# terms

id: PBO:0090907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAG family molecular chaperone regulator Bag101","termid":"PBO:0090907"}


id: PBO:0045801
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endothelin receptor type B","termid":"PBO:0045801"}


id: PBO:0061263
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"notch receptor 3","termid":"PBO:0061263"}


id: PBO:0084428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Major stress-induced structural GPI-cell wall glycoprotein; associates with translating ribosomes, possible role in mitochondrial genome maintenance; ORF contains two distinct variable minisatellites; SED1 has a paralog, SPI1, that arose from the whole genome duplication","termid":"PBO:0084428"}


id: PR:000027580
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A fungal histone H3.2, initiator methionine removed form in Schizosaccharomyces pombe.","definition_xrefs":["PMID:11242054","PMID:20929775","PomBase:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3.2 (Schizosaccharomyces pombe)","termid":"PR:000027572"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3.2, initiator methionine removed form (Schizosaccharomyces pombe)","pombase_gene_id":"SPBC8D2.04","synonyms":[{"name":"Spom-hht2/InitMet-","type":"exact"}],"termid":"PR:000027580"}


id: MONDO:0001862
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pleural cancer","termid":"MONDO:0006294"}],"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":"malignant visceral pleura tumor","secondary_identifiers":["DOID:14033","UMLS:C0153496","SCTID:94140004","MEDGEN:509311"],"synonyms":[{"name":"primary malignant neoplasm of visceral pleura","type":"exact"}],"termid":"MONDO:0001862","xrefs":{"Monarch":{"xref_id":"0001862"}}}


id: PBO:0077962
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ala (anticodon AGC) 15-1","termid":"PBO:0077962"}


id: PBO:0044598
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DDB1 and CUL4 associated factor 6","termid":"PBO:0044598"}


id: GO:0141195
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The formation of facultative heterochromatin into a heterochromatin domain, enriched in histone H3 methylated on lysine 9 (H3K9me), by a process mediated by a Piwi-associated RNA (piRNA).","definition_xrefs":["PMID:26494711"],"gene_count":0,"genotype_count":0,"name":"obsolete piRNA-mediated facultative heterochromatin formation (obsolete GO:0141195)","termid":"GO:0141195"}


id: SO:0002170
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that falls in the region between the 3rd and 6th base after splice junction (5' end of intron).","direct_ancestors":[{"relation_name":"is_a","term_name":"splice_region_variant","termid":"SO:0001630"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splice_donor_region_variant","synonyms":[{"name":"splice donor region variant","type":"exact"}],"termid":"SO:0002170"}


id: GO:0140707
data:
  {"annotated_genes":["SJAG_01745","SJAG_03449","SJAG_03103"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91716,119629,103968],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062239"}]},"cv_name":"molecular_function","definition":"Binding to chromatin and the nuclear inner membrane, in order to establish and maintain the heterochromatin location and organization, or to enable equal segregation of the nuclear membrane during mitosis.","definition_xrefs":["PMID:24184107","PMID:31048766"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane-membrane adaptor activity","termid":"GO:0043495"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01745":null,"SJAG_03103":null,"SJAG_03449":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0003674","GO:0060090","GO:0030674"],"is_obsolete":false,"name":"chromatin-nuclear membrane anchor activity","references_by_uniquename":{"GO_REF:0000107":null,"PMID:24184107":null},"termid":"GO:0140707","terms_by_termid":{"GO:0062239":null}}


id: GO:1902989
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any telomere maintenance via semi-conservative replication that is involved in meiotic cell cycle.","definition_xrefs":["GOC:TermGenie","GO_REF:0000060"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telomere maintenance via semi-conservative replication","termid":"GO:0032201"},{"relation_name":"is_a","term_name":"chromosome organization involved in meiotic cell cycle","termid":"GO:0070192"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0032200"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006260"}],"interesting_parent_ids":["GO:0032200","GO:0007049","GO:0006260","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"meiotic telomere maintenance via semi-conservative replication","synonyms":[{"name":"equal telomere replication involved in meiotic cell cycle","type":"related"},{"name":"telomeric fork progression involved in meiotic cell cycle","type":"narrow"},{"name":"telomeric replication fork progression involved in meiotic cell cycle","type":"narrow"}],"termid":"GO:1902989"}


id: PBO:0053144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lactate dehydrogenase A like 6F, pseudogene","termid":"PBO:0053144"}


id: MONDO:0010570
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An X-linked malformation syndrome characterized by facial asymmetry (particularly orbital), body asymmetry, midline defects (hypertelorism, frontal bossing, broad grooved or bifid nasal tip, cleft lip and/or palate, high arched palate), skeletal anomalies (clavicle pseudoarthrosis, coronal craniosynostosis, various digital and limb anomalies including syndactyly, clinodactyly of the 5th finger, broad thumbs) and ectodermal dysplasias (dental anomalies, grooved nails, wiry hair). Contrary to most X-linked disorders, females are much more severely affected whereas males are asymptomatic or present with a mild phenotype, frequently only displaying hypertelorism.","definition_xrefs":["Orphanet:1520"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"frontonasal dysplasia","termid":"MONDO:0016643"},{"relation_name":"excluded_subClassOf","term_name":"acrofacial dysostosis","termid":"MONDO:0018237"},{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"},{"relation_name":"is_a","term_name":"neurocristopathy","termid":"MONDO:0021635"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"craniofrontonasal syndrome","secondary_identifiers":["MEDGEN:65095","OMIM:304110","DOID:14737","GARD:1578","MESH:C536456","SCTID:715421009","UMLS:C0220767"],"synonyms":[{"name":"CFND","type":"exact"},{"name":"CFNS","type":"exact"},{"name":"Craniofrontonasal Dysplasia","type":"exact"},{"name":"craniofrontonasal dysostosis","type":"related"},{"name":"craniofrontonasal dysplasia","type":"exact"},{"name":"craniofrontonasal dysplasia, X-linked dominant","type":"exact"},{"name":"craniofrontonasal syndrome","type":"exact"}],"termid":"MONDO:0010570","xrefs":{"Monarch":{"xref_id":"0010570"}}}


id: PBO:0073178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"selenoprotein K","termid":"PBO:0073178"}


id: MONDO:0021116
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A biologic subset of breast carcinoma defined by high expression of genes characteristic of luminal epithelial cells, including estrogen receptor (ER), estrogen regulated protein LIV-1, and the transcription factors hepatocyte nuclear factor 3, HNF3A, XBP1, and GATA 3. This subtype of breast cancer is associated with a good prognosis.","definition_xrefs":["NCIT:C53554"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast tumor luminal A or B","termid":"MONDO:0004990"}],"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":"luminal A breast carcinoma","secondary_identifiers":["UMLS:C3642345","MEDGEN:770985"],"synonyms":[{"name":"Luminal A","type":"exact"},{"name":"Luminal A breast cancer","type":"exact"},{"name":"Luminal A breast carcinoma","type":"exact"},{"name":"Luminal A estrogen receptor positive subtype of breast carcinoma","type":"exact"},{"name":"Luminal A oestrogen receptor positive subtype of breast carcinoma","type":"exact"},{"name":"Luminal A subtype of breast carcinoma","type":"exact"}],"termid":"MONDO:0021116","xrefs":{"Monarch":{"xref_id":"0021116"}}}


id: PBO:0044513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYYR1 antisense RNA 1","termid":"PBO:0044513"}


id: PBO:0046053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 subunit F pseudogene 1","termid":"PBO:0046053"}


id: PBO:0060261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myeloma overexpressed","termid":"PBO:0060261"}


id: PBO:0030874
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_amino_acid_import_during_vegetative_growth","termid":"PBO:0030874"}


id: MONDO:0021639
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A glioma arising from the central nervous system. This category includes diffuse astrocytoma, ependymoma, oligodendroglioma, and oligoastrocytoma.","definition_xrefs":["NCIT:C132505"],"direct_ancestors":[{"relation_name":"is_a","term_name":"low grade glioma","termid":"MONDO:0021637"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"grade II glioma","secondary_identifiers":["MEDGEN:1391502","UMLS:C4330050"],"synonyms":[{"name":"WHO grade II glioma","type":"exact"},{"name":"grade II glioma","type":"exact"}],"termid":"MONDO:0021639","xrefs":{"Monarch":{"xref_id":"0021639"}}}


id: MONDO:0958353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of congenital muscular dystrophy characterized by congenital weakness, hypotonia, proximal joint contractures, marked hyperlaxity of the distal joints, attainment of independent ambulation which is subsequently lost and uniform respiratory insufficiency during the teenage years.","definition_xrefs":["Orphanet:646113"],"direct_ancestors":[{"relation_name":"is_a","term_name":"collagen 6-related congenital muscular dystrophy","termid":"MONDO:0958077"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"intermediate collagen VI-related muscular dystrophy","secondary_identifiers":["MEDGEN:1853152","UMLS:C5816698"],"termid":"MONDO:0958353","xrefs":{"Monarch":{"xref_id":"0958353"}}}


id: MONDO:0001105
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypertension caused by the kidney's hormonal response to narrowing or occlusion of the renal arteries.","definition_xrefs":["Wikipedia:Renovascular_hypertension"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary hypertension","termid":"MONDO:0001200"},{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"renal hypertension","secondary_identifiers":["MEDGEN:5700","MESH:D006977","NANDO:2200141","UMLS:C0020544","DOID:1073","EFO:1002039","NANDO:2100016","SCTID:28119000"],"synonyms":[{"name":"renovascular hypertension","type":"narrow"}],"termid":"MONDO:0001105","xrefs":{"Monarch":{"xref_id":"0001105"}}}


id: FYPO:0003331
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a protein kinase activity is decreased during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein kinase activity","termid":"FYPO:0001382"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0001985","FYPO:0000652","FYPO:0000654","FYPO:0000707"],"is_obsolete":false,"name":"decreased protein kinase activity during mitotic interphase","synonyms":[{"name":"reduced protein kinase activity during mitotic interphase","type":"exact"}],"termid":"FYPO:0003331"}


id: GO:0043302
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of leukocyte degranulation.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of immune effector process","termid":"GO:0002699"},{"relation_name":"is_a","term_name":"regulation of leukocyte degranulation","termid":"GO:0043300"},{"relation_name":"is_a","term_name":"positive regulation of regulated secretory pathway","termid":"GO:1903307"},{"relation_name":"positively_regulates","term_name":"leukocyte degranulation","termid":"GO:0043299"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0016192","GO:0008150"],"is_obsolete":false,"name":"positive regulation of leukocyte degranulation","synonyms":[{"name":"activation of leukocyte degranulation","type":"narrow"},{"name":"positive regulation of immune cell degranulation","type":"exact"},{"name":"positive regulation of leucocyte degranulation","type":"exact"},{"name":"stimulation of leukocyte degranulation","type":"narrow"},{"name":"up regulation of leukocyte degranulation","type":"exact"},{"name":"up-regulation of leukocyte degranulation","type":"exact"},{"name":"upregulation of leukocyte degranulation","type":"exact"}],"termid":"GO:0043302"}


id: PBO:0057994
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3918","termid":"PBO:0057994"}


id: MONDO:0005153
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenocarcinoma arising from the cervical epithelium. It accounts for approximately 15% of invasive cervical carcinomas. Increased numbers of sexual partners and human papillomavirus (HPV) infection are risk factors. Grossly, advanced cervical adenocarcinoma may present as an exophytic mass, an ulcerated lesion, or diffuse cervical enlargement. Microscopically, the majority of cervical adenocarcinomas are of the endocervical (mucinous) type.","definition_xrefs":["NCIT:C4029"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"},{"relation_name":"is_a","term_name":"cervical carcinoma","termid":"MONDO:0005131"}],"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 adenocarcinoma","secondary_identifiers":["DOID:3702","ICD10CM:C53.0","MEDGEN:79024","GARD:20488","UMLS:C0279672","SCTID:254887002","icd11.foundation:261293318","Orphanet:213772","EFO:0001416","ONCOTREE:CEAD"],"synonyms":[{"name":"adenocarcinoma - cervix","type":"exact"},{"name":"adenocarcinoma cervix uteri","type":"exact"},{"name":"adenocarcinoma of cervix","type":"exact"},{"name":"adenocarcinoma of cervix uteri","type":"exact"},{"name":"adenocarcinoma of the cervix","type":"exact"},{"name":"adenocarcinoma of the cervix uteri","type":"exact"},{"name":"adenocarcinoma of the uterine cervix","type":"exact"},{"name":"adenocarcinoma of uterine cervix","type":"exact"},{"name":"cervical adenocarcinoma","type":"exact"},{"name":"cervix adenocarcinoma","type":"exact"},{"name":"cervix uteri adenocarcinoma","type":"exact"},{"name":"uterine cervix adenocarcinoma","type":"exact"}],"termid":"MONDO:0005153","xrefs":{"Monarch":{"xref_id":"0005153"}}}


id: PBO:0081028
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger CCCH-type containing 10","termid":"PBO:0081028"}


id: MONDO:0044272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete body mass index quantitative trait locus 9 (obsolete MONDO:0044272)","secondary_identifiers":["OMIM:602025"],"synonyms":[{"name":"BMIQ9","type":"related"},{"name":"body MASS index quantitative trait locus 9","type":"related"},{"name":"obesity, severe, susceptibility to, BMIQ9","type":"exact"},{"name":"obesity, susceptibility to","type":"related"}],"termid":"MONDO:0044272","xrefs":{"Monarch":{"xref_id":"0044272"}}}


id: PBO:0058025
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3975","termid":"PBO:0058025"}


id: MONDO:0007593
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"facial spasm","secondary_identifiers":["OMIM:134300","UMLS:C0278151","MEDGEN:124458"],"synonyms":[{"name":"facial spasm","type":"exact"}],"termid":"MONDO:0007593","xrefs":{"Monarch":{"xref_id":"0007593"}}}


id: FYPO:0005083
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 chromatin at non-coding RNA (ncRNA) genes is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:21151114","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to chromatin during vegetative growth","termid":"FYPO:0001509"}],"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"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0000257","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal protein localization to chromatin at ncRNA gene","synonyms":[{"name":"normal protein localisation to chromatin at ncRNA gene","type":"exact"},{"name":"normal protein localization to chromatin at ncRNA gene during mitotic cell cycle","type":"related"},{"name":"normal protein localization to chromatin at ncRNA gene during vegetative growth","type":"exact"}],"termid":"FYPO:0005083"}


id: GO:1902259
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of delayed rectifier potassium channel activity.","definition_xrefs":["PMID:11299204","GOC:TermGenie","GOC:rl","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of potassium ion transmembrane transporter activity","termid":"GO:1901016"},{"relation_name":"is_a","term_name":"regulation of cation channel activity","termid":"GO:2001257"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of delayed rectifier potassium channel activity","termid":"GO:1902259"}


id: PBO:0041982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCDC26 long non-coding RNA","termid":"PBO:0041982"}


id: GO:0005944
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A class I phosphatidylinositol 3-kinase complex that possesses 1-phosphatidylinositol-4-phosphate 3-kinase activity; comprises a catalytic class IB phosphoinositide 3-kinase (PI3K) subunit and an associated regulatory subunit that is larger than, and unrelated to, the p85 proteins present in class IA complexes. Class IB PI3Ks are stimulated by G-proteins and do not interact with the SH2-domain containing adaptors that bind to Class IA PI3Ks.","definition_xrefs":["PMID:9759495","PMID:9255069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylinositol 3-kinase complex, class I","termid":"GO:0097651"}],"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":"phosphatidylinositol 3-kinase complex, class IB","secondary_identifiers":["GO:0035031"],"synonyms":[{"name":"1-phosphatidylinositol-4-phosphate 3-kinase, class IB complex","type":"exact"},{"name":"1-phosphatidylinositol-4-phosphate kinase, class IB complex","type":"related"},{"name":"class IB PI3K complex","type":"exact"},{"name":"phosphoinositide 3-kinase complex, class IB","type":"exact"}],"termid":"GO:0005944"}


id: GO:0070373
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of signal transduction mediated by the ERK1 and ERK2 cascade.","definition_xrefs":["ISBN:0896039986","ISBN:0121245462","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of MAPK cascade","termid":"GO:0043409"},{"relation_name":"is_a","term_name":"regulation of ERK1 and ERK2 cascade","termid":"GO:0070372"},{"relation_name":"negatively_regulates","term_name":"ERK1 and ERK2 cascade","termid":"GO:0070371"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of ERK1 and ERK2 cascade","synonyms":[{"name":"down regulation of ERK1 and ERK2 cascade","type":"exact"},{"name":"down-regulation of ERK1 and ERK2 cascade","type":"exact"},{"name":"downregulation of ERK1 and ERK2 cascade","type":"exact"},{"name":"inhibition of ERK1 and ERK2 cascade","type":"narrow"},{"name":"negative regulation of ERK cascade","type":"broad"},{"name":"negative regulation of ERK1 and ERK2 signaling pathway","type":"exact"},{"name":"negative regulation of ERK1 and ERK2 signalling pathway","type":"exact"},{"name":"negative regulation of ERK1 cascade","type":"narrow"},{"name":"negative regulation of ERK1/2 cascade","type":"exact"},{"name":"negative regulation of ERK2 cascade","type":"narrow"},{"name":"negative regulation of MAPK1 cascade","type":"narrow"},{"name":"negative regulation of MAPK3 cascade","type":"narrow"}],"termid":"GO:0070373"}


id: GO:1905124
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of glucosylceramidase activity.","definition_xrefs":["GOC:bf","GO_REF:0000059","GOC:PARL","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of glucosylceramidase activity (obsolete GO:1905124)","synonyms":[{"name":"down regulation of D-glucosyl-N-acylsphingosine glucohydrolase activity","type":"exact"},{"name":"down regulation of GlcCer-beta-glucosidase activity","type":"exact"},{"name":"down regulation of acid beta-glucosidase activity","type":"exact"},{"name":"down regulation of beta-D-glucocerebrosidase activity","type":"exact"},{"name":"down regulation of beta-glucocerebrosidase activity","type":"exact"},{"name":"down regulation of beta-glucosylceramidase activity","type":"exact"},{"name":"down regulation of ceramide glucosidase activity","type":"exact"},{"name":"down regulation of glucocerebrosidase activity","type":"exact"},{"name":"down regulation of glucosphingosine glucosylhydrolase activity","type":"exact"},{"name":"down regulation of glucosylceramidase activity","type":"exact"},{"name":"down regulation of glucosylcerebrosidase activity","type":"exact"},{"name":"down regulation of glucosylsphingosine beta-D-glucosidase activity","type":"exact"},{"name":"down regulation of glucosylsphingosine beta-glucosidase activity","type":"exact"},{"name":"down regulation of psychosine hydrolase activity","type":"exact"},{"name":"down-regulation of D-glucosyl-N-acylsphingosine glucohydrolase activity","type":"exact"},{"name":"down-regulation of GlcCer-beta-glucosidase activity","type":"exact"},{"name":"down-regulation of acid beta-glucosidase activity","type":"exact"},{"name":"down-regulation of beta-D-glucocerebrosidase activity","type":"exact"},{"name":"down-regulation of beta-glucocerebrosidase activity","type":"exact"},{"name":"down-regulation of beta-glucosylceramidase activity","type":"exact"},{"name":"down-regulation of ceramide glucosidase activity","type":"exact"},{"name":"down-regulation of glucocerebrosidase activity","type":"exact"},{"name":"down-regulation of glucosphingosine glucosylhydrolase activity","type":"exact"},{"name":"down-regulation of glucosylceramidase activity","type":"exact"},{"name":"down-regulation of glucosylcerebrosidase activity","type":"exact"},{"name":"down-regulation of glucosylsphingosine beta-D-glucosidase activity","type":"exact"},{"name":"down-regulation of glucosylsphingosine beta-glucosidase activity","type":"exact"},{"name":"down-regulation of psychosine hydrolase activity","type":"exact"},{"name":"downregulation of D-glucosyl-N-acylsphingosine glucohydrolase activity","type":"exact"},{"name":"downregulation of GlcCer-beta-glucosidase activity","type":"exact"},{"name":"downregulation of acid beta-glucosidase activity","type":"exact"},{"name":"downregulation of beta-D-glucocerebrosidase activity","type":"exact"},{"name":"downregulation of beta-glucocerebrosidase activity","type":"exact"},{"name":"downregulation of beta-glucosylceramidase activity","type":"exact"},{"name":"downregulation of ceramide glucosidase activity","type":"exact"},{"name":"downregulation of glucocerebrosidase activity","type":"exact"},{"name":"downregulation of glucosphingosine glucosylhydrolase activity","type":"exact"},{"name":"downregulation of glucosylceramidase activity","type":"exact"},{"name":"downregulation of glucosylcerebrosidase activity","type":"exact"},{"name":"downregulation of glucosylsphingosine beta-D-glucosidase activity","type":"exact"},{"name":"downregulation of glucosylsphingosine beta-glucosidase activity","type":"exact"},{"name":"downregulation of psychosine hydrolase activity","type":"exact"},{"name":"inhibition of D-glucosyl-N-acylsphingosine glucohydrolase activity","type":"narrow"},{"name":"inhibition of GlcCer-beta-glucosidase activity","type":"narrow"},{"name":"inhibition of acid beta-glucosidase activity","type":"narrow"},{"name":"inhibition of beta-D-glucocerebrosidase activity","type":"narrow"},{"name":"inhibition of beta-glucocerebrosidase activity","type":"narrow"},{"name":"inhibition of beta-glucosylceramidase activity","type":"narrow"},{"name":"inhibition of ceramide glucosidase activity","type":"narrow"},{"name":"inhibition of glucocerebrosidase activity","type":"narrow"},{"name":"inhibition of glucosphingosine glucosylhydrolase activity","type":"narrow"},{"name":"inhibition of glucosylceramidase activity","type":"narrow"},{"name":"inhibition of glucosylcerebrosidase activity","type":"narrow"},{"name":"inhibition of glucosylsphingosine beta-D-glucosidase activity","type":"narrow"},{"name":"inhibition of glucosylsphingosine beta-glucosidase activity","type":"narrow"},{"name":"inhibition of psychosine hydrolase activity","type":"narrow"},{"name":"negative regulation of D-glucosyl-N-acylsphingosine glucohydrolase activity","type":"exact"},{"name":"negative regulation of GCase activity","type":"exact"},{"name":"negative regulation of GlcCer-beta-glucosidase activity","type":"exact"},{"name":"negative regulation of acid beta-glucosidase activity","type":"exact"},{"name":"negative regulation of beta-D-glucocerebrosidase activity","type":"exact"},{"name":"negative regulation of beta-glucocerebrosidase activity","type":"exact"},{"name":"negative regulation of beta-glucosylceramidase activity","type":"exact"},{"name":"negative regulation of ceramide glucosidase activity","type":"exact"},{"name":"negative regulation of glucocerebrosidase activity","type":"exact"},{"name":"negative regulation of glucosphingosine glucosylhydrolase activity","type":"exact"},{"name":"negative regulation of glucosylcerebrosidase activity","type":"exact"},{"name":"negative regulation of glucosylsphingosine beta-D-glucosidase activity","type":"exact"},{"name":"negative regulation of glucosylsphingosine beta-glucosidase activity","type":"exact"},{"name":"negative regulation of psychosine hydrolase activity","type":"exact"}],"termid":"GO:1905124"}


id: GO:0071290
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 platinum stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to platinum ion","termid":"GO:0070541"},{"relation_name":"is_a","term_name":"cellular response to metal ion","termid":"GO:0071248"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to platinum ion","synonyms":[{"name":"cellular response to platinum","type":"exact"}],"termid":"GO:0071290"}


id: PBO:0040821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bridging integrator 1","termid":"PBO:0040821"}


id: PBO:0087780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit VIIa of cytochrome c oxidase (Complex IV); Complex IV is the terminal member of the mitochondrial inner membrane electron transport chain","termid":"PBO:0087780"}


id: MONDO:0003195
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, serous adenocarcinoma that arises from the lining of the peritoneum. It affects females. The clinical behavior and pathologic characteristics are similar to the serous adenocarcinoma that arises from the ovary.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peritoneal carcinoma","termid":"MONDO:0002113"},{"relation_name":"is_a","term_name":"serous adenocarcinoma","termid":"MONDO:0005278"}],"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":"peritoneal serous adenocarcinoma","secondary_identifiers":["DOID:4901","NCIT:C40023"],"synonyms":[{"name":"peritoneum serous adenocarcinoma","type":"exact"},{"name":"primary peritoneal serous adenocarcinoma","type":"narrow"}],"termid":"MONDO:0003195","xrefs":{"Monarch":{"xref_id":"0003195"}}}


id: PBO:0059290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L42 pseudogene 5","termid":"PBO:0059290"}


id: MONDO:0020362
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inverse Marcus-Gunn phenomenon is a rare congenital synkinesis where jaw opening by the pterygoid muscle (during eating or yawning) causes eyelid drooping from inhibition of the oculomotor nerve to the levator palpebrae superioris. Familial occurrence has been reported.","definition_xrefs":["Orphanet:98951"],"direct_ancestors":[{"relation_name":"is_a","term_name":"jaw-winking syndrome","termid":"MONDO:0007946"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inverse Marcus-Gunn phenomenon","secondary_identifiers":["icd11.foundation:348052110","MEDGEN:1784220","UMLS:C5548210","GARD:19608"],"termid":"MONDO:0020362","xrefs":{"Monarch":{"xref_id":"0020362"}}}


id: PATO:0002243
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality inhering in a fluid (liquid or gas) by virtue of the amount of fluid which passes through a given surface per unit time.","direct_ancestors":[{"relation_name":"is_a","term_name":"flow rate","termid":"PATO:0001574"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fluid flow rate","synonyms":[{"name":"volume flow rate","type":"exact"},{"name":"volumetric flow rate","type":"exact"}],"termid":"PATO:0002243"}


id: FYPO:0008088
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the oscillations of homologous chromosomes which occurs at meiotic metaphase I is abolished.","definition_xrefs":["PMID:33529549"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromosome oscillation at meiotic metaphase I","termid":"FYPO:0008098"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000631"],"is_obsolete":false,"name":"abolished chromosome oscillation at meiotic metaphase I","synonyms":[{"name":"loss of chromosome oscillation at meiotic metaphase I","type":"exact"}],"termid":"FYPO:0008088"}


id: PBO:0116283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Splicing factor, structural and functional homolog of human FAM192A; plays structural role in intermediate spliceosomal C* complex, which executes exon ligation; required for survival upon exposure to K1 killer toxin; proposed to regulate double-strand break repair via non-homologous end-joining","termid":"PBO:0116283"}


id: PBO:0091167
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquinol-cytochrome-c reductase complex, Reiske ISP-associated subunit Qcr10","termid":"PBO:0091167"}


id: GO:0052016
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism resulting in the breakdown of glucan molecules within the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete catabolism by symbiont of host glucan (obsolete GO:0052016)","synonyms":[{"name":"catabolism by organism of host glucan","type":"exact"}],"termid":"GO:0052016"}


id: PBO:0047152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 183 member B, pseudogene","termid":"PBO:0047152"}


id: GO:0018817
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cis-2-oxohept-3-ene-1,7-dioate + H2O = 2,4-dihydroxy-hept-trans-2-ene-1,7-dioate.","definition_xrefs":["UM-BBD_reactionID:r0369"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"2-oxo-hept-3-ene-1,7-dioate hydratase activity","secondary_identifiers":["MetaCyc:HYDROXYHEPTA-DIENEDIOATE-HYDROXY-RXN","RHEA:42072"],"synonyms":[{"name":"2-oxo-hepta-3-ene-1,7-dioate hydratase activity","type":"exact"},{"name":"2-oxo-hepta-3-ene-1,7-dioic acid hydratase activity","type":"exact"},{"name":"HpaH","type":"related"}],"termid":"GO:0018817"}


id: PBO:0071314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L26 pseudogene 37","termid":"PBO:0071314"}


id: PBO:0053722
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 934","termid":"PBO:0053722"}


id: SO:0000132
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A single stranded oligo used for polymerase chain reaction.","direct_ancestors":[{"relation_name":"has_quality","term_name":"reverse","termid":"SO:0001031"},{"relation_name":"is_a","term_name":"primer","termid":"SO:0000112"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reverse_primer","synonyms":[{"name":"DNA reverse primer","type":"exact"},{"name":"reverse DNA primer","type":"exact"},{"name":"reverse primer","type":"exact"},{"name":"reverse primer oligo","type":"exact"},{"name":"reverse primer oligonucleotide","type":"exact"},{"name":"reverse primer sequence","type":"exact"}],"termid":"SO:0000132"}


id: MONDO:0014204
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bilateral striopallidodentate calcinosis","termid":"MONDO:0008947"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0002039"],"is_obsolete":false,"name":"basal ganglia calcification, idiopathic, 5","secondary_identifiers":["OMIM:615483","UMLS:C3809645","GARD:15973","MEDGEN:815975"],"synonyms":[{"name":"IBGC5","type":"related"},{"name":"basal ganglia calcification, idiopathic, 5","type":"exact"},{"name":"basal ganglia calcification, idiopathic, type 5","type":"exact"}],"termid":"MONDO:0014204","xrefs":{"Monarch":{"xref_id":"0014204"}}}


id: GO:1990387
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a lactosyl-ceramide derivative in which a galactose is linked to the galactose via an alpha 1,3 linkage (vs alpha 1,4 for globosides).","definition_xrefs":["GOC:hjd","PMID:22875802"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosphingolipid biosynthetic process","termid":"GO:0006688"},{"relation_name":"is_a","term_name":"ceramide biosynthetic process","termid":"GO:0046513"}],"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":"isogloboside biosynthetic process","termid":"GO:1990387"}


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":["ISBN:0395825172","GOC:jl"],"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"},{"relation_name":"is_a","term_name":"ammonium ion metabolic process","termid":"GO:0097164"}],"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: GO:0070776
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A histone acetyltransferase complex that has histone H3 acetyltransferase and coactivator activities. Subunits of the human complex include MYST3/MOZ, MYST4/MORF, ING5, EAF6 and one of BRPF1, BRD1/BRPF2 and BRPF3.","definition_xrefs":["PMID:18794358"],"direct_ancestors":[{"relation_name":"is_a","term_name":"H3 histone acetyltransferase complex","termid":"GO:0070775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005694","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"MOZ/MORF histone acetyltransferase complex","termid":"GO:0070776"}


id: PBO:0086170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for synthesis of diphthamide; required along with Dph1p, Kti11p, Jjj3p, and Dph5p; diphthamide is a modified histidine residue of translation elongation factor 2 (Eft1p or Eft2p); forms a complex with Dph1p that catalyzes the first step of diphthamide biosynthesis","termid":"PBO:0086170"}


id: GO:0004985
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with an opioid (any narcotic derived from or resembling opium), and transmitting the signal across the membrane by activating an associated G-protein.","definition_xrefs":["GOC:ai","GOC:bf","PMID:20494127"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"G protein-coupled opioid receptor activity","synonyms":[{"name":"opioid receptor activity","type":"broad"}],"termid":"GO:0004985"}


id: MONDO:0000529
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0000529 (obsolete MONDO:0000529)","termid":"MONDO:0000529","xrefs":{"Monarch":{"xref_id":"0000529"}}}


id: PBO:0036406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"folylpolyglutamate synthase Met7 (predicted)","termid":"PBO:0036406"}


id: PBO:0042163
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-C motif chemokine ligand 24","termid":"PBO:0042163"}


id: PR:P21547
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- var1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P21547"],"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":"ribosomal protein var1, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPMIT.08","synonyms":[{"name":"Spom972h-var1","type":"exact"}],"termid":"PR:P21547"}


id: FYPO:0001478
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of guanosine-diphosphatase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal guanosine-diphosphatase activity","termid":"FYPO:0001476"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000654","FYPO:0001985","FYPO:0000707","FYPO:0000661"],"is_obsolete":false,"name":"increased guanosine-diphosphatase activity","synonyms":[{"name":"increased GDPase activity","type":"exact"}],"termid":"FYPO:0001478"}


id: GO:0031761
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a fMet-Leu-Phe receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"fMet-Leu-Phe receptor binding","synonyms":[{"name":"N-formyl peptide receptor binding","type":"exact"},{"name":"fMet-Leu-Phe receptor ligand","type":"narrow"}],"termid":"GO:0031761"}


id: GO:0071523
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process of protein complex assembly in which the arrangement and bonding together of the set of components that form the protein complex is mediated by a TIR domain interaction.","definition_xrefs":["GOC:amm"],"gene_count":0,"genotype_count":0,"name":"obsolete TIR domain-mediated complex assembly (obsolete GO:0071523)","termid":"GO:0071523"}


id: PBO:0052243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium channel tetramerization domain containing 13","termid":"PBO:0052243"}


id: MONDO:0014510
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rhizomelic chondrodysplasia punctate that has material basis in homozygous or compound heterozygous mutation in the FAR1 gene on chromosome 11p15, which is required for the conversion of fatty acyl-CoAs to fatty alcohols, causing reduction or complete loss of FAR1 activity result in peroxisomal FAR1 deficiency.","definition_xrefs":["DOID:0081243"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"is_a","term_name":"chondrodysplasia punctata","termid":"MONDO:0019701"},{"relation_name":"is_a","term_name":"fatty acyl-CoA reductase defects","termid":"MONDO:0100275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0002525","MONDO:0005066","MONDO:0019053"],"is_obsolete":false,"name":"fatty acyl-CoA reductase 1 deficiency","secondary_identifiers":["Orphanet:438178","OMIM:616154","MEDGEN:863781","UMLS:C4015344","GARD:13319"],"synonyms":[{"name":"FAR1 deficiency","type":"exact"},{"name":"PFCRD","type":"related"},{"name":"fatty acyl-CoA reductase 1 deficiency","type":"exact"},{"name":"fatty acyl-CoA reductase 1 disorder","type":"exact"},{"name":"fatty acyl-CoA reductase 1 disorder or fatty acyl-CoA reductase 1 deficiency","type":"exact"},{"name":"peroxisomal fatty acyl-CoA reductase 1 disorder","type":"related"},{"name":"rhizomelic chondrodysplasia punctata type 4","type":"exact"},{"name":"severe intellectual disability-epilepsy-cataract syndrome due to FAR1 deficiency","type":"exact"},{"name":"severe intellectual disability-epilepsy-cataract syndrome due to fatty acyl-CoA reductase 1 deficiency","type":"exact"},{"name":"severe intellectual disability-epilepsy-cataract syndrome due to peroxisomal disorder","type":"exact"}],"termid":"MONDO:0014510","xrefs":{"Monarch":{"xref_id":"0014510"}}}


id: PBO:0029302
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delaminated_cell_wall","termid":"PBO:0029302"}


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


id: GO:1903997
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of non-membrane spanning protein tyrosine kinase activity.","definition_xrefs":["PMID:10518561","GOC:TermGenie","GO_REF:0000059","GOC:BHF","GOC:nc"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of non-membrane spanning protein tyrosine kinase activity (obsolete GO:1903997)","synonyms":[{"name":"activation of ATP:protein-L-tyrosine O-phosphotransferase (non-specific) activity","type":"narrow"},{"name":"activation of Bruton's tyrosine kinase activity","type":"narrow"},{"name":"activation of cytoplasmic protein tyrosine kinase activity","type":"narrow"},{"name":"activation of focal adhesion kinase activity","type":"narrow"},{"name":"activation of janus kinase 1 activity","type":"narrow"},{"name":"activation of janus kinase 2 activity","type":"narrow"},{"name":"activation of janus kinase 3 activity","type":"narrow"},{"name":"activation of non-membrane spanning protein tyrosine kinase activity","type":"narrow"},{"name":"activation of non-specific protein-tyrosine kinase activity","type":"narrow"},{"name":"activation of p60c-src protein tyrosine kinase activity","type":"narrow"},{"name":"positive regulation of ATP:protein-L-tyrosine O-phosphotransferase (non-specific) activity","type":"exact"},{"name":"positive regulation of Bruton's tyrosine kinase activity","type":"narrow"},{"name":"positive regulation of cytoplasmic protein tyrosine kinase activity","type":"narrow"},{"name":"positive regulation of focal adhesion kinase activity","type":"narrow"},{"name":"positive regulation of janus kinase 1 activity","type":"narrow"},{"name":"positive regulation of janus kinase 2 activity","type":"narrow"},{"name":"positive regulation of janus kinase 3 activity","type":"narrow"},{"name":"positive regulation of non-specific protein-tyrosine kinase activity","type":"exact"},{"name":"positive regulation of p60c-src protein tyrosine kinase activity","type":"narrow"},{"name":"up regulation of ATP:protein-L-tyrosine O-phosphotransferase (non-specific) activity","type":"exact"},{"name":"up regulation of Bruton's tyrosine kinase activity","type":"narrow"},{"name":"up regulation of cytoplasmic protein tyrosine kinase activity","type":"narrow"},{"name":"up regulation of focal adhesion kinase activity","type":"narrow"},{"name":"up regulation of janus kinase 1 activity","type":"narrow"},{"name":"up regulation of janus kinase 2 activity","type":"narrow"},{"name":"up regulation of janus kinase 3 activity","type":"narrow"},{"name":"up regulation of non-membrane spanning protein tyrosine kinase activity","type":"exact"},{"name":"up regulation of non-specific protein-tyrosine kinase activity","type":"exact"},{"name":"up regulation of p60c-src protein tyrosine kinase activity","type":"narrow"},{"name":"up-regulation of ATP:protein-L-tyrosine O-phosphotransferase (non-specific) activity","type":"exact"},{"name":"up-regulation of Bruton's tyrosine kinase activity","type":"narrow"},{"name":"up-regulation of cytoplasmic protein tyrosine kinase activity","type":"narrow"},{"name":"up-regulation of focal adhesion kinase activity","type":"narrow"},{"name":"up-regulation of janus kinase 1 activity","type":"narrow"},{"name":"up-regulation of janus kinase 2 activity","type":"narrow"},{"name":"up-regulation of janus kinase 3 activity","type":"narrow"},{"name":"up-regulation of non-membrane spanning protein tyrosine kinase activity","type":"exact"},{"name":"up-regulation of non-specific protein-tyrosine kinase activity","type":"exact"},{"name":"up-regulation of p60c-src protein tyrosine kinase activity","type":"narrow"},{"name":"upregulation of ATP:protein-L-tyrosine O-phosphotransferase (non-specific) activity","type":"exact"},{"name":"upregulation of Bruton's tyrosine kinase activity","type":"narrow"},{"name":"upregulation of cytoplasmic protein tyrosine kinase activity","type":"narrow"},{"name":"upregulation of focal adhesion kinase activity","type":"narrow"},{"name":"upregulation of janus kinase 1 activity","type":"narrow"},{"name":"upregulation of janus kinase 2 activity","type":"narrow"},{"name":"upregulation of janus kinase 3 activity","type":"narrow"},{"name":"upregulation of non-membrane spanning protein tyrosine kinase activity","type":"exact"},{"name":"upregulation of non-specific protein-tyrosine kinase activity","type":"exact"},{"name":"upregulation of p60c-src protein tyrosine kinase activity","type":"narrow"}],"termid":"GO:1903997"}


id: GO:1903145
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any actin filament that is part of a cell cortex of cell tip.","definition_xrefs":["PMID:20807799","GOC:TermGenie","PMID:24954052","GO_REF:0000064"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament","termid":"GO:0005884"},{"relation_name":"part_of","term_name":"cell cortex of cell tip","termid":"GO:0051285"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015629"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005938"}],"interesting_parent_ids":["GO:0005575","GO:0015629","GO:0005938","GO:0005737"],"is_obsolete":false,"name":"actin filament of cell cortex of cell tip","synonyms":[{"name":"actin filament of cell cortex of cell end","type":"exact"},{"name":"microfilament of cell cortex of cell end","type":"exact"},{"name":"microfilament of cell cortex of cell tip","type":"exact"}],"termid":"GO:1903145"}


id: PBO:0054097
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 1450","termid":"PBO:0054097"}


id: PBO:0073150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEC24B antisense RNA 1","termid":"PBO:0073150"}


id: GO:0018547
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the removal of one or more nitrite (NO2-) groups from nitroglycerin or a derivative.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete nitroglycerin reductase activity (obsolete GO:0018547)","secondary_identifiers":["Reactome:R-HSA-9620103"],"synonyms":[{"name":"NG reductase activity","type":"exact"}],"termid":"GO:0018547"}


id: MONDO:0006452
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, usually aggressive, primary thymic carcinoma, characterized by the presence of tumor cells morphologically resembling soft tissue sarcoma.","definition_xrefs":["NCIT:C6463"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"thymus squamous cell carcinoma","termid":"MONDO:0003493"},{"relation_name":"is_a","term_name":"sarcomatoid carcinoma","termid":"MONDO:0006406"},{"relation_name":"is_a","term_name":"thymic carcinoma","termid":"MONDO:0006451"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"thymic sarcomatoid carcinoma","secondary_identifiers":["DOID:8138","EFO:1000577","MEDGEN:234772","UMLS:C1335924"],"synonyms":[{"name":"Thymus sarcomatoid carcinoma","type":"exact"},{"name":"sarcomatoid carcinoma of Thymus","type":"exact"},{"name":"sarcomatoid carcinoma of the Thymus","type":"exact"},{"name":"thymic carcinosarcoma","type":"exact"},{"name":"thymic sarcomatoid carcinoma","type":"exact"},{"name":"thymic spindle cell carcinoma","type":"exact"},{"name":"thymus sarcomatoid carcinoma","type":"exact"}],"termid":"MONDO:0006452","xrefs":{"Monarch":{"xref_id":"0006452"}}}


id: MONDO:0013975
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any pure hair and nail ectodermal dysplasia in which the cause of the disease is a mutation in the KRT74 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pure hair and nail ectodermal dysplasia","termid":"MONDO:0019071"}],"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":"ectodermal dysplasia 7, hair/nail type","secondary_identifiers":["OMIM:614929","GARD:18065","UMLS:C3554117","DOID:0111660","MEDGEN:767031"],"synonyms":[{"name":"ECTD7","type":"related"},{"name":"KRT74 pure hair and nail ectodermal dysplasia","type":"exact"},{"name":"ectodermal dysplasia 7, hair/nail type","type":"exact"},{"name":"pure hair and nail ectodermal dysplasia caused by mutation in KRT74","type":"exact"}],"termid":"MONDO:0013975","xrefs":{"Monarch":{"xref_id":"0013975"}}}


id: PBO:0065514
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein prenyltransferase alpha subunit repeat containing 1","termid":"PBO:0065514"}


id: PBO:0083600
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; identified by fungal homology and RT-PCR","termid":"PBO:0083600"}


id: PBO:0044077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CSTF3 divergent transcript","termid":"PBO:0044077"}


id: PBO:0078292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 25-1","termid":"PBO:0078292"}


id: PBO:0079604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2F pseudogene 1","termid":"PBO:0079604"}


id: PBO:0089338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERMES complex GTPase subunit Gem1","termid":"PBO:0089338"}


id: PBO:0087865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcriptional activator of the basic leucine zipper (bZIP) family; required for transcription of genes involved in resistance to arsenic compounds; directly binds trivalent arsenic (As(III)) as does K. lactis ortholog, KIYAP8","termid":"PBO:0087865"}


id: MONDO:0002542
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm that arises from glial cells in the spinal cord. Representative examples include astrocytoma, oligodendroglioma, and ependymoma.","definition_xrefs":["NCIT:C4534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spinal cord cancer","termid":"MONDO:0003544"},{"relation_name":"is_a","term_name":"malignant glioma","termid":"MONDO:0100342"}],"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":"spinal cord glioma","secondary_identifiers":["MEDGEN:423646","DOID:3185","SCTID:254946004","UMLS:C2937245"],"synonyms":[{"name":"glial neoplasm spinal cord","type":"exact"},{"name":"glial tumor of spinal cord","type":"exact"},{"name":"glial tumour of spinal cord","type":"exact"},{"name":"glioma of spinal cord","type":"exact"},{"name":"malignant glioma of spinal cord","type":"exact"},{"name":"spinal cord glial neoplasm","type":"exact"},{"name":"spinal cord glial tumor","type":"exact"},{"name":"spinal cord glial tumour","type":"exact"},{"name":"spinal cord glioma","type":"exact"},{"name":"spinal cord malignant glioma","type":"exact"}],"termid":"MONDO:0002542","xrefs":{"Monarch":{"xref_id":"0002542"}}}


id: MONDO:0022821
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital benign spinal muscular atrophy dominant","termid":"MONDO:0022821","xrefs":{"Monarch":{"xref_id":"0022821"}}}


id: GO:0160104
data:
  {"annotated_genes":["SJAG_00886"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[61220],"is_not":false,"summary":null,"term":"GO:0160104"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction:guanosine(26) in tRNA + 2 S-adenosyl-L-methionine = 2 H+ + N(2)-dimethylguanosine(26) in tRNA + 2 S-adenosyl-L-homocysteine.","definition_xrefs":["EC:2.1.1.216"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-methyltransferase activity","termid":"GO:0008170"},{"relation_name":"is_a","term_name":"tRNA (guanine) methyltransferase activity","termid":"GO:0016423"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00886":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0140098","GO:0003824","GO:0140101","GO:0003674","GO:0016740","GO:0016741"],"is_obsolete":false,"name":"tRNA (guanine(26)-N2)-dimethyltransferase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["RHEA:43140","Reactome:R-HSA-6782416"],"synonyms":[{"name":"tRNA (guanine(26)-N(2))-dimethyltransferase activity","type":"exact"},{"name":"tRNA (guanosine(26)-N(2))-dimethyltransferase activity","type":"exact"},{"name":"tRNA (m(2)2G26)dimethyltransferase","type":"exact"}],"termid":"GO:0160104","terms_by_termid":{"GO:0160104":null}}


id: PBO:0055944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LRRC52 antisense RNA 1","termid":"PBO:0055944"}


id: MONDO:0020636
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited susceptibility to mycobacterial diseases","termid":"MONDO:0019146"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mendelian susceptibility to mycobacterial diseases due to a complete deficiency","termid":"MONDO:0020636","xrefs":{"Monarch":{"xref_id":"0020636"}}}


id: FYPO:0002243
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of acid phosphatase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal acid phosphatase activity","termid":"FYPO:0001044"},{"relation_name":"is_a","term_name":"increased phosphatase activity","termid":"FYPO:0004415"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000707","FYPO:0000661","FYPO:0000652","FYPO:0000654"],"is_obsolete":false,"name":"increased acid phosphatase activity","termid":"FYPO:0002243"}


id: PATO:0000077
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the whether the bearer's disposition to react to a stimulus or an agent.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality","termid":"PATO:0001018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"response to","synonyms":[{"name":"responsivity","type":"related"}],"termid":"PATO:0000077"}


id: PBO:0063006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"platelet activating factor acetylhydrolase 1b catalytic subunit 2","termid":"PBO:0063006"}


id: PBO:0057556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 671","termid":"PBO:0057556"}


id: PBO:0085764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase of unknown cellular role; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and nucleus; null mutant is sensitive to expression of the top1-T722A allele; not an essential gene; relocalizes from nucleus to cytoplasm upon DNA replication stress","termid":"PBO:0085764"}


id: PBO:0062364
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 X member 1","termid":"PBO:0062364"}


id: GO:1904110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of plus-end directed microfilament motor activity.","definition_xrefs":["GOC:kmv","GO_REF:0000059","GOC:TermGenie","PMID:25717181"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of plus-end directed microfilament motor activity (obsolete GO:1904110)","synonyms":[{"name":"regulation of barbed-end directed actin-filament motor activity","type":"exact"},{"name":"regulation of plus-end directed actin filament motor activity","type":"related"},{"name":"regulation of plus-end directed actin-filament motor activity","type":"exact"}],"termid":"GO:1904110"}


id: PBO:0042849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 58","termid":"PBO:0042849"}


id: PBO:0117440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pheromone-MAPK scaffold Sms1","termid":"PBO:0117440"}


id: FYPO:0000062
data:
  {"alleles_by_uniquename":{"SJAG_01745:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01745","name":"lem2delta","uniquename":"SJAG_01745:allele-1"},"SJAG_01906:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01906","name":"nem1delta","uniquename":"SJAG_01906:allele-1"},"SJAG_02763:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02763","name":"ned1delta","uniquename":"SJAG_02763:allele-1"},"SJAG_02763:allele-2":{"allele_type":"amino_acid_mutation","description":"D422E,D424E","gene_uniquename":"SJAG_02763","name":"ned1cat","synonyms":[{"name":"Catalytic mutant","reference":"PMID:26774782","type":"exact"}],"uniquename":"SJAG_02763:allele-2"},"SJAG_02763:allele-4":{"allele_type":"amino_acid_mutation","description":"S235E; S651E","gene_uniquename":"SJAG_02763","name":"ned1S235E/S651E","synonyms":[{"name":"phosphomimetic","reference":"PMID:26774782","type":"exact"}],"uniquename":"SJAG_02763:allele-4"},"SJAG_02763:allele-5":{"allele_type":"amino_acid_mutation","description":"S499E; 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id: PBO:0035810
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H2A_phosphorylation_during_vegetative_growth","termid":"PBO:0035810"}


id: GO:0002939
data:
  {"annotated_genes":["SJAG_00255","SJAG_04993"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71546,78475],"is_not":false,"summary":null,"term":"GO:0002939"}]},"cv_name":"biological_process","definition":"The process whereby a guanine in tRNA is methylated at position N1 of the guanine.","definition_xrefs":["ISBN:1555811337","ISBN:155581073X"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA methylation","termid":"GO:0030488"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00255":null,"SJAG_04993":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006399"],"is_obsolete":false,"name":"tRNA N1-guanine methylation","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"tRNA m1-guanine biosynthesis","type":"related"}],"termid":"GO:0002939","terms_by_termid":{"GO:0002939":null}}


id: MONDO:0044925
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma arising in the oral cavity. Most oral cavity carcinomas are squamous cell carcinomas of the tongue, buccal mucosa, or gums. Less frequent morphologic variants include mucoepidermoid carcinoma and adenocarcinoma.","definition_xrefs":["NCIT:C8990"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oral cavity cancer","termid":"MONDO:0005515"},{"relation_name":"is_a","term_name":"digestive system carcinoma","termid":"MONDO:0006181"},{"relation_name":"is_a","term_name":"lip and oral cavity carcinoma","termid":"MONDO:0023644"}],"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:0004992","MONDO:0004335"],"is_obsolete":false,"name":"oral cavity carcinoma","secondary_identifiers":["MEDGEN:57468","UMLS:C0151546"],"synonyms":[{"name":"carcinoma of mouth","type":"exact"},{"name":"carcinoma of oral cavity","type":"exact"},{"name":"carcinoma of the oral cavity","type":"exact"},{"name":"mouth carcinoma","type":"exact"},{"name":"oral cavity cancer","type":"broad"},{"name":"oral cavity carcinoma","type":"exact"}],"termid":"MONDO:0044925","xrefs":{"Monarch":{"xref_id":"0044925"}}}


id: PBO:0064787
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase, Mg2+/Mn2+ dependent 1G","termid":"PBO:0064787"}


id: FYPO:0004746
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 heterochromatin assembly involved in chromatin silencing at the centromere outer repeat region does not occur.","definition_xrefs":["GO:0031507","PMID:24240238","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal heterochromatin assembly at centromere outer repeat during vegetative growth","termid":"FYPO:0003098"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"},{"relation_name":"is_a","term_name":"abnormal chromatin remodeling","termid":"FYPO:0006356"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000641"],"is_obsolete":false,"name":"abolished heterochromatin assembly involved in chromatin silencing at centromere outer repeat","synonyms":[{"name":"abolished heterochromatin assembly involved in chromatin silencing at centromere otr","type":"exact"},{"name":"abolished heterochromatin assembly involved in chromatin silencing at centromere outer repeat during mitotic cell cycle","type":"related"},{"name":"abolished heterochromatin assembly involved in chromatin silencing at centromere outer repeat during vegetative growth","type":"exact"},{"name":"abolished heterochromatin assembly involved in chromatin silencing at centromere outer repeat region","type":"exact"},{"name":"abolished heterochromatin assembly involved in chromatin silencing at pericentric region","type":"related"},{"name":"abolished heterochromatin assembly involved in chromatin silencing at pericentromeric region","type":"related"},{"name":"heterochromatin assembly involved in chromatin silencing at centromere outer repeat abolished","type":"exact"}],"termid":"FYPO:0004746"}


id: PBO:0083808
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential protein that promotes the first step of splicing; required for the final stages of spliceosome maturation and activation; interacts with Prp2p, which may release Spp2p from the spliceosome following the first cleavage reaction; stimulates Prp2p ATPase activity","termid":"PBO:0083808"}


id: GO:0018579
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: protocatechuate + O2 = 4-carboxy-2-hydroxymuconate semialdehyde.","definition_xrefs":["EC:1.13.11.8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"protocatechuate 4,5-dioxygenase activity","secondary_identifiers":["MetaCyc:PROTOCATECHUATE-45-DIOXYGENASE-RXN","RHEA:24044","UM-BBD_reactionID:r0144"],"synonyms":[{"name":"protocatechuate 4,5-oxygenase activity","type":"related"},{"name":"protocatechuate:oxygen 4,5-oxidoreductase (decyclizing)","type":"related"},{"name":"protocatechuic 4,5-dioxygenase activity","type":"related"},{"name":"protocatechuic 4,5-oxygenase activity","type":"related"}],"termid":"GO:0018579"}


id: GO:1990553
data:
  {"annotated_genes":["SJAG_03334"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101722],"is_not":false,"summary":null,"term":"GO:1990553"}]},"cv_name":"biological_process","definition":"The process in which 5'-adenylyl sulfate is transported across a mitochondrial membrane, into or out of the mitochondrion.","definition_xrefs":["PMID:24296033"],"direct_ancestors":[{"relation_name":"is_a","term_name":"5'-adenylyl sulfate transmembrane transport","termid":"GO:1902558"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03334":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"mitochondrial 5'-adenylyl sulfate transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990553","terms_by_termid":{"GO:1990553":null}}


id: GO:0045005
data:
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id: MONDO:0043257
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pemphigus foliaceus","termid":"MONDO:0019324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"pemphigus and fogo selvagem","secondary_identifiers":["Orphanet:636955","UMLS:C0263314","GARD:7353","HGNC:3048","MEDGEN:120470","MESH:C535551","SCTID:46459009"],"synonyms":[{"name":"Brazilian pemphigus","type":"related"},{"name":"Brazilian pemphigus foliaceus","type":"exact"},{"name":"FS","type":"related"},{"name":"South American pemphigus","type":"related"},{"name":"amendola's syndrome","type":"related"},{"name":"endemic pemphigus foliaceus","type":"related"},{"name":"fogo selvagem","type":"related"},{"name":"wild fire","type":"related"},{"name":"wildfire pemphigus","type":"related"}],"termid":"MONDO:0043257","xrefs":{"Monarch":{"xref_id":"0043257"}}}


id: PR:Q09772
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA repair and recombination protein RAD54B that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00275","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":"meiotic recombination protein rdh54 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22F3.03c","secondary_identifiers":["UniProtKB:Q09772"],"synonyms":[{"name":"ATP-dependent helicase rdh54 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RAD54 protein homolog 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-RAD54B","type":"exact"},{"name":"meiotically up-regulated gene 34 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09772"}


id: PBO:0088079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin (Ub) chain assembly factor (E4); forms branched Ub chains on substrates destined for degradation, catalyzing K48-linked multi-monoubiquitination of K29-linked Ub chains assembled by the Ub-ligase Ufd4p; involved in the Ub-fusion degradation pathway, OLE membrane fluidity pathway, stress response survival and the ERAD pathway for misfolded proteins, where it promotes ubiquitination and transfer of ERAD substrates to Rad23p; U-box family member; homologous to human Ufd2a and Ufd2b","termid":"PBO:0088079"}


id: PATO:0002467
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer resembling a thin narrow strip.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lathlike","termid":"PATO:0002467"}


id: FYPO:0003910
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 retrotransposon nucleocapsid complexes (also called virus-like particles, VLPs) to the nucleus is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to nucleus during vegetative growth","termid":"FYPO:0001424"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"abolished VLP localization to nucleus during vegetative growth","synonyms":[{"name":"VLP localization to nucleus abolished during vegetative growth","type":"exact"},{"name":"abolished VLP localisation to nucleus during vegetative growth","type":"exact"},{"name":"abolished VLP localization in nucleus during vegetative growth","type":"exact"},{"name":"abolished VLP localization to nucleus during vegetative growth during mitotic cell cycle","type":"related"},{"name":"abolished retrotransposon nucleocapsid localization to nucleus during vegetative growth","type":"exact"},{"name":"abolished virus-like particle localization to nucleus during vegetative growth","type":"exact"}],"termid":"FYPO:0003910"}


id: GO:1903584
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of histone deubiquitination.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:24526689"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone deubiquitination (obsolete GO:1903584)","synonyms":[{"name":"regulation of histone deubiquitinylation","type":"exact"},{"name":"regulation of histone deubiquitylation","type":"exact"}],"termid":"GO:1903584"}


id: GO:0021832
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of cells to one another to form groups of cells involved in cerebral cortex tangential migration.","definition_xrefs":["GOC:cls","PMID:12626695","GOC:dgh","GO_REF:0000021","GOC:dph","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell adhesion via plasma-membrane adhesion molecules","termid":"GO:0098742"},{"relation_name":"part_of","term_name":"cerebral cortex tangential migration using cell-cell interactions","termid":"GO:0021823"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"cell-cell adhesion involved in cerebral cortex tangential migration using cell-cell interactions","termid":"GO:0021832"}


id: GO:0120504
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric complex capable of glycosyltransferase activity required for the elongation of heparan sulfate chains. In humans, the complex consists of EXT1 and EXT2. In Drosophila, the complex consists of ttv and sotv.","definition_xrefs":["GOC:sjm","PMID:36402845","PMID:14998928","PMID:36593275"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"EXT1-EXT2 complex","synonyms":[{"name":"EXT1-EXT2 heparan sulfate biosynthesis complex","type":"exact"},{"name":"exostosin complex","type":"exact"}],"termid":"GO:0120504"}


id: GO:0140162
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism initiates, promotes, or enhances vasodilation via the action of a venom that activates bradykinin-dependent signaling, concomittantly reducing blood pressure in the bitten/stung organism. This can take place via several mechanisms that affect endogenous bradykinin: either increasing its release by kallikrein-like proteases, increasing bradykinin action by potentiation, or inhibiting bradykinin degradation.","definition_xrefs":["PMID:31370142"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated perturbation of G protein-coupled receptor signaling pathway","termid":"GO:0044513"},{"relation_name":"is_a","term_name":"venom-mediated vasodilation","termid":"GO:0044551"}],"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":"venom-mediated vasodilation by activation of bradykinin-dependent signaling","synonyms":[{"name":"venom-mediated vasodilation through activity of bradykinin","type":"exact"}],"termid":"GO:0140162"}


id: PBO:0047385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 22","termid":"PBO:0047385"}


id: GO:0050351
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + trimetaphosphate = 2 H+ + triphosphate.","definition_xrefs":["EC:3.6.1.2","RHEA:11088"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"trimetaphosphatase activity","secondary_identifiers":["KEGG_REACTION:R02504","MetaCyc:TRIMETAPHOSPHATASE-RXN"],"synonyms":[{"name":"inorganic trimetaphosphatase activity","type":"related"},{"name":"trimetaphosphate hydrolase activity","type":"related"}],"termid":"GO:0050351"}


id: PBO:0055487
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 2920","termid":"PBO:0055487"}


id: GO:0170043
data:
  {"annotated_genes":["SJAG_00635","SJAG_00695","SJAG_02972"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019240"},{"annotations":[110888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071269"},{"annotations":[72578],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006592"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of non-proteinogenic amino acids.","definition_xrefs":["GOC:ew"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic acid biosynthetic process","termid":"GO:0046394"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid metabolic process","termid":"GO:0170041"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00635":null,"SJAG_00695":null,"SJAG_02972":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006520"],"is_obsolete":false,"name":"non-proteinogenic amino acid biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"non-proteinogenic amino acid anabolism","type":"exact"},{"name":"non-proteinogenic amino acid formation","type":"exact"},{"name":"non-proteinogenic amino acid synthesis","type":"exact"},{"name":"non-proteinogenic biosynthesis","type":"exact"}],"termid":"GO:0170043","terms_by_termid":{"GO:0006592":null,"GO:0019240":null,"GO:0071269":null}}


id: GO:1904288
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a BAT3 complex.","definition_xrefs":["GOC:TermGenie","GOC:PARL","PMID:23246001","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"BAT3 complex binding","synonyms":[{"name":"BAG6-UBL4A-TRC35 complex binding","type":"exact"},{"name":"BAT3-TRC35-UBL4A complex binding","type":"related"},{"name":"Bag6 complex binding","type":"exact"}],"termid":"GO:1904288"}


id: MOD:01961
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because redundant and identical to MOD:01785. Remap to MOD:01785.","definition_xrefs":["RESID:AA0536#THR","PubMed:17687277","PubMed:16618936","PubMed:17051152","PubMed:18555071"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:01961 O-(L-isoglutamyl)-L-threonine (THR) (obsolete MOD:01961)","synonyms":[{"name":"(2S)-2-amino-5-([(1S,2R)-1-amino-1-carboxypropan-2-yl]oxy)-5-oxopentanoic acid","type":"exact"},{"name":"(2S,3R)-2-amino-3-([(4S)-4-amino-4-carboxybutanoyl]oxy)-propanoic acid","type":"exact"},{"name":"5-(threon-O3-yl)glutamate","type":"exact"},{"name":"O(beta)-(gamma-glutamyl)threonine","type":"exact"},{"name":"O-(L-isoglutamyl)-L-threonine","type":"exact"},{"name":"O3-(isoglutamyl)threonine","type":"exact"}],"termid":"MOD:01961"}


id: PBO:0050114
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 24","termid":"PBO:0050114"}


id: GO:0031036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of a bipolar filament composed of myosin II molecules.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myosin filament assembly","termid":"GO:0031034"},{"relation_name":"is_a","term_name":"myosin II filament organization","termid":"GO:0031038"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0008150","GO:0007010","GO:0044085","GO:0030036","GO:0065003"],"is_obsolete":false,"name":"myosin II filament assembly","synonyms":[{"name":"myosin II polymerization","type":"related"}],"termid":"GO:0031036"}


id: FYPO:0000394
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the G1/S transition of the mitotic cell cycle is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"},{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle phase transition","termid":"FYPO:0005275"}],"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:0000631"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0000631"],"is_obsolete":false,"name":"abnormal mitotic G1/S phase transition","synonyms":[{"name":"abnormal G1/S phase transition during mitotic cell cycle","type":"exact"},{"name":"abnormal cell cycle progression through the G1/S phase transition","type":"exact"},{"name":"abnormal mitotic G1/S cell cycle phase transition","type":"exact"},{"name":"abnormal mitotic G1/S phase transition during vegetative growth","type":"exact"},{"name":"abnormal mitotic cell cycle G1/S phase transition","type":"exact"},{"name":"cell cycle progression through the G1/S phase transition: abnormal","type":"related"}],"termid":"FYPO:0000394"}


id: PR:Q9Y822
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mrpl16 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y822"],"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":"54S ribosomal protein L16, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1105.03c","synonyms":[{"name":"Spom972h-mrpl16","type":"exact"}],"termid":"PR:Q9Y822"}


id: PATO:0001700
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A sleep pattern which has irregular start and/or end times.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sleep pattern","termid":"PATO:0000062"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"irregular sleep pattern","termid":"PATO:0001700"}


id: PBO:0052586
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine rich nucleolar protein 1 pseudogene 4","termid":"PBO:0052586"}


id: GO:0070123
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with transforming growth factor beta to initiate a change in cell activity; facilitates ligand binding to type I and type II TGF-beta receptors.","definition_xrefs":["GOC:BHF","GOC:mah","PMID:9759503"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transforming growth factor beta receptor activity","termid":"GO:0005024"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0004672","GO:0016301","GO:0003824","GO:0140096","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"transforming growth factor beta receptor activity, type III","synonyms":[{"name":"betaglycan","type":"narrow"},{"name":"endoglin","type":"narrow"},{"name":"transforming growth factor beta ligand binding to type III receptor","type":"related"},{"name":"type III TGF-beta receptor activity","type":"exact"},{"name":"type III TGFbeta receptor activity","type":"exact"},{"name":"type III transforming growth factor beta receptor activity","type":"exact"}],"termid":"GO:0070123"}


id: PBO:0039729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apolipoprotein C1","termid":"PBO:0039729"}


id: MONDO:0012485
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the S1PR2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 68","secondary_identifiers":["MEDGEN:324374","GARD:22625","UMLS:C1835854","MESH:C563669","OMIM:610419","DOID:0110519"],"synonyms":[{"name":"DFNB68","type":"narrow"},{"name":"S1PR2 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 68","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 68","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in S1PR2","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 68","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 68","type":"exact"},{"name":"deafness, autosomal recessive 68","type":"narrow"}],"termid":"MONDO:0012485","xrefs":{"Monarch":{"xref_id":"0012485"}}}


id: MONDO:0054739
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Fraser syndrome","termid":"MONDO:0009046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0006025"],"is_obsolete":false,"name":"Fraser syndrome 3","secondary_identifiers":["DOID:0111406","OMIM:617667","UMLS:C4540040","MEDGEN:1621907"],"synonyms":[{"name":"FRASRS3","type":"related"},{"name":"Fraser syndrome 3","type":"exact"}],"termid":"MONDO:0054739","xrefs":{"Monarch":{"xref_id":"0054739"}}}


id: PBO:0041929
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromobox 1 pseudogene 4","termid":"PBO:0041929"}


id: PBO:0085004
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Negative regulator of eIF2 kinase Gcn2p; competes with Gcn2p for binding to Gcn1p; may contribute to regulation of translation in response to starvation via regulation of Gcn2p; binds to monomeric actin and to ribosomes and polyribosomes; ortholog of mammalian IMPACT","termid":"PBO:0085004"}


id: PBO:0054765
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 2177","termid":"PBO:0054765"}


id: PBO:0058061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4281","termid":"PBO:0058061"}


id: GO:1990575
data:
  {"annotated_genes":["SJAG_00543"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[108279],"is_not":false,"summary":null,"term":"GO:1990575"}]},"cv_name":"biological_process","definition":"The process in which L-ornithine is transported across a mitochondrial membrane, into or out of the mitochondrion.","definition_xrefs":["PMID:9237680"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-ornithine transmembrane transport","termid":"GO:1903352"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00543":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"mitochondrial L-ornithine transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0000066"],"synonyms":[{"name":"mitochondrial ornithine transmembrane transport","type":"broad"},{"name":"mitochondrial ornithine transport","type":"related"}],"termid":"GO:1990575","terms_by_termid":{"GO:1990575":null}}


id: GO:1901311
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of gene expression involved in extracellular matrix organization.","definition_xrefs":["GOC:TermGenie","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of gene expression involved in extracellular matrix organization (obsolete GO:1901311)","synonyms":[{"name":"regulation of expression of extracellular matrix proteins","type":"exact"},{"name":"regulation of extracellular matrix protein production","type":"related"}],"termid":"GO:1901311"}


id: PBO:0029066
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_riboflavin_binding","termid":"PBO:0029066"}


id: MONDO:0023206
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A low or intermediate grade well differentiated tumor with neuroendocrine differentiation that arises from the pancreas. It is characterized by the presence of a clinical syndrome that results from hormone hypersecretion.","definition_xrefs":["NCIT:C45840"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatic neuroendocrine tumor","termid":"MONDO:0019954"},{"relation_name":"is_a","term_name":"functioning endocrine neoplasm","termid":"MONDO:0021120"}],"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":"functional pancreatic neuroendocrine tumor","secondary_identifiers":["GARD:22053","UMLS:C1708107","Orphanet:506060","MEDGEN:310778"],"synonyms":[{"name":"functional pancreatic NET","type":"exact"},{"name":"functional pancreatic neuroendocrine tumor","type":"exact"},{"name":"functioning PNET","type":"exact"},{"name":"functioning neuroendocrine tumor of pancreas","type":"related"},{"name":"functioning neuroendocrine tumour of pancreas","type":"related"},{"name":"functioning pancreatic NET","type":"exact"},{"name":"functioning pancreatic endocrine tumor","type":"exact"},{"name":"functioning pancreatic endocrine tumour","type":"exact"},{"name":"functioning pancreatic neuroendocrine tumor","type":"exact"},{"name":"functioning pancreatic neuroendocrine tumour","type":"exact"},{"name":"functioning well differentiated pancreatic endocrine neoplasm","type":"exact"},{"name":"functioning well differentiated pancreatic endocrine tumor","type":"exact"},{"name":"functioning well differentiated pancreatic endocrine tumour","type":"exact"},{"name":"functioning well-differentiated NEN of pancreas","type":"exact"},{"name":"functioning well-differentiated neuroendocrine neoplasm of pancreas","type":"exact"},{"name":"functioning well-differentiated pancreatic NEN","type":"exact"},{"name":"functioning well-differentiated pancreatic neuroendocrine neoplasm","type":"exact"},{"name":"syndromic pancreatic NET","type":"exact"},{"name":"syndromic pancreatic neuroendocrine tumor","type":"exact"},{"name":"syndromic pancreatic neuroendocrine tumour","type":"exact"}],"termid":"MONDO:0023206","xrefs":{"Monarch":{"xref_id":"0023206"}}}


id: GO:0034275
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving kynurenic acid, 4-hydroxyquinoline-2-carboxylic acid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"kynurenic acid metabolic process","synonyms":[{"name":"4-hydroxyquinoline-2-carboxylic acid metabolic process","type":"exact"},{"name":"kynurenic acid metabolism","type":"exact"}],"termid":"GO:0034275"}


id: GO:0008351
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete microtubule severing activity (obsolete GO:0008351)","synonyms":[{"name":"microtubule severing activity","type":"exact"}],"termid":"GO:0008351"}


id: FYPO:0008215
data:
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id: PBO:0043279
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id: PBO:0064638
data:
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id: GO:1902481
data:
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id: GO:0006710
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id: GO:0033554
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id: MONDO:0021086
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the upper or lower gingiva.","definition_xrefs":["NCIT:C3057"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gingival disorder","termid":"MONDO:0002021"},{"relation_name":"is_a","term_name":"odontogenic neoplasm","termid":"MONDO:0021192"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gingival neoplasm","secondary_identifiers":["UMLS:C0017570","SCTID:126792007","MEDGEN:6605"],"synonyms":[{"name":"gingiva neoplasm","type":"exact"},{"name":"gingiva neoplasm (disease)","type":"exact"},{"name":"gingiva tumor","type":"exact"},{"name":"gingiva tumour","type":"exact"},{"name":"gingival neoplasm","type":"exact"},{"name":"gingival tumor","type":"exact"},{"name":"gingival tumour","type":"exact"},{"name":"gum neoplasm","type":"exact"},{"name":"gum tumor","type":"exact"},{"name":"gum tumour","type":"exact"},{"name":"neoplasm of gingiva","type":"exact"},{"name":"neoplasm of gum","type":"exact"},{"name":"neoplasm of the gingiva","type":"exact"},{"name":"neoplasm of the gum","type":"exact"},{"name":"tumor of gingiva","type":"exact"},{"name":"tumor of gum","type":"exact"},{"name":"tumor of the gingiva","type":"exact"},{"name":"tumor of the gum","type":"exact"},{"name":"tumour of gingiva","type":"exact"},{"name":"tumour of gum","type":"exact"},{"name":"tumour of the gingiva","type":"exact"},{"name":"tumour of the gum","type":"exact"}],"termid":"MONDO:0021086","xrefs":{"Monarch":{"xref_id":"0021086"}}}


id: PR:Q9P7K8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A transcription elongation factor SPT4 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03873"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation factor spt4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC21C3.16c","secondary_identifiers":["UniProtKB:Q9P7K8"],"synonyms":[{"name":"Spom972h-SUPT4H1","type":"exact"},{"name":"chromatin elongation factor spt4 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P7K8"}


id: MONDO:0009011
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete constriction rings syndrome (obsolete MONDO:0009011)","termid":"MONDO:0009011","xrefs":{"Monarch":{"xref_id":"0009011"}}}


id: GO:1901671
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of superoxide dismutase activity.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of oxidoreductase activity","termid":"GO:0051353"},{"relation_name":"is_a","term_name":"regulation of superoxide dismutase activity","termid":"GO:1901668"}],"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 superoxide dismutase activity","synonyms":[{"name":"activation of Cu,Zn-SOD","type":"related"},{"name":"activation of Cu-Zn superoxide dismutase activity","type":"narrow"},{"name":"activation of Fe-SOD","type":"related"},{"name":"activation of Mn, Fe superoxide dismutase","type":"narrow"},{"name":"activation of Mn-SOD","type":"related"},{"name":"activation of SOD","type":"related"},{"name":"activation of SOD-1","type":"related"},{"name":"activation of SOD-2","type":"related"},{"name":"activation of SOD-3","type":"related"},{"name":"activation of SOD-4","type":"related"},{"name":"activation of SODF","type":"related"},{"name":"activation of SODS","type":"related"},{"name":"activation of copper, zinc superoxide dismutase activity","type":"narrow"},{"name":"activation of cuprein","type":"related"},{"name":"activation of cytocuprein","type":"related"},{"name":"activation of erythrocuprein","type":"related"},{"name":"activation of ferrisuperoxide dismutase activity","type":"narrow"},{"name":"activation of hemocuprein","type":"related"},{"name":"activation of hepatocuprein","type":"related"},{"name":"activation of iron superoxide dismutase activity","type":"narrow"},{"name":"activation of iron superoxide oxidoreductase","type":"related"},{"name":"activation of manganese superoxide dismutase activity","type":"narrow"},{"name":"activation of manganese superoxide oxidoreductase","type":"related"},{"name":"activation of nickel superoxide dismutase activity","type":"narrow"},{"name":"activation of nickel superoxide oxidoreductase","type":"related"},{"name":"activation of superoxide dismutase I","type":"related"},{"name":"activation of superoxide dismutase II","type":"related"},{"name":"activation of superoxide dismutase activity","type":"narrow"},{"name":"activation of superoxide:superoxide oxidoreductase activity","type":"exact"},{"name":"activation of zinc superoxide oxidoreductase","type":"related"},{"name":"positive regulation of Cu,Zn-SOD","type":"related"},{"name":"positive regulation of Cu-Zn superoxide dismutase activity","type":"narrow"},{"name":"positive regulation of Fe-SOD","type":"related"},{"name":"positive regulation of Mn, Fe superoxide dismutase","type":"narrow"},{"name":"positive regulation of Mn-SOD","type":"related"},{"name":"positive regulation of SOD","type":"related"},{"name":"positive regulation of SOD-1","type":"related"},{"name":"positive regulation of SOD-2","type":"related"},{"name":"positive regulation of SOD-3","type":"related"},{"name":"positive regulation of SOD-4","type":"related"},{"name":"positive regulation of SODF","type":"related"},{"name":"positive regulation of SODS","type":"related"},{"name":"positive regulation of copper, zinc superoxide dismutase activity","type":"narrow"},{"name":"positive regulation of cuprein","type":"related"},{"name":"positive regulation of cytocuprein","type":"related"},{"name":"positive regulation of erythrocuprein","type":"related"},{"name":"positive regulation of ferrisuperoxide dismutase activity","type":"narrow"},{"name":"positive regulation of hemocuprein","type":"related"},{"name":"positive regulation of hepatocuprein","type":"related"},{"name":"positive regulation of iron superoxide dismutase activity","type":"narrow"},{"name":"positive regulation of iron superoxide oxidoreductase","type":"related"},{"name":"positive regulation of manganese superoxide dismutase activity","type":"narrow"},{"name":"positive regulation of manganese superoxide oxidoreductase","type":"related"},{"name":"positive regulation of nickel superoxide dismutase activity","type":"narrow"},{"name":"positive regulation of nickel superoxide oxidoreductase","type":"related"},{"name":"positive regulation of superoxide dismutase I","type":"related"},{"name":"positive regulation of superoxide dismutase II","type":"related"},{"name":"positive regulation of superoxide:superoxide oxidoreductase activity","type":"exact"},{"name":"positive regulation of zinc superoxide oxidoreductase","type":"related"},{"name":"up regulation of Cu,Zn-SOD","type":"related"},{"name":"up regulation of Cu-Zn superoxide dismutase activity","type":"narrow"},{"name":"up regulation of Fe-SOD","type":"related"},{"name":"up regulation of Mn, Fe superoxide dismutase","type":"narrow"},{"name":"up regulation of Mn-SOD","type":"related"},{"name":"up regulation of SOD","type":"related"},{"name":"up regulation of SOD-1","type":"related"},{"name":"up regulation of SOD-2","type":"related"},{"name":"up regulation of SOD-3","type":"related"},{"name":"up regulation of SOD-4","type":"related"},{"name":"up regulation of SODF","type":"related"},{"name":"up regulation of SODS","type":"related"},{"name":"up regulation of copper, zinc superoxide dismutase activity","type":"narrow"},{"name":"up regulation of cuprein","type":"related"},{"name":"up regulation of cytocuprein","type":"related"},{"name":"up regulation of erythrocuprein","type":"related"},{"name":"up regulation of ferrisuperoxide dismutase activity","type":"narrow"},{"name":"up regulation of hemocuprein","type":"related"},{"name":"up regulation of hepatocuprein","type":"related"},{"name":"up regulation of iron superoxide dismutase activity","type":"narrow"},{"name":"up regulation of iron superoxide oxidoreductase","type":"related"},{"name":"up regulation of manganese superoxide dismutase activity","type":"narrow"},{"name":"up regulation of manganese superoxide oxidoreductase","type":"related"},{"name":"up regulation of nickel superoxide dismutase activity","type":"narrow"},{"name":"up regulation of nickel superoxide oxidoreductase","type":"related"},{"name":"up regulation of superoxide dismutase I","type":"related"},{"name":"up regulation of superoxide dismutase II","type":"related"},{"name":"up regulation of superoxide dismutase activity","type":"exact"},{"name":"up regulation of superoxide:superoxide oxidoreductase activity","type":"exact"},{"name":"up regulation of zinc superoxide oxidoreductase","type":"related"},{"name":"up-regulation of Cu,Zn-SOD","type":"related"},{"name":"up-regulation of Cu-Zn superoxide dismutase activity","type":"narrow"},{"name":"up-regulation of Fe-SOD","type":"related"},{"name":"up-regulation of Mn, Fe superoxide dismutase","type":"narrow"},{"name":"up-regulation of Mn-SOD","type":"related"},{"name":"up-regulation of SOD","type":"related"},{"name":"up-regulation of SOD-1","type":"related"},{"name":"up-regulation of SOD-2","type":"related"},{"name":"up-regulation of SOD-3","type":"related"},{"name":"up-regulation of SOD-4","type":"related"},{"name":"up-regulation of SODF","type":"related"},{"name":"up-regulation of SODS","type":"related"},{"name":"up-regulation of copper, zinc superoxide dismutase activity","type":"narrow"},{"name":"up-regulation of cuprein","type":"related"},{"name":"up-regulation of cytocuprein","type":"related"},{"name":"up-regulation of erythrocuprein","type":"related"},{"name":"up-regulation of ferrisuperoxide dismutase activity","type":"narrow"},{"name":"up-regulation of hemocuprein","type":"related"},{"name":"up-regulation of hepatocuprein","type":"related"},{"name":"up-regulation of iron superoxide dismutase activity","type":"narrow"},{"name":"up-regulation of iron superoxide oxidoreductase","type":"related"},{"name":"up-regulation of manganese superoxide dismutase activity","type":"narrow"},{"name":"up-regulation of manganese superoxide oxidoreductase","type":"related"},{"name":"up-regulation of nickel superoxide dismutase activity","type":"narrow"},{"name":"up-regulation of nickel superoxide oxidoreductase","type":"related"},{"name":"up-regulation of superoxide dismutase I","type":"related"},{"name":"up-regulation of superoxide dismutase II","type":"related"},{"name":"up-regulation of superoxide dismutase activity","type":"exact"},{"name":"up-regulation of superoxide:superoxide oxidoreductase activity","type":"exact"},{"name":"up-regulation of zinc superoxide oxidoreductase","type":"related"},{"name":"upregulation of Cu,Zn-SOD","type":"related"},{"name":"upregulation of Cu-Zn superoxide dismutase activity","type":"narrow"},{"name":"upregulation of Fe-SOD","type":"related"},{"name":"upregulation of Mn, Fe superoxide dismutase","type":"narrow"},{"name":"upregulation of Mn-SOD","type":"related"},{"name":"upregulation of SOD","type":"related"},{"name":"upregulation of SOD-1","type":"related"},{"name":"upregulation of SOD-2","type":"related"},{"name":"upregulation of SOD-3","type":"related"},{"name":"upregulation of SOD-4","type":"related"},{"name":"upregulation of SODF","type":"related"},{"name":"upregulation of SODS","type":"related"},{"name":"upregulation of copper, zinc superoxide dismutase activity","type":"narrow"},{"name":"upregulation of cuprein","type":"related"},{"name":"upregulation of cytocuprein","type":"related"},{"name":"upregulation of erythrocuprein","type":"related"},{"name":"upregulation of ferrisuperoxide dismutase activity","type":"narrow"},{"name":"upregulation of hemocuprein","type":"related"},{"name":"upregulation of hepatocuprein","type":"related"},{"name":"upregulation of iron superoxide dismutase activity","type":"narrow"},{"name":"upregulation of iron superoxide oxidoreductase","type":"related"},{"name":"upregulation of manganese superoxide dismutase activity","type":"narrow"},{"name":"upregulation of manganese superoxide oxidoreductase","type":"related"},{"name":"upregulation of nickel superoxide dismutase activity","type":"narrow"},{"name":"upregulation of nickel superoxide oxidoreductase","type":"related"},{"name":"upregulation of superoxide dismutase I","type":"related"},{"name":"upregulation of superoxide dismutase II","type":"related"},{"name":"upregulation of superoxide dismutase activity","type":"exact"},{"name":"upregulation of superoxide:superoxide oxidoreductase activity","type":"exact"},{"name":"upregulation of zinc superoxide oxidoreductase","type":"related"}],"termid":"GO:1901671"}


id: PBO:0086677
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; identified by gene-trapping, microarray analysis, and genome-wide homology searches; mRNA identified as translated by ribosome profiling data; SWAT-GFP, seamless-GFP and mCherry fusion proteins localize to the endoplasmic reticulum; partially overlaps the dubious ORF YBR126W-B","termid":"PBO:0086677"}


id: PBO:0089604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein involved in ribosomal large subunit assembly and maintenance","termid":"PBO:0089604"}


id: PBO:0069289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 545, pseudogene","termid":"PBO:0069289"}


id: PBO:0117046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane bound ghrelin O-acyltransferase MBOAT4","termid":"PBO:0117046"}


id: GO:1902885
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of proteasome-activating ATPase activity.","definition_xrefs":["GO_REF:0000059","GOC:di","GOC:TermGenie","PMID:23995839"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of proteasome-activating ATPase activity (obsolete GO:1902885)","synonyms":[{"name":"regulation of ATPase involved in positive regulation of proteasomal protein catabolic process","type":"exact"},{"name":"regulation of proteasomal ATPase activity","type":"exact"},{"name":"regulation of proteasome channel gating activity","type":"narrow"},{"name":"regulation of proteasome channel opening activity","type":"narrow"}],"termid":"GO:1902885"}


id: MONDO:0010885
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":"angiokeratoma corporis diffusum with arteriovenous fistulas","secondary_identifiers":["MESH:C563940","OMIM:600419","MEDGEN:324953","UMLS:C1838141"],"synonyms":[{"name":"angiokeratoma corporis diffusum with arteriovenous fistulas","type":"exact"}],"termid":"MONDO:0010885","xrefs":{"Monarch":{"xref_id":"0010885"}}}


id: MONDO:0011493
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Stickler syndrome is an inherited vitreoretinopathy characterized by the association of ocular signs with more or less complete forms of Pierre-Robin sequence, bone disorders, and sensorineural deafness (10% of cases). Stickler syndrome type 2 is caused by mutations in the COL11A1 gene (1p21).","definition_xrefs":["Orphanet:828"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Stickler syndrome","termid":"MONDO:0019354"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0005328"],"is_obsolete":false,"name":"Stickler syndrome type 2","secondary_identifiers":["MEDGEN:347615","icd11.foundation:1652024415","DOID:0080675","MESH:C537493","Orphanet:90654","NCIT:C74985","UMLS:C1858084","OMIM:604841","GARD:5020"],"synonyms":[{"name":"COL11A1 Stickler syndrome","type":"exact"},{"name":"STICKLER syndrome, type II","type":"related"},{"name":"STL 2","type":"related"},{"name":"STL2","type":"related"},{"name":"Stickler syndrome caused by mutation in COL11A1","type":"exact"},{"name":"Stickler syndrome type II","type":"exact"},{"name":"Stickler syndrome, beaded vitreous type","type":"related"},{"name":"Stickler syndrome, type 2","type":"related"},{"name":"Stickler syndrome, vitreous type 2","type":"related"}],"termid":"MONDO:0011493","xrefs":{"Monarch":{"xref_id":"0011493"}}}


id: SO:0001961
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A modified DNA cytosine base feature, modified by a formyl group at the 5 carbon.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified_cytosine","termid":"SO:0001963"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5_formylcytosine","secondary_identifiers":["http:http\\://www.pacificbiosciences.com/pdf/WP_Detecting_DNA_Base_Modifications_Using_SMRT_Sequencing.pdf"],"synonyms":[{"name":"5-fC","type":"exact"},{"name":"5-formylcytosine","type":"exact"}],"termid":"SO:0001961"}


id: MONDO:0014642
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any chronic mucocutaneous candidiasis in which the cause of the disease is a mutation in the IL17RC gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic mucocutaneous candidiasis","termid":"MONDO:0015279"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"candidiasis, familial, 9","secondary_identifiers":["OMIM:616445","GARD:16114","MEDGEN:906897","UMLS:C4225324"],"synonyms":[{"name":"CANDF9","type":"related"},{"name":"IL17RC chronic mucocutaneous candidiasis (disease)","type":"exact"},{"name":"candidiasis, familial, 9","type":"exact"},{"name":"candidiasis, familial, type 9","type":"exact"},{"name":"chronic mucocutaneous candidiasis (disease) caused by mutation in IL17RC","type":"exact"}],"termid":"MONDO:0014642","xrefs":{"Monarch":{"xref_id":"0014642"}}}


id: PBO:0032751
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"original gene was in a different frame","termid":"PBO:0032751"}


id: PBO:0067876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 178","termid":"PBO:0067876"}


id: GO:0072110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of glomerular mesangial cells, resulting in the expansion of the population.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell proliferation involved in kidney development","termid":"GO:0072111"},{"relation_name":"part_of","term_name":"glomerular mesangium development","termid":"GO:0072109"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"glomerular mesangial cell proliferation","termid":"GO:0072110"}


id: PBO:0041297
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C2 calcium dependent domain containing 4A","termid":"PBO:0041297"}


id: GO:2000644
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of receptor catabolic process.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of catabolic process","termid":"GO:0009894"},{"relation_name":"is_a","term_name":"regulation of macromolecule metabolic process","termid":"GO:0060255"},{"relation_name":"regulates","term_name":"receptor catabolic process","termid":"GO:0032801"}],"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 receptor catabolic process","synonyms":[{"name":"regulation of receptor breakdown","type":"exact"},{"name":"regulation of receptor catabolism","type":"exact"},{"name":"regulation of receptor degradation","type":"exact"}],"termid":"GO:2000644"}


id: PR:O13738
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A glucosamine 6-phosphate N-acetyltransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR13355:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosamine 6-phosphate N-acetyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC16E8.03","secondary_identifiers":["UniProtKB:O13738"],"synonyms":[{"name":"SPAC16E8.03","type":"related"},{"name":"Spom972h-GNPNAT1","type":"exact"},{"name":"phosphoglucosamine acetylase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"phosphoglucosamine transacetylase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13738"}


id: GO:0019351
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of dethiobiotin, a derivative of biotin in which the sulfur atom has been replaced by two hydrogen atoms.","definition_xrefs":["ISBN:0198506732","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"},{"relation_name":"is_a","term_name":"dethiobiotin metabolic process","termid":"GO:0046450"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"dethiobiotin biosynthetic process","synonyms":[{"name":"desthiobiotin biosynthesis","type":"exact"},{"name":"desthiobiotin biosynthetic process","type":"exact"},{"name":"dethiobiotin anabolism","type":"exact"},{"name":"dethiobiotin biosynthesis","type":"exact"},{"name":"dethiobiotin formation","type":"exact"},{"name":"dethiobiotin synthesis","type":"exact"}],"termid":"GO:0019351"}


id: PBO:0039680
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amyloid beta precursor protein binding family A member 1","termid":"PBO:0039680"}


id: PBO:0031194
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_camptothecin","termid":"PBO:0031194"}


id: MONDO:0018023
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"inherited hemoglobinopathy","termid":"MONDO:0019050"},{"relation_name":"is_a","term_name":"hereditary methemoglobinemia","termid":"MONDO:0018963"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"hemoglobin M disease","secondary_identifiers":["SCTID:74912001","MEDGEN:777099","Orphanet:330041","GARD:13007","MESH:C581942","OMIM:617971","UMLS:C3665425"],"synonyms":[{"name":"M hemoglobinopathy","type":"exact"},{"name":"autosomal dominant methemoglobinemia","type":"related"},{"name":"blue baby syndrome","type":"related"},{"name":"hereditary methemoglobinemia due to haemoglobin mutation","type":"related"},{"name":"hereditary methemoglobinemia due to hemoglobin mutation","type":"related"},{"name":"methemoglobinemia, beta type","type":"exact"},{"name":"methemoglobinemia, beta-globin type","type":"related"}],"termid":"MONDO:0018023","xrefs":{"Monarch":{"xref_id":"0018023"}}}


id: PR:G2TRK9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- new13 gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRK9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein new13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.14","synonyms":[{"name":"Spom972h-new13","type":"exact"}],"termid":"PR:G2TRK9"}


id: SO:0000851
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of a CDS.","definition_xrefs":["SO:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA_region","termid":"SO:0000836"},{"relation_name":"part_of","term_name":"CDS","termid":"SO:0000316"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDS_region","synonyms":[{"name":"CDS region","type":"exact"}],"termid":"SO:0000851"}


id: PBO:0047945
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, distamycin A type, rare, fra(16)(q22.1)","termid":"PBO:0047945"}


id: MONDO:0010386
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any immunodeficiency disease in which the cause of the disease is a mutation in the IKBKG gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"X-linked Mendelian susceptibility to mycobacterial diseases","termid":"MONDO:0017905"},{"relation_name":"is_a","term_name":"inborn error of immunity","termid":"MONDO:0003778"},{"relation_name":"is_a","term_name":"IKBKG-related immunodeficiency with or without ectodermal dysplasia","termid":"MONDO:0100162"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"immunodeficiency 33","secondary_identifiers":["MEDGEN:370376","MESH:C567070","DOID:0112003","OMIM:300584","UMLS:C1970879","OMIM:300636","Orphanet:319612","MESH:C536289","GARD:12915"],"synonyms":[{"name":"IKBKG X-linked mendelian susceptibility to mycobacterial diseases","type":"exact"},{"name":"IKBKG invasive pneumococcal disease, recurrent isolated","type":"exact"},{"name":"IMD33","type":"exact"},{"name":"IPD2","type":"exact"},{"name":"NEMO deficiency syndrome","type":"related"},{"name":"NF-kappa B essential modulator deficiency","type":"related"},{"name":"X-linked MSMD due to IKBKG deficiency","type":"exact"},{"name":"X-linked MSMD due to NEMO deficiency","type":"exact"},{"name":"X-linked mendelian susceptibility to mycobacterial diseases caused by mutation in IKBKG","type":"exact"},{"name":"X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency","type":"exact"},{"name":"X-linked mendelian susceptibility to mycobacterial diseases due to NEMO deficiency","type":"exact"},{"name":"atypical Mycobacteriosis, familial, X-linked 1","type":"related"},{"name":"familial X-linked 1 atypical mycobacteriosis","type":"related"},{"name":"immunodeficiency 33, Mycobacteriosis, X-linked","type":"exact"},{"name":"immunodeficiency 33, X-linked recessive","type":"exact"},{"name":"immunodeficiency type 33","type":"exact"},{"name":"immunodeficiency without anhidrotic ectodermal dysplasia","type":"exact"},{"name":"immunodeficiency, isolated","type":"exact"},{"name":"immunodeficiency, pure","type":"exact"},{"name":"invasive pneumococcal disease, recurrent isolated caused by mutation in IKBKG","type":"exact"},{"name":"invasive pneumococcal disease, recurrent isolated, 2","type":"exact"},{"name":"invasive pneumococcal disease, recurrent isolated, type 2","type":"exact"}],"termid":"MONDO:0010386","xrefs":{"Monarch":{"xref_id":"0010386"}}}


id: MONDO:0100509
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any ciliopathy in which the cause of the disease is biallelic variants in the IFT140 gene.","definition_xrefs":["PMID:26359340","PMID:23418020","PMID:22503633"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliopathy","termid":"MONDO:0005308"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IFT140-related recessive ciliopathy","synonyms":[{"name":"IFT140-related recessive ciliopathy","type":"exact"},{"name":"retinitis pigmentosa 80","type":"narrow"},{"name":"short-rib thoracic dysplasia 9 with or without polydactyly","type":"narrow"}],"termid":"MONDO:0100509","xrefs":{"Monarch":{"xref_id":"0100509"}}}


id: GO:1990964
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex probably required for the internalization of endosomes during actin-coupled endocytosis. Links the site of endocytosis to the cell membrane-associated actin cytoskeleton, coordinating ARP2/3 stimulation at the later stages of endocytosis. Present in the late endocytic coat.","definition_xrefs":["GOC:bhm","PMID:10594004","PMID:11739778"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"actin cytoskeleton-regulatory complex","termid":"GO:1990964"}


id: FYPO:0007382
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of DNA binding at a transcription regulatory region by a gene product is normal (i.e. indistinguishable from wild type). The relevant gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal double-stranded DNA binding","termid":"FYPO:0007542"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000653"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000653","FYPO:0000257"],"is_obsolete":false,"name":"normal transcription regulatory region sequence-specific DNA binding","synonyms":[{"name":"normal promoter binding","type":"related"},{"name":"normal sequence-specific DNA binding at transcription regulatory region","type":"exact"},{"name":"normal transcription regulatory region binding","type":"exact"}],"termid":"FYPO:0007382"}


id: PBO:0081321
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 107","termid":"PBO:0081321"}


id: GO:0040002
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Synthesis and deposition of a collagen and cuticulin-based noncellular, hardened, or membranous secretion from an epithelial sheet. An example of this process is found in Caenorhabditis elegans.","definition_xrefs":["GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cuticle development","termid":"GO:0042335"}],"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":"collagen and cuticulin-based cuticle development","synonyms":[{"name":"collagen and cuticulin-based cuticle anabolism","type":"exact"},{"name":"collagen and cuticulin-based cuticle biosynthetic process","type":"exact"},{"name":"collagen and cuticulin-based cuticle formation","type":"exact"},{"name":"collagen and cuticulin-based cuticle synthesis","type":"exact"}],"termid":"GO:0040002"}


id: PBO:0064658
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A","termid":"PBO:0064658"}


id: PBO:0071086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 88","termid":"PBO:0071086"}


id: MONDO:0017704
data:
  {"annotated_genes":["SJAG_00824","SJAG_02765","SJAG_01184"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85739],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024556"},{"annotations":[87504],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014924"},{"annotations":[87503],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014925"}]},"cv_name":"mondo","definition":"An instance of partial epilepsy 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":"focal epilepsy","termid":"MONDO:0005384"},{"relation_name":"is_a","term_name":"childhood-onset epilepsy syndrome","termid":"MONDO:0020072"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00824":null,"SJAG_01184":null,"SJAG_02765":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"familial partial epilepsy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:309","UMLS:C5680862","GARD:2173","MEDGEN:1826100"],"synonyms":[{"name":"epilepsy, partial, familial","type":"related"},{"name":"hereditary partial epilepsy","type":"exact"}],"termid":"MONDO:0017704","terms_by_termid":{"MONDO:0014924":null,"MONDO:0014925":null,"MONDO:0024556":null},"xrefs":{"Monarch":{"xref_id":"0017704"}}}


id: PBO:0071967
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S6 kinase A6","termid":"PBO:0071967"}


id: GO:0004334
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-fumarylacetoacetate + H2O = acetoacetate + fumarate + H+.","definition_xrefs":["RHEA:10244","EC:3.7.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid carbon-carbon bonds, in ketonic substances","termid":"GO:0016823"}],"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:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"fumarylacetoacetase activity","secondary_identifiers":["UM-BBD_reactionID:r0107","MetaCyc:FUMARYLACETOACETASE-RXN","Reactome:R-HSA-71181","KEGG_REACTION:R01364"],"synonyms":[{"name":"4-fumarylacetoacetate fumarylhydrolase activity","type":"related"},{"name":"beta-diketonase activity","type":"related"},{"name":"fumarylacetoacetate hydrolase activity","type":"related"}],"termid":"GO:0004334"}


id: GO:0090400
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A cellular senescence process associated with the dismantling of a cell as a response to environmental factors such as hydrogen peroxide or X-rays.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular senescence","termid":"GO:0090398"}],"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":"stress-induced premature senescence","synonyms":[{"name":"SIPS","type":"exact"}],"termid":"GO:0090400"}


id: PBO:0088747
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor, zf-fungal binuclear cluster type Gsf1","termid":"PBO:0088747"}


id: MONDO:0011434
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":"psoriasis, susceptibility to","termid":"MONDO:0100171"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"psoriasis 5, susceptibility to","secondary_identifiers":["UMLS:C1858536","DOID:0111282","MEDGEN:347660","OMIM:604316"],"synonyms":[{"name":"PSORS5","type":"exact"},{"name":"psoriasis 5, susceptibility to","type":"exact"},{"name":"psoriasis susceptibility 5","type":"exact"}],"termid":"MONDO:0011434","xrefs":{"Monarch":{"xref_id":"0011434"}}}


id: FYPO:0004894
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of 1,3-beta-D-glucan synthase activity is decreased during sporulation.","definition_xrefs":["PomBase:mah","PMID:11069657"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased 1,3-beta-D-glucan synthase activity","termid":"FYPO:0002159"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000652","FYPO:0000654","FYPO:0000707","FYPO:0001985"],"is_obsolete":false,"name":"decreased 1,3-beta-D-glucan synthase activity during sporulation","synonyms":[{"name":"reduced 1,3-beta-D-glucan synthase activity during sporulation","type":"exact"}],"termid":"FYPO:0004894"}


id: PBO:0084041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPI-glycan remodelase; conserved phosphoesterase domain-containing protein; acts together with Emp24p/Erv25p in cargo exit from the ER; functional ortholog of mammalian GPI-glycan remodelase PGAP5; deletion confers sensitivity to 4-(N-(S-glutathionylacetyl)amino) phenylarsenoxide (GSAO)","termid":"PBO:0084041"}


id: GO:0006601
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of creatine, N-[amino(imino)methyl]-N-methylglycine. Creatine is formed by a process beginning with amidino group transfer from L-arginine to glycine to form guanidinoacetate, followed by methyl group transfer from S-adenosyl-L-methionine to guanidinoacetate; it is then is phosphorylated to form a pool that stores high energy phosphate for the replenishment of ATP during periods of high, or fluctuating energy demand. In animals, most creatine is transported to and used in muscle.","definition_xrefs":["GOC:mah","MetaCyc:GLYCGREAT-PWY"],"direct_ancestors":[{"relation_name":"is_a","term_name":"creatine metabolic process","termid":"GO:0006600"},{"relation_name":"is_a","term_name":"modified amino acid biosynthetic process","termid":"GO:0042398"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"creatine biosynthetic process","synonyms":[{"name":"creatine anabolism","type":"exact"},{"name":"creatine biosynthesis","type":"exact"},{"name":"creatine formation","type":"exact"},{"name":"creatine synthesis","type":"exact"}],"termid":"GO:0006601"}


id: PR:000024855
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A proteolytic cleavage product that is derived from P-factor precursor. In Schizosaccharomyces pombe 972h- the sequence is TYADFLRAYQSWNTFVNPDRPNL, corresponding to amino acids 66-88 or 134-156 of UniProtKB:Q09180-1.","definition_xrefs":["PRO:MSY"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"map2/Clv:P-factor","pombase_gene_id":"SPCC1795.06","synonyms":[{"name":"PomBase_original_PRO_term_name: P-factor","type":"exact"},{"name":"map2/Clv:P-factor","type":"exact"}],"termid":"PR:000024855"}


id: PBO:0065390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein serine kinase H2","termid":"PBO:0065390"}


id: GO:0008727
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: GDP-alpha-D-mannose + H2O = GDP + D-mannose + H+.","definition_xrefs":["MetaCyc:GDPMANMANHYDRO-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mannosidase activity","termid":"GO:0015923"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787","GO:0016798"],"is_obsolete":false,"name":"GDP-mannose mannosyl hydrolase activity","secondary_identifiers":["RHEA:28102"],"termid":"GO:0008727"}


id: PBO:0087392
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S/T kinase and catalytic subunit of DDK (Dbf4-dependent kinase); required for origin firing and replication initiation; phosphorylates MCM subunits and Cdc45 to drive assembly of the pre-IC and the CMG helicase; maintains Cse4p at kinetochores through phosphorylation to regulate chromosome segregation, regulates pre-meiotic replication, meiotic DSB formation, monopolar attachment of homologs during MI through monopolin recruitment and middle meiotic gene expression; HsCDC7 and DBF4 complement","termid":"PBO:0087392"}


id: PBO:0067366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 466, pseudogene","termid":"PBO:0067366"}


id: PR:Q1MTR0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mitochondrial inner membrane protease ATP23 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR21711:SF0","PRO:DNx","OMA:SCHPO04204"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial inner membrane protease atp23 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC320.12","secondary_identifiers":["UniProtKB:Q1MTR0"],"synonyms":[{"name":"Spom972h-XRCC6BP1","type":"exact"}],"termid":"PR:Q1MTR0"}


id: GO:0044627
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process that modulates the frequency, rate or extent of the classical pathway of complement activation, in a different organism.","definition_xrefs":["PMID:20837040","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation of complement activation, classical pathway in another organism (obsolete GO:0044627)","synonyms":[{"name":"modulation of complement activation, classical pathway in other organism","type":"exact"},{"name":"regulation of complement activation, classical pathway in other organism","type":"exact"}],"termid":"GO:0044627"}


id: FYPO:0000922
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of isocitrate dehydrogenase (NAD+) activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal oxidoreductase activity","termid":"FYPO:0000689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000652","FYPO:0000707","FYPO:0001985","FYPO:0000654"],"is_obsolete":false,"name":"abnormal isocitrate dehydrogenase (NAD+) activity","synonyms":[{"name":"abnormal NAD-IDH activity","type":"exact"}],"termid":"FYPO:0000922"}


id: MONDO:0005951
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete sarcocystosis (obsolete MONDO:0005951)","termid":"MONDO:0005951","xrefs":{"Monarch":{"xref_id":"0005951"}}}


id: PBO:0043212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC28 protein kinase regulatory subunit 1B pseudogene 5","termid":"PBO:0043212"}


id: GO:0015204
data:
  {"annotated_genes":["SJAG_02125"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71032],"is_not":false,"summary":null,"term":"GO:0015204"}]},"cv_name":"molecular_function","definition":"Enables the transfer of urea from one side of a membrane to the other. Urea is the water soluble compound H2N-CO-NH2.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide transmembrane transporter activity","termid":"GO:0042887"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02125":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"urea transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-444126","GO:0015287"],"synonyms":[{"name":"urea transporter activity","type":"broad"}],"termid":"GO:0015204","terms_by_termid":{"GO:0015204":null}}


id: GO:0003172
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the sinoatrial valve over time, from its formation to the mature structure.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart valve development","termid":"GO:0003170"}],"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":"sinoatrial valve development","synonyms":[{"name":"SA valve development","type":"exact"}],"termid":"GO:0003172"}


id: SO:0000119
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute to describe a sequence that is regulated.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gene_attribute","termid":"SO:0000401"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulated","termid":"SO:0000119"}


id: MONDO:0021412
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polyp that involves the maxillary sinus.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paranasal sinus disorder","termid":"MONDO:0001735"},{"relation_name":"is_a","term_name":"polyp","termid":"MONDO:0005079"},{"relation_name":"is_a","term_name":"mouth disorder","termid":"MONDO:0006858"},{"relation_name":"is_a","term_name":"disorder of facial skeleton","termid":"MONDO:0023369"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polyp of maxillary sinus","secondary_identifiers":["MEDGEN:120498","UMLS:C0264239","SCTID:29074008","ICD9:471.8","NCIT:C3931"],"synonyms":[{"name":"maxillary antral polyp","type":"exact"},{"name":"maxillary sinus polyp","type":"exact"},{"name":"polyp of the maxillary sinus","type":"exact"}],"termid":"MONDO:0021412","xrefs":{"Monarch":{"xref_id":"0021412"}}}


id: GO:0010184
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of cytokinins, a class of adenine-derived compounds that can function in plants as growth regulators, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone transport","termid":"GO:0009914"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"cytokinin transport","termid":"GO:0010184"}


id: PBO:0086372
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative aryl-alcohol dehydrogenase; involved in oxidative stress response; similar to P. chrysosporium aryl-alcohol dehydrogenase; expression induced in cells treated with the mycotoxin patulin; members of the AAD gene family comprise three pairs (AAD3 + AAD15, AAD6/AAD16 + AAD4, AAD10 + AAD14) whose two genes are more related to one another than to other members of the family","termid":"PBO:0086372"}


id: PBO:0083119
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA Topoisomerase III; conserved protein that functions in a complex with Sgs1p and Rmi1p to relax single-stranded negatively-supercoiled DNA preferentially; DNA catenation/decatenation activity is stimulated by RPA and Sgs1p-Top3p-Rmi1p; involved in telomere stability and regulation of mitotic recombination","termid":"PBO:0083119"}


id: MOD:01879
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts two L-cysteine residues, an L-arginine residue, an L-threonine residue and a copper atom to the methanobactin SB2 copper complex.","definition_xrefs":["RESID:AA0555","PubMed:20961038"],"direct_ancestors":[{"relation_name":"is_a","term_name":"copper containing modified residue","termid":"MOD:00742"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-cysteine residue","termid":"MOD:02067"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"methanobactin SB2 copper complex","synonyms":[{"name":"METAL copper [Cu-methanobactin SB2 complex]","type":"exact"},{"name":"[5-(hydroxy[sulfanyl-kappaS]methylene)-3,5-dihydro-4H-imidazol-4-onato-kappaN1][4-(hydroxy[sulfanyl-kappaS]methylene)-1,3-oxazol-5(4H)-onato-kappaN]copper","type":"exact"},{"name":"methanobactin SB2 copper complex","type":"exact"}],"termid":"MOD:01879"}


id: MONDO:0006235
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An unusual benign or malignant neoplasm characterized by the presence of neoplastic large polygonal cells with granular, eosinophilic cytoplasm which contains abundant lysosomes. It was originally thought to be a tumor originating from muscle cells and was named granular cell myoblastoma. Subsequent studies have suggested a derivation from Schwann cells. It affects females more often than males and it usually presents as a solitary mass. A minority of patients have multiple tumors. It can arise from many anatomic sites including the posterior pituitary gland, skin, oral cavity, esophagus, stomach, heart, mediastinum, and breast.","definition_xrefs":["NCIT:C3474"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nerve sheath neoplasm","termid":"MONDO:0002547"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"granular cell tumor","secondary_identifiers":["ICDO:9580/0","MESH:D016586","MESH:C535558","MEDGEN:88345","SCTID:404035005","ONCOTREE:GCT","GARD:9618","DOID:2411","UMLS:C0085167","EFO:1000284","ICD9:215.9"],"synonyms":[{"name":"Abrikosoff's granulous cell tumor","type":"related"},{"name":"Abrikosoff's granulous cell tumour","type":"related"},{"name":"Abrikosoff's tumor","type":"related"},{"name":"Abrikosoff's tumour","type":"related"},{"name":"Abrikosov's tumor","type":"related"},{"name":"Abrikosov's tumour","type":"related"},{"name":"Abrikosov’s tumor","type":"related"},{"name":"Abrikosov’s tumour","type":"related"},{"name":"Abrikossoff tumor","type":"exact"},{"name":"Abrikossoff tumour","type":"exact"},{"name":"Abrikossoff's tumor","type":"exact"},{"name":"Abrikossoff's tumour","type":"exact"},{"name":"GCT","type":"related"},{"name":"giant granulocellular Abrikosov's tumor","type":"related"},{"name":"giant granulocellular Abrikosov's tumour","type":"related"},{"name":"granular cell myoblastoma","type":"exact"},{"name":"granular cell neoplasm","type":"exact"},{"name":"granular cell nerve sheath tumor","type":"exact"},{"name":"granular cell nerve sheath tumour","type":"exact"},{"name":"granular cell schwannoma","type":"exact"},{"name":"granular cell tumor","type":"exact"},{"name":"granular cell tumor (morphologic abnormality)","type":"exact"},{"name":"granular cell tumor NOS (morphologic abnormality)","type":"narrow"},{"name":"granular cell tumour (morphologic abnormality)","type":"exact"},{"name":"granular cell tumour NOS (morphologic abnormality)","type":"narrow"},{"name":"malignant variant of Abrikosov's tumor","type":"related"},{"name":"malignant variant of Abrikosov's tumour","type":"related"},{"name":"neoplasm of granular cell","type":"narrow"}],"termid":"MONDO:0006235","xrefs":{"Monarch":{"xref_id":"0006235"}}}


id: MONDO:0016251
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete salivary gland type cancer of the breast (obsolete MONDO:0016251)","termid":"MONDO:0016251","xrefs":{"Monarch":{"xref_id":"0016251"}}}


id: PBO:0072110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S13 pseudogene 8","termid":"PBO:0072110"}


id: GO:1900844
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of monodictyphenone biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"negative regulation of secondary metabolite biosynthetic process","termid":"GO:1900377"},{"relation_name":"is_a","term_name":"regulation of monodictyphenone biosynthetic process","termid":"GO:1900843"},{"relation_name":"negatively_regulates","term_name":"monodictyphenone biosynthetic process","termid":"GO:1900815"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0019748"},{"rel_name":"regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0019748"],"is_obsolete":false,"name":"negative regulation of monodictyphenone biosynthetic process","synonyms":[{"name":"down regulation of monodictyphenone biosynthetic process","type":"exact"},{"name":"down-regulation of monodictyphenone biosynthetic process","type":"exact"},{"name":"downregulation of monodictyphenone biosynthetic process","type":"exact"}],"termid":"GO:1900844"}


id: GO:0140233
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a cation by a channel that opens when intracellular cAMP has been bound by the channel complex or one of its constituent parts, to regulate the postsynaptic membrane potential.","definition_xrefs":["GOC:pvn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellularly cAMP-activated cation channel activity","termid":"GO:0005222"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"intracellular cAMP-activated cation channel activity involved in regulation of postsynaptic membrane potential","synonyms":[{"name":"intracellular cAMP activated cation channel activity involved in regulation of postsynaptic membrane potential","type":"exact"}],"termid":"GO:0140233"}


id: GO:0018742
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of the ether in chloro- or hydroxyepoxypropane to produce chloropropane diol or glycerol. Acts on R enantiomers.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete epoxide hydrolase B activity (obsolete GO:0018742)","termid":"GO:0018742"}


id: FYPO:0003205
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A septation phenotype observed in the vegetative growth phase of the life cycle in which a cell forms a primary septum that is thinner than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased septum thickness","termid":"FYPO:0006900"},{"relation_name":"output_of","term_name":"abnormal primary cell septum biogenesis","termid":"FYPO:0003890"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000032","FYPO:0000002","FYPO:0005447","FYPO:0000631","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased primary cell septum thickness","synonyms":[{"name":"decreased primary cell septum thickness during mitotic cell cycle","type":"related"},{"name":"decreased primary cell septum thickness during vegetative growth","type":"exact"},{"name":"decreased primary septum thickness","type":"exact"},{"name":"reduced primary cell septum thickness","type":"exact"},{"name":"thin primary septum","type":"exact"}],"termid":"FYPO:0003205"}


id: MONDO:0014404
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":"Webb-Dattani syndrome","secondary_identifiers":["UMLS:C4014708","OMIM:615926","MEDGEN:863145","Orphanet:370006"],"synonyms":[{"name":"WEBB-Dattani syndrome","type":"related"},{"name":"WEDAS","type":"related"},{"name":"Webb-Dattani syndrome","type":"exact"},{"name":"hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies syndrome","type":"exact"},{"name":"hypothalamo-pituitary-frontotemporal hypoplasia with visual and renal anomalies","type":"related"}],"termid":"MONDO:0014404","xrefs":{"Monarch":{"xref_id":"0014404"}}}


id: GO:0120532
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of a tetrasaccharide linker sequence (xylose-galactose-galactose-glucuronate) on specific serine residues of a core protein, on to which dermatan sulfate, chondroitin sulfate, heparan sulfate or heparin glycosaminoglycans may be assembled to synthesise the corresponding proteoglycan.","definition_xrefs":["MetaCyc:PWY-6557"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein O-linked glycosylation","termid":"GO:0006493"},{"relation_name":"part_of","term_name":"heparan sulfate proteoglycan biosynthetic process","termid":"GO:0015012"},{"relation_name":"part_of","term_name":"heparin proteoglycan biosynthetic process","termid":"GO:0030210"},{"relation_name":"part_of","term_name":"chondroitin sulfate proteoglycan biosynthetic process","termid":"GO:0050650"},{"relation_name":"part_of","term_name":"dermatan sulfate proteoglycan biosynthetic process","termid":"GO:0050651"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006486"}],"interesting_parent_ids":["GO:0008150","GO:0006486"],"is_obsolete":false,"name":"glycosaminoglycan-protein linkage region biosynthetic process","synonyms":[{"name":"Glycosaminoglycan biosynthesis, linkage tetrasaccharide","type":"exact"},{"name":"glycosaminoglycan-protein linkage region biosynthesis","type":"exact"}],"termid":"GO:0120532"}


id: PBO:0000419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sensor for misfolded ER glycoproteins Yos9 (predicted)","termid":"PBO:0000419"}


id: PBO:0060707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit A5 pseudogene 4","termid":"PBO:0060707"}


id: PR:O42653
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC10F6.14c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42653"],"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":"ABC1 family protein C10F6.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC10F6.14c","synonyms":[{"name":"Spom972h-SPAC10F6.14c","type":"exact"}],"termid":"PR:O42653"}


id: PBO:0001705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligosaccharyltransferase epsilon subunit Ost2 (predicted)","termid":"PBO:0001705"}


id: PBO:0067885
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 187","termid":"PBO:0067885"}


id: GO:0044541
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism resulting in the proteolytic processing of an inactive enzyme to an active form in another organism.","definition_xrefs":["GOC:fj","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete zymogen activation in another organism (obsolete GO:0044541)","synonyms":[{"name":"zymogen activation in other organism","type":"exact"}],"termid":"GO:0044541"}


id: MONDO:0019811
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital tricuspid malformation","termid":"MONDO:0020289"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"tricuspid valve agenesis","secondary_identifiers":["UMLS:C0685715","ICD10CM:Q22.4","MEDGEN:672653","GARD:19261","Orphanet:95457"],"synonyms":[{"name":"congenital unguarded tricuspid orifice","type":"exact"}],"termid":"MONDO:0019811","xrefs":{"Monarch":{"xref_id":"0019811"}}}


id: GO:0034424
data:
  {"annotated_genes":["SJAG_03511","SJAG_07012"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[75626,99224],"is_not":false,"summary":null,"term":"GO:0034424"}]},"cv_name":"cellular_component","definition":"A membrane-associated protein complex that is required for a late stage of endosomal transport. In budding yeast, this complex consists of Vps55p and Vps68p proteins.","definition_xrefs":["PMID:18216282"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"part_of","term_name":"endosome membrane","termid":"GO:0010008"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03511":null,"SJAG_07012":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005768"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0032991","GO:0031410","GO:0005768"],"is_obsolete":false,"name":"Vps55/Vps68 complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0034424","terms_by_termid":{"GO:0034424":null}}


id: PBO:0004089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ran GTPase binding protein Hba1","termid":"PBO:0004089"}


id: GO:0047292
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (6AS,11AS)-3,6A,9-trihydroxypterocarpan + dimethylallyl-pyrophosphate = glyceollin + diphosphate.","definition_xrefs":["EC:2.5.1.36"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0016765","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"trihydroxypterocarpan dimethylallyltransferase activity","synonyms":[{"name":"dimethylallyl-diphosphate:(6aS,11aS)-3,6a,9-trihydroxypterocarpan dimethylallyltransferase activity","type":"related"},{"name":"dimethylallyl-diphosphate:(6aS,11aS)-3,6a,9-trihydroxypterocarpan dimethyltransferase activity","type":"related"},{"name":"dimethylallylpyrophosphate:3,6a,9-trihydroxypterocarpan dimethylallyltransferase activity","type":"related"},{"name":"dimethylallylpyrophosphate:trihydroxypterocarpan dimethylallyl transferase activity","type":"related"}],"termid":"GO:0047292"}


id: MONDO:0012902
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 4q12-q13.1.","definition_xrefs":["DOID:0110556","PMID:18279434"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0019497"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 27","secondary_identifiers":["OMIM:612431","UMLS:C3887929","MEDGEN:854637","GARD:18128"],"synonyms":[{"name":"DFNA27","type":"narrow"},{"name":"autosomal dominant deafness 27","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 27","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 27","type":"narrow"},{"name":"deafness, autosomal dominant 27","type":"narrow"}],"termid":"MONDO:0012902","xrefs":{"Monarch":{"xref_id":"0012902"}}}


id: GO:0052511
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism activates, maintains or increases the frequency, rate or extent of the ethylene-mediated defense response of the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by organism of symbiont ethylene-mediated defense response (obsolete GO:0052511)","synonyms":[{"name":"activation by organism of symbiont ethylene-mediated defense response","type":"narrow"},{"name":"induction by organism of symbiont ethylene-mediated defense response","type":"narrow"},{"name":"positive regulation by organism of symbiont ethylene-mediated defense response","type":"exact"},{"name":"upregulation by organism of symbiont ethylene-mediated defense response","type":"narrow"}],"termid":"GO:0052511"}


id: PBO:0086724
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; non-tagged protein is detected in highly purified mitochondria in high-throughput studies; contains a PH domain and binds phosphatidylinositols and phosphatidylethanolamine in a large-scale study; YNL144C has a paralog, YHR131C, that arose from the whole genome duplication","termid":"PBO:0086724"}


id: PBO:0050143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 2 pseudogene 1","termid":"PBO:0050143"}


id: PBO:0039876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho GTPase activating protein 32","termid":"PBO:0039876"}


id: GO:0033621
data:
  {"annotated_genes":["SJAG_00452","SJAG_00456","SJAG_02622","SJAG_04601","SJAG_02720","SJAG_01412","SJAG_01867","SJAG_04768","SJAG_03883","SJAG_02723","SJAG_03745","SJAG_01540","SJAG_04006","SJAG_02382","SJAG_03454"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87851,91155,91231,92227,92608,97085,99451,104662,107824,109617,109636,111683,118498],"is_not":false,"summary":null,"term":"GO:0033621"},{"annotations":[90149],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0120271"},{"annotations":[107029],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0120272"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the selective degradation of meiosis-specific transcripts during vegetative growth, by a mechanism that requires determinant of selective removal (DSR) sequences in the targeted mRNAs and involves a YTH family protein.","definition_xrefs":["PMID:16823445"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear mRNA surveillance","termid":"GO:0071028"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00452":null,"SJAG_00456":null,"SJAG_01412":null,"SJAG_01540":null,"SJAG_01867":null,"SJAG_02382":null,"SJAG_02622":null,"SJAG_02720":null,"SJAG_02723":null,"SJAG_03454":null,"SJAG_03745":null,"SJAG_03883":null,"SJAG_04006":null,"SJAG_04601":null,"SJAG_04768":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016071"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0016071","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"nuclear mRNA surveillance of meiosis-specific transcripts","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"degradation of meiosis-specific transcripts","type":"exact"},{"name":"mRNA breakdown, meiosis-specific transcripts","type":"exact"},{"name":"mRNA catabolism, meiosis-specific transcripts","type":"exact"},{"name":"mRNA degradation, meiosis-specific transcripts","type":"exact"},{"name":"nuclear mRNA catabolic process, meiosis-specific transcripts","type":"exact"},{"name":"nuclear-transcribed mRNA catabolic process, meiosis-specific transcripts","type":"exact"}],"termid":"GO:0033621","terms_by_termid":{"GO:0033621":null,"GO:0120271":null,"GO:0120272":null}}


id: MONDO:0020557
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pleuropulmonary blastoma characterized by a solid pattern and sarcomatous features. It usually follows an aggressive clinical course.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pleuropulmonary blastoma","termid":"MONDO:0011014"}],"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":"pleuropulmonary blastoma type 3","secondary_identifiers":["Orphanet:99935","UMLS:C1710499","GARD:19717","MEDGEN:328132","NCIT:C45628","SCTID:707673006","ICD9:162.9"],"synonyms":[{"name":"type III pleuropulmonary blastoma","type":"exact"}],"termid":"MONDO:0020557","xrefs":{"Monarch":{"xref_id":"0020557"}}}


id: GO:0060053
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Intermediate filament cytoskeletal structure that is made up of neurofilaments. Neurofilaments are specialized intermediate filaments found in neurons.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intermediate filament cytoskeleton","termid":"GO:0045111"}],"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":"neurofilament cytoskeleton","termid":"GO:0060053"}


id: PBO:0034071
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_apparent_orthology_relationship_with","termid":"PBO:0034071"}


id: PBO:0012595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoribosylamine-glycine ligase/phosphoribosylformylglycinamidine cyclo-ligase","termid":"PBO:0012595"}


id: PBO:0043330
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chronic lymphocytic leukemia up-regulated 1","termid":"PBO:0043330"}


id: MONDO:0004563
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polycythemia that is not pathologic.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polycythemia","termid":"MONDO:0005571"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"physiological polycythemia","secondary_identifiers":["MEDGEN:163545","DOID:8431","NCIT:C27311","UMLS:C0856817"],"termid":"MONDO:0004563","xrefs":{"Monarch":{"xref_id":"0004563"}}}


id: PBO:0059705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO2 pseudogene 13","termid":"PBO:0059705"}


id: GO:0016709
data:
  {"annotated_genes":["SJAG_00370","SJAG_03750","SJAG_04608","SJAG_00459"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[109661],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160224"},{"annotations":[57627],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004499"},{"annotations":[77583],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004506"},{"annotations":[88837],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008398"}]},"cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which hydrogen or electrons are transferred from NADH or NADPH and one other donor, and one atom of oxygen is incorporated into one donor.","definition_xrefs":["EC:1.14.13.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00370":null,"SJAG_00459":null,"SJAG_03750":null,"SJAG_04608":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-211951","Reactome:R-HSA-2162187","Reactome:R-HSA-6786239","Reactome:R-HSA-2162194"],"synonyms":[{"name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NADH or NADPH as one donor, and incorporation of one atom of oxygen","type":"related"}],"termid":"GO:0016709","terms_by_termid":{"GO:0004499":null,"GO:0004506":null,"GO:0008398":null,"GO:0160224":null}}


id: MONDO:0013734
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any syndromic microphthalmia in which the cause of the disease is a mutation in the VAX1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic microphthalmia","termid":"MONDO:0016073"}],"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":"microphthalmia, syndromic 11","secondary_identifiers":["OMIM:614402","UMLS:C3553077","MEDGEN:765991","DOID:0111804"],"synonyms":[{"name":"MCOPS11","type":"related"},{"name":"VAX1 syndromic microphthalmia","type":"exact"},{"name":"microphthalmia, syndromic 11","type":"exact"},{"name":"microphthalmia, syndromic type 11","type":"exact"},{"name":"syndromic microphthalmia caused by mutation in VAX1","type":"exact"}],"termid":"MONDO:0013734","xrefs":{"Monarch":{"xref_id":"0013734"}}}


id: GO:0090736
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a meprin and TRAF homology (MATH) domain.","definition_xrefs":["InterPro:IPR002083","PMID:22621901"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"MATH domain binding","termid":"GO:0090736"}


id: GO:2000848
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of corticosteroid hormone secretion.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of steroid hormone secretion","termid":"GO:2000833"},{"relation_name":"is_a","term_name":"regulation of corticosteroid hormone secretion","termid":"GO:2000846"},{"relation_name":"positively_regulates","term_name":"corticosteroid hormone secretion","termid":"GO:0035930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0023052"],"is_obsolete":false,"name":"positive regulation of corticosteroid hormone secretion","synonyms":[{"name":"positive regulation of corticosteroid secretion","type":"related"}],"termid":"GO:2000848"}


id: PBO:0087757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the tRNA splicing endonuclease; tRNA splicing endonuclease (Sen complex) is composed of Sen2p, Sen15p, Sen34p, and Sen54p; Sen complex also cleaves the CBP1 mRNA at the mitochondrial surface; Sen2p contains the active site for tRNA 5' splice site cleavage and has similarity to Sen34p and to Archaeal tRNA splicing endonuclease;","termid":"PBO:0087757"}


id: PBO:0080338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 102 pseudogene","termid":"PBO:0080338"}


id: GO:0031573
data:
  {"annotated_genes":["SJAG_00327","SJAG_00640","SJAG_04332","SJAG_00623","SJAG_05373","SJAG_01708","SJAG_01605","SJAG_03048","SJAG_01677","SJAG_03898","SJAG_04287","SJAG_00429","SJAG_03160","SJAG_03026","SJAG_02771","SJAG_04671","SJAG_02563","SJAG_00364","SJAG_01044"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74279,74801,79178,79553,79785,89484,89529,90808,91796,94904,96372,99720,101223,102720,106992,108037,112113,112420,116443],"is_not":false,"summary":null,"term":"GO:0031573"}]},"cv_name":"biological_process","definition":"A mitotic cell cycle checkpoint that slows DNA synthesis in response to DNA damage by the prevention of new origin firing and the stabilization of slow replication fork progression.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic DNA damage checkpoint signaling","termid":"GO:0044773"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00327":null,"SJAG_00364":null,"SJAG_00429":null,"SJAG_00623":null,"SJAG_00640":null,"SJAG_01044":null,"SJAG_01605":null,"SJAG_01677":null,"SJAG_01708":null,"SJAG_02563":null,"SJAG_02771":null,"SJAG_03026":null,"SJAG_03048":null,"SJAG_03160":null,"SJAG_03898":null,"SJAG_04287":null,"SJAG_04332":null,"SJAG_04671":null,"SJAG_05373":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0023052"],"is_obsolete":false,"name":"mitotic intra-S DNA damage checkpoint signaling","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0072428"],"synonyms":[{"name":"S-phase checkpoint","type":"broad"},{"name":"intra-S DNA damage checkpoint","type":"exact"},{"name":"mitotic intra-S DNA damage checkpoint","type":"exact"},{"name":"signal transduction involved in intra-S DNA damage checkpoint","type":"exact"}],"termid":"GO:0031573","terms_by_termid":{"GO:0031573":null}}


id: GO:0008442
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-hydroxy-2-methylpropanoate + NAD+ = 2-methyl-3-oxopropanoate + NADH + H+.","definition_xrefs":["EC:1.1.1.31"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"3-hydroxyisobutyrate dehydrogenase activity","secondary_identifiers":["Reactome:R-HSA-508473","MetaCyc:3-HYDROXYISOBUTYRATE-DEHYDROGENASE-RXN","RHEA:17681","Reactome:R-HSA-70885"],"termid":"GO:0008442"}


id: PBO:0071230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 71","termid":"PBO:0071230"}


id: GO:0070030
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alphav-beta1 integrin complex bound to osteopontin.","definition_xrefs":["PMID:7592829"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"alphav-beta1 integrin-osteopontin complex","synonyms":[{"name":"ITGAV-ITGB1-SPP1 complex","type":"narrow"}],"termid":"GO:0070030"}


id: PBO:0091195
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Trp","termid":"PBO:0091195"}


id: FYPO:0007057
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 movement of substances via vesicles from recycling endosomes to the Golgi is abnormal.","definition_xrefs":["GO:0071955","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vesicle-mediated transport during vegetative growth","termid":"FYPO:0000213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"abnormal recycling endosome to Golgi transport","synonyms":[{"name":"abnormal recycling endosome to Golgi transport during mitotic cell cycle","type":"related"},{"name":"abnormal recycling endosome to Golgi transport during vegetative growth","type":"exact"}],"termid":"FYPO:0007057"}


id: PBO:0002841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alkyltransferase-like protein Atl1","termid":"PBO:0002841"}


id: PBO:0026761
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_degradation_during_cellular_response_to_UV","termid":"PBO:0026761"}


id: PBO:0064737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 73","termid":"PBO:0064737"}


id: MOD:00810
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O3-mannosylserine.","definition_xrefs":["RESID:AA0402","PubMed:391559"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-glycosyl-L-serine","termid":"MOD:00002"},{"relation_name":"is_a","term_name":"mannosylated residue","termid":"MOD:00595"},{"relation_name":"is_a","term_name":"monohexosylated (Hex1)","termid":"MOD:00761"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"O-mannosyl-L-serine","synonyms":[{"name":"(2S)-2-amino-3-(alpha-D-mannopyranosyloxy)propanoic acid","type":"exact"},{"name":"CARBOHYD O-linked (Hex)","type":"exact"},{"name":"CARBOHYD O-linked (Man) serine","type":"exact"},{"name":"O-glycosylserine","type":"exact"},{"name":"O-mannopyranosylserine","type":"exact"},{"name":"O-mannosyl-L-serine","type":"exact"},{"name":"O3-mannosylserine","type":"exact"},{"name":"OManSer","type":"exact"}],"termid":"MOD:00810"}


id: PR:Q9UTG6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A methionyl-tRNA formyltransferase, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11138:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methionyl-tRNA formyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1805.09c","secondary_identifiers":["UniProtKB:Q9UTG6"],"synonyms":[{"name":"SPAC1805.09c","type":"related"},{"name":"Spom972h-MTFMT","type":"exact"}],"termid":"PR:Q9UTG6"}


id: PBO:0005773
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar membrane zinc transporter (predicted)","termid":"PBO:0005773"}


id: MONDO:0016156
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan","termid":"MONDO:0016155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005066","MONDO:0024322"],"is_obsolete":false,"name":"qualitative or quantitative defects of FKRP","secondary_identifiers":["Orphanet:207119","GARD:20403","UMLS:C5680827","MEDGEN:1842706"],"termid":"MONDO:0016156","xrefs":{"Monarch":{"xref_id":"0016156"}}}


id: FYPO:0006927
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 ratio of the nuclear volume to the total cell volume is lower than normal (the ration observed in wild type is approximately 0.076-0.089).","definition_xrefs":["PMID:31015410","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype during vegetative growth","termid":"FYPO:0004639"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"decreased nucleus:cytoplasm ratio","synonyms":[{"name":"decreased nuclear:cytoplasmic ratio","type":"exact"},{"name":"decreased nuclear:cytoplasmic volume ratio","type":"exact"},{"name":"decreased nucleus:cell volume ratio","type":"exact"},{"name":"decreased nucleus:cytoplasm ratio during mitotic cell cycle","type":"related"},{"name":"decreased nucleus:cytoplasm ratio during vegetative growth","type":"exact"},{"name":"decreased nucleus:cytoplasm volume ratio","type":"exact"},{"name":"reduced nucleus:cytoplasm ratio","type":"exact"}],"termid":"FYPO:0006927"}


id: SO:0001745
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Uniparental disomy is a sequence_alteration where a diploid individual receives two copies for all or part of a chromosome from the mother and no copies of the same chromosome or region from the father.","definition_xrefs":["SO:bm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UPD","termid":"SO:0001744"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maternal_uniparental_disomy","synonyms":[{"name":"maternal uniparental disomy","type":"exact"}],"termid":"SO:0001745"}


id: GO:0003402
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 receptor on the surface of the target cell where activated receptors signal to modulate cytoskeletal elements and control cell polarity that contributes to axis elongation.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete planar cell polarity pathway involved in axis elongation (obsolete GO:0003402)","termid":"GO:0003402"}


id: GO:1902395
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of 1-deoxy-D-xylulose-5-phosphate synthase activity.","definition_xrefs":["PMID:23612965","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of 1-deoxy-D-xylulose-5-phosphate synthase activity (obsolete GO:1902395)","synonyms":[{"name":"regulation of 1-deoxy-D-xylulose-5-phosphate pyruvate-lyase (carboxylating) activity","type":"exact"},{"name":"regulation of 1-deoxyxylulose-5-phosphate synthase activity","type":"exact"},{"name":"regulation of DOXP synthase activity","type":"exact"},{"name":"regulation of DXP-synthase activity","type":"exact"},{"name":"regulation of pyruvate:D-glyceraldehyde-3-phosphate acetaldehydetransferase (decarboxylating)","type":"exact"}],"termid":"GO:1902395"}


id: PBO:0072450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S29 pseudogene 14","termid":"PBO:0072450"}


id: GO:0052372
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which an organism modulates the frequency, rate or extent to which it enters into the host organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological process involved in symbiotic interaction","termid":"GO:0043903"},{"relation_name":"regulates","term_name":"symbiont entry into host","termid":"GO:0044409"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"modulation by symbiont of entry into host","secondary_identifiers":["GO:0052371"],"synonyms":[{"name":"modulation by organism of entry into other organism during symbiotic interaction","type":"related"},{"name":"regulation by organism of entry into other organism during symbiotic interaction","type":"related"},{"name":"regulation by organism of entry into other organism involved in symbiotic interaction","type":"related"}],"termid":"GO:0052372"}


id: FYPO:0007820
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 polyphosphate measured in a cell is too low to detect.","definition_xrefs":["PMID:34147496","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"substance absent from cell during vegetative growth","termid":"FYPO:0001208"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"polyphosphate absent from cell","synonyms":[{"name":"polyphosphate absent from cell during mitotic cell cycle","type":"related"},{"name":"polyphosphate absent from cell during vegetative growth","type":"exact"}],"termid":"FYPO:0007820"}


id: FYPO:0004551
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular response phenotype observed in the vegetative growth phase of the life cycle in which the regulation of the mitotic cell cycle in response to ionizing radiation exposure during mitotic S phase is abnormal. Normally, cell cycle progression is slowed or arrested transiently following exposure to ionizing radiation. The most common abnormality is for the cell cycle to progress as in the absence of ionizing radiation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic cell cycle regulation during cellular response to ionizing radiation","termid":"FYPO:0003489"}],"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000631","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abnormal mitotic cell cycle regulation during cellular response to ionizing radiation during mitotic S phase","synonyms":[{"name":"abnormal cell cycle regulation during cellular response to ionizing radiation during mitotic S phase","type":"exact"},{"name":"abnormal mitotic cell cycle delay following ionizing radiation during mitotic S phase","type":"exact"},{"name":"abnormal mitotic cell cycle regulation during cellular response to IR during mitotic S phase","type":"exact"},{"name":"abnormal mitotic cell cycle regulation during cellular response to ionizing radiation during mitotic S phase during mitotic cell cycle","type":"related"},{"name":"abnormal mitotic cell cycle regulation during cellular response to ionizing radiation during mitotic S phase during vegetative growth","type":"exact"},{"name":"abnormal mitotic cell cycle regulation in response to ionizing radiation during mitotic S phase","type":"exact"}],"termid":"FYPO:0004551"}


id: MONDO:0032920
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":"juvenile arthritis due to defect in LACC1","secondary_identifiers":["GARD:16382","OMIM:618795"],"synonyms":[{"name":"JUVAR","type":"related"},{"name":"JUVENILE ARTHRITIS","type":"related"}],"termid":"MONDO:0032920","xrefs":{"Monarch":{"xref_id":"0032920"}}}


id: PBO:0073472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sarcoglycan beta","termid":"PBO:0073472"}


id: GO:0052875
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: reduced riboflavin + NAD(P)+ = riboflavin + NAD(P)H + 2 H+. This reaction can utilize NADH and NADPH.","definition_xrefs":["EC:1.5.1.41"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor","termid":"GO:0016646"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"riboflavin reductase [NAD(P)H] activity","secondary_identifiers":["KEGG_REACTION:R09750","MetaCyc:RXN-12445","RHEA:31455"],"synonyms":[{"name":"NAD(P)H-FMN reductase activity","type":"related"},{"name":"NAD(P)H-dependent FMN reductase activity","type":"related"},{"name":"NAD(P)H2 dehydrogenase (FMN) activity","type":"related"},{"name":"NAD(P)H2:FMN oxidoreductase activity","type":"related"},{"name":"NAD(P)H:FMN oxidoreductase activity","type":"related"},{"name":"NAD(P)H:riboflavin oxidoreductase activity","type":"related"},{"name":"flavin mononucleotide reductase activity","type":"related"},{"name":"flavine mononucleotide reductase activity","type":"related"},{"name":"riboflavin mononucleotide (reduced nicotinamide adenine dinucleotide) reductase activity","type":"related"},{"name":"riboflavin mononucleotide reductase activity","type":"related"},{"name":"riboflavin reductase (NADH) activity","type":"narrow"},{"name":"riboflavin reductase (NADPH) activity","type":"narrow"},{"name":"riboflavine mononucleotide reductase activity","type":"related"}],"termid":"GO:0052875"}


id: PBO:0090172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium/calmodulin-dependent (CaMKK) protein kinase Ssp1","termid":"PBO:0090172"}


id: PR:Q9UT00
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An extended synaptotagmin-1 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":"uncharacterized protein PYUK71.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPYUK71.03c","secondary_identifiers":["UniProtKB:Q9UT00"],"synonyms":[{"name":"Spom972h-ESYT1","type":"exact"}],"termid":"PR:Q9UT00"}


id: PBO:0089044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diphthamide biosynthesis protein Dph3","termid":"PBO:0089044"}


id: MONDO:0008576
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":"toe, fifth, number of phalanges 1N","secondary_identifiers":["MEDGEN:348255","OMIM:189000","UMLS:C1861062"],"synonyms":[{"name":"toe, fifth, number of phalanges IN","type":"related"},{"name":"toe, fifth, number of phalanges type 1N","type":"exact"}],"termid":"MONDO:0008576","xrefs":{"Monarch":{"xref_id":"0008576"}}}


id: PBO:0026655
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_negative_regulation_of_transcription_by_glucose","termid":"PBO:0026655"}


id: GO:0035628
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the cystic duct over time, from its formation to the mature structure. The cystic duct runs from the gallbladder to the common bile duct.","definition_xrefs":["PMID:20614624"],"direct_ancestors":[{"relation_name":"is_a","term_name":"common bile duct development","termid":"GO:0061009"}],"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":"cystic duct development","termid":"GO:0035628"}


id: GO:0010883
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of lipid storage. Lipid storage is the accumulation and maintenance in cells or tissues of lipids, compounds soluble in organic solvents but insoluble or sparingly soluble in aqueous solvents. Lipid reserves can be accumulated during early developmental stages for mobilization and utilization at later stages of development.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular process","termid":"GO:0050794"},{"relation_name":"regulates","term_name":"lipid storage","termid":"GO:0019915"}],"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 lipid storage","synonyms":[{"name":"regulation of lipid sequestration","type":"narrow"}],"termid":"GO:0010883"}


id: PBO:0068595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 46, pseudogene","termid":"PBO:0068595"}


id: GO:0004952
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with the neurotransmitter dopamine to initiate a change in cell activity.","definition_xrefs":["PMID:21711983","GOC:PARL","IUPHAR_GPCR:1282"],"direct_ancestors":[{"relation_name":"is_a","term_name":"postsynaptic neurotransmitter receptor activity","termid":"GO:0098960"}],"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":"dopamine neurotransmitter receptor activity","termid":"GO:0004952"}


id: FYPO:0006059
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the septin ring is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to cell cortex during vegetative growth","termid":"FYPO:0000928"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"abnormal protein localization to septin ring","synonyms":[{"name":"abnormal protein localisation to septin ring","type":"exact"},{"name":"abnormal protein localization to septin ring during mitotic cell cycle","type":"related"},{"name":"abnormal protein localization to septin ring during vegetative growth","type":"exact"}],"termid":"FYPO:0006059"}


id: PBO:0059208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myoregulin","termid":"PBO:0059208"}


id: MONDO:0007911
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":"lipoprotein, variant of beta","secondary_identifiers":["UMLS:C1835357","OMIM:152400","MEDGEN:322642"],"synonyms":[{"name":"Beta-lipoprotein, Double","type":"related"},{"name":"lipoprotein, variant of beta","type":"exact"}],"termid":"MONDO:0007911","xrefs":{"Monarch":{"xref_id":"0007911"}}}


id: GO:0052530
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism activates, maintains or increases the frequency, rate or extent of the resistance gene-dependent defense response of the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by organism of symbiont resistance gene-dependent defense response (obsolete GO:0052530)","synonyms":[{"name":"positive regulation by organism of defense response in symbiont by specific elicitors","type":"exact"},{"name":"positive regulation by organism of pathogen-race/symbiont plant cultivar-specific resistance in symbiont","type":"exact"},{"name":"positive regulation by organism of symbiont gene-for-gene resistance","type":"exact"},{"name":"positive regulation by organism of symbiont resistance gene-dependent defense response","type":"exact"}],"termid":"GO:0052530"}


id: MONDO:0020786
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete short sleep, familial natural, 2 (obsolete MONDO:0020786)","secondary_identifiers":["OMIM:618591"],"synonyms":[{"name":"FNSS2","type":"related"},{"name":"SHORT SLEEP, FAMILIAL NATURAL, 2","type":"related"},{"name":"short sleep, familial natural, 2","type":"exact"}],"termid":"MONDO:0020786","xrefs":{"Monarch":{"xref_id":"0020786"}}}


id: GO:0007524
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the adult visceral muscle over time, from its formation to the mature structure.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"visceral muscle development","termid":"GO:0007522"}],"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":"adult visceral muscle development","termid":"GO:0007524"}


id: PBO:0059005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MMADHC pseudogene 1","termid":"PBO:0059005"}


id: MONDO:0031646
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":"Braddock-Carey syndrome","secondary_identifiers":["OMIMPS:619980"],"termid":"MONDO:0031646","xrefs":{"Monarch":{"xref_id":"0031646"}}}


id: PBO:0085111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear ubiquitin protein ligase binding protein; may regulate utilization of nonfermentable carbon sources and endocytosis of plasma membrane proteins; overproduction suppresses chs5 spa2 lethality at high temp; ubiquitinated by Rsp5p, deubiquitinated by Ubp2p; CSR2 has a paralog, ECM21, that arose from the whole genome duplication","termid":"PBO:0085111"}


id: PBO:0087549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of RNA polymerase III transcription initiation factor complex; one of six subunits of the RNA polymerase III transcription initiation factor complex (TFIIIC); part of the TauA globular domain of TFIIIC that binds DNA at the BoxA promoter sites of tRNA and similar genes; human homolog is TFIIIC-63","termid":"PBO:0087549"}


id: GO:0036340
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of hardening a chitin-based cuticle by mineral incorporation. For example, the cuticle of crustaceans is hardened by the incorporation of calcium carbonate.","definition_xrefs":["GOC:sart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chitin-based cuticle sclerotization","termid":"GO:0007593"},{"relation_name":"is_a","term_name":"biomineral tissue development","termid":"GO:0031214"}],"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":"chitin-based cuticle sclerotization by biomineralization","synonyms":[{"name":"chitin-based cuticle hardening by biomineralisation","type":"exact"}],"termid":"GO:0036340"}


id: GO:0034978
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains the homeodomain proteins PDX1, PBX1b and MRG1 (MEIS2) and is involved in the transcriptional regulation of pancreatic acinar cell-specific genes.","definition_xrefs":["PMID:11279116","PMID:9710595"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"PDX1-PBX1b-MRG1 complex","synonyms":[{"name":"acinar cell-specific C complex","type":"exact"}],"termid":"GO:0034978"}


id: PBO:0091270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial GTPase related protein Gep3","termid":"PBO:0091270"}


id: GO:0032609
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interferon-gamma due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels. Interferon-gamma is also known as type II interferon.","definition_xrefs":["GOC:add","GOC:mah","PMID:15546383"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"type II interferon production","secondary_identifiers":["GO:0042095","GO:0072643"],"synonyms":[{"name":"IFNG production","type":"exact"},{"name":"interferon-gamma biosynthetic process","type":"narrow"},{"name":"interferon-gamma production","type":"exact"},{"name":"interferon-gamma secretion","type":"narrow"},{"name":"type II IFN production","type":"exact"}],"termid":"GO:0032609"}


id: GO:0160220
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-lactate + ATP + D-alanine = ADP + D-alanyl-(R)-lactate + phosphate.","definition_xrefs":["RHEA:37347"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-oxygen bonds","termid":"GO:0016875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016874","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"D-alanine-(R)-lactate ligase activity","secondary_identifiers":["EC:6.1.2.1","KEGG_REACTION:R09588","MetaCyc:RXN-11298"],"synonyms":[{"name":"D-alanyl-D-lactate ligase activity","type":"exact"}],"termid":"GO:0160220"}


id: PBO:0004133
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mei4 DEpendent protein","termid":"PBO:0004133"}


id: PATO:0002290
data:
  {"annotation_feature_type":"gene","cv_name":"quality","direct_ancestors":[{"relation_name":"is_a","term_name":"physical object quality","termid":"PATO:0001241"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aplastic/hypoplastic","termid":"PATO:0002290"}


id: MONDO:0015039
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lissencephaly with cerebellar hypoplasia type F (LCHf) is a severe form of lissencephaly with cerebellar hypoplasia, characterized by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum.","definition_xrefs":["Orphanet:100016"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lissencephaly with cerebellar hypoplasia","termid":"MONDO:0019450"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"lissencephaly with cerebellar hypoplasia type F","secondary_identifiers":["SCTID:715822007","icd11.foundation:468664200","GARD:19736","MEDGEN:902647","UMLS:C4274989"],"termid":"MONDO:0015039","xrefs":{"Monarch":{"xref_id":"0015039"}}}


id: PBO:0068527
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 128, pseudogene","termid":"PBO:0068527"}


id: GO:1990128
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A protein-DNA complex involved in replication initiation at the origin of replication.","definition_xrefs":["GOC:bhm","PMID:21856207"],"gene_count":0,"genotype_count":0,"name":"obsolete pre-primosome complex involved in replication initiation (obsolete GO:1990128)","synonyms":[{"name":"pre-primosome complex involved in replication initiation","type":"exact"}],"termid":"GO:1990128"}


id: PBO:0049841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HEAT repeat containing 4","termid":"PBO:0049841"}


id: PBO:0082898
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cyclin, interacts with cyclin-dependent kinase Pho85p; member of the Pcl1,2-like subfamily, involved in the regulation of polarized growth and morphogenesis and progression through the cell cycle; localizes to sites of polarized cell growth; PCL2 has a paralog, PCL9, that arose from the whole genome duplication","termid":"PBO:0082898"}


id: PBO:0046417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPHA2 antisense RNA 1","termid":"PBO:0046417"}


id: PBO:0051019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insulin like growth factor binding protein acid labile subunit","termid":"PBO:0051019"}


id: GO:0050603
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: AH(2) + O2 + thiophene-2-carbonyl-CoA = 5-hydroxythiophene-2-carbonyl-CoA + A + H2O + H+.","definition_xrefs":["EC:1.14.99.35","RHEA:18929"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"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:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"thiophene-2-carbonyl-CoA monooxygenase activity","secondary_identifiers":["MetaCyc:1.14.99.35-RXN","UM-BBD_reactionID:r1235","KEGG_REACTION:R05742"],"synonyms":[{"name":"thiophene-2-carbonyl-CoA, hydrogen-donor:oxygen oxidoreductase activity","type":"related"},{"name":"thiophene-2-carboxyl-CoA dehydrogenase activity","type":"related"},{"name":"thiophene-2-carboxyl-CoA hydroxylase activity","type":"related"},{"name":"thiophene-2-carboxyl-CoA monooxygenase activity","type":"related"}],"termid":"GO:0050603"}


id: FYPO:0008066
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through the mitotic cell cycle is no longer arrested during G1 phase when phosphate is removed. Arrest may either occur under conditions where arrest is not a normal occurrence, or may progress differently from normal under conditions where arrest normally does take place.","definition_xrefs":["PMID:36779416"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell cycle arrest in mitotic G1 phase","termid":"FYPO:0005097"}],"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":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000631","FYPO:0001985"],"is_obsolete":false,"name":"abolished cell cycle arrest in mitotic G1 phase in response to phosphate starvation","termid":"FYPO:0008066"}


id: PBO:0071069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 71","termid":"PBO:0071069"}


id: PBO:0067475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 606, pseudogene","termid":"PBO:0067475"}


id: PBO:0090362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial membrane protein, conserved in yeast and apicomplexa","termid":"PBO:0090362"}


id: PBO:0080084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 46","termid":"PBO:0080084"}


id: PBO:0052000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"JAZF zinc finger 1","termid":"PBO:0052000"}


id: PBO:0031655
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_re-entry_into_mitotic_cell_cycle_after_pheromone_arrest","termid":"PBO:0031655"}


id: PBO:0052540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kallikrein related peptidase 13","termid":"PBO:0052540"}


id: PBO:0031527
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_DNA-1,N6-ethenoadenine_N-glycosylase_activity","termid":"PBO:0031527"}


id: PBO:0055954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 66","termid":"PBO:0055954"}


id: GO:0008877
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: alpha-D-glucose 1-phosphate + H2O = D-glucose + phosphate.","definition_xrefs":["EC:3.1.3.10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sugar-phosphatase activity","termid":"GO:0050308"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016788","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"glucose-1-phosphatase activity","secondary_identifiers":["KEGG_REACTION:R00304","MetaCyc:GLUCOSE-1-PHOSPHAT-RXN","RHEA:19933"],"synonyms":[{"name":"D-glucose-1-phosphate phosphohydrolase activity","type":"related"},{"name":"alpha-D-glucose-1-phosphate phosphohydrolase activity","type":"related"}],"termid":"GO:0008877"}


id: GO:0070251
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + pristanate + CoA = AMP + diphosphate + pristanoyl-CoA.","definition_xrefs":["GOC:pde","PMID:10198260"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CoA-ligase activity","termid":"GO:0016405"},{"relation_name":"is_a","term_name":"acid-thiol ligase activity","termid":"GO:0016878"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016874","GO:0003824"],"is_obsolete":false,"name":"pristanate-CoA ligase activity","secondary_identifiers":["Reactome:R-HSA-389632","RHEA:47264"],"synonyms":[{"name":"pristanate:CoA ligase (AMP-forming)","type":"exact"},{"name":"pristanoyl-CoA ligase activity","type":"exact"}],"termid":"GO:0070251"}


id: GO:0061249
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to a mesonephric glomerular capillary. This process pertains to the initial formation of a structure from unspecified parts.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerular capillary formation","termid":"GO:0072104"},{"relation_name":"part_of","term_name":"mesonephric glomerulus vasculature morphogenesis","termid":"GO:0061248"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mesonephric glomerular capillary formation","termid":"GO:0061249"}


id: PBO:0088410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mannosyltransferase complex subunit Alg9","termid":"PBO:0088410"}


id: PBO:0061303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aminopeptidase puromycin sensitive","termid":"PBO:0061303"}


id: PR:G2TRM9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC4H3.17 gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRM9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C4H3.17 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4H3.17","synonyms":[{"name":"Spom972h-SPAC4H3.17","type":"exact"}],"termid":"PR:G2TRM9"}


id: MONDO:0013403
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any visceral heterotaxy in which the cause of the disease is a mutation in the ACVR2B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"visceral heterotaxy","termid":"MONDO:0018677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterotaxy, visceral, 4, autosomal","secondary_identifiers":["OMIM:613751","UMLS:C3151057","MEDGEN:462407"],"synonyms":[{"name":"ACVR2B visceral heterotaxy","type":"exact"},{"name":"HTX4","type":"related"},{"name":"heterotaxy, visceral, 4, autosomal","type":"exact"},{"name":"visceral heterotaxy caused by mutation in ACVR2B","type":"exact"}],"termid":"MONDO:0013403","xrefs":{"Monarch":{"xref_id":"0013403"}}}


id: PBO:0064459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pogo transposable element derived with ZNF domain","termid":"PBO:0064459"}


id: MONDO:0034872
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete large granular lymphocyte leukemia (obsolete MONDO:0034872)","secondary_identifiers":["Orphanet:512034"],"termid":"MONDO:0034872","xrefs":{"Monarch":{"xref_id":"0034872"}}}


id: PBO:0040713
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL6 antisense RNA 1","termid":"PBO:0040713"}


id: PBO:0111485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II CTD S5 small phosphatase Psr1","termid":"PBO:0111485"}


id: PBO:0113475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of tRNA-specific adenosine-34 deaminase; forms a heterodimer with Tad2p that converts adenosine to inosine at the wobble position of several tRNAs; localizes to cytosol, nucleus and peroxisomes","termid":"PBO:0113475"}


id: MONDO:0014250
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial hyperprolactinemia is a rare, genetic endocrine disorder characterized by persistently high prolactin serum levels (not associated with gestation, puerperium, drug intake or pituitary tumor) in multiple affected family members. Clinically it manifests with signs usually observed in hyperprolactinemia, which are: secondary medroxyprogesterone acetate (MPA)-negative amenorrhea and galactorrhea in female patients, and hypogonadism and decreased testosterone level-driven sexual disfunction in male patients. Oligomenorrhea and primary infertility have also been reported in some female patients.","definition_xrefs":["Orphanet:397685"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperprolactinemia","termid":"MONDO:0005804"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial hyperprolactinemia","secondary_identifiers":["OMIM:615555","SCTID:763715007","UMLS:C4706551","MEDGEN:1645317","ICD10CM:E22.1","GARD:17634"],"synonyms":[{"name":"HPRL","type":"related"},{"name":"familial hyperprolactinemia","type":"exact"},{"name":"familial isolated prolactin receptor deficiency","type":"exact"},{"name":"hereditary hyperprolactinemia (disease)","type":"exact"},{"name":"hyperprolactinemia","type":"related"}],"termid":"MONDO:0014250","xrefs":{"Monarch":{"xref_id":"0014250"}}}


id: PBO:0077082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosine kinase with immunoglobulin like and EGF like domains 1","termid":"PBO:0077082"}


id: MONDO:1012606
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any glycogen storage disease that occurs in cats due to a mutation in the GBE1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycogen storage disease, non-human animal","termid":"MONDO:1011419"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycogen storage disease IV, domestic cat","secondary_identifiers":["OMIA:000420-9685"],"synonyms":[{"name":"GSD IV","type":"exact"}],"termid":"MONDO:1012606","xrefs":{"Monarch":{"xref_id":"1012606"}}}


id: MOD:01061
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-carboxymethyl-L-cysteine.","definition_xrefs":["OMSSA:2","DeltaMass:0","DeltaMass:197","Unimod:6#C"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iodoacetic acid derivatized residue","termid":"MOD:00399"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-carboxymethyl-L-cysteine","synonyms":[{"name":"Carboxymethyl","type":"related"},{"name":"Carboxymethyl Cystenyl","type":"exact"},{"name":"Carboxymethyl cysteine","type":"exact"},{"name":"CmC","type":"exact"},{"name":"Iodoacetic acid derivative","type":"related"},{"name":"carboxymethylc","type":"exact"}],"termid":"MOD:01061"}


id: GO:0048608
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The reproductive developmental process whose specific outcome is the progression of somatic structures that will be used in the process of creating new individuals from one or more parents, from their formation to the mature structures.","definition_xrefs":["GOC:isa_complete","GOC:jid","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"reproductive system development","termid":"GO:0061458"}],"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 structure development","termid":"GO:0048608"}


id: PBO:0116310
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospho-2-dehydro-3-deoxyheptonate aldolase Aro3","termid":"PBO:0116310"}


id: FYPO:0004601
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the S-phase DNA damage checkpoint (also known as the intra-S phase DNA damage checkpoint) is normal (i.e. indistinguishable from wild type) when the cell is exposed to hydroxyurea. The S phase DNA damage checkpoint slows progression through S phase in response to DNA damage.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cell cycle regulation during cellular response to hydroxyurea","termid":"FYPO:0001929"},{"relation_name":"is_a","term_name":"normal S-phase DNA damage checkpoint","termid":"FYPO:0003530"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000298","FYPO:0000257","FYPO:0001312","FYPO:0001320","FYPO:0000631"],"is_obsolete":false,"name":"normal S-phase DNA damage checkpoint during cellular response to hydroxyurea","synonyms":[{"name":"normal S-phase DNA damage checkpoint activation during cellular response to hydroxyurea","type":"exact"},{"name":"normal S-phase DNA damage checkpoint during cellular response to HU","type":"exact"},{"name":"normal S-phase DNA damage checkpoint during cellular response to hydroxyurea during mitotic cell cycle","type":"exact"},{"name":"normal S-phase DNA damage checkpoint during cellular response to hydroxyurea during vegetative growth","type":"exact"},{"name":"normal intra-S phase DNA damage checkpoint during cellular response to hydroxyurea","type":"exact"},{"name":"normal mitotic S-phase DNA damage checkpoint during cellular response to hydroxyurea","type":"exact"}],"termid":"FYPO:0004601"}


id: GO:0085022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which an organism effects a change in the structure or function of its host organism, mediated by a substance secreted by a type VI secretion system in the organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete modification by symbiont of host morphology or physiology via protein secreted by type VI secretion system (obsolete GO:0085022)","termid":"GO:0085022"}


id: PBO:0005829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor TFIID complex subunit Taf13 (predicted)","termid":"PBO:0005829"}


id: GO:1904415
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of xenophagy.","definition_xrefs":["PMID:21617041","GOC:pad","GOC:PARL","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to biotic stimulus","termid":"GO:0002831"},{"relation_name":"is_a","term_name":"regulation of macroautophagy","termid":"GO:0016241"},{"relation_name":"is_a","term_name":"regulation of response to external stimulus","termid":"GO:0032101"},{"relation_name":"regulates","term_name":"xenophagy","termid":"GO:0098792"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006914"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006914"],"is_obsolete":false,"name":"regulation of xenophagy","termid":"GO:1904415"}


id: PBO:0087164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase III subunit C25; required for transcription initiation; forms a heterodimer with Rpc17p; paralog of Rpb7p","termid":"PBO:0087164"}


id: PBO:0001281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAD51D-like protein 1","termid":"PBO:0001281"}


id: GO:0016894
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of ester linkages within nucleic acids by creating internal breaks to yield 3'-phosphomonoesters.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 3'-phosphomonoesters (obsolete GO:0016894)","synonyms":[{"name":"3'-endonuclease activity","type":"exact"},{"name":"endoribonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 3'-phosphomonoesters","type":"related"}],"termid":"GO:0016894"}


id: GO:0046146
data:
  {"annotated_genes":["SJAG_03275","SJAG_03098"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[108901,70299],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006729"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving tetrahydrobiopterin, the reduced form of biopterin (2-amino-4-hydroxy-6-(1,2-dihydroxypropyl)-pteridine). It functions as a hydroxylation coenzyme, e.g. in the conversion of phenylalanine to tyrosine.","definition_xrefs":["PMID:21871890"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diol metabolic process","termid":"GO:0034311"},{"relation_name":"is_a","term_name":"pteridine-containing compound metabolic process","termid":"GO:0042558"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03098":null,"SJAG_03275":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"tetrahydrobiopterin metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-1474151"],"synonyms":[{"name":"5,6,7,8-tetrahydrobiopterin metabolic process","type":"exact"},{"name":"tetrahydrobiopterin metabolism","type":"exact"}],"termid":"GO:0046146","terms_by_termid":{"GO:0006729":null}}


id: FYPO:0008309
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a cell divides with a greater surface area than normal (i.e. compared to wild-type cells under the same conditions).","definition_xrefs":["PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable swollen vegetative cell","termid":"FYPO:0002377"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000004","FYPO:0000005","FYPO:0000002"],"is_obsolete":false,"name":"increased cell surface area at division","termid":"FYPO:0008309"}


id: PBO:0082616
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Coiled-coil protein involved in spindle-assembly checkpoint; required for inhibition of karyopherin/importin Pse1p (aka Kap121p) upon spindle assembly checkpoint arrest; phosphorylated by Mps1p upon checkpoint activation which leads to inhibition of anaphase promoting complex activity; forms a complex with Mad2p; gene dosage imbalance between MAD1 and MAD2 leads to chromosome instability","termid":"PBO:0082616"}


id: PBO:0057518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 636","termid":"PBO:0057518"}


id: PBO:0040636
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BARX homeobox 2","termid":"PBO:0040636"}


id: PR:O94609
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A ubiquitin-like modifier-activating enzyme 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10953:SF4","PRO:DNx","OMA:SCHPO03896"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-activating enzyme E1 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1604.21c","secondary_identifiers":["UniProtKB:O94609"],"synonyms":[{"name":"Spom972h-UBA1","type":"exact"},{"name":"poly(A)+ RNA transport protein 3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94609"}


id: PBO:0078823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Pro (anticodon AGG) 2-6","termid":"PBO:0078823"}


id: GO:0003832
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: beta-alanyl-dopamine + H2O = dopamine + beta-alanine.","definition_xrefs":["PMID:16299587","RHEA:73467"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016810","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"beta-alanyl-dopamine hydrolase activity","synonyms":[{"name":"N-beta-alanyl-dopamine hydrolase activity","type":"exact"},{"name":"NBAD hydrolase activity","type":"exact"}],"termid":"GO:0003832"}


id: GO:0061681
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The Entner-Doudoroff pathway that proceeds through a D-gluconate intermediate and yields pyruvate and D-glyceraldehyde-3-phosphate.","definition_xrefs":["GOC:dph","PMID:12921536"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glyceraldehyde-3-phosphate metabolic process","termid":"GO:0019682"},{"relation_name":"is_a","term_name":"Entner-Doudoroff pathway through gluconate","termid":"GO:0061679"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0005975"],"is_obsolete":false,"name":"Entner-Doudoroff pathway through gluconate to D-glyceraldehyde-3-phosphate","secondary_identifiers":["MetaCyc:PWY-2221"],"termid":"GO:0061681"}


id: PBO:0061632
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nudix hydrolase 15","termid":"PBO:0061632"}


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:11875433","Unimod:34#C-term","RESID:AA0318","PubMed:10973948"],"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:0059380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S21 pseudogene 5","termid":"PBO:0059380"}


id: PATO:0001738
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's lacking physically interaction with another entity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dissociated from","synonyms":[{"name":"dissociated","type":"exact"}],"termid":"PATO:0001738"}


id: PBO:0062670
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 Z member 1 pseudogene","termid":"PBO:0062670"}


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


id: PBO:0059494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"macrophage stimulating 1 receptor","termid":"PBO:0059494"}


id: PBO:0070351
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY4 pseudogene 24","termid":"PBO:0070351"}


id: PBO:0016985
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"co-expression of nus1 and rer2 functionally complements a triple deletion of NUS1, RER2 and SRT1 in S. cerevisiae","termid":"PBO:0016985"}


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


id: PBO:0048825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit gamma 10 pseudogene 1","termid":"PBO:0048825"}


id: GO:1905801
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of intraciliary retrograde transport.","definition_xrefs":["PMID:27930654","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of intracellular transport","termid":"GO:0032388"},{"relation_name":"is_a","term_name":"regulation of intraciliary retrograde transport","termid":"GO:1905799"},{"relation_name":"positively_regulates","term_name":"intraciliary retrograde transport","termid":"GO:0035721"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of intraciliary retrograde transport","synonyms":[{"name":"activation of intraciliary retrograde transport","type":"narrow"},{"name":"activation of intraflagellar retrograde transport","type":"narrow"},{"name":"positive regulation of intraflagellar retrograde transport","type":"exact"},{"name":"up regulation of intraciliary retrograde transport","type":"exact"},{"name":"up regulation of intraflagellar retrograde transport","type":"exact"},{"name":"up-regulation of intraciliary retrograde transport","type":"exact"},{"name":"up-regulation of intraflagellar retrograde transport","type":"exact"},{"name":"upregulation of intraciliary retrograde transport","type":"exact"},{"name":"upregulation of intraflagellar retrograde transport","type":"exact"}],"termid":"GO:1905801"}


id: GO:0160174
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A cellular developmental process by which the outer layer of the cell (the cortex) rotates relative to the inner cytoplasm.","definition_xrefs":["PMID:22949618","PMID:25077289","PMID:37983969"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular developmental process","termid":"GO:0048869"}],"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":"cortical rotation","termid":"GO:0160174"}


id: GO:0004667
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: prostaglandin H(2) = prostaglandin D(2).","definition_xrefs":["EC:5.3.99.2","RHEA:10600"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity","termid":"GO:0016860"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"prostaglandin-D synthase activity","secondary_identifiers":["Reactome:R-HSA-2161620","Reactome:R-HSA-2161701","KEGG_REACTION:R02266","MetaCyc:PROSTAGLANDIN-D-SYNTHASE-RXN"],"synonyms":[{"name":"(5,13)-(15S)-9alpha,11alpha-epidioxy-15-hydroxyprosta-5,13-dienoate D-isomerase activity","type":"related"},{"name":"PGD2 synthase activity","type":"related"},{"name":"PGH-PGD isomerase activity","type":"related"},{"name":"prostaglandin D2 synthase activity","type":"related"},{"name":"prostaglandin-H2 D-isomerase activity","type":"related"},{"name":"prostaglandin-R-prostaglandin D isomerase activity","type":"related"}],"termid":"GO:0004667"}


id: PBO:0086753
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; present in a region duplicated between chromosomes XIV and III; YCL001W-B has a paralog, DOM34, that arose from the whole genome duplication","termid":"PBO:0086753"}


id: MONDO:0021272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"primary orthostatic hypotension","termid":"MONDO:0015914"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inherited orthostatic hypotension","secondary_identifiers":["Orphanet:448426","MEDGEN:1842591","GARD:21878","OMIMPS:223360","UMLS:C5681106"],"termid":"MONDO:0021272","xrefs":{"Monarch":{"xref_id":"0021272"}}}


id: GO:1901413
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of tetrapyrrole biosynthetic process from glycine and succinyl-CoA.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of amino acid metabolic process","termid":"GO:0006521"},{"relation_name":"is_a","term_name":"regulation of nucleobase-containing compound metabolic process","termid":"GO:0019219"},{"relation_name":"is_a","term_name":"regulation of phosphate metabolic process","termid":"GO:0019220"},{"relation_name":"is_a","term_name":"regulation of amide metabolic process","termid":"GO:0034248"},{"relation_name":"is_a","term_name":"regulation of sulfur metabolic process","termid":"GO:0042762"},{"relation_name":"is_a","term_name":"regulation of small molecule metabolic process","termid":"GO:0062012"},{"relation_name":"is_a","term_name":"regulation of tetrapyrrole biosynthetic process","termid":"GO:1901463"},{"relation_name":"regulates","term_name":"tetrapyrrole biosynthetic process from glycine and succinyl-CoA","termid":"GO:0033527"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006790"},{"rel_name":"regulates","termid":"GO:0033013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0006520","GO:0008150","GO:0006790","GO:0033013"],"is_obsolete":false,"name":"regulation of tetrapyrrole biosynthetic process from glycine and succinyl-CoA","synonyms":[{"name":"regulation of tetrapyrrole anabolism from glycine and succinyl-CoA","type":"exact"},{"name":"regulation of tetrapyrrole biosynthesis from glycine and succinyl-CoA","type":"exact"},{"name":"regulation of tetrapyrrole formation from glycine and succinyl-CoA","type":"exact"},{"name":"regulation of tetrapyrrole synthesis from glycine and succinyl-CoA","type":"exact"}],"termid":"GO:1901413"}


id: PBO:0110338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BBLN pseudogene 1","termid":"PBO:0110338"}


id: MOD:01856
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that crosslinks two residues by rearrangement and condensation of a cysteine with the carbonyl of the preceding residue to form a 1,3-oxazole-4-carbothionic acid.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxazole/oxazoline ring crosslinked residues","termid":"MOD:01419"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oxazole/oxazoline ring crosslinked residues (Cys)","termid":"MOD:01856"}


id: GO:0048909
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the anterior lateral line nerve over time, form its formation to the mature structure. The anterior lateral line nerve contains efferent axons that innervate hair cells of the ALL and afferent axons that project to an octavolateralis column in the hindbrain. The octavolateralis column consists of the medial octavolateralis nucleus (MON), the caudal octavolateralis nucleus, and the magnocellular nucleus.","definition_xrefs":["ISBN:0125296509","GOC:dgh","GOC:cls","GO_REF:0000021","GOC:jid","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lateral line nerve development","termid":"GO:0048892"},{"relation_name":"part_of","term_name":"anterior lateral line system development","termid":"GO:0048898"}],"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":"anterior lateral line nerve development","secondary_identifiers":["GO:0021734"],"synonyms":[{"name":"ALLN development","type":"exact"},{"name":"nALL development","type":"exact"},{"name":"rostral lateral line nerve development","type":"exact"}],"termid":"GO:0048909"}


id: MONDO:0011118
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute leukemia of ambiguous lineage in which there is a dual population of blasts with each population expressing markers of a distinct lineage (myeloid and lymphoid or B-and T-lymphocyte). (WHO, 2001) -- 2003","definition_xrefs":["NCIT:C6923"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute leukemia of ambiguous lineage","termid":"MONDO:0019460"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"bilineal acute myeloid leukemia","secondary_identifiers":["Orphanet:98836","MEDGEN:87614","UMLS:C0349680"],"synonyms":[{"name":"acute bilineal leukaemia","type":"exact"},{"name":"acute bilineal leukemia","type":"exact"},{"name":"bilineal acute leukaemia","type":"related"},{"name":"bilineal acute leukemia","type":"related"}],"termid":"MONDO:0011118","xrefs":{"Monarch":{"xref_id":"0011118"}}}


id: GO:0001723
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. High molecular weight (100-300 kDa) proteins that associate with intermediate filaments to cross-link them into loose networks.","definition_xrefs":["PMID:9484600","GOC:ajp"],"gene_count":0,"genotype_count":0,"name":"obsolete type II intermediate filament associated protein (obsolete GO:0001723)","synonyms":[{"name":"type II intermediate filament associated protein","type":"exact"}],"termid":"GO:0001723"}


id: MONDO:0019628
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Rieger's anomaly is a congenital ocular defect caused by anterior segment dysgenesis and is characterized by severe anterior chamber deformity with prominent strands and marked atrophy of the iris stroma, with hole or pseudo-hole formation and corectopia. The term covers the association of these iris and pupil anomalies with the features of AxenfeldBs anomaly.","definition_xrefs":["Orphanet:91483"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iridogoniodysgenesis","termid":"MONDO:0011119"}],"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":"Rieger anomaly","secondary_identifiers":["MedDRA:10059198","GARD:16482","UMLS:C0265341","MEDGEN:78558"],"termid":"MONDO:0019628","xrefs":{"Monarch":{"xref_id":"0019628"}}}


id: PBO:0065258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich 23B","termid":"PBO:0065258"}


id: MONDO:0012084
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Aromatic L-amino acid decarboxylase deficiency is a very rare, severe, genetic neurometabolic disorder associated with clinical manifestations related to underproduction of serotonin and dopamine, mainly hypotonia, hypokinesia, ptosis oculogyric crises, and signs of autonomic dysfunction.","definition_xrefs":["Orphanet:35708"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of catecholamine synthesis","termid":"MONDO:0017759"}],"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":"aromatic L-amino acid decarboxylase deficiency","secondary_identifiers":["NORD:2010","ICD9:270.8","icd11.foundation:1134258245","MEDGEN:220945","GARD:770","MESH:C537437","NANDO:1200988","NANDO:2200596","OMIM:608643","UMLS:C1291564","NCIT:C142085","DOID:0090123","SCTID:237922009"],"synonyms":[{"name":"AADC deficiency","type":"exact"},{"name":"Aadc deficiency","type":"related"},{"name":"DDC deficiency","type":"related"},{"name":"Dopa decarboxylase deficiency","type":"related"},{"name":"aromatic L-amino acid decarboxylase deficiency","type":"exact"},{"name":"aromatic L-amino-acid decarboxylase deficiency","type":"exact"},{"name":"aromatic amino acid decarboxylase deficiency","type":"related"}],"termid":"MONDO:0012084","xrefs":{"Monarch":{"xref_id":"0012084"}}}


id: PBO:0013057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudokinase Tea5","termid":"PBO:0013057"}


id: PR:000050518
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A SNF1-like protein kinase ssp2 (Schizosaccharomyces pombe) that has not been phosphorylated at the position equivalent to Thr-189 of the amino acid sequence represented by UniProtKB:O74536. Example: UniProtKB:O74536, Thr-189, MOD:00047.","definition_xrefs":["PMID:22375066","PomBase:VW","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SNF1-like protein kinase ssp2 (Schizosaccharomyces pombe)","termid":"PR:000050516"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ssp2/UnPhos:(T189)","pombase_gene_id":"SPCC74.03c","synonyms":[{"name":"PomBase_original_PRO_term_name: SNF1-like protein kinase ssp2 unphosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-ssp2/UnPhos:1","type":"exact"},{"name":"UniProtKB:O74536, Thr-189, PR:000026291","type":"narrow"},{"name":"ssp2/UnPhos:(T189)","type":"exact"}],"termid":"PR:000050518"}


id: PBO:0070389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ROPN1L antisense RNA 1","termid":"PBO:0070389"}


id: FYPO:0005713
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which cell cycle regulation mediated by the mitotic cytokinesis checkpoint does not occur under conditions that normally trigger the checkpoint signaling and response. Normally, the cytokinesis checkpoint normally delays the G2/M transition of a mitotic cell cycle if cytokinesis was not completed correctly in the previous cell cycle.","definition_xrefs":["PomBase:mah","GO:0044878"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cytokinesis checkpoint","termid":"FYPO:0003830"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000298"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000631","FYPO:0005447","FYPO:0001320","FYPO:0000298","FYPO:0000002"],"is_obsolete":false,"name":"abolished cytokinesis checkpoint","synonyms":[{"name":"abolished cytokinesis checkpoint during mitotic cell cycle","type":"exact"},{"name":"abolished cytokinesis checkpoint during vegetative growth","type":"exact"},{"name":"abolished mitotic cytokinesis checkpoint","type":"exact"}],"termid":"FYPO:0005713"}


id: GO:0075138
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of the symbiont or its cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of detecting oxygen tension in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to host","termid":"GO:0075136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to host oxygen tension environment","synonyms":[{"name":"response of symbiont to host oxygen tension environment","type":"exact"}],"termid":"GO:0075138"}


id: GO:0033852
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-oxoglutarate + 3,5,3'-triiodo-L-thyronine = 3,5,3'-triiodothyropyruvate + L-glutamate.","definition_xrefs":["RHEA:19133","EC:2.6.1.26"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016769","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"thyroid-hormone transaminase activity","secondary_identifiers":["KEGG_REACTION:R03952","MetaCyc:THYROID-HORMONE-AMINOTRANSFERASE-RXN"],"synonyms":[{"name":"3,5-dinitrotyrosine aminotransferase activity","type":"related"},{"name":"3,5-dinitrotyrosine transaminase activity","type":"related"},{"name":"L-3,5,3'-triiodothyronine:2-oxoglutarate aminotransferase activity","type":"related"},{"name":"thyroid hormone aminotransferase activity","type":"related"},{"name":"thyroid-hormone aminotransferase activity","type":"related"}],"termid":"GO:0033852"}


id: GO:0004631
data:
  {"annotated_genes":["SJAG_01474"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74712],"is_not":false,"summary":null,"term":"GO:0004631"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-5-phosphomevalonate + ATP = (R)-5-diphosphomevalonate + ADP + H+.","definition_xrefs":["RHEA:16341","EC:2.7.4.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, phosphate group as acceptor","termid":"GO:0016776"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01474":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016301","GO:0003824"],"is_obsolete":false,"name":"phosphomevalonate kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-191422","KEGG_REACTION:R03245","MetaCyc:PHOSPHOMEVALONATE-KINASE-RXN"],"synonyms":[{"name":"5-phosphomevalonate kinase activity","type":"related"},{"name":"ATP:(R)-5-phosphomevalonate phosphotransferase activity","type":"related"},{"name":"ATP:5-phosphomevalonate phosphotransferase activity","type":"related"},{"name":"mevalonate phosphate kinase activity","type":"related"},{"name":"mevalonate-5-phosphate kinase activity","type":"related"},{"name":"mevalonic acid phosphate kinase activity","type":"related"}],"termid":"GO:0004631","terms_by_termid":{"GO:0004631":null}}


id: GO:0009914
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of hormones into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport","termid":"GO:0006810"},{"relation_name":"is_a","term_name":"regulation of hormone levels","termid":"GO:0010817"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"hormone transport","termid":"GO:0009914"}


id: SO:0001662
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A TATA box core promoter of a gene transcribed by RNA polymerase III.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"TATA_box","termid":"SO:0000174"},{"relation_name":"part_of","term_name":"RNApol_III_promoter","termid":"SO:0000171"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA_polymerase_III_TATA_box","synonyms":[{"name":"RNA polymerase III TATA box","type":"exact"}],"termid":"SO:0001662"}


id: GO:0050316
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dGMP + ATP = dGDP + ADP.","definition_xrefs":["RHEA:12697"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxynucleoside phosphate kinase activity, ATP as phosphate donor","termid":"GO:0047507"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016301"],"is_obsolete":false,"name":"dGMP kinase activity","secondary_identifiers":["MetaCyc:GMKALT-RXN"],"synonyms":[{"name":"ATP:(d)NMP phosphotransferase activity","type":"related"},{"name":"T2-induced deoxynucleotide kinase activity","type":"broad"}],"termid":"GO:0050316"}


id: PBO:0034079
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-member_of","termid":"PBO:0034079"}


id: PBO:0109139
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 3109","termid":"PBO:0109139"}


id: GO:0002071
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process, independent of morphogenetic (shape) change, that is required for a glandular epithelial cell to attain its fully functional state. A glandular epithelial cell is a columnar/cuboidal epithelial cell is a cell found in a two dimensional sheet with a free surface exposed to the lumen of a gland.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"columnar/cuboidal epithelial cell maturation","termid":"GO:0002069"},{"relation_name":"part_of","term_name":"glandular epithelial cell development","termid":"GO:0002068"}],"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":"glandular epithelial cell maturation","termid":"GO:0002071"}


id: MONDO:0019261
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of neuronal ceroid lipofuscinosis (NCL) characterized by onset during the second half of the first year of life and rapid mental and motor deterioration leading to loss of all psychomotor abilities.","definition_xrefs":["Orphanet:79263"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"progressive myoclonus epilepsy","termid":"MONDO:0020074"},{"relation_name":"is_a","term_name":"neuronal ceroid lipofuscinosis","termid":"MONDO:0016295"},{"relation_name":"is_a","term_name":"cerebral lipidosis with dementia","termid":"MONDO:0020143"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005066","MONDO:0002039","MONDO:0002561","MONDO:0002525"],"is_obsolete":false,"name":"infantile neuronal ceroid lipofuscinosis","secondary_identifiers":["NANDO:2201241","MEDGEN:75666","GARD:9447","icd11.foundation:797123687","NORD:1689","SCTID:58258004","UMLS:C0268281","NANDO:1200152"],"synonyms":[{"name":"Classic Infantile CLN1 Disease","type":"exact"},{"name":"Hagberg-Santavuori disease","type":"exact"},{"name":"INCL","type":"exact"},{"name":"Santavuori disease","type":"exact"},{"name":"Santavuori-Haltia disease","type":"exact"},{"name":"infantile NCL","type":"exact"}],"termid":"MONDO:0019261","xrefs":{"Monarch":{"xref_id":"0019261"}}}


id: MONDO:0013107
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing atopic dermatitis that is associated with variation in the region 11q13.5.","definition_xrefs":["MONDO:patterns/inherited_susceptibility","DOID:0110103","PMID:19349984"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"atopic eczema","termid":"MONDO:0004980"},{"relation_name":"is_a","term_name":"dermatitis, atopic, susceptibility to","termid":"MONDO:0100178"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dermatitis, atopic, 7","secondary_identifiers":["MEDGEN:414058","OMIM:613064","UMLS:C2751599","MESH:C567796"],"synonyms":[{"name":"ATOD7","type":"exact"},{"name":"atopic dermatitis 7","type":"exact"},{"name":"atopic dermatitis type 7","type":"exact"},{"name":"dermatitis, ATOPIC, 7","type":"related"},{"name":"dermatitis, atopic, susceptibility to, 7","type":"exact"}],"termid":"MONDO:0013107","xrefs":{"Monarch":{"xref_id":"0013107"}}}


id: PBO:0077360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 100","termid":"PBO:0077360"}


id: GO:1900510
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of pentose catabolic process to ethanol.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of pentose catabolic process to ethanol (obsolete GO:1900510)","synonyms":[{"name":"down regulation of pentose catabolic process to ethanol","type":"exact"},{"name":"down regulation of pentose catabolism to ethanol","type":"exact"},{"name":"down-regulation of pentose catabolic process to ethanol","type":"exact"},{"name":"down-regulation of pentose catabolism to ethanol","type":"exact"},{"name":"downregulation of pentose catabolic process to ethanol","type":"exact"},{"name":"downregulation of pentose catabolism to ethanol","type":"exact"},{"name":"inhibition of pentose catabolic process to ethanol","type":"narrow"},{"name":"inhibition of pentose catabolism to ethanol","type":"exact"},{"name":"negative regulation of pentose catabolism to ethanol","type":"exact"}],"termid":"GO:1900510"}


id: PBO:0051069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy diversity 5-5","termid":"PBO:0051069"}


id: MONDO:0006683
data:
  {"annotated_genes":["SJAG_00663"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86527],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008076"}]},"cv_name":"mondo","definition":"A brachial plexus disorder characterized by regional paresthesia, pain and muscle weakness, and limited movement in the arm or hand.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nerve plexus disorder","termid":"MONDO:0024432"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00663":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"brachial plexus neuropathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D020516","NCIT:C27194","ICD9:353.0","DOID:3690","EFO:1000844","SCTID:3548001","UMLS:C0700251","MEDGEN:148580"],"synonyms":[{"name":"brachial nerve plexus peripheral neuropathy","type":"exact"},{"name":"brachial plexopathy","type":"exact"},{"name":"brachial plexus disorder","type":"exact"},{"name":"peripheral neuropathy of brachial nerve plexus","type":"exact"}],"termid":"MONDO:0006683","terms_by_termid":{"MONDO:0008076":null},"xrefs":{"Monarch":{"xref_id":"0006683"}}}


id: GO:0003360
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the brainstem from its formation to the mature structure. The brainstem is the part of the brain that connects the brain with the spinal cord.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"}],"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":"brainstem development","termid":"GO:0003360"}


id: GO:0032162
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A septin band, i.e. a diffuse ring composed of a series of septin bars running parallel to the long axis of the cell, located at the neck of a shmoo (mating projection).","definition_xrefs":["GOC:mah","PMID:16151244","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"septin band","termid":"GO:0032158"},{"relation_name":"part_of","term_name":"mating projection","termid":"GO:0005937"}],"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":"mating projection septin band","termid":"GO:0032162"}


id: PBO:0043834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cleavage and polyadenylation specific factor 6","termid":"PBO:0043834"}


id: GO:0061139
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regionalization process in which the identity of a bud primordium is specified. Identity is considered to be the aggregate of characteristics by which a structure is recognized.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"},{"relation_name":"part_of","term_name":"morphogenesis of a branching epithelium","termid":"GO:0061138"}],"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":"bud field specification","termid":"GO:0061139"}


id: GO:0016068
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An inflammatory response driven by antigen recognition by antibodies bound to Fc receptors on mast cells or basophils, occurring within minutes after exposure of a sensitized individual to the antigen, and leading to the release of a variety of inflammatory mediators such as histamines.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypersensitivity","termid":"GO:0002524"},{"relation_name":"is_a","term_name":"immunoglobulin mediated immune response","termid":"GO:0016064"}],"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 I hypersensitivity","secondary_identifiers":["Wikipedia:Type_I_hypersensitivity"],"synonyms":[{"name":"immediate hypersensitivity response","type":"exact"}],"termid":"GO:0016068"}


id: PBO:0031545
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_targeting","termid":"PBO:0031545"}


id: FYPO:0000457
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 histone methylation is abnormal. All histone methylation may be affected, or methylation of specific sites on specific histones may be altered.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone modification during vegetative growth","termid":"FYPO:0000330"},{"relation_name":"is_a","term_name":"abnormal protein methylation during vegetative growth","termid":"FYPO:0006122"},{"relation_name":"is_a","term_name":"abnormal histone methylation","termid":"FYPO:0006870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0002274","FYPO:0001985","FYPO:0001320","FYPO:0002494"],"is_obsolete":false,"name":"abnormal histone methylation during vegetative growth","synonyms":[{"name":"abnormal histone methylation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000457"}


id: GO:0004645
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1,4-alpha-D-glucosyl(n) + phosphate = 1,4-alpha-D-glucosyl(n-1) + alpha-D-glucose 1-phosphate.","definition_xrefs":["RHEA:41732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016757","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"1,4-alpha-oligoglucan phosphorylase activity","secondary_identifiers":["EC:2.4.1.1","MetaCyc:RXN0-5184"],"synonyms":[{"name":"1,4-alpha-D-glucan:phosphate alpha-D-glucosyltransferase activity","type":"related"},{"name":"1,4-alpha-glucan phosphorylase activity","type":"related"},{"name":"alpha-glucan phosphorylase","type":"broad"},{"name":"amylopectin phosphorylase","type":"narrow"},{"name":"amylophosphorylase activity","type":"narrow"},{"name":"glucan phosphorylase","type":"narrow"},{"name":"glucosan phosphorylase","type":"narrow"},{"name":"granulose phosphorylase","type":"narrow"},{"name":"muscle phosphorylase","type":"narrow"},{"name":"muscle phosphorylase a and b activity","type":"narrow"},{"name":"myophosphorylase","type":"narrow"},{"name":"polyphosphorylase activity","type":"related"},{"name":"potato phosphorylase","type":"narrow"},{"name":"starch phosphorylase","type":"narrow"}],"termid":"GO:0004645"}


id: MONDO:0014382
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare multiple congenital anomalies syndrome characterized by greater height, mild to moderate intellectual disability and distinctive facial appearance like round face, heavy, horizontal eyebrows and narrow palpebral fissures.","definition_xrefs":["Orphanet:404443"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Tatton-Brown-Rahman overgrowth syndrome","secondary_identifiers":["UMLS:C4014545","DOID:0112339","OMIM:615879","GARD:17674","MEDGEN:862982","SCTID:768843007"],"synonyms":[{"name":"DNMT3A-related overgrowth syndrome","type":"exact"},{"name":"TATTON-BROWN-Rahman syndrome","type":"related"},{"name":"TBRS","type":"related"},{"name":"Tatton Brown Rahman Syndrome","type":"exact"},{"name":"Tatton-Brown-Rahman overgrowth syndrome","type":"exact"},{"name":"tall stature-intellectual disability-facial dysmorphism syndrome","type":"exact"}],"termid":"MONDO:0014382","xrefs":{"Monarch":{"xref_id":"0014382"}}}


id: GO:1900687
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of gerfelin biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"negative regulation of secondary metabolite biosynthetic process","termid":"GO:1900377"},{"relation_name":"is_a","term_name":"regulation of gerfelin biosynthetic process","termid":"GO:1900686"},{"relation_name":"negatively_regulates","term_name":"gerfelin biosynthetic process","termid":"GO:1900578"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0019748"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0044281","GO:0019748","GO:0008150"],"is_obsolete":false,"name":"negative regulation of gerfelin biosynthetic process","synonyms":[{"name":"down regulation of gerfelin anabolism","type":"exact"},{"name":"down regulation of gerfelin biosynthesis","type":"exact"},{"name":"down regulation of gerfelin biosynthetic process","type":"exact"},{"name":"down regulation of gerfelin formation","type":"exact"},{"name":"down regulation of gerfelin synthesis","type":"exact"},{"name":"down-regulation of gerfelin anabolism","type":"exact"},{"name":"down-regulation of gerfelin biosynthesis","type":"exact"},{"name":"down-regulation of gerfelin biosynthetic process","type":"exact"},{"name":"down-regulation of gerfelin formation","type":"exact"},{"name":"down-regulation of gerfelin synthesis","type":"exact"},{"name":"downregulation of gerfelin anabolism","type":"exact"},{"name":"downregulation of gerfelin biosynthesis","type":"exact"},{"name":"downregulation of gerfelin biosynthetic process","type":"exact"},{"name":"downregulation of gerfelin formation","type":"exact"},{"name":"downregulation of gerfelin synthesis","type":"exact"},{"name":"inhibition of gerfelin anabolism","type":"exact"},{"name":"inhibition of gerfelin biosynthesis","type":"exact"},{"name":"inhibition of gerfelin biosynthetic process","type":"narrow"},{"name":"inhibition of gerfelin formation","type":"exact"},{"name":"inhibition of gerfelin synthesis","type":"exact"},{"name":"negative regulation of gerfelin anabolism","type":"exact"},{"name":"negative regulation of gerfelin biosynthesis","type":"exact"},{"name":"negative regulation of gerfelin formation","type":"exact"},{"name":"negative regulation of gerfelin synthesis","type":"exact"}],"termid":"GO:1900687"}


id: GO:0033401
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a UUU codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0060090","GO:0005488","GO:0003723","GO:0003674"],"is_obsolete":false,"name":"UUU codon-amino acid adaptor activity","synonyms":[{"name":"TTT codon-amino acid adaptor activity","type":"exact"},{"name":"phenylalanine tRNA","type":"related"}],"termid":"GO:0033401"}


id: FYPO:0006523
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a smaller than normal proportion of cells in the population remains viable after entering stationary phase following arrest at the mitotic G2/M phase transition of the mitotic cell cycle.","definition_xrefs":["PMID:11598020","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"loss of viability in stationary phase","termid":"FYPO:0000245"},{"relation_name":"is_a","term_name":"loss of viability following cell cycle arrest at mitotic G2/M phase transition","termid":"FYPO:0006522"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003","FYPO:0002057"],"is_obsolete":false,"name":"loss of viability in stationary phase following entry from mitotic G2 phase","synonyms":[{"name":"decreased viability in stationary phase following entry from mitotic G2 phase","type":"exact"},{"name":"loss of cell population viability in stationary phase following entry from mitotic G2 phase","type":"exact"},{"name":"loss of viability following mitotic G2 arrest and stationary phase entry","type":"exact"},{"name":"loss of viability in stationary phase following entry from mitotic G2/M phase transition","type":"exact"},{"name":"loss of viability of following entry into stationary phase from mitotic G2 phase","type":"exact"},{"name":"reduced viability in stationary phase following entry from mitotic G2 phase","type":"related"}],"termid":"FYPO:0006523"}


id: PBO:0026932
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_HMW_ubiquitin_conjugate_level","termid":"PBO:0026932"}


id: PBO:0090993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HbrB family protein involved in TOR signaling Bit2","termid":"PBO:0090993"}


id: MONDO:0030841
data:
  {"annotated_genes":["SJAG_02748"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86148],"is_not":false,"summary":null,"term":"MONDO:0030841"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mismatch repair cancer syndrome","termid":"MONDO:0031219"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02748":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0021190"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0021190"],"is_obsolete":false,"name":"mismatch repair cancer syndrome 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:18363","OMIM:619097","UMLS:C5436807","MEDGEN:1733656"],"synonyms":[{"name":"MMRCS3","type":"exact"},{"name":"mismatch repair cancer syndrome 3","type":"exact"}],"termid":"MONDO:0030841","terms_by_termid":{"MONDO:0030841":null},"xrefs":{"Monarch":{"xref_id":"0030841"}}}


id: GO:0023053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which a mechanical signal causes activation of a receptor.","definition_xrefs":["GOC:mtg_signal"],"gene_count":0,"genotype_count":0,"name":"obsolete signal initiation by mechanical effect (obsolete GO:0023053)","synonyms":[{"name":"signal initiation by mechanical effect","type":"exact"}],"termid":"GO:0023053"}


id: FYECO:0000002
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Any experimental condition specifying the temperature at which the experiment was performed.","definition_xrefs":["PomBase:al"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE FYECO:0000002 temperature (obsolete FYECO:0000002)","termid":"FYECO:0000002"}


id: GO:0016512
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the formation of endothelin 1 by cleavage of the Trp21-Val22 bond in the precursor.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete endothelin-converting enzyme 1 activity (obsolete GO:0016512)","synonyms":[{"name":"ECE-1 activity","type":"related"},{"name":"endothelin-converting enzyme 1 activity","type":"exact"}],"termid":"GO:0016512"}


id: PBO:0075485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPATA31 subfamily D member 3","termid":"PBO:0075485"}


id: MONDO:0005579
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A generalised epilepsy that encompasses several common seizure phenotypes including childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy and epilepsy with generalized tonic-clonic seizures alone. These epilepsy syndromes have polygenic inheritance with or without environmental factors contributing to seizure susceptibility. Seizure types include one or a combination of absence seizures, myoclonic seizures and/or generalized tonic-clonic seizures.","definition_xrefs":["OMIM:600669"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary generalized epilepsy","termid":"MONDO:0100576"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"idiopathic generalized epilepsy","secondary_identifiers":["OMIMPS:600669","EFO:0005917","MESH:C562694","MEDGEN:75725","SCTID:19598007","DOID:1827","UMLS:C0270850"],"synonyms":[{"name":"EIG","type":"exact"},{"name":"IGE","type":"exact"},{"name":"epilepsy, idiopathic generalized","type":"exact"},{"name":"generalized epilepsy","type":"broad"},{"name":"hereditary idiopathic generalized epilepsy","type":"exact"},{"name":"idiopathic generalised epilepsy","type":"exact"},{"name":"idiopathic generalized epilepsy","type":"exact"}],"termid":"MONDO:0005579","xrefs":{"Monarch":{"xref_id":"0005579"}}}


id: GO:0042856
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of eugenol, a colorless, aromatic, liquid hydrocarbon (C10H12O2) found in clove oil.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound catabolic process","termid":"GO:0019336"},{"relation_name":"is_a","term_name":"eugenol metabolic process","termid":"GO:0042854"},{"relation_name":"is_a","term_name":"phenylpropanoid catabolic process","termid":"GO:0046271"},{"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"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"eugenol catabolic process","synonyms":[{"name":"4-allyl-2-methoxyphenol catabolic process","type":"exact"},{"name":"4-allyl-2-methoxyphenol catabolism","type":"exact"},{"name":"eugenic acid catabolic process","type":"exact"},{"name":"eugenic acid catabolism","type":"exact"},{"name":"eugenol breakdown","type":"exact"},{"name":"eugenol catabolism","type":"exact"},{"name":"eugenol degradation","type":"exact"}],"termid":"GO:0042856"}


id: GO:1900067
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cellular response to alkalinity.","definition_xrefs":["GOC:dgf","GOC:TermGenie","PMID:12509465","PMID:17023428"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to stimulus","termid":"GO:0048583"},{"relation_name":"is_a","term_name":"regulation of cellular process","termid":"GO:0050794"},{"relation_name":"regulates","term_name":"cellular response to alkaline pH","termid":"GO:0071469"}],"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 cellular response to alkaline pH","synonyms":[{"name":"regulation of cellular response to alkalinity","type":"broad"},{"name":"regulation of cellular response to basic pH","type":"exact"}],"termid":"GO:1900067"}


id: PBO:0056128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysosomal trafficking regulator","termid":"PBO:0056128"}


id: GO:0004183
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: peptidyl-L-lysine (or peptidyl-L-arginine) + H2O = peptide + L-lysine (or L-arginine). Function is activated by Co2+ and inhibited by 1,10-phenanthroline and other chelating agents.","definition_xrefs":["EC:3.4.17.10"],"gene_count":0,"genotype_count":0,"name":"obsolete carboxypeptidase E activity (obsolete GO:0004183)","synonyms":[{"name":"carboxypeptidase E activity","type":"exact"},{"name":"carboxypeptidase H activity","type":"exact"},{"name":"cobalt-stimulated chromaffin granule carboxypeptidase activity","type":"related"},{"name":"enkephalin convertase activity","type":"narrow"},{"name":"enkephalin precursor carboxypeptidase activity","type":"related"},{"name":"enkephalin-precursor endopeptidase activity","type":"related"},{"name":"insulin granule-associated carboxypeptidase activity","type":"related"},{"name":"membrane-bound carboxypeptidase activity","type":"related"},{"name":"peptidyl-L-lysine(-L-arginine) hydrolase","type":"broad"}],"termid":"GO:0004183"}


id: GO:0005295
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: neutral L-amino acid(out) + Na+(out) = neutral L-amino acid(in) + Na+(in).","definition_xrefs":["TC:2.A.23.3.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid:sodium symporter activity","termid":"GO:0005283"},{"relation_name":"is_a","term_name":"neutral L-amino acid transmembrane transporter activity","termid":"GO:0015175"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"neutral L-amino acid:sodium symporter activity","secondary_identifiers":["GO:0005282"],"synonyms":[{"name":"neutral amino acid-sodium cotransporter","type":"broad"},{"name":"neutral amino acid:sodium symporter activity","type":"exact"},{"name":"sodium/neutral amino acid transporter","type":"broad"}],"termid":"GO:0005295"}


id: MONDO:0018738
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the metanephros.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney benign neoplasm","termid":"MONDO:0002513"}],"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":"benign metanephric tumor","secondary_identifiers":["UMLS:C5681098","MEDGEN:1830110","NCIT:C157748","Orphanet:464359"],"termid":"MONDO:0018738","xrefs":{"Monarch":{"xref_id":"0018738"}}}


id: GO:0015489
data:
  {"annotated_genes":["SJAG_02125"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[71029],"is_not":false,"summary":null,"term":"GO:0015489"}]},"cv_name":"molecular_function","definition":"Enables the transfer of putrescine from one side of a membrane to the other. Putrescine is 1,4-diaminobutane, the polyamine formed by decarboxylation of ornithine and the metabolic precursor of spermidine and spermine.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"polyamine transmembrane transporter activity","termid":"GO:0015203"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02125":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"putrescine transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0015489","terms_by_termid":{"GO:0015489":null}}


id: PBO:0071411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 17","termid":"PBO:0071411"}


id: GO:0090443
data:
  {"annotated_genes":["SJAG_06270","SJAG_00229","SJAG_04455","SJAG_02514","SJAG_03508","SJAG_01790"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[70939,75013,95996,101627,107903,110547],"is_not":false,"summary":null,"term":"GO:0090443"}]},"cv_name":"cellular_component","definition":"A conserved protein phosphatase type 2A complex which contains a protein phosphatase type 2A, a protein phosphatase regulatory subunit, a striatin, an FHA domain protein and other subunits (at least six proteins). In fission yeast this complex negatively regulate the septation initiation network at the spindle pole body.","definition_xrefs":["PMID:22119525","GOC:vw","PMID:21561862"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00229":null,"SJAG_01790":null,"SJAG_02514":null,"SJAG_03508":null,"SJAG_04455":null,"SJAG_06270":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"FAR/SIN/STRIPAK complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"FAR complex","type":"related"},{"name":"SIN inhibitory phosphatase (SIP) complex","type":"exact"},{"name":"SIN inhibitory phosphatase complex","type":"exact"},{"name":"SIP complex","type":"exact"},{"name":"STRIPAK signalling complex","type":"related"},{"name":"striatin interacting phosphatase and kinase complex","type":"exact"}],"termid":"GO:0090443","terms_by_termid":{"GO:0090443":null}}


id: MONDO:0005407
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An eosinophilic esophagitis that starts in childhood.","definition_xrefs":["EFO:0004594"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eosinophilic esophagitis","termid":"MONDO:0005361"}],"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":"childhood eosinophilic esophagitis","synonyms":[{"name":"eosinophilic esophagitis of childhood","type":"exact"},{"name":"paediatric eosinophilic esophagitis","type":"exact"},{"name":"pediatric eosinophilic esophagitis","type":"exact"}],"termid":"MONDO:0005407","xrefs":{"Monarch":{"xref_id":"0005407"}}}


id: GO:0102723
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + curcumin = curcumin monoglucoside + UDP + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete UDP-glucose:curcumin glucosyltransferase activity (obsolete GO:0102723)","termid":"GO:0102723"}


id: MONDO:0013832
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"keratoconus","termid":"MONDO:0015486"}],"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":"keratoconus 8","secondary_identifiers":["OMIM:614628","UMLS:C3553307","MEDGEN:766221"],"synonyms":[{"name":"KTCN8","type":"exact"},{"name":"keratoconus 8","type":"exact"}],"termid":"MONDO:0013832","xrefs":{"Monarch":{"xref_id":"0013832"}}}


id: PBO:0048195
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GABPB1 intronic transcript","termid":"PBO:0048195"}


id: PR:O14268
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC7D4.13c gene.","definition_xrefs":["UniProtKB:O14268","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C7D4.13c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC7D4.13c","synonyms":[{"name":"Spom972h-SPAC7D4.13c","type":"exact"}],"termid":"PR:O14268"}


id: GO:0046360
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of 2-oxobutyrate, the anion of the organic acid 2-oxobutyric acid, which contains a ketone group on carbon 2.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxobutyrate metabolic process","termid":"GO:0046361"},{"relation_name":"is_a","term_name":"short-chain fatty acid biosynthetic process","termid":"GO:0051790"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006629"],"is_obsolete":false,"name":"2-oxobutyrate biosynthetic process","synonyms":[{"name":"2-oxobutyrate anabolism","type":"exact"},{"name":"2-oxobutyrate biosynthesis","type":"exact"},{"name":"2-oxobutyrate formation","type":"exact"},{"name":"2-oxobutyrate synthesis","type":"exact"},{"name":"alpha-ketobutyrate biosynthesis","type":"exact"},{"name":"alpha-ketobutyrate biosynthetic process","type":"exact"}],"termid":"GO:0046360"}


id: PBO:0044155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTDP1 divergent transcript","termid":"PBO:0044155"}


id: GO:0021853
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The migration of GABAergic interneuron precursors from the subpallium to the cerebral cortex.","definition_xrefs":["PMID:12626695","GOC:cls","GOC:dgh","GOC:jid","GOC:dph","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interneuron migration from the subpallium to the cortex","termid":"GO:0021830"},{"relation_name":"is_a","term_name":"interneuron migration","termid":"GO:1904936"},{"relation_name":"part_of","term_name":"cerebral cortex GABAergic interneuron development","termid":"GO:0021894"}],"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":"cerebral cortex GABAergic interneuron migration","termid":"GO:0021853"}


id: PATO:0001917
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial quality inhering in a bearer by virtue of the bearer's being located toward the front and abdomen of an organism relative to another entity.","definition_xrefs":["PATOC:wd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anterior to","termid":"PATO:0001632"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anteroventral to","termid":"PATO:0001917"}


id: MONDO:0002238
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the ascending colon.","direct_ancestors":[{"relation_name":"is_a","term_name":"malignant colon neoplasm","termid":"MONDO:0021063"}],"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":"ascending colon cancer","secondary_identifiers":["SCTID:363412000","MEDGEN:509293","UMLS:C0153439","ICD9:153.6","DOID:218"],"synonyms":[{"name":"Ca ascending colon","type":"exact"},{"name":"ascending colon cancer","type":"exact"},{"name":"cancer of ascending colon","type":"exact"},{"name":"malignant ascending colon neoplasm","type":"exact"},{"name":"malignant neoplasm of ascending colon","type":"exact"},{"name":"malignant neoplasm of right colon","type":"exact"},{"name":"malignant tumor of ascending colon","type":"exact"},{"name":"malignant tumour of ascending colon","type":"exact"}],"termid":"MONDO:0002238","xrefs":{"Monarch":{"xref_id":"0002238"}}}


id: MONDO:0015888
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete other rare diabetes mellitus (obsolete MONDO:0015888)","secondary_identifiers":["Orphanet:181381"],"termid":"MONDO:0015888","xrefs":{"Monarch":{"xref_id":"0015888"}}}


id: MOD:01453
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a source amino acid residue to L-glutamate 5-methyl ester.","definition_xrefs":["RESID:AA0072"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-methylated residue","termid":"MOD:00393"},{"relation_name":"is_a","term_name":"monomethylated residue","termid":"MOD:00599"},{"relation_name":"is_a","term_name":"methylated glutamic acid","termid":"MOD:00713"},{"relation_name":"is_a","term_name":"modified residue that can arise from different natural residues","termid":"MOD:00859"}],"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-glutamic acid 5-methyl ester","synonyms":[{"name":"(2S)-2-amino-5-methoxy-5-oxopentanoic acid","type":"exact"},{"name":"(5)-methyl L-hydrogen glutamate","type":"exact"},{"name":"2-aminopentanedioic acid 5-methyl ester","type":"exact"},{"name":"5-methyl L-2-aminoglutarate","type":"exact"},{"name":"5-methyl L-glutamate","type":"exact"},{"name":"5-methyl esterified L-glutamic acid","type":"exact"},{"name":"L-glutamic acid 5-methyl ester","type":"exact"},{"name":"O-methyl Glutamyl","type":"exact"},{"name":"O5MeGlu","type":"exact"},{"name":"glutamic acid 5-methyl ester","type":"exact"},{"name":"glutamic acid gamma-methyl ester","type":"exact"}],"termid":"MOD:01453"}


id: PBO:0061586
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"netrin G1","termid":"PBO:0061586"}


id: MONDO:0010447
data:
  {"annotated_genes":["SJAG_01047"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87271],"is_not":false,"summary":null,"term":"MONDO:0010447"}]},"cv_name":"mondo","definition":"Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the RPS6KA3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic X-linked intellectual disability","termid":"MONDO:0019181"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01047":null},"genotype_count":0,"is_obsolete":false,"name":"intellectual disability, X-linked 19","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0112019","UMLS:C0796225","OMIM:300844","GARD:22687","MESH:C563141","MEDGEN:208676"],"synonyms":[{"name":"MRX19","type":"related"},{"name":"RPS6KA3 non-syndromic X-linked intellectual disability","type":"exact"},{"name":"intellectual developmental disorder, X-linked 19, X-linked dominant","type":"exact"},{"name":"intellectual disability, X-linked 19","type":"exact"},{"name":"intellectual disability, X-linked type 19","type":"exact"},{"name":"mental retardation, X-linked 19","type":"related"},{"name":"mental retardation, X-linked type 19","type":"exact"},{"name":"non-syndromic X-linked intellectual disability caused by mutation in RPS6KA3","type":"exact"}],"termid":"MONDO:0010447","terms_by_termid":{"MONDO:0010447":null},"xrefs":{"Monarch":{"xref_id":"0010447"}}}


id: MONDO:0018441
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hepatitis delta (obsolete MONDO:0018441)","termid":"MONDO:0018441","xrefs":{"Monarch":{"xref_id":"0018441"}}}


id: GO:1900537
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of glucose homeostasis.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of glucose homeostasis (obsolete GO:1900537)","synonyms":[{"name":"down regulation of glucose homeostasis","type":"exact"},{"name":"down-regulation of glucose homeostasis","type":"exact"},{"name":"downregulation of glucose homeostasis","type":"exact"},{"name":"inhibition of glucose homeostasis","type":"narrow"},{"name":"negative regulation of glucose homeostasis","type":"exact"}],"termid":"GO:1900537"}


id: PBO:0063426
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphodiesterase 4D interacting protein","termid":"PBO:0063426"}


id: PBO:0044223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cortexin 3","termid":"PBO:0044223"}


id: PBO:0031735
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_meiosis","termid":"PBO:0031735"}


id: PBO:0064256
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pleckstrin homology domain containing A4","termid":"PBO:0064256"}


id: GO:0048200
data:
  {"annotated_genes":["SJAG_04391","SJAG_03268"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[118124,71691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048205"}]},"cv_name":"biological_process","definition":"The addition of specific coat proteins to Golgi membranes during the formation of transport vesicles.","definition_xrefs":["GOC:jid","GOC:mah","ISBN:0716731363","PMID:10219233"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle coating","termid":"GO:0006901"},{"relation_name":"part_of","term_name":"Golgi vesicle budding","termid":"GO:0048194"},{"relation_name":"part_of","term_name":"vesicle targeting, to, from or within Golgi","termid":"GO:0048199"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03268":null,"SJAG_04391":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0061024","GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"Golgi transport vesicle coating","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"dictyosome transport vesicle coating","type":"narrow"}],"termid":"GO:0048200","terms_by_termid":{"GO:0048205":null}}


id: MONDO:0011786
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the nasal mucous membranes caused by an IgE-mediated response to external allergens. The inflammation may also involve the mucous membranes of the sinuses, eyes, middle ear, and pharynx. Symptoms include sneezing, nasal congestion, rhinorrhea, and itching. It may lead to fatigue, drowsiness, and malaise thus causing impairment of the quality of life.","definition_xrefs":["NCIT:C79532"],"direct_ancestors":[{"relation_name":"is_a","term_name":"allergic respiratory disease","termid":"MONDO:0000771"},{"relation_name":"is_a","term_name":"rhinitis","termid":"MONDO:0003014"}],"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":"allergic rhinitis","secondary_identifiers":["HP:0003193","icd11.foundation:1711769234","EFO:0005854","ICD9:477","SCTID:61582004","UMLS:C2607914","DOID:4481","ICD9:477.8","MEDGEN:382012","ICD9:477.9"],"synonyms":[{"name":"Alrh","type":"related"},{"name":"Perenial allergic rhinitis","type":"narrow"},{"name":"allergic form of rhinitis","type":"exact"},{"name":"allergic rhinitis","type":"exact"},{"name":"atopic rhinitis","type":"narrow"},{"name":"non-seasonal allergic rhinitis","type":"narrow"},{"name":"perennial allergic rhinitis","type":"narrow"},{"name":"pollenosis","type":"exact"},{"name":"seasonal allergic rhinitis","type":"narrow"}],"termid":"MONDO:0011786","xrefs":{"Monarch":{"xref_id":"0011786"}}}


id: FYPO:0006076
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 mature siRNA measured in a cell is too low to detect.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA absent from cell during vegetative growth","termid":"FYPO:0003161"},{"relation_name":"is_a","term_name":"decreased siRNA level","termid":"FYPO:0004205"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0006551","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"siRNA absent from cell","synonyms":[{"name":"siRNA absent from cell during mitotic cell cycle","type":"related"},{"name":"siRNA absent from cell during vegetative growth","type":"exact"},{"name":"small interfering RNA absent from cell","type":"exact"}],"termid":"FYPO:0006076"}


id: GO:0018143
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of a covalent cross-link between a nucleic acid and a protein.","definition_xrefs":["GOC:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification process","termid":"GO:0036211"}],"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":"nucleic acid-protein covalent cross-linking","termid":"GO:0018143"}


id: PBO:0065030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRDX5 pseudogene 1","termid":"PBO:0065030"}


id: GO:0007464
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the R3/R4 photoreceptors commit to their cell fate. R3 and R4 are paired photoreceptors which contribute the outer rhabdomeres.","definition_xrefs":["PMID:3937883","PMID:3076112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"compound eye photoreceptor fate commitment","termid":"GO:0001752"},{"relation_name":"part_of","term_name":"establishment of ommatidial planar polarity","termid":"GO:0042067"},{"relation_name":"part_of","term_name":"R3/R4 cell differentiation","termid":"GO:0048056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007163"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007163","GO:0008150"],"is_obsolete":false,"name":"R3/R4 cell fate commitment","termid":"GO:0007464"}


id: GO:0036176
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 neutral pH (pH close to 7) stimulus. pH is a measure of the acidity or basicity of an aqueous solution.","definition_xrefs":["GOC:di","Wikipedia:PH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to pH","termid":"GO:0009268"}],"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 neutral pH","termid":"GO:0036176"}


id: MONDO:0015910
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare constitutional hemolytic anemia (obsolete MONDO:0015910)","secondary_identifiers":["Orphanet:182043"],"synonyms":[{"name":"rare familial constitutional hemolytic anemia","type":"related"},{"name":"rare genetic constitutional hemolytic anemia","type":"related"}],"termid":"MONDO:0015910","xrefs":{"Monarch":{"xref_id":"0015910"}}}


id: PBO:0047730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"formin binding protein 1","termid":"PBO:0047730"}


id: MONDO:0014595
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 SIK1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"infantile spasms","termid":"MONDO:0018097"},{"relation_name":"is_a","term_name":"early myoclonic encephalopathy","termid":"MONDO:0016022"},{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0005027"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 30","secondary_identifiers":["UMLS:C4225360","MEDGEN:898954","GARD:16093","OMIM:616341","DOID:0080465"],"synonyms":[{"name":"DEE30","type":"exact"},{"name":"EIEE30","type":"exact"},{"name":"SIK1 early infantile epileptic encephalopathy","type":"exact"},{"name":"developmental and epileptic encephalopathy 30","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in SIK1","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 30","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 30","type":"exact"}],"termid":"MONDO:0014595","xrefs":{"Monarch":{"xref_id":"0014595"}}}


id: MOD:00640
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative","definition_xrefs":["Unimod:333"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"},{"relation_name":"is_a","term_name":"phosphorus containing modified residue","termid":"MOD:00861"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6-N-biotinylaminohexyl isopropyl phosphorofluoridate","synonyms":[{"name":"6-N-biotinylaminohexyl isopropyl phosphate","type":"related"},{"name":"Can-FP-biotin","type":"related"}],"termid":"MOD:00640"}


id: PBO:0090827
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaphase-promoting complex platform subcomplex scaffold TPR subunit Apc5","termid":"PBO:0090827"}


id: GO:0033314
data:
  {"annotated_genes":["SJAG_02771","SJAG_01044","SJAG_01010","SJAG_03927","SJAG_04287","SJAG_01605","SJAG_02266","SJAG_02098","SJAG_00364","SJAG_01205","SJAG_03026","SJAG_03695","SJAG_03160","SJAG_02563","SJAG_04671","SJAG_02074","SJAG_01076"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71520,72830,75127,79180,79841,91794,94326,99550,99717,100904,106990,109694,112419,116441,117186,117487,117659],"is_not":false,"summary":null,"term":"GO:0033314"}]},"cv_name":"biological_process","definition":"A signal transduction process that contributes to a mitotic DNA replication checkpoint.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA replication checkpoint signaling","termid":"GO:0000076"},{"relation_name":"is_a","term_name":"mitotic DNA integrity checkpoint signaling","termid":"GO:0044774"},{"relation_name":"is_a","term_name":"mitotic G2/M transition checkpoint","termid":"GO:0044818"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00364":null,"SJAG_01010":null,"SJAG_01044":null,"SJAG_01076":null,"SJAG_01205":null,"SJAG_01605":null,"SJAG_02074":null,"SJAG_02098":null,"SJAG_02266":null,"SJAG_02563":null,"SJAG_02771":null,"SJAG_03026":null,"SJAG_03160":null,"SJAG_03695":null,"SJAG_03927":null,"SJAG_04287":null,"SJAG_04671":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0044772"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0044772"}],"interesting_parent_ids":["GO:0023052","GO:0008150","GO:0044772","GO:0007049"],"is_obsolete":false,"name":"mitotic DNA replication checkpoint signaling","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0072446","GO:0072443","GO:0072459","GO:0031574"],"synonyms":[{"name":"S-M DNA replication checkpoint","type":"exact"},{"name":"S-M checkpoint","type":"exact"},{"name":"S-phase checkpoint","type":"broad"},{"name":"mitotic DNA replication checkpoint","type":"exact"},{"name":"mitotic cell cycle DNA replication checkpoint","type":"exact"},{"name":"signal transduction involved in S-M checkpoint","type":"exact"},{"name":"signal transduction involved in mitotic DNA replication checkpoint","type":"narrow"},{"name":"signal transduction involved in mitotic G2/M transition decatenation checkpoint","type":"related"}],"termid":"GO:0033314","terms_by_termid":{"GO:0033314":null}}


id: PBO:0031870
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved in Fungi","termid":"PBO:0031870"}


id: MONDO:0030673
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"complex hereditary spastic paraplegia","termid":"MONDO:0015150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"spastic paraplegia 86, autosomal recessive","secondary_identifiers":["OMIM:619735","MEDGEN:1801286","UMLS:C5676910","Orphanet:631085","DOID:0112342"],"synonyms":[{"name":"SPG86","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 86","type":"exact"},{"name":"spastic paraplegia 86, autosomal recessive","type":"exact"}],"termid":"MONDO:0030673","xrefs":{"Monarch":{"xref_id":"0030673"}}}


id: PBO:0075758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine and arginine repetitive matrix 1","termid":"PBO:0075758"}


id: PBO:0061043
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NIPA2 pseudogene 4","termid":"PBO:0061043"}


id: PBO:0001406
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"overlapping genome wide occupancy in coding regions Nap1/Hrp1/Hrp3","termid":"PBO:0001406"}


id: GO:0004858
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of dUTP pyrophosphatase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme inhibitor activity","termid":"GO:0004857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0004857"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140678"}],"interesting_parent_ids":["GO:0140678","GO:0030234","GO:0003674","GO:0004857","GO:0098772"],"is_obsolete":false,"name":"dUTP pyrophosphatase inhibitor activity","termid":"GO:0004858"}


id: GO:0090573
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex, located in the nucleus, that possesses activity that prevents or downregulates transcription from a RNA polymerase IV promoter.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription repressor complex","termid":"GO:0017053"},{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005634"],"is_obsolete":false,"name":"RNA polymerase IV transcription repressor complex","termid":"GO:0090573"}


id: GO:0060477
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The phosphorylation of peptidyl-serine to form peptidyl-O-phospho-L-serine that is part of the acrosome reaction.","definition_xrefs":["GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-serine phosphorylation involved in acrosome reaction (obsolete GO:0060477)","termid":"GO:0060477"}


id: PBO:0080284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 47 pseudogene","termid":"PBO:0080284"}


id: MONDO:0022909
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cutis laxa osteoporosis","termid":"MONDO:0022909","xrefs":{"Monarch":{"xref_id":"0022909"}}}


id: GO:0018787
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-chlorobenzoyl-CoA + H2O = 4-hydroxybenzoyl-CoA + chloride + H+.","definition_xrefs":["RHEA:14853"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid halide bonds, in C-halide compounds","termid":"GO:0019120"}],"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:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"4-chlorobenzoyl-CoA dehalogenase activity","secondary_identifiers":["EC:3.8.1.7","UM-BBD_enzymeID:r0140","MetaCyc:3.8.1.7-RXN"],"synonyms":[{"name":"4-chlorobenzoyl CoA chlorohydrolase activity","type":"related"}],"termid":"GO:0018787"}


id: GO:0150202
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of transport across blood-brain barrier.","definition_xrefs":["PMID:30280653","GOC:aruk","PMID:29377008","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transport","termid":"GO:0051051"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of transport across blood-brain barrier","termid":"GO:0150200"},{"relation_name":"negatively_regulates","term_name":"transport across blood-brain barrier","termid":"GO:0150104"},{"relation_name":"part_of","term_name":"negative regulation of vascular permeability","termid":"GO:0043116"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of transport across blood-brain barrier","termid":"GO:0150202"}


id: PBO:0069714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 994, pseudogene","termid":"PBO:0069714"}


id: GO:0047546
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-hydroxypyridine + AH(2) + O2 = 2,5-dihydroxypyridine + A + H2O.","definition_xrefs":["EC:1.14.99.26","RHEA:16973"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"2-hydroxypyridine 5-monooxygenase activity","secondary_identifiers":["KEGG_REACTION:R03206","MetaCyc:2-HYDROXYPYRIDINE-5-MONOOXYGENASE-RXN"],"synonyms":[{"name":"2-hydroxypyridine oxygenase activity","type":"related"},{"name":"2-hydroxypyridine,hydrogen-donor:oxygen oxidoreductase (5-hydroxylating)","type":"related"}],"termid":"GO:0047546"}


id: PBO:0058703
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6831","termid":"PBO:0058703"}


id: PBO:0113449
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of both RNase MRP and nuclear RNase P; RNase MRP cleaves pre-rRNA, while nuclear RNase P cleaves tRNA precursors to generate mature 5' ends and facilitates turnover of nuclear RNAs; increases the activity and thermal stability of the RNase P complex, along with Pop2p; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0113449"}


