identifiers":["Wikipedia:Specific_granule"],"synonyms":[{"name":"secondary granule","type":"exact"}],"termid":"GO:0042581"}


id: PBO:0045084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"delta like canonical Notch ligand 1","termid":"PBO:0045084"}


id: PBO:0051601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 24","termid":"PBO:0051601"}


id: GO:0160036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of postsynaptic density assembly.","definition_xrefs":["PMID:17626212"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of postsynaptic density assembly","termid":"GO:0099151"},{"relation_name":"is_a","term_name":"positive regulation of organelle assembly","termid":"GO:1902117"},{"relation_name":"is_a","term_name":"positive regulation of postsynaptic density organization","termid":"GO:1905876"},{"relation_name":"positively_regulates","term_name":"postsynaptic density assembly","termid":"GO:0097107"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"positive regulation of postsynaptic density assembly","termid":"GO:0160036"}


id: GO:0140930
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: D-fructose(out) + Na+(out) = D-fructose(in) + Na+(in).","definition_xrefs":["PMID:23451068","PMID:22212718"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fructose transmembrane transporter activity","termid":"GO:0005353"},{"relation_name":"is_a","term_name":"carbohydrate:monoatomic cation symporter activity","termid":"GO:0005402"},{"relation_name":"is_a","term_name":"solute:sodium symporter activity","termid":"GO:0015370"}],"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:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"fructose:sodium symporter activity","termid":"GO:0140930"}


id: GO:0000470
data:
  {"annotated_genes":["SJAG_00537","SJAG_01811","SJAG_02275","SJAG_04890","SJAG_05223","SJAG_02417","SJAG_03425","SJAG_05190","SJAG_04330","SJAG_01366","SJAG_02374","SJAG_00882","SJAG_03789","SJAG_01606","SJAG_00722","SJAG_00752","SJAG_01551","SJAG_04492","SJAG_00689","SJAG_02894","SJAG_04108","SJAG_01821","SJAG_04669","SJAG_01581","SJAG_02830","SJAG_03012","SJAG_00749","SJAG_04289","SJAG_02427"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73540,74344,77111,77291,80820,81246,81365],"is_not":false,"summary":null,"term":"GO:0000470"},{"annotations":[93648,73419,96911,106069],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000448"},{"annotations":[80609,74185,99927,75231,72260,73128,76733,62653,80091,102007,99894,75395,75943,81629,74211,77135,75575,77804],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000463"}]},"cv_name":"biological_process","definition":"Any process involved in the maturation of a precursor Large SubUnit (LSU) ribosomal RNA (rRNA) molecule into a mature LSU-rRNA molecule.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA processing","termid":"GO:0006364"},{"relation_name":"part_of","term_name":"ribosomal large subunit biogenesis","termid":"GO:0042273"}],"gene_count":29,"genes_by_uniquename":{"SJAG_00537":null,"SJAG_00689":null,"SJAG_00722":null,"SJAG_00749":null,"SJAG_00752":null,"SJAG_00882":null,"SJAG_01366":null,"SJAG_01551":null,"SJAG_01581":null,"SJAG_01606":null,"SJAG_01811":null,"SJAG_01821":null,"SJAG_02275":null,"SJAG_02374":null,"SJAG_02417":null,"SJAG_02427":null,"SJAG_02830":null,"SJAG_02894":null,"SJAG_03012":null,"SJAG_03425":null,"SJAG_03789":null,"SJAG_04108":null,"SJAG_04289":null,"SJAG_04330":null,"SJAG_04492":null,"SJAG_04669":null,"SJAG_04890":null,"SJAG_05190":null,"SJAG_05223":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0042254"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0042254","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"maturation of LSU-rRNA","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0000470","terms_by_termid":{"GO:0000448":null,"GO:0000463":null,"GO:0000470":null}}


id: GO:0045148
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of a single N-terminal amino acid residue from a tripeptide.","definition_xrefs":["EC:3.4.11.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminopeptidase activity","termid":"GO:0004177"},{"relation_name":"is_a","term_name":"tripeptidase activity","termid":"GO:0034701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0008233","GO:0003674","GO:0003824","GO:0140096","GO:0016787"],"is_obsolete":false,"name":"tripeptide aminopeptidase activity","secondary_identifiers":["MetaCyc:3.4.11.4-RXN"],"synonyms":[{"name":"alanine-phenylalanine-proline arylamidase activity","type":"related"},{"name":"aminoexotripeptidase activity","type":"related"},{"name":"aminotripeptidase activity","type":"exact"},{"name":"imidoendopeptidase activity","type":"related"},{"name":"lymphopeptidase activity","type":"related"},{"name":"peptidase B","type":"related"},{"name":"peptidase T","type":"exact"}],"termid":"GO:0045148"}


id: PBO:0047927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, aphidicolin type, common, fra(11)(p13)","termid":"PBO:0047927"}


id: GO:0030500
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of bone mineralization.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ossification","termid":"GO:0030278"},{"relation_name":"is_a","term_name":"regulation of biomineral tissue development","termid":"GO:0070167"},{"relation_name":"regulates","term_name":"bone mineralization","termid":"GO:0030282"}],"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 bone mineralization","termid":"GO:0030500"}


id: GO:1905847
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cellular response to oxidopamine.","definition_xrefs":["PMID:23721876","GOC:TermGenie","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 response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of cellular response to oxidopamine","termid":"GO:1905846"},{"relation_name":"negatively_regulates","term_name":"cellular response to oxidopamine","termid":"GO:1905842"}],"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 cellular response to oxidopamine","synonyms":[{"name":"down regulation of cellular response to oxidopamine","type":"exact"},{"name":"down-regulation of cellular response to oxidopamine","type":"exact"},{"name":"downregulation of cellular response to oxidopamine","type":"exact"},{"name":"inhibition of cellular response to oxidopamine","type":"narrow"}],"termid":"GO:1905847"}


id: GO:0005783
data:
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id: PBO:0082186
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id: MONDO:0008505
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id: PBO:0111056
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id: PBO:0048857
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id: PBO:0011148
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id: PBO:0061269
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id: PBO:0043761
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id: MONDO:0002667
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id: PBO:0054471
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id: MONDO:0010201
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id: MONDO:0018478
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id: PBO:0051422
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id: PBO:0001970
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id: PBO:0039039
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id: PATO:0001762
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id: PBO:0046503
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id: MOD:00827
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id: GO:0050072
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id: GO:0045333
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{"annotated_genes":["SJAG_01062","SJAG_07006","SJAG_07003","SJAG_01895","SJAG_MIT09","SJAG_05204","SJAG_MIT20","SJAG_06621","SJAG_04843","SJAG_02158","SJAG_00976","SJAG_00605","SJAG_01763","SJAG_02107","SJAG_03290","SJAG_03064","SJAG_01539","SJAG_01671","SJAG_00080","SJAG_04334","SJAG_03903","SJAG_01490","SJAG_02646","SJAG_MIT37","SJAG_01922","SJAG_03114","SJAG_00915","SJAG_01753","SJAG_00438","SJAG_02592","SJAG_05629","SJAG_03310","SJAG_03588","SJAG_MIT15","SJAG_00133","SJAG_00839","SJAG_01310","SJAG_00698","SJAG_01524","SJAG_01630","SJAG_03920","SJAG_03813","SJAG_01402","SJAG_04152","SJAG_02464","SJAG_MIT13","SJAG_07007","SJAG_03660","SJAG_03373","SJAG_01190","SJAG_02398","SJAG_00836","SJAG_04495","SJAG_00985","SJAG_00542","SJAG_02744","SJAG_02504","SJAG_00866","SJAG_03925","SJAG_01355","SJAG_03163","SJAG_06382","SJAG_02433","SJAG_02105","SJAG_03828","SJAG_00461","SJAG_03490","SJAG_02796","SJAG_02945","SJAG_04122","SJAG_02598","SJAG_02006","SJAG_02135","SJAG_06622","SJAG_MIT03","SJAG_02009","SJAG_00755","SJAG_02564","SJAG_00027","SJAG_02369","SJAG_01077","SJAG_MIT04","SJAG_00601","SJAG_04192","SJAG_04048","SJAG_00260"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111376,107417,100213,111379,111374,107418,107419,111375,111380,118347,111378,96474,74323,105336,107787,105593,107788,111377,99942,79726],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061621"},{"annotations":[90555],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061613"},{"annotations":[73729,110262,76141,117458,121073,121103,80762,116226,78336,121051,62712],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0006123"},{"annotations":[98668,114852],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0006120"},{"annotations":[118755,90761,91132,115190],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006121"},{"annotations":[62678,75652,74066,115397,119689,121078,77572,77654,78335,106031],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0006122"},{"annotations":[105605,94801,103775,104991,106978,121090,91076,95227,109783,121084,95818,117844,110766,105631,121096,109875,96797],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0042776"},{"annotations":[89365,100979,75235,89802,80983,74600,76495],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006086"},{"annotations":[113873,99574,96323,111674],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1903715"},{"annotations":[72122,108707,81167,77719,63681,67928,72634,73648,78698,76301,75043,75994,65640,77222,62362],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006099"}]},"cv_name":"biological_process","definition":"The enzymatic release of energy from inorganic and organic compounds (especially carbohydrates and fats) which either requires oxygen (aerobic respiration) or does not (anaerobic respiration).","definition_xrefs":["ISBN:0198506732","ISBN:0140513590","GOC:das"],"direct_ancestors":[{"relation_name":"is_a","term_name":"energy derivation by oxidation of organic 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id: MONDO:0013213
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":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hearing loss, cisplatin-induced, susceptibility to","secondary_identifiers":["MEDGEN:413752","OMIM:613290","UMLS:C2750088"],"synonyms":[{"name":"CIHL","type":"exact"},{"name":"hearing loss, cisplatin-induced, susceptibility to","type":"exact"}],"termid":"MONDO:0013213","xrefs":{"Monarch":{"xref_id":"0013213"}}}


id: PBO:0067915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 217","termid":"PBO:0067915"}


id: PBO:0070086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear variant sequence with SNRPE pseudogene sequence","termid":"PBO:0070086"}


id: GO:0005727
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Circular DNA structures that are not part of a chromosome.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular anatomical structure","termid":"GO:0005622"},{"relation_name":"part_of","term_name":"extrachromosomal DNA","termid":"GO:0046821"}],"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":"extrachromosomal circular DNA","termid":"GO:0005727"}


id: PBO:0054256
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 1640","termid":"PBO:0054256"}


id: PBO:0031259
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_meiotic_telomere_clustering","termid":"PBO:0031259"}


id: GO:0042354
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving L-fucose, 6-deoxy-L-galactose, a sugar that occurs in fucans, a class of polysaccharides in seaweeds, especially Fucus species, and in the cell wall matrix of higher plants.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fucose metabolic process","termid":"GO:0006004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0005975"],"is_obsolete":false,"name":"L-fucose metabolic process","synonyms":[{"name":"L-fucose metabolism","type":"exact"}],"termid":"GO:0042354"}


id: MOD:01024
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-proline residue to one of several monohydroxylated proline residues, including 3-hydroxy-L-proline and 4-hydroxy-L-proline.","definition_xrefs":["OMSSA:62","Unimod:35#P","DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monohydroxylated residue","termid":"MOD:00425"},{"relation_name":"is_a","term_name":"residues isobaric at 113.047678 Da","termid":"MOD:00594"},{"relation_name":"is_a","term_name":"hydroxylated proline","termid":"MOD:00678"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monohydroxylated proline","synonyms":[{"name":"Hy1Pro","type":"exact"},{"name":"Hydroxyproline","type":"exact"},{"name":"Hyp","type":"exact"},{"name":"Oxidation","type":"related"},{"name":"hydroxylationp","type":"exact"}],"termid":"MOD:01024"}


id: MONDO:0009128
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":"dwarfism, intellectual disability, and eye abnormality","secondary_identifiers":["UMLS:C0796076","MEDGEN:208664","MESH:C535809","Orphanet:2650","OMIM:223540"],"synonyms":[{"name":"Mollica syndrome","type":"related"},{"name":"dwarfism, intellectual disability, and eye abnormality","type":"exact"},{"name":"dwarfism, mental retardation, and eye abnormality","type":"exact"}],"termid":"MONDO:0009128","xrefs":{"Monarch":{"xref_id":"0009128"}}}


id: PomGeneEx:0000014
data:
  {"annotation_feature_type":"gene","cv_name":"PomGeneExRNA","definition":"A gene expression qualifier that indicates that an RNA is present under a given set of conditions or at an indicated time.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"present","termid":"PomGeneEx:0000005"},{"relation_name":"is_a","term_name":"RNA expression level","termid":"PomGeneEx:0000009"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA present","synonyms":[{"name":"RNA expression present","type":"exact"}],"termid":"PomGeneEx:0000014"}


id: GO:0010149
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A preprogrammed process associated with the dismantling of an anatomical structure and an overall decline in metabolism. This may include the breakdown of organelles, membranes and other cellular components. An example of this process is found in Arabidopsis thaliana, when older leaves or floral organs are shed.","definition_xrefs":["ISBN:0387987819","GOC:mtg_sensu"],"gene_count":0,"genotype_count":0,"name":"obsolete senescence (obsolete GO:0010149)","secondary_identifiers":["Wikipedia:Senescence"],"synonyms":[{"name":"senescence","type":"exact"}],"termid":"GO:0010149"}


id: PBO:0056557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"minichromosome maintenance complex component 5","termid":"PBO:0056557"}


id: GO:1903927
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a cyanide stimulus.","definition_xrefs":["GOC:TermGenie","PMID:21854848","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to cyanide","termid":"GO:1903927"}


id: PBO:0073398
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SET pseudogene 1","termid":"PBO:0073398"}


id: PBO:0050782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-hydroxytryptamine receptor 1F","termid":"PBO:0050782"}


id: MONDO:0007124
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An ectodermal dysplasia syndrome with defining features of ankyloblepharon filiforme adnatum (AFA), ectodermal abnormalities and a cleft lip and/or palate.","definition_xrefs":["Orphanet:1071"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome or malformation associated with head and neck malformations (obsolete MONDO:0015501)","termid":"MONDO:0015501"},{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"},{"relation_name":"is_a","term_name":"TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations","termid":"MONDO:1040001"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005497"],"is_obsolete":false,"name":"ankyloblepharon-ectodermal defects-cleft lip/palate syndrome","secondary_identifiers":["NORD:738","MESH:C535847","GARD:6571","DOID:0090119","MEDGEN:98032","OMIM:106260","SCTID:55821006","UMLS:C0406709"],"synonyms":[{"name":"AEC Syndrome","type":"exact"},{"name":"AEC syndrome","type":"exact"},{"name":"Ankyloblepharon ectodermal defects cleft lip/palate","type":"related"},{"name":"Ankyloblepharon-ectodermal defects-cleft lip and palate syndrome","type":"exact"},{"name":"Hay-Wells syndrome","type":"exact"},{"name":"Rapp-Hodgkins syndrome","type":"related"},{"name":"Seres-Santamaria Arimany Muniz syndrome","type":"related"},{"name":"ankyloblepharon-ectodermal defects-cleft LIP/palate","type":"related"},{"name":"cleft palate, ankyloblepharon, alveolar synechiae, and ectodermal defects","type":"related"}],"termid":"MONDO:0007124","xrefs":{"Monarch":{"xref_id":"0007124"}}}


id: MONDO:0005404
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A medical condition characterized by long-term fatigue and other symptoms that limit a person's ability to carry out ordinary daily activities.","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"muscle tissue disorder","termid":"MONDO:0003939"},{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"},{"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:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"myalgic encephalomeyelitis/chronic fatigue syndrome","secondary_identifiers":["ICD9:780.79","MEDGEN:5130","DOID:8544","EFO:0004540","ICD9:780.71","NCIT:C3037","MESH:D015673","Orphanet:1983","SCTID:51771007","UMLS:C0015674"],"synonyms":[{"name":"CFS","type":"exact"},{"name":"Postviral fatigue syndrome","type":"exact"},{"name":"chronic fatigue immune dysfunction syndrome","type":"exact"},{"name":"chronic fatigue syndrome","type":"exact"},{"name":"myalgic encephalitis","type":"exact"},{"name":"myalgic encephalomyelitis","type":"exact"},{"name":"systemic exertion intolerance disease","type":"exact"}],"termid":"MONDO:0005404","xrefs":{"Monarch":{"xref_id":"0005404"}}}


id: GO:0043748
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-succinylbenzoate + H2O = 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate.","definition_xrefs":["PMID:8335646"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"O-succinylbenzoate synthase activity","secondary_identifiers":["EC:4.2.1.113","RHEA:10196"],"termid":"GO:0043748"}


id: PR:Q9P801
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC777.17c gene.","definition_xrefs":["UniProtKB:Q9P801","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":"L9-like mitochondrial ribosomal protein SPCC777.17c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC777.17c","synonyms":[{"name":"54S ribosomal protein L9, mitochondrial (Schizosaccharomyces pombe 972h-)","type":"related"},{"name":"Spom972h-SPCC777.17c","type":"exact"}],"termid":"PR:Q9P801"}


id: PBO:0001040
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulated by Mbx1","termid":"PBO:0001040"}


id: FYPO:0000312
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a normal germ tube, and undergoes septation, but does not go on to form a viable dividing cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division, with normal germ tube morphology","termid":"FYPO:0000310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"inviable after spore germination with normal, septated germ tube morphology","synonyms":[{"name":"inviable following spore germination with normal, septated germ tube morphology","type":"exact"},{"name":"inviable germinated spore with normal, septated germ tube morphology","type":"exact"},{"name":"lethal after spore germination with normal, septated germ tube morphology","type":"exact"}],"termid":"FYPO:0000312"}


id: GO:0002218
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that initiates an innate immune response. Innate immune responses are defense responses mediated by germline encoded components that directly recognize components of potential pathogens. Examples of this process include activation of the hypersensitive response of Arabidopsis thaliana and activation of any NOD or TLR signaling pathway in vertebrate species.","definition_xrefs":["GOC:add","GOC:mtg_sensu","PMID:15199967","PMID:16177805","GO_REF:0000022","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"activation of immune response","termid":"GO:0002253"},{"relation_name":"is_a","term_name":"positive regulation of innate immune response","termid":"GO:0045089"}],"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":"activation of innate immune response","secondary_identifiers":["GO:0002219"],"termid":"GO:0002218"}


id: PBO:0063037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"p21 (RAC1) activated kinase 4","termid":"PBO:0063037"}


id: PBO:0050665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HSPA2 and ZBTB1 antisense RNA 1","termid":"PBO:0050665"}


id: MONDO:0017279
data:
  {"annotated_genes":["SJAG_01229","SJAG_04404","SJAG_04757","SJAG_00063","SJAG_02106","SJAG_03866","SJAG_16459","SJAG_04545"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87706,87707],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014796"},{"annotations":[88107,88108],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011658"},{"annotations":[87716,87715],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014233"},{"annotations":[88869,88868],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011706"}]},"cv_name":"mondo","definition":"A form of Parkinson disease (PD) characterized by an age of onset between 21-45 years, rigidity, painful cramps followed by tremor, bradykinesia, dystonia, gait complaints and falls, and other non-motor symptoms. A slow disease progression and a more pronounced response to dopaminergic therapy are also observed in most YOPD forms.","definition_xrefs":["Orphanet:2828"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"primary orthostatic hypotension","termid":"MONDO:0015914"},{"relation_name":"is_a","term_name":"Parkinson disease","termid":"MONDO:0005180"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00063":null,"SJAG_01229":null,"SJAG_02106":null,"SJAG_03866":null,"SJAG_04404":null,"SJAG_04545":null,"SJAG_04757":null,"SJAG_16459":null},"genotype_count":0,"is_obsolete":false,"name":"young-onset Parkinson disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:715345007","UMLS:C4275179","MEDGEN:907947","GARD:16610","DOID:0060894"],"synonyms":[{"name":"YOPD","type":"exact"},{"name":"early-onset Parkinson disease","type":"exact"},{"name":"early-onset Parkinson's disease","type":"related"}],"termid":"MONDO:0017279","terms_by_termid":{"MONDO:0011658":null,"MONDO:0011706":null,"MONDO:0014233":null,"MONDO:0014796":null},"xrefs":{"Monarch":{"xref_id":"0017279"}}}


id: GO:0015188
data:
  {"annotated_genes":["SJAG_02029","SJAG_04725"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[104758,112014],"is_not":false,"summary":null,"term":"GO:0015188"}]},"cv_name":"molecular_function","definition":"Enables the transfer of L-isoleucine from one side of a membrane to the other. L-isoleucine is (2R*,3R*)-2-amino-3-methylpentanoic acid.","definition_xrefs":["GOC:mtg_transport","GOC:ai","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"neutral L-amino acid transmembrane transporter activity","termid":"GO:0015175"},{"relation_name":"is_a","term_name":"L-amino acid transmembrane transporter activity","termid":"GO:0015179"},{"relation_name":"is_a","term_name":"branched-chain amino acid transmembrane transporter activity","termid":"GO:0015658"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02029":null,"SJAG_04725":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"L-isoleucine transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"L-isoleucine transporter activity","type":"broad"},{"name":"isoleucine/valine:sodium symporter activity","type":"narrow"},{"name":"leucine/isoleucine/valine porter activity","type":"narrow"},{"name":"leucine/valine/isoleucine permease activity","type":"narrow"}],"termid":"GO:0015188","terms_by_termid":{"GO:0015188":null}}


id: PBO:0051371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 3D-25 (pseudogene)","termid":"PBO:0051371"}


id: PBO:0030790
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_volume_spheroid_vegetative_cell","termid":"PBO:0030790"}


id: PBO:0056675
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myocyte enhancer factor 2A","termid":"PBO:0056675"}


id: MONDO:0014853
data:
  {"annotated_genes":["SJAG_02348"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87550],"is_not":false,"summary":null,"term":"MONDO:0014853"}]},"cv_name":"mondo","definition":"Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MCM2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02348":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 70","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:18145","UMLS:C4310775","MEDGEN:934742","DOID:0110592","OMIM:616968"],"synonyms":[{"name":"DFNA70","type":"narrow"},{"name":"MCM2 autosomal dominant nonsyndromic deafness","type":"narrow"},{"name":"autosomal dominant deafness 70","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 70","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness caused by mutation in MCM2","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 70","type":"narrow"},{"name":"autosomal dominant nonsyndromic hearing loss 70","type":"exact"},{"name":"deafness, autosomal dominant 70","type":"narrow"},{"name":"deafness, autosomal dominant type 70","type":"narrow"}],"termid":"MONDO:0014853","terms_by_termid":{"MONDO:0014853":null},"xrefs":{"Monarch":{"xref_id":"0014853"}}}


id: PBO:0068968
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 212, pseudogene","termid":"PBO:0068968"}


id: MONDO:0041755
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"twin to twin transfusion syndrome","termid":"MONDO:0019805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0002280"],"is_obsolete":false,"name":"twin reversal arterial perfusion syndrome","secondary_identifiers":["MEDGEN:736778","UMLS:C1562817","SCTID:417006004"],"synonyms":[{"name":"twin reversal arterial perfusion syndrome","type":"exact"}],"termid":"MONDO:0041755","xrefs":{"Monarch":{"xref_id":"0041755"}}}


id: GO:0090437
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a socket cell, a shoot epidermal cell that surrounds a trichome and provides its support.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant epidermal cell differentiation","termid":"GO:0090627"},{"relation_name":"part_of","term_name":"plant epidermis development","termid":"GO:0090558"}],"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":"socket cell differentiation","termid":"GO:0090437"}


id: PBO:0045450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydropyrimidinase like 3","termid":"PBO:0045450"}


id: MONDO:0011399
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited hemoglobinopathy characterized by impaired synthesis of alpha-globin chains leading to a variable clinical picture depending on the number of affected alleles.","definition_xrefs":["Orphanet:846"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thalassemia","termid":"MONDO:0000984"}],"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":"alpha thalassemia spectrum","secondary_identifiers":["DOID:1099","MEDGEN:1434","UMLS:C0002312","ICD9:282.43","SCTID:68913001","icd11.foundation:531667506","ICD9:282.49","GARD:621","NANDO:2201273","MESH:D017085","ICD10CM:D56.0","OMIM:604131","MedDRA:10043390","NCIT:C34368"],"synonyms":[{"name":"A-thalassemia","type":"related"},{"name":"alpha thalassaemia","type":"exact"},{"name":"alpha thalassemia spectrum","type":"exact"},{"name":"alpha-thalassemia","type":"exact"},{"name":"alpha-thalassemia trait","type":"related"},{"name":"thalassemia, alpha-","type":"exact"},{"name":"thalassemias, alpha-","type":"exact"}],"termid":"MONDO:0011399","xrefs":{"Monarch":{"xref_id":"0011399"}}}


id: PBO:0004292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleosome assembly protein Nap2 (predicted)","termid":"PBO:0004292"}


id: GO:0102948
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate + a glucosylated glucose acceptor = isoorientin + a non glucosylated glucose acceptor.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete luteolin C-glucosyltransferase activity (obsolete GO:0102948)","termid":"GO:0102948"}


id: PBO:0053475
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 445","termid":"PBO:0053475"}


id: FYPO:0008362
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which cells in a population contain variable numbers of lipid droplets. Some cells may contain more or less lipid droplets than normal, while others may lack any detectable lipid droplets.","definition_xrefs":["PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population phenotype","termid":"FYPO:0000003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000003"],"is_obsolete":false,"name":"variable cellular lipid droplet content","termid":"FYPO:0008362"}


id: FYPO:0005057
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which meiotic DNA double-strand break clipping does not occur. Meiotic DNA double-strand break clipping is the process by which SPO11/Rec12-oligonucleotide complexes are removed from 5' DNA double-strand breaks induced during meiosis.","definition_xrefs":["PomBase:mah","GO:1990898","PMID:26130711"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic recombination","termid":"FYPO:0000008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000631","FYPO:0000002","FYPO:0000293"],"is_obsolete":false,"name":"abolished meiotic DNA double-strand break clipping","synonyms":[{"name":"meiotic DNA double-strand break clipping abolished","type":"exact"}],"termid":"FYPO:0005057"}


id: PBO:0046036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 4","termid":"PBO:0046036"}


id: SO:0001942
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 20th residue (a lysine), from the start of the H2B histone protein is acetylated.","definition_xrefs":["EBI:nj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_2B_acetylation_site","termid":"SO:0002143"}],"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":"H2BK20_acetylation_site","synonyms":[{"name":"H2BK20 acetylation site","type":"exact"},{"name":"H2BK20ac","type":"exact"}],"termid":"SO:0001942"}


id: FYPO:0000206
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A transcription regulation phenotype observed in the vegetative growth phase of the life cycle in which chromatin silencing at ribosomal DNA repeats is abnormal. Chromatin silencing is the observed effect of processes that repress transcription in a region of the genome that is normally assembled into heterochromatin.","definition_xrefs":["PomBase:vw","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin silencing","termid":"FYPO:0000144"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"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:0005447","FYPO:0001985","FYPO:0006551","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal chromatin silencing at rDNA","synonyms":[{"name":"abnormal chromatin silencing at rDNA during mitotic cell cycle","type":"related"},{"name":"abnormal chromatin silencing at rDNA during vegetative growth","type":"exact"},{"name":"abnormal chromatin silencing at ribosomal DNA","type":"exact"}],"termid":"FYPO:0000206"}


id: PATO:0000462
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality denoting the lack of an entity.","definition_xrefs":["thefreedictionary.:thefreedictionary."],"direct_ancestors":[{"relation_name":"is_a","term_name":"amount","termid":"PATO:0000070"},{"relation_name":"reciprocal_of","term_name":"lacking processual parts","termid":"PATO:0001558"},{"relation_name":"reciprocal_of","term_name":"lacks all parts of type","termid":"PATO:0002000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"absent","secondary_identifiers":["PATO:0001996"],"synonyms":[{"name":"absence","type":"exact"},{"name":"absent from organism","type":"exact"}],"termid":"PATO:0000462"}


id: PBO:0058935
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIS18 binding protein 1","termid":"PBO:0058935"}


id: PBO:0061793
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"outer dynein arm docking complex subunit 4","termid":"PBO:0061793"}


id: PBO:0076517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taste 2 receptor member 19","termid":"PBO:0076517"}


id: FYPO:0000328
data:
  {"alleles_by_uniquename":{"SJAG_00610:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00610","name":"pck2delta","uniquename":"SJAG_00610:allele-1"},"SJAG_01787:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01787","name":"pck1delta","uniquename":"SJAG_01787:allele-1"},"SJAG_04551:allele-2":{"allele_type":"amino_acid_insertion","description":"82-NITCIYDLDIIINPYNFNEVYIYEE-105","gene_uniquename":"SJAG_04551","name":"Pmk1Sj(ins82-105)","uniquename":"SJAG_04551:allele-2"},"SJAG_04551:allele-4":{"allele_type":"partial_amino_acid_deletion","description":"Pmk1 from S. pombe with deleted residues 82-105","gene_uniquename":"SJAG_04551","name":"Pmk1Sp(delta82-105)","uniquename":"SJAG_04551:allele-4"},"SJAG_04697:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04697","name":"gms1delta","uniquename":"SJAG_04697:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002033"},{"annotations":[121239,121243],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001838"},{"annotations":[121166],"is_not":false,"rel_names":["output_of"],"summary":null,"term":"FYPO:0003727"},{"annotations":[121233],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001038"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle that affects protein metabolism in the cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal metabolic process during vegetative growth","termid":"FYPO:0001363"},{"relation_name":"is_a","term_name":"abnormal protein metabolic process","termid":"FYPO:0002274"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00610":null,"SJAG_01787":null,"SJAG_04551":null,"SJAG_04697":null},"genotype_count":5,"genotypes_by_uniquename":{"Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sj(ins82-105)(82-NITCIYDLDIIINPYNFNEVYIYEE-105)","display_uniquename":"Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-2","expression":"Not assayed or wild type"}]}]},"Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type":{"display_name":"Pmk1Sp(delta82-105)(Pmk1 from S. pombe with deleted residues 82-105 Δaa)","display_uniquename":"Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04551:allele-4","expression":"Not assayed or wild type"}]}]},"gms1delta":{"display_name":"gms1delta","display_uniquename":"gms1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04697:allele-1","expression":"Null"}]}]},"pck1delta":{"display_name":"pck1delta","display_uniquename":"pck1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01787:allele-1","expression":"Null"}]}]},"pck2delta":{"display_name":"pck2delta","display_uniquename":"pck2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00610:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0002274","FYPO:0001985"],"is_obsolete":false,"name":"abnormal protein metabolic process during vegetative growth","references_by_uniquename":{"PMID:34198697":null,"PMID:36058798":null},"single_locus_annotated_genes":["SJAG_04551","SJAG_00610","SJAG_01787","SJAG_04697"],"single_locus_genotype_uniquenames":["gms1delta","Pmk1Sj(ins82-105)-82-NITCIYDLDIIINPYNFNEVYIYEE-105-amino_acid_insertion-expression-not_assayed_or_wild_type","Pmk1Sp(delta82-105)-Pmk1_from_S._pombe_with_deleted_residues_82-105-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","pck1delta","pck2delta"],"synonyms":[{"name":"abnormal cellular protein metabolic process during vegetative growth","type":"exact"},{"name":"abnormal protein metabolic process during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000328","terms_by_termid":{"FYPO:0001038":null,"FYPO:0001838":null,"FYPO:0002033":null,"FYPO:0003727":null,"FYPO_EXT:0000001":null}}


id: PBO:0075546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPECC1L-ADORA2A readthrough (NMD candidate)","termid":"PBO:0075546"}


id: PBO:0077896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetrapeptide repeat homeobox 1 pseudogene 1","termid":"PBO:0077896"}


id: MONDO:0010115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thoracic malformation","termid":"MONDO:0015929"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thoracic dysplasia-hydrocephalus syndrome","secondary_identifiers":["UMLS:C1848864","MESH:C564774","OMIM:273730","Orphanet:1861","MEDGEN:338562","GARD:5180"],"synonyms":[{"name":"thoracic dysplasia hydrocephalus syndrome","type":"related"},{"name":"thoracic dysplasia-hydrocephalus syndrome","type":"exact"}],"termid":"MONDO:0010115","xrefs":{"Monarch":{"xref_id":"0010115"}}}


id: PBO:0076065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STPG2 antisense RNA 1","termid":"PBO:0076065"}


id: PBO:0117242
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongation factor methyltransferase Efm7","termid":"PBO:0117242"}


id: PBO:0030348
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-incomplete,_unequal_mitotic_sister_chromatid_segregation","termid":"PBO:0030348"}


id: PR:Q9Y803
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An RNA-binding protein EIF1AD that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["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":"S1-like domain-containing protein C146.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC146.08c","secondary_identifiers":["UniProtKB:Q9Y803"],"synonyms":[{"name":"Spom972h-EIF1AD","type":"exact"}],"termid":"PR:Q9Y803"}


id: MONDO:1012347
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"facial eczema, non-human animal","termid":"MONDO:1011746"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"facial eczema, sheep","secondary_identifiers":["OMIA:001276-9940"],"termid":"MONDO:1012347","xrefs":{"Monarch":{"xref_id":"1012347"}}}


id: PBO:0029961
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cytochrome-c_oxidase_activity","termid":"PBO:0029961"}


id: PBO:0005729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wtf element Wtf19","termid":"PBO:0005729"}


id: PBO:0041216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1D nuclear receptor corepressor pseudogene 4","termid":"PBO:0041216"}


id: FYECO:0000183
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which alpha-tocopherol was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ alpha-tocopherol","synonyms":[{"name":"vitamin E added","type":"related"}],"termid":"FYECO:0000183"}


id: PBO:0003400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inducer of sexual development Sds23/Moc1","termid":"PBO:0003400"}


id: PBO:0038353
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-stem_parasite_of","termid":"PBO:0038353"}


id: MONDO:0002974
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm involving the cervix.","definition_xrefs":["NCIT:C9311"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uterine cancer","termid":"MONDO:0002715"},{"relation_name":"is_a","term_name":"uterine cervix neoplasm","termid":"MONDO:0021230"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"cervical cancer","secondary_identifiers":["ICD10CM:C53","OMIM:603956","ICD9:180","MEDGEN:890252","SCTID:363354003","UMLS:C4048328","DOID:4362","ICD9:180.9","ICD9:180.8"],"synonyms":[{"name":"cancer of uterine cervix","type":"exact"},{"name":"cervical cancer, somatic","type":"exact"},{"name":"cervical neoplasm","type":"broad"},{"name":"cervix cancer","type":"exact"},{"name":"cervix uteri cancer","type":"exact"},{"name":"malignant cervical neoplasm","type":"exact"},{"name":"malignant cervical tumor","type":"exact"},{"name":"malignant cervical tumour","type":"exact"},{"name":"malignant cervix neoplasm","type":"exact"},{"name":"malignant cervix tumor","type":"exact"},{"name":"malignant cervix tumour","type":"exact"},{"name":"malignant cervix uteri neoplasm","type":"exact"},{"name":"malignant cervix uteri tumor","type":"exact"},{"name":"malignant cervix uteri tumour","type":"exact"},{"name":"malignant neoplasm of cervix","type":"exact"},{"name":"malignant neoplasm of cervix uteri","type":"exact"},{"name":"malignant neoplasm of the cervix","type":"exact"},{"name":"malignant neoplasm of the cervix uteri","type":"exact"},{"name":"malignant neoplasm of the uterine cervix","type":"exact"},{"name":"malignant neoplasm of uterine cervix","type":"exact"},{"name":"malignant tumor of cervix","type":"exact"},{"name":"malignant tumor of cervix uteri","type":"exact"},{"name":"malignant tumor of the cervix","type":"exact"},{"name":"malignant tumor of the cervix uteri","type":"exact"},{"name":"malignant tumor of the uterine cervix","type":"exact"},{"name":"malignant tumor of uterine cervix","type":"exact"},{"name":"malignant tumour of cervix","type":"exact"},{"name":"malignant tumour of cervix uteri","type":"exact"},{"name":"malignant tumour of the cervix","type":"exact"},{"name":"malignant tumour of the cervix uteri","type":"exact"},{"name":"malignant tumour of the uterine cervix","type":"exact"},{"name":"malignant tumour of uterine cervix","type":"exact"},{"name":"malignant uterine cervix neoplasm","type":"exact"},{"name":"malignant uterine cervix tumor","type":"exact"},{"name":"malignant uterine cervix tumour","type":"exact"},{"name":"tumor of the cervix uteri","type":"broad"},{"name":"tumour of the cervix uteri","type":"broad"},{"name":"uterine cervical neoplasm","type":"broad"},{"name":"uterine cervix cancer","type":"exact"}],"termid":"MONDO:0002974","xrefs":{"Monarch":{"xref_id":"0002974"}}}


id: FYPO:0005105
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which Lys63-specific deubiquitinase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished peptidase activity","termid":"FYPO:0000669"},{"relation_name":"is_a","term_name":"abnormal Lys63-specific deubiquitinase activity","termid":"FYPO:0005104"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0001985","FYPO:0000707","FYPO:0000652","FYPO:0000661"],"is_obsolete":false,"name":"abolished Lys63-specific deubiquitinase activity","synonyms":[{"name":"Lys63-specific deubiquitinase activity abolished","type":"exact"}],"termid":"FYPO:0005105"}


id: PBO:0066239
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 46","termid":"PBO:0066239"}


id: MONDO:1012226
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"progressive retinal atrophy, non-human animal","termid":"MONDO:1011977"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progressive retinal atrophy, dog","secondary_identifiers":["OMIA:000830-9615"],"termid":"MONDO:1012226","xrefs":{"Monarch":{"xref_id":"1012226"}}}


id: PBO:0000560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"karyopherin Kap111 (predicted)","termid":"PBO:0000560"}


id: PBO:0078444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor gamma joining 2","termid":"PBO:0078444"}


id: SO:0001369
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"5_carboxymethylaminomethyluridine 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":"five_carboxymethylaminomethyluridine","secondary_identifiers":["RNAMOD:077"],"synonyms":[{"name":"5-carboxymethylaminomethyluridine","type":"exact"},{"name":"cmnm5U","type":"exact"},{"name":"five carboxymethylaminomethyluridine","type":"exact"}],"termid":"SO:0001369"}


id: PBO:0074252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier organic anion transporter family member 1B3","termid":"PBO:0074252"}


id: PBO:0031127
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_proline_nitrogen_source","termid":"PBO:0031127"}


id: GO:0045244
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric enzyme complex, usually composed of an alpha and beta chain. Functions in the TCA cycle, hydrolyzing succinyl-CoA into succinate and CoA, thereby forming GTP.","definition_xrefs":["PMID:27487822","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"succinate-CoA ligase complex","termid":"GO:0042709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0032991"],"is_obsolete":false,"name":"succinate-CoA ligase complex (GDP-forming)","secondary_identifiers":["GO:0008325","GO:0045245"],"synonyms":[{"name":"succinyl-CoA synthetase, GDP-forming","type":"exact"}],"termid":"GO:0045244"}


id: PBO:0039140
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ajuba LIM protein","termid":"PBO:0039140"}


id: GO:0050040
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-lactate + O2 = acetate + CO2 + H2O.","definition_xrefs":["EC:1.13.12.4","RHEA:16513"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of one atom of oxygen (internal monooxygenases or internal mixed function oxidases)","termid":"GO:0016703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"lactate 2-monooxygenase activity","secondary_identifiers":["KEGG_REACTION:R00319","MetaCyc:RXN-19631"],"synonyms":[{"name":"(S)-lactate:oxygen 2-oxidoreductase (decarboxylating)","type":"related"},{"name":"L-lactate monooxygenase activity","type":"related"},{"name":"L-lactate-2-monooxygenase activity","type":"related"},{"name":"lactate monooxygenase activity","type":"related"},{"name":"lactate oxidase activity","type":"related"},{"name":"lactate oxidative decarboxylase activity","type":"related"},{"name":"lactate oxygenase activity","type":"related"},{"name":"lactic oxidase activity","type":"related"},{"name":"lactic oxygenase activity","type":"related"}],"termid":"GO:0050040"}


id: PBO:0027134
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_telomere-nuclear_envelope_distance_during_mitotic_G2_phase","termid":"PBO:0027134"}


id: SO:0000365
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region encoding an integrase which acts at a site adjacent to it (attI_site) to insert DNA which must include but is not limited to an attC_site.","definition_xrefs":["SO:as"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integrated_mobile_genetic_element","termid":"SO:0001039"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integron","secondary_identifiers":["http://en.wikipedia.org/wiki/Integron"],"termid":"SO:0000365"}


id: PBO:0084700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial glycerol-3-phosphate dehydrogenase; expression is repressed by both glucose and cAMP and derepressed by non-fermentable carbon sources in a Snf1p, Rsf1p, Hap2/3/4/5 complex dependent manner","termid":"PBO:0084700"}


id: PBO:0084654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Minor orotate phosphoribosyltransferase (OPRTase) isozyme; catalyzes the fifth enzymatic step in the de novo biosynthesis of pyrimidines, converting orotate into orotidine-5'-phosphate; URA10 has a paralog, URA5, that arose from the whole genome duplication","termid":"PBO:0084654"}


id: MOD:00009
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that removes a residue, or inserts or replaces a residue with a natural, standard or nonstandard, encoded residue.","definition_xrefs":["RESID:AA0000","PubMed:6692818"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by amino acid modified","termid":"MOD:01157"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"natural residue","synonyms":[{"name":"Res","type":"exact"},{"name":"alpha-amino acid","type":"exact"}],"termid":"MOD:00009"}


id: PBO:0081512
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 418","termid":"PBO:0081512"}


id: GO:0034740
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains TFIIIC, topoisomerase 1, and Sub1/PC4. Characterized in human, the complex is involved in regulating transcription from RNA polymerase III (Pol III) promoters. Topoisomerase 1 and Sub1 enhance the accuracy of transcription termination, and promote reinitiation by Pol III.","definition_xrefs":["PMID:9660958"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase III transcription regulator complex","termid":"GO:0090576"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"TFIIIC-TOP1-SUB1 complex","synonyms":[{"name":"TFIIIC-Topoisomerase 1-PC4 complex","type":"exact"}],"termid":"GO:0034740"}


id: GO:0031603
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The core complex of a proteasome located in the cytosol of a cell.","definition_xrefs":["GOC:mah","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteasome core complex","termid":"GO:0005839"},{"relation_name":"part_of","term_name":"cytosolic proteasome complex","termid":"GO:0031597"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005829"},{"rel_name":"part_of","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005829","GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"cytosolic proteasome core complex","termid":"GO:0031603"}


id: PBO:0070034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1331, pseudogene","termid":"PBO:0070034"}


id: PBO:0069099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 346, pseudogene","termid":"PBO:0069099"}


id: PBO:0045817
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 7","termid":"PBO:0045817"}


id: PBO:0080685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain, phosphoinositide interacting 2","termid":"PBO:0080685"}


id: PBO:0068024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 329","termid":"PBO:0068024"}


id: PBO:0071932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S4X pseudogene 9","termid":"PBO:0071932"}


id: GO:0102698
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,6-trans-farnesyl diphosphate = (+)-5-epi-aristolochene + diphosphoric acid.","definition_xrefs":["GOC:pz","EC:4.2.3.61"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"5-epi-aristolochene synthase activity","secondary_identifiers":["RHEA:28635","MetaCyc:RXN-4781"],"termid":"GO:0102698"}


id: GO:1905199
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disaggregation of a manchette into its constituent components.","definition_xrefs":["GOC:TermGenie","PMID:24440897","PMID:26792866","GOC:krc","GO_REF:0000079","PMID:22319670"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component disassembly","termid":"GO:0022411"},{"relation_name":"part_of","term_name":"spermatid development","termid":"GO:0007286"}],"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":"manchette disassembly","termid":"GO:1905199"}


id: GO:0033166
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A multilayered extraembryonic matrix that functions as a substrate for cell adhesion through early development. It is thought to protect and lubricate the embryo, stabilize the blastomeres during morphogenesis, and regulate nutrient intake. The major constituent of the hyaline layer is the protein hyalin. This matrix has been found in echinoderms.","definition_xrefs":["PMID:1721506","PMID:9473317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specialized extracellular matrix","termid":"GO:0140047"}],"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":"hyaline layer","termid":"GO:0033166"}


id: PBO:0066356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reticulocalbin 3","termid":"PBO:0066356"}


id: PBO:0060153
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-RNR2 like 1 (pseudogene)","termid":"PBO:0060153"}


id: MONDO:0012117
data:
  {"annotated_genes":["SJAG_00334"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88358],"is_not":false,"summary":null,"term":"MONDO:0012117"},{"annotations":[89197],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009890"}]},"cv_name":"mondo","definition":"A form of congenital disorders of N-linked glycosylation characterized by progressive microcephaly, hypotonia, developmental delay, drug-resistant infantile epilepsy, and hepatomegaly. Additional features that may be observed include failure to thrive, pericardial effusion, renal cysts, skeletal dysplasia, facial dysmorphism (frontal bossing, hypertelorism, depressed nasal bridge, low-seated ears, large mouth) and hydrops fetalis. The disease is caused by loss-of-function mutations in the gene ALG9 (11q23).","definition_xrefs":["Orphanet:79328"],"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_00334":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"ALG9-congenital disorder of glycosylation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080564","OMIM:608776","UMLS:C2931006","SCTID:720978005","GARD:9839","MEDGEN:443955","MESH:C535750"],"synonyms":[{"name":"ALG9-CDG","type":"exact"},{"name":"ALG9-CDG (CDG-IL)","type":"related"},{"name":"ALG9-congenital disorder of glycosylation","type":"exact"},{"name":"CDG 1L","type":"related"},{"name":"CDG IL","type":"related"},{"name":"CDG syndrome type IL","type":"exact"},{"name":"CDG-IL","type":"exact"},{"name":"CDG1L","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type 1L","type":"exact"},{"name":"carbohydrate deficient glycoprotein syndrome type IL","type":"related"},{"name":"congenital disorder of glycosylation type 1L","type":"exact"},{"name":"congenital disorder of glycosylation type IL","type":"related"},{"name":"congenital disorder of glycosylation, type IL","type":"related"},{"name":"mannosyltransferase 7-9 deficiency","type":"exact"}],"termid":"MONDO:0012117","terms_by_termid":{"MONDO:0009890":null,"MONDO:0012117":null},"xrefs":{"Monarch":{"xref_id":"0012117"}}}


id: MONDO:0021720
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete fetal alcohol spectrum disorders (obsolete MONDO:0021720)","termid":"MONDO:0021720","xrefs":{"Monarch":{"xref_id":"0021720"}}}


id: FYPO:0004989
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which centromere clustering is abnormal during one or both meiotic nuclear divisions, such that one or more centromeres is associated with the spindle pole body (SPB) during prophase. Normally, centromeres and SPBs associate after prophase, but not earlier.","definition_xrefs":["PomBase:mah","PMID:15298676"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic centromere clustering","termid":"FYPO:0004086"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0000002","FYPO:0005447","FYPO:0000631","FYPO:0000641"],"is_obsolete":false,"name":"abnormal meiotic centromere clustering resulting in centromere-spindle pole body colocalization during prophase","synonyms":[{"name":"abnormal centromere clustering during meiosis resulting in centromere-spindle pole body colocalization during prophase","type":"exact"},{"name":"abnormal chromosome retrieval during meiosis resulting in centromere-spindle pole body colocalization during prophase","type":"related"},{"name":"abnormal kinetochore retrieval during meiosis resulting in centromere-spindle pole body colocalization during prophase","type":"related"},{"name":"abnormal meiotic centromere clustering resulting in centromere-SPB colocalization during prophase","type":"exact"},{"name":"abnormal meiotic centromere clustering resulting in centromere-spindle pole body colocalisation during prophase","type":"exact"},{"name":"abnormal meiotic centromere clustering resulting in centromere-spindle pole body colocalization during meiotic prophase","type":"exact"},{"name":"abnormal meiotic centromere clustering resulting in premature centromere-spindle pole body colocalization","type":"related"},{"name":"centromeres colocalized with SPB during meiosis","type":"exact"},{"name":"centromeres colocalized with SPB during meiotic cell cycle","type":"related"},{"name":"centromeres colocalized with spindle pole body during meiosis","type":"exact"},{"name":"centromeres colocalized with spindle pole body during meiotic cell cycle","type":"related"}],"termid":"FYPO:0004989"}


id: FYPO:0004382
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 a single kinetochore becomes attached to both spindle poles, and sister chromatids do not move towards the spindle poles at the same time during mitosis prior to completion of chromosome segregation.","definition_xrefs":["PMID:20935472","PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"lagging mitotic chromosomes","termid":"FYPO:0000228"},{"relation_name":"has_part","term_name":"merotelic kinetochore attachment during mitosis","termid":"FYPO:0004381"},{"relation_name":"is_a","term_name":"abnormal attachment of mitotic spindle microtubules to kinetochore","termid":"FYPO:0004213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"part_of","termid":"FYPO:0000641"},{"rel_name":"has_part","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000641","FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000337","FYPO:0000138","FYPO:0000631"],"is_obsolete":false,"name":"meroterically attached lagging mitotic chromosomes","synonyms":[{"name":"abnormal mitotic sister chromatid segregation, with merotelic kinetochore attachment and lagging mitotic chromosomes","type":"exact"},{"name":"lagging mitotic chromosomes with merotelic kinetochore attachment","type":"exact"},{"name":"lagging mitotic sister chromatids, with merotelic kinetochore attachment","type":"exact"},{"name":"merotelic kinetochore attachment with lagging mitotic chromosomes","type":"exact"},{"name":"meroterically attached lagging mitotic chromosomes during mitotic cell cycle","type":"related"},{"name":"meroterically attached lagging mitotic chromosomes during vegetative growth","type":"exact"}],"termid":"FYPO:0004382"}


id: PBO:0062367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily A member 2 pseudogene","termid":"PBO:0062367"}


id: GO:0038015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which internalization of an insulin receptor activates or increases the frequency, rate or extent of the insulin receptor signaling pathway. Endocytosis of activated receptors can concentrate receptors within endosomes and allow the insulin receptor to phosphorylate substrates that are spatially distinct from those accessible at the plasma membrane.","definition_xrefs":["GOC:signaling","PMID:9609114","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of signal transduction by receptor internalization","termid":"GO:0038010"},{"relation_name":"is_a","term_name":"insulin receptor internalization","termid":"GO:0038016"},{"relation_name":"is_a","term_name":"positive regulation of insulin receptor signaling pathway","termid":"GO:0046628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0016192","GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of insulin receptor signaling pathway by insulin receptor internalization","synonyms":[{"name":"positive regulation of insulin receptor signalling pathway by insulin receptor internalization","type":"exact"}],"termid":"GO:0038015"}


id: GO:1901913
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of capsule organization.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"regulates","term_name":"capsule organization","termid":"GO:0045230"}],"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 capsule organization","synonyms":[{"name":"regulation of capsule organisation","type":"exact"},{"name":"regulation of capsule organization and biogenesis","type":"related"}],"termid":"GO:1901913"}


id: MONDO:0000817
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0000817 (obsolete MONDO:0000817)","termid":"MONDO:0000817","xrefs":{"Monarch":{"xref_id":"0000817"}}}


id: PBO:0046744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exocyst complex component 3","termid":"PBO:0046744"}


id: PBO:0091583
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human RAD1","termid":"PBO:0091583"}


id: SO:0000750
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An origin_of_replication that is used for the amplification of a chromosomal nucleic acid sequence.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"origin_of_replication","termid":"SO:0000296"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amplification_origin","synonyms":[{"name":"amplification origin","type":"exact"}],"termid":"SO:0000750"}


id: PBO:0045161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein axonemal intermediate chain 1","termid":"PBO:0045161"}


id: GO:0007253
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The selective interaction of the transcription factor NF-kappaB with specific molecules in the cytoplasm, thereby inhibiting its translocation into the nucleus.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete cytoplasmic sequestering of NF-kappaB (obsolete GO:0007253)","synonyms":[{"name":"cytoplasmic NF-kappaB retention","type":"exact"},{"name":"cytoplasmic NF-kappaB sequestration","type":"exact"},{"name":"cytoplasmic NF-kappaB storage","type":"exact"},{"name":"cytoplasmic retention of NF-kappaB","type":"exact"},{"name":"cytoplasmic sequestration of NF-kappaB","type":"exact"},{"name":"cytoplasmic storage of NF-kappaB","type":"exact"},{"name":"maintenance of NF-kappaB location in cytoplasm","type":"exact"}],"termid":"GO:0007253"}


id: GO:2000739
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mesenchymal stem cell differentiation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of stem cell differentiation","termid":"GO:2000736"},{"relation_name":"regulates","term_name":"mesenchymal stem cell differentiation","termid":"GO:0072497"}],"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 mesenchymal stem cell differentiation","termid":"GO:2000739"}


id: PR:Q09795
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An Xaa-Pro aminopeptidase 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00285"],"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 peptidase C22G7.01c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22G7.01c","secondary_identifiers":["UniProtKB:Q09795"],"synonyms":[{"name":"Spom972h-XPNPEP1","type":"exact"}],"termid":"PR:Q09795"}


id: PBO:0005719
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hereditary leiomyomatosis","termid":"PBO:0005719"}


id: PBO:0051448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 4-60","termid":"PBO:0051448"}


id: GO:0045707
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of salivary gland determination in an adult organism.","definition_xrefs":["GOC:go_curators","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of salivary gland boundary specification","termid":"GO:0045704"},{"relation_name":"regulates","term_name":"adult salivary gland boundary specification","termid":"GO:0007434"}],"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 adult salivary gland boundary specification","synonyms":[{"name":"regulation of adult salivary gland determination","type":"exact"}],"termid":"GO:0045707"}


id: PBO:0045083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"delta like non-canonical Notch ligand 2","termid":"PBO:0045083"}


id: FYPO:0007914
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic sister chromatid separation occurs during mitotic metaphase.","definition_xrefs":["PomBase:vw","PMID:10398680"],"direct_ancestors":[{"relation_name":"is_a","term_name":"premature mitotic sister chromatid separation","termid":"FYPO:0000416"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0000631","FYPO:0001985","FYPO:0000337","FYPO:0000002","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"mitotic sister chromatid separation during metaphase","termid":"FYPO:0007914"}


id: GO:1905001
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of membrane repolarization during atrial cardiac muscle cell action potential.","definition_xrefs":["PMID:21098446","GOC:TermGenie","GO_REF:0000058","GOC:mtg_cardiac_conduct_nov11","GOC:rph","GOC:BHF","GOC:BHF_miRNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of membrane repolarization during atrial cardiac muscle cell action potential","termid":"GO:1905000"},{"relation_name":"is_a","term_name":"negative regulation of membrane repolarization during cardiac muscle cell action potential","termid":"GO:1905032"},{"relation_name":"negatively_regulates","term_name":"membrane repolarization during atrial cardiac muscle cell action potential","termid":"GO:0098914"}],"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 membrane repolarization during atrial cardiac muscle cell action potential","synonyms":[{"name":"down regulation of atrial repolarization","type":"related"},{"name":"down regulation of electrocardiogram QRS complex","type":"related"},{"name":"down regulation of membrane repolarization during atrial cardiac muscle cell action potential","type":"exact"},{"name":"down-regulation of atrial repolarization","type":"related"},{"name":"down-regulation of electrocardiogram QRS complex","type":"related"},{"name":"down-regulation of membrane repolarization during atrial cardiac muscle cell action potential","type":"exact"},{"name":"downregulation of atrial repolarization","type":"related"},{"name":"downregulation of electrocardiogram QRS complex","type":"related"},{"name":"downregulation of membrane repolarization during atrial cardiac muscle cell action potential","type":"exact"},{"name":"inhibition of atrial repolarization","type":"related"},{"name":"inhibition of electrocardiogram QRS complex","type":"related"},{"name":"inhibition of membrane repolarization during atrial cardiac muscle cell action potential","type":"narrow"},{"name":"negative regulation of atrial repolarization","type":"related"},{"name":"negative regulation of electrocardiogram QRS complex","type":"related"}],"termid":"GO:1905001"}


id: GO:0033966
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-benzylformamide + H2O = formate + benzylamine.","definition_xrefs":["EC:3.5.1.91"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016810","GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"N-substituted formamide deformylase activity","secondary_identifiers":["MetaCyc:3.5.1.91-RXN","RHEA:12096"],"synonyms":[{"name":"N-benzylformamide amidohydrolase activity","type":"related"},{"name":"NfdA","type":"related"}],"termid":"GO:0033966"}


id: PBO:0038520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily F member 2 pseudogene 2","termid":"PBO:0038520"}


id: PBO:0090890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA exonuclease Rrp17","termid":"PBO:0090890"}


id: PBO:0056643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit 15 pseudogene 4","termid":"PBO:0056643"}


id: MONDO:0033618
data:
  {"annotated_genes":["SJAG_03597"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87638],"is_not":false,"summary":null,"term":"MONDO:0033618"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03597":null},"genotype_count":0,"is_obsolete":false,"name":"Vissers-Bodmer syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0081397","MEDGEN:1776566","OMIM:619033","UMLS:C5436647"],"synonyms":[{"name":"VIBOS","type":"exact"}],"termid":"MONDO:0033618","terms_by_termid":{"MONDO:0033618":null},"xrefs":{"Monarch":{"xref_id":"0033618"}}}


id: GO:0032790
data:
  {"annotated_genes":["SJAG_01497","SJAG_02096","SJAG_03428","SJAG_00188","SJAG_04283","SJAG_02746","SJAG_03189","SJAG_03232","SJAG_03106","SJAG_00898","SJAG_04862","SJAG_05000","SJAG_01074"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72696,76433,106666],"is_not":false,"summary":null,"term":"GO:0032790"},{"annotations":[116409],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140708"},{"annotations":[71734,105087,65565,107600,80077,118086,78511,105565,77246],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072344"}]},"cv_name":"biological_process","definition":"The disaggregation of a ribosome into its constituent components; includes the dissociation of ribosomal subunits.","definition_xrefs":["GOC:vk","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle disassembly","termid":"GO:1903008"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00188":null,"SJAG_00898":null,"SJAG_01074":null,"SJAG_01497":null,"SJAG_02096":null,"SJAG_02746":null,"SJAG_03106":null,"SJAG_03189":null,"SJAG_03232":null,"SJAG_03428":null,"SJAG_04283":null,"SJAG_04862":null,"SJAG_05000":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"ribosome disassembly","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"ribosome dissociation factor","type":"related"},{"name":"ribosome recycling","type":"narrow"}],"termid":"GO:0032790","terms_by_termid":{"GO:0032790":null,"GO:0072344":null,"GO:0140708":null}}


id: MONDO:0002444
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A subtype of depression characterized by the inability to find pleasure in positive things combined with physical agitation, insomnia, or decreased appetite.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"depressive disorder","termid":"MONDO:0002050"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"melancholia","secondary_identifiers":["UMLS:C0025193","EFO:1002014","NCIT:C34812","DOID:2848","MEDGEN:6288"],"synonyms":[{"name":"depression with melancholic features","type":"exact"},{"name":"melancholic depression","type":"exact"}],"termid":"MONDO:0002444","xrefs":{"Monarch":{"xref_id":"0002444"}}}


id: GO:0002572
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a pro-T cell. Pro-T cells are the earliest stage of the T cell lineage but are not fully committed.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoid progenitor cell differentiation","termid":"GO:0002320"},{"relation_name":"part_of","term_name":"T cell differentiation","termid":"GO:0030217"}],"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":"pro-T cell differentiation","synonyms":[{"name":"pro-T lymphocyte differentiation","type":"exact"}],"termid":"GO:0002572"}


id: MONDO:0016666
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"rheumatic disorder","termid":"MONDO:0005554"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unexplained long-lasting fever/inflammatory syndrome","secondary_identifiers":["MEDGEN:1842329","Orphanet:251332","GARD:20699","UMLS:C5679630"],"termid":"MONDO:0016666","xrefs":{"Monarch":{"xref_id":"0016666"}}}


id: PBO:0059341
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S10","termid":"PBO:0059341"}


id: PBO:0109639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinoic acid early transcript 1F (pseudogene)","termid":"PBO:0109639"}


id: PATO:0002422
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Pertaining to the individual parts making up an aggregate fruit like a many-lobed \\\"berry,\\\" such as a raspberry.","definition_xrefs":["wikipedia:https://en.wikipedia.org/wiki/Acinus"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acinar","termid":"PATO:0002422"}


id: PBO:0064058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 92","termid":"PBO:0064058"}


id: MONDO:0000164
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete corneal dystrophy, Fuchs endothelial (obsolete MONDO:0000164)","termid":"MONDO:0000164","xrefs":{"Monarch":{"xref_id":"0000164"}}}


id: MONDO:0010154
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trigonocephaly-bifid nose-acral anomalies syndrome is characterized by trigonocephaly, brachycephaly, bulbous nose (bifid at the tip), micrognathia, macrostomia, hypotonia and relatively broad metatarsals and phalanges.","definition_xrefs":["Orphanet:3368"],"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":"trigonocephaly-bifid nose-acral anomalies syndrome","secondary_identifiers":["MESH:C564759","GARD:5126","MEDGEN:341296","OMIM:275595","UMLS:C1848743"],"synonyms":[{"name":"trigonobrachycephaly, bulbous bifid nose, macrostomia, micrognathia, acral anomalies, and hypotonia","type":"related"},{"name":"trigonobrachycephaly, bulbous bifid nose, micrognathia, and abnormalities of the hands and feet","type":"related"},{"name":"trigonocephaly - bifid nose - acral anomalies","type":"related"}],"termid":"MONDO:0010154","xrefs":{"Monarch":{"xref_id":"0010154"}}}


id: MONDO:1010792
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited syndrome characterized by hypotrichosis (sparseness of hair), hypo- or an-hidrosis (reduced ability to sweat), and hypodontia (congenital absence of teeth) in cattle due to a variation in the EDAR gene.","definition_xrefs":["PMID:28904385"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anhidrotic ectodermal dysplasia EDAR-related, cattle","secondary_identifiers":["OMIA:002128-9913"],"termid":"MONDO:1010792","xrefs":{"Monarch":{"xref_id":"1010792"}}}


id: GO:0048858
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a cell projection are generated and organized.","definition_xrefs":["GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"is_a","term_name":"cell projection organization","termid":"GO:0030030"},{"relation_name":"part_of","term_name":"cell morphogenesis","termid":"GO:0000902"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell projection morphogenesis","termid":"GO:0048858"}


id: GO:1902902
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of autophagosome assembly.","definition_xrefs":["GOC:autophagy","GOC:TermGenie","GO_REF:0000058","GOC:als","PMID:21975012"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of macroautophagy","termid":"GO:0016242"},{"relation_name":"is_a","term_name":"negative regulation of organelle assembly","termid":"GO:1902116"},{"relation_name":"is_a","term_name":"regulation of autophagosome assembly","termid":"GO:2000785"},{"relation_name":"negatively_regulates","term_name":"autophagosome assembly","termid":"GO:0000045"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0006914"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006914"}],"interesting_parent_ids":["GO:0006914","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"negative regulation of autophagosome assembly","synonyms":[{"name":"down regulation of PAS formation","type":"narrow"},{"name":"down regulation of autophagic vacuole assembly","type":"exact"},{"name":"down regulation of autophagic vacuole formation","type":"related"},{"name":"down regulation of autophagosome biosynthesis","type":"exact"},{"name":"down regulation of autophagosome formation","type":"exact"},{"name":"down-regulation of PAS formation","type":"narrow"},{"name":"down-regulation of autophagic vacuole assembly","type":"exact"},{"name":"down-regulation of autophagic vacuole formation","type":"related"},{"name":"down-regulation of autophagosome biosynthesis","type":"exact"},{"name":"down-regulation of autophagosome formation","type":"exact"},{"name":"downregulation of PAS formation","type":"narrow"},{"name":"downregulation of autophagic vacuole assembly","type":"exact"},{"name":"downregulation of autophagic vacuole formation","type":"related"},{"name":"downregulation of autophagosome biosynthesis","type":"exact"},{"name":"downregulation of autophagosome formation","type":"exact"},{"name":"inhibition of PAS formation","type":"narrow"},{"name":"inhibition of autophagic vacuole assembly","type":"narrow"},{"name":"inhibition of autophagic vacuole formation","type":"related"},{"name":"inhibition of autophagosome biosynthesis","type":"narrow"},{"name":"inhibition of autophagosome formation","type":"narrow"},{"name":"negative regulation of PAS formation","type":"narrow"},{"name":"negative regulation of autophagic vacuole assembly","type":"exact"},{"name":"negative regulation of autophagic vacuole formation","type":"related"},{"name":"negative regulation of autophagosome biosynthesis","type":"exact"},{"name":"negative regulation of autophagosome formation","type":"exact"}],"termid":"GO:1902902"}


