# terms

id: PBO:0069435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 700, pseudogene","termid":"PBO:0069435"}


id: PBO:0005219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L12.1/L12A","termid":"PBO:0005219"}


id: GO:0097477
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a lateral motor column neuron from one site to another. A lateral motor column neuron is a motor neuron that is generated only on limb levels and send axons into the limb mesenchyme.","definition_xrefs":["PMID:20711475","GOC:yaf","CL:0011002"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spinal cord motor neuron migration","termid":"GO:0097476"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lateral motor column neuron migration","termid":"GO:0097477"}


id: MONDO:0800375
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"DEND syndrome","termid":"MONDO:0019207"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005015"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005015","MONDO:0019254","MONDO:0004335","MONDO:0037792"],"is_obsolete":false,"name":"developmental delay, epilepsy, and neonatal diabetes 1","secondary_identifiers":["UMLS:C5394597","MEDGEN:1709191"],"synonyms":[{"name":"DEND1","type":"exact"}],"termid":"MONDO:0800375","xrefs":{"Monarch":{"xref_id":"0800375"}}}


id: PBO:0052863
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 5-6","termid":"PBO:0052863"}


id: PBO:0002076
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heavy metal ion homeostasis protein (predicted)","termid":"PBO:0002076"}


id: MONDO:0033115
data:
  {"annotated_genes":["SJAG_00059"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84953],"is_not":false,"summary":null,"term":"MONDO:0033115"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive cerebellar ataxia","termid":"MONDO:0015244"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00059":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"spinocerebellar ataxia, autosomal recessive 25","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:617584","DOID:0080259","UMLS:C4539808","MEDGEN:1618081"],"synonyms":[{"name":"SCAR25","type":"related"},{"name":"autosomal recessive spinocerebellar ataxia 25","type":"related"},{"name":"spinocerebellar ataxia, autosomal recessive 25","type":"exact"}],"termid":"MONDO:0033115","terms_by_termid":{"MONDO:0033115":null},"xrefs":{"Monarch":{"xref_id":"0033115"}}}


id: PBO:0045046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DKKL1 pseudogene 1","termid":"PBO:0045046"}


id: PATO:0001828
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A biological sex quality inhering in an individual or a population by virtue of having internal reproductive organs of male and external sexual characteristics of female.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pseudohermaphrodite","termid":"PATO:0001827"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"male pseudohermaphrodite","termid":"PATO:0001828"}


id: GO:0018631
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-phenylacetate + O2 + reduced [NADPH--hemoprotein reductase] = (2-hydroxyphenyl)acetate + H+ + H2O + oxidized [NADPH--hemoprotein reductase].","definition_xrefs":["RHEA:53392"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO: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":"phenylacetate 2-hydroxylase activity","secondary_identifiers":["UM-BBD_reactionID:r0036","EC:1.14.14.54"],"synonyms":[{"name":"phenylacetate hydroxylase activity","type":"exact"}],"termid":"GO:0018631"}


id: MOD:00015
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a source amino acid residue to an L-glutamic acid.","definition_xrefs":["PubMed:4922541","DeltaMass:0","RESID:AA0006","ChEBI:29972","PubMed:1881881","PubMed:957425","PubMed:9326660","PubMed:4565668","PubMed:6692818"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified residue that can arise from different natural residues","termid":"MOD:00859"},{"relation_name":"is_a","term_name":"natural, standard, encoded residue","termid":"MOD:01441"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-glutamic acid residue","synonyms":[{"name":"(2S)-2-aminopentanedioic acid","type":"exact"},{"name":"1-aminopropane-1,3-dicarboxylic acid","type":"exact"},{"name":"2-aminoglutaric acid","type":"exact"},{"name":"2-azanylpentanedioic acid","type":"exact"},{"name":"Glu","type":"exact"},{"name":"L-glutamic acid","type":"exact"},{"name":"alpha-aminoglutaric acid","type":"exact"},{"name":"glutaminic acid","type":"exact"}],"termid":"MOD:00015"}


id: MONDO:0015601
data:
  {"annotated_genes":["SJAG_05239"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85446],"is_not":false,"summary":null,"term":"MONDO:0015601"}]},"cv_name":"mondo","definition":"X-linked intellectual deficit, Van Esch type is characterized by mild to moderate intellectual deficit associated with low birth weight, short stature, microcephaly and variable hypergonadotropic hypogonadism.","definition_xrefs":["Orphanet:163976"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05239":null},"genotype_count":0,"is_obsolete":false,"name":"X-linked intellectual disability, van Esch type","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:301030","DOID:0111840","UMLS:C4305072","SCTID:718914002","GARD:17008","MEDGEN:930741"],"synonyms":[{"name":"VEODS","type":"exact"},{"name":"Van Esch-O'Driscoll syndrome","type":"exact"},{"name":"Van Esch-O'Driscoll syndrome, X-linked recessive","type":"exact"},{"name":"mental retardation, X-Linked, syndromic, Van Esch-O'Driscoll type","type":"exact"}],"termid":"MONDO:0015601","terms_by_termid":{"MONDO:0015601":null},"xrefs":{"Monarch":{"xref_id":"0015601"}}}


id: PBO:0028972
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_plasma_membrane","termid":"PBO:0028972"}


id: PBO:0089932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial RNA-binding protein","termid":"PBO:0089932"}


id: PBO:0081787
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 714","termid":"PBO:0081787"}


id: PBO:0027161
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_meiotic_spindle_pole_body_during_meiosis_I","termid":"PBO:0027161"}


id: PBO:0074067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 42","termid":"PBO:0074067"}


id: PBO:0089869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF1754 family, human FAM32A homolog, implicated in mRNA splicing","termid":"PBO:0089869"}


id: GO:0140767
data:
  {"annotated_genes":["SJAG_02651","SJAG_03651","SJAG_02162","SJAG_00262","SJAG_00656","SJAG_03218","SJAG_02822","SJAG_00192","SJAG_01022","SJAG_04035","SJAG_00651","SJAG_00117","SJAG_01617","SJAG_02753","SJAG_03535","SJAG_01392","SJAG_01068"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[101250,117955],"is_not":false,"summary":null,"term":"GO:0140767"},{"annotations":[99134,104344,106697,116195,97273,108550,97964,106677,100963,95045,115092,115241,104069,110483,116297],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990756"}]},"cv_name":"molecular_function","definition":"An adaptor that brings together an enzyme and its substrate. Adaptors recruit the substrate to its enzyme, thus contributing to substrate selection and specificity.","definition_xrefs":["PMID:34358446","PMID:16250895"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-macromolecule adaptor activity","termid":"GO:0030674"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00117":null,"SJAG_00192":null,"SJAG_00262":null,"SJAG_00651":null,"SJAG_00656":null,"SJAG_01022":null,"SJAG_01068":null,"SJAG_01392":null,"SJAG_01617":null,"SJAG_02162":null,"SJAG_02651":null,"SJAG_02753":null,"SJAG_02822":null,"SJAG_03218":null,"SJAG_03535":null,"SJAG_03651":null,"SJAG_04035":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0030674","GO:0060090","GO:0003674"],"is_obsolete":false,"name":"enzyme-substrate adaptor activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-202137"],"synonyms":[{"name":"protein substrate chaperone activity","type":"related"},{"name":"protein-substrate adaptor activity","type":"broad"}],"termid":"GO:0140767","terms_by_termid":{"GO:0140767":null,"GO:1990756":null}}


id: GO:0010086
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the embryonic root are generated and organized.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"root morphogenesis","termid":"GO:0010015"},{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"}],"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":"embryonic root morphogenesis","termid":"GO:0010086"}


id: MONDO:0859141
data:
  {"annotated_genes":["SJAG_03938"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86039],"is_not":false,"summary":null,"term":"MONDO:0859141"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurodevelopmental disorder","termid":"MONDO:0700092"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03938":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 dysmorphic facies and cerebellar hypoplasia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1786150","UMLS:C5543332","OMIM:619306","GARD:18545"],"termid":"MONDO:0859141","terms_by_termid":{"MONDO:0859141":null},"xrefs":{"Monarch":{"xref_id":"0859141"}}}


id: PBO:0078417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gly (anticodon GCC) 1-3","termid":"PBO:0078417"}


id: FYPO:0004902
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is elongated, has more than one septum and more than one nucleus, and is curved along the long axis.","definition_xrefs":["PomBase:mah","PMID:25530312"],"direct_ancestors":[{"relation_name":"is_a","term_name":"elongated multinucleate vegetative cell","termid":"FYPO:0000133"},{"relation_name":"is_a","term_name":"elongated multiseptate vegetative cell","termid":"FYPO:0000223"},{"relation_name":"is_a","term_name":"multinucleate multiseptate vegetative cell","termid":"FYPO:0001252"},{"relation_name":"is_a","term_name":"curved elongated vegetative cell","termid":"FYPO:0005103"}],"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":"has_part","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000631","FYPO:0000005","FYPO:0000032","FYPO:0000002"],"is_obsolete":false,"name":"curved, elongated, multinucleate multiseptate vegetative cell","synonyms":[{"name":"curved, elongated, multinucleate multiseptate cell during vegetative growth","type":"exact"},{"name":"curved, elongated, multinucleate multiseptate vegetative cell during mitotic cell cycle","type":"related"},{"name":"curved, long, multinucleate multiseptate cell","type":"exact"}],"termid":"FYPO:0004902"}


id: GO:0001527
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Extracellular matrix components occurring independently or along with elastin. Thought to have force-bearing functions in tendon. In addition to fibrillins, microfibrils may contain other associated proteins.","definition_xrefs":["PMID:27026396"],"direct_ancestors":[{"relation_name":"is_a","term_name":"supramolecular fiber","termid":"GO:0099512"},{"relation_name":"part_of","term_name":"extracellular matrix","termid":"GO:0031012"}],"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":"microfibril","synonyms":[{"name":"extended fibrils","type":"exact"},{"name":"fibrillin","type":"related"}],"termid":"GO:0001527"}


id: PBO:0078021
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 11","termid":"PBO:0078021"}


id: GO:0009717
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of isoflavonoids, a group of water-soluble phenolic derivatives, isomeric with flavonoids.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenylpropanoid biosynthetic process","termid":"GO:0009699"},{"relation_name":"is_a","term_name":"isoflavonoid metabolic process","termid":"GO:0046287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"isoflavonoid biosynthetic process","synonyms":[{"name":"isoflavonoid anabolism","type":"exact"},{"name":"isoflavonoid biosynthesis","type":"exact"},{"name":"isoflavonoid formation","type":"exact"},{"name":"isoflavonoid synthesis","type":"exact"}],"termid":"GO:0009717"}


id: PBO:0087418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit 8 of the F0 sector of mitochondrial F1F0 ATP synthase; encoded on the mitochondrial genome; ATP8 and ATP6 mRNAs are not translated in the absence of the F1 sector of ATPase","termid":"PBO:0087418"}


id: MONDO:0002700
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete epithelioid trophoblastic tumor (obsolete MONDO:0002700)","termid":"MONDO:0002700","xrefs":{"Monarch":{"xref_id":"0002700"}}}


id: GO:0140017
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A histone reader that recognizes a histone H3 crotonylated at lysine 18.","definition_xrefs":["PMID:27105114"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3 reader activity","termid":"GO:0140006"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0140566"},{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0060090","GO:0003674","GO:0030674","GO:0140566"],"is_obsolete":false,"name":"histone H3K18cr reader activity","synonyms":[{"name":"H3K18cr modified histone binding","type":"narrow"}],"termid":"GO:0140017"}


id: MOD:00869
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-aspartic acid residue to L-alanine.","definition_xrefs":["PubMed:17138938","RESID:AA0001#ASP"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-alanine residue","termid":"MOD:00010"},{"relation_name":"is_a","term_name":"modified L-aspartic acid residue","termid":"MOD:00904"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-alanine residue (Asp)","synonyms":[{"name":"(2S)-2-aminopropanoic acid","type":"exact"},{"name":"2-aminopropionic acid","type":"exact"},{"name":"2-azanylpropanoic acid","type":"exact"},{"name":"Asp(Ala)","type":"exact"},{"name":"L-alanine","type":"exact"},{"name":"MOD_RES Beta-decarboxylated aspartate","type":"exact"},{"name":"alpha-alanine","type":"exact"},{"name":"alpha-aminopropionic acid","type":"exact"}],"termid":"MOD:00869"}


id: MONDO:0016914
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of chromosome 16","termid":"MONDO:0016878"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of the long arm of chromosome 16","secondary_identifiers":["UMLS:C4736186","icd11.foundation:324314539","MEDGEN:1790033","GARD:20835","Orphanet:262128"],"synonyms":[{"name":"partial deletion of chromosome 16q","type":"exact"},{"name":"partial deletion of the long arm of chromosome type 16","type":"exact"},{"name":"partial monosomy of chromosome 16q","type":"exact"},{"name":"partial monosomy of the long arm of chromosome 16","type":"exact"}],"termid":"MONDO:0016914","xrefs":{"Monarch":{"xref_id":"0016914"}}}


id: MONDO:0005702
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A subcutaneous mycosis that is a chronic subcutaneous fungal infection, which presents as nodular or verrucoid, ulcerated, or crusted skin lesions on exposed areas of skin caused by Fonsecaea pedrosoi, Fonsecaea compacta, Cladophialophora carrionii or Phialophora verrucosa. Histological examination reveals muriform cells (with perpendicular septations) or thick walled, dark-colored, rounded forms (copper pennies) that are characteristic of this infection.","definition_xrefs":["EFO:0007207"],"gene_count":0,"genotype_count":0,"name":"obsolete chromoblastomycosis (obsolete MONDO:0005702)","termid":"MONDO:0005702","xrefs":{"Monarch":{"xref_id":"0005702"}}}


id: MONDO:0017997
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Telecanthus-hypertelorism-strabismus-pes cavus syndrome is characterized by telecanthus, hypertelorism, strabismus, pes cavus and other variable anomalies. It has been described in a father and his son. The son also had hypospadias, bilateral inguinal hernia, clinodactyly and camptodactyly of the fingers, and radiographic findings including flared metaphyses of the long bones and osteopenia.","definition_xrefs":["Orphanet:3293"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"telecanthus-hypertelorism-strabismus-pes cavus syndrome","secondary_identifiers":["GARD:18791"],"termid":"MONDO:0017997","xrefs":{"Monarch":{"xref_id":"0017997"}}}


id: PR:O43120
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- uap2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O43120"],"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":"splicing factor U2AF-associated protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1289.02c","synonyms":[{"name":"Spom972h-uap2","type":"exact"},{"name":"cold sensitive U2 snRNA suppressor 2 homolog (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O43120"}


id: PBO:0059448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Myb/SANT DNA binding domain containing 2","termid":"PBO:0059448"}


id: GO:1905888
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cellular response to very-low-density lipoprotein particle stimulus.","definition_xrefs":["GOC:aruk","GOC:bc","GOC:TermGenie","PMID:7592957","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of cellular response to very-low-density lipoprotein particle stimulus","termid":"GO:1905890"},{"relation_name":"negatively_regulates","term_name":"cellular response to very-low-density lipoprotein particle stimulus","termid":"GO:0090731"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of cellular response to very-low-density lipoprotein particle stimulus","synonyms":[{"name":"down regulation of cellular response to VLDL particle stimulus","type":"exact"},{"name":"down regulation of cellular response to very-low-density lipoprotein particle stimulus","type":"exact"},{"name":"down-regulation of cellular response to VLDL particle stimulus","type":"exact"},{"name":"down-regulation of cellular response to very-low-density lipoprotein particle stimulus","type":"exact"},{"name":"downregulation of cellular response to VLDL particle stimulus","type":"exact"},{"name":"downregulation of cellular response to very-low-density lipoprotein particle stimulus","type":"exact"},{"name":"inhibition of cellular response to VLDL particle stimulus","type":"narrow"},{"name":"inhibition of cellular response to very-low-density lipoprotein particle stimulus","type":"narrow"},{"name":"negative regulation of cellular response to VLDL particle stimulus","type":"exact"}],"termid":"GO:1905888"}


id: MONDO:0019522
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Recessive dystrophic epidermolysis bullosa (RDEB)-generalized other, also known as RDEB non-Hallopeau-Siemens type, is a subtype of DEB characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities.","definition_xrefs":["Orphanet:89842"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermolysis bullosa dystrophica","termid":"MONDO:0006543"}],"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":"recessive dystrophic epidermolysis bullosa-generalized other","secondary_identifiers":["MEDGEN:1392226","GARD:12794","UMLS:C4511044"],"synonyms":[{"name":"RDEB generalisata mitis","type":"exact"},{"name":"RDEB, generalised intermediate","type":"exact"},{"name":"RDEB, generalized intermediate","type":"exact"},{"name":"RDEB, non-Hallopeau-Siemens type","type":"exact"},{"name":"RDEB-O","type":"exact"},{"name":"RDEB-generalized other","type":"exact"},{"name":"autosomal recessive dystrophic epidermolysis bullosa generalisata mitis","type":"exact"},{"name":"autosomal recessive dystrophic epidermolysis bullosa, generalised other","type":"exact"},{"name":"autosomal recessive dystrophic epidermolysis bullosa, generalized other","type":"exact"},{"name":"generalised mitis RDEB","type":"exact"},{"name":"generalized mitis RDEB","type":"exact"},{"name":"recessive dystrophic epidermolysis bullosa, generalised intermediate","type":"related"},{"name":"recessive dystrophic epidermolysis bullosa, generalized intermediate","type":"related"},{"name":"recessive dystrophic epidermolysis bullosa, non-Hallopeau-Siemens type","type":"exact"}],"termid":"MONDO:0019522","xrefs":{"Monarch":{"xref_id":"0019522"}}}


id: GO:0038027
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by apolipoprotein A-I binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:bf","GOC:signaling","PMID:16443932"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell surface receptor signaling pathway","termid":"GO:0007166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"apolipoprotein A-I-mediated signaling pathway","synonyms":[{"name":"apolipoprotein A-I-mediated signalling pathway","type":"exact"}],"termid":"GO:0038027"}


id: PBO:0084524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of the ChAPs family (Chs5p-Arf1p-binding proteins); members include Bch1p, Bch2p, Bud7p, and Chs6p; ChAPs family proteins form the exomer complex with Chs5p to mediate export of specific cargo proteins, including Chs3p, from the Golgi to the plasma membrane; BUD7 has a paralog, BCH1, that arose from the whole genome duplication","termid":"PBO:0084524"}


id: GO:0052612
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: adonirubin + a reduced electron acceptor + oxygen = 3S,3'S-astaxanthin + an oxidized electron acceptor + H2O.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete adonirubin 3-hydroxylase activity (obsolete GO:0052612)","synonyms":[{"name":"beta-carotene hydroxylase activity","type":"broad"},{"name":"carotene beta-ring hydroxylase activity","type":"broad"}],"termid":"GO:0052612"}


id: PBO:0059096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mortality factor 4 like 1 pseudogene 2","termid":"PBO:0059096"}


id: MONDO:0021208
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"alopecia","termid":"MONDO:0004907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endocrine alopecia","secondary_identifiers":["SCTID:54539003","UMLS:C0002176","ICD9:704.09","MEDGEN:507423"],"termid":"MONDO:0021208","xrefs":{"Monarch":{"xref_id":"0021208"}}}


id: PBO:0041755
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclase associated actin cytoskeleton regulatory protein 1","termid":"PBO:0041755"}


id: PBO:0049910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hexosaminidase subunit beta","termid":"PBO:0049910"}


id: PBO:0087951
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Translation initiation factor eIF5; functions as both a GTPase-activating protein (GAP) that stimulates the hydrolysis of GTP bound to eIF-2, as part of the 43S preinitiation complex, and as a GDP dissociation inhibitor (GDI) to prevent recycling of eIF2; human ortholog eIF5 complements the yeast null mutant","termid":"PBO:0087951"}


id: PBO:0084446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mannitol dehydrogenase; deletion suppresses mutation of mpt5; DSF1 has a paralog, MAN2, that arose from a segmental duplication","termid":"PBO:0084446"}


id: MONDO:1010127
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dermatomyositis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polymyositis, non-human animal","termid":"MONDO:1010203"},{"relation_name":"is_a","term_name":"connective tissue disorder, non-human animal","termid":"MONDO:1011309"},{"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":"dermatomyositis, non-human animal","secondary_identifiers":["OMIA:000270"],"termid":"MONDO:1010127","xrefs":{"Monarch":{"xref_id":"1010127"}}}


id: MONDO:0800130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoinflammatory syndrome characterized by onset of various autoimmune features usually in the first decades of life, although later onset has been reported. Typical features include autoimmune cytopenia, hemolytic anemia, thrombocytopenia, and lymphadenopathy. More variable features may include autoimmune thyroiditis, psoriasis or eczema, nephritis, hepatitis, and symptoms of systemic lupus erythematosus (SL). Some patients may have recurrent infections or exacerbation of the disease with acute infection. Laboratory studies show variable findings, often decreased numbers of naive B cells, lymphopenia with skewed subsets, hypogammaglobulinemia, presence of autoantibodies, and a hyperinflammatory state. The disorder shows autosomal dominant inheritance with incomplete penetrance.","definition_xrefs":["OMIM:619375"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoinflammatory syndrome","termid":"MONDO:0019751"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autoinflammatory syndrome with immunodeficiency","secondary_identifiers":["UMLS:C5543547","MEDGEN:1784363"],"termid":"MONDO:0800130","xrefs":{"Monarch":{"xref_id":"0800130"}}}


id: PBO:0063546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"platelet and endothelial cell adhesion molecule 1","termid":"PBO:0063546"}


id: PBO:0067459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 584, pseudogene","termid":"PBO:0067459"}


id: PBO:0063249
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin alpha 14 pseudogene","termid":"PBO:0063249"}


id: PBO:0060079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 26","termid":"PBO:0060079"}


id: GO:0014741
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of muscle hypertrophy.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle hypertrophy","termid":"GO:0014743"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"muscle hypertrophy","termid":"GO:0014896"}],"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 muscle hypertrophy","termid":"GO:0014741"}


id: PBO:0000345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNARE","termid":"PBO:0000345"}


id: GO:0003701
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Functions to initiate or regulate RNA polymerase I transcription.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete RNA polymerase I transcription factor activity (obsolete GO:0003701)","synonyms":[{"name":"RNA polymerase I transcription factor activity","type":"exact"}],"termid":"GO:0003701"}


id: SO:0000952
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An origin of vegetative replication in plasmids and phages.","definition_xrefs":["SO:as"],"direct_ancestors":[{"relation_name":"is_a","term_name":"origin_of_replication","termid":"SO:0000296"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oriV","synonyms":[{"name":"origin of vegetative replication","type":"exact"}],"termid":"SO:0000952"}


id: GO:0090401
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A cellular senescence process associated with the dismantling of a cell as a response to viral infection.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete viral-induced premature senescence (obsolete GO:0090401)","termid":"GO:0090401"}


id: PBO:0084108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HDEL receptor; an integral membrane protein that binds to the HDEL motif in proteins destined for retention in the endoplasmic reticulum; has a role in maintenance of normal levels of ER-resident proteins","termid":"PBO:0084108"}


id: PBO:0067200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 265, pseudogene","termid":"PBO:0067200"}


id: PBO:0030652
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cell_cycle_arrest_in_mitotic_G2_phase_during_starvation","termid":"PBO:0030652"}


id: PR:C6Y4B7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC227.19c gene.","definition_xrefs":["UniProtKB:C6Y4B7","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C227.19c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC227.19c","synonyms":[{"name":"Spom972h-SPAC227.19c","type":"exact"}],"termid":"PR:C6Y4B7"}


id: PBO:0039717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apolipoprotein B mRNA editing enzyme catalytic subunit 3A","termid":"PBO:0039717"}


id: PBO:0076677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation factor A1 pseudogene 2","termid":"PBO:0076677"}


id: GO:0060932
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized structural and/or functional features of a cell of the His-Purkinje system. These cells form the fibers regulate cardiac muscle contraction in the ventricles.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac muscle cell differentiation","termid":"GO:0055007"},{"relation_name":"part_of","term_name":"His-Purkinje system development","termid":"GO:0003164"}],"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":"His-Purkinje system cell differentiation","termid":"GO:0060932"}


id: PBO:0036100
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_biotinylation_during_vegetative_growth","termid":"PBO:0036100"}


id: GO:0004489
data:
  {"annotated_genes":["SJAG_01466","SJAG_03712"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[96146,97915],"is_not":false,"summary":null,"term":"GO:0004489"},{"annotations":[97916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106312"},{"annotations":[96147,97917],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106313"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-methyltetrahydrofolate + NAD(P)+ = 5,10-methylenetetrahydrofolate + NAD(P)H + H+.","definition_xrefs":["EC:1.5.1.20","PMID:26872964"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor","termid":"GO:0016646"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01466":null,"SJAG_03712":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"methylenetetrahydrofolate reductase (NAD(P)H) activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R07168","Reactome:R-HSA-200676","GO:0008702","KEGG_REACTION:R01224","MetaCyc:1.5.1.20-RXN"],"synonyms":[{"name":"5,10-CH(2)-H(4)folate reductase activity","type":"related"},{"name":"5,10-CH2-H4folate reductase activity","type":"related"},{"name":"5,10-methylenetetrahydrofolate reductase (FADH(2)) activity","type":"related"},{"name":"5,10-methylenetetrahydrofolate reductase (FADH) activity","type":"exact"},{"name":"5,10-methylenetetrahydrofolate reductase (FADH2) activity","type":"exact"},{"name":"5,10-methylenetetrahydrofolate reductase (NADPH) activity","type":"related"},{"name":"5,10-methylenetetrahydrofolate reductase activity","type":"broad"},{"name":"5,10-methylenetetrahydrofolic acid reductase activity","type":"broad"},{"name":"5,10-methylenetetrahydropteroylglutamate reductase activity","type":"related"},{"name":"5-methyltetrahydrofolate:(acceptor) oxidoreductase activity","type":"related"},{"name":"5-methyltetrahydrofolate:NAD oxidoreductase activity","type":"related"},{"name":"5-methyltetrahydrofolate:NAD(+) oxidoreductase activity","type":"related"},{"name":"5-methyltetrahydrofolate:NAD(P)+ oxidoreductase activity","type":"related"},{"name":"5-methyltetrahydrofolate:NAD+ oxidoreductase activity","type":"related"},{"name":"5-methyltetrahydrofolate:NADP(+) oxidoreductase activity","type":"related"},{"name":"5-methyltetrahydrofolate:NADP+ oxidoreductase activity","type":"related"},{"name":"MTHFR activity","type":"broad"},{"name":"MetF","type":"related"},{"name":"N(5),N(10)-methylenetetrahydrofolate reductase activity","type":"broad"},{"name":"N(5,10)-methylenetetrahydrofolate reductase activity","type":"broad"},{"name":"N5,10-methylenetetrahydrofolate reductase activity","type":"related"},{"name":"N5,N10-methylenetetrahydrofolate reductase activity","type":"related"},{"name":"methylenetetrahydrofolate (reduced nicotinamide adenine dinucleotide phosphate) reductase activity","type":"related"},{"name":"methylenetetrahydrofolate (reduced riboflavin adenine dinucleotide) reductase activity","type":"related"},{"name":"methylenetetrahydrofolate reductase (NADPH(2)) activity","type":"related"},{"name":"methylenetetrahydrofolate reductase (NADPH2)","type":"related"},{"name":"methylenetetrahydrofolate reductase [NAD(P)H]","type":"related"},{"name":"methylenetetrahydrofolate reductase activity","type":"broad"},{"name":"methylenetetrahydrofolic acid reductase activity","type":"broad"}],"termid":"GO:0004489","terms_by_termid":{"GO:0004489":null,"GO:0106312":null,"GO:0106313":null}}


id: GO:0031173
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of otoliths during embryogenesis with completion in early postembryonic development. Formation occurs by precipitation of specific crystal forms of calcium carbonate around an organic core of extracellular matrix proteins. Otoconia (otoliths) are small (~10 micron) dense extracellular particles present in the otolith end organs of the vertebrate inner ear.","definition_xrefs":["GOC:dsf","PMID:15581873"],"direct_ancestors":[{"relation_name":"is_a","term_name":"otolith mineralization","termid":"GO:0045299"}],"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":"otolith mineralization completed early in development","synonyms":[{"name":"otoconia mineralization","type":"exact"},{"name":"otoconium mineralization","type":"exact"}],"termid":"GO:0031173"}


id: PBO:0067070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 98, pseudogene","termid":"PBO:0067070"}


id: GO:0062170
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways, including anabolism and catabolism, by which living organisms transform lutein.","definition_xrefs":["PMID:24397433"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xanthophyll metabolic process","termid":"GO:0016122"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"lutein metabolic process","synonyms":[{"name":"lutein metabolism","type":"exact"}],"termid":"GO:0062170"}


id: GO:0031997
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to the N-terminus of a protein that has the potential to be, or has been, modified by N-terminal myristoylation. Binding affinity is typically altered by myristoylation; for example, N-terminal myristoylation of HIV Nef increases its affinity for calmodulin.","definition_xrefs":["GOC:dl","PMID:15632291","GOC:jsg"],"gene_count":0,"genotype_count":0,"name":"obsolete N-terminal myristoylation domain binding (obsolete GO:0031997)","termid":"GO:0031997"}


id: MOD:00717
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-phenylalanine residue to a methylated phenylalanine, such as N-methyl-L-phenylalanine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylated residue","termid":"MOD:00427"},{"relation_name":"is_a","term_name":"modified L-phenylalanine residue","termid":"MOD:00914"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"methylated phenylalanine","synonyms":[{"name":"MePhe","type":"exact"}],"termid":"MOD:00717"}


id: PBO:0028540
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-secondary_cell_septum_absent_from_cell_during_vegetative_growth","termid":"PBO:0028540"}


id: MONDO:0002044
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ectropion","termid":"MONDO:0002043"}],"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":"spastic ectropion","secondary_identifiers":["MEDGEN:509843","SCTID:80846000","DOID:1571","ICD9:374.13","UMLS:C0155195"],"termid":"MONDO:0002044","xrefs":{"Monarch":{"xref_id":"0002044"}}}


id: PBO:0062723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 51 subfamily V member 1","termid":"PBO:0062723"}


id: GO:0016751
data:
  {"annotated_genes":["SJAG_03163"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[111520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004149"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of a succinyl group to a sulfur atom on the acceptor molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-acyltransferase activity","termid":"GO:0016417"},{"relation_name":"is_a","term_name":"succinyltransferase activity","termid":"GO:0016748"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03163":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:0016746"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016746","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"S-succinyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0016751","terms_by_termid":{"GO:0004149":null}}


id: MONDO:0859764
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurofibromatosis/schwannomatosis","termid":"MONDO:0859008"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mosaic NF2-related schwannomatosis","secondary_identifiers":["MEDGEN:1843426","Orphanet:634475","UMLS:C5816778"],"termid":"MONDO:0859764","xrefs":{"Monarch":{"xref_id":"0859764"}}}


id: GO:0043607
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of formamide, the simplest amide, HCONH2, derived from formic acid.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"},{"relation_name":"is_a","term_name":"formamide metabolic process","termid":"GO:0043606"}],"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":"formamide biosynthetic process","termid":"GO:0043607"}


id: GO:0030415
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Stops, prevents or reduces the activity of the enzyme carboxypeptidase A.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete carboxypeptidase A inhibitor activity (obsolete GO:0030415)","synonyms":[{"name":"carboxypeptidase A inhibitor activity","type":"exact"}],"termid":"GO:0030415"}


id: PBO:0003465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F1-ATPase gamma subunit (predicted)","termid":"PBO:0003465"}


id: GO:0006367
data:
  {"annotated_genes":["SJAG_00095","SJAG_03441","SJAG_02589","SJAG_03900","SJAG_01403","SJAG_04205","SJAG_03668","SJAG_04368","SJAG_03206","SJAG_02773","SJAG_03579","SJAG_04596","SJAG_03145","SJAG_03285","SJAG_04213","SJAG_03107","SJAG_00159","SJAG_03618","SJAG_00641","SJAG_00746","SJAG_02101","SJAG_01658","SJAG_00342","SJAG_01436","SJAG_00087","SJAG_02768","SJAG_03061","SJAG_03431","SJAG_01713","SJAG_04989","SJAG_03944","SJAG_03694","SJAG_01110","SJAG_04097","SJAG_02174","SJAG_03622","SJAG_05313","SJAG_04030","SJAG_01711","SJAG_04099","SJAG_00872","SJAG_04576","SJAG_00650","SJAG_01710","SJAG_02447","SJAG_00441","SJAG_00735","SJAG_00540","SJAG_03787","SJAG_04977","SJAG_02981","SJAG_01771","SJAG_02458","SJAG_00769","SJAG_00440","SJAG_00995","SJAG_00896","SJAG_04705","SJAG_01622","SJAG_02066","SJAG_04194","SJAG_04894","SJAG_00868","SJAG_01465","SJAG_02798","SJAG_03590","SJAG_02254","SJAG_00150","SJAG_00045","SJAG_04005","SJAG_04852","SJAG_05192","SJAG_05020","SJAG_05341","SJAG_03884","SJAG_03211","SJAG_07011","SJAG_04274","SJAG_02541","SJAG_01808","SJAG_05203","SJAG_01111","SJAG_00581","SJAG_01325","SJAG_02391","SJAG_03599","SJAG_00184","SJAG_00758","SJAG_00766","SJAG_00297","SJAG_00873","SJAG_02549","SJAG_02303","SJAG_03421","SJAG_02500","SJAG_01653","SJAG_03776","SJAG_02466","SJAG_03839","SJAG_01765","SJAG_00512","SJAG_02385","SJAG_04613","SJAG_00116","SJAG_00119","SJAG_01016","SJAG_00739","SJAG_01952","SJAG_01475","SJAG_02869","SJAG_04758","SJAG_02872","SJAG_02691","SJAG_00458","SJAG_02314","SJAG_00349","SJAG_02849","SJAG_04038","SJAG_01611","SJAG_04917","SJAG_00584","SJAG_01230","SJAG_03255","SJAG_03576","SJAG_01513","SJAG_01207","SJAG_00741","SJAG_02494","SJAG_02571","SJAG_01523","SJAG_02927","SJAG_00901","SJAG_03033","SJAG_00909","SJAG_00421","SJAG_03095","SJAG_02846","SJAG_03366","SJAG_03758","SJAG_04654","SJAG_03752","SJAG_04647","SJAG_00743","SJAG_02329","SJAG_01804","SJAG_00904","SJAG_02170","SJAG_04420","SJAG_04614","SJAG_02906","SJAG_03573","SJAG_04755","SJAG_04820","SJAG_02551"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[86904,87858,88119,88795,89402,89421,89771,91542,91684,93014,93412,93601,93653,94885,95081,95533,96300,96314,97114,99715,100502,101266,101785,102637,103100,104934,104974,105512,105707,105840,106366,107142,107164,107356,107945,108183,108441,108734,111534,112412,113672,114177,114242,114274,114421,114514,114584,114831,117005],"is_not":false,"summary":null,"term":"GO:0006367"},{"annotations":[89221,114630],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0045899"},{"annotations":[118367,86972,105839,108209,105706,95367,105161,108182,93955,93845,114176,90194,103162,89879,102901,114741,98180,98528,101447,94884,105511,108494],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0060261"},{"annotations":[88794,88118,114241,114830,87857,116785,86903,95532,107958,66878,89420,93651],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051123"},{"annotations":[94148,107925,90210,98008,108527,112593,111203,87175,93717,98646,101052,112576,115148,117006,88007,102852,106909,92299,89308,102268,110062,114163,116895,117054,106367,106215,93641,93015,111996,113838,107346,93661,106796,115733,88390,109927,115794,87318,107147,100468,93689,96589,97321,116349,95390,115983,95396,103335,105239,112420,114832,93814,94951,98173,108927,89581,90922,112761,113676,116711,104499,113749,88623,94976,117402,87674,95949,104491,93517,108803,113665,87497,88796,105097,114699,114451,96154,93627,114846,116985,102603,87859,90224,109040,98891,97742,90103,104042,91807,93281],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045815"},{"annotations":[89422],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0001174"}]},"cv_name":"biological_process","definition":"A transcription initiation process that takes place at a RNA polymerase II gene promoter. 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id: FYPO:0002823
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 mitotic spindle pole body does not occur during interphase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to mitotic spindle pole body","termid":"FYPO:0000941"}],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000138","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abolished protein localization to mitotic spindle pole body during interphase","synonyms":[{"name":"abolished protein localization to spindle pole body during interphase during mitotic cell cycle","type":"related"},{"name":"protein absent from mitotic spindle pole body during interphase","type":"related"},{"name":"protein localisation to mitotic spindle pole body abolished during interphase","type":"exact"},{"name":"protein localization to mitotic SPB abolished during interphase","type":"exact"},{"name":"protein localization to mitotic spindle pole body abolished during interphase","type":"exact"},{"name":"protein localization to spindle pole body abolished during interphase during vegetative growth","type":"exact"}],"termid":"FYPO:0002823"}


id: PBO:0041053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bromodomain containing 7 pseudogene 4","termid":"PBO:0041053"}


id: GO:0039501
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any viral process that results in the inhibition of host cell type I interferon production. Type I interferons include the interferon-alpha, beta, delta, episilon, zeta, kappa, tau, and omega gene families.","definition_xrefs":["GOC:sp","GOC:add","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host type I interferon production (obsolete GO:0039501)","synonyms":[{"name":"negative regulation by virus of host type I interferon production","type":"exact"},{"name":"suppression by virus of host interferon type I production","type":"exact"},{"name":"suppression by virus of host type I IFN production","type":"exact"}],"termid":"GO:0039501"}


id: GO:0019918
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of methylation of peptidyl-arginine to form peptidyl-N(omega),N'(omega)-dimethyl-L-arginine.","definition_xrefs":["RESID:AA0069","RESID:AA0067"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-arginine omega-N-methylation","termid":"GO:0035247"}],"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":"peptidyl-arginine methylation, to symmetrical-dimethyl arginine","termid":"GO:0019918"}


id: PBO:0054945
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 2359","termid":"PBO:0054945"}


id: PBO:0026789
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_number_of_heterothallic_h-_cells","termid":"PBO:0026789"}


id: PBO:0018221
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae TRF4","termid":"PBO:0018221"}


id: MONDO:0009564
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Marden-Walker syndrome (MWS) is a malformation syndrome characterized by multiple joint contractures (arthrogryposis), a mask-like face with blepharophimosis, micrognathia, high-arched or cleft palate, low-set ears, decreased muscular bulk, kyphoscoliosis and arachnodactyly.","definition_xrefs":["Orphanet:2461"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome or malformation associated with head and neck malformations (obsolete MONDO:0015501)","termid":"MONDO:0015501"},{"relation_name":"is_a","term_name":"ciliopathy","termid":"MONDO:0005308"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"arthrogryposis multiplex congenita","termid":"MONDO:0015168"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Marden-Walker syndrome","secondary_identifiers":["OMIM:248700","icd11.foundation:1983460876","SCTID:449824004","UMLS:C0796033","MESH:C535910","NORD:1402","ICD9:759.89","MEDGEN:163206","GARD:6973"],"synonyms":[{"name":"MARDEN-WALKER syndrome","type":"related"},{"name":"MWKS","type":"related"},{"name":"Marden Walker Syndrome","type":"exact"},{"name":"Marden-Walker syndrome","type":"exact"},{"name":"Mws","type":"related"},{"name":"connective tissue disorder Marden Walker type","type":"related"}],"termid":"MONDO:0009564","xrefs":{"Monarch":{"xref_id":"0009564"}}}


id: PBO:0025536
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"argininosuccinic aciduria","termid":"PBO:0025536"}


id: PBO:0067698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5.8S ribosomal pseudogene 6","termid":"PBO:0067698"}


id: GO:0009921
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The protein complex associated with the plasma membrane of certain plant cells (e.g. root cortex, epidermal cells) that functions to transport auxin out of the cell.","definition_xrefs":["PMID:9843496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"auxin efflux carrier complex","termid":"GO:0009921"}


id: FYPO:0007059
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 late endosomes is decreased.","definition_xrefs":["PomBase:mah","PMID:31341193"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to endosome","termid":"FYPO:0007587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"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:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to late endosome","synonyms":[{"name":"decreased protein localisation to late endosome","type":"exact"},{"name":"decreased protein localization to PVE","type":"exact"},{"name":"decreased protein localization to late endosome during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to late endosome during vegetative growth","type":"exact"},{"name":"decreased protein localization to prevacuolar compartment","type":"exact"},{"name":"decreased protein localization to prevacuolar endosome","type":"exact"},{"name":"reduced protein localization to late endosome","type":"exact"}],"termid":"FYPO:0007059"}


id: GO:0061138
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a branched epithelium are generated and organized.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphogenesis of a branching structure","termid":"GO:0001763"},{"relation_name":"is_a","term_name":"morphogenesis of an epithelium","termid":"GO:0002009"}],"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":"morphogenesis of a branching epithelium","termid":"GO:0061138"}


id: PBO:0050153
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 3 pseudogene 9","termid":"PBO:0050153"}


id: PBO:0047176
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 197 Y-linked member 9","termid":"PBO:0047176"}


id: GO:0140587
data:
  {"annotated_genes":["SJAG_00698"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[111333],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140585"}]},"cv_name":"molecular_function","definition":"Bridging together two DNA loop anchors together, maintaining a chromatin loop.","definition_xrefs":["PMID:32213323"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromatin DNA binding","termid":"GO:0031490"},{"relation_name":"is_a","term_name":"DNA-DNA tethering activity","termid":"GO:0106260"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00698":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003677"}],"interesting_parent_ids":["GO:0060090","GO:0003674","GO:0005488","GO:0003677"],"is_obsolete":false,"name":"chromatin loop anchoring activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DNA loop binding","type":"exact"},{"name":"chromosomal loop binding","type":"exact"}],"termid":"GO:0140587","terms_by_termid":{"GO:0140585":null}}


id: MONDO:0013765
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any coronary artery disease in which the cause of the disease is a mutation in the MMP3 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":"coronary heart disease, susceptibility to, 6","secondary_identifiers":["UMLS:C3280913","OMIM:614466","MEDGEN:482543"],"synonyms":[{"name":"CHDS6","type":"related"},{"name":"MMP3 coronary artery disease","type":"exact"},{"name":"coronary artery disease caused by mutation in MMP3","type":"exact"},{"name":"coronary heart disease, susceptibility to, 6","type":"exact"},{"name":"coronary heart disease, susceptibility to, type 6","type":"exact"},{"name":"susceptibility to coronary heart disease 6","type":"related"}],"termid":"MONDO:0013765","xrefs":{"Monarch":{"xref_id":"0013765"}}}


id: MOD:01396
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-proline residue to a 5-hydroxy-3-methyl-L-proline.","definition_xrefs":["PubMed:8557573","PubMed:7592021","RESID:AA0473"],"direct_ancestors":[{"relation_name":"has_functional_parent","term_name":"monohydroxylated proline","termid":"MOD:01024"},{"relation_name":"has_functional_parent","term_name":"monomethylated proline","termid":"MOD:01417"},{"relation_name":"is_a","term_name":"modified L-proline residue","termid":"MOD:00915"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-hydroxy-3-methyl-L-proline (Pro)","synonyms":[{"name":"(2S,3S,5Xi)-5-hydroxy-3-methylpyrrolidine-2-carboxylic acid","type":"exact"},{"name":"5-hydroxy-3-methyl-L-proline","type":"exact"},{"name":"5-hydroxy-3-methylproline","type":"exact"},{"name":"5Hy3MePro","type":"exact"},{"name":"MOD_RES 5-hydroxy-3-methylproline (Ile)","type":"exact"},{"name":"beta-methyl-delta-hydroxyproline","type":"exact"}],"termid":"MOD:01396"}


id: GO:0060601
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a branch forms along the side of an epithelium.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphogenesis of an epithelium","termid":"GO:0002009"},{"relation_name":"part_of","term_name":"morphogenesis of a branching epithelium","termid":"GO:0061138"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lateral sprouting from an epithelium","termid":"GO:0060601"}


id: PBO:0018147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane protein involved in inositol lipid-mediated signaling Sfk1 (predicted)","termid":"PBO:0018147"}


id: PBO:0045770
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"extracellular matrix protein 1 pseudogene 1","termid":"PBO:0045770"}


id: GO:0110037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of nematode male tail tip morphogenesis, the process in which the anatomical structure of the adult male tail tip is generated and organized.","definition_xrefs":["PMID:28068334","GOC:rz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of anatomical structure morphogenesis","termid":"GO:0022603"},{"relation_name":"regulates","term_name":"nematode male tail tip morphogenesis","termid":"GO:0045138"}],"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 nematode male tail tip morphogenesis","termid":"GO:0110037"}


id: PBO:0079338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis-specific transcript, Y-linked 23","termid":"PBO:0079338"}


id: PBO:0047340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FBN1 divergent transcript","termid":"PBO:0047340"}


id: PBO:0047146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 180 member B","termid":"PBO:0047146"}


id: GO:0019824
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A subform of peroxisome that corresponds to an intermediate in a peroxisome assembly pathway, which operates by conversion of peroxisomal subforms in the direction P1, P2 -> P3 -> P4 -> P5 -> P6. P6 peroxisomes are distinguished from the other subforms on the bases of buoyant density and protein content, and are equivalent to mature peroxisomes.","definition_xrefs":["PMID:10629216"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxisome","termid":"GO:0005777"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005777"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005777"],"is_obsolete":false,"name":"P6 peroxisome","synonyms":[{"name":"peroxisome vesicle","type":"broad"}],"termid":"GO:0019824"}


id: PBO:0065867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB24, member RAS oncogene family","termid":"PBO:0065867"}


id: GO:0045562
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of TRAIL (TNF-related apoptosis inducing ligand) receptor 2.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of TRAIL receptor 2 biosynthetic process (obsolete GO:0045562)","synonyms":[{"name":"regulation of TRAIL receptor 2 anabolism","type":"exact"},{"name":"regulation of TRAIL receptor 2 biosynthesis","type":"exact"},{"name":"regulation of TRAIL receptor 2 formation","type":"exact"},{"name":"regulation of TRAIL receptor 2 synthesis","type":"exact"}],"termid":"GO:0045562"}


id: FYPO:0002581
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 any tRNA processing intermediates with 3' extensions measured in the nucleus is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered tRNA or precursor level","termid":"FYPO:0005999"},{"relation_name":"is_a","term_name":"increased ncRNA level during vegetative growth","termid":"FYPO:0008146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"increased level of nuclear tRNA processing intermediates with 3' extensions","synonyms":[{"name":"increased accumulation of nuclear tRNA processing intermediates with 3' extensions","type":"related"},{"name":"increased level of nuclear tRNA processing intermediates with 3' extensions during mitotic cell cycle","type":"related"},{"name":"increased level of nuclear tRNA processing intermediates with 3' extensions during vegetative growth","type":"exact"}],"termid":"FYPO:0002581"}


id: PBO:0086947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Receptor protein involved in selective autophagy during starvation; specifically involved in the transport of cargo protein alpha-mannosidase (Ams1p); Atg19p paralog","termid":"PBO:0086947"}


id: PBO:0072389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS27A pseudogene 15","termid":"PBO:0072389"}


id: PBO:0088348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH-dependent reductase for Dph3, Cbr1","termid":"PBO:0088348"}


id: PBO:0084683
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial cardiolipin-specific phospholipase; functions upstream of Taz1p to generate monolyso-cardiolipin; transcription increases upon genotoxic stress; involved in restricting Ty1 transposition; has homology to mammalian CGI-58","termid":"PBO:0084683"}


id: MONDO:0004404
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"T-lymphoblastic leukemia/lymphoma resistant to treatment","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"precursor T-lymphoblastic lymphoma/leukemia","termid":"MONDO:0003537"},{"relation_name":"is_a","term_name":"refractory hematologic cancer","termid":"MONDO:0004111"}],"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":"refractory precursor T-lymphoblastic lymphoma/leukemia","secondary_identifiers":["UMLS:C0854859","DOID:7936","MEDGEN:167728","NCIT:C8696"],"synonyms":[{"name":"precursor T lymphoblastic lymphoma/leukemia refractory","type":"exact"},{"name":"refractory T lymphoblastic leukemia/lymphoma","type":"exact"},{"name":"refractory precursor T-lymphoblastic lymphoma/leukemia","type":"exact"}],"termid":"MONDO:0004404","xrefs":{"Monarch":{"xref_id":"0004404"}}}


id: GO:0140533
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process by which a symbiont inhibits or disrupts the host's RNAi-mediated antiviral immune response. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:17693253"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host innate immune response","termid":"GO:0052170"}],"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 RNAi-mediated antiviral immune response","synonyms":[{"name":"suppression of host RNAi-mediated antiviral immune response","type":"exact"},{"name":"suppression of host RNAi-mediated antiviral immunity","type":"exact"},{"name":"suppression of host RNAi-mediated gene silencing","type":"exact"}],"termid":"GO:0140533"}


id: PBO:0028918
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_transcription_during_glucose_starvation","termid":"PBO:0028918"}


id: PATO:0000438
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A variability quality inhering in a bearer by virtue of the bearer's lacking or not exhibiting variation.","definition_xrefs":["Dictionary:http://dictionary.reference.com/"],"direct_ancestors":[{"relation_name":"is_a","term_name":"variability","termid":"PATO:0001303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"invariant","synonyms":[{"name":"constant","type":"related"},{"name":"uniform","type":"exact"}],"termid":"PATO:0000438"}


id: PBO:0051224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable IGHV8-51-1 (non-functional)","termid":"PBO:0051224"}


id: PBO:0064639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pro-platelet basic protein pseudogene 2","termid":"PBO:0064639"}


id: MOD:00465
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-phenylalanine residue to a dihydroxyphenylalanine.","definition_xrefs":["PubMed:3734192","RESID:AA0146#var","PubMed:1610822","PubMed:9252331","Unimod:425#F","PubMed:1903612","OMSSA:39"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dihydroxylated residue","termid":"MOD:00428"},{"relation_name":"is_a","term_name":"modified L-phenylalanine residue","termid":"MOD:00914"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydroxyphenylalanine (Phe)","synonyms":[{"name":"Dioxidation","type":"related"},{"name":"dihydroxy","type":"related"},{"name":"dihydroxyf","type":"exact"}],"termid":"MOD:00465"}


id: GO:1900002
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of anthocyanin catabolic process.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catabolic process","termid":"GO:0009896"},{"relation_name":"is_a","term_name":"positive regulation of anthocyanin metabolic process","termid":"GO:0031539"},{"relation_name":"is_a","term_name":"regulation of anthocyanin catabolic process","termid":"GO:1900000"},{"relation_name":"positively_regulates","term_name":"anthocyanin-containing compound catabolic process","termid":"GO:0046284"}],"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 anthocyanin catabolic process","synonyms":[{"name":"positive regulation of anthocyanin breakdown","type":"exact"},{"name":"positive regulation of anthocyanin catabolism","type":"exact"},{"name":"positive regulation of anthocyanin degradation","type":"exact"},{"name":"up regulation of anthocyanin breakdown","type":"exact"},{"name":"up regulation of anthocyanin catabolic process","type":"related"},{"name":"up regulation of anthocyanin catabolism","type":"exact"},{"name":"up regulation of anthocyanin degradation","type":"exact"}],"termid":"GO:1900002"}


id: MONDO:0017142
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hemorrhagic disorder due to a qualitative platelet defect (obsolete MONDO:0017142)","secondary_identifiers":["Orphanet:275736"],"synonyms":[{"name":"rare bleeding disorder due to a constitutional thrombopathy","type":"exact"},{"name":"rare bleeding disorder due to a qualitative platelet defect","type":"exact"},{"name":"rare coagulopathy due to a constitutional thrombopathy","type":"exact"},{"name":"rare coagulopathy due to a qualitative platelet defect","type":"exact"},{"name":"rare hemorrhagic disorder due to a constitutional thrombopathy","type":"exact"},{"name":"rare hemorrhagic disorder due to a qualitative platelet defect","type":"exact"}],"termid":"MONDO:0017142","xrefs":{"Monarch":{"xref_id":"0017142"}}}


id: PBO:0085296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pheromone-regulated protein; predicted to have 4 transmembrane segments and a coiled coil domain; regulated by Ste12p; required for efficient nuclear fusion","termid":"PBO:0085296"}


id: GO:0018107
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The phosphorylation of peptidyl-threonine to form peptidyl-O-phospho-L-threonine.","definition_xrefs":["RESID:AA0038"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein phosphorylation","termid":"GO:0006468"},{"relation_name":"is_a","term_name":"peptidyl-threonine modification","termid":"GO:0018210"}],"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":"peptidyl-threonine phosphorylation","termid":"GO:0018107"}


id: GO:0015591
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of D-ribose from one side of a membrane to the other. As beta-D-ribofuranose, D-ribose forms the glycose group of all ribonucleosides, ribonucleotides and ribonucleic acids, and also of ribose phosphates, various glycosides, some coenzymes and some forms of vitamin B12.","definition_xrefs":["GOC:mtg_transport","ISBN:0198506732","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentose transmembrane transporter activity","termid":"GO:0015146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"D-ribose transmembrane transporter activity","termid":"GO:0015591"}


id: MOD:01345
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue to 2-amino-3-oxobutanoic acid.","definition_xrefs":["OMSSA:23","Unimod:401#T","PubMed:12716131","PubMed:9252331"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-threonine residue","termid":"MOD:00917"},{"relation_name":"is_a","term_name":"didehydrogenated residue","termid":"MOD:01888"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2-amino-3-oxobutanoic acid","synonyms":[{"name":"2-amino-3-ketobutyric acid","type":"exact"},{"name":"2-amino-3-oxo-butanoic_acid","type":"related"},{"name":"3-ketobutyrine","type":"exact"},{"name":"Didehydro","type":"related"},{"name":"twoamino3oxobutanoicacid","type":"exact"}],"termid":"MOD:01345"}


id: GO:0046591
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process, occurring in the embryo, by which the anatomical structures of the leg joint are generated and organized. A leg joint is a flexible region that separates the rigid sections of a leg to allow movement in a controlled manner.","definition_xrefs":["PMID:12051824","GOC:bf","ISBN:0582227089"],"gene_count":0,"genotype_count":0,"name":"obsolete embryonic leg joint morphogenesis (obsolete GO:0046591)","synonyms":[{"name":"embryonic leg joint morphogenesis","type":"exact"}],"termid":"GO:0046591"}


id: PBO:0011516
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unbinds SPAC11H11.04 with force 120 pN at probe speed 1.74 um/s","termid":"PBO:0011516"}


id: PBO:0067228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 299, pseudogene","termid":"PBO:0067228"}


id: MONDO:0011699
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory bowel disease that has material basis in variation in the chromosome region 16p.","definition_xrefs":["PMID:11752413","DOID:0110904"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory bowel disease","termid":"MONDO:0005265"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005046"],"is_obsolete":false,"name":"inflammatory bowel disease 8","secondary_identifiers":["MESH:C564682","OMIM:606668","UMLS:C1847719","MEDGEN:335753"],"synonyms":[{"name":"IBD8","type":"exact"},{"name":"inflammatory bowel disease 8","type":"exact"},{"name":"inflammatory bowel disease type 8","type":"exact"}],"termid":"MONDO:0011699","xrefs":{"Monarch":{"xref_id":"0011699"}}}


id: MONDO:0021009
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from the salivary glands. It is the most common primary carcinoma of the salivary glands and usually presents as a firm and painless mass. It is characterized by the presence of epidermoid cells, mucus producing cells, and cells of intermediate type. The majority of cases have a favorable outcome.","definition_xrefs":["NCIT:C5908"],"direct_ancestors":[{"relation_name":"is_a","term_name":"salivary gland carcinoma","termid":"MONDO:0000521"},{"relation_name":"is_a","term_name":"oral cavity mucoepidermoid carcinoma","termid":"MONDO:0044964"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"salivary gland mucoepidermoid carcinoma","secondary_identifiers":["DOID:0081293","MEDGEN:277630","SCTID:423708008","UMLS:C1335903"],"synonyms":[{"name":"mucoepidermoid carcinoma of salivary gland","type":"exact"},{"name":"mucoepidermoid carcinoma of the salivary gland","type":"exact"},{"name":"saliva-secreting gland mucoepidermoid carcinoma","type":"exact"},{"name":"salivary gland mucoepidermoid carcinoma","type":"exact"}],"termid":"MONDO:0021009","xrefs":{"Monarch":{"xref_id":"0021009"}}}


id: MONDO:0001293
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm that affects the subglottic area of the larynx. The vast majority of cases are squamous cell carcinomas.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"subglottis neoplasm","termid":"MONDO:0000933"},{"relation_name":"is_a","term_name":"larynx cancer","termid":"MONDO:0002352"}],"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":"subglottis cancer","secondary_identifiers":["SCTID:363430007","DOID:11472","ICD9:161.2","NCIT:C3546","UMLS:C0153485","ICD10CM:C32.2","MEDGEN:57562"],"synonyms":[{"name":"Ca larynx - subglottis","type":"exact"},{"name":"cancer of subglottis","type":"exact"},{"name":"malignant neoplasm of subglottis","type":"exact"},{"name":"malignant neoplasm of the subglottis","type":"exact"},{"name":"malignant subglottic neoplasm","type":"exact"},{"name":"malignant subglottic tumor","type":"exact"},{"name":"malignant subglottic tumour","type":"exact"},{"name":"malignant subglottis neoplasm","type":"exact"},{"name":"malignant subglottis tumor","type":"exact"},{"name":"malignant subglottis tumour","type":"exact"},{"name":"malignant tumor of subglottis","type":"exact"},{"name":"malignant tumor of the subglottis","type":"exact"},{"name":"malignant tumour of subglottis","type":"exact"},{"name":"malignant tumour of the subglottis","type":"exact"},{"name":"subglottis cancer","type":"exact"}],"termid":"MONDO:0001293","xrefs":{"Monarch":{"xref_id":"0001293"}}}


id: MONDO:0006236
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete granular cell tumor of the neurohypophysis (obsolete MONDO:0006236)","termid":"MONDO:0006236","xrefs":{"Monarch":{"xref_id":"0006236"}}}


id: GO:0005902
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Thin cylindrical membrane-covered projections on the surface of an animal cell containing a core bundle of actin filaments. Present in especially large numbers on the absorptive surface of intestinal cells.","definition_xrefs":["ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin-based cell projection","termid":"GO:0098858"}],"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":"microvillus","secondary_identifiers":["NIF_Subcellular:sao671419673","Wikipedia:Microvillus"],"synonyms":[{"name":"microvilli","type":"related"}],"termid":"GO:0005902"}


id: PR:Q9UUF4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC17A3.02 gene.","definition_xrefs":["UniProtKB:Q9UUF4","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":"altered inheritance of mitochondria protein 19 homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17A3.02","synonyms":[{"name":"Spom972h-SPBC17A3.02","type":"exact"}],"termid":"PR:Q9UUF4"}


id: GO:0048007
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an antigen-presenting cell expresses lipid antigen of exogenous origin in association with an MHC class Ib protein complex on its cell surface. Class Ib here refers to non-classical class I molecules, such as those of the CD1 family.","definition_xrefs":["PMID:15928680","GOC:add","PMID:15928678","PMID:10375559"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antigen processing and presentation of exogenous antigen","termid":"GO:0019884"},{"relation_name":"is_a","term_name":"antigen processing and presentation of lipid antigen via MHC class Ib","termid":"GO:0048003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"antigen processing and presentation, exogenous lipid antigen via MHC class Ib","synonyms":[{"name":"antigen presentation, exogenous peptide antigen","type":"exact"},{"name":"exogenous lipid antigen processing and presentation via MHC class Ib","type":"exact"}],"termid":"GO:0048007"}


id: PBO:0055463
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 2896","termid":"PBO:0055463"}


id: MOD:00954
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that crosslinks two residues with a covalent bond and the loss of water.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"crosslinked residues","termid":"MOD:00033"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crosslinked residues with loss of water","termid":"MOD:00954"}


id: MONDO:0000243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dermatophyte infection of the hair that infects the hair surface.","definition_xrefs":["Wikipedia:Exothrix"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatophytosis","termid":"MONDO:0004678"}],"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":"ectothrix infectious disease","secondary_identifiers":["DOID:0050097"],"termid":"MONDO:0000243","xrefs":{"Monarch":{"xref_id":"0000243"}}}


id: PBO:0017477
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-contains_process","termid":"PBO:0017477"}


id: MONDO:0010316
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"FG syndrome","termid":"MONDO:0002010"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FG syndrome 3","secondary_identifiers":["MEDGEN:375687","OMIM:300406","UMLS:C1845567"],"synonyms":[{"name":"FG syndrome 3","type":"exact"},{"name":"FGS3","type":"related"}],"termid":"MONDO:0010316","xrefs":{"Monarch":{"xref_id":"0010316"}}}


id: PBO:0080726
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WT1 interacting protein","termid":"PBO:0080726"}


id: GO:1902815
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of N,N'-diacetylchitobiose into a cell or organelle.","definition_xrefs":["PMID:9405618","GOC:am","GOC:TermGenie","GO_REF:0000073"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate derivative transport","termid":"GO:1901264"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"N,N'-diacetylchitobiose import","termid":"GO:1902815"}


id: GO:0098503
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of removing a 3' phosphate group from a DNA molecule.","definition_xrefs":["GOC:DOS"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA 3' dephosphorylation (obsolete GO:0098503)","termid":"GO:0098503"}


id: MONDO:0020009
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare nervous system disease.","gene_count":0,"genotype_count":0,"name":"obsolete rare neurologic disease (obsolete MONDO:0020009)","secondary_identifiers":["Orphanet:98006"],"synonyms":[{"name":"rare nervous system disease","type":"exact"},{"name":"rare nervous system disorder","type":"exact"}],"termid":"MONDO:0020009","xrefs":{"Monarch":{"xref_id":"0020009"}}}


id: GO:1905645
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of FACT complex assembly.","definition_xrefs":["GO_REF:0000058","PMID:20889714","GOC:TermGenie"],"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 FACT complex assembly","termid":"GO:1905644"},{"relation_name":"negatively_regulates","term_name":"FACT complex assembly","termid":"GO:1905635"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"negatively_regulates","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0065003"],"is_obsolete":false,"name":"negative regulation of FACT complex assembly","synonyms":[{"name":"down regulation of FACT complex assembly","type":"exact"},{"name":"down regulation of FACT complex formation","type":"exact"},{"name":"down regulation of Facilitates chromatin transcription complex assembly","type":"exact"},{"name":"down regulation of Facilitates chromatin transcription complex formation","type":"exact"},{"name":"down-regulation of FACT complex assembly","type":"exact"},{"name":"down-regulation of FACT complex formation","type":"exact"},{"name":"down-regulation of Facilitates chromatin transcription complex assembly","type":"exact"},{"name":"down-regulation of Facilitates chromatin transcription complex formation","type":"exact"},{"name":"downregulation of FACT complex assembly","type":"exact"},{"name":"downregulation of FACT complex formation","type":"exact"},{"name":"downregulation of Facilitates chromatin transcription complex assembly","type":"exact"},{"name":"downregulation of Facilitates chromatin transcription complex formation","type":"exact"},{"name":"inhibition of FACT complex assembly","type":"narrow"},{"name":"inhibition of FACT complex formation","type":"narrow"},{"name":"inhibition of Facilitates chromatin transcription complex assembly","type":"narrow"},{"name":"inhibition of Facilitates chromatin transcription complex formation","type":"narrow"},{"name":"negative regulation of FACT complex formation","type":"exact"},{"name":"negative regulation of Facilitates chromatin transcription complex assembly","type":"exact"},{"name":"negative regulation of Facilitates chromatin transcription complex formation","type":"exact"}],"termid":"GO:1905645"}


id: GO:0019724
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved with the carrying out of an immune response by a B cell, through, for instance, the production of antibodies or cytokines, or antigen presentation to T cells.","definition_xrefs":["GOC:add","ISBN:0781735149","GO_REF:0000022"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphocyte mediated immunity","termid":"GO:0002449"},{"relation_name":"is_a","term_name":"adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains","termid":"GO:0002460"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"B cell mediated immunity","synonyms":[{"name":"B lymphocyte mediated immune effector process","type":"exact"},{"name":"B lymphocyte mediated immunity","type":"exact"},{"name":"B-cell mediated immune effector process","type":"exact"},{"name":"B-cell mediated immunity","type":"exact"},{"name":"B-lymphocyte mediated immune effector process","type":"exact"},{"name":"B-lymphocyte mediated immunity","type":"exact"}],"termid":"GO:0019724"}


id: PBO:0059037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"matrix metallopeptidase 25","termid":"PBO:0059037"}


id: MONDO:0016845
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 21","termid":"MONDO:0016919"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"21q22.11q22.12 microdeletion syndrome","secondary_identifiers":["UMLS:C5192593","GARD:20779","Orphanet:261323","MEDGEN:1681958"],"synonyms":[{"name":"21q22.11-q22.12 microdeletion syndrome","type":"exact"},{"name":"Del(21)(q22.11q22.12)","type":"exact"},{"name":"monosomy 21q22.11-q22.12","type":"exact"},{"name":"monosomy 21q22.11q22.12","type":"exact"}],"termid":"MONDO:0016845","xrefs":{"Monarch":{"xref_id":"0016845"}}}


id: GO:0003138
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that results in the delineation of a specific region of the lateral mesoderm into the area which will form the primary beating heart tube. In mammals the primary heart field gives rise to the left ventricle.","definition_xrefs":["GOC:mtg_heart","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart field specification","termid":"GO:0003128"}],"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 heart field specification","synonyms":[{"name":"FHS specification","type":"exact"},{"name":"first heart field specification","type":"exact"}],"termid":"GO:0003138"}


id: GO:0001533
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A type of plasma membrane that has been modified through addition of distinct intracellular and extracellular components, including ceramide, found in cornifying epithelial cells (corneocytes).","definition_xrefs":["PMID:11112355","PMID:11590230","GOC:add","PMID:15803139"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane","termid":"GO:0005886"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"cornified envelope","termid":"GO:0001533"}


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


id: PBO:0058666
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6794","termid":"PBO:0058666"}


id: MONDO:0005623
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammatory disease of the thyroid gland due to autoimmune responses leading to lymphocytic infiltration of the gland. It is characterized by the presence of circulating thyroid antigen-specific T-cells and thyroid autoantibodies. The clinical signs can range from hypothyroidism to thyrotoxicosis depending on the type of autoimmune thyroiditis.","definition_xrefs":["MESH:D013967"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disorder of endocrine system","termid":"MONDO:0000569"},{"relation_name":"is_a","term_name":"thyroiditis","termid":"MONDO:0004126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune thyroid disease","secondary_identifiers":["UMLS:C0920350","EFO:0006812","Wikipedia:Autoimmune_thyroiditis","MEDGEN:183088"],"synonyms":[{"name":"autoimmune thyroid gland inflammation","type":"exact"},{"name":"autoimmune thyroiditides","type":"related"},{"name":"autoimmune thyroiditis","type":"related"},{"name":"lymphocytic thyroiditides","type":"related"},{"name":"lymphocytic thyroiditis","type":"related"},{"name":"lymphomatous thyroiditides","type":"related"},{"name":"lymphomatous thyroiditis","type":"related"},{"name":"thyroiditides, autoimmune","type":"related"},{"name":"thyroiditides, lymphocytic","type":"related"},{"name":"thyroiditides, lymphomatous","type":"related"},{"name":"thyroiditis, lymphocytic","type":"related"},{"name":"thyroiditis, lymphomatous","type":"related"}],"termid":"MONDO:0005623","xrefs":{"Monarch":{"xref_id":"0005623"}}}


id: PBO:0083041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Delta subunit of the translation initiation factor eIF2B; the guanine-nucleotide exchange factor for eIF2; activity subsequently regulated by phosphorylated eIF2; first identified as a negative regulator of GCN4 expression","termid":"PBO:0083041"}


id: FYPO:0005070
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. An inviable phenotype observed in the vegetative growth phase of the life cycle in which a cell undergoes septation despite abolished mitotic sister chromatid separation, producing inviable daughter cells, and in which the septum forms in a position that partitions the nucleus into one compartment. Cell separation may or may not be completed.","definition_xrefs":["PomBase:mah","PomBase:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete cut with abolished mitotic sister chromatid separation, with mononucleate and anucleate compartment formation (obsolete FYPO:0005070)","synonyms":[{"name":"cut with abolished mitotic sister chromatid separation and anucleate cell formation","type":"exact"},{"name":"cut with abolished mitotic sister chromatid separation, with mononucleate and anucleate compartment formation during mitotic cell cycle","type":"related"},{"name":"cut with abolished mitotic sister chromatid separation, with mononucleate and anucleate compartment formation during vegetative growth","type":"exact"},{"name":"monoseptate vegetative cell with mononucleate and anucleate compartments following abolished mitotic sister chromatid separation","type":"exact"},{"name":"septation following abolished mitotic sister chromatid separation, with mononucleate and anucleate compartment formation","type":"exact"}],"termid":"FYPO:0005070"}


id: MONDO:0100346
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Primary microcephaly refers to the clinical finding of a head circumference more than than 3 standard deviations (SD) below the age- and sex-related mean, present at birth. Primary microcephaly is a static developmental anomaly, distinguished from secondary microcephaly, which refers to a progressive neurodegenerative condition. Microcephaly is a disorder of fetal brain growth; individuals with microcephaly have small brains and almost always have intellectual disability, although rare individuals with mild microcephaly (-3 SD) and normal intelligence have been reported. Additional clinical features may include short stature or mild seizures. These clinical features include Seckel syndrome, a rare autosomal recessive disorder characterized by intrauterine growth retardation, dwarfism, microcephaly with intellectual disability.","definition_xrefs":["PMID:9128935"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive primary microcephaly","termid":"MONDO:0016660"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0006025"],"is_obsolete":false,"name":"microcephaly with or without short stature","termid":"MONDO:0100346","xrefs":{"Monarch":{"xref_id":"0100346"}}}


id: PATO:0002119
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality which is held by a bearer when the latter exhibits an excessive accumulation of intracellular fluid.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"composition","termid":"PATO:0000025"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydropic","termid":"PATO:0002119"}


id: MONDO:0000308
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A systemic mycosis that arises from infection in an immunologically normal host.","direct_ancestors":[{"relation_name":"is_a","term_name":"systemic mycosis","termid":"MONDO:0000256"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary systemic mycosis","secondary_identifiers":["DOID:0050292"],"termid":"MONDO:0000308","xrefs":{"Monarch":{"xref_id":"0000308"}}}


id: GO:0048587
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of short-day photoperiodism, where the response associated with the photoperiodism is flowering. Flowering is defined by the switch from the vegetative to the reproductive phase.","definition_xrefs":["ISBN:0582015952","ISBN:0697037754","GOC:jid","ISBN:0709408862","GOC:pj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of photoperiodism, flowering","termid":"GO:2000028"},{"relation_name":"regulates","term_name":"short-day photoperiodism, flowering","termid":"GO:0048575"}],"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 short-day photoperiodism, flowering","termid":"GO:0048587"}


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: PBO:0050959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon lambda 2","termid":"PBO:0050959"}


id: PBO:0000427
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA Z4","termid":"PBO:0000427"}


id: GO:0006617
data:
  {"annotated_genes":["SJAG_01759","SJAG_01282","SJAG_02456"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91138,113808,114574],"is_not":false,"summary":null,"term":"GO:0006617"}]},"cv_name":"biological_process","definition":"The process in which SRP binds to the signal peptide in a nascent protein, causing protein elongation to pause, during cotranslational membrane targeting.","definition_xrefs":["ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"},{"relation_name":"part_of","term_name":"SRP-dependent cotranslational protein targeting to membrane","termid":"GO:0006614"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01282":null,"SJAG_01759":null,"SJAG_02456":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006605"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150","GO:0006605"],"is_obsolete":false,"name":"SRP-dependent cotranslational protein targeting to membrane, signal sequence recognition","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"SRP-dependent cotranslational membrane targeting, signal sequence recognition","type":"exact"},{"name":"SRP-dependent cotranslational protein-membrane targeting, signal sequence recognition","type":"exact"},{"name":"signal sequence recognition during SRP-dependent cotranslational protein targeting to membrane","type":"exact"}],"termid":"GO:0006617","terms_by_termid":{"GO:0006617":null}}


id: GO:0030296
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Increases the activity of a protein tyrosine kinase, an enzyme which phosphorylates a tyrosyl phenolic group on a protein.","definition_xrefs":["GOC:ai","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase activator activity","termid":"GO:0030295"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0030234","GO:0003674","GO:0140677","GO:0098772"],"is_obsolete":false,"name":"protein tyrosine kinase activator activity","termid":"GO:0030296"}


id: PBO:0077455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMEM183A pseudogene 5","termid":"PBO:0077455"}


id: GO:0070844
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of polyubiquitinated proteins in a cell, including the movement of proteins between specific compartments or structures within a cell.","definition_xrefs":["PMID:14675537","GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein transport","termid":"GO:0006886"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"polyubiquitinated protein transport","synonyms":[{"name":"polyubiquitylated protein transport","type":"exact"}],"termid":"GO:0070844"}


id: PBO:0056791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MFF divergent transcript","termid":"PBO:0056791"}


id: PBO:0038424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-2-macroglobulin like 1","termid":"PBO:0038424"}


id: MONDO:0022975
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diaphragmatic agenesis radial aplasia omphalocele","termid":"MONDO:0022975","xrefs":{"Monarch":{"xref_id":"0022975"}}}


id: PBO:0083872
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein of unknown function; predicted to be part of an SCF ubiquitin protease complex; involved in regulating protein levels of sulfur metabolism enzymes; may interact with ribosomes, based on co-purification experiments","termid":"PBO:0083872"}


id: PBO:0077347
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 87B","termid":"PBO:0077347"}


id: GO:0005427
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a oligopeptide from one side of a membrane to the other, up its concentration gradient. The transporter binds the solute and undergoes a series of conformational changes. Transport works equally well in either direction and is driven by proton movement.","definition_xrefs":["GOC:mtg_transport","OMIM:600544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary active transmembrane transporter activity","termid":"GO:0015291"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"proton-dependent oligopeptide secondary active transmembrane transporter activity","synonyms":[{"name":"hydrogen/oligopeptide symporter","type":"related"},{"name":"proton-dependent oligopeptide transporter activity","type":"exact"}],"termid":"GO:0005427"}


id: PBO:0049787
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex group 22 (gene/pseudogene)","termid":"PBO:0049787"}


id: PBO:0085022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nicotinic acid mononucleotide adenylyltransferase; catalyzes the transfer of the adenylyl moiety of ATP to nicotinamide mononucleotide to form NAD; involved in pathways of NAD biosynthesis, including the de novo, NAD(+) salvage, and nicotinamide riboside salvage pathways; homolog of human NMNAT; NMA1 has a paralog, NMA2, that arose from the whole genome duplication","termid":"PBO:0085022"}


id: GO:0140881
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of the chemical reactions and pathways resulting in the formation of the fungal metabolite terrein.","definition_xrefs":["PMID:25852654","PMID:24816227"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of secondary metabolite biosynthetic process","termid":"GO:1900378"},{"relation_name":"is_a","term_name":"positive regulation of alcohol biosynthetic process","termid":"GO:1902932"},{"relation_name":"positively_regulates","term_name":"terrein biosynthetic process","termid":"GO:0140880"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0019748"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0019748"],"is_obsolete":false,"name":"positive regulation terrein biosynthetic process","termid":"GO:0140881"}


id: PBO:0041590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carbonic anhydrase 4","termid":"PBO:0041590"}


id: GO:0060405
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of penile erection. Penile erection is the hardening, enlarging and rising of the penis which often occurs in the sexually aroused male and enables sexual intercourse. Achieved by increased inflow of blood into the vessels of erectile tissue, and decreased outflow.","definition_xrefs":["GOC:dph","GOC:add","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"penile erection","termid":"GO:0043084"}],"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 penile erection","termid":"GO:0060405"}


id: PBO:0110169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial and nuclear tRNA (guanine-N2-)-methyltransferase Trm1","termid":"PBO:0110169"}


id: PBO:0062291
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 M member 2 pseudogene","termid":"PBO:0062291"}


id: PR:O13784
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rps2401 gene.","definition_xrefs":["UniProtKB:O13784","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S24-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17G6.06","synonyms":[{"name":"Spom972h-rps2401","type":"exact"}],"termid":"PR:O13784"}


id: PBO:0001253
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.5.3.1","termid":"PBO:0001253"}


id: GO:0097180
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex that contains a serine protease inhibitor and a protease; formation of the complex inhibits serine protease activity.","definition_xrefs":["PMID:6323392","GOC:ans"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protease inhibitor complex","termid":"GO:0097179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"serine protease inhibitor complex","synonyms":[{"name":"serine-type endopeptidase inhibitor complex","type":"exact"},{"name":"serpin complex","type":"exact"}],"termid":"GO:0097180"}


id: PBO:0002030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha SNAP (predicted)","termid":"PBO:0002030"}


id: PBO:0027662
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_proteasomal_ubiquitin-dependent_protein_degradation","termid":"PBO:0027662"}


id: RO:0002313
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Holds between p and c when p is a localization process (localization covers maintenance of localization as well as its establishment)  and the outcome of this process is to regulate the localization of c.","direct_ancestors":[{"relation_name":"is_a","term_name":"has_participant","termid":"RO:0000057"},{"relation_name":"is_a","term_name":"related_via_localization_to","termid":"RO:0002337"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transports_or_maintains_localization_of","termid":"RO:0002313"}


id: FYPO:0000105
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 cyclosporin A. Cells stop growing (and may die) at a concentration of cyclosporin A 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:0005447"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0001985","FYPO:0002683","FYPO:0000139","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to cyclosporin A","synonyms":[{"name":"hypersensitive to cyclosporin A","type":"exact"},{"name":"sensitive to cyclosporin A during mitotic cell cycle","type":"related"},{"name":"sensitive to cyclosporin A during vegetative growth","type":"exact"},{"name":"sensitive to cyclosporine","type":"exact"}],"termid":"FYPO:0000105"}


id: MONDO:0024472
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infectious disease of the Mediterranean area, the Crimea, Africa, and India, caused by infection with rickettsia conorii subsp. coronorii.","definition_xrefs":["PMID:18760001"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Rickettsia conorii infectious disease","termid":"MONDO:0005677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"boutonneuse fever","secondary_identifiers":["GARD:19031","icd11.foundation:1771381430","ICD9:082.1","SCTID:186774005","Orphanet:101334","DOID:14095","MedDRA:10006045","MEDGEN:14205","Orphanet:83313","UMLS:C0006060","MESH:D001907"],"synonyms":[{"name":"African tick typhus","type":"exact"},{"name":"Conor and Bruch's disease","type":"exact"},{"name":"Kenya fever","type":"exact"},{"name":"Kenya tick typhus","type":"exact"},{"name":"Kenyan tick typhus","type":"exact"},{"name":"Mediterranean spotted fever","type":"exact"},{"name":"Mediterranean tick fever","type":"exact"},{"name":"Rickettsia conorii spotted fever","type":"broad"},{"name":"South African tick-bite fever","type":"exact"},{"name":"boutonneuse disease","type":"exact"},{"name":"boutonneuse fever","type":"exact"},{"name":"fievre boutonneuse","type":"exact"},{"name":"marseilles fever","type":"exact"},{"name":"tick typhus due to rickettsia conorii","type":"exact"}],"termid":"MONDO:0024472","xrefs":{"Monarch":{"xref_id":"0024472"}}}


id: PR:O14136
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A peroxisomal membrane protein PEX13 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR19332: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":"peroxisomal membrane protein pex13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3C7.10","secondary_identifiers":["UniProtKB:O14136"],"synonyms":[{"name":"SPAC3C7.10","type":"related"},{"name":"Spom972h-PEX13","type":"exact"},{"name":"peroxin-13 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14136"}


id: FYPO:0001831
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of phosphoglycerate mutase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"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:0001985","FYPO:0000707","FYPO:0000661","FYPO:0000654","FYPO:0000652"],"is_obsolete":false,"name":"abnormal phosphoglycerate mutase activity","termid":"FYPO:0001831"}


id: FYPO:0003981
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of glutathione transferase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal glutathione transferase activity","termid":"FYPO:0003980"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000654","FYPO:0001985","FYPO:0000661","FYPO:0000652"],"is_obsolete":false,"name":"increased glutathione transferase activity","termid":"FYPO:0003981"}


id: MONDO:0019431
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Portal vein thrombosis (PVT) is associated with acute (recent) or chronic (long-standing) thrombosis of the portal system.","definition_xrefs":["Orphanet:854"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liver disorder","termid":"MONDO:0005154"}],"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:0004335","MONDO:0002515"],"is_obsolete":false,"name":"primitive portal vein thrombosis","secondary_identifiers":["GARD:18707","MedDRA:10036206","ICD10CM:I81"],"synonyms":[{"name":"non-cirrhotic portal vein thrombosis","type":"exact"}],"termid":"MONDO:0019431","xrefs":{"Monarch":{"xref_id":"0019431"}}}


id: GO:0016045
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a stimulus from a bacterium is received and converted into a molecular signal.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to bacterium","termid":"GO:0009617"},{"relation_name":"is_a","term_name":"detection of other organism","termid":"GO:0098543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of bacterium","secondary_identifiers":["GO:0009598","GO:0009681"],"synonyms":[{"name":"detection of bacteria","type":"exact"},{"name":"perception of bacteria","type":"related"},{"name":"perception of bacterium","type":"related"}],"termid":"GO:0016045"}


id: PBO:0031740
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_mating_type_switching","termid":"PBO:0031740"}


id: MONDO:1010003
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Narcolepsy that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"narcolepsy, non-human animal","secondary_identifiers":["OMIA:000703"],"termid":"MONDO:1010003","xrefs":{"Monarch":{"xref_id":"1010003"}}}


id: PBO:0058614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6746","termid":"PBO:0058614"}


id: PBO:0048778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanine monophosphate synthase","termid":"PBO:0048778"}


id: FYPO:0000063
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which DNA recombination is abnormal. DNA recombination is a process that results in reassortment of genes, producing gene combinations different from those that were present in the parents.","definition_xrefs":["GO:0006310","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA metabolism phenotype","termid":"FYPO:0000293"},{"relation_name":"is_a","term_name":"abnormal metabolic process","termid":"FYPO:0000860"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000293"],"is_obsolete":false,"name":"abnormal DNA recombination","synonyms":[{"name":"abnormal recombination","type":"exact"},{"name":"recombination defects","type":"exact"}],"termid":"FYPO:0000063"}


id: GO:0003974
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-N-acetyl-D-glucosamine = UDP-N-acetyl-D-galactosamine.","definition_xrefs":["EC:5.1.3.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"racemase and epimerase activity, acting on carbohydrates and derivatives","termid":"GO:0016857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"UDP-N-acetylglucosamine 4-epimerase activity","secondary_identifiers":["MetaCyc:UDP-N-ACETYLGLUCOSAMINE-4-EPIMERASE-RXN","RHEA:20517"],"synonyms":[{"name":"UDP acetylglucosamine epimerase activity","type":"related"},{"name":"UDP-GlcNAc 4-epimerase activity","type":"related"},{"name":"UDP-N-acetyl-D-glucosamine 4-epimerase activity","type":"related"},{"name":"uridine 5'-diphospho-N-acetylglucosamine-4-epimerase activity","type":"related"},{"name":"uridine diphosphate N-acetylglucosamine-4-epimerase activity","type":"related"},{"name":"uridine diphosphoacetylglucosamine epimerase activity","type":"related"}],"termid":"GO:0003974"}


id: PBO:0070223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 156 pseudogene","termid":"PBO:0070223"}


id: PBO:0004022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial PPR repeat protein Ppr3","termid":"PBO:0004022"}


id: GO:1903024
data:
  {"annotated_genes":["SJAG_02169"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90242],"is_not":false,"summary":null,"term":"GO:1903024"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of formation of an ascospore-type prospore membrane.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:11405625"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular component biogenesis","termid":"GO:0044089"},{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"is_a","term_name":"positive regulation of ascospore formation","termid":"GO:0075296"},{"relation_name":"is_a","term_name":"regulation of ascospore-type prospore membrane formation","termid":"GO:1903023"},{"relation_name":"positively_regulates","term_name":"ascospore-type prospore membrane formation","termid":"GO:0032120"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02169":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0030437"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0061024"},{"rel_name":"positively_regulates","termid":"GO:0030437"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0030437","GO:0061024","GO:0007049"],"is_obsolete":false,"name":"positive regulation of ascospore-type prospore membrane formation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of FSM assembly","type":"narrow"},{"name":"activation of FSM biosynthesis","type":"narrow"},{"name":"activation of FSM formation","type":"narrow"},{"name":"activation of ascospore-type prospore membrane assembly","type":"narrow"},{"name":"activation of forespore membrane biosynthesis","type":"narrow"},{"name":"activation of forespore membrane formation","type":"narrow"},{"name":"positive regulation of FSM assembly","type":"exact"},{"name":"positive regulation of FSM biosynthesis","type":"exact"},{"name":"positive regulation of FSM formation","type":"exact"},{"name":"positive regulation of ascospore-type prospore membrane assembly","type":"related"},{"name":"positive regulation of forespore membrane biosynthesis","type":"exact"},{"name":"positive regulation of forespore membrane formation","type":"exact"},{"name":"up regulation of FSM assembly","type":"exact"},{"name":"up regulation of FSM biosynthesis","type":"exact"},{"name":"up regulation of FSM formation","type":"exact"},{"name":"up regulation of ascospore-type prospore membrane assembly","type":"exact"},{"name":"up regulation of forespore membrane biosynthesis","type":"exact"},{"name":"up regulation of forespore membrane formation","type":"exact"},{"name":"up-regulation of FSM assembly","type":"exact"},{"name":"up-regulation of FSM biosynthesis","type":"exact"},{"name":"up-regulation of FSM formation","type":"exact"},{"name":"up-regulation of ascospore-type prospore membrane assembly","type":"exact"},{"name":"up-regulation of forespore membrane biosynthesis","type":"exact"},{"name":"up-regulation of forespore membrane formation","type":"exact"},{"name":"upregulation of FSM assembly","type":"exact"},{"name":"upregulation of FSM biosynthesis","type":"exact"},{"name":"upregulation of FSM formation","type":"exact"},{"name":"upregulation of ascospore-type prospore membrane assembly","type":"exact"},{"name":"upregulation of forespore membrane biosynthesis","type":"exact"},{"name":"upregulation of forespore membrane formation","type":"exact"}],"termid":"GO:1903024","terms_by_termid":{"GO:1903024":null}}


id: GO:0052753
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: propan-2-ol + coenzyme F420 = acetone + reduced coenzyme F420.","definition_xrefs":["PMID:15016352","PMID:8706724","GOC:mengo_curators","PMID:1879431"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on CH-OH group of donors","termid":"GO:0016614"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"propan-2-ol:coenzyme F420 oxidoreductase activity","synonyms":[{"name":"F420-dependent propan-2-ol dehydrogenase activity","type":"exact"},{"name":"F420-dependent secondary alcohol dehydrogenase activity","type":"broad"},{"name":"isopropanol:coenzyme F420 oxidoreductase activity","type":"exact"}],"termid":"GO:0052753"}


id: MONDO:0001772
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"rectal disorder","termid":"MONDO:0001593"}],"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":"ulcer of anus and rectum","secondary_identifiers":["DOID:13662","ICD10CM:K62.6","UMLS:C0400832","MEDGEN:1843457","ICD9:569.41"],"synonyms":[{"name":"anal and rectal ulcer","type":"exact"}],"termid":"MONDO:0001772","xrefs":{"Monarch":{"xref_id":"0001772"}}}


id: MONDO:0013845
data:
  {"annotated_genes":["SJAG_00321"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85833],"is_not":false,"summary":null,"term":"MONDO:0013845"}]},"cv_name":"mondo","definition":"Any auriculocondylar syndrome in which the cause of the disease is a mutation in the PLCB4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auriculocondylar syndrome","termid":"MONDO:0000107"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00321":null},"genotype_count":0,"is_obsolete":false,"name":"auriculocondylar syndrome 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:766318","OMIM:614669","UMLS:C3553404","GARD:15831"],"synonyms":[{"name":"ARCND2","type":"related"},{"name":"AURICULOCONDYLAR syndrome 2","type":"related"},{"name":"Auriculocondylar syndrome 2","type":"exact"},{"name":"Auriculocondylar syndrome type 2","type":"exact"},{"name":"PLCB4 auriculocondylar syndrome","type":"exact"},{"name":"auriculocondylar syndrome caused by mutation in PLCB4","type":"exact"}],"termid":"MONDO:0013845","terms_by_termid":{"MONDO:0013845":null},"xrefs":{"Monarch":{"xref_id":"0013845"}}}


id: MONDO:0019893
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal monosomy 19p13.3 is a rare chromosomal anomaly associated with a wide range of phenotypic features depending on the size of the deletion. It may present with intrauterine growth retardation, failure to thrive, global developmental delay, dysmorphic features (such as broad forehead, midface retrusion, broad nasal bridge, micrognathia, smooth philtrum, low-set, dysplastic ears), congenital anomalies (such as atrial septal defect, gastrointestinal anomalies, renal and urogenital malformations, agenesis of the corpus callosum) and other clinical features (such as hearing loss, visual impairment and immune dysregulation).","definition_xrefs":["Orphanet:96129"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of the short arm of chromosome 19","termid":"MONDO:0016897"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal monosomy 19p13.3","secondary_identifiers":["GARD:19326","MEDGEN:1665859","UMLS:C4749277"],"synonyms":[{"name":"distal deletion 19p","type":"exact"},{"name":"telomeric deletion 19p","type":"exact"}],"termid":"MONDO:0019893","xrefs":{"Monarch":{"xref_id":"0019893"}}}


id: GO:0140049
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of endocardial cushion to mesenchymal transition.","definition_xrefs":["GOC:BHF","GOC:BHF_miRNA","GOC:rph","PMID:21778427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardiac epithelial to mesenchymal transition","termid":"GO:0062042"},{"relation_name":"regulates","term_name":"endocardial cushion to mesenchymal transition","termid":"GO:0090500"}],"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 endocardial cushion to mesenchymal transition","termid":"GO:0140049"}


id: MONDO:0004286
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually slow-growing epithelial neoplasm with ductal differentiation that arises from the exocrine pancreas and grows mostly within the pancreatic ducts. Grossly, it is characterized by the presence of intraductal masses. Morphologically, there is proliferation of mucin-producing cells within the pancreatic ducts, intraductal accumulation of mucin, and a papillary growth pattern. It may be associated with the presence of an invasive carcinoma. It usually occurs in older patients. Signs and symptoms include epigastric pain, weight loss, jaundice, chronic pancreatitis, and diabetes mellitus.","definition_xrefs":["NCIT:C38342"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant exocrine pancreas neoplasm","termid":"MONDO:0002116"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"pancreatic intraductal papillary-mucinous neoplasm","secondary_identifiers":["UMLS:C4511687","MEDGEN:1373306","DOID:7575","ONCOTREE:IPMN"],"synonyms":[{"name":"IPMN","type":"exact"},{"name":"intraductal papillary mucinous neoplasm","type":"related"},{"name":"pancreatic IPMN","type":"exact"},{"name":"pancreatic intraductal papillary-mucinous neoplasm","type":"exact"},{"name":"pancreatic intraductal papillary-mucinous tumor","type":"exact"},{"name":"pancreatic intraductal papillary-mucinous tumour","type":"exact"}],"termid":"MONDO:0004286","xrefs":{"Monarch":{"xref_id":"0004286"}}}


id: PBO:0060786
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B11 pseudogene 1","termid":"PBO:0060786"}


id: MONDO:0004488
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenomyoma that arises from the cervix and is characterized by the presence of a glandular component exhibiting architectural complexity.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervical adenomyoma","termid":"MONDO:0003238"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cervical atypical polypoid adenomyoma","secondary_identifiers":["NCIT:C40234","UMLS:C1516409","DOID:8179","MEDGEN:273123"],"termid":"MONDO:0004488","xrefs":{"Monarch":{"xref_id":"0004488"}}}


id: PATO:0001878
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's consisting of two curves, in opposite directions. S-shaped.","definition_xrefs":["PATOC:CJM"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sigmoid","synonyms":[{"name":"S-shaped","type":"exact"},{"name":"sigmoidal","type":"exact"}],"termid":"PATO:0001878"}


id: MONDO:0016277
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cervical cancer","termid":"MONDO:0002974"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant mixed epithelial and mesenchymal tumor of cervix uteri","secondary_identifiers":["GARD:20490","Orphanet:213782","MEDGEN:1843195","UMLS:C5679806","ICD10CM:C53.0"],"synonyms":[{"name":"cervical malignant mixed epithelial and mesenchymal tumor","type":"exact"},{"name":"cervical malignant mixed epithelial and mesenchymal tumour","type":"exact"},{"name":"mixed epithelial and mesenchymal cancer of cervix uteri","type":"exact"}],"termid":"MONDO:0016277","xrefs":{"Monarch":{"xref_id":"0016277"}}}


id: GO:0071979
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell motility in which contractile cytoskeletal elements alter cell shape, resulting in the smooth movement of a cell through a liquid medium.","definition_xrefs":["PMID:18461074"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell swimming","termid":"GO:0071975"}],"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":"cytoskeleton-mediated cell swimming","synonyms":[{"name":"cytoskeleton-mediated swimming motility","type":"exact"}],"termid":"GO:0071979"}


id: FYPO:0004147
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of pyridoxine:NADP 4-dehydrogenase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal pyridoxine:NADP 4-dehydrogenase activity","termid":"FYPO:0004145"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000652","FYPO:0001985","FYPO:0000707","FYPO:0000661"],"is_obsolete":false,"name":"increased pyridoxine:NADP 4-dehydrogenase activity","termid":"FYPO:0004147"}


id: PBO:0027366
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mislocalized_actin_cortical_patches","termid":"PBO:0027366"}


id: PBO:0038364
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-directly_regulated_by","termid":"PBO:0038364"}


id: MONDO:0017264
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Syndromic recessive X-linked ichthyosis (RXLI) refers to the cases of RXLI that are associated with extracutaneous manifestations as part of a syndrome.","definition_xrefs":["Orphanet:281090"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"is_a","term_name":"X-linked ichthyosis syndrome","termid":"MONDO:0017269"}],"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":"syndromic recessive X-linked ichthyosis","secondary_identifiers":["GARD:17302","MEDGEN:904038","SCTID:717041008","UMLS:C4274085"],"synonyms":[{"name":"recessive X-linked ichthyosis with extracutaneous manifestations","type":"exact"},{"name":"syndrome associated with recessive X-linked ichthyosis","type":"exact"},{"name":"syndromic RXLI","type":"exact"},{"name":"syndromic X-linked ichthyosis","type":"exact"},{"name":"syndromic recessive X-linked ichthyosis","type":"exact"}],"termid":"MONDO:0017264","xrefs":{"Monarch":{"xref_id":"0017264"}}}


id: MONDO:0020510
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic syringomyelia is a rare, non-syndromic central nervous system malformation characterized by a longitudinally oriented fluid-filled cavity inside the spinal cord parenchyma or the central canal, without any readily identifiably cause. It is usually associated with pain, sensory and/or musculoskeletal disturbances, but it can also be an incidental and asymptomatic finding.","definition_xrefs":["Orphanet:99858"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary syringomyelia","termid":"MONDO:0020508"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"idiopathic syringomyelia","secondary_identifiers":["UMLS:C4511700","SCTID:725001004","GARD:19693","icd11.foundation:1218010255","MEDGEN:1378771"],"termid":"MONDO:0020510","xrefs":{"Monarch":{"xref_id":"0020510"}}}


id: GO:0030812
data:
  {"annotated_genes":["SJAG_05314","SJAG_00685"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72605,75583],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045820"}]},"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 breakdown of nucleotides.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of catabolic process","termid":"GO:0009895"},{"relation_name":"is_a","term_name":"regulation of nucleotide catabolic process","termid":"GO:0030811"},{"relation_name":"is_a","term_name":"negative regulation of nucleotide metabolic process","termid":"GO:0045980"},{"relation_name":"negatively_regulates","term_name":"nucleotide catabolic process","termid":"GO:0009166"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00685":null,"SJAG_05314":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0055086"},{"rel_name":"negatively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"negative regulation of nucleotide catabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"negative regulation of nucleotide catabolism","type":"exact"},{"name":"negative regulation of nucleotide degradation","type":"exact"},{"name":"down regulation of nucleotide catabolic process","type":"exact"},{"name":"down-regulation of nucleotide catabolic process","type":"exact"},{"name":"downregulation of nucleotide catabolic process","type":"exact"},{"name":"inhibition of nucleotide catabolic process","type":"narrow"},{"name":"negative regulation of nucleotide breakdown","type":"exact"}],"termid":"GO:0030812","terms_by_termid":{"GO:0045820":null}}


id: PBO:0040790
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beaded filament structural protein 1","termid":"PBO:0040790"}


id: GO:0048540
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the bursa of Fabricius over time, from its formation to the mature structure. The bursa of Fabricius is an organ found in birds involved in B cell differentiation.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hematopoietic or lymphoid organ development","termid":"GO:0048534"}],"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":"bursa of Fabricius development","termid":"GO:0048540"}


id: MONDO:0030689
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease","termid":"MONDO:0015626"}],"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":"Charcot-Marie-Tooth disease, demyelinating, IIA 1H","secondary_identifiers":["MEDGEN:1804752","OMIM:619764","UMLS:C5676926"],"synonyms":[{"name":"CMT1H","type":"exact"},{"name":"Charcot-Marie-Tooth disease, demyelinating, IIA 1H","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, IIA 1H","type":"exact"},{"name":"hereditary motor and sensory neuropathy, 1h","type":"exact"},{"name":"neuropathy, hereditary, with or without age-related macular degeneration","type":"exact"}],"termid":"MONDO:0030689","xrefs":{"Monarch":{"xref_id":"0030689"}}}


id: GO:0140862
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a ubiquitin molecule to histone 2A at the lysine-119 residue.","definition_xrefs":["PMID:28624371","PMID:22844243","PMID:25470042"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H2A ubiquitin ligase activity","termid":"GO:0141053"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004842"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0019787"}],"interesting_parent_ids":["GO:0004842","GO:0003824","GO:0016740","GO:0019787","GO:0016746","GO:0003674","GO:0140096"],"is_obsolete":false,"name":"histone H2AK119 ubiquitin ligase activity","synonyms":[{"name":"histone H2A-K119 ubiquitin ligase activity","type":"exact"},{"name":"histone ubiquitin ligase activity (H2A-K119 specific)","type":"exact"}],"termid":"GO:0140862"}


id: PBO:0018156
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nse5Ts Suppressor","termid":"PBO:0018156"}


id: PBO:0001784
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2',3'-cyclic-nucleotide 3'-phosphodiesterase (predicted)","termid":"PBO:0001784"}


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


id: GO:0106197
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the translocation of inorganic anions llinked to the hydrolysis of a diphosphate.","definition_xrefs":["GOC:hjd"],"gene_count":0,"genotype_count":0,"name":"obsolete translocase activity acting on inorganic anions linked to the hydrolysis of a diphosphate (obsolete GO:0106197)","termid":"GO:0106197"}


id: MONDO:0044717
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"},{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 4","termid":"MONDO:0016903"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4q25 proximal deletion syndrome","secondary_identifiers":["MEDGEN:1814447","UMLS:C5680087","GARD:22048","Orphanet:502437"],"synonyms":[{"name":"proximal del(4)(q25)","type":"exact"},{"name":"proximal monosomy 4q25","type":"exact"}],"termid":"MONDO:0044717","xrefs":{"Monarch":{"xref_id":"0044717"}}}


id: PBO:0076643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transforming growth factor beta regulator 4","termid":"PBO:0076643"}


id: GO:0060152
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The microtubule-based process in which a peroxisome is transported to, and/or maintained in, a specific location. A peroxisome is a small membrane-bounded organelle that uses dioxygen (O2) to oxidize organic molecules.","definition_xrefs":["GOC:dph","PMID:16449325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule-based process","termid":"GO:0007017"},{"relation_name":"is_a","term_name":"peroxisome localization","termid":"GO:0060151"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"microtubule-based peroxisome localization","synonyms":[{"name":"microtubule-based peroxisome localisation","type":"exact"}],"termid":"GO:0060152"}


id: PBO:0059109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MORN repeat containing 5","termid":"PBO:0059109"}


id: PBO:0042523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase 2 associated protein 2 pseudogene 1","termid":"PBO:0042523"}


id: MONDO:0016068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fibrochondrogenesis is a rare, neonatally lethal, rhizomelic chondrodysplasia. Eleven cases have been reported. The face is distinctive and characterized by protuberant eyes, flat midface, flat small nose with anteverted nares and a small mouth with long upper lip. Cleft palate, micrognathia and bifid tongue can occur. The limbs show marked shortness of all segments with relatively normal hands and feet. No internal anomalies other than omphalocele have been reported. Transmission is probably autosomal recessive. Recurrence in a consanguineous family (affecting both sexes) and concordance of affected male twins have been reported.","direct_ancestors":[{"relation_name":"is_a","term_name":"osteochondrodysplasia","termid":"MONDO:0005516"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"fibrochondrogenesis","secondary_identifiers":["SCTID:17144009","DOID:0060465","OMIMPS:228520","NANDO:2201016","Orphanet:2021","icd11.foundation:1412541453","MEDGEN:82700","UMLS:C0265282","MESH:C562524","GARD:2321"],"termid":"MONDO:0016068","xrefs":{"Monarch":{"xref_id":"0016068"}}}


id: GO:1901994
data:
  {"annotated_genes":["SJAG_04287","SJAG_00364","SJAG_01082","SJAG_04259","SJAG_02771","SJAG_03854","SJAG_01330","SJAG_04126","SJAG_01837","SJAG_04280","SJAG_01515","SJAG_03327"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105785,113941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905318"},{"annotations":[115503,90940,106081],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033315"},{"annotations":[116112,105786,101287],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033316"},{"annotations":[115452,111015],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110031"},{"annotations":[98198],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902103"},{"annotations":[113226],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905326"},{"annotations":[100826],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1905325"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of meiotic cell cycle phase transition.","definition_xrefs":["GOC:mtg_cell_cycle","PMID:22841721","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of meiotic cell cycle","termid":"GO:0051447"},{"relation_name":"is_a","term_name":"negative regulation of cell cycle phase transition","termid":"GO:1901988"},{"relation_name":"is_a","term_name":"regulation of meiotic cell cycle phase transition","termid":"GO:1901993"},{"relation_name":"negatively_regulates","term_name":"meiotic cell cycle phase transition","termid":"GO:0044771"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00364":null,"SJAG_01082":null,"SJAG_01330":null,"SJAG_01515":null,"SJAG_01837":null,"SJAG_02771":null,"SJAG_03327":null,"SJAG_03854":null,"SJAG_04126":null,"SJAG_04259":null,"SJAG_04280":null,"SJAG_04287":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"negative regulation of meiotic cell cycle phase transition","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of cell cycle transition","type":"broad"},{"name":"down regulation of meiotic cell cycle phase transition","type":"exact"},{"name":"down-regulation of cell cycle transition","type":"broad"},{"name":"down-regulation of meiotic cell cycle phase transition","type":"exact"},{"name":"downregulation of cell cycle transition","type":"broad"},{"name":"downregulation of meiotic cell cycle phase transition","type":"exact"},{"name":"inhibition of cell cycle transition","type":"broad"},{"name":"inhibition of meiotic cell cycle phase transition","type":"narrow"},{"name":"negative regulation of cell cycle transition","type":"broad"}],"termid":"GO:1901994","terms_by_termid":{"GO:0033315":null,"GO:0033316":null,"GO:0110031":null,"GO:1902103":null,"GO:1905318":null,"GO:1905325":null,"GO:1905326":null}}


id: MONDO:0019583
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Localized lichen myxedematosus (LM) with mixed features of different subtypes is a form of atypical lichen myxedematosus, characterized by mixed features of the 5 subtypes of localized LM which are: discrete papular LM, acral persistent papular mucinosis, self-healing papular mucinosis, papular mucinosis of infancy, and nodular LM.","definition_xrefs":["Orphanet:90398"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atypical lichen myxedematosus","termid":"MONDO:0019447"}],"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":"localized lichen myxedematosus with mixed features of different subtypes","secondary_identifiers":["GARD:19142","MEDGEN:1843441","UMLS:C5681465"],"termid":"MONDO:0019583","xrefs":{"Monarch":{"xref_id":"0019583"}}}


id: FYECO:0000343
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which ammonium sulfate was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ (NH4)2SO4","synonyms":[{"name":"+ ammonium sulfate","type":"exact"}],"termid":"FYECO:0000343"}


id: PBO:0089248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Smc5-6 complex non-SMC SUMO ligase subunit Nse2","termid":"PBO:0089248"}


id: PBO:0063794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHD finger protein 21B","termid":"PBO:0063794"}


id: GO:0015994
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving chlorophyll, any compound of magnesium complexed in a porphyrin (tetrapyrrole) ring and which functions as a photosynthetic pigment.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porphyrin-containing compound metabolic process","termid":"GO:0006778"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0033013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0033013","GO:0008150"],"is_obsolete":false,"name":"chlorophyll metabolic process","synonyms":[{"name":"chlorophyll metabolism","type":"exact"}],"termid":"GO:0015994"}


id: RO:0003002
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Holds between protein a (a transcription factor) and DNA element b if and only if a diminishes the process of transcription of b.","direct_ancestors":[{"relation_name":"is_a","term_name":"activity_directly_negatively_regulates_activity_of","termid":"RO:0002449"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"represses_expression_of","termid":"RO:0003002"}


id: GO:0060912
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process involved in the specification of cardiac cell identity. Once specification has taken place, a cell will be committed to differentiate down a specific pathway if left in its normal environment.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate specification","termid":"GO:0001708"},{"relation_name":"part_of","term_name":"cardiac cell fate commitment","termid":"GO:0060911"}],"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 cell fate specification","synonyms":[{"name":"cardiocyte cell fate specification","type":"exact"}],"termid":"GO:0060912"}


id: GO:0070327
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of thyroid hormone into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone transport","termid":"GO:0009914"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"thyroid hormone transport","synonyms":[{"name":"thyroxine transport","type":"narrow"},{"name":"triiodothyronine transport","type":"narrow"}],"termid":"GO:0070327"}


id: GO:0035235
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by glutamate binding to a glutamate receptor on the surface of the target cell, followed by the movement of ions through a channel in the receptor complex, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["ISBN:0198506732","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glutamate receptor signaling pathway","termid":"GO:0007215"},{"relation_name":"is_a","term_name":"ligand-gated ion channel signaling pathway","termid":"GO:1990806"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"ionotropic glutamate receptor signaling pathway","synonyms":[{"name":"ionotropic glutamate receptor signalling pathway","type":"exact"}],"termid":"GO:0035235"}


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


id: PBO:0075559
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPG7 matrix AAA peptidase subunit, paraplegin","termid":"PBO:0075559"}


id: PBO:0083536
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified ORF YAP1802/YGR241C","termid":"PBO:0083536"}


id: PR:P87240
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- not2 gene.","definition_xrefs":["UniProtKB:P87240","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":"general negative regulator of transcription subunit 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC4G3.15c","synonyms":[{"name":"Spom972h-not2","type":"exact"}],"termid":"PR:P87240"}


id: FYPO:0004969
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell growth phenotype in which vegetative cell population growth is cell population growth is normal (i.e. indistinguishable from wild type) under conditions of phosphate starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0000003","FYPO:0002058","FYPO:0002057","FYPO:0002060","FYPO:0000257"],"is_obsolete":false,"name":"normal vegetative cell population growth during phosphate starvation","synonyms":[{"name":"normal vegetative cell population growth during phosphate depletion","type":"exact"},{"name":"normal vegetative cell population growth during phosphate deprivation","type":"exact"},{"name":"normal vegetative cell population growth during phosphate limitation","type":"exact"},{"name":"normal vegetative cell population growth in response to phosphate starvation","type":"exact"}],"termid":"FYPO:0004969"}


id: MONDO:1011040
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any oculocutaneous albinism that occurs in cattle due to a mutation in the SLC45A2 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oculocutaneous albinism, non-human animal","termid":"MONDO:1012579"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oculocutaneous albinism, SLC45A2-related, cattle","secondary_identifiers":["OMIA:001821-9913"],"synonyms":[{"name":"coat color albinism, oculocutaneous type IV, cattle","type":"related"}],"termid":"MONDO:1011040","xrefs":{"Monarch":{"xref_id":"1011040"}}}


id: PBO:0084503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Meiosis-specific protein that localizes to chromosomes; prevents synapsis between nonhomologous chromosomes and ensures synapsis between homologs; forms complex with Mnd1p to promote homolog pairing and meiotic double-strand break repair; heterodimer of Hop2p-Mnd1p stimulates the Dmc1p-mediated strand invasion","termid":"PBO:0084503"}


id: GO:0051710
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the cytolysis by an organism of cells in another organism.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cytolysis in another organism (obsolete GO:0051710)","synonyms":[{"name":"regulation of cytolysis in other organism","type":"exact"},{"name":"regulation of cytolysis of cells of another organism","type":"exact"}],"termid":"GO:0051710"}


id: GO:1901066
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of syringal lignin.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lignin biosynthetic process","termid":"GO:0009809"},{"relation_name":"is_a","term_name":"syringal lignin metabolic process","termid":"GO:1901064"}],"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:0019748","GO:0008150"],"is_obsolete":false,"name":"syringal lignin biosynthetic process","synonyms":[{"name":"S-lignin biosynthetic process","type":"exact"},{"name":"syringal lignin anabolism","type":"exact"},{"name":"syringal lignin biosynthesis","type":"exact"},{"name":"syringal lignin formation","type":"exact"},{"name":"syringal lignin synthesis","type":"exact"}],"termid":"GO:1901066"}


id: MONDO:0000534
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A mucoepidermoid carcinoma that involves the trachea.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucoepidermoid carcinoma","termid":"MONDO:0003036"},{"relation_name":"is_a","term_name":"trachea carcinoma","termid":"MONDO:0003184"}],"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":"trachea mucoepidermoid carcinoma","secondary_identifiers":["DOID:0050919","MEDGEN:835970","SCTID:707379000","UMLS:C3873401"],"synonyms":[{"name":"trachea mucoepidermoid carcinoma","type":"exact"}],"termid":"MONDO:0000534","xrefs":{"Monarch":{"xref_id":"0000534"}}}


id: GO:0042409
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + caffeoyl-CoA = S-adenosyl-L-homocysteine + feruloyl-CoA.","definition_xrefs":["EC:2.1.1.104"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-methyltransferase activity","termid":"GO:0008171"},{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016741","GO:0003824"],"is_obsolete":false,"name":"caffeoyl-CoA O-methyltransferase activity","secondary_identifiers":["MetaCyc:CAFFEOYL-COA-O-METHYLTRANSFERASE-RXN","RHEA:16925"],"synonyms":[{"name":"S-adenosyl-L-methionine:caffeoyl-CoA 3-O-methyltransferase activity","type":"related"},{"name":"caffeoyl CoA:S-adenosyl-L-methionine O-methyltransferase activity","type":"exact"},{"name":"caffeoyl coenzyme A methyltransferase activity","type":"exact"},{"name":"caffeoyl-CoA 3-O-methyltransferase activity","type":"exact"},{"name":"trans-caffeoyl-CoA 3-O-methyltransferase activity","type":"related"}],"termid":"GO:0042409"}


id: PBO:0086438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative K+/H+ antiporter; involved in intracellular cation homeostasis; promotes copper binding to Fet3p multicopper oxidase; localized to Golgi vesicles and detected in highly purified mitochondria in high-throughput studies","termid":"PBO:0086438"}


id: GO:1990956
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a fibroblast guided by a specific chemical concentration gradient. Movement may be towards a higher concentration (positive chemotaxis) or towards a lower concentration (negative chemotaxis).","definition_xrefs":["PMID:8760137","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell chemotaxis","termid":"GO:0060326"}],"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":"fibroblast chemotaxis","termid":"GO:1990956"}


id: PBO:0012831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exosome subunit Rrp40","termid":"PBO:0012831"}


id: PBO:0056433
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MARK2 pseudogene 6","termid":"PBO:0056433"}


id: PBO:0062484
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 A member 3 pseudogene","termid":"PBO:0062484"}


id: MONDO:0014599
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the COL4A3BP gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant non-syndromic intellectual disability","termid":"MONDO:0015802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"intellectual disability, autosomal dominant 34","secondary_identifiers":["UMLS:C4225156","MEDGEN:907277","OMIM:616351","DOID:0070064"],"synonyms":[{"name":"COL4A3BP autosomal dominant non-syndromic intellectual disability","type":"exact"},{"name":"MRD34","type":"exact"},{"name":"autosomal dominant intellectual disability 34","type":"exact"},{"name":"autosomal dominant mental retardation 34","type":"exact"},{"name":"autosomal dominant non-syndromic intellectual disability 34","type":"related"},{"name":"autosomal dominant non-syndromic intellectual disability caused by mutation in COL4A3BP","type":"exact"},{"name":"intellectual developmental disorder, autosomal dominant 34","type":"exact"},{"name":"intellectual disability, autosomal dominant 34","type":"exact"},{"name":"intellectual disability, autosomal dominant type 34","type":"exact"},{"name":"mental retardation, autosomal dominant 34","type":"related"},{"name":"mental retardation, autosomal dominant type 34","type":"exact"}],"termid":"MONDO:0014599","xrefs":{"Monarch":{"xref_id":"0014599"}}}


id: PBO:0041593
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carbonic anhydrase 5B","termid":"PBO:0041593"}


id: PBO:0044921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DiGeorge syndrome critical region gene 6 like","termid":"PBO:0044921"}


id: PBO:0109223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin gamma complex component 4","termid":"PBO:0109223"}


id: GO:0033089
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of T cell differentiation in the thymus.","definition_xrefs":["GOC:mah","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of T cell differentiation in thymus","termid":"GO:0033081"},{"relation_name":"is_a","term_name":"positive regulation of T cell differentiation","termid":"GO:0045582"},{"relation_name":"positively_regulates","term_name":"T cell differentiation in thymus","termid":"GO:0033077"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"positive regulation of T cell differentiation in thymus","synonyms":[{"name":"positive regulation of T cell development in thymus","type":"related"},{"name":"positive regulation of thymic T cell differentiation","type":"exact"},{"name":"positive regulation of thymocyte cell differentiation","type":"exact"},{"name":"positive regulation of thymocyte differentiation","type":"exact"}],"termid":"GO:0033089"}


id: GO:0099069
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The initial, indirect interaction between a synaptic vesicle membrane and a the preseynaptic membrane active zone. This interaction is mediated by tethering factors (or complexes), which interact with both membranes. This process is distinct from and prior to synaptic vesicle priming and fusion.","definition_xrefs":["GOC:rn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle tethering involved in exocytosis","termid":"GO:0090522"},{"relation_name":"part_of","term_name":"synaptic vesicle docking","termid":"GO:0016081"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0140056"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0140056","GO:0008150","GO:0006810","GO:0016192","GO:0023052"],"is_obsolete":false,"name":"synaptic vesicle tethering involved in synaptic vesicle exocytosis","termid":"GO:0099069"}


id: GO:0047550
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-hydroxyadipate + NAD+ = 2-oxoadipate + H+ + NADH.","definition_xrefs":["RHEA:14793","EC:1.1.1.172"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"2-oxoadipate reductase activity","secondary_identifiers":["MetaCyc:2-OXOADIPATE-REDUCTASE-RXN","KEGG_REACTION:R01932"],"synonyms":[{"name":"2-hydroxyadipate:NAD+ 2-oxidoreductase activity","type":"related"},{"name":"2-ketoadipate reductase activity","type":"related"},{"name":"alpha-ketoadipate reductase activity","type":"related"}],"termid":"GO:0047550"}


id: PBO:0071095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 97","termid":"PBO:0071095"}


id: GO:0060193
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of lipase activity, the hydrolysis of a lipid or phospholipid.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of hydrolase activity","termid":"GO:0051345"}],"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 lipase activity","termid":"GO:0060193"}


id: MONDO:0024891
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"meningitis","termid":"MONDO:0021108"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-infectious meningitis","secondary_identifiers":["UMLS:C5539586","SCTID:230155003","MEDGEN:1783059"],"synonyms":[{"name":"non-infective meningitis","type":"exact"}],"termid":"MONDO:0024891","xrefs":{"Monarch":{"xref_id":"0024891"}}}


id: PBO:0055024
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 2439","termid":"PBO:0055024"}


id: MONDO:0100424
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acute myeloid leukemia that has the chromosomal anomaly NRAS gene mutation. (A change in the structure of the NRAS gene.)","definition_xrefs":["NCIT:C41381"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"acute myeloid leukemia, NRAS gene mutation","synonyms":[{"name":"AML, N-RAS Gene Mutation","type":"exact"},{"name":"AML, NRAS gene mutation","type":"exact"},{"name":"AML, Neuroblastoma RAS Viral Oncogene Homolog Gene Mutation","type":"exact"}],"termid":"MONDO:0100424","xrefs":{"Monarch":{"xref_id":"0100424"}}}


id: MONDO:0009622
data:
  {"annotated_genes":["SJAG_01076"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86776],"is_not":false,"summary":null,"term":"MONDO:0009622"}]},"cv_name":"mondo","definition":"Jawad syndrome is a rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by congenital microcephaly with facial dysmorphism (sloping forehead, prominent nose, mild retrognathia), moderate to severe, non-progressive intellectual disability and symmetrical digital malformations of variable degree, including brachydactyly of the fifth fingers with single flexion crease, clinodactyly, syndactyly, polydactyly and hallux valgus. Congenital anonychia and white café au lait-like spots on the skin of hands and feet are also associated.","definition_xrefs":["Orphanet:313795"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01076":null},"genotype_count":0,"is_obsolete":false,"name":"Jawad syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:810673","UMLS:C0796063","OMIM:251255","GARD:17410"],"synonyms":[{"name":"JAWAD syndrome","type":"related"},{"name":"JWDS","type":"related"},{"name":"Jawad syndrome","type":"exact"},{"name":"Kelly syndrome","type":"related"},{"name":"microcephaly with intellectual disability and digital anomalies","type":"related"},{"name":"microcephaly with mental retardation and digital anomalies","type":"related"}],"termid":"MONDO:0009622","terms_by_termid":{"MONDO:0009622":null},"xrefs":{"Monarch":{"xref_id":"0009622"}}}


id: MOD:01347
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A modification produced in a non-enzymatic reaction between a carbohydrate carbonyl group (C1 of aldohexose or C2 of fructose) and an L-lysine residue to form a Schiff-base or an Amadori ketosamine lysine adduct.","definition_xrefs":["DeltaMass:0","Unimod:41#K","PubMed:15279557"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycated residue","termid":"MOD:00767"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"hexose glycated L-lysine","synonyms":[{"name":"Hex","type":"related"},{"name":"Hexose","type":"related"}],"termid":"MOD:01347"}


id: GO:0120148
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A structure in a host cell comprised of a core structure (in most organisms, a pair of centrioles) and peripheral material from which a microtubule-based structure, such as a spindle apparatus, is organized. Centrosomes occur close to the nucleus during interphase in many eukaryotic cells, though in animal cells it changes continually during the cell-division cycle.","definition_xrefs":["ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cytoskeleton","termid":"GO:0044163"}],"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":"host cell centrosome","synonyms":[{"name":"host centrosome","type":"exact"}],"termid":"GO:0120148"}


id: GO:1901655
data:
  {"annotated_genes":["SJAG_02960","SJAG_01162"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104514],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140041"},{"annotations":[104693],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036245"}]},"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 ketone stimulus.","definition_xrefs":["GOC:pr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to ketone","termid":"GO:1901654"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01162":null,"SJAG_02960":null},"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 ketone","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1901655","terms_by_termid":{"GO:0036245":null,"GO:0140041":null}}


id: SO:0001634
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant located within a half KB of the end of a gene.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"downstream_gene_variant","termid":"SO:0001632"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"500B_downstream_variant","synonyms":[{"name":"500B downstream variant","type":"exact"},{"name":"near-gene-3","type":"exact"}],"termid":"SO:0001634"}


id: PBO:0051125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 1/OR16-3 (pseudogene)","termid":"PBO:0051125"}


id: FYPO:0004701
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a cell does not alter the timing or rate of cell division when shifted from one nitrogen source to another. Normally, cell division is delayed upon shifting from a poor to a rich nitrogen source, and accelerated upon shifting from a rich to a poor nitrogen source.","definition_xrefs":["PMID:689088","PomBase:mah","PMID:872891"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population phenotype","termid":"FYPO:0000003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000003"],"is_obsolete":false,"name":"abolished cell division timing change upon nitrogen source shift","synonyms":[{"name":"abolished cell division rate change upon nitrogen source shift","type":"related"},{"name":"abolished change in cell division rate upon nitrogen source shift","type":"related"},{"name":"abolished change in cell division timing upon nitrogen source shift","type":"exact"},{"name":"abolished nutritional modulation of cell division","type":"related"},{"name":"unchanged cell division timing upon nitrogen source shift","type":"related"}],"termid":"FYPO:0004701"}


id: PBO:0068932
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 175, pseudogene","termid":"PBO:0068932"}


id: GO:0035481
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the series of molecular signals initiated by binding of an extracellular ligand to a Notch receptor on the surface of the target cell that contributes to heart induction.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of Notch signaling pathway involved in heart induction (obsolete GO:0035481)","synonyms":[{"name":"positive regulation of Notch signalling pathway involved in heart induction","type":"exact"}],"termid":"GO:0035481"}


id: PBO:0049059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 65","termid":"PBO:0049059"}


id: PBO:0091639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"extracellular phospholipase","termid":"PBO:0091639"}


id: MONDO:0005889
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete orthomyxoviridae infectious disease (obsolete MONDO:0005889)","termid":"MONDO:0005889","xrefs":{"Monarch":{"xref_id":"0005889"}}}


id: GO:0022872
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 + mannitol(out) = protein histidine + mannitol phosphate(in). This differs from primary and secondary active transport in that the solute is modified during transport.","definition_xrefs":["ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-N(PI)-phosphohistidine-sugar phosphotransferase activity","termid":"GO:0008982"},{"relation_name":"is_a","term_name":"mannitol transmembrane transporter activity","termid":"GO:0015575"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"protein-N(PI)-phosphohistidine-mannitol phosphotransferase system transmembrane transporter activity","synonyms":[{"name":"mannitol PTS transporter activity","type":"exact"}],"termid":"GO:0022872"}


id: GO:0002291
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The change in morphology and behavior of a mature or immature T cell resulting from exposure to an antigen for which its T cell receptor is specific bound to an MHC molecule on an antigen presenting cell, leading to the initiation or perpetuation of an immune response.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell activation involved in immune response","termid":"GO:0002286"}],"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":"T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell","synonyms":[{"name":"T lymphocyte activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell","type":"exact"},{"name":"T-cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell","type":"exact"},{"name":"T-lymphocyte activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell","type":"exact"}],"termid":"GO:0002291"}


id: GO:1904465
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of matrix metallopeptidase secretion.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:8679543"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein secretion","termid":"GO:0050709"},{"relation_name":"is_a","term_name":"regulation of matrix metallopeptidase secretion","termid":"GO:1904464"},{"relation_name":"negatively_regulates","term_name":"matrix metallopeptidase secretion","termid":"GO:1990773"}],"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 matrix metallopeptidase secretion","synonyms":[{"name":"down regulation of MMP secretion","type":"exact"},{"name":"down regulation of matrix metallopeptidase secretion","type":"exact"},{"name":"down regulation of matrix metalloproteinase secretion","type":"narrow"},{"name":"down-regulation of MMP secretion","type":"exact"},{"name":"down-regulation of matrix metallopeptidase secretion","type":"exact"},{"name":"down-regulation of matrix metalloproteinase secretion","type":"narrow"},{"name":"downregulation of MMP secretion","type":"exact"},{"name":"downregulation of matrix metallopeptidase secretion","type":"exact"},{"name":"downregulation of matrix metalloproteinase secretion","type":"narrow"},{"name":"inhibition of MMP secretion","type":"narrow"},{"name":"inhibition of matrix metallopeptidase secretion","type":"narrow"},{"name":"inhibition of matrix metalloproteinase secretion","type":"narrow"},{"name":"negative regulation of MMP secretion","type":"exact"},{"name":"negative regulation of matrix metalloproteinase secretion","type":"narrow"}],"termid":"GO:1904465"}


id: MONDO:0004100
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lung carcinoma characterized by a combination of small cell carcinoma and squamous cell carcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung neuroendocrine neoplasm","termid":"MONDO:0005454"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lung mixed small cell and squamous cell carcinoma","secondary_identifiers":["UMLS:C1334788","MEDGEN:235331","NCIT:C9423","DOID:7081"],"synonyms":[{"name":"combined small cell and squamous cell lung carcinoma","type":"exact"},{"name":"mixed small cell and squamous cell carcinoma of lung","type":"related"},{"name":"mixed small cell and squamous cell carcinoma of the lung","type":"exact"},{"name":"small cell and large cell carcinoma of the lung","type":"related"},{"name":"small cell and squamous cell carcinoma of lung","type":"exact"},{"name":"small cell and squamous cell carcinoma of the lung","type":"exact"},{"name":"small cell and squamous cell lung carcinoma","type":"exact"}],"termid":"MONDO:0004100","xrefs":{"Monarch":{"xref_id":"0004100"}}}


id: PBO:0028614
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_ADP_binding","termid":"PBO:0028614"}


id: FYPO:0003143
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of protein measured in a cell during a cellular response to methyl methanesulfonate is lower than normal. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein level during vegetative growth","termid":"FYPO:0001324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"decreased protein level during cellular response to methyl methanesulfonate","synonyms":[{"name":"decreased protein accumulation during cellular response to methyl methanesulfonate","type":"related"},{"name":"decreased protein level during cellular response to MMS","type":"exact"},{"name":"decreased protein level during cellular response to methyl methanesulfonate during mitotic cell cycle","type":"related"},{"name":"decreased protein level during cellular response to methyl methanesulfonate during vegetative growth","type":"exact"},{"name":"decreased protein level during cellular response to methyl methanesulphonate","type":"exact"},{"name":"reduced protein level during cellular response to methyl methanesulfonate","type":"exact"}],"termid":"FYPO:0003143"}


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


id: PBO:0054381
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 1777","termid":"PBO:0054381"}


id: PBO:0059960
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 5","termid":"PBO:0059960"}


id: MONDO:0000415
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An electroclinical syndrome with onset in adolescence and adulthood.","definition_xrefs":["PMID:20196795","DOID:0050705"],"direct_ancestors":[{"relation_name":"is_a","term_name":"electroclinical syndrome","termid":"MONDO:0000411"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"adolescence-adult electroclinical syndrome","termid":"MONDO:0000415","xrefs":{"Monarch":{"xref_id":"0000415"}}}


id: GO:0150089
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 a synapse between a multiple synapse bouton and one or more dendritic spines.","definition_xrefs":["GOC:bc","PMID:22028887","PMID:7482800","PMID:10586883","PMID:11248111","GOC:aruk","PMID:29774619","PMID:11466428","PMID:18501438","PMID:8366344"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synapse organization","termid":"GO:0050808"}],"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":"multiple spine synapse organization","synonyms":[{"name":"multi-synapse organisation","type":"broad"},{"name":"multi-synapse organization","type":"broad"},{"name":"multi-synaptic organisation","type":"broad"},{"name":"multi-synaptic organization","type":"broad"},{"name":"multiple spine synapse organisation","type":"exact"},{"name":"multisynapse organisation","type":"broad"},{"name":"multisynapse organization","type":"broad"},{"name":"multisynaptic organisation","type":"broad"},{"name":"multisynaptic organization","type":"broad"}],"termid":"GO:0150089"}


id: PBO:0077645
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF alpha induced protein 2","termid":"PBO:0077645"}


id: PR:O74556
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC970.02 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74556"],"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":"mannan endo-1,6-alpha-mannosidase C970.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC970.02","synonyms":[{"name":"Spom972h-SPCC970.02","type":"exact"},{"name":"endo-alpha-1->6-D-mannanase C970.02 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74556"}


id: PBO:0040498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aurora kinase A interacting protein 1","termid":"PBO:0040498"}


id: MONDO:0020029
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare genetic heart disease.","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic cardiac disease (obsolete MONDO:0020029)","secondary_identifiers":["Orphanet:98054"],"synonyms":[{"name":"rare genetic heart disease","type":"exact"}],"termid":"MONDO:0020029","xrefs":{"Monarch":{"xref_id":"0020029"}}}


id: PBO:0012060
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galactose-specific flocculin Gsf2","termid":"PBO:0012060"}


id: PR:O13768
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A TFIIH basal transcription factor complex helicase XPB subunit that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11274:SF0","PRO:DNx","OMA:SCHPO00720"],"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":"DNA repair helicase ercc3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17A5.06","secondary_identifiers":["UniProtKB:O13768"],"synonyms":[{"name":"Spom972h-ERCC3","type":"exact"}],"termid":"PR:O13768"}


id: MOD:01019
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydroxymethylphenyl linker","synonyms":[{"name":"HMP","type":"exact"}],"termid":"MOD:01019"}


id: PBO:0002286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein methyltransferase Mtq2 (predicted)","termid":"PBO:0002286"}


id: GO:0050460
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NH3 + NAD+ + H2O = hydroxylamine + NADH + H+.","definition_xrefs":["MetaCyc:HYDROXYLAMINE-REDUCTASE-NADH-RXN","EC:1.7.1.10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor","termid":"GO:0046857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"hydroxylamine reductase (NADH) activity","secondary_identifiers":["RHEA:20581"],"synonyms":[{"name":"N-hydroxy amine reductase activity","type":"related"},{"name":"NADH-hydroxylamine reductase activity","type":"related"},{"name":"NADH2:hydroxylamine oxidoreductase activity","type":"related"},{"name":"NADH:hydroxylamine oxidoreductase activity","type":"related"},{"name":"ammonium dehydrogenase activity","type":"related"},{"name":"ammonium:NAD+ oxidoreductase activity","type":"related"},{"name":"hydroxylamine reductase (NADH2)","type":"related"}],"termid":"GO:0050460"}


id: GO:1900974
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of tatiopterin biosynthetic process.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biosynthetic process","termid":"GO:0009889"},{"relation_name":"is_a","term_name":"regulation of tatiopterin metabolic process","termid":"GO:1900977"},{"relation_name":"regulates","term_name":"tatiopterin biosynthetic process","termid":"GO:1900870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0042559"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0042559","GO:0008150"],"is_obsolete":false,"name":"regulation of tatiopterin biosynthetic process","synonyms":[{"name":"regulation of tatiopterin anabolism","type":"exact"},{"name":"regulation of tatiopterin biosynthesis","type":"exact"},{"name":"regulation of tatiopterin formation","type":"exact"},{"name":"regulation of tatiopterin synthesis","type":"exact"}],"termid":"GO:1900974"}


id: MONDO:0020558
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant Charcot-Marie-Tooth disease, type 2K (CMT2K) is an axonal CMT peripheral sensorimotor polyneuropathy.","definition_xrefs":["Orphanet:99944"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 2","termid":"MONDO:0018993"}],"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":"autosomal dominant Charcot-Marie-Tooth disease type 2K","secondary_identifiers":["MEDGEN:334294","NCIT:C133886","UMLS:C1842984","SCTID:719512003","GARD:9199"],"synonyms":[{"name":"CMT2K","type":"exact"},{"name":"Charcot-Marie-Tooth disease type 2K","type":"exact"}],"termid":"MONDO:0020558","xrefs":{"Monarch":{"xref_id":"0020558"}}}


id: GO:0043385
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a mycotoxin, any poisonous substance produced by a fungus.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toxin metabolic process","termid":"GO:0009404"}],"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:0019748","GO:0008150"],"is_obsolete":false,"name":"mycotoxin metabolic process","synonyms":[{"name":"mycotoxin metabolism","type":"exact"}],"termid":"GO:0043385"}


id: GO:0060797
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by an extracellular ligand binding to a transforming growth factor beta receptor on the surface of a target cell, which contributes to an unspecified cell adopting a mesoderm fate.","definition_xrefs":["GOC:sdb_2009","GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete transforming growth factor beta receptor signaling pathway involved in primary germ layer cell fate commitment (obsolete GO:0060797)","synonyms":[{"name":"transforming growth factor beta receptor signalling pathway involved in primary germ layer cell fate commitment","type":"exact"}],"termid":"GO:0060797"}


id: PBO:0000973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urease accessory protein UreD (predicted)","termid":"PBO:0000973"}


id: PBO:0034494
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H2B-K119_ubiquitination_at_double-strand_break_site","termid":"PBO:0034494"}


id: PBO:0028279
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_pericentric_heterochromatin","termid":"PBO:0028279"}


id: MONDO:0700247
data:
  {"annotated_genes":["SJAG_04938"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014296"}]},"cv_name":"mondo","definition":"Group of diseases encompassing a spectrum of disorders characterized by Warburg Micro Syndrome (characterized by eye, nervous system, and endocrine abnormalities) and Martsolf Syndrome phenotypes (characterized by similar – but milder – findings). To date Warburg micro syndrome comprises >96% of reported individuals with genetically defined RAB18 deficiency. The hallmark ophthalmologic findings are bilateral congenital cataracts, usually accompanied by microphthalmia, microcornea (diameter <10), and small atonic pupils. Poor vision despite early cataract surgery likely results from progressive optic atrophy and cortical visual impairment. Individuals with Warburg micro syndrome have severe to profound intellectual disability (ID); those with Martsolf syndrome have mild to moderate ID. Some individuals with RAB18 deficiency also have epilepsy. In Warburg micro syndrome, a progressive ascending spastic paraplegia typically begins with spastic diplegia and contractures during the first year, followed by upper-limb involvement leading to spastic quadriplegia after about age five years, often eventually causing breathing difficulties. In Martsolf syndrome infantile hypotonia is followed primarily by slowly progressive lower-limb spasticity. Hypogonadism – when present – manifests in both syndromes, in males as micropenis and/or cryptorchidism and in females as hypoplastic labia minora, clitoral hypoplasia, and small introitus.","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic microphthalmia","termid":"MONDO:0016073"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04938":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"RAB18 deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4750414","MEDGEN:1650928"],"synonyms":[{"name":"Warburg micro spectrum","type":"exact"}],"termid":"MONDO:0700247","terms_by_termid":{"MONDO:0014296":null},"xrefs":{"Monarch":{"xref_id":"0700247"}}}


id: GO:0097015
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. All of the contents of a bacterial-type flagellum, excluding the plasma membrane surrounding the flagellum.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete bacterial-type flagellar cytoplasm (obsolete GO:0097015)","synonyms":[{"name":"bacterial-type flagellum cytoplasm","type":"exact"}],"termid":"GO:0097015"}


id: GO:0140489
data:
  {"annotated_genes":["SJAG_03835","SJAG_02886","SJAG_02609","SJAG_00856","SJAG_01756","SJAG_01215"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[110037,116635,105918,108316,109073,99579],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140490"}]},"cv_name":"molecular_function","definition":"The action of a molecule that provides a shape or a sequence mimicking or complementary to the final product, providing template for copying the original molecule's shape or sequence.","definition_xrefs":["GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_function","termid":"GO:0003674"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00856":null,"SJAG_01215":null,"SJAG_01756":null,"SJAG_02609":null,"SJAG_02886":null,"SJAG_03835":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"molecular template activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140489","terms_by_termid":{"GO:0140490":null}}


id: GO:1905041
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of epithelium regeneration.","definition_xrefs":["GOC:BHF","GOC:BHF_miRNA","GOC:rph","GO_REF:0000058","GOC:TermGenie","PMID:23221517"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental growth","termid":"GO:0048638"},{"relation_name":"regulates","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":"regulation of epithelium regeneration","synonyms":[{"name":"regulation of regeneration of epithelium","type":"exact"}],"termid":"GO:1905041"}


id: PBO:0071911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 50","termid":"PBO:0071911"}


id: PBO:0090923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial asparagine-tRNA ligase Slm5","termid":"PBO:0090923"}


id: MONDO:0005514
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nanophthalmia is a severe form of microphthalmia characterized by a small eye with a short axial length, severe hyperopia, an elevated lens/eye ratio, and a high incidence of angle-closure glaucoma.","definition_xrefs":["Orphanet:35612"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"isolated anophthalmia-microphthalmia syndrome","termid":"MONDO:0016764"},{"relation_name":"is_a","term_name":"microphthalmia","termid":"MONDO:0021129"}],"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":"nanophthalmia","secondary_identifiers":["OMIMPS:600165","SCTID:716775009","UMLS:C4274282","GARD:16637","MEDGEN:901455","DOID:0080634"],"termid":"MONDO:0005514","xrefs":{"Monarch":{"xref_id":"0005514"}}}


id: PBO:0078413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gly (CCC) 7-1","termid":"PBO:0078413"}


id: GO:0006015
data:
  {"annotated_genes":["SJAG_04970","SJAG_04882","SJAG_03811"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97210,109380,114400],"is_not":false,"summary":null,"term":"GO:0006015"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of 5-phosphoribose 1-diphosphate, also known as 5-phosphoribosyl-1-pyrophosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribose phosphate biosynthetic process","termid":"GO:0046390"},{"relation_name":"is_a","term_name":"5-phosphoribose 1-diphosphate metabolic process","termid":"GO:0046391"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03811":null,"SJAG_04882":null,"SJAG_04970":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"5-phosphoribose 1-diphosphate biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-73843"],"synonyms":[{"name":"5-phosphoribose 1-diphosphate anabolism","type":"exact"},{"name":"5-phosphoribose 1-diphosphate biosynthesis","type":"exact"},{"name":"5-phosphoribose 1-diphosphate formation","type":"exact"},{"name":"5-phosphoribose 1-diphosphate synthesis","type":"exact"},{"name":"5-phosphoribosyl-1-pyrophosphate biosynthesis","type":"exact"},{"name":"5-phosphoribosyl-1-pyrophosphate biosynthetic process","type":"exact"},{"name":"PRPP biosynthetic process","type":"exact"}],"termid":"GO:0006015","terms_by_termid":{"GO:0006015":null}}


id: PBO:0040923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basonuclin 1","termid":"PBO:0040923"}


id: PBO:0059689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 55","termid":"PBO:0059689"}


id: PBO:0079326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis-specific transcript, Y-linked 14","termid":"PBO:0079326"}


id: PBO:0064078
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 112","termid":"PBO:0064078"}


id: GO:0075153
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont organism modulates the frequency, rate or extent of its transmembrane receptor-mediated signal transduction as a result of detecting molecules of its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transmembrane receptor-mediated signal transduction in response to host (obsolete GO:0075153)","synonyms":[{"name":"regulation of symbiont transmembrane receptor-mediated signal transduction in response to host","type":"exact"}],"termid":"GO:0075153"}


id: PBO:0012856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exosome subunit Rrp43","termid":"PBO:0012856"}


id: PBO:0009107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase I core factor complex subunit Rrn7","termid":"PBO:0009107"}


id: GO:0002154
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A nuclear receptor-mediated signaling pathway initiated by a thyroid hormone  binding to an intracellular receptor of the nuclear receptor protein family, and ending with regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone-mediated signaling pathway","termid":"GO:0009755"},{"relation_name":"is_a","term_name":"nuclear receptor-mediated signaling pathway","termid":"GO:0141193"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"thyroid hormone receptor signaling pathway","synonyms":[{"name":"thyroid hormone mediated signalling pathway","type":"exact"}],"termid":"GO:0002154"}


id: PR:O74862
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An rRNA-processing protein UTP23 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04892","PANTHER:PTHR12416: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":"rRNA-processing protein utp23 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC18.12c","secondary_identifiers":["UniProtKB:O74862"],"synonyms":[{"name":"Spom972h-UTP23","type":"exact"},{"name":"U three protein 23 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74862"}


id: PBO:0075718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorcin","termid":"PBO:0075718"}


id: PBO:0050561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histidine rich glycoprotein","termid":"PBO:0050561"}


id: PBO:0036457
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystathionine gamma-synthase Met3","termid":"PBO:0036457"}


id: MONDO:0012716
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spondyloepiphyseal dysplasia, Cantu type is an extremely rare type of spondyloepiphyseal dysplasia described in about 5 patients to date and characterized by clinical signs including short stature, peculiar facies with blepharophimosis, upward slanted eyes, abundant eyebrows and eyelashes, coarse voice, and short hands and feet (brachymetacarpalia, brachymetatarsalia and brachyphalangia).","definition_xrefs":["Orphanet:163654"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"spondyloepiphyseal dysplasia, Cantu type","secondary_identifiers":["DOID:0112287","SCTID:718765003","UMLS:C2673649","GARD:10629","OMIM:611717","MEDGEN:435975","MESH:C567128","icd11.foundation:897226700"],"synonyms":[{"name":"SED-BDS","type":"exact"},{"name":"Sed-BDS","type":"related"},{"name":"Tatoo dysplasia","type":"related"},{"name":"fantasy Island syndrome","type":"related"},{"name":"spondyloepiphyseal dysplasia-brachydactyly and distinctive speech","type":"related"},{"name":"spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome","type":"exact"},{"name":"tattoo dysplasia","type":"exact"}],"termid":"MONDO:0012716","xrefs":{"Monarch":{"xref_id":"0012716"}}}


id: PBO:0068523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 119, pseudogene","termid":"PBO:0068523"}


id: PBO:0012574
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongated at low pH","termid":"PBO:0012574"}


id: MONDO:0021653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cutaneous mucinosis","termid":"MONDO:0002523"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"cutaneous focal mucinosis","secondary_identifiers":["ICD9:701.8","MEDGEN:590585","UMLS:C0406659","SCTID:110981005"],"synonyms":[{"name":"focal mucinoses","type":"related"},{"name":"focal mucinosis","type":"related"}],"termid":"MONDO:0021653","xrefs":{"Monarch":{"xref_id":"0021653"}}}


id: GO:0017028
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Strengthening of a bond between proteins. Proteins are large molecules composed of one or more chains of amino acids. The amino acids are joined in a specific order by peptide bonds.","definition_xrefs":["GOC:jid"],"gene_count":0,"genotype_count":0,"name":"obsolete protein stabilization activity (obsolete GO:0017028)","synonyms":[{"name":"protein stabilization activity","type":"exact"}],"termid":"GO:0017028"}


id: GO:0140022
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A giant secretory organelle that comprises a bulb-shape capsule containing a coiled hollow tubule structure attached to it. A cnida defines the phylum Cnidaria.","definition_xrefs":["Wikipedia:Cnida#Structure_and_function"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"}],"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":"cnida","synonyms":[{"name":"cnidae (plural)","type":"exact"}],"termid":"GO:0140022"}


id: PBO:0001098
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multi-copy suppressor of Chk1","termid":"PBO:0001098"}


id: PBO:0002249
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.1.40","termid":"PBO:0002249"}


id: GO:0036253
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. 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 amiloride stimulus.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete response to amiloride (obsolete GO:0036253)","termid":"GO:0036253"}


id: GO:0017195
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The acetylation of the N-terminal lysine of proteins to form the derivative N2-acetyl-L-lysine. The occurrence of this modification has not been confirmed.","definition_xrefs":["RESID:AA0048"],"gene_count":0,"genotype_count":0,"name":"obsolete N-terminal peptidyl-lysine N2-acetylation (obsolete GO:0017195)","termid":"GO:0017195"}


id: GO:0030027
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A thin sheetlike process extended by the leading edge of a migrating cell or extending cell process; contains a dense meshwork of actin filaments.","definition_xrefs":["ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection","termid":"GO:0120025"},{"relation_name":"part_of","term_name":"cell leading edge","termid":"GO:0031252"}],"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":"lamellipodium","secondary_identifiers":["Wikipedia:Lamellipodia"],"termid":"GO:0030027"}


id: PBO:0077753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocase of outer mitochondrial membrane 5","termid":"PBO:0077753"}


id: GO:0051100
data:
  {"annotated_genes":["SJAG_03088","SJAG_04887"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94792,104620],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904530"}]},"cv_name":"biological_process","definition":"Any process that stops or reduces the rate or extent of binding, the selective interaction of a molecule with one or more specific sites on another molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of molecular function","termid":"GO:0044092"},{"relation_name":"is_a","term_name":"regulation of binding","termid":"GO:0051098"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03088":null,"SJAG_04887":null},"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 binding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of binding","type":"exact"},{"name":"down-regulation of binding","type":"exact"},{"name":"downregulation of binding","type":"exact"},{"name":"inhibition of binding","type":"narrow"}],"termid":"GO:0051100","terms_by_termid":{"GO:1904530":null}}


id: PBO:0081989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and SCAN domain containing 18","termid":"PBO:0081989"}


id: PBO:0029336
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_phosphorylation","termid":"PBO:0029336"}


id: GO:0007444
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the imaginal disc over time, from its formation to the metamorphosis to form adult structures. Imaginal discs are epithelial infoldings in the larvae of holometabolous insects that develop into adult structures (legs, antennae, wings, etc.).","definition_xrefs":["GOC:bf","ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ development","termid":"GO:0048513"}],"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":"imaginal disc development","termid":"GO:0007444"}


id: MONDO:0017103
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare genetic developmental defect during embryogenesis (obsolete MONDO:0015960)","termid":"MONDO:0015960"},{"relation_name":"excluded_subClassOf","term_name":"obsolete genetic nervous system disorder (obsolete MONDO:0019117)","termid":"MONDO:0019117"},{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"encephaloclastic disorder","secondary_identifiers":["icd11.foundation:1436588898","MEDGEN:1843179","UMLS:C5680772","Orphanet:269190","GARD:20987"],"termid":"MONDO:0017103","xrefs":{"Monarch":{"xref_id":"0017103"}}}


id: PBO:0030103
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_threonine_level","termid":"PBO:0030103"}


id: MONDO:0032788
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":"cerebellar atrophy with seizures and variable developmental delay","secondary_identifiers":["UMLS:C5193132","MEDGEN:1683734","OMIM:618501"],"synonyms":[{"name":"CASVDD","type":"related"},{"name":"CEREBELLAR ATROPHY WITH SEIZURES AND VARIABLE DEVELOPMENTAL DELAY","type":"related"}],"termid":"MONDO:0032788","xrefs":{"Monarch":{"xref_id":"0032788"}}}


id: MONDO:0008853
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Barber Say syndrome (BSS) is a rare ectodermal dysplasia with neonatal onset characterized by congenital generalized hypertrichosis, atrophic skin, ectropion and microstomia.","definition_xrefs":["Orphanet:1231"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertrichosis of eyelid","termid":"MONDO:0001334"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"},{"relation_name":"is_a","term_name":"congenital entropion","termid":"MONDO:0020159"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005093"],"is_obsolete":false,"name":"Barber-Say syndrome","secondary_identifiers":["icd11.foundation:37248895","DOID:0060549","GARD:819","MESH:C537908","MEDGEN:230818","NORD:875","UMLS:C1319466","OMIM:209885","SCTID:408537003"],"synonyms":[{"name":"BARBER-SAY syndrome","type":"related"},{"name":"BBRSAY","type":"related"},{"name":"Barber Say syndrome","type":"related"},{"name":"Barber-Say syndrome","type":"exact"},{"name":"Brown Séquard Syndrome","type":"exact"},{"name":"Bss","type":"related"},{"name":"hypertrichosis atrophic skin ectropion macrostomia","type":"related"},{"name":"hypertrichosis, atrophic skin, ectropion, and macrostomia","type":"related"},{"name":"hypertrichosis-atrophic skin-ectropion-macrostomia syndrome","type":"exact"}],"termid":"MONDO:0008853","xrefs":{"Monarch":{"xref_id":"0008853"}}}


id: GO:0031365
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The alteration of the N-terminal amino acid residue in a protein.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification process","termid":"GO:0036211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"N-terminal protein amino acid modification","secondary_identifiers":["GO:0018409"],"synonyms":[{"name":"peptide or protein amino-terminal blocking","type":"related"},{"name":"peptide/protein amino-terminal blocking","type":"related"}],"termid":"GO:0031365"}


id: MONDO:0003257
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A low-grade neoplasm that arises from the neurohypophysis. It includes the granular cell tumor of the neurohypophysis and pituicytoma.","definition_xrefs":["NCIT:C7157"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pituitary tumor","termid":"MONDO:0017611"},{"relation_name":"is_a","term_name":"neuroendocrine disorder","termid":"MONDO:0100070"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"posterior pituitary gland neoplasm","secondary_identifiers":["DOID:5048","MEDGEN:235368","UMLS:C1334957"],"synonyms":[{"name":"Neurohypophysis neoplasm","type":"exact"},{"name":"Neurohypophysis tumor","type":"exact"},{"name":"Neurohypophysis tumour","type":"exact"},{"name":"PITUICYTOMA, benign","type":"exact"},{"name":"neoplasm of neurohypophysis","type":"exact"},{"name":"neurohypophysis neoplasm","type":"exact"},{"name":"neurohypophysis neoplasm (disease)","type":"exact"},{"name":"neurohypophysis tumor","type":"exact"},{"name":"neurohypophysis tumour","type":"exact"},{"name":"posterior pituitary gland neoplasm","type":"exact"},{"name":"posterior pituitary gland tumor","type":"exact"},{"name":"posterior pituitary gland tumour","type":"exact"},{"name":"posterior pituitary neoplasm","type":"exact"},{"name":"posterior pituitary tumor","type":"exact"},{"name":"posterior pituitary tumour","type":"exact"},{"name":"tumor of neurohypophysis","type":"exact"},{"name":"tumour of neurohypophysis","type":"exact"}],"termid":"MONDO:0003257","xrefs":{"Monarch":{"xref_id":"0003257"}}}


id: GO:0006047
data:
  {"annotated_genes":["SJAG_00978","SJAG_04728","SJAG_00519","SJAG_01443","SJAG_03723"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87708,88049,58139,102180,102274],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006048"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving UDP-N-acetylglucosamine, a substance composed of N-acetylglucosamine, a common structural unit of oligosaccharides, in glycosidic linkage with uridine diphosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino sugar metabolic process","termid":"GO:0006040"},{"relation_name":"is_a","term_name":"nucleotide-sugar metabolic process","termid":"GO:0009225"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00519":null,"SJAG_00978":null,"SJAG_01443":null,"SJAG_03723":null,"SJAG_04728":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:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"UDP-N-acetylglucosamine metabolic process","references_by_uniquename":{"GO_REF:0000041":null,"GO_REF:0000107":null},"synonyms":[{"name":"UDP-N-acetylglucosamine metabolism","type":"exact"}],"termid":"GO:0006047","terms_by_termid":{"GO:0006048":null}}


id: MOD:01427
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because redundant and identical to MOD:00819. Remap to MOD:00819.","definition_xrefs":["PubMed:18688235"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:01427 2-aminobutanoic acid (Abu) (obsolete MOD:01427)","synonyms":[{"name":"Abu","type":"exact"}],"termid":"MOD:01427"}


id: MONDO:0026782
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete chondrodysplasia punctata 2, X-linked dominant (obsolete MONDO:0026782)","termid":"MONDO:0026782","xrefs":{"Monarch":{"xref_id":"0026782"}}}


id: GO:0044346
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any apoptotic process in a fibroblast, a connective tissue cell which secretes an extracellular matrix rich in collagen and other macromolecules.","definition_xrefs":["CL:0000057","GOC:jl","GOC:mtg_apoptosis","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apoptotic process","termid":"GO:0006915"}],"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":"fibroblast apoptotic process","synonyms":[{"name":"fibroblast apoptosis","type":"narrow"}],"termid":"GO:0044346"}


id: PBO:0002844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent DNA helicase Snf21","termid":"PBO:0002844"}


id: PBO:0085900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; may be involved in mitochondrial DNA maintenance; required for slowed DNA synthesis-induced filamentous growth","termid":"PBO:0085900"}


id: GO:1902696
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glycine to isobutanol.","definition_xrefs":["PMID:23642236","GOC:mengo_curators","GOC:TermGenie","GO_REF:0000093"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycine catabolic process","termid":"GO:0006546"},{"relation_name":"is_a","term_name":"isobutanol metabolic process","termid":"GO:1901960"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0044248","GO:0008150","GO:0006520"],"is_obsolete":false,"name":"glycine catabolic process to isobutanol","secondary_identifiers":["GO:1990293"],"synonyms":[{"name":"glycine breakdown to isobutanol","type":"exact"},{"name":"glycine catabolism to isobutanol","type":"exact"},{"name":"glycine degradation to isobutanol","type":"exact"}],"termid":"GO:1902696"}


id: PR:O14281
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC8C9.12c gene.","definition_xrefs":["UniProtKB:O14281","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized mitochondrial carrier C8C9.12c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC8C9.12c","synonyms":[{"name":"Spom972h-SPAC8C9.12c","type":"exact"}],"termid":"PR:O14281"}


id: MONDO:0015583
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The 2p21 microdeletion syndrome consists of cystinuria, neonatal seizures, hypotonia, severe growth and developmental delay, facial dysmorphism, and lactic acidemia.","definition_xrefs":["Orphanet:163693"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hypotonia-cystinuria syndrome","termid":"MONDO:0011669"},{"relation_name":"excluded_subClassOf","term_name":"partial deletion of the long arm of chromosome 2","termid":"MONDO:0016901"},{"relation_name":"is_a","term_name":"partial deletion of the short arm of chromosome 2","termid":"MONDO:0016884"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2p21 microdeletion syndrome","secondary_identifiers":["DECIPHER:87","MEDGEN:930206","UMLS:C4304537","SCTID:719652007","GARD:16999"],"synonyms":[{"name":"2p21 deletion syndrome","type":"exact"},{"name":"2p21 microdeletion syndrome","type":"exact"},{"name":"Del(2)(p21)","type":"exact"},{"name":"monosomy 2p21","type":"exact"}],"termid":"MONDO:0015583","xrefs":{"Monarch":{"xref_id":"0015583"}}}


id: GO:0071258
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 gravitational stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to gravity","termid":"GO:0009629"},{"relation_name":"is_a","term_name":"cellular response to abiotic stimulus","termid":"GO:0071214"}],"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 gravity","synonyms":[{"name":"cellular response to gravitational stimulus","type":"exact"}],"termid":"GO:0071258"}


id: PBO:0054569
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 1971","termid":"PBO:0054569"}


id: RO:HOM0000068
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Xenology that is characterized by multiple horizontal transfer events, resulting in the presence of two or more copies of the foreign gene in the host genome.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_xenology_relationship_with","termid":"RO:HOM0000018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_paraxenology_relationship_with","synonyms":[{"name":"duplicate xenology","type":"exact"},{"name":"multiple xenology","type":"exact"},{"name":"paraxenologous to","type":"exact"}],"termid":"RO:HOM0000068"}


id: MONDO:0019396
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare glomerular disease characterized by abnormal accumulation of type III collagen within the mesangium and subendothelial space of the glomerulus. Clinically it usually manifests with proteinuria (often in the nephrotic range), microscopic hematuria, peripheral edema and/or hypertension. In some cases progression to end-stage renal failure is observed.","definition_xrefs":["Orphanet:84087"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary glomerular disease (obsolete MONDO:0019724)","termid":"MONDO:0019724"},{"relation_name":"is_a","term_name":"glomerular disorder","termid":"MONDO:0019722"}],"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":"collagen type III glomerulopathy","secondary_identifiers":["ICD9:583.89","GARD:19048","UMLS:C3872695","MEDGEN:836996","SCTID:708127008"],"synonyms":[{"name":"Collagenofibrotic glomerulopathy","type":"exact"}],"termid":"MONDO:0019396","xrefs":{"Monarch":{"xref_id":"0019396"}}}


id: PBO:0058937
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic spindle positioning","termid":"PBO:0058937"}


id: PBO:0078441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor gamma constant 1","termid":"PBO:0078441"}


id: GO:0150119
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein localization to cell-cell junction.","definition_xrefs":["GOC:aruk","GOC:bc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to cell-cell junction","termid":"GO:0150106"},{"relation_name":"is_a","term_name":"negative regulation of protein localization","termid":"GO:1903828"},{"relation_name":"negatively_regulates","term_name":"protein localization to cell-cell junction","termid":"GO:0150105"}],"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 protein localization to cell-cell junction","synonyms":[{"name":"negative regulation of protein localisation to cell-cell junction","type":"exact"}],"termid":"GO:0150119"}


id: MONDO:0017921
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hearing loss-familial salivary gland insensitivity to aldosterone syndrome is characterized by bilateral moderate-to-severe sensorineural hearing loss and salivary gland insensitivity to aldosterone resulting in hyponatremia. It has been described in two brothers. Transmission appeared to be autosomal recessive.","definition_xrefs":["Orphanet:3225"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hearing loss-familial salivary gland insensitivity to aldosterone syndrome","secondary_identifiers":["UMLS:C2931369","MEDGEN:419395","GARD:18788","MESH:C536927","SCTID:716239006"],"synonyms":[{"name":"Tungland-Bellman syndrome","type":"exact"},{"name":"Tunglang savage Bellman syndrome","type":"related"},{"name":"hearing loss and familial salivary gland insensitivity to aldosterone","type":"related"},{"name":"hearing loss insensitivity to aldosterone","type":"related"}],"termid":"MONDO:0017921","xrefs":{"Monarch":{"xref_id":"0017921"}}}


id: PBO:0049311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutathione S-transferase theta 1","termid":"PBO:0049311"}


id: MONDO:0003591
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare malignant adipose tissue neoplasm of the fat cells surrounding the kidney, usually of the well-differentiated or myxoid type. It may be associated with tuberous sclerosis.","definition_xrefs":["NCIT:C6185"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney sarcoma","termid":"MONDO:0002930"},{"relation_name":"is_a","term_name":"liposarcoma","termid":"MONDO:0005060"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0004992"],"is_obsolete":false,"name":"kidney liposarcoma","secondary_identifiers":["MEDGEN:235546","UMLS:C1335745","DOID:5699"],"synonyms":[{"name":"kidney liposarcoma","type":"exact"},{"name":"liposarcoma of kidney","type":"exact"},{"name":"liposarcoma of the kidney","type":"exact"},{"name":"renal liposarcoma","type":"exact"}],"termid":"MONDO:0003591","xrefs":{"Monarch":{"xref_id":"0003591"}}}


id: PR:Q5FC18
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sgf11 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q5FC18"],"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":"SAGA-associated factor 11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC57A10.14","synonyms":[{"name":"Spom972h-sgf11","type":"exact"}],"termid":"PR:Q5FC18"}


id: GO:0043523
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the occurrence or rate of cell death by apoptotic process in neurons.","definition_xrefs":["GOC:mtg_apoptosis","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of apoptotic process","termid":"GO:0042981"},{"relation_name":"regulates","term_name":"neuron apoptotic process","termid":"GO:0051402"}],"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 neuron apoptotic process","synonyms":[{"name":"regulation of apoptosis of neuronal cells","type":"exact"},{"name":"regulation of apoptosis of neurons","type":"exact"},{"name":"regulation of neuron apoptosis","type":"narrow"},{"name":"regulation of neuron programmed cell death","type":"exact"},{"name":"regulation of neuronal cell programmed cell death","type":"exact"},{"name":"regulation of programmed cell death of neuronal cells","type":"exact"},{"name":"regulation of programmed cell death, neurons","type":"exact"}],"termid":"GO:0043523"}


id: PBO:0061296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuropeptides B and W receptor 1","termid":"PBO:0061296"}


id: GO:0033156
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of oligogalacturonides into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharide transport","termid":"GO:0015772"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"oligogalacturonide transport","termid":"GO:0033156"}


id: SO:0001437
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A non-polar, hydorophobic amino acid encoded by the codons CTN (CTT, CTC, CTA and CTG), TTA and TTG.","direct_ancestors":[{"relation_name":"is_a","term_name":"amino_acid","termid":"SO:0001237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine","synonyms":[{"name":"L","type":"exact"},{"name":"Leu","type":"exact"}],"termid":"SO:0001437"}


id: MONDO:0007208
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Boomerang dysplasia (BD) is a rare lethal skeletal dysplasia characterized by severe short-limbed dwarfism, dislocated joints, club feet, distinctive facies and diagnostic x-ray findings of underossified and dysplastic long tubular bones, with a boomerang-like bowing.","definition_xrefs":["Orphanet:1263"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with multiple joint dislocations (obsolete MONDO:0019700)","termid":"MONDO:0019700"},{"relation_name":"is_a","term_name":"osteochondrodysplasia","termid":"MONDO:0005516"},{"relation_name":"is_a","term_name":"filamin-related bone disorder","termid":"MONDO:0019690"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"Boomerang dysplasia","secondary_identifiers":["OMIM:112310","MEDGEN:96579","MESH:C536573","DOID:0050680","SCTID:254054000","icd11.foundation:423736259","ICD9:756.9","UMLS:C0432201","GARD:933"],"synonyms":[{"name":"Boomerang dysplasia","type":"exact"},{"name":"Boomerang-like skeletal dysplasia","type":"related"},{"name":"dwarfism with short, bowed, rigid limbs and characteristic facies","type":"related"}],"termid":"MONDO:0007208","xrefs":{"Monarch":{"xref_id":"0007208"}}}


id: GO:0098565
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The side (leaflet) of the endosome membrane that faces the lumen.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lumenal side of membrane","termid":"GO:0098576"},{"relation_name":"part_of","term_name":"endosome membrane","termid":"GO:0010008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005768"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005768","GO:0005737","GO:0005575","GO:0031410"],"is_obsolete":false,"name":"lumenal side of endosome membrane","synonyms":[{"name":"internal leaflet of endosome membrane","type":"exact"},{"name":"internal side of endosome membrane","type":"exact"}],"termid":"GO:0098565"}


id: PBO:0082116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Acetyl-coA synthetase isoform; along with Acs2p, acetyl-coA synthetase isoform is the nuclear source of acetyl-coA for histone acetylation; expressed during growth on nonfermentable carbon sources and under aerobic conditions","termid":"PBO:0082116"}


id: PBO:0065383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pregnancy specific beta-1-glycoprotein 10, pseudogene","termid":"PBO:0065383"}


id: PBO:0058158
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4453","termid":"PBO:0058158"}


id: GO:0060040
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a bipolar cell, the last neuron to be generated in the retina.","definition_xrefs":["GOC:bf","GOC:tb","GOC:dph","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glutamatergic neuron differentiation","termid":"GO:1905962"},{"relation_name":"part_of","term_name":"neural retina development","termid":"GO:0003407"},{"relation_name":"part_of","term_name":"retina morphogenesis in camera-type eye","termid":"GO:0060042"}],"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":"retinal bipolar neuron differentiation","termid":"GO:0060040"}


id: MONDO:0010911
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Prolactinoma is a usually benign neoplasm of the pituitary gland that results in hyperprolactinemia. The most common clinical manifestations are amenorrhea and infertility in women; and impotence, decreased libido and infertility in men.","definition_xrefs":["Orphanet:2965"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prolactin producing pituitary tumor","termid":"MONDO:0003430"},{"relation_name":"is_a","term_name":"familial isolated pituitary adenoma","termid":"MONDO:0017824"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prolactin-producing pituitary gland adenoma","secondary_identifiers":["DOID:5394","ICDO:8271/0","GARD:4508","ICD10CM:E22.1","NANDO:1200378","NCIT:C3342","MEDGEN:10936","MedDRA:10036832","ICD10CM:D35.2","OMIM:600634","EFO:1000496","SCTID:134209002","UMLS:C0033375","MESH:D015175"],"synonyms":[{"name":"Forbes-Albright syndrome (formerly)","type":"related"},{"name":"PRL producing pituitary gland adenoma","type":"exact"},{"name":"PRL-secreting pituitary adenoma","type":"exact"},{"name":"PRLoma","type":"exact"},{"name":"familial prolactinoma","type":"exact"},{"name":"lactotrope adenoma","type":"exact"},{"name":"lactotroph adenoma","type":"exact"},{"name":"lactotroph cell adenoma","type":"exact"},{"name":"pituitary adenoma, prolactin-secreting","type":"exact"},{"name":"pituitary gland prolactinoma","type":"exact"},{"name":"pituitary lactotrophic adenoma","type":"exact"},{"name":"pituitary prolactinoma","type":"exact"},{"name":"prolactin producing adenoma of pituitary","type":"exact"},{"name":"prolactin producing adenoma of pituitary gland","type":"exact"},{"name":"prolactin producing adenoma of the pituitary","type":"exact"},{"name":"prolactin producing adenoma of the pituitary gland","type":"exact"},{"name":"prolactin producing pituitary adenoma","type":"exact"},{"name":"prolactin producing pituitary gland adenoma","type":"exact"},{"name":"prolactin secreting adenoma","type":"exact"},{"name":"prolactin secreting adenoma of pituitary","type":"exact"},{"name":"prolactin secreting adenoma of pituitary gland","type":"exact"},{"name":"prolactin secreting adenoma of the pituitary","type":"exact"},{"name":"prolactin secreting adenoma of the pituitary gland","type":"exact"},{"name":"prolactin secreting pituitary adenoma","type":"exact"},{"name":"prolactin secreting pituitary gland adenoma","type":"exact"},{"name":"prolactin-producing pituitary gland adenoma","type":"exact"},{"name":"prolactin-secreting pituitary adenoma","type":"exact"},{"name":"prolactinoma","type":"exact"},{"name":"prolactinoma of pituitary","type":"exact"},{"name":"prolactinoma of pituitary gland","type":"exact"},{"name":"prolactinoma of the pituitary","type":"exact"},{"name":"prolactinoma of the pituitary gland","type":"exact"},{"name":"prolactinoma, familial","type":"related"}],"termid":"MONDO:0010911","xrefs":{"Monarch":{"xref_id":"0010911"}}}


id: PBO:0062264
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 F member 1","termid":"PBO:0062264"}


id: GO:0072666
data:
  {"annotated_genes":["SJAG_04552","SJAG_01360","SJAG_02117","SJAG_04024","SJAG_00821","SJAG_03892","SJAG_05303","SJAG_03976","SJAG_03970","SJAG_01488","SJAG_03385","SJAG_00181","SJAG_01981","SJAG_00204","SJAG_00108","SJAG_02912","SJAG_03756","SJAG_00380","SJAG_04349","SJAG_00416","SJAG_03783","SJAG_01367","SJAG_01586","SJAG_16459","SJAG_01229","SJAG_04936","SJAG_01242","SJAG_01088","SJAG_00208","SJAG_01281","SJAG_02584","SJAG_04912","SJAG_03250","SJAG_05210","SJAG_04489"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90579,91011,91145,112750,87525,105223,87638,113893,87603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120113"},{"annotations":[90515],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044395"},{"annotations":[91625,103549,106208,96900,88422,101621,89692,100613,103530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006623"},{"annotations":[91508,91797,87641,91014,97459,87472,104445,114154,90070,95468,91148,115834,108833,106837,106029,110087,110918,100383,109253],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043328"}]},"cv_name":"biological_process","definition":"The directed movement of a protein to a specific location in a vacuole.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of protein localization to organelle","termid":"GO:0072594"},{"relation_name":"is_a","term_name":"protein localization to vacuole","termid":"GO:0072665"}],"gene_count":35,"genes_by_uniquename":{"SJAG_00108":null,"SJAG_00181":null,"SJAG_00204":null,"SJAG_00208":null,"SJAG_00380":null,"SJAG_00416":null,"SJAG_00821":null,"SJAG_01088":null,"SJAG_01229":null,"SJAG_01242":null,"SJAG_01281":null,"SJAG_01360":null,"SJAG_01367":null,"SJAG_01488":null,"SJAG_01586":null,"SJAG_01981":null,"SJAG_02117":null,"SJAG_02584":null,"SJAG_02912":null,"SJAG_03250":null,"SJAG_03385":null,"SJAG_03756":null,"SJAG_03783":null,"SJAG_03892":null,"SJAG_03970":null,"SJAG_03976":null,"SJAG_04024":null,"SJAG_04349":null,"SJAG_04489":null,"SJAG_04552":null,"SJAG_04912":null,"SJAG_04936":null,"SJAG_05210":null,"SJAG_05303":null,"SJAG_16459":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"establishment of protein localization to vacuole","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"establishment of protein localisation to vacuole","type":"exact"}],"termid":"GO:0072666","terms_by_termid":{"GO:0006623":null,"GO:0043328":null,"GO:0044395":null,"GO:0120113":null}}


id: PATO:0002282
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A mobility which is relative high.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"mobile","termid":"PATO:0000299"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased mobility","termid":"PATO:0002282"}


id: FYPO:0006415
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A spindle phenotype in which the meiotic spindles in adjacent dividing nuclei overlap during meiosis II.","definition_xrefs":["PomBase:mah","PMID:27304859"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic spindle","termid":"FYPO:0000734"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000054","FYPO:0000002","FYPO:0001985","FYPO:0000120","FYPO:0002399"],"is_obsolete":false,"name":"overlapping meiosis II spindles","synonyms":[{"name":"overlapping spindles at meiosis II","type":"exact"},{"name":"overlapping spindles during second meiotic nuclear division","type":"exact"}],"termid":"FYPO:0006415"}


id: GO:0016334
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any cellular process that results in the specification, formation or maintenance of a polarized follicular epithelial sheet.","definition_xrefs":["GOC:bf","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment or maintenance of cell polarity","termid":"GO:0007163"},{"relation_name":"part_of","term_name":"morphogenesis of follicular epithelium","termid":"GO:0016333"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0007163","GO:0008150"],"is_obsolete":false,"name":"establishment or maintenance of polarity of follicular epithelium","termid":"GO:0016334"}


id: GO:0032129
data:
  {"annotated_genes":["SJAG_00581"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[108930],"is_not":false,"summary":null,"term":"GO:0032129"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: histone H3 N6-acetyl-L-lysine (position 9) + H2O = histone H3 L-lysine (position 9) + acetate. This reaction represents the removal of an acetyl group from lysine at position 9 of the histone H3 protein.","definition_xrefs":["PMID:28450737"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3K deacetylase activity","termid":"GO:0141050"},{"relation_name":"is_a","term_name":"histone deacetylase activity, hydrolytic mechanism","termid":"GO:0141221"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00581":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0033558"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0019213"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140096","GO:0003824","GO:0016810","GO:0033558","GO:0019213","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"histone H3K9 deacetylase activity, hydrolytic mechanism","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"histone H3-K9 deacetylase activity","type":"exact"},{"name":"histone H3K9 deacetylase activity","type":"broad"},{"name":"histone deacetylase activity (H3-K9 specific)","type":"exact"}],"termid":"GO:0032129","terms_by_termid":{"GO:0032129":null}}


id: PBO:0045941
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ephrin B1","termid":"PBO:0045941"}


id: GO:0030255
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which proteins are transferred into the extracellular milieu or directly into host cells, via the type IV protein secretion system.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein secretion","termid":"GO:0009306"},{"relation_name":"is_a","term_name":"secretion by the type IV secretion system","termid":"GO:0044097"},{"relation_name":"is_a","term_name":"protein transmembrane transport","termid":"GO:0071806"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"protein secretion by the type IV secretion system","synonyms":[{"name":"protein secretion by the T4SS","type":"exact"},{"name":"protein secretion by the type IV protein secretion system","type":"exact"},{"name":"type IV protein secretion system","type":"narrow"}],"termid":"GO:0030255"}


id: PBO:0052452
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KLF transcription factor 4","termid":"PBO:0052452"}


id: PBO:0055194
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 2619","termid":"PBO:0055194"}


id: PBO:0060912
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NEXN antisense RNA 1","termid":"PBO:0060912"}


id: PBO:0069179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 433, pseudogene","termid":"PBO:0069179"}


id: FYPO:0002767
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 terbinafine 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:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002682"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0002682","FYPO:0000139","FYPO:0000003"],"is_obsolete":false,"name":"resistance to terbinafine","synonyms":[{"name":"resistance to terbinafine during mitotic cell cycle","type":"related"},{"name":"resistance to terbinafine during vegetative growth","type":"exact"},{"name":"resistant to terbinafine","type":"exact"}],"termid":"FYPO:0002767"}


id: PBO:0089647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pig-F/3-ketosphinganine reductase fusion protein","termid":"PBO:0089647"}


id: GO:1990303
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A ubiquitin ligase complex consisting of UBR1 and RAD6 components. It polyubiquitinates proteins containing non-acetylated N-terminal residues causing their subsequent degradation by the proteasome as part of the Ac/N-End Rule pathway. It recognizes non-acetylated N-terminal methionine if it is followed by a hydrophobic residue. Additionally, it acts in an N-end rule independent manner as a component of a novel quality control pathway for proteins synthesized on cytosolic ribosomes.","definition_xrefs":["GOC:bhm","PMID:19531475"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"UBR1-RAD6 ubiquitin ligase complex","synonyms":[{"name":"UBR1-RAD6 complex","type":"exact"}],"termid":"GO:1990303"}


id: GO:0021951
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The creation and reception of signals that guide a precerebellar neuron towards their signals, where this process is involved in tangential migration.","definition_xrefs":["GOC:cls","GOC:dgh","GOC:dph","GOC:jid","PMID:15157725","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive chemotaxis","termid":"GO:0050918"},{"relation_name":"part_of","term_name":"brainstem precerebellar neuron precursor migration","termid":"GO:0021949"}],"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":"chemoattraction involved in precerebellar neuron migration","synonyms":[{"name":"positive chemotaxis involved in precerebellar neuron migration","type":"exact"}],"termid":"GO:0021951"}


id: PBO:0061950
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily A member 2","termid":"PBO:0061950"}


id: MONDO:1011869
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinal dysmyelination, non-human animal","secondary_identifiers":["OMIA:001247"],"termid":"MONDO:1011869","xrefs":{"Monarch":{"xref_id":"1011869"}}}


id: MONDO:0019955
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"6cm and approximately 1/3 have metastasized at the time of diagnosis. It often co-occurs with Zollinger-Ellison syndrome or multiple endocrine neoplasia type 1 (MEN 1).","definition_xrefs":["Orphanet:97261"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatic neuroendocrine tumor","termid":"MONDO:0019954"}],"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":"GRFoma","secondary_identifiers":["MEDGEN:577391","icd11.foundation:1245945716","UMLS:C0346406","GARD:19356"],"synonyms":[{"name":"GRF tumor","type":"exact"},{"name":"GRF tumour","type":"exact"},{"name":"Growth hormone releasing factor tumor","type":"exact"},{"name":"Growth hormone releasing factor tumour","type":"exact"}],"termid":"MONDO:0019955","xrefs":{"Monarch":{"xref_id":"0019955"}}}


id: MONDO:0800420
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast cancer, familial, susceptibility to, 3","secondary_identifiers":["UMLS:C3150660","MEDGEN:462010"],"termid":"MONDO:0800420","xrefs":{"Monarch":{"xref_id":"0800420"}}}


id: GO:0043053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Entry into the facultative diapause of the dauer (enduring) larval stage of nematode development.","definition_xrefs":["PMID:10077613","GOC:cab1","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"entry into diapause","termid":"GO:0055115"},{"relation_name":"part_of","term_name":"dauer larval development","termid":"GO:0040024"}],"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":"dauer entry","synonyms":[{"name":"nematode entry into dormancy","type":"exact"}],"termid":"GO:0043053"}


id: PBO:0003856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-directed RNA polymerase I complex subunit Rpa2","termid":"PBO:0003856"}


id: PR:O42922
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC16A3.17c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42922"],"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 MFS-type transporter C16A3.17c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16A3.17c","synonyms":[{"name":"Spom972h-SPBC16A3.17c","type":"exact"}],"termid":"PR:O42922"}


id: GO:0052344
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a symbiont activates, maintains or increases the frequency, rate or extent of the production of phytoalexins as part of the defense response of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by symbiont of host phytoalexin production (obsolete GO:0052344)","synonyms":[{"name":"activation by symbiont of host phytoalexin production","type":"narrow"},{"name":"positive regulation by organism of phytoalexin production in other organism involved in symbiotic interaction","type":"broad"},{"name":"stimulation by symbiont of host phytoalexin production","type":"narrow"},{"name":"up regulation by symbiont of host phytoalexin production","type":"exact"},{"name":"up-regulation by symbiont of host phytoalexin production","type":"exact"},{"name":"upregulation by symbiont of host phytoalexin production","type":"exact"}],"termid":"GO:0052344"}


id: GO:0003322
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a pancreatic A cell over time, from its formation to the mature structure. A pancreatic A cell is a cell in the pancreas that secretes glucagon.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glandular epithelial cell development","termid":"GO:0002068"},{"relation_name":"part_of","term_name":"pancreatic A cell differentiation","termid":"GO:0003310"}],"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":"pancreatic A cell development","synonyms":[{"name":"pancreatic alpha cell development","type":"exact"}],"termid":"GO:0003322"}


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


id: PBO:0026650
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_binding_during_cellular_response_to_methyl_methanesulfonate","termid":"PBO:0026650"}


id: FYPO:0002163
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the fungal-type cell wall is thinner than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell wall thickness during vegetative growth","termid":"FYPO:0006745"}],"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:0002946"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0002946"],"is_obsolete":false,"name":"decreased cell wall thickness during vegetative growth","synonyms":[{"name":"decreased cell wall thickness during mitotic cell cycle","type":"related"},{"name":"reduced cell wall thickness during vegetative growth","type":"exact"},{"name":"thin cell wall during vegetative growth","type":"exact"}],"termid":"FYPO:0002163"}


id: GO:1901569
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of fatty acid derivative.","definition_xrefs":["GOC:pr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid catabolic process","termid":"GO:0016042"},{"relation_name":"is_a","term_name":"fatty acid derivative metabolic process","termid":"GO:1901568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"fatty acid derivative catabolic process","synonyms":[{"name":"fatty acid derivative breakdown","type":"exact"},{"name":"fatty acid derivative catabolism","type":"exact"},{"name":"fatty acid derivative degradation","type":"exact"}],"termid":"GO:1901569"}


id: GO:0044618
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism effects a change in the relaxation of smooth muscle in the uterus of a second organism.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation of relaxation of smooth muscle in another organism","termid":"GO:0044617"},{"relation_name":"is_a","term_name":"regulation of uterine smooth muscle relaxation","termid":"GO:1900719"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"modulation of relaxation of uterine smooth muscle in another organism","synonyms":[{"name":"modulation of relaxation of uterine smooth muscle in other organism","type":"exact"},{"name":"regulation of relaxation of uterine smooth muscle in other organism","type":"exact"}],"termid":"GO:0044618"}


id: GO:0033968
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (7R)-7-(4-carboxybutanamido)cephalosporanate + H2O = (7R)-7-aminocephalosporanate + glutarate.","definition_xrefs":["EC:3.5.1.93"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0016810","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"glutaryl-7-aminocephalosporanic-acid acylase activity","secondary_identifiers":["RHEA:23508","MetaCyc:3.5.1.93-RXN"],"synonyms":[{"name":"(7R)-7-(4-carboxybutanamido)cephalosporanate amidohydrolase activity","type":"related"},{"name":"7beta-(4-carboxybutanamido)cephalosporanic acid acylase activity","type":"related"},{"name":"CA","type":"related"},{"name":"GA","type":"related"},{"name":"GCA","type":"related"},{"name":"GL-7-ACA acylase activity","type":"related"},{"name":"cephalosporin C acylase activity","type":"related"},{"name":"cephalosporin acylase activity","type":"related"},{"name":"glutaryl-7-ACA acylase activity","type":"related"},{"name":"glutaryl-7-aminocephalosporanic acid acylase activity","type":"related"}],"termid":"GO:0033968"}


id: PBO:0068449
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 23, pseudogene","termid":"PBO:0068449"}


id: PBO:0078075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocation associated membrane protein 1 like 1","termid":"PBO:0078075"}


id: GO:0120116
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of mature glucagon by proteolysis of the precursor proglucagon.","definition_xrefs":["PMID:28719828"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide hormone processing","termid":"GO:0016486"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051604"}],"interesting_parent_ids":["GO:0008150","GO:0051604","GO:0010467"],"is_obsolete":false,"name":"glucagon processing","secondary_identifiers":["Reactome:R-HSA-381771"],"termid":"GO:0120116"}


id: MOD:01447
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-methionine residue to N-(dihydroxymethyl)-L-methionine (not known as a natural, post-translational modification process).","definition_xrefs":["PubMed:12595263","RESID:AA0493","PubMed:9159480"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-methionine residue","termid":"MOD:00913"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-(dihydroxymethyl)-L-methionine (Met)","synonyms":[{"name":"(2S)-2-[(dihydroxymethyl)amino]-4-(methylsulfanyl)butanoic acid","type":"exact"},{"name":"N-(dihydroxymethyl)-L-methionine","type":"exact"},{"name":"N-formyl-L-methionine hydrate","type":"exact"},{"name":"N-orthoformylmethionine","type":"exact"}],"termid":"MOD:01447"}


id: MONDO:0016775
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lichen planus (LP) pemphigoides is a rare cross-over syndrome between lichen planus and bullous pemphigoid.","definition_xrefs":["Orphanet:254478"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lichen planus","termid":"MONDO:0006572"}],"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":"lichen planus pemphigoides","secondary_identifiers":["SCTID:238653005","GARD:12677","MEDGEN:590352","icd11.foundation:1373932539","UMLS:C0406369"],"synonyms":[{"name":"LP pemphigoides","type":"exact"}],"termid":"MONDO:0016775","xrefs":{"Monarch":{"xref_id":"0016775"}}}


id: GO:0070445
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of oligodendrocyte progenitor proliferation.","definition_xrefs":["GOC:mah","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neural precursor cell proliferation","termid":"GO:2000177"},{"relation_name":"regulates","term_name":"oligodendrocyte progenitor proliferation","termid":"GO:0070444"}],"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 oligodendrocyte progenitor proliferation","synonyms":[{"name":"regulation of oligodendrocyte precursor proliferation","type":"exact"}],"termid":"GO:0070445"}


id: MONDO:0005794
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Virus diseases caused by the herpesviridae.","definition_xrefs":["MESH:D006566"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Herpesviridae infectious disease","secondary_identifiers":["EFO:0007309","SCTID:23513009"],"synonyms":[{"name":"Herpesviridae caused disease or disorder","type":"exact"},{"name":"Herpesviridae disease or disorder","type":"exact"},{"name":"Herpesviridae infection","type":"related"},{"name":"Herpesviridae infections","type":"exact"},{"name":"Herpesvirus infection","type":"related"},{"name":"Herpesvirus infections","type":"related"},{"name":"herpes infection","type":"related"},{"name":"herpesvirus infection","type":"exact"},{"name":"infection, Herpesviridae","type":"related"},{"name":"infection, Herpesvirus","type":"related"},{"name":"infections, Herpesviridae","type":"related"},{"name":"infections, Herpesvirus","type":"related"}],"termid":"MONDO:0005794","xrefs":{"Monarch":{"xref_id":"0005794"}}}


id: GO:0001014
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The synthesis of small nucleolar RNA (snoRNA) from a DNA template by RNA polymerase III, originating at a type 2 RNA polymerase III promoter.","definition_xrefs":["GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription by RNA polymerase III","termid":"GO:0006383"},{"relation_name":"is_a","term_name":"sno(s)RNA transcription","termid":"GO:0009302"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0016074"}],"interesting_parent_ids":["GO:0006351","GO:0010467","GO:0008150","GO:0016074"],"is_obsolete":false,"name":"snoRNA transcription by RNA polymerase III","synonyms":[{"name":"snoRNA transcription from a type 2 RNA polymerase III promoter","type":"narrow"}],"termid":"GO:0001014"}


id: MONDO:0004078
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An intrahepatic cholangiocarcinoma that produces abundant mucin.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrahepatic bile duct mucinous adenocarcinoma","termid":"MONDO:0002739"},{"relation_name":"is_a","term_name":"intrahepatic cholangiocarcinoma","termid":"MONDO:0003210"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992","MONDO:0002515"],"is_obsolete":false,"name":"mucinous intrahepatic cholangiocarcinoma","secondary_identifiers":["NCIT:C41618","MEDGEN:270842","DOID:7024","UMLS:C1513718"],"synonyms":[{"name":"mucin-producing intrahepatic cholangiocarcinoma","type":"exact"},{"name":"mucinous intrahepatic cholangiocarcinoma","type":"exact"}],"termid":"MONDO:0004078","xrefs":{"Monarch":{"xref_id":"0004078"}}}


id: PBO:0082659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the CCR4-NOT transcriptional complex; CCR4-NOT is involved in regulation of gene expression; component of the major cytoplasmic deadenylase, which is involved in mRNA poly(A) tail shortening","termid":"PBO:0082659"}


id: PBO:0036050
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H3-K9_dimethylation_at_centromere_during_vegetative_growth","termid":"PBO:0036050"}


id: PBO:0074054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 25 member 34","termid":"PBO:0074054"}


id: PBO:0031736
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_mitotic_recombination","termid":"PBO:0031736"}


id: MONDO:0012604
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any isolated microphthalmia in which the cause of the disease is a mutation in the RAX gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated microphthalmia","termid":"MONDO:0000062"},{"relation_name":"is_a","term_name":"isolated anophthalmia-microphthalmia syndrome","termid":"MONDO:0016764"}],"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":"isolated microphthalmia 3","secondary_identifiers":["MESH:C567025","DOID:0060842","UMLS:C5774181","OMIM:611038","MEDGEN:1823955"],"synonyms":[{"name":"MCOP3","type":"exact"},{"name":"RAX isolated microphthalmia","type":"exact"},{"name":"isolated microphthalmia 3","type":"exact"},{"name":"isolated microphthalmia caused by mutation in RAX","type":"exact"},{"name":"isolated microphthalmia caused by mutation in rax","type":"exact"},{"name":"isolated microphthalmia type 3","type":"exact"},{"name":"microphthalmia, isolated 3","type":"related"},{"name":"microphthalmia, isolated type 3","type":"exact"},{"name":"rax isolated microphthalmia","type":"exact"}],"termid":"MONDO:0012604","xrefs":{"Monarch":{"xref_id":"0012604"}}}


id: PBO:0028590
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_vegetative_cell_growth","termid":"PBO:0028590"}


id: GO:0003870
data:
  {"annotated_genes":["SJAG_03961","SJAG_00097"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77986,95280],"is_not":false,"summary":null,"term":"GO:0003870"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: glycine + H+ + succinyl-CoA = 5-aminolevulinate + CO2 + CoA.","definition_xrefs":["EC:2.3.1.37","RHEA:12921"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-succinyltransferase activity","termid":"GO:0016749"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00097":null,"SJAG_03961":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016746","GO:0016740"],"is_obsolete":false,"name":"5-aminolevulinate synthase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:5-AMINOLEVULINIC-ACID-SYNTHASE-RXN","Reactome:R-HSA-189442","KEGG_REACTION:R00830"],"synonyms":[{"name":"5-aminolevulinate synthetase activity","type":"related"},{"name":"5-aminolevulinic acid synthase activity","type":"related"},{"name":"5-aminolevulinic acid synthetase activity","type":"related"},{"name":"ALA synthase activity","type":"related"},{"name":"ALA synthetase activity","type":"related"},{"name":"ALAS activity","type":"related"},{"name":"alpha-aminolevulinic acid synthase activity","type":"related"},{"name":"aminolevulinate synthase activity","type":"related"},{"name":"aminolevulinate synthetase activity","type":"related"},{"name":"aminolevulinic acid synthase activity","type":"related"},{"name":"aminolevulinic acid synthetase activity","type":"related"},{"name":"aminolevulinic synthetase activity","type":"related"},{"name":"delta-ALA synthetase activity","type":"related"},{"name":"delta-aminolevulinate synthase activity","type":"related"},{"name":"delta-aminolevulinate synthetase activity","type":"related"},{"name":"delta-aminolevulinic acid synthase activity","type":"related"},{"name":"delta-aminolevulinic acid synthetase activity","type":"related"},{"name":"delta-aminolevulinic synthetase activity","type":"related"},{"name":"succinyl-CoA:glycine C-succinyltransferase (decarboxylating)","type":"related"}],"termid":"GO:0003870","terms_by_termid":{"GO:0003870":null}}


id: MONDO:0000714
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete crest syndrome (obsolete MONDO:0000714)","termid":"MONDO:0000714","xrefs":{"Monarch":{"xref_id":"0000714"}}}


id: GO:0031120
data:
  {"annotated_genes":["SJAG_00566","SJAG_00083","SJAG_00088","SJAG_03572","SJAG_01234","SJAG_04754"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89523,94857,100656,105698,105759,113736],"is_not":false,"summary":null,"term":"GO:0031120"}]},"cv_name":"biological_process","definition":"The intramolecular conversion of uridine to pseudouridine in an snRNA molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pseudouridine synthesis","termid":"GO:0001522"},{"relation_name":"is_a","term_name":"snRNA modification","termid":"GO:0040031"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00083":null,"SJAG_00088":null,"SJAG_00566":null,"SJAG_01234":null,"SJAG_03572":null,"SJAG_04754":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0016073"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016073","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"snRNA pseudouridine synthesis","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0031120","terms_by_termid":{"GO:0031120":null}}


id: PBO:0058138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4436a","termid":"PBO:0058138"}


id: PBO:0074835
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 30","termid":"PBO:0074835"}


id: PBO:0071244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 85","termid":"PBO:0071244"}


id: GO:0070221
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A sulfide oxidation process that proceeds via the reaction catalyzed by sulfide:quinone oxidoreductase.","definition_xrefs":["MetaCyc:P222-PWY"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfide oxidation","termid":"GO:0019418"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006790","GO:0008150"],"is_obsolete":false,"name":"sulfide oxidation, using sulfide:quinone oxidoreductase","secondary_identifiers":["Reactome:R-HSA-1614517"],"synonyms":[{"name":"sulfide oxidation, using sulfide-quinone reductase","type":"exact"},{"name":"sulphide oxidation, using sulfide:quinone oxidoreductase","type":"exact"}],"termid":"GO:0070221"}


id: RO:0002354
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"output_of","termid":"RO:0002353"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"formed_as_result_of","termid":"RO:0002354"}


id: GO:0106172
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane of a COPI-coated endocytic vesicle.","definition_xrefs":["GOC:pde","PMID:29535154"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic vesicle lumen","termid":"GO:0060205"},{"relation_name":"part_of","term_name":"COPI-coated vesicle","termid":"GO:0030137"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0031410","GO:0005575"],"is_obsolete":false,"name":"COPI-coated vesicle lumen","termid":"GO:0106172"}


id: PBO:0090840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA processing protein Rrp12-like","termid":"PBO:0090840"}


id: GO:0031526
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the plasma membrane surrounding the brush border.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell projection membrane","termid":"GO:0031253"},{"relation_name":"part_of","term_name":"brush border","termid":"GO:0005903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886"],"is_obsolete":false,"name":"brush border membrane","termid":"GO:0031526"}


id: GO:0021903
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the neural tube is divided into specific regions along the rostrocaudal axis.","definition_xrefs":["GOC:cls","PMID:11262869","GOC:jid","GOC:dgh","GOC:dph","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anterior/posterior pattern specification","termid":"GO:0009952"},{"relation_name":"part_of","term_name":"neural tube patterning","termid":"GO:0021532"}],"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":"rostrocaudal neural tube patterning","synonyms":[{"name":"anterior-posterior neural tube patterning","type":"related"}],"termid":"GO:0021903"}


id: MONDO:0019187
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Axenfeld-Rieger syndrome (ARS) is a generic term used to designate overlapping genetic disorders, in which the major physical condition is anterior segment dysgenesis of the eye. Patients with ARS may also present with multiple variable congenital anomalies.","definition_xrefs":["Orphanet:782"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"iridogoniodysgenesis","termid":"MONDO:0011119"},{"relation_name":"excluded_subClassOf","term_name":"obsolete non-syndromic developmental defect of the eye (obsolete MONDO:0015217)","termid":"MONDO:0015217"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic anorectal malformation (obsolete MONDO:0015246)","termid":"MONDO:0015246"},{"relation_name":"excluded_subClassOf","term_name":"non-acquired combined pituitary hormone deficiency","termid":"MONDO:0018762"},{"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":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"neurocristopathy","termid":"MONDO:0021635"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Axenfeld-Rieger syndrome","secondary_identifiers":["DOID:14686","GARD:5701","NCIT:C131001","OMIMPS:180500","NORD:1670","ICD9:743.44","MedDRA:10059255","UMLS:C3495488","MESH:C535679","MEDGEN:501192","SCTID:47507006"],"synonyms":[{"name":"Axenfeld syndrome","type":"exact"},{"name":"Axenfeldt-Rieger syndrome","type":"exact"},{"name":"Hagedoom syndrome","type":"related"},{"name":"RGS - Rieger syndrome","type":"exact"},{"name":"Rieger syndrome","type":"exact"},{"name":"Rieger's anomaly","type":"exact"},{"name":"anomaly, Rieger's","type":"exact"},{"name":"goniodysgenesis hypodontia","type":"related"},{"name":"iridogoniodysgenesis with somatic anomalies","type":"related"}],"termid":"MONDO:0019187","xrefs":{"Monarch":{"xref_id":"0019187"}}}


id: GO:0007178
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by an extracellular ligand binding to a receptor on the surface of the target cell where the receptor possesses serine/threonine kinase activity, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:signaling","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme-linked receptor protein signaling pathway","termid":"GO:0007167"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"cell surface receptor protein serine/threonine kinase signaling pathway","synonyms":[{"name":"transmembrane receptor protein serine/threonine kinase signaling pathway","type":"broad"},{"name":"transmembrane receptor protein serine/threonine kinase signalling pathway","type":"exact"}],"termid":"GO:0007178"}


id: PBO:0089331
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-type ATPase V0 subunit d","termid":"PBO:0089331"}


id: PBO:0080579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 5","termid":"PBO:0080579"}


id: PBO:0088520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial carrier, 2-oxoadipate/2-oxoglutarate","termid":"PBO:0088520"}


id: PBO:0088871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNARE associated Golgi protein","termid":"PBO:0088871"}


id: GO:0009264
data:
  {"annotated_genes":["SJAG_04487"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98490],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035863"},{"annotations":[98492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046081"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a deoxyribonucleotide, a compound consisting of deoxyribonucleoside (a base linked to a deoxyribose sugar) esterified with a phosphate group at either the 3' or 5'-hydroxyl group of the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide catabolic process","termid":"GO:0009166"},{"relation_name":"is_a","term_name":"deoxyribonucleotide metabolic process","termid":"GO:0009262"},{"relation_name":"is_a","term_name":"carbohydrate derivative catabolic process","termid":"GO:1901136"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04487":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:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"deoxyribonucleotide catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"deoxyribonucleotide breakdown","type":"exact"},{"name":"deoxyribonucleotide catabolism","type":"exact"},{"name":"deoxyribonucleotide degradation","type":"exact"}],"termid":"GO:0009264","terms_by_termid":{"GO:0035863":null,"GO:0046081":null}}


id: PBO:0087509
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of heterodimeric nuclear SUMO activating enzyme E1 with Uba2p; activates Smt3p (SUMO) before its conjugation to proteins (sumoylation), which may play a role in protein targeting; essential for viability; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0087509"}


id: MONDO:0021223
data:
  {"annotated_genes":["SJAG_04699","SJAG_02231","SJAG_01620","SJAG_02426","SJAG_02261","SJAG_02226","SJAG_00260","SJAG_04206","SJAG_00980","SJAG_01837","SJAG_02049","SJAG_02187","SJAG_02748","SJAG_03920","SJAG_01082","SJAG_03453","SJAG_04394"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86011,86008,86013,86007,86010,86009,86014,86012,86859],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0005575"},{"annotations":[86575,86576],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0001056"},{"annotations":[86336,86335],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011719"},{"annotations":[86169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007256"},{"annotations":[85899],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007356"},{"annotations":[84720],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012249"},{"annotations":[85170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013699"},{"annotations":[85172],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013710"},{"annotations":[85182,85183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008018"}]},"cv_name":"mondo","definition":"A neoplasm (disease) that involves the digestive system.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm","termid":"MONDO:0005070"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00260":null,"SJAG_00980":null,"SJAG_01082":null,"SJAG_01620":null,"SJAG_01837":null,"SJAG_02049":null,"SJAG_02187":null,"SJAG_02226":null,"SJAG_02231":null,"SJAG_02261":null,"SJAG_02426":null,"SJAG_02748":null,"SJAG_03453":null,"SJAG_03920":null,"SJAG_04206":null,"SJAG_04394":null,"SJAG_04699":null},"genotype_count":0,"is_obsolete":false,"name":"digestive system neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:4846","EFO:0008549","MESH:D005770","NCIT:C3052","UMLS:C0017185"],"synonyms":[{"name":"GI neoplasm","type":"exact"},{"name":"GI system neoplasm","type":"exact"},{"name":"GI system tumor","type":"exact"},{"name":"GI system tumour","type":"exact"},{"name":"GI tumor","type":"exact"},{"name":"GI tumour","type":"exact"},{"name":"digestive neoplasm","type":"exact"},{"name":"digestive system neoplasm (disease)","type":"exact"},{"name":"digestive system tumor","type":"exact"},{"name":"digestive system tumour","type":"exact"},{"name":"digestive tumor","type":"exact"},{"name":"digestive tumour","type":"exact"},{"name":"gastrointestinal neoplasm","type":"exact"},{"name":"gastrointestinal system neoplasm","type":"exact"},{"name":"gastrointestinal system tumor","type":"exact"},{"name":"gastrointestinal system tumour","type":"exact"},{"name":"gastrointestinal tumor","type":"exact"},{"name":"gastrointestinal tumour","type":"exact"},{"name":"neoplasm of GI system","type":"exact"},{"name":"neoplasm of digestive system","type":"exact"},{"name":"neoplasm of gastrointestinal system","type":"exact"},{"name":"neoplasm of the GI system","type":"exact"},{"name":"neoplasm of the digestive system","type":"exact"},{"name":"neoplasm of the gastrointestinal system","type":"exact"},{"name":"tumor of GI system","type":"exact"},{"name":"tumor of digestive system","type":"exact"},{"name":"tumor of gastrointestinal system","type":"exact"},{"name":"tumor of the GI system","type":"exact"},{"name":"tumor of the digestive system","type":"exact"},{"name":"tumor of the gastrointestinal system","type":"exact"},{"name":"tumour of GI system","type":"exact"},{"name":"tumour of digestive system","type":"exact"},{"name":"tumour of gastrointestinal system","type":"exact"},{"name":"tumour of the GI system","type":"exact"},{"name":"tumour of the digestive system","type":"exact"},{"name":"tumour of the gastrointestinal system","type":"exact"}],"termid":"MONDO:0021223","terms_by_termid":{"MONDO:0001056":null,"MONDO:0005575":null,"MONDO:0007256":null,"MONDO:0007356":null,"MONDO:0008018":null,"MONDO:0011719":null,"MONDO:0012249":null,"MONDO:0013699":null,"MONDO:0013710":null},"xrefs":{"Monarch":{"xref_id":"0021223"}}}


id: PR:O94656
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- atg16 gene.","definition_xrefs":["UniProtKB:O94656","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":"autophagy protein 16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC405.05","synonyms":[{"name":"Spom972h-atg16","type":"exact"}],"termid":"PR:O94656"}


id: PBO:0056007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LSM4 homolog, U6 small nuclear RNA and mRNA degradation associated","termid":"PBO:0056007"}


id: MONDO:0011228
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":"creases, infra-auricular cutaneous, with tall stature and advanced bone age","secondary_identifiers":["MEDGEN:356259","MESH:C566543","UMLS:C1865360","OMIM:602472"],"synonyms":[{"name":"creases, infra-auricular cutaneous, with tall stature and advanced bone age","type":"exact"}],"termid":"MONDO:0011228","xrefs":{"Monarch":{"xref_id":"0011228"}}}


id: MONDO:0010544
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the NHS gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset non-syndromic cataract","termid":"MONDO:0011060"}],"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":"cataract 40","secondary_identifiers":["MESH:C535338","MEDGEN:886621","DOID:0110272","OMIM:302200","UMLS:C4049004"],"synonyms":[{"name":"CTRCT40","type":"exact"},{"name":"NHS early-onset non-syndromic cataract","type":"exact"},{"name":"cataract 40","type":"exact"},{"name":"cataract 40 X-linked","type":"exact"},{"name":"cataract 40 with or without microcornea","type":"exact"},{"name":"cataract 40, X-linked","type":"related"},{"name":"cataract congenital X-linked","type":"related"},{"name":"cataract type 40","type":"exact"},{"name":"cataract, congenital total, with posterior sutural opacities in heterozygotes","type":"related"},{"name":"cataract, congenital, X-linked","type":"related"},{"name":"cataract, congenital, with microcornea or slight microphthalmia","type":"related"},{"name":"early-onset non-syndromic cataract caused by mutation in NHS","type":"exact"}],"termid":"MONDO:0010544","xrefs":{"Monarch":{"xref_id":"0010544"}}}


id: MONDO:0006971
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tumors or cancer of the sigmoid colon.","definition_xrefs":["MESH:D012811"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colonic neoplasm","termid":"MONDO:0005401"}],"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":"sigmoid neoplasm","secondary_identifiers":["UMLS:C0037073","DOID:1896","EFO:1001181","MEDGEN:20753","MedDRA:10026456","SCTID:126845000","ICD9:153.3"],"synonyms":[{"name":"neoplasm of sigmoid colon","type":"exact"},{"name":"sigmoid colon neoplasm","type":"exact"},{"name":"sigmoid colon neoplasm (disease)","type":"exact"},{"name":"sigmoid colon tumor","type":"exact"},{"name":"sigmoid colon tumour","type":"exact"},{"name":"tumor of sigmoid colon","type":"exact"},{"name":"tumour of sigmoid colon","type":"exact"}],"termid":"MONDO:0006971","xrefs":{"Monarch":{"xref_id":"0006971"}}}


id: FYPO:0006562
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 RNA measured in a cell during G2 phase of the mitotic cell cycle is higher than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased RNA level during vegetative growth","termid":"FYPO:0000825"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0006551","FYPO:0005447"],"is_obsolete":false,"name":"increased RNA level during mitotic G2 phase","synonyms":[{"name":"increased RNA accumulation during mitotic G2 phase","type":"related"},{"name":"increased RNA level during G2 phase of mitotic cell cycle","type":"exact"},{"name":"increased RNA level during mitotic G2 phase during vegetative growth","type":"exact"},{"name":"increased mRNA level during mitotic G2 phase","type":"narrow"},{"name":"increased transcript level during mitotic G2 phase","type":"exact"}],"termid":"FYPO:0006562"}


id: PBO:0077476
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 198B (pseudogene)","termid":"PBO:0077476"}


id: PBO:0066528
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RANBP2 like and GRIP domain containing 4","termid":"PBO:0066528"}


id: PBO:0017469
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-ends_during","termid":"PBO:0017469"}


id: PBO:0002479
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.1.1.8","termid":"PBO:0002479"}


id: PBO:0057641
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1233-1","termid":"PBO:0057641"}


id: MONDO:0003295
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition characterized by the presence of numerous small benign smooth muscle neoplasms located throughout the body.","definition_xrefs":["NCIT:C3748"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leiomyomatosis","secondary_identifiers":["MESH:D018231","ICDO:8890/1","DOID:5138","MEDGEN:60203","UMLS:C0206654"],"synonyms":[{"name":"leiomyomatosis","type":"exact"},{"name":"leiomyomatosis, no ICD-O subtype","type":"exact"},{"name":"leiomyomatosis, no ICD-O subtype (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0003295","xrefs":{"Monarch":{"xref_id":"0003295"}}}


id: MONDO:0016680
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An anaplastic astrocytoma (grade III astrocytic tumor) or glioblastoma (grade IV astrocytic tumor).","definition_xrefs":["NCIT:C102897"],"direct_ancestors":[{"relation_name":"is_a","term_name":"astrocytic tumor","termid":"MONDO:0021636"},{"relation_name":"is_a","term_name":"malignant glioma","termid":"MONDO:0100342"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"high grade astrocytic tumor","secondary_identifiers":["MEDGEN:769639","Orphanet:251561","GARD:20704","UMLS:C3640999"],"synonyms":[{"name":"high grade astrocytic neoplasm","type":"exact"},{"name":"high grade astrocytic tumor","type":"exact"},{"name":"high-grade astrocytic neoplasm","type":"exact"},{"name":"high-grade astrocytic tumor","type":"exact"},{"name":"high-grade astrocytic tumour","type":"exact"},{"name":"high-grade astrocytoma","type":"related"}],"termid":"MONDO:0016680","xrefs":{"Monarch":{"xref_id":"0016680"}}}


id: MONDO:1010862
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lysosomal storage disease that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal storage disease, non-human animal","termid":"MONDO:1010171"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysosomal storage disease, cattle","secondary_identifiers":["OMIA:000616-9913"],"termid":"MONDO:1010862","xrefs":{"Monarch":{"xref_id":"1010862"}}}


id: MOD:01595
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"The protein modification reporter fragment produced by an Applied Biosystems iTRAQ8plex-114 reagent derivatized residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"iTRAQ8plex-114 reporter+balance reagent acylated residue","termid":"MOD:01535"},{"relation_name":"is_a","term_name":"iTRAQ8plex reporter fragment","termid":"MOD:01593"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ8plex-114 reporter fragment","synonyms":[{"name":"4-methyl-1-methylidenepiperazin-1-ium","type":"exact"}],"termid":"MOD:01595"}


id: GO:0039556
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to MDA-5, a cytoplasmic pattern recognition receptor that initiates an antiviral signaling pathway upon binding to viral dsRNA.","definition_xrefs":["PMID:19019954"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"MDA-5 binding","synonyms":[{"name":"MDA5 binding","type":"exact"}],"termid":"GO:0039556"}


id: GO:0061179
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of the regulated release of insulin that contributes to the response of a cell to glucose.","definition_xrefs":["GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of insulin secretion","termid":"GO:0046676"},{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of insulin secretion involved in cellular response to glucose stimulus","termid":"GO:0061178"},{"relation_name":"negatively_regulates","term_name":"insulin secretion involved in cellular response to glucose stimulus","termid":"GO:0035773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0006810","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of insulin secretion involved in cellular response to glucose stimulus","synonyms":[{"name":"negative regulation of insulin secretion in response to glucose","type":"related"},{"name":"negative regulation of insulin secretion involved in cellular response to glucose","type":"exact"}],"termid":"GO:0061179"}


id: PR:O14239
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rax2 gene.","definition_xrefs":["UniProtKB:O14239","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":"polarized growth protein rax2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6F6.06c","synonyms":[{"name":"Spom972h-rax2","type":"exact"},{"name":"revert to axial protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14239"}


id: PBO:0004536
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA processing protein Rrp12-like (predicted)","termid":"PBO:0004536"}


id: PBO:0082374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Basic leucine zipper (bZIP) transcription factor (ATF/CREB1 homolog); regulates the unfolded protein response, via UPRE binding, and membrane biogenesis; ER stress-induced splicing pathway triggers efficient Hac1p translation; two functional forms of Hac1p are produced; translation initiation is repressed under non-stress conditions; protein abundance increases in response to DNA replication stress","termid":"PBO:0082374"}


id: MONDO:0700012
data:
  {"annotated_genes":["SJAG_03424","SJAG_01548"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85251,85250],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007925"}]},"cv_name":"mondo","definition":"Chromosomal disorder in which chromosome 5 is affected.","definition_xrefs":["MONDO:patterns/chromosome_type"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal anomaly","termid":"MONDO:0020049"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01548":null,"SJAG_03424":null},"genotype_count":0,"is_obsolete":false,"name":"chromosome 5 disorder","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0700012","terms_by_termid":{"MONDO:0007925":null},"xrefs":{"Monarch":{"xref_id":"0700012"}}}


id: PBO:0041852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caspase 1 pseudogene 2","termid":"PBO:0041852"}


id: PR:P40373
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ATP phosphoribosyltransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01785"],"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":"ATP phosphoribosyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC25G10.05c","secondary_identifiers":["UniProtKB:P40373"],"synonyms":[{"name":"ATP-PRT (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ATP-PRTase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-hisG","type":"exact"}],"termid":"PR:P40373"}


id: internal:obsolete_name
data:
  {"annotation_feature_type":"gene","cv_name":"synonym_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"obsolete_name","termid":"internal:obsolete_name"}


id: PR:O14157
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- myp2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14157"],"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":"myosin type-2 heavy chain 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4A8.05c","synonyms":[{"name":"Spom972h-myp2","type":"exact"},{"name":"myosin type II heavy chain 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14157"}


id: GO:1903063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of reverse cholesterol transport.","definition_xrefs":["GOC:BHF","GOC:rl","PMID:23931754","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cholesterol transport","termid":"GO:0032375"},{"relation_name":"is_a","term_name":"regulation of reverse cholesterol transport","termid":"GO:1903062"},{"relation_name":"negatively_regulates","term_name":"reverse cholesterol transport","termid":"GO:0043691"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of reverse cholesterol transport","synonyms":[{"name":"down regulation of reverse cholesterol transport","type":"exact"},{"name":"down-regulation of reverse cholesterol transport","type":"exact"},{"name":"downregulation of reverse cholesterol transport","type":"exact"},{"name":"inhibition of reverse cholesterol transport","type":"narrow"}],"termid":"GO:1903063"}


id: PBO:0067357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 455, pseudogene","termid":"PBO:0067357"}


id: PBO:0031133
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_regulation_of_translation_in_response_to_nitrogen_starvation","termid":"PBO:0031133"}


id: PBO:0056371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase 8","termid":"PBO:0056371"}


id: FYPO:0003486
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 region of a chromosome at which a DNA double-strand break has occurred is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to double-strand break site","termid":"FYPO:0002473"},{"relation_name":"is_a","term_name":"abolished protein localization to chromosome during vegetative growth","termid":"FYPO:0002841"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"abolished protein localization to double-strand break site","synonyms":[{"name":"abolished protein localisation to double-strand break site","type":"exact"},{"name":"abolished protein localization to double-strand break site during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to double-strand break site during vegetative growth","type":"exact"},{"name":"abolished protein localization to site of double-strand break","type":"exact"},{"name":"protein localization to double-strand break site abolished","type":"exact"}],"termid":"FYPO:0003486"}


id: PBO:0044876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DENN domain containing 5A","termid":"PBO:0044876"}


id: PBO:0090606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3-H4 chaperone, CAF assembly factor (CAF-1) complex subunit A Pcf1","termid":"PBO:0090606"}


id: MONDO:0019469
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"T-cell large granular lymphocyte leukemia (T-cell LGL leukemia) is a lymphoproliferative malignancy that arises from the mature T-cell (CD3+) lineage.","definition_xrefs":["Orphanet:86872"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"B-cell chronic lymphocytic leukemia","termid":"MONDO:0004948"},{"relation_name":"is_a","term_name":"mature T-cell and NK-cell non-Hodgkin lymphoma","termid":"MONDO:0000430"},{"relation_name":"is_a","term_name":"chronic leukemia","termid":"MONDO:0001014"},{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"},{"relation_name":"is_a","term_name":"lymphoid leukemia","termid":"MONDO:0005402"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"T-cell large granular lymphocyte leukemia","secondary_identifiers":["icd11.foundation:83430037","ICD9:204.80","MedDRA:10065862","NCIT:C4664","MEDGEN:363038","ICDO:9768/1","ICDO:9831/1","ICDO:9831/3","UMLS:C1955861","GARD:9812","ONCOTREE:TLGL","SCTID:277569004","DOID:0050751"],"synonyms":[{"name":"LGL leukaemia","type":"related"},{"name":"LGL leukemia","type":"related"},{"name":"LGLL","type":"exact"},{"name":"T gamma lymphoproliferative disorder","type":"exact"},{"name":"T-LGL","type":"exact"},{"name":"T-LGL leukaemia","type":"exact"},{"name":"T-LGL leukemia","type":"exact"},{"name":"T-cell LGL leukaemia","type":"exact"},{"name":"T-cell LGL leukemia","type":"exact"},{"name":"T-cell large gran. lymph. leuk.","type":"exact"},{"name":"T-cell large granular lymphocyte leukemia","type":"exact"},{"name":"T-cell large granular lymphocytic leukaemia","type":"exact"},{"name":"T-cell large granular lymphocytic leukemia","type":"exact"},{"name":"T-gamma lymphoproliferative disorder","type":"exact"},{"name":"TLGL","type":"related"},{"name":"Tgamma large granular lymphocyte leukaemia","type":"exact"},{"name":"Tgamma large granular lymphocyte leukemia","type":"exact"},{"name":"large cell granular lymphogenous leukaemia","type":"exact"},{"name":"large cell granular lymphogenous leukemia","type":"exact"},{"name":"large cell granular lymphoid leukaemia","type":"exact"},{"name":"large cell granular lymphoid leukemia","type":"exact"},{"name":"large granular lymphocyte leukaemia","type":"related"},{"name":"large granular lymphocyte leukemia","type":"related"},{"name":"large granular lymphocytic leukaemia","type":"exact"},{"name":"large granular lymphocytic leukemia","type":"exact"},{"name":"large granular lymphocytosis","type":"exact"},{"name":"leukemia, large granular LYMPHOCYTIC, malignant","type":"exact"},{"name":"proliferation of large granular lymphocytes","type":"exact"}],"termid":"MONDO:0019469","xrefs":{"Monarch":{"xref_id":"0019469"}}}


id: PBO:0055784
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LONRF2 pseudogene 4","termid":"PBO:0055784"}


id: GO:2000526
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any positive regulation of glycoprotein biosynthetic process that is involved in immunological synapse formation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of glycoprotein biosynthetic process","termid":"GO:0010560"},{"relation_name":"part_of","term_name":"immunological synapse formation","termid":"GO:0001771"}],"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 glycoprotein biosynthetic process involved in immunological synapse formation","synonyms":[{"name":"positive regulation of glycoprotein biosynthetic process of formation of immunological synapse","type":"exact"},{"name":"positive regulation of glycoprotein biosynthetic process of immunological synapse formation","type":"exact"}],"termid":"GO:2000526"}


id: PBO:0039416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angel homolog 1","termid":"PBO:0039416"}


id: MONDO:0009698
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Unverricht-Lundborg disease (ULD) is a rare progressive myoclonic epilepsy disorder characterized by action- and stimulus-sensitive myoclonus, and tonic-clonic seizures with ataxia, but with only a mild cognitive decline over time.","definition_xrefs":["Orphanet:308"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"},{"relation_name":"is_a","term_name":"progressive myoclonus epilepsy","termid":"MONDO:0020074"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"Unverricht-Lundborg syndrome","secondary_identifiers":["DOID:0111452","MedDRA:10054895","DOID:3535","OMIM:254800","SCTID:230423006","UMLS:C0751785","NANDO:1200954","GARD:3876","MESH:D020194","MEDGEN:155923","NANDO:2200880"],"synonyms":[{"name":"Baltic myoclonic epilepsy","type":"related"},{"name":"EPM1","type":"related"},{"name":"PME type 1","type":"exact"},{"name":"ULD","type":"exact"},{"name":"Uld","type":"related"},{"name":"Unverricht - Lundborg disease","type":"exact"},{"name":"Unverricht's disease","type":"exact"},{"name":"Unverricht-Lundborg disease","type":"exact"},{"name":"Unverricht-Lundborg syndrome","type":"exact"},{"name":"epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)","type":"exact"},{"name":"epilepsy, progressive myoclonic type 1","type":"related"},{"name":"epilepsy, progressive myoclonic, 1","type":"related"},{"name":"epilepsy, progressive myoclonic, 1A","type":"related"},{"name":"epilepsy, progressive myoclonus 1","type":"related"},{"name":"myoclonic epilepsy of Unverricht and Lundborg","type":"related"},{"name":"myoclonus progressive epilepsy of Unverricht and Lundborg","type":"related"},{"name":"progressive myoclonic epilepsy","type":"related"},{"name":"progressive myoclonic epilepsy type 1","type":"exact"},{"name":"progressive myoclonus epilepsy Baltic myoclonic epilepsy","type":"related"},{"name":"progressive myoclonus epilepsy type 1","type":"exact"}],"termid":"MONDO:0009698","xrefs":{"Monarch":{"xref_id":"0009698"}}}


id: PR:O94619
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- adn2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94619"],"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":"adhesion defective protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1289.10c","synonyms":[{"name":"LisH domain-containing protein adn2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-adn2","type":"exact"}],"termid":"PR:O94619"}


id: PBO:0088417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis protein Tsr1","termid":"PBO:0088417"}


id: FYPO:0005720
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 chromosome recapture is normal (i.e. indistinguishable from wild type) during metaphase of mitosis. Chromosome recapture is the reattachment of chromosomes which have become detached from the spindle.","definition_xrefs":["PMID:17881496","GO:1990942","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"},{"relation_name":"is_a","term_name":"localization phenotype during vegetative growth","termid":"FYPO:0001337"},{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"},{"relation_name":"is_a","term_name":"normal cell cycle process","termid":"FYPO:0006915"}],"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:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000138","FYPO:0000002","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal mitotic metaphase chromosome recapture","synonyms":[{"name":"normal chromosome recapture during mitotic metaphase","type":"exact"},{"name":"normal kinetochore retrieval in mitotic metaphase","type":"exact"},{"name":"normal mitotic kinetochore retrieval","type":"exact"},{"name":"normal mitotic metaphase chromosome recapture during vegetative growth","type":"exact"},{"name":"normal mitotic metaphase chromosome retrieval to SPB","type":"exact"},{"name":"normal mitotic metaphase chromosome retrieval to the spindle pole body","type":"exact"},{"name":"normal mitotic sister kinetochore recapture","type":"exact"}],"termid":"FYPO:0005720"}


id: PBO:0001504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase epsilon subunit Dpb3","termid":"PBO:0001504"}


id: PBO:0109050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metabolism induced tumor activator 1","termid":"PBO:0109050"}


id: PBO:0091121
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial glutamyl-tRNA amidotransferase complex subunit Gta3","termid":"PBO:0091121"}


id: PBO:0026891
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_kinetochore","termid":"PBO:0026891"}


id: PBO:0073771
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 4 member 4","termid":"PBO:0073771"}


id: MONDO:0004982
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the pancreas.","definition_xrefs":["NCIT:C3306"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreas disorder","termid":"MONDO:0002356"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"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":"pancreatitis","secondary_identifiers":["EFO:0000278","DOID:4989","MESH:D010195","SCTID:75694006","MEDGEN:14586","UMLS:C0030305"],"synonyms":[{"name":"inflammation of pancreas","type":"exact"},{"name":"pancreas inflammation","type":"exact"}],"termid":"MONDO:0004982","xrefs":{"Monarch":{"xref_id":"0004982"}}}


id: GO:0045689
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of antipodal cell differentiation.","definition_xrefs":["GOC:go_curators","GOC:mtg_plant"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell differentiation","termid":"GO:0045596"},{"relation_name":"is_a","term_name":"regulation of antipodal cell differentiation","termid":"GO:0045688"},{"relation_name":"negatively_regulates","term_name":"antipodal cell differentiation","termid":"GO:0009557"}],"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 antipodal cell differentiation","synonyms":[{"name":"down regulation of antipodal cell differentiation","type":"exact"},{"name":"down-regulation of antipodal cell differentiation","type":"exact"},{"name":"downregulation of antipodal cell differentiation","type":"exact"},{"name":"inhibition of antipodal cell differentiation","type":"narrow"}],"termid":"GO:0045689"}


id: PBO:0029605
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_transporter_activity","termid":"PBO:0029605"}


id: SO:0000192
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An intron that is the most 3-prime in a given transcript.","direct_ancestors":[{"relation_name":"is_a","term_name":"intron","termid":"SO:0000188"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_prime_intron","synonyms":[{"name":"3' intron","type":"exact"},{"name":"3' intron sequence","type":"related"},{"name":"three prime intron","type":"exact"}],"termid":"SO:0000192"}


id: GO:0050003
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5,10-methylenetetrahydrofolate + dCMP = 2'-deoxy-5-methyl-5'-cytidylate + 7,8-dihydrofolate.","definition_xrefs":["EC:2.1.1.54","RHEA:11568"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-methyltransferase activity","termid":"GO:0008169"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016741","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"deoxycytidylate C-methyltransferase activity","secondary_identifiers":["MetaCyc:DEOXYCYTIDYLATE-C-METHYLTRANSFERASE-RXN","KEGG_REACTION:R01670"],"synonyms":[{"name":"5,10-methylenetetrahydrofolate:dCMP C-methyltransferase activity","type":"related"},{"name":"dCMP methyltransferase activity","type":"related"},{"name":"deoxycytidylate methyltransferase activity","type":"related"}],"termid":"GO:0050003"}


id: PBO:0042805
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ceramide kinase","termid":"PBO:0042805"}


id: FYPO:0001864
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which conjugation takes place in cells that are not subject to glucose starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mating","termid":"FYPO:0000031"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000301"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000301","FYPO:0001985"],"is_obsolete":false,"name":"mating without glucose starvation","synonyms":[{"name":"conjugation without glucose starvation","type":"exact"},{"name":"mating in the absence of glucose starvation","type":"exact"},{"name":"mating without glucose depletion","type":"exact"},{"name":"mating without glucose deprivation","type":"exact"}],"termid":"FYPO:0001864"}


id: PBO:0005695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein, rrm type","termid":"PBO:0005695"}


id: PBO:0084050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase-activating protein for Gpa1p; regulates desensitization to alpha factor pheromone; also required to prevent receptor-independent signaling of the mating pathway; member of the RGS (regulator of G-protein signaling) family","termid":"PBO:0084050"}


id: MONDO:0000609
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete sideroblastic anemia with spinocerebellar ataxia (obsolete MONDO:0000609)","termid":"MONDO:0000609","xrefs":{"Monarch":{"xref_id":"0000609"}}}


id: MONDO:0004964
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Aggressive nodal or extranodal mature (peripheral) T-cell lymphomas that do not belong to the better defined entities of the remainder of mature T-cell lymphomas. This category includes the following variants: lymphoepithelioid cell variant (Lennert's lymphoma), follicular variant, and T-zone variant.","definition_xrefs":["NCIT:C4340"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoma","termid":"MONDO:0005062"},{"relation_name":"is_a","term_name":"neoplasm of mature T-cells or NK-cells","termid":"MONDO:0005169"}],"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":"peripheral T-cell lymphoma, not otherwise specified","secondary_identifiers":["icd11.foundation:855224800","NANDO:2200028","ONCOTREE:PTCL","EFO:0000211"],"synonyms":[{"name":"PTCL","type":"related"},{"name":"peripheral T-cell lymphoma, not otherwise specified","type":"exact"}],"termid":"MONDO:0004964","xrefs":{"Monarch":{"xref_id":"0004964"}}}


id: PBO:0048375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgi associated RAB2 interactor 1A","termid":"PBO:0048375"}


id: FYPO:0008062
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of chromatin binding to the chromatin central core by a gene product (usually a protein) in a mutant is increased. The affected gene product may be encoded by the mutated gene, or by a different gene, and may normally bind DNA, protein, or both in chromatin.","definition_xrefs":["PMID:15908586"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased chromatin binding","termid":"FYPO:0002980"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000702"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000702","FYPO:0000707","FYPO:0001985"],"is_obsolete":false,"name":"increased chromatin binding at centromere central core","termid":"FYPO:0008062"}


id: PBO:0054511
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 1911","termid":"PBO:0054511"}


id: MONDO:0003757
data:
  {"annotated_genes":["SJAG_03866","SJAG_04628","SJAG_00773","SJAG_01537","SJAG_04110","SJAG_04537","SJAG_04145","SJAG_00564","SJAG_03457","SJAG_04292","SJAG_01857","SJAG_00308","SJAG_05289","SJAG_00660","SJAG_04506","SJAG_01530","SJAG_04123","SJAG_02306","SJAG_04913","SJAG_01854","SJAG_04325","SJAG_00199","SJAG_02322","SJAG_03895","SJAG_04757","SJAG_03320","SJAG_02615","SJAG_01848","SJAG_04566","SJAG_01159"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84546,84547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014702"},{"annotations":[86518,86519],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014975"},{"annotations":[86785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030669"},{"annotations":[84966],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014567"},{"annotations":[85181],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009748"},{"annotations":[85234],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011489"},{"annotations":[86587],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011532"},{"annotations":[84706],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010043"},{"annotations":[84711,84710,84709],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012256"},{"annotations":[84596],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012476"},{"annotations":[84716],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012453"},{"annotations":[86570],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012866"},{"annotations":[85840],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012787"},{"annotations":[86028,86029],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008438"},{"annotations":[86288],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012928"},{"annotations":[84812,84814,84813],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014018"},{"annotations":[84811],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014020"},{"annotations":[85173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014305"},{"annotations":[85157],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014282"},{"annotations":[84643],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014644"},{"annotations":[85648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014882"},{"annotations":[86019,86020],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011006"},{"annotations":[84627],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014679"},{"annotations":[86273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012651"},{"annotations":[86059],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957221"},{"annotations":[85569],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957958"},{"annotations":[86227],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032906"},{"annotations":[85571],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030482"},{"annotations":[85615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030512"},{"annotations":[86367,86366],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031019"},{"annotations":[85864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957308"},{"annotations":[85865],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957309"}]},"cv_name":"mondo","definition":"Complete paralysis of the lower half of the body including both legs, often caused by damage to the spinal cord.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"central nervous system 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lower","type":"exact"},{"name":"severe or complete loss of motor function in the lower extremities and lower portions of the trunk","type":"related"}],"termid":"MONDO:0003757","terms_by_termid":{"MONDO:0008438":null,"MONDO:0009748":null,"MONDO:0010043":null,"MONDO:0011006":null,"MONDO:0011489":null,"MONDO:0011532":null,"MONDO:0012256":null,"MONDO:0012453":null,"MONDO:0012476":null,"MONDO:0012651":null,"MONDO:0012787":null,"MONDO:0012866":null,"MONDO:0012928":null,"MONDO:0014018":null,"MONDO:0014020":null,"MONDO:0014282":null,"MONDO:0014305":null,"MONDO:0014567":null,"MONDO:0014644":null,"MONDO:0014679":null,"MONDO:0014702":null,"MONDO:0014882":null,"MONDO:0014975":null,"MONDO:0030482":null,"MONDO:0030512":null,"MONDO:0030669":null,"MONDO:0031019":null,"MONDO:0032906":null,"MONDO:0957221":null,"MONDO:0957308":null,"MONDO:0957309":null,"MONDO:0957958":null},"xrefs":{"Monarch":{"xref_id":"0003757"}}}


id: PBO:0038846
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase with thrombospondin type 1 motif 15","termid":"PBO:0038846"}


id: GO:0004962
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with endothelin and transmitting the signal across the membrane by activating an associated G-protein; promotes the exchange of GDP for GTP on the alpha subunit of a heterotrimeric G-protein complex.","definition_xrefs":["IUPHAR_RECEPTOR:2263","GOC:dph","GOC:signaling","GOC:bf","IUPHAR_GPCR:1283","IUPHAR_RECEPTOR:2265"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled peptide receptor activity","termid":"GO:0008528"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"endothelin receptor activity","secondary_identifiers":["GO:0001599","GO:0001600"],"synonyms":[{"name":"endothelin-A receptor activity","type":"narrow"},{"name":"endothelin-B receptor activity","type":"narrow"}],"termid":"GO:0004962"}


id: GO:0051363
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of linking a protein to peptidoglycan via a carboxy terminal alanine carboxyl group through a pentaglycyl peptide to the lysine or diaminopimelic acid of the peptidoglycan.","definition_xrefs":["PMID:9086265","PMID:8163519","RESID:AA0383"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidoglycan-protein cross-linking via L-alanyl-pentaglycyl-murein (obsolete GO:0051363)","termid":"GO:0051363"}


id: PBO:0038882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylate cyclase 8","termid":"PBO:0038882"}


id: GO:0046709
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of IDP, inosine 5'-diphosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleotide catabolic process","termid":"GO:0009154"},{"relation_name":"is_a","term_name":"purine ribonucleoside diphosphate catabolic process","termid":"GO:0009181"},{"relation_name":"is_a","term_name":"IDP metabolic process","termid":"GO:0046707"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"IDP catabolic process","synonyms":[{"name":"IDP breakdown","type":"exact"},{"name":"IDP catabolism","type":"exact"},{"name":"IDP degradation","type":"exact"}],"termid":"GO:0046709"}


id: PBO:0044898
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deoxyribose-phosphate aldolase","termid":"PBO:0044898"}


id: MONDO:0020545
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Staphylococcal toxic shock syndrome (staphylococcal TSS) is an acute disease mediated by the production of superantigenic toxins, characterized by high fever, skin rash followed by skin peeling, hypotension, vomiting, diarrhea and potentially leading to multisystem organ failure and caused by a Staphylococcus aureus bacterial infection.","definition_xrefs":["Orphanet:99919"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toxic shock syndrome","termid":"MONDO:0001881"},{"relation_name":"is_a","term_name":"staphylococcal toxemia","termid":"MONDO:0017592"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"staphylococcal toxic-shock syndrome","secondary_identifiers":["UMLS:C3714602","SCTID:240450004","ICD9:040.89","MedDRA:10044250","GARD:19710","icd11.foundation:788554020","MEDGEN:811401"],"synonyms":[{"name":"Staphylococcus caused toxic shock syndrome","type":"exact"},{"name":"Staphylococcus toxic shock syndrome","type":"exact"},{"name":"staphylococcal TSS","type":"exact"}],"termid":"MONDO:0020545","xrefs":{"Monarch":{"xref_id":"0020545"}}}


id: PBO:0062633
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 11 subfamily I member 1 pseudogene","termid":"PBO:0062633"}


id: FYPO:0000827
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which one or more cell cycle phase transitions begins earlier than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell cycle","termid":"FYPO:0000011"},{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000631","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"premature cell cycle phase transition","synonyms":[{"name":"advanced cell cycle phase transition","type":"exact"},{"name":"premature cell cycle phase transition during mitotic cell cycle","type":"related"},{"name":"premature cell cycle phase transition during vegetative growth","type":"exact"},{"name":"premature cell cycle progression","type":"exact"},{"name":"premature cell cycle progression during vegetative growth","type":"exact"}],"termid":"FYPO:0000827"}


id: PATO:0000458
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000458 presence value (obsolete PATO:0000458)","termid":"PATO:0000458"}


id: PBO:0044038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondroitin sulfate proteoglycan 4 pseudogene 10","termid":"PBO:0044038"}


id: PBO:0058165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR4458 host gene","termid":"PBO:0058165"}


id: PBO:0062693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 51 subfamily B member 4","termid":"PBO:0062693"}


id: GO:0097280
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Histamine release triggered by the binding of an antigen to an immunoglobulin bound to the cell surface.","definition_xrefs":["PMID:1719184","GOC:add","PMID:11490155","GOC:rv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory response to antigenic stimulus","termid":"GO:0002437"},{"relation_name":"is_a","term_name":"histamine secretion involved in inflammatory response","termid":"GO:0002441"},{"relation_name":"is_a","term_name":"response to histamine","termid":"GO:0034776"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179","GO:0023052"],"is_obsolete":false,"name":"histamine secretion mediated by immunoglobulin","termid":"GO:0097280"}


id: GO:0072662
data:
  {"annotated_genes":["SJAG_05315","SJAG_02034","SJAG_02693","SJAG_02619","SJAG_03324","SJAG_04763","SJAG_03781","SJAG_04857","SJAG_05950","SJAG_00891","SJAG_00702","SJAG_04428","SJAG_02797","SJAG_00326","SJAG_02997","SJAG_01165","SJAG_03440"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110843,95973,89948,109504,97736,104711,101752,89737],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016558"},{"annotations":[102577,96459,111301],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016560"},{"annotations":[98078,116749,114745,100798],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016562"},{"annotations":[89940,94929,110844],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045046"},{"annotations":[102578,89949,89941,94930,96460],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006625"}]},"cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained at, a location in a peroxisome.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxisome organization","termid":"GO:0007031"},{"relation_name":"is_a","term_name":"protein localization to organelle","termid":"GO:0033365"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00326":null,"SJAG_00702":null,"SJAG_00891":null,"SJAG_01165":null,"SJAG_02034":null,"SJAG_02619":null,"SJAG_02693":null,"SJAG_02797":null,"SJAG_02997":null,"SJAG_03324":null,"SJAG_03440":null,"SJAG_03781":null,"SJAG_04428":null,"SJAG_04763":null,"SJAG_04857":null,"SJAG_05315":null,"SJAG_05950":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0007031"}],"interesting_parent_ids":["GO:0007031","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"protein localization to peroxisome","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"protein localisation to peroxisome","type":"exact"}],"termid":"GO:0072662","terms_by_termid":{"GO:0006625":null,"GO:0016558":null,"GO:0016560":null,"GO:0016562":null,"GO:0045046":null}}


id: GO:0002566
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which immune receptor genes are diversified through somatic mutation.","definition_xrefs":["PMID:16102575","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatic diversification of immune receptors","termid":"GO:0002200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"somatic diversification of immune receptors via somatic mutation","termid":"GO:0002566"}


id: PBO:0077330
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 67","termid":"PBO:0077330"}


id: PBO:0065254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich 20G","termid":"PBO:0065254"}


id: PBO:0005541
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"target of lithium","termid":"PBO:0005541"}


id: PBO:0056676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myocyte enhancer factor 2A pseudogene 1","termid":"PBO:0056676"}


id: GO:0050249
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3'-phospho-5'-adenylyl sulfate + Renilla luciferin = adenosine 3',5'-diphosphate + H+ + luciferyl sulfate.","definition_xrefs":["EC:2.8.2.10","RHEA:20481"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfotransferase activity","termid":"GO:0008146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016782"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0016782","GO:0003674"],"is_obsolete":false,"name":"Renilla-luciferin sulfotransferase activity","secondary_identifiers":["KEGG_REACTION:R03138","MetaCyc:RENILLA-LUCIFERIN-SULFOTRANSFERASE-RXN"],"synonyms":[{"name":"3'-phosphoadenylyl-sulfate:Renilla luciferin sulfotransferase activity","type":"related"},{"name":"Renilla-luciferin sulphotransferase activity","type":"exact"},{"name":"luciferin sulfokinase (3'-phosphoadenylyl sulfate:luciferin sulfotransferase)","type":"related"},{"name":"luciferin sulfokinase activity","type":"related"},{"name":"luciferin sulfotransferase activity","type":"broad"}],"termid":"GO:0050249"}


id: GO:0035809
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the amount of urine excreted from the body over a unit of time.","definition_xrefs":["GOC:mtg_25march11","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal system process","termid":"GO:0003014"},{"relation_name":"is_a","term_name":"regulation of body fluid levels","termid":"GO:0050878"}],"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 urine volume","synonyms":[{"name":"regulation of urinary volume","type":"exact"},{"name":"regulation of urine flow","type":"exact"}],"termid":"GO:0035809"}


id: PBO:0077532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 245","termid":"PBO:0077532"}


id: GO:0036203
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 10beta-hydroxytaxa-4(20),11-dien-5alpha-yl acetate + O2 + NADPH + H+ = 10beta,14beta-dihydroxytaxa-4(20),11-dien-5alpha-yl acetate + NADP+ + H2O.","definition_xrefs":["EC:1.14.13.146"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"taxoid 14-beta-hydroxylase activity","secondary_identifiers":["RHEA:31971","KEGG_REACTION:R09867"],"termid":"GO:0036203"}


id: GO:0071975
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell motility that results in the smooth movement of a cell through a liquid medium.","definition_xrefs":["PMID:18461074"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell motility","termid":"GO:0048870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell swimming","synonyms":[{"name":"cell swimming motility","type":"exact"}],"termid":"GO:0071975"}


id: PBO:0085259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peripheral peroxisomal membrane peroxin; required for the regulation of peroxisome size and maintenance, recruits GTPase Rho1p to peroxisomes, induced by oleate, interacts with Pex27p; PEX25 has a paralog, PEX27, that arose from the whole genome duplication","termid":"PBO:0085259"}


id: GO:1905228
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of adhesion of symbiont to host epithelial cell.","definition_xrefs":["GOC:TermGenie","PMID:15659068","GO_REF:0000058"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of adhesion of symbiont to host epithelial cell (obsolete GO:1905228)","synonyms":[{"name":"activation of adhesion of symbiont to host epithelial cell","type":"narrow"},{"name":"up regulation of adhesion of symbiont to host epithelial cell","type":"exact"},{"name":"up-regulation of adhesion of symbiont to host epithelial cell","type":"exact"},{"name":"upregulation of adhesion of symbiont to host epithelial cell","type":"exact"}],"termid":"GO:1905228"}


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":["MESH:C564012","OMIM:598500","GARD:15313","UMLS:C1838782","DOID:0080583","MEDGEN:325511"],"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:0004337
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-consensus GC donor","termid":"PBO:0004337"}


id: PBO:0076874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed 26","termid":"PBO:0076874"}


id: GO:0021549
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the cerebellum over time, from its formation to the mature structure. The cerebellum is the portion of the brain in the back of the head between the cerebrum and the pons. In mice, the cerebellum controls balance for walking and standing, modulates the force and range of movement and is involved in the learning of motor skills.","definition_xrefs":["GOC:dph","GOC:jid","ISBN:0838580343","GO_REF:0000021","GOC:cls","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"metencephalon development","termid":"GO:0022037"}],"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":"cerebellum development","termid":"GO:0021549"}


id: MONDO:0000009
data:
  {"annotated_genes":["SJAG_03703","SJAG_02431","SJAG_04312","SJAG_03204","SJAG_02093","SJAG_02091","SJAG_04887","SJAG_04621"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85910],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957580"},{"annotations":[85645,85646,85647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018794"},{"annotations":[85885,85886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015912"},{"annotations":[84683],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014078"},{"annotations":[86253],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014518"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hemorrhagic disease","termid":"MONDO:0002243"},{"relation_name":"is_a","term_name":"blood platelet disease","termid":"MONDO:0002245"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":8,"genes_by_uniquename":{"SJAG_02091":null,"SJAG_02093":null,"SJAG_02431":null,"SJAG_03204":null,"SJAG_03703":null,"SJAG_04312":null,"SJAG_04621":null,"SJAG_04887":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"inherited bleeding disorder, platelet-type","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0005818","MEDGEN:610","OMIMPS:231200","DOID:2218"],"synonyms":[{"name":"bleeding disorder, platelet-type","type":"exact"},{"name":"blood platelet disease","type":"broad"},{"name":"platelet disorder","type":"broad"},{"name":"thrombocytopathy","type":"related"}],"termid":"MONDO:0000009","terms_by_termid":{"MONDO:0014078":null,"MONDO:0014518":null,"MONDO:0015912":null,"MONDO:0018794":null,"MONDO:0957580":null},"xrefs":{"Monarch":{"xref_id":"0000009"}}}


id: PBO:0077076
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIAM1 antisense RNA 1","termid":"PBO:0077076"}


id: PBO:0071361
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L29 pseudogene 20","termid":"PBO:0071361"}


id: MONDO:0002767
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A rare thrombophilia disorder characterized by deficiency of protein C. It results in venous thromboembolism.","definition_xrefs":["NCIT:C99025"],"gene_count":0,"genotype_count":0,"name":"obsolete protein C deficiency (obsolete MONDO:0002767)","termid":"MONDO:0002767","xrefs":{"Monarch":{"xref_id":"0002767"}}}


id: GO:0070252
data:
  {"annotated_genes":["SJAG_00750"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[117081],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033275"}]},"cv_name":"biological_process","definition":"The actin filament-based process in which cytoplasmic actin filaments slide past one another resulting in contraction of all or part of the cell body.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament-based movement","termid":"GO:0030048"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00750":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"actin-mediated cell contraction","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0070252","terms_by_termid":{"GO:0033275":null}}


id: MONDO:0009468
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic intracranial hypertension is a neurological disorder characterized by isolated increased intracranial pressure manifesting with recurrent and persistent headaches, nausea, vomiting, progressive and transient obstruction of the visual field, papilledema. Visual loss can be irreversible.","definition_xrefs":["Orphanet:238624"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracranial hypertension","termid":"MONDO:0006810"},{"relation_name":"is_a","term_name":"cerebrovascular disorder","termid":"MONDO:0011057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudotumor cerebri","secondary_identifiers":["NORD:1294","OMIM:243200","GARD:4561","SCTID:68267002","ICD9:348.2","DOID:11459","EFO:1001132","NCIT:C85035","MEDGEN:18732","UMLS:C0033845","MedDRA:10037149","MESH:D011559"],"synonyms":[{"name":"IIH","type":"exact"},{"name":"Idiopathic Intracranial Hypertension","type":"exact"},{"name":"benign intracran. hypt.","type":"exact"},{"name":"benign intracranial hypertension","type":"exact"},{"name":"idiopathic intracranial hypertension","type":"exact"},{"name":"intracranial hypertension, idiopathic","type":"related"},{"name":"pseudotumor cerebri","type":"exact"}],"termid":"MONDO:0009468","xrefs":{"Monarch":{"xref_id":"0009468"}}}


id: PBO:0002296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-aminolevulinate synthase (predicted)","termid":"PBO:0002296"}


id: MONDO:0022939
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete deafness hyperuricemia neurologic ataxia (obsolete MONDO:0022939)","termid":"MONDO:0022939","xrefs":{"Monarch":{"xref_id":"0022939"}}}


id: MONDO:0006416
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A Burkitt lymphoma that arises from the small intestine.","definition_xrefs":["NCIT:C27409"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system cancer","termid":"MONDO:0000621"},{"relation_name":"is_a","term_name":"small intestine lymphoma","termid":"MONDO:0001852"},{"relation_name":"is_a","term_name":"Burkitt lymphoma","termid":"MONDO:0007243"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005570","MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"small intestinal Burkitt lymphoma","secondary_identifiers":["MEDGEN:277650","UMLS:C1335991"],"synonyms":[{"name":"Burkitt lymphoma of small intestine","type":"exact"},{"name":"Burkitts lymphoma of small intestine","type":"exact"},{"name":"primary small intestinal Burkitt's lymphoma","type":"exact"},{"name":"small intestinal Burkitt lymphoma","type":"exact"},{"name":"small intestinal Burkitt's lymphoma","type":"exact"},{"name":"small intestine Burkitt lymphoma","type":"exact"},{"name":"small intestine Burkitt's lymphoma","type":"exact"},{"name":"small intestine Burkitts lymphoma","type":"exact"}],"termid":"MONDO:0006416","xrefs":{"Monarch":{"xref_id":"0006416"}}}


id: GO:0052106
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which a community of single-celled organisms living in intimate contact with a host organism monitors population density by detecting the concentration of small diffusible signal molecules. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete quorum sensing involved in interaction with host (obsolete GO:0052106)","synonyms":[{"name":"quorum sensing during interaction with host","type":"related"}],"termid":"GO:0052106"}


id: PBO:0001773
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-CSL","termid":"PBO:0001773"}


id: MONDO:0029141
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Usher syndrome","termid":"MONDO:0019501"}],"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":"Usher syndrome, type 4","secondary_identifiers":["UMLS:C4748364","MEDGEN:1648315","OMIM:618144"],"synonyms":[{"name":"USH4","type":"related"},{"name":"Usher syndrome, type IV","type":"exact"}],"termid":"MONDO:0029141","xrefs":{"Monarch":{"xref_id":"0029141"}}}


id: PATO:0001257
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Pink color having high brightness and moderate saturation.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pink","termid":"PATO:0000954"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"light deep pink","termid":"PATO:0001257"}


id: PBO:0067572
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 727, pseudogene","termid":"PBO:0067572"}


id: GO:0004911
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with interleukin-2 and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:jl","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor activity","termid":"GO:0004896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"interleukin-2 receptor activity","synonyms":[{"name":"IL-2 receptor activity","type":"exact"},{"name":"IL-2R","type":"exact"}],"termid":"GO:0004911"}


id: GO:0002304
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a gamma-delta intraepithelial T cell. Intraepithelial T cells are found among epithelial cells in mucosal areas and have distinct phenotypes and developmental pathways.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gamma-delta T cell differentiation","termid":"GO:0042492"}],"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":"gamma-delta intraepithelial T cell differentiation","synonyms":[{"name":"gamma-delta intraepithelial T cell development","type":"related"},{"name":"gamma-delta intraepithelial T lymphocyte differentiation","type":"exact"},{"name":"gamma-delta intraepithelial T-cell differentiation","type":"exact"},{"name":"gamma-delta intraepithelial T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0002304"}


id: PBO:0012270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteiasome complex subunit beta 7 (predicted)","termid":"PBO:0012270"}


id: MONDO:1012283
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tremor syndrome with central axonopathy, non-human animal","termid":"MONDO:1011862"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tremor syndrome with central axonopathy, dog","secondary_identifiers":["OMIA:001017-9615"],"termid":"MONDO:1012283","xrefs":{"Monarch":{"xref_id":"1012283"}}}


id: PBO:0041979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 22","termid":"PBO:0041979"}


id: MONDO:0700082
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosomal disorder in which (part or full) chromosome 21 is attached to another chromosome, resulting in the presence of a third copy of part of full chromosome 21 genetic material. A Robertsonian translocation is a structural chromosomal anomaly in which two acrocentric chromosomes break, resulting in the fusion of the nonhomologous chromosomes’ long arms to form a single, large chromosome.","definition_xrefs":["PMID:23097978","PMID:29956287","PMID:1831959"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translocation Down syndrome","termid":"MONDO:0700128"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Robertsonian translocation Down syndrome","secondary_identifiers":["UMLS:C5707615","MEDGEN:1816520","NCIT:C188150"],"termid":"MONDO:0700082","xrefs":{"Monarch":{"xref_id":"0700082"}}}


id: FYPO:0002430
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a cell that undergoes two or more rounds of cell division, and then dies.","definition_xrefs":["PomBase:al","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination","termid":"FYPO:0000316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000004"],"is_obsolete":false,"name":"inviable after spore germination, multiple cell divisions","synonyms":[{"name":"inviable following spore germination, multiple cell divisions","type":"exact"},{"name":"inviable germinated spore, multiple cell divisions","type":"exact"},{"name":"lethal after spore germination, multiple cell divisions","type":"exact"}],"termid":"FYPO:0002430"}


id: GO:0004244
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the maturation of mitochondrial precursor proteins delivered to the intermembrane space.","definition_xrefs":["PMID:12191769"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial inner membrane peptidase activity (obsolete GO:0004244)","synonyms":[{"name":"IMP","type":"broad"},{"name":"mitochondrial inner membrane peptidase activity","type":"exact"}],"termid":"GO:0004244"}


id: GO:1903113
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of copper ion transmembrane transporter activity.","definition_xrefs":["GOC:bhm","PMID:23122209","GOC:TermGenie","GO_REF:0000088"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter complex","termid":"GO:1902495"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"copper ion transmembrane transporter complex","termid":"GO:1903113"}


