# terms

id: MONDO:0020121
data:
  {"annotated_genes":["SJAG_04228","SJAG_04053","SJAG_03715","SJAG_02096","SJAG_01939","SJAG_02043","SJAG_00831","SJAG_04316","SJAG_01918","SJAG_04601","SJAG_04003","SJAG_01491","SJAG_02431","SJAG_02396","SJAG_03188","SJAG_00804","SJAG_03815","SJAG_03703","SJAG_03470","SJAG_02103","SJAG_05219","SJAG_04567","SJAG_02919","SJAG_00044","SJAG_03145"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87505],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0021018"},{"annotations":[87613],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012034"},{"annotations":[87020],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012248"},{"annotations":[88503,88502],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013162"},{"annotations":[87771],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014142"},{"annotations":[87114],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014023"},{"annotations":[87961],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014896"},{"annotations":[87707,87706],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008409"},{"annotations":[86984],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013049"},{"annotations":[87982],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008030"},{"annotations":[88604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010912"},{"annotations":[88178],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011246"},{"annotations":[87581,87582],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009682"},{"annotations":[88400],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957270"},{"annotations":[87678,87676,87677],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009364"},{"annotations":[87764],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014140"},{"annotations":[88497,88496],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013154"},{"annotations":[87074],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033556"},{"annotations":[88501],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013159"},{"annotations":[87769],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014141"},{"annotations":[88500,88499],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013160"},{"annotations":[87084,87085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008050"},{"annotations":[88036,88037,88038],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012130"},{"annotations":[87934],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014877"},{"annotations":[88074],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011266"},{"annotations":[87445],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958176"},{"annotations":[87621],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014800"},{"annotations":[87265],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010684"}]},"cv_name":"mondo","definition":"Muscular dystrophy (MD) refers to a group of more than 30 genetic diseases characterized by progressive weakness and degeneration of the skeletal muscles that control movement. Some forms of MD are seen in newborns, infants or children, while others have late-onset and may not appear until middle age or later. The disorders differ in terms of the distribution and extent of muscle weakness (some forms of MD also affect cardiac muscle), age of onset, rate of progression, and pattern of inheritance. The prognosis for people with MD varies according to the type and progression of the disorder. There is no specific treatment to stop or reverse any form of MD. Treatment is supportive and may include physical therapy, respiratory therapy, speech therapy, orthopedic appliances used for support, corrective orthopedic surgery, and medicationsincluding corticosteroids, anticonvulsants (seizure medications), immunosuppressants, and antibiotics. Some individuals may need assisted ventilation to treat respiratory muscle weaknessor a pacemaker for cardiac (heart)abnormalities.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"pulmonary disease, chronic obstructive, susceptibility to","termid":"MONDO:0100167"},{"relation_name":"is_a","term_name":"myopathy","termid":"MONDO:0005336"},{"relation_name":"is_a","term_name":"hereditary neuromuscular disease","termid":"MONDO:0100546"},{"relation_name":"is_a","term_name":"hereditary skeletal muscle disorder","termid":"MONDO:0700223"}],"gene_count":25,"genes_by_uniquename":{"SJAG_00044":null,"SJAG_00804":null,"SJAG_00831":null,"SJAG_01491":null,"SJAG_01918":null,"SJAG_01939":null,"SJAG_02043":null,"SJAG_02096":null,"SJAG_02103":null,"SJAG_02396":null,"SJAG_02431":null,"SJAG_02919":null,"SJAG_03145":null,"SJAG_03188":null,"SJAG_03470":null,"SJAG_03703":null,"SJAG_03715":null,"SJAG_03815":null,"SJAG_04003":null,"SJAG_04053":null,"SJAG_04228":null,"SJAG_04316":null,"SJAG_04567":null,"SJAG_04601":null,"SJAG_05219":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"muscular dystrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:359.1","SCTID:73297009","NANDO:1200486","MedDRA:10028356","ICD10CM:G71.0","NANDO:2100233","MEDGEN:44527","GARD:7922","icd11.foundation:1464662404","MESH:D009136","DOID:9884","NCIT:C84910","Orphanet:98473","UMLS:C0026850"],"termid":"MONDO:0020121","terms_by_termid":{"MONDO:0008030":null,"MONDO:0008050":null,"MONDO:0008409":null,"MONDO:0009364":null,"MONDO:0009682":null,"MONDO:0010684":null,"MONDO:0010912":null,"MONDO:0011246":null,"MONDO:0011266":null,"MONDO:0012034":null,"MONDO:0012130":null,"MONDO:0012248":null,"MONDO:0013049":null,"MONDO:0013154":null,"MONDO:0013159":null,"MONDO:0013160":null,"MONDO:0013162":null,"MONDO:0014023":null,"MONDO:0014140":null,"MONDO:0014141":null,"MONDO:0014142":null,"MONDO:0014800":null,"MONDO:0014877":null,"MONDO:0014896":null,"MONDO:0021018":null,"MONDO:0033556":null,"MONDO:0957270":null,"MONDO:0958176":null},"xrefs":{"Monarch":{"xref_id":"0020121"}}}


id: PBO:0081402
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 250","termid":"PBO:0081402"}


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


id: MONDO:0010204
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lysosomal acid lipase deficiency (obsolete MONDO:0010204)","termid":"MONDO:0010204","xrefs":{"Monarch":{"xref_id":"0010204"}}}


id: FYPO:0003951
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of tyrosine residues in one or more specific proteins, or of specific protein sites, occurs to a greater extent than normal during a cellular response to heat.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete increased protein tyrosine phosphorylation during cellular response to heat (obsolete FYPO:0003951)","synonyms":[{"name":"increased peptidyl-tyrosine phosphorylation during cellular response to heat","type":"exact"},{"name":"increased protein tyrosine phosphorylation during cellular response to heat during mitotic cell cycle","type":"related"},{"name":"increased protein tyrosine phosphorylation during cellular response to heat during vegetative growth","type":"exact"},{"name":"increased tyrosine phosphorylation during cellular response to heat","type":"exact"}],"termid":"FYPO:0003951"}


id: GO:0070980
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of biphenyl, a toxic aromatic hydrocarbon used as a heat transfer agent, as a fungistat in packaging citrus fruits and in plant disease control. Biphenyl can be chlorinated with 1-10 chlorine molecules to form polychlorinated biphenyls (PCBs).","definition_xrefs":["PMID:16339959","PMID:16310831"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biphenyl metabolic process","termid":"GO:0018879"},{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"}],"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":"biphenyl catabolic process","synonyms":[{"name":"biphenyl breakdown","type":"exact"},{"name":"biphenyl catabolism","type":"exact"},{"name":"biphenyl degradation","type":"exact"}],"termid":"GO:0070980"}


id: PBO:0029810
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_spore_with_abnormal_shape","termid":"PBO:0029810"}


id: GO:0098641
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Any cadherin binding that occurs as part of the process of cell-cell adhesion.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cadherin binding","termid":"GO:0045296"},{"relation_name":"is_a","term_name":"cell-cell adhesion mediator activity","termid":"GO:0098632"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0098631"}],"interesting_parent_ids":["GO:0098631","GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"cadherin binding involved in cell-cell adhesion","termid":"GO:0098641"}


id: MONDO:0800210
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"juvenile open angle glaucoma","termid":"MONDO:0020367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"glaucoma 1, open angle, l","synonyms":[{"name":"GLC1L","type":"exact"}],"termid":"MONDO:0800210","xrefs":{"Monarch":{"xref_id":"0800210"}}}


id: GO:1902999
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of phospholipid efflux.","definition_xrefs":["GO_REF:0000058","PMID:12042316","GOC:sjp","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of phospholipid efflux","termid":"GO:1902994"},{"relation_name":"is_a","term_name":"negative regulation of phospholipid transport","termid":"GO:2001139"},{"relation_name":"negatively_regulates","term_name":"phospholipid efflux","termid":"GO:0033700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of phospholipid efflux","synonyms":[{"name":"down regulation of phospholipid efflux","type":"exact"},{"name":"down regulation of phospholipid export","type":"exact"},{"name":"down-regulation of phospholipid efflux","type":"exact"},{"name":"down-regulation of phospholipid export","type":"exact"},{"name":"downregulation of phospholipid efflux","type":"exact"},{"name":"downregulation of phospholipid export","type":"exact"},{"name":"inhibition of phospholipid efflux","type":"narrow"},{"name":"inhibition of phospholipid export","type":"narrow"},{"name":"negative regulation of phospholipid export","type":"exact"}],"termid":"GO:1902999"}


id: FYPO:0007808
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of valproic acid than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002682"}],"interesting_parent_ids":["FYPO:0002682","FYPO:0000139","FYPO:0001985","FYPO:0005447","FYPO:0000003"],"is_obsolete":false,"name":"resistance to valproic acid","synonyms":[{"name":"resistance to valproic acid during mitotic cell cycle","type":"related"},{"name":"resistance to valproic acid during vegetative growth","type":"exact"}],"termid":"FYPO:0007808"}


id: PBO:0071934
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S4X pseudogene 11","termid":"PBO:0071934"}


id: PBO:0056152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule actin crosslinking factor 1","termid":"PBO:0056152"}


id: SO:0000955
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Structural unit composed of a self-replicating, double-stranded DNA molecule.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"double","termid":"SO:0000985"},{"relation_name":"is_a","term_name":"DNA_chromosome","termid":"SO:0000954"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double_stranded_DNA_chromosome","synonyms":[{"name":"double stranded DNA chromosome","type":"exact"}],"termid":"SO:0000955"}


id: MONDO:0016824
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, multifocal, nodular and well-circumscribed neoplasm usually seen as a congenital neoplasm or in the first year of life. It is characterized by a biphasic growth pattern and is composed of small, undifferentiated mesenchymal cells associated with branching thin-walled vessels and more mature neoplastic spindle cells with abundant eosinophilic cytoplasm in a collagenous stroma.","definition_xrefs":["NCIT:C3742"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete muscular tumor (obsolete MONDO:0016123)","termid":"MONDO:0016123"},{"relation_name":"excluded_subClassOf","term_name":"obsolete rare skin tumor or hamartoma (obsolete MONDO:0019300)","termid":"MONDO:0019300"},{"relation_name":"is_a","term_name":"benign perivascular tumor","termid":"MONDO:0003342"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"},{"relation_name":"is_a","term_name":"benign soft tissue neoplasm","termid":"MONDO:0044335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infantile myofibromatosis","secondary_identifiers":["MEDGEN:140933","NORD:1301","Orphanet:2591","UMLS:C0432284","ONCOTREE:IMS","OMIMPS:228550","ICDO:8824/1","DOID:0080109","MESH:D018224","GARD:2998"],"synonyms":[{"name":"IMS","type":"related"},{"name":"infantile hemangiopericytoma","type":"exact"},{"name":"infantile myofibromatosis","type":"exact"},{"name":"multicentric myofibromatosis","type":"exact"},{"name":"myofibromatosis","type":"exact"}],"termid":"MONDO:0016824","xrefs":{"Monarch":{"xref_id":"0016824"}}}


id: PBO:0062375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily A member 18 pseudogene","termid":"PBO:0062375"}


id: PBO:0058543
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6089","termid":"PBO:0058543"}


id: PBO:0067837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 139","termid":"PBO:0067837"}


id: MOD:00018
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a source amino acid residue to an L-histidine.","definition_xrefs":["DeltaMass:0","PubMed:6876174","ChEBI:29979","PubMed:14342316","PubMed:2722967","PubMed:6129252","PubMed:5460889","PubMed:512","PubMed:6692818","RESID:AA0009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"natural, standard, encoded residue","termid":"MOD:01441"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-histidine residue","synonyms":[{"name":"(2S)-2-amino-3-(1H-imidazol-4-yl)propanoic acid","type":"exact"},{"name":"(2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid [tautomer]","type":"exact"},{"name":"2-azanyl-3-(1H-imidazol-4-yl)propanoic acid","type":"exact"},{"name":"2-azanyl-3-(1H-imidazol-5-yl)propanoic acid [tautomer]","type":"exact"},{"name":"4-(2-amino-2-carboxyethyl)imidazole","type":"exact"},{"name":"His","type":"exact"},{"name":"L-histidine","type":"exact"},{"name":"alpha-amino-beta-(4-imidazole)propionic acid","type":"exact"},{"name":"glyoxaline-5-alanine","type":"exact"}],"termid":"MOD:00018"}


id: PBO:0056274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAN1B1 divergent transcript","termid":"PBO:0056274"}


id: GO:0071446
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 salicylic acid stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to salicylic acid","termid":"GO:0009751"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to salicylic acid stimulus","synonyms":[{"name":"cellular response to salicylate stimulus","type":"exact"}],"termid":"GO:0071446"}


id: GO:0051335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The reformation of the nuclear membrane during meiosis II.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic nuclear membrane reassembly","termid":"GO:0051333"},{"relation_name":"part_of","term_name":"meiosis II","termid":"GO:0007135"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0140013"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0007049","GO:0140013","GO:0061024"],"is_obsolete":false,"name":"meiosis II nuclear membrane reassembly","synonyms":[{"name":"meiosis II nuclear envelope reassembly","type":"related"}],"termid":"GO:0051335"}


id: GO:0015137
data:
  {"annotated_genes":["SJAG_01872"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071913"}]},"cv_name":"molecular_function","definition":"Enables the transfer of citrate, 2-hydroxy-1,2,3-propanetricarboxylate, from one side of a membrane to the other.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tricarboxylic acid transmembrane transporter activity","termid":"GO:0015142"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01872":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"citrate transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-433104","TC:2.A.29.7.2"],"synonyms":[{"name":"tricarboxylate transport protein","type":"related"}],"termid":"GO:0015137","terms_by_termid":{"GO:0071913":null}}


id: MONDO:0010633
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"},{"relation_name":"is_a","term_name":"hereditary glaucoma","termid":"MONDO:0018174"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"iris hypoplasia with glaucoma","secondary_identifiers":["MEDGEN:326993","OMIM:308500","MESH:C535538","GARD:9171","UMLS:C1839928"],"synonyms":[{"name":"IHG","type":"related"},{"name":"iris hypoplasia and glaucoma","type":"related"},{"name":"iris hypoplasia with glaucoma","type":"exact"}],"termid":"MONDO:0010633","xrefs":{"Monarch":{"xref_id":"0010633"}}}


id: GO:1904427
data:
  {"annotated_genes":["SJAG_04551"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104076],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905665"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of calcium ion transmembrane transport.","definition_xrefs":["PMID:22910094","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of calcium ion transport","termid":"GO:0051928"},{"relation_name":"is_a","term_name":"regulation of calcium ion transmembrane transport","termid":"GO:1903169"},{"relation_name":"is_a","term_name":"positive regulation of cation transmembrane transport","termid":"GO:1904064"},{"relation_name":"positively_regulates","term_name":"calcium ion transmembrane transport","termid":"GO:0070588"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04551":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of calcium ion transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of calcium ion membrane transport","type":"narrow"},{"name":"activation of calcium ion transmembrane transport","type":"narrow"},{"name":"activation of transmembrane calcium transport","type":"narrow"},{"name":"positive regulation of calcium ion membrane transport","type":"exact"},{"name":"positive regulation of transmembrane calcium transport","type":"exact"},{"name":"up regulation of calcium ion membrane transport","type":"exact"},{"name":"up regulation of calcium ion transmembrane transport","type":"exact"},{"name":"up regulation of transmembrane calcium transport","type":"exact"},{"name":"up-regulation of calcium ion membrane transport","type":"exact"},{"name":"up-regulation of calcium ion transmembrane transport","type":"exact"},{"name":"up-regulation of transmembrane calcium transport","type":"exact"},{"name":"upregulation of calcium ion membrane transport","type":"exact"},{"name":"upregulation of calcium ion transmembrane transport","type":"exact"},{"name":"upregulation of transmembrane calcium transport","type":"exact"}],"termid":"GO:1904427","terms_by_termid":{"GO:1905665":null}}


id: GO:0033668
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont inhibits or disrupts the normal execution of host apoptosis, leading to a decrease in the frequency, rate or extent of apoptosis in the host cell. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host programmed cell death","termid":"GO:0052041"},{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host apoptosis","termid":"GO:0052150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host apoptosis","secondary_identifiers":["Reactome:R-HSA-9635465","GO:0039650"],"synonyms":[{"name":"down regulation by organism of host apoptotic programmed cell death","type":"exact"},{"name":"down-regulation by organism of host apoptotic programmed cell death","type":"exact"},{"name":"downregulation by organism of host apoptotic programmed cell death","type":"exact"},{"name":"inhibition by organism of host apoptotic programmed cell death","type":"exact"},{"name":"negative regulation by symbiont of host apoptosis","type":"exact"},{"name":"negative regulation by symbiont of host apoptotic process","type":"exact"},{"name":"negative regulation by virus of host apoptosis","type":"narrow"},{"name":"suppression by symbiont of host apoptotic process","type":"exact"},{"name":"suppression by virus of host apoptosis","type":"narrow"}],"termid":"GO:0033668"}


id: GO:0051260
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of creating protein oligomers, compounds composed of a small number, usually between three and ten, of identical component monomers. Oligomers may be formed by the polymerization of a number of monomers or the depolymerization of a large protein polymer.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein complex oligomerization","termid":"GO:0051259"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"protein homooligomerization","synonyms":[{"name":"protein homooligomer assembly","type":"exact"},{"name":"protein homooligomer biosynthesis","type":"exact"},{"name":"protein homooligomer biosynthetic process","type":"exact"},{"name":"protein homooligomer formation","type":"exact"},{"name":"protein homooligomerization activity","type":"related"}],"termid":"GO:0051260"}


id: GO:0031788
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a motilin 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:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"motilin receptor binding","synonyms":[{"name":"motilin receptor ligand","type":"narrow"}],"termid":"GO:0031788"}


id: GO:0010220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or induces the rate of the vernalization response, by which induction of flowering is normally caused by extended exposure to cold temperatures.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vernalization response","termid":"GO:0010219"},{"relation_name":"is_a","term_name":"positive regulation of response to stimulus","termid":"GO:0048584"},{"relation_name":"positively_regulates","term_name":"vernalization response","termid":"GO:0010048"}],"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 vernalization response","synonyms":[{"name":"activation of vernalization response","type":"narrow"},{"name":"stimulation of vernalization response","type":"narrow"},{"name":"up regulation of vernalization response","type":"exact"},{"name":"up-regulation of vernalization response","type":"exact"},{"name":"upregulation of vernalization response","type":"exact"}],"termid":"GO:0010220"}


id: PBO:0041046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bromodomain containing 3","termid":"PBO:0041046"}


id: PBO:0077085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TP53 induced glycolysis regulatory phosphatase","termid":"PBO:0077085"}


id: MONDO:0031697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic intractable diarrhea of infancy (obsolete MONDO:0031697)","secondary_identifiers":["Orphanet:363300"],"termid":"MONDO:0031697","xrefs":{"Monarch":{"xref_id":"0031697"}}}


id: MOD:00369
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O-acetyl-L-serine.","definition_xrefs":["PubMed:7309355","PubMed:14730666","PubMed:11857757","ChEBI:17981","PubMed:11999733","PubMed:12175151","PubMed:15350136","PubMed:489587","PubMed:16731519","Unimod:1#S","RESID:AA0364"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acetylated residue","termid":"MOD:00644"},{"relation_name":"is_a","term_name":"acetylated L-serine","termid":"MOD:00647"},{"relation_name":"is_a","term_name":"O3-acylated L-serine","termid":"MOD:02003"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-acetyl-L-serine","synonyms":[{"name":"(2S)-3-(acetyloxy)-2-aminopropanoic acid","type":"exact"},{"name":"Acetyl","type":"related"},{"name":"Acetylation","type":"related"},{"name":"MOD_RES O-acetylserine","type":"exact"},{"name":"O-acetyl-L-serine","type":"exact"},{"name":"O-acetylated L-serine","type":"exact"},{"name":"O-acetylserine","type":"exact"},{"name":"OAcSer","type":"exact"},{"name":"serine acetate ester","type":"exact"}],"termid":"MOD:00369"}


id: PBO:0067972
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 274","termid":"PBO:0067972"}


id: GO:0015316
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 nitrite/nitrate porter activity (obsolete GO:0015316)","synonyms":[{"name":"nitrite/nitrate porter activity","type":"exact"}],"termid":"GO:0015316"}


id: GO:0090384
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The initial attachment of a phagosome membrane to a lysosome membrane. Docking requires only that the proteins come close enough to interact and adhere.","definition_xrefs":["GOC:kmv","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle docking","termid":"GO:0048278"},{"relation_name":"part_of","term_name":"phagolysosome assembly","termid":"GO:0001845"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140056"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0016192","GO:0044085","GO:0140056","GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"phagosome-lysosome docking","synonyms":[{"name":"lysosome recruitment to phagosome","type":"exact"}],"termid":"GO:0090384"}


id: RO:0002254
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x has developmental contribution from y iff x has some part z such that z develops from y","direct_ancestors":[{"relation_name":"is_a","term_name":"developmentally_preceded_by","termid":"RO:0002258"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_developmental_contribution_from","termid":"RO:0002254"}


id: GO:0006721
data:
  {"annotated_genes":["SJAG_00624","SJAG_03352","SJAG_04499","SJAG_03349","SJAG_04307","SJAG_03715","SJAG_00580","SJAG_04865","SJAG_01474","SJAG_02719","SJAG_04568","SJAG_00413","SJAG_03360"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[76066,81904,96332,111457,116906,103811,90560,115742,108484,101513],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010142"},{"annotations":[78266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045338"},{"annotations":[101514,111458],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033386"},{"annotations":[67802,62532],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016104"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving terpenoids, any member of a class of compounds characterized by an isoprenoid chemical structure and including derivatives with various functional groups.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoprenoid metabolic process","termid":"GO:0006720"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00413":null,"SJAG_00580":null,"SJAG_00624":null,"SJAG_01474":null,"SJAG_02719":null,"SJAG_03349":null,"SJAG_03352":null,"SJAG_03360":null,"SJAG_03715":null,"SJAG_04307":null,"SJAG_04499":null,"SJAG_04568":null,"SJAG_04865":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"terpenoid metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"terpenoid metabolism","type":"exact"}],"termid":"GO:0006721","terms_by_termid":{"GO:0010142":null,"GO:0016104":null,"GO:0033386":null,"GO:0045338":null}}


id: GO:1902384
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving glycyrrhetinate.","definition_xrefs":["GOC:TermGenie","PMID:22128119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentacyclic triterpenoid metabolic process","termid":"GO:0019742"},{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006629"],"is_obsolete":false,"name":"glycyrrhetinate metabolic process","synonyms":[{"name":"glycyrrhetinate metabolism","type":"exact"}],"termid":"GO:1902384"}


id: MONDO:0011197
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary thermosensitive neuropathy is a rare, demyelinating, hereditary motor and sensory neuropathy characterized by reversible episodes of ascending muscle weakness, paresthesias and areflexia triggered by a febrile episode, with or without pressure palsy.","definition_xrefs":["Orphanet:84093"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary motor and sensory neuropathy","termid":"MONDO:0015358"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"hereditary thermosensitive neuropathy","secondary_identifiers":["GARD:16731","OMIM:602107","icd11.foundation:1124144144","MEDGEN:355568","MESH:C566575","SCTID:715645004","UMLS:C1865856"],"synonyms":[{"name":"neuropathy, hereditary thermosensitive","type":"related"}],"termid":"MONDO:0011197","xrefs":{"Monarch":{"xref_id":"0011197"}}}


id: PR:Q9C0Z8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAPB1E7.11c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9C0Z8"],"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 PB1E7.11c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB1E7.11c","synonyms":[{"name":"Spom972h-SPAPB1E7.11c","type":"exact"}],"termid":"PR:Q9C0Z8"}


id: PBO:0049797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperpolarization activated cyclic nucleotide gated potassium channel 3","termid":"PBO:0049797"}


id: MONDO:1011191
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Synovial chondromatosis that occurs in great horned owl.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"synovial chondromatosis, non-human animal","termid":"MONDO:1010304"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synovial chondromatosis, great horned owl","secondary_identifiers":["OMIA:001174-56268"],"termid":"MONDO:1011191","xrefs":{"Monarch":{"xref_id":"1011191"}}}


id: GO:0008301
data:
  {"annotated_genes":["SJAG_04009","SJAG_04036","SJAG_05153","SJAG_04855","SJAG_00247"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91965,117029],"is_not":false,"summary":null,"term":"GO:0008301"},{"annotations":[104215],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110035"},{"annotations":[109013,110785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044377"}]},"cv_name":"molecular_function","definition":"The activity of binding selectively and non-covalently to and distorting the original structure of DNA, typically a straight helix, into a bend, or increasing the bend if the original structure was intrinsically bent due to its sequence.","definition_xrefs":["PMID:10710711","GOC:vw","PMID:19037758","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA binding","termid":"GO:0003677"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00247":null,"SJAG_04009":null,"SJAG_04036":null,"SJAG_04855":null,"SJAG_05153":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003677","GO:0003674"],"is_obsolete":false,"name":"DNA binding, bending","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DNA bending activity","type":"exact"},{"name":"DNA bending involving DNA binding","type":"exact"}],"termid":"GO:0008301","terms_by_termid":{"GO:0008301":null,"GO:0044377":null,"GO:0110035":null}}


id: MONDO:0003896
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A capillary hemangioma arising from the breast.","definition_xrefs":["NCIT:C5210"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"breast angiomatosis","termid":"MONDO:0002064"},{"relation_name":"is_a","term_name":"capillary hemangioma","termid":"MONDO:0002407"},{"relation_name":"is_a","term_name":"breast hemangioma","termid":"MONDO:0003126"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast capillary hemangioma","secondary_identifiers":["UMLS:C1332619","DOID:6491","MEDGEN:231963"],"synonyms":[{"name":"breast capillary angioma","type":"exact"},{"name":"breast capillary hemangioma","type":"exact"},{"name":"capillary angioma of breast","type":"exact"},{"name":"capillary angioma of the breast","type":"exact"},{"name":"capillary hemangioma of breast","type":"exact"},{"name":"capillary hemangioma of the breast","type":"exact"}],"termid":"MONDO:0003896","xrefs":{"Monarch":{"xref_id":"0003896"}}}


id: GO:1901745
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving prephenate(2-).","definition_xrefs":["GOC:TermGenie","GOC:yaf","PMID:16752890"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid metabolic process","termid":"GO:0043648"}],"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:0008150","GO:0044281"],"is_obsolete":false,"name":"prephenate(2-) metabolic process","synonyms":[{"name":"prephenate metabolism","type":"exact"},{"name":"prephenate(2-) metabolism","type":"exact"}],"termid":"GO:1901745"}


id: FYPO:0004199
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 occurrence of protein degradation is increased during mitosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein degradation during vegetative growth","termid":"FYPO:0000847"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0002274","FYPO:0001985"],"is_obsolete":false,"name":"increased protein degradation during mitosis","synonyms":[{"name":"increased protein breakdown during mitosis","type":"exact"},{"name":"increased protein catabolic process during mitosis","type":"exact"},{"name":"increased protein catabolism during mitosis","type":"exact"},{"name":"increased protein degradation during mitosis during mitotic cell cycle","type":"related"},{"name":"increased protein degradation during mitosis during vegetative growth","type":"exact"},{"name":"increased protein degradation during mitotic M phase","type":"related"},{"name":"increased protein degradation during mitotic nuclear division","type":"exact"}],"termid":"FYPO:0004199"}


id: PBO:0088738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3.3-H4 chaperone, HIR complex subunit Hip3","termid":"PBO:0088738"}


id: PBO:0081401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF248 antisense RNA 1","termid":"PBO:0081401"}


id: PBO:0004693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA replication factor C complex subunit Rfc1","termid":"PBO:0004693"}


id: MONDO:0019434
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Systemic-onset juvenile idiopathic arthritis is marked by the severity of the extra-articular manifestations (fever, cutaneous eruptions) and by an equal sex ratio.","definition_xrefs":["Orphanet:85414"],"direct_ancestors":[{"relation_name":"is_a","term_name":"juvenile idiopathic arthritis","termid":"MONDO:0011429"},{"relation_name":"is_a","term_name":"autoinflammatory syndrome","termid":"MONDO:0019751"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"systemic-onset juvenile idiopathic arthritis","secondary_identifiers":["icd11.foundation:504387587","GARD:10966","MEDGEN:346934","MESH:C565798","EFO:1001999","SCTID:201796004","UMLS:C1858558","NANDO:1200470","NANDO:2201055","NCIT:C119031"],"synonyms":[{"name":"SoJIA","type":"exact"},{"name":"Still disease","type":"exact"},{"name":"Still's disease (formerly)","type":"related"},{"name":"sJIA","type":"exact"},{"name":"systemic juvenile idiopathic arthritis","type":"related"},{"name":"systemic onset juvenile idiopathic arthritis","type":"related"},{"name":"systemic onset juvenile rheumatoid arthritis","type":"related"},{"name":"systemic polyarthritis","type":"exact"},{"name":"systemic-onset JIA","type":"exact"}],"termid":"MONDO:0019434","xrefs":{"Monarch":{"xref_id":"0019434"}}}


id: PBO:0069270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 526, pseudogene","termid":"PBO:0069270"}


id: PBO:0059270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L34","termid":"PBO:0059270"}


id: PBO:0069604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 881, pseudogene","termid":"PBO:0069604"}


id: PBO:0053402
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 332","termid":"PBO:0053402"}


id: GO:1901907
data:
  {"annotated_genes":["SJAG_04870"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[81045],"is_not":false,"summary":null,"term":"GO:1901907"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of diadenosine pentaphosphate.","definition_xrefs":["GOC:TermGenie","PMID:10090752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diadenosine polyphosphate catabolic process","termid":"GO:0015961"},{"relation_name":"is_a","term_name":"diadenosine pentaphosphate metabolic process","termid":"GO:1901906"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04870":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"diadenosine pentaphosphate catabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"diadenosine pentaphosphate catabolism","type":"exact"},{"name":"diadenosyl pentaphosphate breakdown","type":"exact"},{"name":"diadenosyl pentaphosphate catabolic process","type":"exact"},{"name":"diadenosyl pentaphosphate catabolism","type":"exact"},{"name":"diadenosyl pentaphosphate degradation","type":"exact"}],"termid":"GO:1901907","terms_by_termid":{"GO:1901907":null}}


id: PBO:0051858
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron-sulfur cluster assembly 1 pseudogene 4","termid":"PBO:0051858"}


id: MONDO:0007049
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":"acroleukopathy, symmetric","secondary_identifiers":["MEDGEN:350143","MESH:C566322","OMIM:102000","UMLS:C1863342"],"synonyms":[{"name":"acroleukopathy, symmetric","type":"exact"}],"termid":"MONDO:0007049","xrefs":{"Monarch":{"xref_id":"0007049"}}}


id: GO:0008572
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: ATP + H2O = ADP + phosphate. The hydrolysis of ATP required for the ATP-dependent assembly of nucleosome cores, in decondensation of sperm chromatin and in other histone-involving processes.","definition_xrefs":["EC:3.6.4.11"],"gene_count":0,"genotype_count":0,"name":"obsolete nucleoplasmin ATPase activity (obsolete GO:0008572)","synonyms":[{"name":"nucleoplasmin ATPase activity","type":"exact"}],"termid":"GO:0008572"}


id: PR:O14318
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- php4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14318"],"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":"CCAAT-binding factor complex subunit php4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16E9.01c","synonyms":[{"name":"Spom972h-php4","type":"exact"}],"termid":"PR:O14318"}


id: PBO:0055698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LLGL scribble cell polarity complex component 1","termid":"PBO:0055698"}


id: PBO:0080067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 32 pseudogene 4","termid":"PBO:0080067"}


id: MONDO:0011917
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any focal segmental glomerulosclerosis in which the cause of the disease is a mutation in the CD2AP gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"focal segmental glomerulosclerosis 3, susceptibility to","secondary_identifiers":["DOID:0112245","MEDGEN:335850","OMIM:607832","UMLS:C1842982"],"synonyms":[{"name":"CD2AP focal segmental glomerulosclerosis","type":"exact"},{"name":"FSGS3","type":"related"},{"name":"focal segmental glomerulosclerosis 3, susceptibility to","type":"exact"},{"name":"focal segmental glomerulosclerosis caused by mutation in CD2AP","type":"exact"},{"name":"glomerulosclerosis, focal segmental, 3","type":"exact"},{"name":"glomerulosclerosis, focal segmental, 3, susceptibility to","type":"related"},{"name":"susceptibility to focal segmental glomerulosclerosis 3","type":"related"}],"termid":"MONDO:0011917","xrefs":{"Monarch":{"xref_id":"0011917"}}}


id: PBO:0049579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3.3 histone B","termid":"PBO:0049579"}


id: GO:0140288
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A SWI/SNF subcomplex that incorporates two mutually exclusive paralogs, GLTSCR1 (glioma tumor suppressor candidate region gene 1) or GLTSCR1L (GLTSCR1-like), BRD9 (bromodomain-containing 9) and the BAF subunits BAF155, BAF60, SS18, BAF53a, and BRG1/BRM.","definition_xrefs":["PMID:29374058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SWI/SNF superfamily-type complex","termid":"GO:0070603"}],"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:0005694"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005694","GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"GBAF complex","termid":"GO:0140288"}


id: MONDO:0016668
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sickle beta thalassemia is an inherited condition that affects hemoglobin, the protein in red blood cells that carries oxygen to different parts of the body.It is a type of sickle cell disease. Affected people have a differentchange (mutation) in each copy of their HBB gene: onethat causes red blood cells to form a 'sickle' or crescent shape and a second that is associated with beta thalassemia, a blood disorder that reduces the production of hemoglobin. Depending on the beta thalassemia mutation, people may have no normal hemoglobin (called sickle beta zero thalassemia) or a reduced amount of normal hemoglobin (called sickle beta plus thalassemia). The presence of sickle-shaped red blood cells, which often breakdown prematurely and can get stuck in blood vessels, combined with the reduction or absence of mature redblood cells leads to the many signs and symptoms of sickle beta thalassemia. Features, which may include anemia (low levels of red blood cells), repeated infections, and frequent episodes of pain, generally develop in early childhood and vary in severity depending on the amount of normal hemoglobin made. Sickle beta thalassemia is inherited in an autosomal recessive manner. Treatment is supportive and depends on the signs and symptoms present in each person.","definition_xrefs":["GARD:0010333"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"inherited hemoglobinopathy","termid":"MONDO:0019050"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"sickle cell-beta-thalassemia disease syndrome","secondary_identifiers":["GARD:10333","MedDRA:10040655","MedDRA:10055579","NCIT:C95539","Orphanet:251359","SCTID:127041004"],"synonyms":[{"name":"Haemoglobin sickle-beta thalassemia","type":"related"},{"name":"Hb S beta-thalassemia","type":"related"},{"name":"Hb S-Beta thalassemia","type":"exact"},{"name":"HbS - beta-thalassemia","type":"related"},{"name":"HbS-beta-thalassemia syndrome","type":"exact"},{"name":"Hemoglobin sickle-beta thalassemia","type":"related"},{"name":"S-Beta thalassemia","type":"exact"},{"name":"sickle beta thalassemia","type":"related"},{"name":"sickle cell - beta-thalassemia disease","type":"related"},{"name":"sickle cell-Beta thalassemia","type":"exact"},{"name":"sickle cell-Beta-thalassemia","type":"exact"},{"name":"sickle cell-beta-thalassemia disease syndrome","type":"exact"}],"termid":"MONDO:0016668","xrefs":{"Monarch":{"xref_id":"0016668"}}}


id: PBO:0043400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CMKLR2 antisense RNA","termid":"PBO:0043400"}


id: MONDO:0001573
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Friedreich ataxia (obsolete MONDO:0001573)","termid":"MONDO:0001573","xrefs":{"Monarch":{"xref_id":"0001573"}}}


id: GO:0051004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the activity of the enzyme lipoprotein lipase.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of lipoprotein lipase activity (obsolete GO:0051004)","termid":"GO:0051004"}


id: GO:1900379
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of asperthecin biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ketone biosynthetic process","termid":"GO:0010566"},{"relation_name":"is_a","term_name":"regulation of secondary metabolite biosynthetic process","termid":"GO:1900376"},{"relation_name":"regulates","term_name":"asperthecin biosynthetic process","termid":"GO:0036184"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0019748"],"is_obsolete":false,"name":"regulation of asperthecin biosynthetic process","synonyms":[{"name":"regulation of asperthecin biosynthesis","type":"exact"},{"name":"regulation of asperthecin formation","type":"exact"},{"name":"regulation of asperthecin synthesis","type":"exact"}],"termid":"GO:1900379"}


id: GO:0016917
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with gamma-aminobutyric acid (GABA), and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity. (GABA, 4-aminobutyrate) is an amino acid which acts as a neurotransmitter in some organisms.","definition_xrefs":["PMID:10637650","GOC:jl","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane signaling receptor activity","termid":"GO:0004888"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"GABA receptor activity","synonyms":[{"name":"4-aminobutanoate receptor activity","type":"exact"},{"name":"4-aminobutyrate receptor activity","type":"exact"},{"name":"GABA binding","type":"exact"},{"name":"gamma-aminobutyrate binding","type":"exact"},{"name":"gamma-aminobutyric acid binding","type":"exact"},{"name":"gamma-aminobutyric acid receptor activity","type":"exact"}],"termid":"GO:0016917"}


id: PBO:0049779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex group 13 pseudogene","termid":"PBO:0049779"}


id: PBO:0090852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carboxylic acid transmembrane transporter Tna1","termid":"PBO:0090852"}


id: MONDO:0018391
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete male infertility with spermatogenesis disorder (obsolete MONDO:0018391)","secondary_identifiers":["Orphanet:399775"],"termid":"MONDO:0018391","xrefs":{"Monarch":{"xref_id":"0018391"}}}


id: PBO:0014270
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae CAR1","termid":"PBO:0014270"}


id: GO:0120302
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which an organism changes its pigmentation (lightening in response to a brighter environment or darkening in response to a dimmer environment) in response to a change in light intensity.","definition_xrefs":["GOC:cvs","GOC:krc","PMID:10493760","PMID:29239123","PMID:32898924"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to light intensity","termid":"GO:0009642"},{"relation_name":"is_a","term_name":"regulation of pigmentation","termid":"GO:0120305"}],"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":"background adaptation","termid":"GO:0120302"}


id: GO:1901545
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 raffinose stimulus.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to carbohydrate","termid":"GO:0009743"}],"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 raffinose","termid":"GO:1901545"}


id: MONDO:0010153
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trichoodontoonychial dysplasia is a rare ectodermal dysplasia syndrome characterized by severe generalized hypotrichosis, parietal alopecia, secondary anodontia resulting from enamel hypoplasia, onychodystrophy, bone deficiency in the frontoparietal region and skin manifestations (incl. nevus pigmentosus, papules, ephelides, palmoplantar keratosis, supernumerary nipples, abnormal dermatoglyphics). There have been no further descriptions in the literature since 1983.","definition_xrefs":["Orphanet:3355"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"trichoodontoonychial dysplasia","secondary_identifiers":["GARD:5267","SCTID:766813000","MEDGEN:481087","UMLS:C3279457","OMIM:275450","MESH:C564760"],"synonyms":[{"name":"trichoodontoonychial dysplasia with bone deficiency","type":"related"},{"name":"trichoodontoonychial dysplasia with bone deficiency in frontoparietal region","type":"exact"}],"termid":"MONDO:0010153","xrefs":{"Monarch":{"xref_id":"0010153"}}}


id: GO:0019603
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The degradation of toluene to form p-hydroxybenzoate; the first step in the pathway is the oxidation of toluene to form 4-hydroxytoluene (4-cresol).","definition_xrefs":["MetaCyc:TOLUENE-DEG-4-OH-PWY"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toluene oxidation","termid":"GO:0019600"}],"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":"toluene oxidation via 4-hydroxytoluene","termid":"GO:0019603"}


id: PBO:0068164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 471","termid":"PBO:0068164"}


id: GO:0035320
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Determination of the site in the cell of an imaginal disc-derived wing at which a prehair initiates outgrowth. Restriction of prehair initiation to the distalmost part of a cell is essential to ensure that each wing epithelial cell produces one adult hair that points distally.","definition_xrefs":["PMID:8947551","ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of proximal/distal cell polarity","termid":"GO:0022606"},{"relation_name":"part_of","term_name":"establishment of imaginal disc-derived wing hair orientation","termid":"GO:0001737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007163"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007163","GO:0008150"],"is_obsolete":false,"name":"imaginal disc-derived wing hair site selection","synonyms":[{"name":"prehair localization","type":"related"},{"name":"wing hair site selection","type":"exact"}],"termid":"GO:0035320"}


id: PR:O42939
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A SUMO-activating enzyme subunit 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10953:SF5","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":"ubiquitin-activating enzyme E1-like (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16H5.03c","secondary_identifiers":["UniProtKB:O42939"],"synonyms":[{"name":"SPBC16H5.03c","type":"related"},{"name":"Spom972h-UBA2","type":"exact"},{"name":"pmt3-activating enzyme subunit 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O42939"}


id: PBO:0002458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP phosphoribosyltransferase","termid":"PBO:0002458"}


id: GO:0098977
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Synaptic transmission that results in an inhibitory postsynaptic potential.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemical synaptic transmission","termid":"GO:0007268"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"inhibitory chemical synaptic transmission","termid":"GO:0098977"}


id: GO:0060512
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a prostate gland are generated and organized.","definition_xrefs":["GOC:dph","PMID:18977204"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"gland morphogenesis","termid":"GO:0022612"},{"relation_name":"part_of","term_name":"prostate gland development","termid":"GO:0030850"}],"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":"prostate gland morphogenesis","termid":"GO:0060512"}


id: PBO:0034391
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-relation_between_structure_and_stage","termid":"PBO:0034391"}


id: GO:0006380
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete poly-A binding (obsolete GO:0006380)","synonyms":[{"name":"poly-A binding","type":"exact"}],"termid":"GO:0006380"}


id: PR:O94504
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- trx2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94504"],"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":"thioredoxin-2, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC12D12.07c","synonyms":[{"name":"Spom972h-trx2","type":"exact"},{"name":"Trx-2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94504"}


id: PBO:0090707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RhoGAP Rga5","termid":"PBO:0090707"}


id: PBO:0074083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC25A53 pseudogene 1","termid":"PBO:0074083"}


id: GO:2001117
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a tetrahydromethanopterin.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methanopterin-containing compound metabolic process","termid":"GO:2001115"}],"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":"tetrahydromethanopterin metabolic process","synonyms":[{"name":"tetrahydromethanopterin metabolism","type":"exact"}],"termid":"GO:2001117"}


id: MONDO:0044675
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with decreased bone density (obsolete MONDO:0019704)","termid":"MONDO:0019704"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LRP5-related primary osteoporosis","secondary_identifiers":["MEDGEN:1798664","GARD:22031","Orphanet:498481","UMLS:C5567241"],"termid":"MONDO:0044675","xrefs":{"Monarch":{"xref_id":"0044675"}}}


id: GO:0045565
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of TRAIL (TNF-related apoptosis inducing ligand) receptor 1.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of TRAIL receptor 1 biosynthetic process (obsolete GO:0045565)","synonyms":[{"name":"down regulation of TRAIL receptor 1 biosynthetic process","type":"exact"},{"name":"down-regulation of TRAIL receptor 1 biosynthetic process","type":"exact"},{"name":"downregulation of TRAIL receptor 1 biosynthetic process","type":"exact"},{"name":"inhibition of TRAIL receptor 1 biosynthetic process","type":"narrow"},{"name":"negative regulation of TRAIL receptor 1 anabolism","type":"exact"},{"name":"negative regulation of TRAIL receptor 1 biosynthesis","type":"exact"},{"name":"negative regulation of TRAIL receptor 1 formation","type":"exact"},{"name":"negative regulation of TRAIL receptor 1 synthesis","type":"exact"}],"termid":"GO:0045565"}


id: PR:Q9P327
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of any of the following genes in Schizosaccharomyces pombe 972h-: SPAC977.09c/SPBC1348.10c.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P327"],"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":"lysophospholipase C977.09c/C1348.10c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1348.10c","synonyms":[{"name":"Spom972h-SPBC1348.10c","type":"exact"},{"name":"phospholipase B (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P327"}


id: PBO:0072295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S24 pseudogene 13","termid":"PBO:0072295"}


id: GO:0042834
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Interacting selectively and non-covalently, in a non-covalent manner, with peptidoglycan, any of a class of glycoconjugates found in bacterial cell walls.","definition_xrefs":["PMID:14698226","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosaminoglycan binding","termid":"GO:0005539"}],"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:0005488","GO:0003674"],"is_obsolete":false,"name":"peptidoglycan binding","termid":"GO:0042834"}


id: GO:0047019
data:
  {"annotated_genes":["SJAG_01869"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[93702],"is_not":false,"summary":null,"term":"GO:0047019"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: indole-3-ethanol + NADP+ = (indol-3-yl)acetaldehyde + H+ + NADPH.","definition_xrefs":["EC:1.1.1.191","RHEA:17037"],"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":1,"genes_by_uniquename":{"SJAG_01869":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"indole-3-acetaldehyde reductase (NADPH) activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:1.1.1.191-RXN","KEGG_REACTION:R02680"],"synonyms":[{"name":"(indol-3-yl)ethanol:NADP+ oxidoreductase activity","type":"related"},{"name":"indole-3-ethanol:NADP+ oxidoreductase activity","type":"related"},{"name":"indoleacetaldehyde (reduced nicotinamide adenine dinucleotide phosphate) reductase activity","type":"related"}],"termid":"GO:0047019","terms_by_termid":{"GO:0047019":null}}


id: PBO:0034243
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_functional_equivalence_relationship_with","termid":"PBO:0034243"}


id: PBO:0044327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYCS pseudogene 7","termid":"PBO:0044327"}


id: GO:0019825
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to oxygen (O2).","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small molecule binding","termid":"GO:0036094"}],"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:0005488","GO:0003674"],"is_obsolete":false,"name":"oxygen binding","synonyms":[{"name":"cytochrome P450","type":"narrow"},{"name":"cytochrome P450 activity","type":"related"}],"termid":"GO:0019825"}


id: PBO:0026888
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitotic_sister_chromatid_segregation_with_lagging_chromosomes_and_decreased_rate_of_mitotic_spindle_elongation","termid":"PBO:0026888"}


id: PBO:0046779
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EXTL3 antisense RNA 1","termid":"PBO:0046779"}


id: MONDO:0032628
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  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex I deficiency, nuclear type","termid":"MONDO:0100223"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial complex 1 deficiency, nuclear type 24","secondary_identifiers":["GARD:16328","MEDGEN:1648364","UMLS:C4748803","OMIM:618245","DOID:0112079"],"synonyms":[{"name":"MC1DN24","type":"related"},{"name":"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 24","type":"related"}],"termid":"MONDO:0032628","xrefs":{"Monarch":{"xref_id":"0032628"}}}


id: PBO:0069881
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1169, pseudogene","termid":"PBO:0069881"}


id: MOD:00841
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  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification produced by formation of an adduct with an isothiocyanate compound.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isothiocyanate reagent derivatized residue","termid":"MOD:00841"}


id: PR:O00084
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ure2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O00084"],"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":"urease (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1952.11c","synonyms":[{"name":"Spom972h-ure2","type":"exact"},{"name":"urea amidohydrolase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O00084"}


id: PBO:0061337
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear pore complex interacting protein family member B15","termid":"PBO:0061337"}


id: PR:Q9UTP0
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl3002 gene.","definition_xrefs":["UniProtKB:Q9UTP0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L30-2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1250.05","synonyms":[{"name":"Spom972h-rpl3002","type":"exact"}],"termid":"PR:Q9UTP0"}


id: MONDO:0004107
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id: MONDO:0013141
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  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete autosomal dominant macrothrombocytopenia TUBB1-related (obsolete MONDO:0013141)","secondary_identifiers":["NANDO:2200667"],"termid":"MONDO:0013141","xrefs":{"Monarch":{"xref_id":"0013141"}}}


id: MONDO:0005530
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Disorders related or resulting from abuse or mis-use of opioids.","definition_xrefs":["MESH:D009293"],"direct_ancestors":[{"relation_name":"is_a","term_name":"drug dependence","termid":"MONDO:0005303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"opiate dependence","secondary_identifiers":["ICD9:304.0","UMLS:C0524662","ICD9:304.00","DOID:2559","MEDGEN:99372","EFO:0005611","SCTID:75544000"],"synonyms":[{"name":"narcotism","type":"related"},{"name":"opioid dependence","type":"exact"},{"name":"opioid type dependence","type":"exact"}],"termid":"MONDO:0005530","xrefs":{"Monarch":{"xref_id":"0005530"}}}


id: GO:0007238
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of Pbs2 (obsolete GO:0007238)","synonyms":[{"name":"activation of Pbs2","type":"exact"}],"termid":"GO:0007238"}


id: PBO:0044957
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dehydrogenase/reductase 4","termid":"PBO:0044957"}


id: PBO:0071401
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L31 pseudogene 7","termid":"PBO:0071401"}


id: PBO:0075478
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPATA31 subfamily A member 6","termid":"PBO:0075478"}


id: PBO:0050114
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  {"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: PBO:0013085
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase Prp16","termid":"PBO:0013085"}


id: PBO:0001453
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylate kinase Adk1","termid":"PBO:0001453"}


id: MONDO:0020288
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id: GO:0140010
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id: GO:0043651
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id: GO:1990157
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id: MONDO:0000720
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id: PBO:0049502
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id: SO:0000097
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id: MONDO:0019056
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id: GO:0003861
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  {"annotated_genes":["SJAG_03243"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[59633],"is_not":false,"summary":null,"term":"GO:0003861"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: (2R,3S)-3-isopropylmalate = (2S)-2-isopropylmalate.","definition_xrefs":["EC:4.2.1.33"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03243":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"3-isopropylmalate dehydratase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["MetaCyc:3-ISOPROPYLMALISOM-RXN","RHEA:32287"],"synonyms":[{"name":"(2R,3S)-3-isopropylmalate hydro-lyase (2-isopropylmaleate-forming)","type":"related"},{"name":"(2R,3S)-3-isopropylmalate hydro-lyase activity","type":"related"},{"name":"alpha-IPM isomerase activity","type":"related"},{"name":"alpha-isopropylmalate isomerase activity","type":"related"},{"name":"beta-isopropylmalate dehydratase activity","type":"related"},{"name":"isopropylmalate isomerase activity","type":"related"}],"termid":"GO:0003861","terms_by_termid":{"GO:0003861":null}}


id: PBO:0052962
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kynureninase pseudogene 2","termid":"PBO:0052962"}


id: GO:0070654
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regrowth of a sensory epithelium following its loss or destruction.","definition_xrefs":["GOC:dsf","PMID:19381250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelium regeneration","termid":"GO:1990399"}],"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":"sensory epithelium regeneration","termid":"GO:0070654"}


id: GO:1900581
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of (17Z)-protosta-17(20),24-dien-3beta-ol.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid biosynthetic process","termid":"GO:0006694"},{"relation_name":"is_a","term_name":"tetracyclic triterpenoid biosynthetic process","termid":"GO:0010686"},{"relation_name":"is_a","term_name":"secondary metabolite biosynthetic process","termid":"GO:0044550"},{"relation_name":"is_a","term_name":"(17Z)-protosta-17(20),24-dien-3beta-ol metabolic process","termid":"GO:1900579"},{"relation_name":"is_a","term_name":"secondary alcohol biosynthetic process","termid":"GO:1902653"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0019748","GO:0044281","GO:0006629","GO:0008150"],"is_obsolete":false,"name":"(17Z)-protosta-17(20),24-dien-3beta-ol biosynthetic process","synonyms":[{"name":"(17Z)-protosta-17(20),24-dien-3beta-ol anabolism","type":"exact"},{"name":"(17Z)-protosta-17(20),24-dien-3beta-ol biosynthesis","type":"exact"},{"name":"(17Z)-protosta-17(20),24-dien-3beta-ol formation","type":"exact"},{"name":"(17Z)-protosta-17(20),24-dien-3beta-ol synthesis","type":"exact"}],"termid":"GO:1900581"}


id: MONDO:0008888
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete non-syndromic respiratory or mediastinal malformation (obsolete MONDO:0015221)","termid":"MONDO:0015221"},{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Williams-Campbell syndrome","secondary_identifiers":["MEDGEN:137939","UMLS:C0340231","GARD:21731","ICD9:748.3","SCTID:54203008","icd11.foundation:766574679","NANDO:2201040","Orphanet:411501","OMIM:211450"],"synonyms":[{"name":"BRONCHOMALACIA","type":"related"},{"name":"Williams-Campbell syndrome","type":"exact"}],"termid":"MONDO:0008888","xrefs":{"Monarch":{"xref_id":"0008888"}}}


id: GO:0033049
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving clavulanic acid, (2R,3Z,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"lactam metabolic process","termid":"GO:0072338"}],"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":"clavulanic acid metabolic process","synonyms":[{"name":"clavulanic acid metabolism","type":"exact"}],"termid":"GO:0033049"}


id: PBO:0017444
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-produces","termid":"PBO:0017444"}


id: GO:1990889
data:
  {"annotated_genes":["SJAG_00545"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[109887],"is_not":false,"summary":null,"term":"GO:1990889"}]},"cv_name":"molecular_function","definition":"A histone reader that recognizes a histone H4 trimethylated at lysine 20.","definition_xrefs":["PMID:20943666","PMID:22150589"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H4 reader activity","termid":"GO:0140008"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00545":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0140566"}],"interesting_parent_ids":["GO:0140566","GO:0030674","GO:0060090","GO:0003674"],"is_obsolete":false,"name":"histone H4K20me3 reader activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"H4K20me3 modified histone binding","type":"narrow"}],"termid":"GO:1990889","terms_by_termid":{"GO:1990889":null}}


id: PBO:0030881
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_chromatin_organization_during_vegetative_growth","termid":"PBO:0030881"}


id: GO:0000084
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle phase, following G1, during which DNA synthesis takes place as part of a mitotic cell cycle.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S phase","termid":"GO:0051320"},{"relation_name":"part_of","term_name":"mitotic interphase","termid":"GO:0051329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0051329"}],"interesting_parent_ids":["GO:0008150","GO:0051329"],"is_obsolete":false,"name":"mitotic S phase","synonyms":[{"name":"S phase of mitotic cell cycle","type":"exact"},{"name":"S-phase of mitotic cell cycle","type":"exact"}],"termid":"GO:0000084"}


id: GO:0102867
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2 H+ + MoO2-molybdopterin cofactor(2-) + L-cysteine = thio-molybdenum cofactor + L-alanine + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete molybdenum cofactor sulfurtransferase activity (obsolete GO:0102867)","termid":"GO:0102867"}


id: PBO:0078305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asp (anticodon GTC) 2-10","termid":"PBO:0078305"}


id: PBO:0044160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTDSPL2 divergent transcript","termid":"PBO:0044160"}


id: PR:O94460
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A queuine tRNA-ribosyltransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00369","PANTHER:PTHR11962: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":"queuine tRNA-ribosyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1687.19c","secondary_identifiers":["UniProtKB:O94460"],"synonyms":[{"name":"Spom972h-QTRT1","type":"exact"},{"name":"guanine insertion enzyme (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"tRNA-guanine transglycosylase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94460"}


id: GO:1904076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of estrogen biosynthetic process.","definition_xrefs":["PMID:24530842","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hormone biosynthetic process","termid":"GO:0046885"},{"relation_name":"is_a","term_name":"regulation of steroid biosynthetic process","termid":"GO:0050810"},{"relation_name":"regulates","term_name":"estrogen biosynthetic process","termid":"GO:0006703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"regulation of estrogen biosynthetic process","synonyms":[{"name":"regulation of estrogen anabolism","type":"exact"},{"name":"regulation of estrogen biosynthesis","type":"exact"},{"name":"regulation of estrogen formation","type":"exact"},{"name":"regulation of estrogen synthesis","type":"exact"},{"name":"regulation of oestrogen biosynthesis","type":"exact"},{"name":"regulation of oestrogen biosynthetic process","type":"exact"}],"termid":"GO:1904076"}


id: MONDO:0002899
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neuroblastoma in which the differentiating neuroblasts constitute more than five-percent of the tumor cells.","definition_xrefs":["NCIT:C42048"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroblastoma","termid":"MONDO:0005072"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"differentiating neuroblastoma","secondary_identifiers":["DOID:4160","MEDGEN:268734","UMLS:C1511934"],"synonyms":[{"name":"differentiating neuroblastoma","type":"exact"}],"termid":"MONDO:0002899","xrefs":{"Monarch":{"xref_id":"0002899"}}}


id: FYPO:0004269
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 dissolution of the cell septum edging material is abnormal; may result in the formation of chains of attached cells.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell separation after cytokinesis","termid":"FYPO:0000164"},{"relation_name":"is_a","term_name":"abnormal cellular component organization during vegetative growth","termid":"FYPO:0001353"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"abnormal cell septum edging catabolic process","synonyms":[{"name":"abnormal cell septum edging catabolic process during mitotic cell cycle","type":"related"},{"name":"abnormal cell septum edging catabolic process during vegetative growth","type":"exact"},{"name":"abnormal cell septum edging catabolism","type":"exact"},{"name":"abnormal cell septum edging hydrolysis","type":"exact"},{"name":"chained cells","type":"related"}],"termid":"FYPO:0004269"}


id: GO:0103089
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-(6'-methylthio)hexylmalate = 3-(6'-methylthio)hexylmalate.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete methylthiohexylmalate isomerase activity (obsolete GO:0103089)","termid":"GO:0103089"}


id: MONDO:0859347
data:
  {"annotated_genes":["SJAG_00134"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87440],"is_not":false,"summary":null,"term":"MONDO:0859347"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00134":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620191","MEDGEN:1824058","UMLS:C5774285"],"termid":"MONDO:0859347","terms_by_termid":{"MONDO:0859347":null},"xrefs":{"Monarch":{"xref_id":"0859347"}}}


id: GO:0008389
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: coumarin + O2 + NADPH + H+ = hydroxycoumarin + H2O + NADP+.","definition_xrefs":["PMID:10490589","PMID:2733794"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"coumarin 7-hydroxylase activity","secondary_identifiers":["Reactome:R-HSA-211881","Reactome:R-HSA-76453"],"synonyms":[{"name":"cytochrome P450 CYP2A5","type":"narrow"}],"termid":"GO:0008389"}


id: PBO:0004081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protoheme IX farnesyltransferase (predicted)","termid":"PBO:0004081"}


id: PATO:0002463
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of some aspect of the bearer extending to the position of another entity.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"extends to","termid":"PATO:0002463"}


id: GO:0000970
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A tRNA exon ligation process in which the splice junction phosphate is derived from exogenous GTP. This type of ligation to rejoin the 5' and 3' exons of a tRNA is observed in the yeast Saccharomyces cerevisiae where the ligation reaction also produces a 2'-phosphate at the splice junction which is subsequently removed as part of the ligation process.","definition_xrefs":["PMID:18217203","GOC:krc","PMID:9299409"],"gene_count":0,"genotype_count":0,"name":"obsolete tRNA exon ligation utilizing GTP as source of linkage phosphate (obsolete GO:0000970)","termid":"GO:0000970"}


id: GO:0070626
data:
  {"annotated_genes":["SJAG_02850"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78755],"is_not":false,"summary":null,"term":"GO:0070626"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido)succinate = fumarate + 5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamide.","definition_xrefs":["RHEA:23920"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amidine-lyase activity","termid":"GO:0016842"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02850":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"(S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido) succinate lyase (fumarate-forming) activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:AICARSYN-RXN","Reactome:R-HSA-73828","KEGG_REACTION:R04559","Reactome:R-HSA-73800"],"synonyms":[{"name":"(S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido)succinate AMP-lyase (fumarate-forming) activity","type":"related"},{"name":"SAICAR-lyase (fumarate forming) activity","type":"related"},{"name":"adenylosuccinase activity","type":"broad"},{"name":"adenylosuccinate lyase activity","type":"broad"},{"name":"succino AMP-lyase activity","type":"broad"}],"termid":"GO:0070626","terms_by_termid":{"GO:0070626":null}}


id: FYPO:0006347
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to mechlorethamine. Cells stop growing (and may die) at a concentration of mechlorethamine that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002683","FYPO:0000139","FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to mechlorethamine","synonyms":[{"name":"hypersensitive to mechlorethamine","type":"exact"},{"name":"sensitive to 2-chloro-N-(2-chloroethyl)-N-methylethanamine","type":"exact"},{"name":"sensitive to HN2","type":"exact"},{"name":"sensitive to bis(2-chloroethyl)methylamine","type":"exact"},{"name":"sensitive to mechlorethamine during mitotic cell cycle","type":"related"},{"name":"sensitive to mechlorethamine during vegetative growth","type":"exact"}],"termid":"FYPO:0006347"}


id: FYPO:0005979
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 actin filament bundle organization is abnormal. The process normally results in the assembly, arrangement of constituent parts, or disassembly of an actin filament bundle. Actin filament bundles are assemblies of actin filaments organized along a single axis.","definition_xrefs":["PomBase:mah","GO:0061572"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actin filament organization during vegetative growth","termid":"FYPO:0000727"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0004803"},{"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"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0004803","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abnormal actin filament bundle organization","synonyms":[{"name":"abnormal actin filament bundle organisation during vegetative growth","type":"exact"},{"name":"abnormal actin filament bundle organization during mitotic cell cycle","type":"related"},{"name":"abnormal actin filament bundle organization during vegetative growth","type":"exact"}],"termid":"FYPO:0005979"}


id: PBO:0082585
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chromatin-binding ATPase that regulates histone gene expression; only bromodomain-containing AAA-ATPase in yeast; bromodomain interacts with N-terminal tail of histone H3; relocalizes to cytosol in response to hypoxia; human ortholog ANCCA is coactivator of both estrogen and androgen receptors, and increased expression of ANCCA is associated with breast and prostate cancers with poor prognoses","termid":"PBO:0082585"}


id: PBO:0080242
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 5 (gene/pseudogene)","termid":"PBO:0080242"}


id: GO:0090029
data:
  {"annotated_genes":["SJAG_00990"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95204],"is_not":false,"summary":null,"term":"GO:0090029"}]},"cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of pheromone-dependent signal transduction during conjugation with cellular fusion, a signal transduction process resulting in the relay, amplification or dampening of a signal generated in response to pheromone exposure in organisms that undergo conjugation with cellular fusion.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of pheromone-dependent signal transduction involved in conjugation with cellular fusion","termid":"GO:0010969"},{"relation_name":"is_a","term_name":"negative regulation of signal transduction involved in conjugation with cellular fusion","termid":"GO:0060240"},{"relation_name":"negatively_regulates","term_name":"pheromone-dependent signal transduction involved in conjugation with cellular fusion","termid":"GO:0000750"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00990":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0000747"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0000747","GO:0023052"],"is_obsolete":false,"name":"negative regulation of pheromone-dependent signal transduction involved in conjugation with cellular fusion","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0090029","terms_by_termid":{"GO:0090029":null}}


id: SO:0001519
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An inversion event that does not include the centromere.","direct_ancestors":[{"relation_name":"is_a","term_name":"inversion_attribute","termid":"SO:0001517"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paracentric","termid":"SO:0001519"}


id: GO:1900667
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of endocrocin biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ketone biosynthetic process","termid":"GO:0010566"},{"relation_name":"is_a","term_name":"regulation of secondary metabolite biosynthetic process","termid":"GO:1900376"},{"relation_name":"regulates","term_name":"endocrocin biosynthetic process","termid":"GO:1900602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0019748"],"is_obsolete":false,"name":"regulation of endocrocin biosynthetic process","synonyms":[{"name":"regulation of endocrocin anabolism","type":"exact"},{"name":"regulation of endocrocin biosynthesis","type":"exact"},{"name":"regulation of endocrocin formation","type":"exact"},{"name":"regulation of endocrocin synthesis","type":"exact"}],"termid":"GO:1900667"}


id: PBO:0012541
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-regulates_o_acts_on_population_of","termid":"PBO:0012541"}


id: PBO:0088651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19S proteasome regulatory subunit Rpn8","termid":"PBO:0088651"}


id: PBO:0081090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger DHHC-type palmitoyltransferase 20","termid":"PBO:0081090"}


id: PBO:0052071
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"katanin catalytic subunit A1","termid":"PBO:0052071"}


id: PBO:0062229
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily B member 2","termid":"PBO:0062229"}


id: PBO:0071585
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36a pseudogene 1","termid":"PBO:0071585"}


id: PR:Q10349
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A phosphoserine aminotransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01578","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":"phosphoserine aminotransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1F12.07","secondary_identifiers":["UniProtKB:Q10349"],"synonyms":[{"name":"PSAT (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PSAT1","type":"exact"},{"name":"phosphohydroxythreonine aminotransferase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10349"}


id: MONDO:0019699
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete slender bone dysplasia (obsolete MONDO:0019699)","secondary_identifiers":["icd11.foundation:691657602","Orphanet:93440"],"termid":"MONDO:0019699","xrefs":{"Monarch":{"xref_id":"0019699"}}}


id: FYPO:0006552
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the cytoplasm is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to cytoplasm","termid":"FYPO:0006098"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"increased protein localization to cytoplasm","synonyms":[{"name":"increased protein localisation to cytoplasm","type":"exact"},{"name":"increased protein localization to cytoplasm during mitotic cell cycle","type":"related"},{"name":"increased protein localization to cytoplasm during vegetative growth","type":"exact"}],"termid":"FYPO:0006552"}


id: GO:0021870
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a neuroblast acquires specialized structural and/or functional features of a Cajal-Retzius cell, one of a transient population of pioneering neurons in the cerebral cortex. These cells are slender bipolar cells of the developing marginal zone. One feature of these cells in mammals is that they express the Reelin gene.","definition_xrefs":["GOC:jid","GO_REF:0000021","GOC:cls","GOC:dph","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral cortex neuron differentiation","termid":"GO:0021895"}],"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":"Cajal-Retzius cell differentiation","termid":"GO:0021870"}


id: GO:0044777
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A homotetrameric protein complex that is essential for DNA replication. It supercoils the single-stranded DNA preventing DNA duplexing before the polymerase holoenzyme passes and synthesizes the complementary strand. It is also involved in DNA recombination and repair.","definition_xrefs":["UniProt:P0AGE0","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"nucleoid","termid":"GO:0009295"}],"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:0005575","GO:0032991"],"is_obsolete":false,"name":"single-stranded DNA-binding protein complex","synonyms":[{"name":"SSB complex","type":"exact"}],"termid":"GO:0044777"}


id: PBO:0070968
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L18 pseudogene 6","termid":"PBO:0070968"}


id: GO:0001573
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving ceramide oligosaccharides carrying in addition to other sugar residues, one or more sialic acid residues.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ceramide metabolic process","termid":"GO:0006672"},{"relation_name":"is_a","term_name":"glycosphingolipid metabolic process","termid":"GO:0006687"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"ganglioside metabolic process","synonyms":[{"name":"ganglioside metabolism","type":"exact"}],"termid":"GO:0001573"}


id: PBO:0059837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MTFR1 pseudogene 1","termid":"PBO:0059837"}


id: PBO:0066396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"receptor accessory protein 6","termid":"PBO:0066396"}


id: PBO:0068894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 136, pseudogene","termid":"PBO:0068894"}


id: PBO:0085541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein component of the small (40S) ribosomal subunit; interacts with Kti11p; deletion causes hypersensitivity to zymocin; homologous to mammalian ribosomal protein S7, no bacterial homolog; RPS7A has a paralog, RPS7B, that arose from the whole genome duplication","termid":"PBO:0085541"}


id: GO:0102479
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: quercetin-7-olate + UDP-D-galactose = quercetin 3-O-beta-D-galactopyranoside + UDP(3-) + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete quercetin 3-O-beta:-D-galactosyltransferase activity (obsolete GO:0102479)","termid":"GO:0102479"}


id: MONDO:0007886
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign smooth muscle neoplasm arising from the body of the uterus. It is characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.","definition_xrefs":["NCIT:C3434"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"},{"relation_name":"is_a","term_name":"fibroma","termid":"MONDO:0005167"},{"relation_name":"is_a","term_name":"benign neoplasm of corpus uteri","termid":"MONDO:0021525"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uterine corpus leiomyoma","secondary_identifiers":["DOID:13223","ICD9:218","ICD9:218.9","MESH:D047708","ONCOTREE:ULM","OMIM:150699","HP:0000131","SCTID:95315005","UMLS:C0042133","MEDGEN:21801","NCIT:C7052","EFO:0000731"],"synonyms":[{"name":"UL","type":"related"},{"name":"body of uterus fibroid","type":"exact"},{"name":"body of uterus leiomyoma","type":"exact"},{"name":"corpus uteri fibroid","type":"exact"},{"name":"corpus uteri leiomyoma","type":"exact"},{"name":"fibroid of body of uterus","type":"exact"},{"name":"fibroid of corpus uteri","type":"exact"},{"name":"fibroid of the body of uterus","type":"exact"},{"name":"fibroid of the corpus uteri","type":"exact"},{"name":"fibroid of the uterine body","type":"exact"},{"name":"fibroid of the uterine corpus","type":"exact"},{"name":"fibroid of uterine body","type":"exact"},{"name":"fibroid of uterine corpus","type":"exact"},{"name":"leiomyoma of body of uterus","type":"exact"},{"name":"leiomyoma of corpus uteri","type":"exact"},{"name":"leiomyoma of the body of uterus","type":"exact"},{"name":"leiomyoma of the corpus uteri","type":"exact"},{"name":"leiomyoma of the uterine body","type":"exact"},{"name":"leiomyoma of the uterine corpus","type":"exact"},{"name":"leiomyoma of uterine body","type":"exact"},{"name":"leiomyoma of uterine corpus","type":"exact"},{"name":"leiomyoma, uterine","type":"related"},{"name":"plexiform leiomyoma","type":"exact"},{"name":"uterine body fibroid","type":"exact"},{"name":"uterine body leiomyoma","type":"exact"},{"name":"uterine corpus fibroid","type":"exact"},{"name":"uterine corpus leiomyoma","type":"exact"},{"name":"uterine corpus leiomyomata","type":"exact"},{"name":"uterine fibroid","type":"exact"},{"name":"uterine leiomyoma","type":"related"},{"name":"uterus fibroma","type":"related"}],"termid":"MONDO:0007886","xrefs":{"Monarch":{"xref_id":"0007886"}}}


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


id: MONDO:0014373
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any nephrotic syndrome in which the cause of the disease is a mutation in the EMP2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial idiopathic steroid-resistant nephrotic syndrome","termid":"MONDO:0019006"}],"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":"nephrotic syndrome, type 10","secondary_identifiers":["UMLS:C4014507","DOID:0080386","MEDGEN:862944","OMIM:615861"],"synonyms":[{"name":"EMP2 nephrotic syndrome","type":"exact"},{"name":"NPHS10","type":"related"},{"name":"nephrotic syndrome caused by mutation in EMP2","type":"exact"},{"name":"nephrotic syndrome, type 10","type":"exact"}],"termid":"MONDO:0014373","xrefs":{"Monarch":{"xref_id":"0014373"}}}


id: GO:0099187
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of cytoskeletal structures and their associated proteins in the presynaptic cytoskeleton.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoskeleton organization","termid":"GO:0007010"},{"relation_name":"part_of","term_name":"presynapse organization","termid":"GO:0099172"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0007010","GO:0008150"],"is_obsolete":false,"name":"presynaptic cytoskeleton organization","termid":"GO:0099187"}


id: GO:0047419
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + N-acetyl-D-galactosamine 6-phosphate = acetate + D-galactosamine 6-phosphate.","definition_xrefs":["RHEA:18149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"},{"relation_name":"is_a","term_name":"deacetylase activity","termid":"GO:0019213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0019213"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0019213","GO:0016787","GO:0016810","GO:0003824"],"is_obsolete":false,"name":"N-acetylgalactosamine-6-phosphate deacetylase activity","secondary_identifiers":["MetaCyc:3.5.1.80-RXN"],"termid":"GO:0047419"}


id: GO:0030146
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of renal water excretion.","definition_xrefs":["ISBN:0198506732","GOC:mah","GOC:mtg_cardio"],"gene_count":0,"genotype_count":0,"name":"obsolete diuresis (obsolete GO:0030146)","secondary_identifiers":["Wikipedia:Diuresis"],"synonyms":[{"name":"diuresis","type":"exact"},{"name":"positive regulation of renal water excretion","type":"exact"},{"name":"renal water excretion","type":"broad"}],"termid":"GO:0030146"}


id: PBO:0086713
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; mutant has long chronological lifespan; has homology to Staphylococcus aureus nuclease; GFP-fusion protein localizes to mitochondria; is induced in response to the DNA-damaging agent MMS","termid":"PBO:0086713"}


id: MONDO:0005502
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dengue fever (DF), caused by dengue virus, is an arboviral disease characterized by an initial non-specific febrile illness that can sometimes progress to more severe forms manifesting capillary leakage and hemorrhage (dengue hemorrhagic fever, or DHF) and shock (dengue shock syndrome, or DSS).","definition_xrefs":["Orphanet:99828"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"arbovirus fever","termid":"MONDO:0018093"},{"relation_name":"is_a","term_name":"Flaviviridae infectious disease","termid":"MONDO:0005763"},{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dengue disease","secondary_identifiers":["MEDGEN:3721","SCTID:38362002","MESH:D003715","ICD9:061","EFO:0005547","UMLS:C0011311","NCIT:C34528","DOID:12205","GARD:6254","MedDRA:10012310"],"synonyms":[{"name":"DF","type":"exact"},{"name":"Dengue","type":"exact"},{"name":"Dengue fever","type":"exact"},{"name":"Dengue virus caused disease or disorder","type":"exact"},{"name":"Dengue virus disease or disorder","type":"exact"},{"name":"Dengue virus infection","type":"exact"},{"name":"Dengue virus infectious disease","type":"exact"},{"name":"Philippine hemorrhagic fever","type":"related"},{"name":"Singapore hemorrhagic fever","type":"related"},{"name":"Thai hemorrhagic fever","type":"related"},{"name":"break bone fever","type":"exact"},{"name":"breakbone fever","type":"exact"},{"name":"classic dengue","type":"exact"},{"name":"classical dengue","type":"related"},{"name":"hemorrhagic dengue","type":"related"}],"termid":"MONDO:0005502","xrefs":{"Monarch":{"xref_id":"0005502"}}}


id: GO:0071179
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of the intracellular domain of Notch1 (ICN1), the DNA-binding transcription factor RBP-Jkappa, and the transcriptional coactivator Mastermind-like-3 (MAML3); the complex is involved in transcriptional activation in response to Notch-mediated signaling.","definition_xrefs":["PMID:12370315"],"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":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"MAML3-RBP-Jkappa-ICN1 complex","synonyms":[{"name":"MAML3-RBP-Jkappa-Notch1 complex","type":"exact"}],"termid":"GO:0071179"}


id: MOD:00410
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-(N-isopropylcarboxamidomethyl)-L-cysteine.","definition_xrefs":["PubMed:11465505","OMSSA:84","PubMed:8465942","Unimod:17#C"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"},{"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-(N-isopropylcarboxamidomethyl)-L-cysteine","synonyms":[{"name":"N-isopropylcarboxamidomethyl","type":"related"},{"name":"NIPCAM","type":"related"},{"name":"nipcam","type":"exact"}],"termid":"MOD:00410"}


id: GO:2000272
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of a signaling receptor activity.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signaling receptor activity","termid":"GO:0010469"},{"relation_name":"is_a","term_name":"negative regulation of molecular function","termid":"GO:0044092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of signaling receptor activity","synonyms":[{"name":"negative regulation of receptor activity","type":"broad"},{"name":"negative regulation of signalling receptor activity","type":"exact"}],"termid":"GO:2000272"}


id: FYPO:0004953
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the presence, distribution, or morphology of the prospore membrane is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component","termid":"FYPO:0000287"},{"relation_name":"output_of","term_name":"abnormal prospore membrane formation","termid":"FYPO:0001914"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000121"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000002","FYPO:0000121","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abnormal prospore membrane","synonyms":[{"name":"abnormal forespore membrane","type":"exact"}],"termid":"FYPO:0004953"}


id: GO:0140972
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of AIM2 inflammasome complex assembly.","definition_xrefs":["PMID:33467177"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein-containing complex assembly","termid":"GO:0031333"},{"relation_name":"is_a","term_name":"regulation of AIM2 inflammasome complex assembly","termid":"GO:0140971"},{"relation_name":"negatively_regulates","term_name":"AIM2 inflammasome complex assembly","termid":"GO:0140970"},{"relation_name":"part_of","term_name":"negative regulation of inflammasome-mediated signaling pathway","termid":"GO:0141086"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"negative regulation of AIM2 inflammasome complex assembly","termid":"GO:0140972"}


id: GO:0046037
data:
  {"annotated_genes":["SJAG_00964","SJAG_04849","SJAG_06634","SJAG_04634","SJAG_01298"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[65332],"is_not":false,"summary":null,"term":"GO:0046037"},{"annotations":[63868,59782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006177"},{"annotations":[77410,103122],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032263"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving GMP, guanosine monophosphate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleotide metabolic process","termid":"GO:0009150"},{"relation_name":"is_a","term_name":"purine ribonucleoside monophosphate metabolic process","termid":"GO:0009167"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00964":null,"SJAG_01298":null,"SJAG_04634":null,"SJAG_04849":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"GMP metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"GMP metabolism","type":"exact"}],"termid":"GO:0046037","terms_by_termid":{"GO:0006177":null,"GO:0032263":null,"GO:0046037":null}}


id: PBO:0060823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nectin cell adhesion molecule 1","termid":"PBO:0060823"}


id: MONDO:0014474
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive limb-girdle muscular dystrophy in which the cause of the disease is a mutation in the ISPD gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy, type C","termid":"MONDO:0000173"},{"relation_name":"is_a","term_name":"autosomal recessive limb-girdle muscular dystrophy","termid":"MONDO:0015152"},{"relation_name":"is_a","term_name":"myopathy caused by variation in CRPPA","termid":"MONDO:0100530"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0002320","MONDO:0005336","MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"autosomal recessive limb-girdle muscular dystrophy type 2U","secondary_identifiers":["OMIM:616052","GARD:17519","Orphanet:352479","UMLS:C5190987","MEDGEN:1683417","DOID:0110295"],"synonyms":[{"name":"ISPD autosomal recessive limb-girdle muscular dystrophy","type":"exact"},{"name":"LGMD2U","type":"exact"},{"name":"MDDGC7","type":"exact"},{"name":"autosomal recessive limb-girdle muscular dystrophy caused by mutation in ISPD","type":"exact"},{"name":"autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency","type":"exact"},{"name":"muscular dystrophy limb-girdle type 2U","type":"exact"},{"name":"muscular dystrophy, limb-girdle, type 2U","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy (limb-girdle) type C7","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7","type":"related"}],"termid":"MONDO:0014474","xrefs":{"Monarch":{"xref_id":"0014474"}}}


id: MONDO:0006926
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with bacteria of the genus haemophilus.","definition_xrefs":["MESH:D006192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial infectious disease","termid":"MONDO:0005113"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"haemophilus infectious disease","secondary_identifiers":["EFO:1001127","NCIT:C34654","SCTID:41659003"],"synonyms":[{"name":"Haemophilus caused disease or disorder","type":"exact"},{"name":"Haemophilus disease or disorder","type":"exact"},{"name":"Haemophilus infection","type":"related"},{"name":"Haemophilus infectious disease","type":"exact"},{"name":"Hemophilus infection","type":"related"},{"name":"Hemophilus infections","type":"related"},{"name":"haemophilus infectious disease","type":"exact"},{"name":"infection, Haemophilus","type":"related"},{"name":"infection, Hemophilus","type":"related"},{"name":"infections, Haemophilus","type":"related"},{"name":"infections, Hemophilus","type":"related"}],"termid":"MONDO:0006926","xrefs":{"Monarch":{"xref_id":"0006926"}}}


id: GO:0046249
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of alpha-pinene, a monoterpene that may be a significant factor affecting bacterial activities in nature.","definition_xrefs":["PMID:14736461","PMID:29414896","PMID:10192895"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-pinene metabolic process","termid":"GO:0018867"},{"relation_name":"is_a","term_name":"pinene catabolic process","termid":"GO:0033074"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"alpha-pinene catabolic process","synonyms":[{"name":"alpha-pinene breakdown","type":"exact"},{"name":"alpha-pinene catabolism","type":"exact"},{"name":"alpha-pinene degradation","type":"exact"}],"termid":"GO:0046249"}


id: PBO:0076017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine kinase 11","termid":"PBO:0076017"}


id: PBO:0004404
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.3.1.158","termid":"PBO:0004404"}


id: PBO:0027153
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_vacuolar_histidine_level","termid":"PBO:0027153"}


id: PBO:0053695
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 895","termid":"PBO:0053695"}


id: FYPO:0001275
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the binding of one protein to another occurs to a lower extent than normal during a cellular response to hypoxia. The relevant proteins may include the one encoded by the mutated gene, or may both be encoded by different genes.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein-protein interaction","termid":"FYPO:0001645"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000707","FYPO:0001985","FYPO:0000702"],"is_obsolete":false,"name":"decreased protein-protein interaction during cellular response to hypoxia","synonyms":[{"name":"decreased protein binding during cellular response to hypoxia","type":"exact"},{"name":"decreased protein-protein interaction in response to hypoxia","type":"related"},{"name":"reduced protein-protein interaction during cellular response to hypoxia","type":"exact"}],"termid":"FYPO:0001275"}


id: GO:0036479
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of peroxidase.","definition_xrefs":["GOC:bf","GOC:PARL"],"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:0098772"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0004857"}],"interesting_parent_ids":["GO:0030234","GO:0140678","GO:0004857","GO:0098772","GO:0003674"],"is_obsolete":false,"name":"peroxidase inhibitor activity","termid":"GO:0036479"}


id: MONDO:0005302
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A mental disorder characterized by inattention, easy distraction, careless mistakes and avoidance of tasks that require sustained mental focus. These behaviors can lead to maladaptive consequences in the affected individual's life.","definition_xrefs":["NCIT:C35092"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"oppositional defiant disorder","termid":"MONDO:0000495"},{"relation_name":"excluded_subClassOf","term_name":"specific developmental disorder","termid":"MONDO:0000592"},{"relation_name":"is_a","term_name":"attention deficit-hyperactivity disorder","termid":"MONDO:0007743"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"attention deficit hyperactivity disorder, inattentive type","secondary_identifiers":["SCTID:406506008","ICD9:314.9","ICD9:314.8","UMLS:C0339002","ICD9:314.01","DOID:1094","MEDGEN:473060","MESH:D001289"],"synonyms":[{"name":"ADD","type":"exact"},{"name":"ADHD","type":"exact"},{"name":"attention deficit disorder","type":"exact"},{"name":"attention deficit hyperactivity disorder, inattentive/distractible type","type":"exact"},{"name":"attention deficit hyperactivity disorder, predominantly inattentive type","type":"exact"},{"name":"hyperkinetic disorder","type":"exact"}],"termid":"MONDO:0005302","xrefs":{"Monarch":{"xref_id":"0005302"}}}


id: PBO:0113221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA-binding protein; interacts with the UBA domain of mRNA export factor Mex67p; participates in the export of Msn2/4 stress-dependent mRNAs; partially redundant function with paralog PES4 in the steady-state expression, translational timing and localization of a subset of Ndt80-dependent mRNAs that are protected until translated near the end of meiosis II; redundant role with PES4 in sporulation; shuttles between the nucleus and cytoplasm, localizes to stress granules and the prospore membrane","termid":"PBO:0113221"}


id: GO:0034662
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains ezrin, Na+/H+ exchanger regulatory factor (NHERF, also called EBP50), and two copies of the cystic fibrosis transmembrane conductance regulator (CFTR). The CFTR molecules interact with NHERF via their cytoplasmic tail domains; the complex is thought to link the CFTR channel to the actin cytoskeleton and contribute to the regulation of channel activity.","definition_xrefs":["PMID:16926444","PMID:16129695","PMID:16798722"],"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":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005886","GO:0032991"],"is_obsolete":false,"name":"CFTR-NHERF-ezrin complex","termid":"GO:0034662"}


id: GO:0097291
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A renal system process in which phosphate ions are taken up from the collecting ducts and proximal and distal loops of the nephron. In non-mammalian species, absorption may occur in related structures.","definition_xrefs":["GOC:lb","PMID:22506049","PMID:18784102"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal absorption","termid":"GO:0070293"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"renal phosphate ion absorption","synonyms":[{"name":"renal phosphate absorption","type":"exact"}],"termid":"GO:0097291"}


id: GO:1903056
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of melanosome organization.","definition_xrefs":["PMID:24769727","GO_REF:0000058","GOC:BHF","GOC:rl","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of organelle organization","termid":"GO:0033043"},{"relation_name":"regulates","term_name":"melanosome organization","termid":"GO:0032438"}],"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 melanosome organization","synonyms":[{"name":"regulation of melanosome organisation","type":"exact"},{"name":"regulation of melanosome organization and biogenesis","type":"related"}],"termid":"GO:1903056"}


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


id: PBO:0043430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cornichon family AMPA receptor auxiliary protein 2","termid":"PBO:0043430"}


id: GO:0019680
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of L-methylmalonyl-CoA, the L-enantiomer of 2-carboxypropanoyl-CoA.","definition_xrefs":["GOC:mah","GOC:ai","GOC:jsg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-methylmalonyl-CoA metabolic process","termid":"GO:0046491"},{"relation_name":"is_a","term_name":"acyl-CoA biosynthetic process","termid":"GO:0071616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150","GO:0006790"],"is_obsolete":false,"name":"L-methylmalonyl-CoA biosynthetic process","secondary_identifiers":["MetaCyc:PWY0-43"],"synonyms":[{"name":"L-methylmalonyl-CoA anabolism","type":"exact"},{"name":"L-methylmalonyl-CoA biosynthesis","type":"exact"},{"name":"L-methylmalonyl-CoA formation","type":"exact"},{"name":"L-methylmalonyl-CoA synthesis","type":"exact"}],"termid":"GO:0019680"}


id: GO:0004956
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with prostaglandin D (PGD(2)) to initiate a change in cell activity.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostaglandin receptor activity","termid":"GO:0004955"}],"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":"prostaglandin D receptor activity","synonyms":[{"name":"PGD receptor activity","type":"related"},{"name":"PGD(2) receptor activity","type":"exact"}],"termid":"GO:0004956"}


id: PBO:0069814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1100, pseudogene","termid":"PBO:0069814"}


id: MONDO:0009989
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete enhanced S-cone syndrome (obsolete MONDO:0009989)","termid":"MONDO:0009989","xrefs":{"Monarch":{"xref_id":"0009989"}}}


id: MONDO:0009604
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"methemoglobin reductase deficiency","secondary_identifiers":["UMLS:C0472786","MESH:C563171","GARD:3909","MEDGEN:501116","OMIM:250700","SCTID:234397008"],"synonyms":[{"name":"NADPH-dependent methemoglobin reductase deficiency","type":"related"},{"name":"TPNH-methemoglobin reductase deficiency","type":"related"},{"name":"methemoglobin reductase deficiency","type":"exact"}],"termid":"MONDO:0009604","xrefs":{"Monarch":{"xref_id":"0009604"}}}


id: GO:0032096
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of a response to a food stimulus.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to food","termid":"GO:0032095"},{"relation_name":"is_a","term_name":"negative regulation of response to nutrient levels","termid":"GO:0032108"},{"relation_name":"negatively_regulates","term_name":"response to food","termid":"GO:0032094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of response to food","synonyms":[{"name":"down regulation of response to food","type":"exact"},{"name":"down-regulation of response to food","type":"exact"},{"name":"downregulation of response to food","type":"exact"},{"name":"inhibition of response to food","type":"narrow"}],"termid":"GO:0032096"}


id: PBO:0044877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DENN domain containing 5B","termid":"PBO:0044877"}


id: PBO:0081153
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZFP91 pseudogene 1","termid":"PBO:0081153"}


id: GO:0120076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of endocardial cushion cell differentiation.","definition_xrefs":["GOC:rph","GOC:BHF","GOC:BHF_miRNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of endocardial cushion cell differentiation","termid":"GO:0120074"},{"relation_name":"is_a","term_name":"negative regulation of cardiocyte differentiation","termid":"GO:1905208"},{"relation_name":"negatively_regulates","term_name":"endocardial cushion cell differentiation","termid":"GO:0061443"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of endocardial cushion cell differentiation","termid":"GO:0120076"}


id: PBO:0078263
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 2-1","termid":"PBO:0078263"}


id: PBO:0084204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Homeobox-domain protein; with Mcm1p, represses a-specific genes in haploids; acts with A1p to repress transcription of haploid-specific genes in diploids; one of two genes encoded by the MATalpha mating type cassette","termid":"PBO:0084204"}


id: GO:1904535
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of telomeric loop disassembly.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:22579284","GOC:BHF_telomere","GOC:nc","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of telomere maintenance","termid":"GO:0032206"},{"relation_name":"is_a","term_name":"regulation of telomeric loop disassembly","termid":"GO:1904533"},{"relation_name":"positively_regulates","term_name":"telomeric loop disassembly","termid":"GO:0090657"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0032200"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"positively_regulates","termid":"GO:0006259"},{"rel_name":"positively_regulates","termid":"GO:0032200"}],"interesting_parent_ids":["GO:0032200","GO:0008150","GO:0006259"],"is_obsolete":false,"name":"positive regulation of telomeric loop disassembly","synonyms":[{"name":"activation of T loop disassembly","type":"narrow"},{"name":"activation of telomeric loop disassembly","type":"narrow"},{"name":"positive regulation of T loop disassembly","type":"exact"},{"name":"up regulation of T loop disassembly","type":"exact"},{"name":"up regulation of telomeric loop disassembly","type":"exact"},{"name":"up-regulation of T loop disassembly","type":"exact"},{"name":"up-regulation of telomeric loop disassembly","type":"exact"},{"name":"upregulation of T loop disassembly","type":"exact"},{"name":"upregulation of telomeric loop disassembly","type":"exact"}],"termid":"GO:1904535"}


id: PBO:0080912
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YWHAQ pseudogene 1","termid":"PBO:0080912"}


id: PBO:0109381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed transcript, Y-linked 12","termid":"PBO:0109381"}


id: GO:1901326
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 tetracycline stimulus.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to alcohol","termid":"GO:0097305"},{"relation_name":"is_a","term_name":"response to ketone","termid":"GO:1901654"}],"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 tetracycline","termid":"GO:1901326"}


id: PBO:0066257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBMX2 pseudogene 5","termid":"PBO:0066257"}


id: GO:0044074
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which a symbiont organism stops, prevents, or reduces the frequency, rate or extent of translation, the chemical reactions and pathways resulting in the formation of a protein, in its host organism.","definition_xrefs":["MITRE:tk"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation by symbiont of host translation (obsolete GO:0044074)","synonyms":[{"name":"negative regulation of host translation by symbiont","type":"exact"}],"termid":"GO:0044074"}


id: MONDO:0006224
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic polyp that arises from the stomach and is characterized by the presence of connective tissue stroma overgrowth and cystic formations.","definition_xrefs":["NCIT:C4373"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastrointestinal hamartoma","termid":"MONDO:0006231"},{"relation_name":"is_a","term_name":"gastric neoplasm","termid":"MONDO:0021085"}],"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":"gastric hamartomatous polyp","secondary_identifiers":["MEDGEN:90961","EFO:1000271","SCTID:235685007","UMLS:C0341225"],"synonyms":[{"name":"gastric hamartomatous polyp","type":"exact"},{"name":"hamartoma of stomach","type":"exact"},{"name":"hamartoma of the stomach","type":"exact"},{"name":"stomach hamartoma (disease)","type":"exact"}],"termid":"MONDO:0006224","xrefs":{"Monarch":{"xref_id":"0006224"}}}


id: MONDO:0100110
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"},{"relation_name":"is_a","term_name":"adenoviridae infectious disease","termid":"MONDO:0043479"},{"relation_name":"is_a","term_name":"urinary tract infection","termid":"MONDO:0100338"}],"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":"adenovirus renal infection","termid":"MONDO:0100110","xrefs":{"Monarch":{"xref_id":"0100110"}}}


id: PBO:0086581
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; deletion mutant is fluconazole resistant and has long chronological lifespan","termid":"PBO:0086581"}


id: PR:O13791
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- slt1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13791"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein slt1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17G6.13","synonyms":[{"name":"Spom972h-slt1","type":"exact"}],"termid":"PR:O13791"}


id: MONDO:0010237
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked intellectual disability-plagiocephaly syndrome is characterized by severe intellectual deficit, brachycephaly, plagiocephaly, prominent forehead and coarse facial features. It has been described in two males from one family. Two females belonging to the same family displayed moderate intellectual deficit but no craniofacial dysmorphism.","definition_xrefs":["Orphanet:2898"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"},{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0002320"],"is_obsolete":false,"name":"X-linked intellectual disability-plagiocephaly syndrome","secondary_identifiers":["MESH:C537512","OMIM:300064","SCTID:719812008","GARD:2765","UMLS:C2931516","MEDGEN:419824"],"synonyms":[{"name":"Hyde Forster McCarthy Berry syndrome","type":"related"},{"name":"Hyde Forster-McCarthy-Berry syndrome","type":"exact"},{"name":"intellectual disability, X-linked Hyde-Forster type","type":"related"},{"name":"intellectual disability, X-linked, Hyde-Forster type","type":"related"},{"name":"intellectual disability, X-linked, with craniofacial dysmorphism","type":"related"},{"name":"intellectual disability, plagiocephaly, brachycephaly, prominent forehead, and coarse facial features","type":"related"},{"name":"mental retardation, X-linked Hyde-Forster type","type":"related"},{"name":"mental retardation, X-linked, Hyde-Forster type","type":"related"},{"name":"mental retardation, X-linked, with craniofacial dysmorphism","type":"related"},{"name":"mental retardation, plagiocephaly, brachycephaly, prominent forehead, and coarse facial features","type":"related"},{"name":"plagiocephaly and X-linked intellectual disability","type":"related"},{"name":"plagiocephaly and X-linked mental retardation","type":"related"}],"termid":"MONDO:0010237","xrefs":{"Monarch":{"xref_id":"0010237"}}}


id: PBO:0044055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystatin SA","termid":"PBO:0044055"}


id: PBO:0053385
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 312","termid":"PBO:0053385"}


id: MONDO:0019686
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete type 2 collagen-related bone disorder (obsolete MONDO:0019686)","termid":"MONDO:0019686","xrefs":{"Monarch":{"xref_id":"0019686"}}}


id: PBO:0039985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor like GTPase 6","termid":"PBO:0039985"}


id: MONDO:0018808
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"biliary tract disorder","termid":"MONDO:0004868"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"Caroli syndrome","secondary_identifiers":["DOID:0081394","GARD:21976","NANDO:2200934","MEDGEN:1814547","UMLS:C5700203","Orphanet:480520"],"termid":"MONDO:0018808","xrefs":{"Monarch":{"xref_id":"0018808"}}}


id: PBO:0027514
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_localization_to_nucleolus_during_mitosis","termid":"PBO:0027514"}


id: GO:0008923
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-lysine + H+ = cadaverine + CO2.","definition_xrefs":["RHEA:22352"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"lysine decarboxylase activity","secondary_identifiers":["KEGG_REACTION:R00462","MetaCyc:LYSDECARBOX-RXN","EC:4.1.1.18"],"synonyms":[{"name":"L-lysine carboxy-lyase activity","type":"related"}],"termid":"GO:0008923"}


id: PBO:0081739
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 670","termid":"PBO:0081739"}


id: GO:0140331
data:
  {"annotated_genes":["SJAG_00669","SJAG_02516","SJAG_03050"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[60410,63629,70236],"is_not":false,"summary":null,"term":"GO:0140331"}]},"cv_name":"biological_process","definition":"The movement of an aminophospholipid molecule from one leaflet of a membrane bilayer to the opposite leaflet.","definition_xrefs":["GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminophospholipid transport","termid":"GO:0015917"},{"relation_name":"is_a","term_name":"phospholipid translocation","termid":"GO:0045332"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00669":null,"SJAG_02516":null,"SJAG_03050":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150","GO:0061024"],"is_obsolete":false,"name":"aminophospholipid translocation","references_by_uniquename":{"GO_REF:0000108":null},"termid":"GO:0140331","terms_by_termid":{"GO:0140331":null}}


id: GO:1905027
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of membrane depolarization during AV node cell action potential.","definition_xrefs":["GOC:TermGenie","GOC:BHF","GOC:rph","GO_REF:0000058","PMID:19726871","GOC:BHF_miRNA","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of AV node cell action potential","termid":"GO:0098904"},{"relation_name":"is_a","term_name":"regulation of membrane depolarization during cardiac muscle cell action potential","termid":"GO:1900825"},{"relation_name":"regulates","term_name":"membrane depolarization during AV node cell action potential","termid":"GO:0086045"}],"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 membrane depolarization during AV node cell action potential","synonyms":[{"name":"regulation of membrane depolarization during AV node cardiac muscle cell action potential","type":"exact"},{"name":"regulation of membrane depolarization during atrioventricular node cardiac muscle cell action potential","type":"exact"}],"termid":"GO:1905027"}


id: PBO:0000946
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expression induced by UV","termid":"PBO:0000946"}


id: PBO:0080877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"yippee like 3","termid":"PBO:0080877"}


id: GO:0009964
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of flavonoids.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biosynthetic process","termid":"GO:0009890"},{"relation_name":"is_a","term_name":"regulation of flavonoid biosynthetic process","termid":"GO:0009962"},{"relation_name":"negatively_regulates","term_name":"flavonoid biosynthetic process","termid":"GO:0009813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of flavonoid biosynthetic process","synonyms":[{"name":"down regulation of flavonoid biosynthetic process","type":"exact"},{"name":"down-regulation of flavonoid biosynthetic process","type":"exact"},{"name":"downregulation of flavonoid biosynthetic process","type":"exact"},{"name":"inhibition of flavonoid biosynthetic process","type":"narrow"},{"name":"negative regulation of flavonoid anabolism","type":"exact"},{"name":"negative regulation of flavonoid biosynthesis","type":"exact"},{"name":"negative regulation of flavonoid formation","type":"exact"},{"name":"negative regulation of flavonoid synthesis","type":"exact"}],"termid":"GO:0009964"}


id: GO:0047963
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: choloyl-CoA + glycine = CoA + glycocholate.","definition_xrefs":["EC:2.3.1.65","MetaCyc:GLYCINE-N-CHOLOYLTRANSFERASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"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:0003824","GO:0003674","GO:0016746","GO:0016740"],"is_obsolete":false,"name":"glycine N-choloyltransferase activity","secondary_identifiers":["RHEA:14001"],"synonyms":[{"name":"BACAT activity","type":"related"},{"name":"BAT activity","type":"related"},{"name":"amino acid N-choloyltransferase activity","type":"related"},{"name":"bile acid-CoA:amino acid N-acyltransferase activity","type":"related"},{"name":"choloyl-CoA:glycine N-choloyltransferase activity","type":"related"},{"name":"cholyl-CoA glycine-taurine N-acyltransferase activity","type":"related"},{"name":"cholyl-CoA:taurine N-acyltransferase activity","type":"related"},{"name":"glycine--taurine N-acyltransferase activity","type":"related"}],"termid":"GO:0047963"}


id: PBO:0040069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrestin 3","termid":"PBO:0040069"}


id: PBO:0040909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMS1 pseudogene 13","termid":"PBO:0040909"}


id: GO:0097327
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an antineoplastic agent stimulus. An antineoplastic agent is a substance that inhibits or prevents the proliferation of neoplasms.","definition_xrefs":["GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to antineoplastic agent","termid":"GO:0097327"}


id: PBO:0085338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphoglucomutase, minor isoform; catalyzes the conversion from glucose-1-phosphate to glucose-6-phosphate, which is a key step in hexose metabolism; PGM1 has a paralog, PGM2, that arose from the whole genome duplication","termid":"PBO:0085338"}


id: PBO:0054160
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 1527","termid":"PBO:0054160"}


id: PBO:0066150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBBP4 pseudogene 6","termid":"PBO:0066150"}


id: GO:0018876
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving benzonitrile. Benzonitrile is used as a solvent and chemical intermediate in the pharmaceutical, dyestuffs and rubber industries. It is highly toxic and harmful in contact with skin.","definition_xrefs":["UM-BBD_pathwayID:bzn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"},{"relation_name":"is_a","term_name":"nitrile metabolic process","termid":"GO:0050898"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"benzonitrile metabolic process","synonyms":[{"name":"benzonitrile metabolism","type":"exact"}],"termid":"GO:0018876"}


id: PBO:0036116
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_rate_of_actin_filament-based_movement","termid":"PBO:0036116"}


id: PBO:0042350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD84 molecule","termid":"PBO:0042350"}


id: PBO:0071694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L38","termid":"PBO:0071694"}


id: PBO:0068985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 229, pseudogene","termid":"PBO:0068985"}


id: GO:0003209
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the cardiac atrium is generated and organized. A cardiac atrium receives blood from a vein and pumps it to a cardiac ventricle.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac chamber morphogenesis","termid":"GO:0003206"},{"relation_name":"part_of","term_name":"cardiac atrium development","termid":"GO:0003230"}],"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":"cardiac atrium morphogenesis","termid":"GO:0003209"}


id: PBO:0027052
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-long_astral_microtubules_during_mitotic_anaphase_A","termid":"PBO:0027052"}


id: GO:0009581
data:
  {"annotated_genes":["SJAG_02258"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110411],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050982"}]},"cv_name":"biological_process","definition":"The series of events in which an external stimulus is received by a cell and converted into a molecular signal.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to external stimulus","termid":"GO:0009605"},{"relation_name":"is_a","term_name":"detection of stimulus","termid":"GO:0051606"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02258":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of external stimulus","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"perception of external stimulus","type":"related"}],"termid":"GO:0009581","terms_by_termid":{"GO:0050982":null}}


id: MONDO:1011659
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system disorder, non-human animal","termid":"MONDO:1011311"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gastric dilatation volvulus syndrome, non-human animal","secondary_identifiers":["OMIA:000404"],"termid":"MONDO:1011659","xrefs":{"Monarch":{"xref_id":"1011659"}}}


id: FYPO:0003463
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which alpha,alpha-trehalase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished catalytic activity","termid":"FYPO:0000664"},{"relation_name":"is_a","term_name":"abnormal alpha,alpha-trehalase activity","termid":"FYPO:0001479"}],"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:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000661","FYPO:0001985","FYPO:0000654","FYPO:0000652"],"is_obsolete":false,"name":"abolished alpha,alpha-trehalase activity","synonyms":[{"name":"abolished neutral trehalase activity","type":"exact"},{"name":"abolished trehalase activity","type":"broad"},{"name":"alpha,alpha-trehalase activity abolished","type":"exact"}],"termid":"FYPO:0003463"}


id: MONDO:0014466
data:
  {"annotated_genes":["SJAG_02791"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88723],"is_not":false,"summary":null,"term":"MONDO:0014466"}]},"cv_name":"mondo","definition":"Any Neu-Laxova syndrome in which the cause of the disease is a mutation in the PSAT1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Neu-Laxova syndrome","termid":"MONDO:0000179"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02791":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736","MONDO:0002320"],"is_obsolete":false,"name":"Neu-Laxova syndrome 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080075","MEDGEN:863456","UMLS:C4015019","Orphanet:583602","GARD:22335","OMIM:616038"],"synonyms":[{"name":"NEU-Laxova syndrome 2","type":"related"},{"name":"NLS2","type":"related"},{"name":"Neu-Laxova syndrome 2","type":"exact"},{"name":"Neu-Laxova syndrome caused by mutation in PSAT1","type":"exact"},{"name":"Neu-Laxova syndrome due to phosphoserine aminotransferase deficiency","type":"exact"},{"name":"Neu-Laxova syndrome type 2","type":"exact"},{"name":"PSAT1 Neu-Laxova syndrome","type":"exact"},{"name":"phosphoserine aminotransferase deficiency, prenatal form","type":"exact"}],"termid":"MONDO:0014466","terms_by_termid":{"MONDO:0014466":null},"xrefs":{"Monarch":{"xref_id":"0014466"}}}


id: MONDO:0009000
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial reactive perforating collagenosis is a very rare genetic skin disease characterized by transepidermal elimination of collagen fibers presenting as recurrent spontaneously involuting keratotic papules or nodules.","definition_xrefs":["Orphanet:79147"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermis disorder","termid":"MONDO:0021154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"familial reactive perforating collagenosis","secondary_identifiers":["icd11.foundation:563155724","MEDGEN:347504","OMIM:216700","GARD:13331","MESH:C565687","UMLS:C1857624"],"synonyms":[{"name":"RPC","type":"related"},{"name":"collagenosis, familial reactive perforating","type":"related"},{"name":"inherited reactive perforating collagenosis","type":"related"}],"termid":"MONDO:0009000","xrefs":{"Monarch":{"xref_id":"0009000"}}}


id: GO:1904104
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of convergent extension involved in gastrulation.","definition_xrefs":["GO_REF:0000058","GOC:dph","PMID:24892953","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of convergent extension involved in gastrulation","termid":"GO:1904103"},{"relation_name":"is_a","term_name":"negative regulation of morphogenesis of an epithelium","termid":"GO:1905331"},{"relation_name":"negatively_regulates","term_name":"convergent extension involved in gastrulation","termid":"GO:0060027"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of convergent extension involved in gastrulation","synonyms":[{"name":"down regulation of convergent extension involved in gastrulation","type":"exact"},{"name":"down-regulation of convergent extension involved in gastrulation","type":"exact"},{"name":"downregulation of convergent extension involved in gastrulation","type":"exact"},{"name":"inhibition of convergent extension involved in gastrulation","type":"narrow"}],"termid":"GO:1904104"}


id: SO:0002334
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A stop codon with the DNA sequence TAA.","direct_ancestors":[{"relation_name":"is_a","term_name":"stop_codon","termid":"SO:0000319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ochre_stop_codon","synonyms":[{"name":"Ochre stop codon","type":"exact"}],"termid":"SO:0002334"}


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


id: MONDO:0015566
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"2q24 microdeletion syndrome is a chromosomal anomaly consisting of a partial long arm deletion of chromosome 2 and characterized clinically by a wide range of manifestations (depending on the specific region deleted) which can include seizures, microcephaly, dysmorphic features, cleft palate, eye abnormalities (coloboma, cataract and microphthalmia), growth retardation, failure to thrive, heart defects, limb anomalies, developmental delay and autism.","definition_xrefs":["Orphanet:1617"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete chromosomal anomaly with cataract (obsolete MONDO:0020226)","termid":"MONDO:0020226"},{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 2","termid":"MONDO:0016901"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2q24 microdeletion syndrome","secondary_identifiers":["SCTID:719658006","UMLS:C2931816","GARD:3746","MESH:C538316","MEDGEN:419168"],"synonyms":[{"name":"2q24 deletion","type":"related"},{"name":"Del(2)(q24)","type":"exact"},{"name":"chromosome 2q24 microdeletion syndrome","type":"related"},{"name":"deletion 2q24","type":"related"},{"name":"monosomy 2q24","type":"exact"}],"termid":"MONDO:0015566","xrefs":{"Monarch":{"xref_id":"0015566"}}}


id: GO:0002523
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The movement of a leukocyte within or between different tissues and organs of the body contributing to an inflammatory response.","definition_xrefs":["PMID:7507411","GOC:add","ISBN:0781735149","PMID:14680625","PMID:14708592","PMID:8600538"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte migration","termid":"GO:0050900"},{"relation_name":"part_of","term_name":"inflammatory response","termid":"GO:0006954"}],"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":"leukocyte migration involved in inflammatory response","synonyms":[{"name":"immune cell migration during inflammatory response","type":"related"},{"name":"immune cell trafficking during inflammatory response","type":"related"},{"name":"leucocyte migration during inflammatory response","type":"related"},{"name":"leucocyte trafficking during inflammatory response","type":"related"},{"name":"leukocyte migration during inflammatory response","type":"related"},{"name":"leukocyte trafficking during inflammatory response","type":"related"}],"termid":"GO:0002523"}


id: MONDO:0700000
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the ALG9 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant polycystic kidney disease","termid":"MONDO:0004691"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0000426"],"is_obsolete":false,"name":"ALG9-associated autosomal dominant polycystic kidney disease","synonyms":[{"name":"ALG9 autosomal dominant polycystic kidney disease","type":"exact"},{"name":"ALG9 related autosomal dominant polycystic kidney disease","type":"exact"},{"name":"ALG9-associated ADPKD","type":"exact"},{"name":"ALG9-associated autosomal dominant polycystic kidney disease","type":"exact"},{"name":"Autosomal Dominant Polycystic Kidney Disease - ALG9","type":"exact"},{"name":"autosomal dominant polycystic kidney disease caused by mutation in ALG9","type":"exact"}],"termid":"MONDO:0700000","xrefs":{"Monarch":{"xref_id":"0700000"}}}


id: GO:2000560
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of CD24 biosynthetic process.","definition_xrefs":["GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of CD24 production (obsolete GO:2000560)","synonyms":[{"name":"positive regulation of CD24 anabolism","type":"exact"},{"name":"positive regulation of CD24 biosynthesis","type":"exact"},{"name":"positive regulation of CD24 biosynthetic process","type":"exact"},{"name":"positive regulation of CD24 formation","type":"exact"},{"name":"positive regulation of CD24 synthesis","type":"exact"}],"termid":"GO:2000560"}


id: PBO:0043530
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cordon-bleu WH2 repeat protein like 1","termid":"PBO:0043530"}


id: PBO:0000757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein, human WDR55 family, involved in ribosome biogenesis (predicted)","termid":"PBO:0000757"}


id: MONDO:0012521
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Herpes simplex virus encephalitis (HSE) is caused by the infection of the central nervous system by Herpes simplex virus (HSV) that could have a devastating clinical course and a potentially fatal outcome particularly with delay or lack of treatment. HSV often involves the frontal and temporal lobes, usually asymmetrically, resulting in personality changes, cognitive impairment, aphasia, seizures, and focal weakness.","definition_xrefs":["Orphanet:1930"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete infectious disease with epilepsy (obsolete MONDO:0015659)","termid":"MONDO:0015659"},{"relation_name":"excluded_subClassOf","term_name":"obsolete hereditary predisposition to infections (obsolete MONDO:0015979)","termid":"MONDO:0015979"},{"relation_name":"excluded_subClassOf","term_name":"obsolete infectious disease with dementia (obsolete MONDO:0020141)","termid":"MONDO:0020141"},{"relation_name":"is_a","term_name":"herpes simplex infectious disease","termid":"MONDO:0004609"},{"relation_name":"is_a","term_name":"viral encephalitis","termid":"MONDO:0006009"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"herpes simplex encephalitis","secondary_identifiers":["ICD10EXP:B00.4+","icd11.foundation:320069644","NANDO:2200772","NORD:1087","GARD:6649","NCIT:C84762","ICD10EXP:G05.1*","MEDGEN:75794","MESH:D020803","UMLS:C0276226"],"synonyms":[{"name":"Encephalitis, Herpes Simplex","type":"exact"},{"name":"HSE","type":"exact"},{"name":"HSV encephalitis","type":"exact"},{"name":"HSVE","type":"exact"},{"name":"Herpes simplex meningo-encephalitis","type":"exact"},{"name":"Herpes simplex neuroinvasion","type":"exact"},{"name":"Herpes simplex virus encephalitis","type":"related"},{"name":"Simplexvirus caused infectious encephalitis","type":"exact"},{"name":"Simplexvirus infectious encephalitis","type":"exact"},{"name":"herpetic encephalitis","type":"exact"}],"termid":"MONDO:0012521","xrefs":{"Monarch":{"xref_id":"0012521"}}}


id: FYPO:0006475
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a short mitotic spindle assembles, and may begin elongation, but does not elongate normally or completely, and eventually collapses. Upon collapse the spindle may break or shrink.","definition_xrefs":["PMID:15147872","PomBase:mah","PMID:25375240","PMID:23885124","PMID:27697865"],"direct_ancestors":[{"relation_name":"is_a","term_name":"unstable mitotic spindle","termid":"FYPO:0006048"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0000002","FYPO:0001320","FYPO:0000054","FYPO:0000641","FYPO:0001985","FYPO:0000337","FYPO:0005447"],"is_obsolete":false,"name":"mitotic spindle collapse","synonyms":[{"name":"broken mitotic spindle","type":"related"},{"name":"mitotic spindle breakage","type":"exact"},{"name":"mitotic spindle collapse during vegetative growth","type":"exact"},{"name":"spindle collapse during mitosis","type":"exact"},{"name":"spindle collapse during mitotic cell cycle","type":"related"}],"termid":"FYPO:0006475"}


id: GO:0160137
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: uridine(2457) in 23S rRNA = pseudouridine(2457) in 23S rRNA.","definition_xrefs":["EC:5.4.99.20","RHEA:38871"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA pseudouridine synthase activity","termid":"GO:0120159"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"}],"interesting_parent_ids":["GO:0003674","GO:0140098","GO:0016853","GO:0003824"],"is_obsolete":false,"name":"23S rRNA pseudouridine(2457) synthase activity","termid":"GO:0160137"}


id: GO:0071770
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components, including (phenyl)phthiocerol, phthiodiolone, phthiotriol dimycocerosate and diphthioceranate, to form the DIM/DIP layer of the Actinobacterium-type cell wall.","definition_xrefs":["GOC:mah","PMID:3149973","PMID:15653820","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"part_of","term_name":"Actinobacterium-type cell wall biogenesis","termid":"GO:0071766"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0071554"],"is_obsolete":false,"name":"DIM/DIP cell wall layer assembly","synonyms":[{"name":"DIM cell wall layer assembly","type":"exact"},{"name":"DIM/DIP cell wall layer biogenesis","type":"related"},{"name":"PDIM cell wall layer assembly","type":"exact"}],"termid":"GO:0071770"}


id: PBO:0040529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beta-2-microglobulin regulator","termid":"PBO:0040529"}


id: GO:0015863
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of xanthosine, xanthine riboside, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside transport","termid":"GO:0015858"}],"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:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"xanthosine transport","termid":"GO:0015863"}


id: PBO:0084284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Integral membrane protein required for ER to Golgi transport; localized to the Golgi, the ER, and COPII vesicles; interacts with Yip1p and Yif1p","termid":"PBO:0084284"}


id: PBO:0060770
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B5 pseudogene 1","termid":"PBO:0060770"}


id: GO:0071940
data:
  {"annotated_genes":["SJAG_04868","SJAG_00974","SJAG_03013","SJAG_01321"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90072,90566,93654,92118],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030476"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a fungal-type cell wall.","definition_xrefs":["GOC:vw","GOC:mah","PMID:19646873"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fungal-type cell wall organization","termid":"GO:0031505"},{"relation_name":"is_a","term_name":"cell wall assembly","termid":"GO:0070726"},{"relation_name":"part_of","term_name":"fungal-type cell wall biogenesis","termid":"GO:0009272"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00974":null,"SJAG_01321":null,"SJAG_03013":null,"SJAG_04868":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0008150","GO:0071554","GO:0044085"],"is_obsolete":false,"name":"fungal-type cell wall assembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"fungal-type cell wall formation","type":"related"}],"termid":"GO:0071940","terms_by_termid":{"GO:0030476":null}}


id: GO:0060888
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The pattern specification process that results in the subdivision of the epidermis of the limb in space to define a volume in which specific patterns of basal cell, spinous cell and granular cells will differentiate giving rise to the layers of the limb epidermis.","definition_xrefs":["GOC:tb","GOC:dph","GOC:sdb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"},{"relation_name":"is_a","term_name":"limb epidermis development","termid":"GO:0060887"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"limb epidermis stratification","termid":"GO:0060888"}


id: GO:0070742
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a C2H2-type zinc finger domain of a protein. The C2H2 zinc finger is the classical zinc finger domain, in which two conserved cysteines and histidines co-ordinate a zinc ion.","definition_xrefs":["GOC:mah","GOC:BHF","Pfam:PF00096"],"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:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"C2H2 zinc finger domain binding","termid":"GO:0070742"}


id: FYPO:0001727
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 L-glutamine measured in the cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular amino acid level","termid":"FYPO:0003985"}],"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:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased cellular glutamine level","synonyms":[{"name":"decreased cellular L-glutamine level","type":"exact"},{"name":"decreased cellular glutamine level during mitotic cell cycle","type":"related"},{"name":"decreased cellular glutamine level during vegetative growth","type":"exact"},{"name":"decreased level of glutamine in cell","type":"exact"},{"name":"reduced cellular glutamine level","type":"exact"},{"name":"reduced level of glutamine in cell","type":"exact"}],"termid":"FYPO:0001727"}


id: PBO:0073611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"siah E3 ubiquitin protein ligase 2","termid":"PBO:0073611"}


id: GO:0140754
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in intracellular membranes are reorganized by viral proteins that perturb membrane integrity and can cause an extensive rearrangement of cellular membranes, forming membranous webs, which are thought to be the site of replication or certain viruses, for example the HPV virus.","definition_xrefs":["PMID:19376974"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host membrane","termid":"GO:0141171"}],"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":"reorganization of cellular membranes to establish viral sites of replication","termid":"GO:0140754"}


id: MONDO:0014977
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive condition caused by pathogenic variant(s) of the POGLUT1 gene, encoding protein O-glucosyltransferase 1. It is characterized by progressive muscular dystrophy, primarily affecting the proximal muscles, resulting in difficulty walking. A characteristic finding of “inside-to-outside” fatty degeneration on muscle imaging has been noted in patients.","definition_xrefs":["PMID:1897643","PMID:27807076","NCIT:C142082","PMID:30055862"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"autosomal recessive limb-girdle muscular dystrophy","termid":"MONDO:0015152"},{"relation_name":"is_a","term_name":"disorder of protein O-glycosylation","termid":"MONDO:0017741"}],"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:0005336"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005066","MONDO:0024322","MONDO:0005336","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive limb-girdle muscular dystrophy type 2R1","secondary_identifiers":["MONDO:0018817","DOID:0080762","MEDGEN:934627","OMIM:617232","GARD:17869","Orphanet:480682","UMLS:C4310660"],"synonyms":[{"name":"LGMD2Z","type":"exact"},{"name":"POGLUT1 autosomal recessive limb-girdle muscular dystrophy","type":"exact"},{"name":"autosomal recessive limb-girdle muscular dystrophy caused by mutation in POGLUT1","type":"exact"},{"name":"autosomal recessive limb-girdle muscular dystrophy type 2Z","type":"exact"},{"name":"limb-girdle muscular dystrophy type 2Z","type":"exact"},{"name":"muscular dystrophy, limb-girdle, autosomal recessive 21","type":"exact"},{"name":"muscular dystrophy, limb-girdle, type 2Z","type":"exact"}],"termid":"MONDO:0014977","xrefs":{"Monarch":{"xref_id":"0014977"}}}


id: PBO:0060695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit A3 pseudogene 3","termid":"PBO:0060695"}


id: PBO:0089945
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin-like protein","termid":"PBO:0089945"}


id: MONDO:0006964
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Overproduction of parathyroid hormone in response to influence external to the parathyroid glands.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperparathyroidism","termid":"MONDO:0001741"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secondary hyperparathyroidism","secondary_identifiers":["UMLS:C0020503","HP:0000867","SCTID:91478007","MedDRA:10020708","icd11.foundation:1442752937","EFO:1001173","MEDGEN:9368","NCIT:C113335","MESH:D006962","DOID:12466"],"synonyms":[{"name":"secondary hyperparathyroidism","type":"exact"},{"name":"secondary hyperparathyroidism (disease)","type":"exact"},{"name":"secondary hyperparathyroidism NOS","type":"narrow"}],"termid":"MONDO:0006964","xrefs":{"Monarch":{"xref_id":"0006964"}}}


id: PBO:0054803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 2216","termid":"PBO:0054803"}


id: PBO:0041613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cdk5 and Abl enzyme substrate 1","termid":"PBO:0041613"}


id: PBO:0085975
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; previously annotated as two separate ORFs, YDR474C and YDR475C, which were merged as a result of corrections to the systematic reference sequence; JIP4 has a paralog, YOR019W, that arose from the whole genome duplication","termid":"PBO:0085975"}


id: GO:0006460
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-prolyl isomerase B reaction (obsolete GO:0006460)","synonyms":[{"name":"peptidyl-prolyl isomerase B reaction","type":"exact"}],"termid":"GO:0006460"}


id: GO:0032449
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex comprising Bcl10, MALT1 and a CARD domain-containing protein (CARD9, CARD10 or CARD11); plays a role in signal transduction during NF-kappaB activation.","definition_xrefs":["PMID:30467369","PMID:12909454"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"}],"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":"CBM complex","synonyms":[{"name":"CARMA1-BCL10-Malt1 complex","type":"exact"}],"termid":"GO:0032449"}


id: PBO:0068142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 449","termid":"PBO:0068142"}


id: MONDO:0044244
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete nail low-sulfur protein (obsolete MONDO:0044244)","secondary_identifiers":["OMIM:161080"],"synonyms":[{"name":"nail LOW-sulfur PROTEIN","type":"related"}],"termid":"MONDO:0044244","xrefs":{"Monarch":{"xref_id":"0044244"}}}


id: PBO:0039764
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alu-mediated CDKN1A/p21 transcriptional regulator","termid":"PBO:0039764"}


id: FYPO:0004314
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 CENP-A containing chromatin is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to centromeric chromatin","termid":"FYPO:0005072"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000002","FYPO:0000257","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization to CENP-A containing chromatin","synonyms":[{"name":"normal protein localisation to CENP-A containing chromatin","type":"exact"},{"name":"normal protein localization to CENP-A containing chromatin during mitotic cell cycle","type":"related"},{"name":"normal protein localization to CENP-A containing chromatin during vegetative growth","type":"exact"},{"name":"normal protein localization to centromeric core region chromatin","type":"exact"}],"termid":"FYPO:0004314"}


id: PR:O59817
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- efr3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59817"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein efr3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC794.08","synonyms":[{"name":"Spom972h-efr3","type":"exact"}],"termid":"PR:O59817"}


id: PBO:0003889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis protein Rrs1 (predicted)","termid":"PBO:0003889"}


id: MONDO:0100427
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A characteristic of a diseae in which it does not result from diagnostic and therapeutic procedures undertaken on a patient.","definition_xrefs":["PMID:27407693"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iatrogenic or non-iatrogenic","termid":"MONDO:0100369"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-iatrogenic","termid":"MONDO:0100427","xrefs":{"Monarch":{"xref_id":"0100427"}}}


id: MONDO:0010800
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Wolfram syndrome","termid":"MONDO:0018105"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Wolfram syndrome, mitochondrial form","secondary_identifiers":["GARD:15313","MEDGEN:325511","MESH:C564012","OMIM:598500","UMLS:C1838782","DOID:0080583"],"synonyms":[{"name":"Didmoad syndrome, mitochondrial form","type":"related"},{"name":"Wolfram syndrome, mitochondrial form","type":"exact"},{"name":"diabetes insipidus and mellitus with optic atrophy and deafness, mitochondrial form","type":"related"}],"termid":"MONDO:0010800","xrefs":{"Monarch":{"xref_id":"0010800"}}}


id: PBO:0044380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYP1B1 antisense RNA 1","termid":"PBO:0044380"}


id: FYPO:0002181
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A mixed population phenotype in which all cells in a population are inviable, and the population includes a mixture of germinated spores and spheroid vegetative cells. The spheroid cells arise from division of some of the germinated spores, and may form a microcolony of up to 64 cells.","definition_xrefs":["PomBase:vw","PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable mixed population including germinated spores and spheroid cells (obsolete FYPO:0002181)","synonyms":[{"name":"inviable mixed population including germinated spores and rounded cells","type":"exact"}],"termid":"FYPO:0002181"}


id: GO:0031962
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a nuclear mineralocorticoid receptor.","definition_xrefs":["GOC:mah","PMID:12511169"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear receptor binding","termid":"GO:0016922"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"nuclear mineralocorticoid receptor binding","synonyms":[{"name":"mineralocorticoid receptor binding","type":"broad"}],"termid":"GO:0031962"}


id: PBO:0041081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BRK1 pseudogene 2","termid":"PBO:0041081"}


id: MONDO:0018352
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma arising from the penis. It occurs chiefly in the squamous epithelium of the glans, coronal sulcus, and foreskin. Etiologic factors include phimosis, lichen sclerosus, smoking, ultraviolet irradiation, history of warts or condylomas, and lack of circumcision. Human papilloma virus is present in a subset of penile squamous cell carcinomas. Patients may present with an exophytic or flat ulcerative mass in the glans or a large primary tumor with inguinal nodal and skin metastases. Morphologic variants include the basaloid carcinoma, warty (condylomatous) carcinoma, verrucous carcinoma, and sarcomatoid (spindle cell) carcinoma. (WHO, 2004)","definition_xrefs":["NCIT:C7729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell carcinoma","termid":"MONDO:0005096"},{"relation_name":"is_a","term_name":"penile carcinoma","termid":"MONDO:0006360"}],"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":"squamous cell carcinoma of penis","secondary_identifiers":["DOID:5518","UMLS:C0238348","GARD:21639","icd11.foundation:186592209","ONCOTREE:PSCC","Orphanet:398058","MEDGEN:116057","SCTID:403468003"],"synonyms":[{"name":"PSCC","type":"related"},{"name":"epidermoid carcinoma of penis","type":"exact"},{"name":"epidermoid carcinoma of the penis","type":"exact"},{"name":"epidermoid cell carcinoma of penis","type":"exact"},{"name":"epidermoid cell carcinoma of the penis","type":"exact"},{"name":"penile epidermoid carcinoma","type":"exact"},{"name":"penile epidermoid cell carcinoma","type":"exact"},{"name":"penile squamous car.(epidermoid)","type":"exact"},{"name":"penile squamous carcinoma (epidermoid)","type":"exact"},{"name":"penile squamous cell cancer","type":"exact"},{"name":"penile squamous cell carcinoma","type":"exact"},{"name":"penis squamous cell carcinoma","type":"exact"},{"name":"squamous cell carcinoma of penis","type":"exact"},{"name":"squamous cell carcinoma of the penis","type":"exact"}],"termid":"MONDO:0018352","xrefs":{"Monarch":{"xref_id":"0018352"}}}


id: GO:0031314
data:
  {"annotated_genes":["SJAG_01249","SJAG_00933","SJAG_00576","SJAG_00230","SJAG_00852","SJAG_01043","SJAG_03456","SJAG_00721","SJAG_05398","SJAG_04000","SJAG_03563","SJAG_04642"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[61192,62763,64730,66254,92750,103205,108158,108817,110128,111483],"is_not":false,"summary":null,"term":"GO:0031314"},{"annotations":[102377,105693],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099616"}]},"cv_name":"cellular_component","definition":"The component of mitochondrial inner membrane consisting of gene products and protein complexes that are loosely bound to one of its surfaces, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:mah","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrinsic component of organelle membrane","termid":"GO:0031312"},{"relation_name":"part_of","term_name":"mitochondrial inner membrane","termid":"GO:0005743"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00230":null,"SJAG_00576":null,"SJAG_00721":null,"SJAG_00852":null,"SJAG_00933":null,"SJAG_01043":null,"SJAG_01249":null,"SJAG_03456":null,"SJAG_03563":null,"SJAG_04000":null,"SJAG_04642":null,"SJAG_05398":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005739"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005739","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"extrinsic component of mitochondrial inner membrane","references_by_uniquename":{"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"extrinsic to mitochondrial inner membrane","type":"narrow"}],"termid":"GO:0031314","terms_by_termid":{"GO:0031314":null,"GO:0099616":null}}


id: PBO:0054466
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 1865","termid":"PBO:0054466"}


id: MOD:00044
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-histidine residue to tele-phospho-L-histidine (N-tau-phospho-L-histidine, 1'-phospho-L-histidine).","definition_xrefs":["PubMed:6692818","PubMed:11038361","PubMed:5642389","RESID:AA0035"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphorylated L-histidine","termid":"MOD:00890"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00696"}],"interesting_parent_ids":["MOD:00696"],"is_obsolete":false,"name":"1'-phospho-L-histidine","synonyms":[{"name":"(2S)-2-amino-3-(1-phosphono-1H-imidazol-4-yl)propanoic acid","type":"exact"},{"name":"1'-phospho-L-histidine","type":"exact"},{"name":"2-azanyl-3-(1-phosphono-1H-imidazol-4-yl)propanoic acid","type":"exact"},{"name":"ACT_SITE Tele-phosphohistidine intermediate","type":"exact"},{"name":"MOD_RES Tele-phosphohistidine","type":"exact"},{"name":"N(tau)-phosphohistidine","type":"exact"},{"name":"N1-phosphonohistidine","type":"exact"},{"name":"NE2-phosphonohistidine","type":"exact"},{"name":"NtPHis","type":"exact"},{"name":"Ntau-phosphorylated L-histidine","type":"exact"},{"name":"Phospho","type":"related"},{"name":"Phosphorylation","type":"related"},{"name":"histidine-3-phosphate","type":"related"},{"name":"histidine-N(epsilon)-phosphate","type":"exact"},{"name":"histidine-N1'-phosphate","type":"exact"},{"name":"tele-phosphohistidine","type":"exact"}],"termid":"MOD:00044"}


id: PBO:0080880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"yippee like 5","termid":"PBO:0080880"}


id: FYPO:0008264
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which a protein kinase activity is absent during a cellular response to  oxidative stress.","definition_xrefs":["PMID:24498240"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein kinase activity","termid":"FYPO:0001384"}],"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:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0001985","FYPO:0000652","FYPO:0000654","FYPO:0000707"],"is_obsolete":false,"name":"abolished protein kinase activity in response to oxidative stress","termid":"FYPO:0008264"}


id: PATO:0000732
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000732 body tone value (obsolete PATO:0000732)","termid":"PATO:0000732"}


id: PR:Q9USU3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- fbh1 gene.","definition_xrefs":["UniProtKB:Q9USU3","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":"F-box DNA helicase protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC336.01","synonyms":[{"name":"Spom972h-fbh1","type":"exact"}],"termid":"PR:Q9USU3"}


id: MONDO:0005112
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm that arises from mesothelial cells in the pleura and shows a diffuse growth pattern. It arises on the parietal and sometimes visceral pleura as multiple small nodules that later become confluent and invade the chest wall adipose tissue and muscle. Asbestos exposure is the main cause for the development of pleural malignant mesothelioma. It usually affects patients over sixty years of age. The latency period is long. Patients usually present with pleural effusion, dyspnea and chest wall pain. Additional signs and symptoms include chills, sweating, weight loss, and weakness. Morphologic variants include epithelioid, desmoplastic, sarcomatoid, and biphasic mesothelioma. The clinical course is usually aggressive.","definition_xrefs":["NCIT:C7376"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pleural mesothelioma","termid":"MONDO:0003308"},{"relation_name":"is_a","term_name":"malignant mesothelioma","termid":"MONDO:0006292"},{"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 pleural mesothelioma","secondary_identifiers":["MEDGEN:208810","SCTID:254645002","EFO:0000770","UMLS:C0812413","DOID:7474"],"synonyms":[{"name":"malignant mesothelioma of pleura","type":"exact"},{"name":"malignant mesothelioma of the pleura","type":"exact"},{"name":"malignant pleural mesothelioma","type":"exact"},{"name":"pleura mesothelioma","type":"broad"},{"name":"pleural diffuse malignant mesothelioma","type":"exact"},{"name":"pleural malignant mesothelioma","type":"exact"}],"termid":"MONDO:0005112","xrefs":{"Monarch":{"xref_id":"0005112"}}}


id: PBO:0074621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 20B","termid":"PBO:0074621"}


id: GO:1902785
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an undecane stimulus.","definition_xrefs":["GOC:mengo_curators","GO_REF:0000071","PMID:23826995","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to alkane","termid":"GO:1902779"},{"relation_name":"is_a","term_name":"response to undecane","termid":"GO:1902784"}],"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 undecane","termid":"GO:1902785"}


id: PBO:0071766
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein lateral stalk subunit P1 pseudogene 13","termid":"PBO:0071766"}


id: PBO:0069309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 565, pseudogene","termid":"PBO:0069309"}


id: GO:0042425
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of choline (2-hydroxyethyltrimethylammonium), an amino alcohol that occurs widely in living organisms as a constituent of certain types of phospholipids and in the neurotransmitter acetylcholine.","definition_xrefs":["GOC:jl","ISBN:0192801023"],"direct_ancestors":[{"relation_name":"is_a","term_name":"choline metabolic process","termid":"GO:0019695"},{"relation_name":"is_a","term_name":"biogenic amine biosynthetic process","termid":"GO:0042401"}],"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":"choline biosynthetic process","secondary_identifiers":["MetaCyc:PWY-4762"],"synonyms":[{"name":"choline anabolism","type":"exact"},{"name":"choline biosynthesis","type":"exact"},{"name":"choline formation","type":"exact"},{"name":"choline synthesis","type":"exact"}],"termid":"GO:0042425"}


id: PBO:0029841
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_maintenance_of_protein_localization_to_heterochromatin_at_centromere_outer_repeat","termid":"PBO:0029841"}


id: PBO:0082793
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the U2 snRNP; required for the first catalytic step of splicing and for spliceosomal assembly; interacts with Rds3p and is required for Mer1p-activated splicing; diploid mutants have a specific defect in MATa1 pre-mRNA splicing which leads to haploid gene expression in diploids","termid":"PBO:0082793"}


id: GO:0007600
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events required for an organism to receive a sensory stimulus, convert it to a molecular signal, and recognize and characterize the signal. This is a neurological process.","definition_xrefs":["GOC:dph","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system process","termid":"GO:0050877"}],"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":"sensory perception","secondary_identifiers":["Reactome:R-HSA-9709957","Wikipedia:Perception"],"termid":"GO:0007600"}


id: PBO:0086664
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 expression profiling and mass spectrometry","termid":"PBO:0086664"}


id: GO:0032841
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to calcitonin, a peptide hormone responsible for reducing serum calcium levels by inhibiting osteoclastic bone reabsorption and promoting renal calcium excretion. It is synthesized and released by the C cells of the thyroid.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcitonin family binding","termid":"GO:0097644"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"calcitonin binding","termid":"GO:0032841"}


id: PBO:0027416
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cell_population_growth_during_glucose_starvation","termid":"PBO:0027416"}


id: PBO:0057750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1909","termid":"PBO:0057750"}


id: GO:0035911
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the descending aorta are generated and organized. The descending aorta is the portion of the aorta in a two-pass circulatory system from the arch of aorta to the point where it divides into the common iliac arteries. In a two-pass circulatory system blood passes twice through the heart to supply the body once.","definition_xrefs":["GOC:bf","GOC:dgh","UBERON:0001514","MA:0002571","Wikipedia:Descending_aorta"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"descending aorta development","termid":"GO:0035906"},{"relation_name":"part_of","term_name":"aorta morphogenesis","termid":"GO:0035909"}],"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":"descending aorta morphogenesis","termid":"GO:0035911"}


id: PBO:0000351
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing associated factor Dre4","termid":"PBO:0000351"}


id: PBO:0081609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 532","termid":"PBO:0081609"}


id: GO:0014910
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of smooth muscle cell migration.","definition_xrefs":["GOC:mtg_muscle","CL:0000192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell migration","termid":"GO:0030334"},{"relation_name":"regulates","term_name":"smooth muscle cell migration","termid":"GO:0014909"}],"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 smooth muscle cell migration","termid":"GO:0014910"}


id: MONDO:1011755
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sebaceous adenitis, non-human animal","secondary_identifiers":["OMIA:001563"],"termid":"MONDO:1011755","xrefs":{"Monarch":{"xref_id":"1011755"}}}


id: PBO:0029940
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-dispersed_actin_cortical_patch_localization_during_mitotic_interphase","termid":"PBO:0029940"}


id: PBO:0005172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinetochore protein Mis18","termid":"PBO:0005172"}


id: GO:0097297
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that initiates the activity of an inactive cysteine-type endopeptidase involved in the execution phase of apoptosis.","definition_xrefs":["GOC:mtg_apoptosis"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of cysteine-type endopeptidase activity involved in execution phase of apoptosis (obsolete GO:0097297)","synonyms":[{"name":"activation of effector caspase activity","type":"narrow"}],"termid":"GO:0097297"}


id: MONDO:0014190
data:
  {"annotated_genes":["SJAG_00997","SJAG_04885"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87751,87752],"is_not":false,"summary":null,"term":"MONDO:0014190"}]},"cv_name":"mondo","definition":"Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the ELAC2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00997":null,"SJAG_04885":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"combined oxidative phosphorylation defect type 17","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0111496","Orphanet:369913","OMIM:615440","UMLS:C3809526","GARD:17589","MEDGEN:815856"],"synonyms":[{"name":"COXPD17","type":"exact"},{"name":"ELAC2 combined oxidative phosphorylation deficiency","type":"exact"},{"name":"combined oxidative phosphorylation deficiency 17","type":"related"},{"name":"combined oxidative phosphorylation deficiency caused by mutation in ELAC2","type":"exact"},{"name":"combined oxidative phosphorylation deficiency type 17","type":"exact"}],"termid":"MONDO:0014190","terms_by_termid":{"MONDO:0014190":null},"xrefs":{"Monarch":{"xref_id":"0014190"}}}


id: GO:1905289
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of CAMKK-AMPK signaling cascade.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:22128786"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of calcium-mediated signaling","termid":"GO:0050848"},{"relation_name":"regulates","term_name":"CAMKK-AMPK signaling cascade","termid":"GO:0061762"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of CAMKK-AMPK signaling cascade","synonyms":[{"name":"regulation of stress-activated AMP-activated protein kinase signaling cascade","type":"related"}],"termid":"GO:1905289"}


id: FYPO:0001034
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of tunicamycin than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000139","FYPO:0002682","FYPO:0000003","FYPO:0005447"],"is_obsolete":false,"name":"resistance to tunicamycin","synonyms":[{"name":"resistance to tunicamycin during mitotic cell cycle","type":"related"},{"name":"resistance to tunicamycin during vegetative growth","type":"exact"},{"name":"resistant to TM","type":"exact"},{"name":"resistant to tunicamycin","type":"exact"}],"termid":"FYPO:0001034"}


id: PBO:0078039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 29","termid":"PBO:0078039"}


id: MONDO:0015619
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A urogenital tract malformation that is not part of a larger syndrome.","definition_xrefs":["MONDO:patterns/isolated"],"gene_count":0,"genotype_count":0,"name":"obsolete non-syndromic urogenital tract malformation (obsolete MONDO:0015619)","secondary_identifiers":["Orphanet:165704"],"synonyms":[{"name":"isolated urogenital tract malformation","type":"exact"},{"name":"nonsyndromic urogenital tract malformation","type":"exact"}],"termid":"MONDO:0015619","xrefs":{"Monarch":{"xref_id":"0015619"}}}


id: MONDO:0859224
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":"intellectual disability and myopathy syndrome","secondary_identifiers":["OMIM:619719","MEDGEN:1808193","UMLS:C5676904"],"termid":"MONDO:0859224","xrefs":{"Monarch":{"xref_id":"0859224"}}}


id: PBO:0052861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 5-4","termid":"PBO:0052861"}


id: PBO:0059076
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"molybdenum cofactor synthesis 3 pseudogene 2","termid":"PBO:0059076"}


id: FYPO:0004080
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 phosphorylation of serine at position 10 of histone H3 is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone phosphorylation during vegetative growth","termid":"FYPO:0002591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0005447","FYPO:0002274","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased histone H3-S10 phosphorylation during vegetative growth","synonyms":[{"name":"increased histone H3 phosphorylation at S10 during vegetative growth","type":"exact"},{"name":"increased histone H3-S10 phosphorylation during mitotic cell cycle","type":"related"},{"name":"increased histone H3S10 phosphorylation during vegetative growth","type":"exact"}],"termid":"FYPO:0004080"}


id: SO:0000994
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region that has a known consensus sequence.","direct_ancestors":[{"relation_name":"has_quality","term_name":"consensus","termid":"SO:0000993"},{"relation_name":"is_a","term_name":"experimental_feature","termid":"SO:0001410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"consensus_region","synonyms":[{"name":"consensus region","type":"exact"}],"termid":"SO:0000994"}


id: PR:Q9USM3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sfh1 gene.","definition_xrefs":["UniProtKB:Q9USM3","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":"chromatin structure-remodeling complex subunit sfh1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC16A11.14","synonyms":[{"name":"RSC complex subunit sfh1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SNF5 homolog 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-sfh1","type":"exact"}],"termid":"PR:Q9USM3"}


id: PBO:0073729
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stem-loop binding protein","termid":"PBO:0073729"}


id: PR:Q09787
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC13G6.09 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09787"],"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 C13G6.09 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13G6.09","synonyms":[{"name":"Spom972h-SPAC13G6.09","type":"exact"}],"termid":"PR:Q09787"}


id: MONDO:0011012
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"African iron overload is a rare disorder described in sub-Saharan African populations and is characterized by iron overload due to excess dietary iron intake and possibly genetic factors, leading to hepatic portal fibrosis and micronodular cirrhosis.","definition_xrefs":["Orphanet:139507"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hemochromatosis","termid":"MONDO:0006507"}],"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":"African iron overload","secondary_identifiers":["SCTID:66576001","DOID:0111033","OMIM:601195","UMLS:C0268063","icd11.foundation:869212237","GARD:8495","MEDGEN:75649","MESH:C537904","NORD:740"],"synonyms":[{"name":"African iron overload","type":"exact"},{"name":"Bantu siderosis","type":"exact"},{"name":"hereditary iron overload and African Americans","type":"related"},{"name":"iron overload in Africa","type":"exact"}],"termid":"MONDO:0011012","xrefs":{"Monarch":{"xref_id":"0011012"}}}


id: MONDO:0031439
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":"short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies","secondary_identifiers":["OMIMPS:617877"],"termid":"MONDO:0031439","xrefs":{"Monarch":{"xref_id":"0031439"}}}


id: MONDO:0009345
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Histidinemia is a rare metabolic disorder characterized by elevated histidine levels in blood, urine, and cerebrospinal fluid, generally with no clinical repercussions.","definition_xrefs":["Orphanet:2157"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of histidine metabolism","termid":"MONDO:0019228"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"histidinemia","secondary_identifiers":["GARD:6661","MEDGEN:113135","ICD10CM:E70.41","OMIM:235800","SCTID:410058007","icd11.foundation:261052955","MESH:C538320","NORD:1245","UMLS:C0220992","DOID:0060168"],"synonyms":[{"name":"HIS deficiency","type":"exact"},{"name":"Hal deficiency","type":"exact"},{"name":"Histidinuria","type":"exact"},{"name":"histidase deficiency","type":"exact"},{"name":"histidine ammonia-lyase deficiency","type":"exact"},{"name":"histidinemia","type":"exact"},{"name":"histidinuria","type":"exact"},{"name":"hyperhistidinemia","type":"exact"}],"termid":"MONDO:0009345","xrefs":{"Monarch":{"xref_id":"0009345"}}}


id: GO:1990684
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A macromolecular complex containing separate protein, lipid and RNA molecules. Separate in this context means not covalently bound to each other.","definition_xrefs":["GOC:vesicles","PMID:21423178","PMID:22028337","PMID:23559634"],"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":"protein-lipid-RNA complex","synonyms":[{"name":"miRNA-lipoprotein complex","type":"related"}],"termid":"GO:1990684"}


id: PBO:0028735
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_L-ergothioneine_level_during_vegetative_growth","termid":"PBO:0028735"}


id: SO:0001507
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A collection of one or more sequences of an individual.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_part","term_name":"sequence_alteration","termid":"SO:0001059"},{"relation_name":"is_a","term_name":"sequence_collection","termid":"SO:0001260"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"variant_collection","synonyms":[{"name":"variant collection","type":"related"}],"termid":"SO:0001507"}


id: GO:0032727
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of interferon-alpha production.","definition_xrefs":["PMID:15546383","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of type I interferon production","termid":"GO:0032481"},{"relation_name":"is_a","term_name":"regulation of interferon-alpha production","termid":"GO:0032647"},{"relation_name":"positively_regulates","term_name":"interferon-alpha production","termid":"GO:0032607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of interferon-alpha production","secondary_identifiers":["GO:1902741","GO:0045356"],"synonyms":[{"name":"activation of interferon-alpha production","type":"narrow"},{"name":"positive regulation of interferon-alpha biosynthetic process","type":"narrow"},{"name":"positive regulation of interferon-alpha secretion","type":"narrow"},{"name":"stimulation of interferon-alpha production","type":"narrow"},{"name":"up regulation of interferon-alpha production","type":"exact"},{"name":"up-regulation of interferon-alpha production","type":"exact"},{"name":"upregulation of interferon-alpha production","type":"exact"}],"termid":"GO:0032727"}


id: PBO:0048331
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde 3 phosphate dehydrogenase pseudogene 42","termid":"PBO:0048331"}


id: PBO:0072442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S29 pseudogene 6","termid":"PBO:0072442"}


id: GO:1900800
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving cspyrone B1.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary metabolic process","termid":"GO:0019748"},{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"},{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"},{"relation_name":"is_a","term_name":"lactone metabolic process","termid":"GO:1901334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0019748"],"is_obsolete":false,"name":"cspyrone B1 metabolic process","synonyms":[{"name":"cspyrone B1 metabolism","type":"exact"}],"termid":"GO:1900800"}


id: PBO:0046710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ETV7 and PTX1 antisense RNA 1","termid":"PBO:0046710"}


id: PBO:0029081
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_spindle_pole_body","termid":"PBO:0029081"}


id: MONDO:0011479
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition characterized by development of symptoms while standing. It is an autonomic nervous system disorder and the symptoms are relieved once the person sits back down. Symptoms include heart.","definition_xrefs":["EFO:1000645"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart conduction disease","termid":"MONDO:0000992"},{"relation_name":"is_a","term_name":"inherited orthostatic hypotension","termid":"MONDO:0021272"},{"relation_name":"is_a","term_name":"cardiogenetic disease","termid":"MONDO:0100547"}],"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":"postural orthostatic tachycardia syndrome","secondary_identifiers":["Orphanet:443236","DOID:0111154","MEDGEN:226970","NCIT:C85020","SCTID:371073003","GARD:13591","icd11.foundation:1533647472","MESH:D054972","OMIM:604715","UMLS:C1299624"],"synonyms":[{"name":"POTS","type":"exact"},{"name":"Soldiers heart","type":"related"},{"name":"familial orthostatic tachycardia due to norepinephrine transporter deficiency","type":"exact"},{"name":"irritable heart","type":"exact"},{"name":"neurocirculatory asthenia","type":"related"},{"name":"orhtostatic intolerance","type":"exact"},{"name":"orthostatic intolerance","type":"related"},{"name":"orthostatic intolerance due to NET deficiency","type":"exact"},{"name":"postural tachycardia syndrome due to NET deficiency","type":"exact"},{"name":"soldiers heart","type":"exact"}],"termid":"MONDO:0011479","xrefs":{"Monarch":{"xref_id":"0011479"}}}


id: PBO:0039588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anoctamin 6","termid":"PBO:0039588"}


id: GO:0061708
data:
  {"annotated_genes":["SJAG_00358"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[61302],"is_not":false,"summary":null,"term":"GO:0061708"}]},"cv_name":"molecular_function","definition":"Catalysis of 5-taurinomethyluridine in tRNA + a [protein]-S-sulfanylcysteine + ATP + a reduced electron acceptor = a 5-taurinomethyl-2-thiouridine in tRNA + a [protein]-L-cysteine + AMP + an oxidized electron acceptor + diphosphate + H+.","definition_xrefs":["PMID:15509579","GOC:dph","RHEA:47040"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfurtransferase activity","termid":"GO:0016783"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a tRNA","termid":"GO:0140101"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00358":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0140101","GO:0003674","GO:0003824","GO:0016782","GO:0140098"],"is_obsolete":false,"name":"tRNA-5-taurinomethyluridine 2-sulfurtransferase","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["EC:2.8.1.14","Reactome:R-HSA-6787447","MetaCyc:RXN-16821"],"termid":"GO:0061708","terms_by_termid":{"GO:0061708":null}}


id: GO:0010361
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which blue light modulates the frequency, rate or extent of anion channel activity.","definition_xrefs":["PMID:17319842","GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of anion channel activity by blue light (obsolete GO:0010361)","synonyms":[{"name":"regulation by blue light of anion channel activity","type":"exact"}],"termid":"GO:0010361"}


id: PBO:0090536
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane ammonium transmembrane transporter Amt1","termid":"PBO:0090536"}


id: FYECO:0000328
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"LNB medium is a Low Nutrient medium containing yeast nitrogen base without amino acids, glucose, salts and vitamins.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping defined medium","termid":"FYECO:0000013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LNB glucose medium","termid":"FYECO:0000328"}


id: GO:0070792
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of Hulle cells over time, from their formation to the mature structures. Hulle cells are specialized multinucleate cells that originate from a nest-like aggregation of hyphae during sexual development and serve as nurse cells to the developing cleistothecium, or fruiting body.","definition_xrefs":["PMID:19210625"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"cell development","termid":"GO:0048468"},{"relation_name":"part_of","term_name":"cleistothecium development","termid":"GO:0070791"}],"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":"Hulle cell development","synonyms":[{"name":"Huelle cell development","type":"exact"},{"name":"Hulle cell formation","type":"narrow"}],"termid":"GO:0070792"}


id: GO:0031402
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a sodium ion (Na+).","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkali metal ion binding","termid":"GO:0031420"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0046872"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0046872","GO:0005488"],"is_obsolete":false,"name":"sodium ion binding","synonyms":[{"name":"Na+ ion binding","type":"exact"}],"termid":"GO:0031402"}


id: PBO:0044824
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 110","termid":"PBO:0044824"}


id: GO:1901903
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of tyrocidine.","definition_xrefs":["GOC:yaf","PMID:9352938","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catabolic process","termid":"GO:0009056"},{"relation_name":"is_a","term_name":"tyrocidine metabolic process","termid":"GO:1901902"}],"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":"tyrocidine catabolic process","synonyms":[{"name":"tyrocidine breakdown","type":"exact"},{"name":"tyrocidine catabolism","type":"exact"},{"name":"tyrocidine degradation","type":"exact"}],"termid":"GO:1901903"}


id: PR:Q10659
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spo14 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10659"],"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":"membrane glycoprotein spo14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3H7.01","synonyms":[{"name":"SEC12-like protein (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-spo14","type":"exact"},{"name":"sporulation-specific protein 14 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10659"}


id: MONDO:0008699
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Achalasia-microcephaly is an extremely rare genetic syndrome, reported in a few families to date, characterized by the association of microcephaly, intellectual deficit and achalasia (with symptoms of coughing, dysphagia, vomiting, failure to thrive and aspiration appearing in infancy/early-childhood). Antenatal exposure to Mefloquine was reported in one simplex case. An autosomal recessive inheritance has been proposed.","definition_xrefs":["Orphanet:929"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"achalasia microcephaly syndrome","secondary_identifiers":["SCTID:718573009","GARD:456","MESH:C536010","MEDGEN:349753","DOID:0050796","UMLS:C1860212","OMIM:200450"],"synonyms":[{"name":"achalasia microcephaly","type":"exact"},{"name":"achalasia-microcephaly syndrome","type":"exact"}],"termid":"MONDO:0008699","xrefs":{"Monarch":{"xref_id":"0008699"}}}


id: PBO:0067260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 334, pseudogene","termid":"PBO:0067260"}


id: PBO:0012299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human LYAR homolog","termid":"PBO:0012299"}


id: PBO:0065939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rac GTPase activating protein 1 pseudogene 1","termid":"PBO:0065939"}


id: PBO:0069621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 898, pseudogene","termid":"PBO:0069621"}


id: GO:0030896
data:
  {"annotated_genes":["SJAG_02771","SJAG_01605","SJAG_03026"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[74741,75668,80716],"is_not":false,"summary":null,"term":"GO:0030896"}]},"cv_name":"cellular_component","definition":"Conserved heterotrimeric complex of PCNA-like proteins that is loaded onto DNA at sites of DNA damage.","definition_xrefs":["PMID:12531008"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"condensed nuclear chromosome","termid":"GO:0000794"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01605":null,"SJAG_02771":null,"SJAG_03026":null},"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:0005694"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005694","GO:0005634"],"is_obsolete":false,"name":"checkpoint clamp complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"CCC","type":"exact"},{"name":"Rad9-Hus1-Rad1 (9-1-1) clamp complex","type":"exact"}],"termid":"GO:0030896","terms_by_termid":{"GO:0030896":null}}


id: MONDO:0020231
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cardiac disease with cataract (obsolete MONDO:0020231)","secondary_identifiers":["Orphanet:98647"],"termid":"MONDO:0020231","xrefs":{"Monarch":{"xref_id":"0020231"}}}


id: MONDO:0009275
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neonatal hemochromatosis is a disease in which too much iron builds up inthe body. In this form of hemochromatosis the iron overload begins before birth. This disease tends to progress rapidly and is characterized by liver damage that is apparent at birth or in the first day of life. There are a number of other forms of hemochromatosis. To learn more about these other forms click on the disease names listed below: Hemochromatosis type 1 Hemochromatosis type 2 Hemochromatosis type 3 Hemochromatosis type 4","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hemochromatosis","termid":"MONDO:0006507"}],"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":"neonatal hemochromatosis","secondary_identifiers":["UMLS:C0268059","MEDGEN:82768","NORD:1494","NCIT:C129980","OMIM:231100","MESH:C536394","GARD:7172","Orphanet:446"],"synonyms":[{"name":"Nh","type":"related"},{"name":"Nhc","type":"related"},{"name":"alloimmune Hepatitis, congenital","type":"related"},{"name":"giant cell Hepatitis","type":"related"},{"name":"giant cell Hepatitis (formerly)","type":"related"},{"name":"giant cell Hepatitis, formerly","type":"related"},{"name":"hemochromatosis neonatal","type":"related"},{"name":"hemochromatosis, neonatal","type":"related"},{"name":"idiopathic neonatal hemochromatosis","type":"related"},{"name":"neonatal Hepatitis","type":"related"},{"name":"neonatal Hepatitis, formerly","type":"related"},{"name":"neonatal hepatitis (formerly)","type":"related"}],"termid":"MONDO:0009275","xrefs":{"Monarch":{"xref_id":"0009275"}}}


id: GO:0022881
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the PEP-dependent, phosphoryl transfer-driven transport of substances across a membrane. The transport happens by catalysis of the reaction: protein N-phosphohistidine + N-acetylgalactosamine(out) = protein histidine + N-acetylgalactosamine phosphate(in). This differs from primary and secondary active transport in that the solute is modified during transport.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-N(PI)-phosphohistidine-sugar phosphotransferase activity","termid":"GO:0008982"},{"relation_name":"is_a","term_name":"N-acetylgalactosamine transmembrane transporter activity","termid":"GO:0015571"},{"relation_name":"is_a","term_name":"D-glucose transmembrane transporter activity","termid":"GO:0055056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"protein-N(PI)-phosphohistidine-N-acetylgalactosamine phosphotransferase system transporter activity","synonyms":[{"name":"N-acetylgalactosamine PTS transporter activity","type":"exact"}],"termid":"GO:0022881"}


id: GO:0044044
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. An interaction with the host organism mediated by a substance on the surface of the other (symbiont) organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["MITRE:tk"],"gene_count":0,"genotype_count":0,"name":"obsolete interaction with host via substance in symbiont surface (obsolete GO:0044044)","termid":"GO:0044044"}


id: GO:0031850
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a delta-type opioid receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"opioid receptor binding","termid":"GO:0031628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"delta-type opioid receptor binding","synonyms":[{"name":"delta-type opioid receptor ligand","type":"narrow"},{"name":"enkephalin receptor binding","type":"related"}],"termid":"GO:0031850"}


id: MONDO:0008995
data:
  {"annotated_genes":["SJAG_02289"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88061],"is_not":false,"summary":null,"term":"MONDO:0008995"}]},"cv_name":"mondo","definition":"Yunis-Varon syndrome is a rare condition that affects many different parts of the body. Signs and symptoms are generally present from birth and may include underdeveloped or absent collarbones (clavicles); large fontanelles; characteristic facial features; hypotonia (reduced muscle tone) and/or abnormalities of the fingers and toes. Affected people may also experience feeding difficulties, breathing problems, brain malformations, heart defects, skeletal abnormalities, developmental delay, and/or intellectual disability. Yunis-Varon syndrome is caused by changes (mutations) in the FIG4 gene and isinherited in an autosomal recessive manner. Treatment is based on the signs and symptoms present in each person.","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02289":null},"genotype_count":0,"is_obsolete":false,"name":"Yunis-Varon syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0060589","OMIM:216340","NORD:1875","icd11.foundation:1696991249","Orphanet:3472","UMLS:C1857663","MEDGEN:341818","MESH:C536719","GARD:331"],"synonyms":[{"name":"YVS","type":"related"},{"name":"Yunis Varon Syndrome","type":"exact"},{"name":"Yunis Varon syndrome","type":"exact"},{"name":"Yunis-Varon syndrome","type":"exact"},{"name":"Yunis-Varón syndrome","type":"exact"},{"name":"cleidocranial dysplasia with micrognathia, absent thumbs, and distal Aphalangia","type":"related"},{"name":"cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia","type":"exact"},{"name":"cleidocranial dysplasia-micrognathia-absent thumbs syndrome","type":"exact"}],"termid":"MONDO:0008995","terms_by_termid":{"MONDO:0008995":null},"xrefs":{"Monarch":{"xref_id":"0008995"}}}


id: GO:1905340
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein localization to kinetochore.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:22581055"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization","termid":"GO:0032880"},{"relation_name":"regulates","term_name":"protein localization to kinetochore","termid":"GO:0034501"}],"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 protein localization to kinetochore","synonyms":[{"name":"regulation of condensin localization to kinetochore","type":"narrow"},{"name":"regulation of protein localisation to kinetochore","type":"exact"}],"termid":"GO:1905340"}


id: PBO:0029612
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_tapered_cell","termid":"PBO:0029612"}


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:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"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: PBO:0065862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB19, member RAS oncogene family","termid":"PBO:0065862"}


id: PBO:0076697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation regulator 1 like","termid":"PBO:0076697"}


id: PBO:0067001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 5, pseudogene","termid":"PBO:0067001"}


id: PBO:0087905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcription factor, activates transcription of stress response genes; nuclear localization is positively regulated by calcineurin-mediated dephosphorylation; rapidly localizes to the nucleus under blue light stress; can be activated in stochastic pulses of nuclear localization in response to calcium","termid":"PBO:0087905"}


id: FYPO:0003168
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which protein farnesyltransferase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished catalytic activity","termid":"FYPO:0000664"},{"relation_name":"is_a","term_name":"abnormal protein farnesyltransferase activity","termid":"FYPO:0003167"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000661","FYPO:0000654","FYPO:0000707","FYPO:0000652"],"is_obsolete":false,"name":"abolished protein farnesyltransferase activity","synonyms":[{"name":"protein farnesyltransferase activity abolished","type":"exact"}],"termid":"FYPO:0003168"}


id: MONDO:0003457
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ovarian serous adenofibroma (obsolete MONDO:0003457)","termid":"MONDO:0003457","xrefs":{"Monarch":{"xref_id":"0003457"}}}


id: PBO:0061577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurotrimin","termid":"PBO:0061577"}


id: PBO:0120063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wtf meiotic drive antidote Wtf23 OR wtf meiotic drive poison Wtf23","termid":"PBO:0120063"}


id: MONDO:0006767
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dilatation of the vessels in the antrum of the stomach. It is associated with portal hypertension, scleroderma, and chronic renal failure. It may cause gastric bleeding.","definition_xrefs":["NCIT:C84724"],"direct_ancestors":[{"relation_name":"is_a","term_name":"capillary disorder","termid":"MONDO:0001574"},{"relation_name":"is_a","term_name":"vascular ectasia","termid":"MONDO:0021658"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gastric antral vascular ectasia","secondary_identifiers":["MEDGEN:82753","DOID:2493","MedDRA:10051585","UMLS:C0267211","EFO:1000945","SCTID:43935004","MESH:D020252"],"synonyms":[{"name":"GAVE","type":"exact"},{"name":"watermelon stomach","type":"exact"}],"termid":"MONDO:0006767","xrefs":{"Monarch":{"xref_id":"0006767"}}}


id: GO:0008410
data:
  {"annotated_genes":["SJAG_02769","SJAG_02985"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77214,78559],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008775"},{"annotations":[93322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008260"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of a coenzyme A (CoA) group from one compound (donor) to another (acceptor).","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring sulphur-containing groups","termid":"GO:0016782"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02769":null,"SJAG_02985":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016782"],"is_obsolete":false,"name":"CoA-transferase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["EC:2.8.3.-"],"termid":"GO:0008410","terms_by_termid":{"GO:0008260":null,"GO:0008775":null}}


id: PBO:0089638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell wall beta-glucosidase Adg3","termid":"PBO:0089638"}


id: MONDO:1012031
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital blindness, non-human animal","termid":"MONDO:1011975"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital blindness, pig","secondary_identifiers":["OMIA:000115-9823"],"termid":"MONDO:1012031","xrefs":{"Monarch":{"xref_id":"1012031"}}}


id: PATO:0001744
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A radiation quality inhering in a bearer by virtue of what the bearer receives as a result of being exposed to ionizing radiation.","definition_xrefs":["hps:hps"],"direct_ancestors":[{"relation_name":"is_a","term_name":"radiation quality","termid":"PATO:0001739"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"radiation exposure","termid":"PATO:0001744"}


id: PBO:0076730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"treacle ribosome biogenesis factor 1","termid":"PBO:0076730"}


id: GO:1902790
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving undecan-2-one.","definition_xrefs":["GOC:TermGenie","PMID:4950559","GO_REF:0000068","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"}],"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":"undecan-2-one metabolic process","synonyms":[{"name":"undecan-2-one metabolism","type":"exact"}],"termid":"GO:1902790"}


id: GO:0031024
data:
  {"annotated_genes":["SJAG_03052","SJAG_03264"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104257,114758],"is_not":false,"summary":null,"term":"GO:0031024"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components, including gamma-tubulin and other proteins, to form an interphase microtubule organizing center.","definition_xrefs":["PMID:15068790","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"is_a","term_name":"microtubule organizing center organization","termid":"GO:0031023"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03052":null,"SJAG_03264":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0000226"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0007010","GO:0000226"],"is_obsolete":false,"name":"interphase microtubule organizing center assembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"interphase microtubule organising center biosynthesis","type":"exact"},{"name":"interphase microtubule organising center formation","type":"exact"},{"name":"interphase microtubule organizing center biogenesis","type":"related"},{"name":"interphase microtubule organizing centre assembly","type":"exact"}],"termid":"GO:0031024","terms_by_termid":{"GO:0031024":null}}


id: PBO:0055882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LRRC7 antisense RNA 1","termid":"PBO:0055882"}


id: GO:0120161
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cold-induced thermogenesis.","definition_xrefs":["PMID:27876809"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of metabolic process","termid":"GO:0019222"},{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"regulates","term_name":"cold-induced thermogenesis","termid":"GO:0106106"}],"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 cold-induced thermogenesis","synonyms":[{"name":"regulation of CIT","type":"related"}],"termid":"GO:0120161"}


id: MONDO:0001033
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"corneal ulcer","termid":"MONDO:0004577"}],"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":"mycotic corneal ulcer","secondary_identifiers":["ICD9:370.05","icd11.foundation:1756043578","UMLS:C0155071","SCTID:397977001","DOID:10440","MEDGEN:509769"],"termid":"MONDO:0001033","xrefs":{"Monarch":{"xref_id":"0001033"}}}


id: PBO:0090053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane LMBR1-like multi-pass membrane protein, human LMBRD2 ortholog, implicated in signalling","termid":"PBO:0090053"}


id: PBO:0042118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 190","termid":"PBO:0042118"}


id: GO:0052171
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The increase in size or mass of an organism, or the progression of an organism from an initial condition to a later condition, occurring when the organism is in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete growth or development during symbiotic interaction (obsolete GO:0052171)","synonyms":[{"name":"growth or development during symbiotic interaction","type":"exact"}],"termid":"GO:0052171"}


id: GO:0060271
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The assembly of a cilium, a specialized eukaryotic organelle that consists of a filiform extrusion of the cell surface. Each cilium is bounded by an extrusion of the cytoplasmic membrane, and contains a regular longitudinal array of microtubules, anchored basally in a centriole.","definition_xrefs":["GOC:cilia","PMID:27350441","GOC:pr","PMID:13978319","ISBN:0198506732","GOC:BHF","GOC:vw","GOC:dph","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cilium organization","termid":"GO:0044782"},{"relation_name":"is_a","term_name":"organelle assembly","termid":"GO:0070925"},{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection assembly","termid":"GO:0120031"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"cilium assembly","secondary_identifiers":["GO:0042384","Reactome:R-HSA-5617833"],"synonyms":[{"name":"ciliogenesis","type":"exact"},{"name":"cilium biogenesis","type":"related"},{"name":"cilium formation","type":"exact"},{"name":"cilium morphogenesis","type":"related"},{"name":"cilium organization","type":"related"},{"name":"microtubule-based flagellum assembly","type":"exact"}],"termid":"GO:0060271"}


id: MONDO:1010721
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any deficiency in fumarylacetoacetate hydrolase that occurs in rabbits due to a mutation in the FAH gene created by genetic engineering or gene editing. Fumarylacetoacetate hydrolase is an enzyme that catalyzes the last step of tyrosine metabolism.","definition_xrefs":["OMIA:002078-9986"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"metabolic disease, non-human animal","termid":"MONDO:1011331"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tyrosinemia type 1, FAH-related, rabbit","synonyms":[{"name":"tyrosinemia type I, rabbit","type":"related"}],"termid":"MONDO:1010721","xrefs":{"Monarch":{"xref_id":"1010721"}}}


id: MONDO:0001450
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete arachnoiditis (obsolete MONDO:0001450)","termid":"MONDO:0001450","xrefs":{"Monarch":{"xref_id":"0001450"}}}


id: GO:0017113
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5,6-dihydrouracil + NADP+ = uracil + NADPH + H+.","definition_xrefs":["EC:1.3.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"gene_count":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":"dihydropyrimidine dehydrogenase (NADP+) activity","secondary_identifiers":["MetaCyc:1.3.1.2-RXN","Reactome:R-HSA-73585","Reactome:R-HSA-73616","RHEA:18093"],"synonyms":[{"name":"4,5-dihydrothymine: oxidoreductase activity","type":"related"},{"name":"5,6-dihydrouracil:NADP+ 5-oxidoreductase activity","type":"related"},{"name":"DHPDH","type":"related"},{"name":"DHU dehydrogenase activity","type":"related"},{"name":"DPD","type":"related"},{"name":"dehydrogenase, dihydrouracil (nicotinamide adenine dinucleotide phosphate)","type":"related"},{"name":"dihydropyrimidine dehydrogenase activity","type":"exact"},{"name":"dihydrothymine dehydrogenase activity","type":"related"},{"name":"dihydrouracil dehydrogenase (NADP)","type":"related"},{"name":"dihydrouracil dehydrogenase (NADP+) activity","type":"related"},{"name":"hydropyrimidine dehydrogenase activity","type":"related"}],"termid":"GO:0017113"}


id: MONDO:0019219
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of biogenic amine metabolism and transport","termid":"MONDO:0019250"}],"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":"inborn disorder of neurotransmitter metabolism and transport","secondary_identifiers":["MEDGEN:1842206","Orphanet:79169","UMLS:C5681289","GARD:18950"],"synonyms":[{"name":"disorder of neurotransmitter metabolism and transport","type":"related"}],"termid":"MONDO:0019219","xrefs":{"Monarch":{"xref_id":"0019219"}}}


id: MONDO:0001118
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A spotted fever that has material basis in Rickettsia australis, which is transmitted by ticks (Ixodes holocyclus). The infection has symptom fever, has symptom headache, has symptom myalgia, has symptom maculopapular rash, and has symptom lymphadenopathy.","definition_xrefs":["DOID:10784"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spotted fever","termid":"MONDO:0001195"},{"relation_name":"is_a","term_name":"tick-borne infectious disease","termid":"MONDO:0025294"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Queensland tick typhus","secondary_identifiers":["MEDGEN:755996","ICD9:082.3","SCTID:68981009","UMLS:C2979888"],"synonyms":[{"name":"Australian tick typhus","type":"related"},{"name":"North Queensland tick typhus","type":"related"},{"name":"Rickettsia australis spotted fever","type":"exact"}],"termid":"MONDO:0001118","xrefs":{"Monarch":{"xref_id":"0001118"}}}


id: PBO:0052920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 19-3","termid":"PBO:0052920"}


id: PBO:0062538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 9 subfamily G member 3 pseudogene","termid":"PBO:0062538"}


id: MONDO:0004137
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0004137 (obsolete MONDO:0004137)","termid":"MONDO:0004137","xrefs":{"Monarch":{"xref_id":"0004137"}}}


id: PR:P87228
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A D-3-phosphoglycerate dehydrogenase SerA that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO04328"],"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":"D-3-phosphoglycerate dehydrogenase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC364.07","secondary_identifiers":["UniProtKB:P87228"],"synonyms":[{"name":"3-PGDH (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-serA","type":"exact"}],"termid":"PR:P87228"}


id: GO:0097687
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A horn-shaped dinoflagellate antapex found in thecate species.","definition_xrefs":["PMID:7002229","GOC:at"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dinoflagellate antapex","termid":"GO:0097684"}],"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":"dinoflagellate antapical horn","termid":"GO:0097687"}


id: PBO:0062529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily U member 9","termid":"PBO:0062529"}


id: PBO:0047200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 217 member A","termid":"PBO:0047200"}


id: GO:0097386
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A prolongation or process extending from a glial cell.","definition_xrefs":["GOC:mc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection","termid":"GO:0120025"}],"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":"glial cell projection","synonyms":[{"name":"glial process","type":"related"},{"name":"glial projection","type":"related"}],"termid":"GO:0097386"}


id: MONDO:0005521
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete shigellosis (obsolete MONDO:0005521)","termid":"MONDO:0005521","xrefs":{"Monarch":{"xref_id":"0005521"}}}


id: GO:0097728
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A motile cilium where the axoneme has a ring of nine outer microtubule doublets but no central microtubules (and is therefore called a 9+0 axoneme).","definition_xrefs":["GOC:cilia","PMID:10330409","PMID:22118931"],"direct_ancestors":[{"relation_name":"is_a","term_name":"motile cilium","termid":"GO:0031514"}],"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":"9+0 motile cilium","synonyms":[{"name":"motile 9+0 cilium","type":"exact"},{"name":"nodal cilium","type":"narrow"}],"termid":"GO:0097728"}


id: MONDO:0000912
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 14q12.","definition_xrefs":["DOID:0110507","PMID:8944017"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 5","secondary_identifiers":["UMLS:C1833319","OMIM:600792","MEDGEN:331485","GARD:22585","MESH:C563444"],"synonyms":[{"name":"DFNB5","type":"narrow"},{"name":"autosomal recessive deafness 5","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 5","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 5","type":"narrow"},{"name":"deafness, autosomal recessive 5","type":"narrow"},{"name":"neurosensory nonsyndromic recessive deafness 5","type":"narrow"}],"termid":"MONDO:0000912","xrefs":{"Monarch":{"xref_id":"0000912"}}}


id: PBO:0058240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR4527 host gene","termid":"PBO:0058240"}


id: FYPO:0006942
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of lipid binding by a gene product (usually a protein) in a mutant is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal molecular function","termid":"FYPO:0000706"},{"relation_name":"is_a","term_name":"binding phenotype","termid":"FYPO:0001092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000257"],"is_obsolete":false,"name":"normal lipid binding","termid":"FYPO:0006942"}


id: GO:0090515
data:
  {"annotated_genes":["SJAG_03256"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105765],"is_not":false,"summary":null,"term":"GO:0090515"}]},"cv_name":"biological_process","definition":"The directed movement of L-glutamate into the vacuole across the vacuolar membrane.","definition_xrefs":["GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-glutamate transmembrane transport","termid":"GO:0015813"},{"relation_name":"is_a","term_name":"glutamate transmembrane import into vacuole","termid":"GO:0090454"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03256":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179","GO:0055085"],"is_obsolete":false,"name":"L-glutamate transmembrane import into vacuole","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0090515","terms_by_termid":{"GO:0090515":null}}


id: MONDO:0013124
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"pelvic organ prolapse","termid":"MONDO:0000082"},{"relation_name":"excluded_subClassOf","term_name":"peeling skin syndrome","termid":"MONDO:0019347"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pelvic organ prolapse, susceptibility to, 2","secondary_identifiers":["OMIM:613088","MEDGEN:416523","UMLS:C2751314"],"synonyms":[{"name":"Pvop2","type":"related"},{"name":"pelvic organ prolapse, susceptibility to, 2","type":"exact"},{"name":"pelvic organ prolapse, susceptibility to, type 2","type":"exact"}],"termid":"MONDO:0013124","xrefs":{"Monarch":{"xref_id":"0013124"}}}


id: PBO:0054414
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 1810","termid":"PBO:0054414"}


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


id: PBO:0017809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vitamin H transmembrane transporter Vht1","termid":"PBO:0017809"}


id: MONDO:1012403
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"contractural arachnodactyly, non-human animal","termid":"MONDO:1011800"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"contractural arachnodactyly, cattle","secondary_identifiers":["OMIA:001511-9913"],"synonyms":[{"name":"Fawn calf syndrome","type":"exact"}],"termid":"MONDO:1012403","xrefs":{"Monarch":{"xref_id":"1012403"}}}


id: FYPO:0006628
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of phosphatidylinositol-4-phosphate measured in the plasma membrane is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased phosphatidylinositol phosphate level in plasma membrane","termid":"FYPO:0006222"},{"relation_name":"is_a","term_name":"decreased cellular phosphatidylinositol-4-phosphate level","termid":"FYPO:0006775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased phosphatidylinositol-4-phosphate level in plasma membrane","synonyms":[{"name":"decreased 1-phosphatidyl-1D-myo-inositol 4-phosphate level in plasma membrane","type":"exact"},{"name":"decreased phosphatidylinositol-4-phosphate level in cell membrane","type":"exact"},{"name":"decreased phosphatidylinositol-4-phosphate level in plasma membrane during mitotic cell cycle","type":"related"},{"name":"decreased phosphatidylinositol-4-phosphate level in plasma membrane during vegetative growth","type":"exact"},{"name":"decreased plasma membrane PI(5)P level","type":"exact"},{"name":"decreased plasma membrane phosphatidylinositol-4-phosphate level","type":"exact"},{"name":"reduced phosphatidylinositol-4-phosphate level in plasma membrane","type":"exact"}],"termid":"FYPO:0006628"}


id: PBO:0048682
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GLI family zinc finger 1","termid":"PBO:0048682"}


id: GO:0120227
data:
  {"annotated_genes":["SJAG_01458"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77692],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036042"}]},"cv_name":"molecular_function","definition":"Binding to an acyl-CoA, a thioester that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of any carboxylic acid.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide binding","termid":"GO:0033218"},{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"},{"relation_name":"is_a","term_name":"nucleoside phosphate binding","termid":"GO:1901265"},{"relation_name":"is_a","term_name":"heterocyclic compound binding","termid":"GO:1901363"},{"relation_name":"is_a","term_name":"sulfur compound binding","termid":"GO:1901681"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01458":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"acyl-CoA binding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"acyl binding","type":"broad"},{"name":"acyl-coenzyme A binding","type":"exact"}],"termid":"GO:0120227","terms_by_termid":{"GO:0036042":null}}


id: PBO:0043978
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CSAG family member 4 (pseudogene)","termid":"PBO:0043978"}


id: GO:0003676
data:
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id: GO:0042627
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A large lipoprotein particle (diameter 75-1200 nm) composed of a central core of triglycerides and cholesterol surrounded by a protein-phospholipid coating. The proteins include one molecule of apolipoprotein B-48 and may include a variety of apolipoproteins, including APOAs, APOCs and APOE. Chylomicrons are found in blood or lymph and carry lipids from the intestines into other body tissues.","definition_xrefs":["GOC:jl","PMID:10580165","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma lipoprotein particle","termid":"GO:0034358"}],"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:0005576"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005576"],"is_obsolete":false,"name":"chylomicron","secondary_identifiers":["Wikipedia:Chylomicron"],"termid":"GO:0042627"}


id: MONDO:0008873
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"microcephalic osteodysplastic primordial dwarfism","termid":"MONDO:0000060"},{"relation_name":"is_a","term_name":"microcephalic osteodysplastic primordial dwarfism types I and III","termid":"MONDO:0016994"},{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"microcephalic osteodysplastic primordial dwarfism, type 3","secondary_identifiers":["OMIM:210730","MEDGEN:349167","MESH:C537320","GARD:15145","UMLS:C1859439"],"synonyms":[{"name":"Mopd 3","type":"related"},{"name":"Mopd, Caroline Crachami type","type":"related"},{"name":"Mopd, Sicilian fairy type","type":"related"},{"name":"microcephalic osteodysplastic primordial dwarfism, Caroline Crachami type","type":"related"},{"name":"microcephalic osteodysplastic primordial dwarfism, Sicilian fairy type","type":"related"},{"name":"microcephalic osteodysplastic primordial dwarfism, type III","type":"related"},{"name":"osteodysplastic primordial dwarfism, type 3","type":"related"}],"termid":"MONDO:0008873","xrefs":{"Monarch":{"xref_id":"0008873"}}}


id: GO:0072245
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a metanephric glomerular parietal epithelial cell. Metanephric glomerular parietal epithelial cells are specialized epithelial cells that form tight junctions as a barrier to protein transport.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerular parietal epithelial cell differentiation","termid":"GO:0072139"},{"relation_name":"is_a","term_name":"metanephric glomerular epithelial cell differentiation","termid":"GO:0072312"}],"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":"metanephric glomerular parietal epithelial cell differentiation","termid":"GO:0072245"}


id: FYPO:0005566
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a new growth zone forms along the lateral portion of the cell (often in the middle) before septation, such that a single cell grows in the form of the letter T. Cell length is normal.","definition_xrefs":["PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell shape","termid":"FYPO:0001126"},{"relation_name":"output_of","term_name":"abnormal cell polarity","termid":"FYPO:0005568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005568"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0005568","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"T-shaped cell","synonyms":[{"name":"cell morphology, T shaped","type":"exact"}],"termid":"FYPO:0005566"}


id: FYPO:0000043
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 glucan biosynthesis is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process phenotype during vegetative growth","termid":"FYPO:0001331"},{"relation_name":"is_a","term_name":"abnormal glucan synthesis","termid":"FYPO:0007904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abnormal glucan synthesis during vegetative growth","synonyms":[{"name":"abnormal glucan synthesis during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000043"}


id: PBO:0109611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glioma stem cell association long noncoding RNA","termid":"PBO:0109611"}


id: PBO:0041901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CBARP divergent transcript","termid":"PBO:0041901"}


id: PR:O13674
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug24 gene.","definition_xrefs":["UniProtKB:O13674","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 24 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC74.09","synonyms":[{"name":"Spom972h-mug24","type":"exact"}],"termid":"PR:O13674"}


id: GO:0055038
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a recycling endosome.","definition_xrefs":["PMID:16246101","PMID:15601896","GOC:jid","GOC:rph","PMID:10930469"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endosome membrane","termid":"GO:0010008"},{"relation_name":"part_of","term_name":"recycling endosome","termid":"GO:0055037"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005768"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005768","GO:0005737","GO:0031410"],"is_obsolete":false,"name":"recycling endosome membrane","termid":"GO:0055038"}


id: GO:0097105
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a presynaptic membrane, including any proteins associated with the membrane, but excluding other cellular components. A presynaptic membrane is a specialized area of membrane of the axon terminal that faces the plasma membrane of the neuron or muscle fiber with which the axon terminal establishes a synaptic junction.","definition_xrefs":["PMID:15797875","GOC:sjp","GOC:BHF","PMID:18550748","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane assembly","termid":"GO:0071709"},{"relation_name":"is_a","term_name":"presynaptic membrane organization","termid":"GO:0097090"},{"relation_name":"part_of","term_name":"presynapse assembly","termid":"GO:0099054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0061024","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"presynaptic membrane assembly","synonyms":[{"name":"pre-synaptic membrane assembly","type":"exact"}],"termid":"GO:0097105"}


id: PBO:0039822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor guanine nucleotide exchange factor 2","termid":"PBO:0039822"}


id: PBO:0063501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate dehydrogenase phosphatase catalytic subunit 2","termid":"PBO:0063501"}


id: GO:0042618
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving poly-hydroxybutyrate (PHB), a polymer of beta-hydroxybutyrate and a common storage material of prokaryotic cells.","definition_xrefs":["GOC:jl","PMID:18640095"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poly(hydroxyalkanoate) metabolic process","termid":"GO:1901440"}],"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":"poly-hydroxybutyrate metabolic process","synonyms":[{"name":"PHB metabolic process","type":"exact"},{"name":"PHB metabolism","type":"exact"},{"name":"poly-hydroxybutyrate metabolism","type":"exact"}],"termid":"GO:0042618"}


id: GO:1903641
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of gastrin-induced gastric acid secretion.","definition_xrefs":["PMID:11123201","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of gastric acid secretion","termid":"GO:0060454"},{"relation_name":"is_a","term_name":"regulation of gastrin-induced gastric acid secretion","termid":"GO:1903639"},{"relation_name":"positively_regulates","term_name":"gastrin-induced gastric acid secretion","termid":"GO:0001698"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of gastrin-induced gastric acid secretion","synonyms":[{"name":"activation of gastrin-induced gastric acid secretion","type":"narrow"},{"name":"up regulation of gastrin-induced gastric acid secretion","type":"exact"},{"name":"up-regulation of gastrin-induced gastric acid secretion","type":"exact"},{"name":"upregulation of gastrin-induced gastric acid secretion","type":"exact"}],"termid":"GO:1903641"}


id: GO:1900587
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of arugosin.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary metabolite biosynthetic process","termid":"GO:0044550"},{"relation_name":"is_a","term_name":"arugosin metabolic process","termid":"GO:1900585"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"arugosin biosynthetic process","synonyms":[{"name":"arugosin anabolism","type":"exact"},{"name":"arugosin biosynthesis","type":"exact"},{"name":"arugosin formation","type":"exact"},{"name":"arugosin synthesis","type":"exact"}],"termid":"GO:1900587"}


id: PBO:0067920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 222","termid":"PBO:0067920"}


id: GO:0034618
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to 2-amino-5-(carbamimidamido)pentanoic acid.","definition_xrefs":["GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid binding","termid":"GO:0016597"},{"relation_name":"is_a","term_name":"carboxylic acid binding","termid":"GO:0031406"},{"relation_name":"is_a","term_name":"cation binding","termid":"GO:0043169"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"arginine binding","synonyms":[{"name":"Arg binding","type":"exact"},{"name":"aminopentanoic acid binding","type":"related"}],"termid":"GO:0034618"}


id: MOD:00196
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-cysteine residue and a glycine residue to form L-cysteine 5-imidazolinone glycine.","definition_xrefs":["RESID:AA0188","PubMed:1537807"],"direct_ancestors":[{"relation_name":"is_a","term_name":"5-imidazolinone ring crosslinked residues (Gly)","termid":"MOD:01882"},{"relation_name":"is_a","term_name":"crosslinked L-cysteine residue","termid":"MOD:02044"},{"relation_name":"is_a","term_name":"crosslinked glycine residue","termid":"MOD:02047"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"L-cysteine 5-imidazolinone glycine","synonyms":[{"name":"(2-[(1R)-1-amino-2-sulfanylethyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl)acetic acid","type":"exact"},{"name":"2-[1-amino-2-sulfanylethyl]-1-carboxymethyl-1-imidazolin-5-one","type":"exact"},{"name":"4-methylidene-imidazole-5-one (MIO) active site","type":"exact"},{"name":"CROSSLNK 5-imidazolinone (Cys-Gly)","type":"exact"},{"name":"L-cysteine 5-imidazolinone glycine","type":"exact"},{"name":"XLNK-1Cys-NGly(Imidazole)","type":"exact"},{"name":"cysteinyl-5-imidazolinone glycine","type":"exact"},{"name":"para-hydroxybenzylidene-imidazolidinone chromophore","type":"exact"}],"termid":"MOD:00196"}


id: PBO:0070701
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L9 pseudogene 5","termid":"PBO:0070701"}


id: GO:0071390
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 ecdysone stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to ecdysone","termid":"GO:0035075"},{"relation_name":"is_a","term_name":"cellular response to sterol","termid":"GO:0036315"},{"relation_name":"is_a","term_name":"cellular response to alcohol","termid":"GO:0097306"},{"relation_name":"is_a","term_name":"cellular response to ketone","termid":"GO:1901655"}],"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 ecdysone","termid":"GO:0071390"}


id: MONDO:0008255
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":"platelet factor 3 deficiency","secondary_identifiers":["MEDGEN:356931","OMIM:173450","MESH:C566798","UMLS:C1868256"],"synonyms":[{"name":"platelet factor 3 deficiency","type":"exact"}],"termid":"MONDO:0008255","xrefs":{"Monarch":{"xref_id":"0008255"}}}


id: PBO:0110481
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 3124","termid":"PBO:0110481"}


id: MONDO:0007175
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":"PR interval, variation in","secondary_identifiers":["MEDGEN:463601","OMIM:108980","UMLS:C3152251"],"synonyms":[{"name":"Atrioventricular conduction time, variation in","type":"related"},{"name":"PR interval, variation in","type":"exact"},{"name":"PR interval, variation type in","type":"exact"}],"termid":"MONDO:0007175","xrefs":{"Monarch":{"xref_id":"0007175"}}}


id: PBO:0040856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bridge-like lipid transfer protein family member 2","termid":"PBO:0040856"}


id: PBO:0083770
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential, non-ATPase regulatory subunit of the 26S proteasome lid; required for the assembly and activity of the 26S proteasome; the human homolog (S9 protein) partially rescues Rpn6p depletion; protein abundance increases in response to DNA replication stress","termid":"PBO:0083770"}


id: PBO:0005382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase activating protein Gyp2 (predicted)","termid":"PBO:0005382"}


id: PBO:0072953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"saccharopine dehydrogenase (putative)","termid":"PBO:0072953"}


id: MONDO:1012157
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Megaesophagus that occurs in llama.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"megaesophagus, non-human animal","termid":"MONDO:1011660"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"megaesophagus, llama","secondary_identifiers":["OMIA:000631-9844"],"termid":"MONDO:1012157","xrefs":{"Monarch":{"xref_id":"1012157"}}}


id: MONDO:0024552
data:
  {"annotated_genes":["SJAG_04008","SJAG_03199"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87782,87783],"is_not":false,"summary":null,"term":"MONDO:0024552"}]},"cv_name":"mondo","definition":"Any microphthalmia with linear skin defects syndrome in which the cause of the disease is a mutation in the HCCS gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"linear skin defects with multiple congenital anomalies","termid":"MONDO:0010672"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03199":null,"SJAG_04008":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005328"],"is_obsolete":false,"name":"linear skin defects with multiple congenital anomalies 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0796070","MEDGEN:163210","DOID:0111808","OMIM:309801"],"synonyms":[{"name":"HCCS microphthalmia with linear skin defects syndrome","type":"exact"},{"name":"LSDMCA1","type":"related"},{"name":"Midas syndrome","type":"related"},{"name":"linear skin defects with multiple congenital anomalies 1","type":"exact"},{"name":"linear skin defects with multiple congenital anomalies 1, X-linked dominant","type":"exact"},{"name":"microphthalmia with linear skin defects","type":"related"},{"name":"microphthalmia with linear skin defects syndrome caused by mutation in HCCS","type":"exact"},{"name":"microphthalmia, dermal aplasia, and sclerocornea","type":"related"},{"name":"microphthalmia, syndromic 7","type":"related"}],"termid":"MONDO:0024552","terms_by_termid":{"MONDO:0024552":null},"xrefs":{"Monarch":{"xref_id":"0024552"}}}


id: GO:0032704
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of interleukin-20 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine production","termid":"GO:0001818"},{"relation_name":"is_a","term_name":"regulation of interleukin-20 production","termid":"GO:0032664"},{"relation_name":"negatively_regulates","term_name":"interleukin-20 production","termid":"GO:0032624"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of interleukin-20 production","secondary_identifiers":["GO:0045388"],"synonyms":[{"name":"down regulation of interleukin-20 production","type":"exact"},{"name":"down-regulation of interleukin-20 production","type":"exact"},{"name":"downregulation of interleukin-20 production","type":"exact"},{"name":"inhibition of interleukin-20 production","type":"narrow"},{"name":"negative regulation of IL-20 production","type":"exact"},{"name":"negative regulation of interleukin-20 biosynthetic process","type":"narrow"}],"termid":"GO:0032704"}


id: GO:0050201
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-fucose + ATP = beta-L-fucose 1-phosphate + ADP + 2 H+.","definition_xrefs":["EC:2.7.1.52","RHEA:13241"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"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:0016301"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0016301","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"fucokinase activity","secondary_identifiers":["Reactome:R-HSA-6787540","MetaCyc:FUCOKINASE-RXN","KEGG_REACTION:R03161"],"synonyms":[{"name":"ATP:6-deoxy-L-galactose 1-phosphotransferase activity","type":"related"},{"name":"ATP:beta-L-fucose 1-phosphotransferase activity","type":"related"},{"name":"L-fucokinase activity","type":"related"},{"name":"L-fucose kinase activity","type":"related"},{"name":"fucokinase (phosphorylating) activity","type":"related"},{"name":"fucose kinase activity","type":"related"}],"termid":"GO:0050201"}


