# terms

id: GO:1990245
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H2A by the addition of a phosphate group to a threonine residue at position 120 of the histone.","definition_xrefs":["PMID:24140421"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H2A-T120 phosphorylation (obsolete GO:1990245)","synonyms":[{"name":"histone H2A phosphorylation at T120","type":"exact"},{"name":"histone H2AT120 phosphorylation","type":"exact"}],"termid":"GO:1990245"}


id: GO:0010812
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of cell-substrate adhesion. Cell-substrate adhesion is the attachment of a cell to the underlying substrate via adhesion molecules.","definition_xrefs":["GOC:pf","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell adhesion","termid":"GO:0007162"},{"relation_name":"is_a","term_name":"regulation of cell-substrate adhesion","termid":"GO:0010810"},{"relation_name":"negatively_regulates","term_name":"cell-substrate adhesion","termid":"GO:0031589"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"negative regulation of cell-substrate adhesion","termid":"GO:0010812"}


id: MONDO:0011881
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any striate palmoplantar keratoderma in which the cause of the disease is a mutation in the KRT1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"striate palmoplantar keratoderma","termid":"MONDO:0018865"}],"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":"keratosis palmoplantaris striata 3","secondary_identifiers":["MEDGEN:418996","DOID:0081110","GARD:9173","UMLS:C2931123","OMIM:607654","MESH:C536163"],"synonyms":[{"name":"KRT1 striate palmoplantar keratoderma","type":"exact"},{"name":"PPKS3","type":"related"},{"name":"keratoderma palmoplantar striate form 3","type":"related"},{"name":"keratoderma, palmoplantar, striate form 3","type":"related"},{"name":"keratosis palmoplantaris striata III","type":"related"},{"name":"keratosis palmoplantaris striata type 3","type":"exact"},{"name":"striate palmoplantar keratoderma 3","type":"related"},{"name":"striate palmoplantar keratoderma caused by mutation in KRT1","type":"exact"}],"termid":"MONDO:0011881","xrefs":{"Monarch":{"xref_id":"0011881"}}}


id: PBO:0063889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol glycan anchor biosynthesis class P pseudogene 2","termid":"PBO:0063889"}


id: PBO:0060295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYL6 pseudogene 3","termid":"PBO:0060295"}


id: MONDO:0700014
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosomal disorder in which chromosome 7 is affected.","definition_xrefs":["MONDO:patterns/chromosome_type"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal anomaly","termid":"MONDO:0020049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 7 disorder","termid":"MONDO:0700014","xrefs":{"Monarch":{"xref_id":"0700014"}}}


id: PBO:0080483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"von Willebrand factor A domain containing 3A","termid":"PBO:0080483"}


id: FYPO:0006710
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, occurs to a lower extent than normal during a cellular response to a pH above 7.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein phosphorylation during vegetative growth","termid":"FYPO:0001838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0002494","FYPO:0002274","FYPO:0001320","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein phosphorylation during cellular response to alkaline pH","synonyms":[{"name":"decreased protein phosphorylation during cellular response to alkaline pH during mitotic cell cycle","type":"related"},{"name":"decreased protein phosphorylation during cellular response to alkaline pH during vegetative growth","type":"exact"},{"name":"decreased protein phosphorylation during cellular response to high pH","type":"exact"},{"name":"decreased protein phosphorylation in high pH","type":"related"},{"name":"reduced protein phosphorylation during cellular response to alkaline pH","type":"exact"}],"termid":"FYPO:0006710"}


id: GO:0030458
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:elh"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of MAPKKK (mating sensu Fungi) (obsolete GO:0030458)","synonyms":[{"name":"activation of MAPKKK (mating sensu Fungi)","type":"exact"}],"termid":"GO:0030458"}


id: PR:O43027
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rga6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O43027"],"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":"rho-GTPase-activating protein 6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC354.13","synonyms":[{"name":"Spom972h-rga6","type":"exact"}],"termid":"PR:O43027"}


id: MONDO:0008757
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The most severe form of alopecia areata, an inflammatory disease of the hair follicle, which is characterized by a complete loss of hair of the scalp and all the hair-bearing areas of the body.","definition_xrefs":["Orphanet:701"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alopecia, isolated","termid":"MONDO:0000005"}],"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":"alopecia universalis congenita","secondary_identifiers":["MEDGEN:349262","SCTID:86166000","DOID:0050634","MESH:C537055","ICD9:704.09","MedDRA:10001767","OMIM:203655","UMLS:C1859877","GARD:614"],"synonyms":[{"name":"ALUNC","type":"related"},{"name":"AU","type":"related"},{"name":"alopecia areata universalis","type":"related"},{"name":"alopecia universalis","type":"related"},{"name":"alopecia universalis congenita","type":"exact"},{"name":"atrichia, generalised","type":"exact"},{"name":"atrichia, generalized","type":"exact"}],"termid":"MONDO:0008757","xrefs":{"Monarch":{"xref_id":"0008757"}}}


id: MONDO:0017191
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"sporadic pheochromocytoma/secreting paraganglioma","termid":"MONDO:0017190"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sporadic pheochromocytoma","secondary_identifiers":["Orphanet:276624"],"termid":"MONDO:0017191","xrefs":{"Monarch":{"xref_id":"0017191"}}}


id: PBO:0063534
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDZ domain containing ring finger 3","termid":"PBO:0063534"}


id: GO:1901340
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of store-operated calcium channel activity.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of calcium ion transmembrane transporter activity","termid":"GO:1901020"},{"relation_name":"is_a","term_name":"regulation of store-operated calcium channel activity","termid":"GO:1901339"},{"relation_name":"is_a","term_name":"negative regulation of cation channel activity","termid":"GO:2001258"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"negative regulation of store-operated calcium channel activity","synonyms":[{"name":"down regulation of store-operated calcium channel activity","type":"exact"},{"name":"down-regulation of store-operated calcium channel activity","type":"exact"},{"name":"downregulation of store-operated calcium channel activity","type":"exact"},{"name":"inhibition of store-operated calcium channel activity","type":"narrow"}],"termid":"GO:1901340"}


id: MONDO:0008321
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":"pruritus, hereditary localized","secondary_identifiers":["OMIM:177100","UMLS:C1867499","MEDGEN:356792","MESH:C566754"],"synonyms":[{"name":"pruritus, hereditary localized","type":"exact"}],"termid":"MONDO:0008321","xrefs":{"Monarch":{"xref_id":"0008321"}}}


id: PBO:0076198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO2 pseudogene 7","termid":"PBO:0076198"}


id: PBO:0081257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 26","termid":"PBO:0081257"}


id: GO:0102671
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (+)-6a-hydroxymaackiain + S-adenosyl-L-methionine = H+ + (+)-pisatin + S-adenosyl-L-homocysteine.","definition_xrefs":["GOC:pz","EC:2.1.1.270"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase activity","termid":"GO:0008168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016741","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"6a-hydroxymaackiain-3-O-methyltransferase activity","secondary_identifiers":["MetaCyc:RXN-4002","RHEA:35471"],"termid":"GO:0102671"}


id: FYECO:0000375
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which streptonigrin was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ streptonigrin","termid":"FYECO:0000375"}


id: MONDO:0017350
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited metabolic disease that is has its basis in the disruption of tryptophan metabolic process.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of amino acid metabolism","termid":"MONDO:0004736"},{"relation_name":"is_a","term_name":"inborn disorder of amino acid and other organic acid metabolism","termid":"MONDO:0019189"},{"relation_name":"is_a","term_name":"disorder of organic acid metabolism","termid":"MONDO:0045022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"inborn disorder of tryptophan metabolism","secondary_identifiers":["GARD:21154","MEDGEN:22506","icd11.foundation:282654317","SCTID:5181007","Orphanet:289829","ICD9:270.2","UMLS:C0041254"],"synonyms":[{"name":"disorder of tryptophan metabolism","type":"related"},{"name":"inborn error of tryptophan metabolic process","type":"exact"},{"name":"inborn tryptophan metabolic process disorder","type":"exact"},{"name":"rare inborn error of tryptophan metabolic process","type":"exact"}],"termid":"MONDO:0017350","xrefs":{"Monarch":{"xref_id":"0017350"}}}


id: GO:0008113
data:
  {"annotated_genes":["SJAG_00419"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[94763],"is_not":false,"summary":null,"term":"GO:0008113"}]},"cv_name":"molecular_function","definition":"Catalysis of the reactions: peptide-L-methionine + thioredoxin disulfide + H2O = peptide-L-methionine (S)-S-oxide + thioredoxin, and L-methionine + thioredoxin disulfide + H2O = L-methionine (S)-S-oxide + thioredoxin. Can act on oxidized methionine in peptide linkage with specificity for the S enantiomer. Thioredoxin disulfide is the oxidized form of thioredoxin.","definition_xrefs":["PMID:11169920","GOC:vw","EC:1.8.4.11","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor","termid":"GO:0016671"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00419":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"peptide-methionine (S)-S-oxide reductase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:RXN-8668","Reactome:R-HSA-1222363","RHEA:14217","Reactome:R-HSA-5676940","GO:0033742","GO:0072561"],"synonyms":[{"name":"MsrA","type":"related"},{"name":"methionine S-oxide reductase (S-form oxidizing) activity","type":"related"},{"name":"methionine S-oxide reductase activity","type":"broad"},{"name":"methionine sulfoxide (protein) reductase activity","type":"exact"},{"name":"methionine sulfoxide reductase A activity","type":"related"},{"name":"methionine sulfoxide reductase activity","type":"broad"},{"name":"methionine sulphoxide reductase A activity","type":"related"},{"name":"peptide Met(O) reductase activity","type":"related"},{"name":"peptide methionine sulfoxide reductase activity","type":"related"},{"name":"peptide-L-methionine:thioredoxin-disulfide S-oxidoreductase [L-methionine (S)-S-oxide-forming] activity","type":"related"},{"name":"peptide-methionine-(S)-S-oxide reductase activity","type":"exact"},{"name":"protein-methionine-S-oxide reductase activity","type":"exact"}],"termid":"GO:0008113","terms_by_termid":{"GO:0008113":null}}


id: MONDO:1010118
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Systemic lupus erythematosus that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder, non-human animal","termid":"MONDO:0700106"},{"relation_name":"is_a","term_name":"connective tissue disorder, non-human animal","termid":"MONDO:1011309"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"systemic lupus erythematosus, non-human animal","secondary_identifiers":["OMIA:000968"],"termid":"MONDO:1010118","xrefs":{"Monarch":{"xref_id":"1010118"}}}


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: PBO:0055139
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 2558","termid":"PBO:0055139"}


id: PBO:0082523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cell-cycle checkpoint S/T protein kinase; required for transient G2/M arrest after DNA damage, damage-induced transcription, and nuclear-to-cytoplasmic redistribution of Rnr2p-Rnr4p after genotoxic stress and iron deprivation; phosphorylates repair protein Rad55p, transcriptional repressor Sml1p, superoxide dismutase, and ribonucleotide reductase inhibitors Crt1p and Dif1p; functions in the Mec1p pathway to regulate dNTP pools and telomere length; postreplicative repair role","termid":"PBO:0082523"}


id: MONDO:0002012
data:
  {"annotated_genes":["SJAG_00947","SJAG_01199"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84884],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013661"},{"annotations":[85905],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010184"}]},"cv_name":"mondo","definition":"A rare autosomal recessive inherited disorder caused by mutations of the MUT, MMAA, MMAB, MMADHC, and MCEE genes. It is characterized by abnormalities in the metabolism of lipids and proteins. Signs and symptoms usually appear early in life and vary from mild to life threatening. They include vomiting, dehydration, hypotonia, developmental delays, hepatomegaly, lethargy, intellectual disabilities, and chronic kidney disease.","definition_xrefs":["NCIT:C98986"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn organic aciduria","termid":"MONDO:0000688"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00947":null,"SJAG_01199":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"methylmalonic acidemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0268583","ICD9:270.7","NANDO:2200491","ICD10CM:E71.120","SCTID:42393006","NANDO:1200793","MEDGEN:120654","DOID:14749","GARD:7033","MESH:C537358"],"synonyms":[{"name":"METHYLMALONICACIDURIA due to methylmalonic CoA mutase deficiency","type":"narrow"},{"name":"METHYLMALONICACIDURIA, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin--Cbl A","type":"narrow"},{"name":"METHYLMALONICACIDURIA, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin--Cbl B","type":"narrow"},{"name":"methylmalonic acidemia, cblA type","type":"narrow"},{"name":"methylmalonic acidemia, cblB type","type":"narrow"},{"name":"methylmalonic aciduria","type":"exact"},{"name":"methylmalonic aciduria cblB type","type":"narrow"},{"name":"methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency","type":"narrow"},{"name":"methylmalonic aciduria mut type","type":"narrow"},{"name":"methylmalonic aciduria type cblA","type":"narrow"},{"name":"methylmalonic aciduria type cblB","type":"narrow"},{"name":"methylmalonic aciduria, mut type","type":"narrow"},{"name":"methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblA type","type":"narrow"},{"name":"methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB type","type":"narrow"}],"termid":"MONDO:0002012","terms_by_termid":{"MONDO:0010184":null,"MONDO:0013661":null},"xrefs":{"Monarch":{"xref_id":"0002012"}}}


id: MOD:01008
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively substitutes a benzyl (phenylmethyl) group for a hydrogen atom.","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benzyl (Bzl) and benzyl ester (OBzl) modified residue","termid":"MOD:01008"}


id: PBO:0066171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBIS pseudogene 4","termid":"PBO:0066171"}


id: MONDO:0014361
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autism spectrum disorder due to AUTS2 deficiency is a rare genetic syndromic intellectual disability characterized by global developmental delay and borderline to severe intellectual disability, autism spectrum disorder with obsessive behavior, stereotypies, hyperactivity but frequently friendly and affable personality, feeding difficulties, short stature, muscular hypotonia, microcephaly, characteristic dysmorphic features (hypertelorism, high arched eyebrows, ptosis, deep and/or broad nasal bridge, broad/prominent nasal tip, short and/or upturned philtrum, narrow mouth, and micrognathia), and skeletal anomalies (kyphosis and/or scoliosis, arthrogryposis, slender habitus and extremities). Other clinical features may include hernias, congenital heart defects, cryptorchidism and seizures.","definition_xrefs":["Orphanet:352490"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"autosomal dominant non-syndromic intellectual disability","termid":"MONDO:0015802"},{"relation_name":"is_a","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"intellectual disability, autosomal dominant","termid":"MONDO:0100172"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0000426"],"is_obsolete":false,"name":"autism spectrum disorder due to AUTS2 deficiency","secondary_identifiers":["DOID:0070056","MEDGEN:862872","OMIM:615834","UMLS:C4014435","GARD:17520"],"synonyms":[{"name":"ASD due to AUTS2 deficiency","type":"exact"},{"name":"AUTS2 syndrome","type":"exact"},{"name":"MRD26","type":"exact"},{"name":"autism spectrum disorder due to AUTS2 deficiency","type":"exact"},{"name":"autosomal dominant mental retardation 26","type":"exact"},{"name":"autosomal dominant non-syndromic intellectual disability 26","type":"exact"},{"name":"intellectual developmental disorder, autosomal dominant 26","type":"exact"},{"name":"intellectual disability type 26","type":"exact"},{"name":"mental retardation, autosomal dominant 26","type":"exact"},{"name":"mental retardation, autosomal dominant type 26","type":"exact"}],"termid":"MONDO:0014361","xrefs":{"Monarch":{"xref_id":"0014361"}}}


id: PBO:0041282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1QTNF7 antisense RNA 1","termid":"PBO:0041282"}


id: GO:1900866
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a glycolate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:pr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid transport","termid":"GO:0015718"},{"relation_name":"is_a","term_name":"organic hydroxy compound transport","termid":"GO:0015850"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"glycolate transport","termid":"GO:1900866"}


id: GO:0045543
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a gibberellin + 2-oxoglutarate + O2 = a 2-beta-hydroxygibberellin + succinate + CO2.","definition_xrefs":["EC:1.14.11.13","PMID:32652020"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxoglutarate-dependent dioxygenase activity","termid":"GO:0016706"}],"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":"gibberellin 2-beta-dioxygenase activity","synonyms":[{"name":"gibberellin 2-beta-hydroxylase activity","type":"related"},{"name":"gibberellin 2-oxidase activity","type":"exact"},{"name":"gibberellin 2beta-dioxygenase activity","type":"related"},{"name":"gibberellin 2beta-hydroxylase activity","type":"related"}],"termid":"GO:0045543"}


id: PBO:0050922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IFITM3 pseudogene 5","termid":"PBO:0050922"}


id: PBO:0086416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative GTPase; associates with free 60S ribosomal subunits in the nucleolus and is required for 60S ribosomal subunit biogenesis; constituent of 66S pre-ribosomal particles; member of the ODN family of nucleolar G-proteins","termid":"PBO:0086416"}


id: PATO:0001367
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A surface feature shape quality inhering in a bearer by virtue of the bearer's having deeply undulating edges forming lobes.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"surface feature shape","termid":"PATO:0001925"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lobate","termid":"PATO:0001367"}


id: PBO:0091442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial conserved fungal protein Rrg8","termid":"PBO:0091442"}


id: GO:0000076
data:
  {"annotated_genes":["SJAG_01605","SJAG_03160","SJAG_04671","SJAG_01010","SJAG_00364","SJAG_01205","SJAG_02074","SJAG_03927","SJAG_02771","SJAG_02098","SJAG_03026","SJAG_01076","SJAG_02266","SJAG_02563","SJAG_04287","SJAG_03695","SJAG_01044"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105773,115193,90635],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033315"},{"annotations":[98551,105776,116235,115195,106993,93159,111175,90636,93138,91728,99722,102497,88327,115936,116404,98385,108466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033314"}]},"cv_name":"biological_process","definition":"A signal transduction process that contributes to a DNA replication checkpoint, that prevents the initiation of nuclear division until DNA replication is complete, thereby ensuring that progeny inherit a full complement of the genome.","definition_xrefs":["PMID:12537518","GOC:rn","GOC:curators","PMID:11728327"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA integrity checkpoint signaling","termid":"GO:0031570"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00364":null,"SJAG_01010":null,"SJAG_01044":null,"SJAG_01076":null,"SJAG_01205":null,"SJAG_01605":null,"SJAG_02074":null,"SJAG_02098":null,"SJAG_02266":null,"SJAG_02563":null,"SJAG_02771":null,"SJAG_03026":null,"SJAG_03160":null,"SJAG_03695":null,"SJAG_03927":null,"SJAG_04287":null,"SJAG_04671":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0007049"],"is_obsolete":false,"name":"DNA replication checkpoint signaling","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0072437"],"synonyms":[{"name":"DNA replication checkpoint","type":"exact"},{"name":"signal transduction involved in DNA replication checkpoint","type":"exact"}],"termid":"GO:0000076","terms_by_termid":{"GO:0033314":null,"GO:0033315":null}}


id: GO:0062200
data:
  {"annotated_genes":["SJAG_03637","SJAG_04461","SJAG_00333","SJAG_00661","SJAG_00317","SJAG_00236"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90343,99363,104520,111609,112183,117909],"is_not":false,"summary":null,"term":"GO:0062200"}]},"cv_name":"biological_process","definition":"An intracellular signaling cascade that starts with the activation of S. cerevisiae Kic1p, which activate Mob2p and Cbk1p. Cbk1p phosphorylates Ace2p, which results in its nuclear translocation, where it regulates transcription of genes involved in polarity and morphogenesis.","definition_xrefs":["PMID:20826805","PMID:15731009","PMID:22629372","PMID:16096637","PMID:23212898","PMID:20805322","PMID:21246752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular signal transduction","termid":"GO:0035556"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00236":null,"SJAG_00317":null,"SJAG_00333":null,"SJAG_00661":null,"SJAG_03637":null,"SJAG_04461":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"RAM/MOR signaling","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"MOR signaling pathway","type":"narrow"},{"name":"RAM signaling pathway","type":"narrow"},{"name":"RAM/MOR signaling pathway","type":"exact"},{"name":"morphogenesis Orb6 network","type":"exact"}],"termid":"GO:0062200","terms_by_termid":{"GO:0062200":null}}


id: MONDO:0001880
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"glossitis","termid":"MONDO:0006771"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"median rhomboid glossitis","secondary_identifiers":["icd11.foundation:598142773","SCTID:7522008","ICD9:750.19","DOID:14111","ICD10CM:K14.2","ICD9:529.2","UMLS:C0155963","MEDGEN:510155"],"synonyms":[{"name":"persistent tuberculum impar","type":"exact"}],"termid":"MONDO:0001880","xrefs":{"Monarch":{"xref_id":"0001880"}}}


id: FYECO:0000346
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Any set of experimental conditions that places all cells in a culture into the same growth stage (e.g. cell cycle phase).","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping experimental environment","termid":"FYECO:0000132"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synchronous culture","termid":"FYECO:0000346"}


id: PBO:0027242
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-unequal_nucleolus_inheritance","termid":"PBO:0027242"}


id: MONDO:0016610
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acquired idiopathic inflammatory myopathy","termid":"MONDO:0020122"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"idiopathic eosinophilic myositis","secondary_identifiers":["GARD:20664","Orphanet:247724","UMLS:C4755301","MEDGEN:1659844"],"synonyms":[{"name":"idiopathic eosinophilia-associated myopathy","type":"exact"}],"termid":"MONDO:0016610","xrefs":{"Monarch":{"xref_id":"0016610"}}}


id: GO:0032357
data:
  {"annotated_genes":["SJAG_02261"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[94067],"is_not":false,"summary":null,"term":"GO:0032357"}]},"cv_name":"molecular_function","definition":"Binding to a DNA region containing an oxidized purine residue.","definition_xrefs":["GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidized DNA binding","termid":"GO:0032356"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02261":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003677"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003677","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"oxidized purine DNA binding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"oxidised purine DNA binding","type":"exact"},{"name":"oxidized purine base DNA binding","type":"exact"},{"name":"oxidized purine nucleobase DNA binding","type":"exact"}],"termid":"GO:0032357","terms_by_termid":{"GO:0032357":null}}


id: FYPO:0003766
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 mitochondrial DNA molecules are interlinked by unresolved recombination junctions.","definition_xrefs":["PMID:10954073","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromosome morphology during vegetative growth","termid":"FYPO:0000848"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"output_of","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000654","FYPO:0000641","FYPO:0000661","FYPO:0000002","FYPO:0000707","FYPO:0000652","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"aggregated mtDNA","synonyms":[{"name":"aggregated mitochondrial DNA","type":"exact"},{"name":"aggregated mitochondrial chromosomes","type":"exact"},{"name":"aggregated mtDNA during mitotic cell cycle","type":"related"},{"name":"aggregated mtDNA during vegetative growth","type":"exact"},{"name":"fused mitochondrial chromosomes","type":"related"},{"name":"fused mtDNA","type":"related"},{"name":"interlinked mtDNA","type":"exact"}],"termid":"FYPO:0003766"}


id: MONDO:0002908
data:
  {"annotated_genes":["SJAG_02012","SJAG_04495","SJAG_00092","SJAG_02013","SJAG_00464","SJAG_04394","SJAG_02426","SJAG_04192","SJAG_04206","SJAG_04334","SJAG_03266","SJAG_00214","SJAG_02000","SJAG_03247"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86567,86568],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014488"},{"annotations":[85719,85718],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011236"},{"annotations":[86047],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011717"},{"annotations":[86491],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014674"},{"annotations":[84369,84368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007453"},{"annotations":[85638,85639],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100165"},{"annotations":[84991],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009949"},{"annotations":[85019],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014221"},{"annotations":[84367,86494,84363,84365,86495,84366,84364,86493],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0005148"}]},"cv_name":"mondo","definition":"A metabolic disorder characterized by abnormal blood glucose levels.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease","termid":"MONDO:0005066"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00092":null,"SJAG_00214":null,"SJAG_00464":null,"SJAG_02000":null,"SJAG_02012":null,"SJAG_02013":null,"SJAG_02426":null,"SJAG_03247":null,"SJAG_03266":null,"SJAG_04192":null,"SJAG_04206":null,"SJAG_04334":null,"SJAG_04394":null,"SJAG_04495":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"glucose metabolism disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C53655","SCTID:126877002","MEDGEN:226229","UMLS:C1257958","DOID:4194","ICD9:271.8","EFO:0009406","MESH:D044882"],"synonyms":[{"name":"disorder of glucose metabolism","type":"exact"},{"name":"glucose metabolism disorder","type":"exact"}],"termid":"MONDO:0002908","terms_by_termid":{"MONDO:0005148":null,"MONDO:0007453":null,"MONDO:0009949":null,"MONDO:0011236":null,"MONDO:0011717":null,"MONDO:0014221":null,"MONDO:0014488":null,"MONDO:0014674":null,"MONDO:0100165":null},"xrefs":{"Monarch":{"xref_id":"0002908"}}}


id: PBO:0082607
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Co-chaperone that binds and regulates Hsp90 family chaperones; plays a role in determining prion variants; important for pp60v-src activity in yeast; homologous to the mammalian p23 proteins, and like p23 can regulate telomerase activity; protein abundance increases in response to DNA replication stress","termid":"PBO:0082607"}


id: PBO:0053129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lactase","termid":"PBO:0053129"}


id: GO:0045626
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of T-helper 1 cell differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of T-helper 1 type immune response","termid":"GO:0002826"},{"relation_name":"is_a","term_name":"negative regulation of T-helper cell differentiation","termid":"GO:0045623"},{"relation_name":"is_a","term_name":"regulation of T-helper 1 cell differentiation","termid":"GO:0045625"},{"relation_name":"negatively_regulates","term_name":"T-helper 1 cell differentiation","termid":"GO:0045063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"negative regulation of T-helper 1 cell differentiation","synonyms":[{"name":"down regulation of T-helper 1 cell differentiation","type":"exact"},{"name":"down-regulation of T-helper 1 cell differentiation","type":"exact"},{"name":"downregulation of T-helper 1 cell differentiation","type":"exact"},{"name":"inhibition of T-helper 1 cell differentiation","type":"narrow"},{"name":"negative regulation of T-helper 1 cell development","type":"related"}],"termid":"GO:0045626"}


id: PBO:0004865
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.4.2.18","termid":"PBO:0004865"}


id: GO:0006664
data:
  {"annotated_genes":["SJAG_00295","SJAG_00846","SJAG_04924","SJAG_03672","SJAG_01227","SJAG_02168","SJAG_00506","SJAG_04881","SJAG_03801","SJAG_04119","SJAG_02488","SJAG_06425","SJAG_00068","SJAG_04165","SJAG_06383","SJAG_02804","SJAG_04975","SJAG_04913","SJAG_02913","SJAG_04878","SJAG_03953","SJAG_02523","SJAG_01860","SJAG_03292","SJAG_03066","SJAG_05327","SJAG_03115","SJAG_05278","SJAG_03506","SJAG_01570","SJAG_05311","SJAG_03878","SJAG_04337","SJAG_02776","SJAG_01416","SJAG_00831"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88759,87863,111493,97297,115269,110742,90429,102951,100790,106706,109079,99479,90602,114345,98065,107736,92284,93711,92728,86653,99413,102218,88135,113920,92195,113072,97858,91428,102889,116366],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006506"},{"annotations":[96697],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006676"},{"annotations":[94927,94447,91005,89946,111671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051999"},{"annotations":[91006,111672],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006675"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving glycolipids, a class of 1,2-di-O-acylglycerols joined at oxygen 3 by a glycosidic linkage to a carbohydrate part (usually a mono-, di- or tri-saccharide). Some substances classified as bacterial glycolipids have the sugar group acylated by one or more fatty acids and the glycerol group may be absent.","definition_xrefs":["ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane lipid metabolic process","termid":"GO:0006643"},{"relation_name":"is_a","term_name":"liposaccharide metabolic process","termid":"GO:1903509"}],"gene_count":36,"genes_by_uniquename":{"SJAG_00068":null,"SJAG_00295":null,"SJAG_00506":null,"SJAG_00831":null,"SJAG_00846":null,"SJAG_01227":null,"SJAG_01416":null,"SJAG_01570":null,"SJAG_01860":null,"SJAG_02168":null,"SJAG_02488":null,"SJAG_02523":null,"SJAG_02776":null,"SJAG_02804":null,"SJAG_02913":null,"SJAG_03066":null,"SJAG_03115":null,"SJAG_03292":null,"SJAG_03506":null,"SJAG_03672":null,"SJAG_03801":null,"SJAG_03878":null,"SJAG_03953":null,"SJAG_04119":null,"SJAG_04165":null,"SJAG_04337":null,"SJAG_04878":null,"SJAG_04881":null,"SJAG_04913":null,"SJAG_04924":null,"SJAG_04975":null,"SJAG_05278":null,"SJAG_05311":null,"SJAG_05327":null,"SJAG_06383":null,"SJAG_06425":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"glycolipid metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"glycolipid metabolism","type":"exact"}],"termid":"GO:0006664","terms_by_termid":{"GO:0006506":null,"GO:0006675":null,"GO:0006676":null,"GO:0051999":null}}


id: PBO:0092015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Phenylalanine (gaa), mitochondrial","termid":"PBO:0092015"}


id: GO:0044511
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with the resultant modulation of receptor activity in of the bitten organism.","definition_xrefs":["GOC:jl","GOC:fj","PMID:8405712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"envenomation resulting in modulation of process in another organism","termid":"GO:0035738"}],"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":"envenomation resulting in modulation of receptor activity in another organism","synonyms":[{"name":"envenomation resulting in modulation of receptor activity in other organism","type":"exact"}],"termid":"GO:0044511"}


id: GO:0061752
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to long non-coding RNA molecules transcribed from subtelomeric regions in most eukaryotes. Telomeric repeat-containing RNA (TERRA) molecules consist of subtelomeric-derived sequences and G-rich telomeric repeats.","definition_xrefs":["GOC:jbu","PMID:20655916","GOC:BHF","GOC:BHF_telomere","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA binding","termid":"GO:0003723"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0003723"],"is_obsolete":false,"name":"telomeric repeat-containing RNA binding","synonyms":[{"name":"TERRA binding","type":"exact"}],"termid":"GO:0061752"}


id: PBO:0039574
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat and sterile alpha motif domain containing 1B","termid":"PBO:0039574"}


id: GO:0060721
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of spongiotrophoblast cell proliferation.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell proliferation involved in embryonic placenta development","termid":"GO:0060723"},{"relation_name":"regulates","term_name":"spongiotrophoblast cell proliferation","termid":"GO:0060720"}],"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 spongiotrophoblast cell proliferation","termid":"GO:0060721"}


id: GO:1903019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of glycoprotein metabolic process.","definition_xrefs":["GOC:rl","PMID:23544079","GO_REF:0000058","GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein metabolic process","termid":"GO:0051248"},{"relation_name":"is_a","term_name":"regulation of glycoprotein metabolic process","termid":"GO:1903018"},{"relation_name":"negatively_regulates","term_name":"glycoprotein metabolic process","termid":"GO:0009100"}],"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 glycoprotein metabolic process","synonyms":[{"name":"down regulation of glycoprotein metabolic process","type":"exact"},{"name":"down regulation of glycoprotein metabolism","type":"exact"},{"name":"down-regulation of glycoprotein metabolic process","type":"exact"},{"name":"down-regulation of glycoprotein metabolism","type":"exact"},{"name":"downregulation of glycoprotein metabolic process","type":"exact"},{"name":"downregulation of glycoprotein metabolism","type":"exact"},{"name":"inhibition of glycoprotein metabolic process","type":"narrow"},{"name":"inhibition of glycoprotein metabolism","type":"narrow"},{"name":"negative regulation of glycoprotein metabolism","type":"exact"}],"termid":"GO:1903019"}


id: PBO:0051511
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IKAROS family zinc finger 1","termid":"PBO:0051511"}


id: PBO:0005206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"frataxin (predicted)","termid":"PBO:0005206"}


id: PATO:0000371
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000371 distance value (obsolete PATO:0000371)","termid":"PATO:0000371"}


id: GO:0061274
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the mesonephric distal tubule over time, from its formation to the mature structure. The mesonephric distal tubule is a mesonephric nephron tubule that begins at the terminal segment of the proximal tubule and ends at the mesonephric connecting tubule.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesonephric nephron tubule development","termid":"GO:0061242"},{"relation_name":"is_a","term_name":"distal tubule development","termid":"GO:0072017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mesonephric distal tubule development","termid":"GO:0061274"}


id: PBO:0046411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ependymin related 1","termid":"PBO:0046411"}


id: GO:0043856
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The function of binding to an anti-sigma factor and stopping, preventing or reducing the rate of its activity.","definition_xrefs":["PMID:15576799","GOC:jl","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription regulator activity","termid":"GO:0140110"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140110"}],"interesting_parent_ids":["GO:0003674","GO:0140110"],"is_obsolete":false,"name":"anti-sigma factor antagonist activity","synonyms":[{"name":"anti-anti-sigma factor activity","type":"exact"}],"termid":"GO:0043856"}


id: MONDO:0012802
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oculoauricular syndrome, Schorderet type is a rare, genetic developmental defect during embryogenesis characterized by various ophthalmic anomalies (including congenital microphthalmia, microcornea, cataract, anterior segment dysgenesis, ocular coloboma and early onset rod-cone dystrophy), and abnormal external ears (low-set pinna with crumpled helix, narrow intertragic incisure, abnormal bridge connecting the crus of the helix and the anthelix, narrow external acoustic meatus, and lobule aplasia).","definition_xrefs":["Orphanet:157962"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic microphthalmia","termid":"MONDO:0016073"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"oculoauricular syndrome","secondary_identifiers":["UMLS:C2677500","GARD:16988","DOID:0060482","MEDGEN:393758","MESH:C567416","OMIM:612109"],"synonyms":[{"name":"OCACS","type":"related"},{"name":"Schorderet-Munier-Franceschetti syndrome","type":"related"},{"name":"microphthalmia, microcornea, anterior segment dysgenesis, cataract, ocular coloboma, retinal pigment epithelium abnormalities, Rod-cone dystrophy, and anomalies of the external Ear","type":"related"},{"name":"oculoauricular syndrome","type":"exact"},{"name":"oculoauricular syndrome, Schorderet type","type":"related"}],"termid":"MONDO:0012802","xrefs":{"Monarch":{"xref_id":"0012802"}}}


id: PBO:0089821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase I general transcription initiation factor subunit Rrn7","termid":"PBO:0089821"}


id: PBO:0066783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 81","termid":"PBO:0066783"}


id: GO:0019532
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of oxalate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Oxalate, or ethanedioic acid, occurs in many plants and is highly toxic to animals.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid transport","termid":"GO:0006835"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"oxalate transport","synonyms":[{"name":"ethanedioate transport","type":"exact"},{"name":"ethanedioic acid transport","type":"exact"},{"name":"oxalic acid transport","type":"exact"}],"termid":"GO:0019532"}


id: MONDO:0012583
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tooth agenesis","termid":"MONDO:0005486"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tooth agenesis, selective, 5","secondary_identifiers":["MESH:C565757","UMLS:C1858210","OMIM:610926","GARD:18248","MEDGEN:346764"],"synonyms":[{"name":"STHAG5","type":"exact"},{"name":"he-Zhao deficiency","type":"related"},{"name":"hypodontia/oligodontia 5","type":"related"},{"name":"tooth agenesis, selective, 5","type":"exact"}],"termid":"MONDO:0012583","xrefs":{"Monarch":{"xref_id":"0012583"}}}


id: PR:O60184
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ssn6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O60184"],"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 transcriptional corepressor ssn6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC23E6.09","synonyms":[{"name":"Spom972h-ssn6","type":"exact"}],"termid":"PR:O60184"}


id: GO:2000011
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of adaxial/abaxial pattern formation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"regulates","term_name":"adaxial/abaxial pattern specification","termid":"GO:0009955"}],"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 adaxial/abaxial pattern formation","synonyms":[{"name":"regulation of adaxial/abaxial pattern specification","type":"related"}],"termid":"GO:2000011"}


id: GO:1901612
data:
  {"annotated_genes":["SJAG_00368","SJAG_03563"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[105371,105751],"is_not":false,"summary":null,"term":"GO:1901612"}]},"cv_name":"molecular_function","definition":"Binding to cardiolipin.","definition_xrefs":["GOC:TermGenie","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylglycerol binding","termid":"GO:1901611"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00368":null,"SJAG_03563":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0008289"],"is_obsolete":false,"name":"cardiolipin binding","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1901612","terms_by_termid":{"GO:1901612":null}}


id: PBO:0090718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19S proteasome base subcomplex ATPase subunit Rpt3","termid":"PBO:0090718"}


id: GO:2000793
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any cell proliferation that is involved in heart valve development.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population proliferation","termid":"GO:0008283"},{"relation_name":"part_of","term_name":"heart valve development","termid":"GO:0003170"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell proliferation involved in heart valve development","synonyms":[{"name":"cell proliferation of cardiac valve development","type":"exact"},{"name":"cell proliferation of heart valve development","type":"exact"}],"termid":"GO:2000793"}


id: PATO:0001209
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001209 absolute function (obsolete PATO:0001209)","termid":"PATO:0001209"}


id: PBO:0061876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oocyte secreted protein 1","termid":"PBO:0061876"}


id: PBO:0065282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich and Gla domain 2","termid":"PBO:0065282"}


id: FYPO:0006956
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 deferrichrome measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"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:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased cellular deferrichrome level","synonyms":[{"name":"increased cellular deferrichrome level during mitotic cell cycle","type":"related"},{"name":"increased cellular deferrichrome level during vegetative growth","type":"exact"},{"name":"increased cellular deferriferrichrome level","type":"exact"},{"name":"increased deferrichrome accumulation","type":"related"}],"termid":"FYPO:0006956"}


id: PBO:0029674
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_elongated_multinucleate_vegetative_cell_with_abnormal_septum_morphology","termid":"PBO:0029674"}


id: PBO:0078892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gln (anticodon CTG) 4-1","termid":"PBO:0078892"}


id: GO:0033693
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The assembly of neurofilaments into bundles, in which the filaments are longitudinally oriented, with numerous crossbridges between them. Neurofilament bundles may be cross-linked to each other, to membrane-bounded organelles or other cytoskeletal structures such as microtubules.","definition_xrefs":["PMID:11034913","PMID:11264295"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intermediate filament bundle assembly","termid":"GO:0045110"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0007010","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"neurofilament bundle assembly","synonyms":[{"name":"NF bundle assembly","type":"exact"}],"termid":"GO:0033693"}


id: PBO:0057394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548f-2","termid":"PBO:0057394"}


id: MONDO:0054791
data:
  {"annotated_genes":["SJAG_02665"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85231],"is_not":false,"summary":null,"term":"MONDO:0054791"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02665":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"leukodystrophy, hypomyelinating, 16","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070405","OMIM:617964","MEDGEN:1631337","UMLS:C4693779"],"synonyms":[{"name":"HLD16","type":"related"},{"name":"leukodystrophy, hypomyelinating, 16","type":"exact"}],"termid":"MONDO:0054791","terms_by_termid":{"MONDO:0054791":null},"xrefs":{"Monarch":{"xref_id":"0054791"}}}


id: PBO:0072809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterile alpha motif domain containing 4B","termid":"PBO:0072809"}


id: GO:0021710
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which neuroblasts acquire specialized structural and/or functional features that characterize the mature cerebellar stellate cell. Differentiation includes the processes involved in commitment of a neuroblast to a cerebellar stellate cell fate. A cerebellar stellate cell is an inhibitory GABAergic interneuron found in the cerebellar cortex.","definition_xrefs":["GO_REF:0000021","GOC:dph","GOC:cls","GOC:jid","PMID:15157725","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation in hindbrain","termid":"GO:0021533"},{"relation_name":"is_a","term_name":"central nervous system neuron differentiation","termid":"GO:0021953"},{"relation_name":"part_of","term_name":"cerebellar molecular layer formation","termid":"GO:0021688"}],"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":"cerebellar stellate cell differentiation","termid":"GO:0021710"}


id: GO:0052704
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The pathway resulting in the formation of ergothioneine from histidine via a set of steps in which gamma-glutamyl-hercynylcysteine sulfoxide is formed as an intermediate.","definition_xrefs":["PMID:5484456","PMID:4276459"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ergothioneine biosynthetic process","termid":"GO:0052699"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006790"],"is_obsolete":false,"name":"ergothioneine biosynthesis from histidine via gamma-glutamyl-hercynylcysteine sulfoxide","secondary_identifiers":["Wikipedia:Ergothioneine"],"synonyms":[{"name":"ergothioneine biosynthesis from histidine via N-alpha,N-alpha,N-alpha-trimethyl-L-histidine","type":"broad"}],"termid":"GO:0052704"}


id: PBO:0045542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydrouridine synthase 2","termid":"PBO:0045542"}


id: PBO:0003384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"replication fork protection complex subunit Swi1","termid":"PBO:0003384"}


id: RO:0002429
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"involved_in_regulation_of","termid":"RO:0002428"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"involved_in_positive_regulation_of","termid":"RO:0002429"}


id: MONDO:0024864
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"posterior uveal melanoma","termid":"MONDO:0003927"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004992"],"is_obsolete":false,"name":"medium/large size posterior uveal melanoma","secondary_identifiers":["NCIT:C9090","MEDGEN:124525","UMLS:C0278868"],"synonyms":[{"name":"medium/large size posterior uveal melanoma","type":"exact"}],"termid":"MONDO:0024864","xrefs":{"Monarch":{"xref_id":"0024864"}}}


id: MONDO:0018051
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Jessner lymphocytic infiltration of the skin (JLIS) is a chronic benign cutaneous disease characterized by asymptomatic non-scaly erythematous papules or plaques on the face and neck.","definition_xrefs":["Orphanet:33314"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"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":"Jessner lymphocytic infiltration of the skin","secondary_identifiers":["MEDGEN:663150","icd11.foundation:1624135677","NORD:1384","GARD:6940","UMLS:C0580181"],"synonyms":[{"name":"Jessner disease","type":"related"},{"name":"Jessner-Kanof lymphocytic infiltration of the skin","type":"exact"},{"name":"Jessner-Kanof syndrome","type":"related"},{"name":"Lymphocytic Infiltrate of Jessner","type":"exact"},{"name":"benign chronic T-cell infiltrative disorder","type":"related"},{"name":"benign lymphocytic infiltration","type":"related"},{"name":"lymphocytic infiltrate of Jessner","type":"related"}],"termid":"MONDO:0018051","xrefs":{"Monarch":{"xref_id":"0018051"}}}


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


id: GO:0032965
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of collagen, any of a group of fibrous proteins of very high tensile strength that form the main component of connective tissue in animals.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biosynthetic process","termid":"GO:0009889"},{"relation_name":"is_a","term_name":"regulation of collagen metabolic process","termid":"GO:0010712"},{"relation_name":"regulates","term_name":"collagen biosynthetic process","termid":"GO:0032964"}],"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 collagen biosynthetic process","synonyms":[{"name":"regulation of collagen anabolism","type":"exact"},{"name":"regulation of collagen biosynthesis","type":"exact"},{"name":"regulation of collagen formation","type":"exact"},{"name":"regulation of collagen synthesis","type":"exact"}],"termid":"GO:0032965"}


id: FYPO:0006230
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of translational initiation in the cytoplasm is decreased during a cellular response to oxidative stress.","definition_xrefs":["PMID:16278445","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cytoplasmic translational initiation","termid":"FYPO:0003125"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0006551"],"is_obsolete":false,"name":"decreased cytoplasmic translational initiation during cellular response to oxidative stress","synonyms":[{"name":"decreased cytoplasmic translation initiation during cellular response to oxidative stress","type":"exact"},{"name":"decreased cytoplasmic translational initiation during cellular response to oxidative stress during mitotic cell cycle","type":"related"},{"name":"decreased cytoplasmic translational initiation during cellular response to oxidative stress during vegetative growth","type":"exact"},{"name":"decreased cytoplasmic translational initiation during oxidative stress response","type":"exact"},{"name":"reduced cytoplasmic translational initiation during cellular response to oxidative stress","type":"exact"}],"termid":"FYPO:0006230"}


id: PBO:0089731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pleckstrin homology domain protein Opy1","termid":"PBO:0089731"}


id: PBO:0001304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic cohesin complex, non-SMC subunit Psc3","termid":"PBO:0001304"}


id: PBO:0078159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha variable 37 (pseudogene)","termid":"PBO:0078159"}


id: GO:0033417
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a CUU codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0060090","GO:0003723"],"is_obsolete":false,"name":"CUU codon-amino acid adaptor activity","synonyms":[{"name":"CTT codon-amino acid adaptor activity","type":"exact"},{"name":"leucine tRNA","type":"related"}],"termid":"GO:0033417"}


id: MONDO:0020384
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Niemann-Pick disease, type E is a poorly defined adult-onset and non-neuronopathic form of Niemann-Pick disease.","definition_xrefs":["Orphanet:99022"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Niemann-Pick disease","termid":"MONDO:0001982"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0002561"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0002525","MONDO:0005066","MONDO:0002561"],"is_obsolete":false,"name":"Niemann-Pick disease type E","secondary_identifiers":["MEDGEN:82781","SCTID:73399005","UMLS:C0268248"],"termid":"MONDO:0020384","xrefs":{"Monarch":{"xref_id":"0020384"}}}


id: PBO:0039611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANTXR like pseudogene 1","termid":"PBO:0039611"}


id: PBO:0030222
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_guanosine-diphosphatase_activity","termid":"PBO:0030222"}


id: PBO:0046248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ELOVL fatty acid elongase 4","termid":"PBO:0046248"}


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


id: GO:0047404
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + 3-D-glucuronosyl-N2-,6-disulfo-beta-D-glucosamine = glucuronate + N2,6-disulfo-D-glucosamine.","definition_xrefs":["EC:3.2.1.56"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0016798","GO:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"glucuronosyl-disulfoglucosamine glucuronidase activity","secondary_identifiers":["MetaCyc:RXN-16484","RHEA:15073"],"synonyms":[{"name":"3-D-glucuronsyl-2-N,6-disulfo-beta-D-glucosamine glucuronohydrolase activity","type":"related"},{"name":"3-D-glucuronsyl-N2,6-disulfo-beta-D-glucosamine glucuronohydrolase activity","type":"related"},{"name":"glucuronosyl-disulphoglucosamine glucuronidase activity","type":"exact"}],"termid":"GO:0047404"}


id: FYECO:0000051
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which linolenic acid 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":"+ fatty acid","termid":"FYECO:0000042"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ linolenic acid","termid":"FYECO:0000051"}


id: GO:0019633
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of shikimate, (3R,4S,5R)--3,4,5-trihydroxycyclohex-1-ene-1-carboxylate, the anion of shikimic acid.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shikimate metabolic process","termid":"GO:0019632"},{"relation_name":"is_a","term_name":"monocarboxylic acid catabolic process","termid":"GO:0072329"},{"relation_name":"is_a","term_name":"organic hydroxy compound catabolic process","termid":"GO:1901616"}],"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:0044248"}],"interesting_parent_ids":["GO:0044248","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"shikimate catabolic process","secondary_identifiers":["MetaCyc:SHIKIMATEDEG-PWY"],"synonyms":[{"name":"shikimate breakdown","type":"exact"},{"name":"shikimate catabolism","type":"exact"},{"name":"shikimate degradation","type":"exact"}],"termid":"GO:0019633"}


id: PBO:0054425
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 1821","termid":"PBO:0054425"}


id: PBO:0051786
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IQ motif containing F4, pseudogene","termid":"PBO:0051786"}


id: PBO:0077077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIAM Rac1 associated GEF 2","termid":"PBO:0077077"}


id: GO:0046205
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of nor-spermidine, a compound related to spermidine, N-(3-aminopropyl)-1,4-diaminobutane.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyamine catabolic process","termid":"GO:0006598"},{"relation_name":"is_a","term_name":"nor-spermidine metabolic process","termid":"GO:0046204"}],"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":"nor-spermidine catabolic process","synonyms":[{"name":"nor-spermidine breakdown","type":"exact"},{"name":"nor-spermidine catabolism","type":"exact"},{"name":"nor-spermidine degradation","type":"exact"}],"termid":"GO:0046205"}


id: GO:0007561
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The eversion (turning inside out) of imaginal discs from their peripodial sacs, resulting in movement of the epithelium to the outside of the larval epidermis.","definition_xrefs":["PMID:11494317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"imaginal disc morphogenesis","termid":"GO:0007560"}],"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 eversion","termid":"GO:0007561"}


id: FYPO:0006807
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the glycan moiety of a glycoprotein found at the cell surface contains a lower amount of galactose residues than normal. In wild-type cells, glycoprotein glycans contain mannose and galactose residues in a 1:1.2 ratio, and the galactose residues are connected by alpha-1,2 linkages.","definition_xrefs":["PMID:9839953","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased galactose level in glycoprotein glycan","termid":"FYPO:0003354"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0002274"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0003290"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0002494"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0003290","FYPO:0002274","FYPO:0002494","FYPO:0001320","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased galactose level in cell surface glycoprotein glycan","synonyms":[{"name":"decreased cell surface protein glycan galactosylation","type":"related"},{"name":"decreased galactose level in cell surface glycoprotein oligosaccharide","type":"related"},{"name":"decreased galactose level in glycoprotein glycan at cell surface","type":"exact"},{"name":"decreased level of alpha 1,2-linked galactose residues in cell surface glycoprotein glycan","type":"exact"},{"name":"reduced galactose level in cell surface glycoprotein glycan","type":"exact"}],"termid":"FYPO:0006807"}


id: PBO:0034144
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_within-species_paralogy_relationship_with","termid":"PBO:0034144"}


id: MONDO:0019303
data:
  {"annotated_genes":["SJAG_04114","SJAG_02818","SJAG_00566","SJAG_02362","SJAG_04540","SJAG_02396","SJAG_02200","SJAG_03457","SJAG_04934","SJAG_05979","SJAG_04631","SJAG_00660","SJAG_01836","SJAG_03125","SJAG_01745","SJAG_03855","SJAG_02194","SJAG_03898","SJAG_00120","SJAG_01378","SJAG_05329","SJAG_04995"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86457,86456],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009053"},{"annotations":[86091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015026"},{"annotations":[85786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957264"},{"annotations":[85264],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019569"},{"annotations":[85299],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019570"},{"annotations":[85132],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007485"},{"annotations":[84333],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014690"},{"annotations":[85378],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008030"},{"annotations":[84292],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0800029"},{"annotations":[85182],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014157"},{"annotations":[85743],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859147"},{"annotations":[86114],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010457"},{"annotations":[85789],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957261"},{"annotations":[85788],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957263"},{"annotations":[85557],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957294"},{"annotations":[85388],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013878"},{"annotations":[84516],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014612"},{"annotations":[86351],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030690"},{"annotations":[85852],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013755"},{"annotations":[86056],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0016368"},{"annotations":[84290,84291],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0016369"},{"annotations":[86067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010196"},{"annotations":[85390],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009910"}]},"cv_name":"mondo","definition":"Changes in the organism associated with senescence, occurring at an accelerated rate.","definition_xrefs":["MESH:D019588"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"skin disorder","termid":"MONDO:0005093"},{"relation_name":"is_a","term_name":"human disease","termid":"MONDO:0700096"}],"gene_count":22,"genes_by_uniquename":{"SJAG_00120":null,"SJAG_00566":null,"SJAG_00660":null,"SJAG_01378":null,"SJAG_01745":null,"SJAG_01836":null,"SJAG_02194":null,"SJAG_02200":null,"SJAG_02362":null,"SJAG_02396":null,"SJAG_02818":null,"SJAG_03125":null,"SJAG_03457":null,"SJAG_03855":null,"SJAG_03898":null,"SJAG_04114":null,"SJAG_04540":null,"SJAG_04631":null,"SJAG_04934":null,"SJAG_04995":null,"SJAG_05329":null,"SJAG_05979":null},"genotype_count":0,"in_subsets":["pombe_mondo_slim"],"is_obsolete":false,"name":"premature aging syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:79389","UMLS:C0231341","GARD:19017","MedDRA:10063493","MEDGEN:65416"],"synonyms":[{"name":"premature ageing","type":"related"},{"name":"premature aging","type":"related"}],"termid":"MONDO:0019303","terms_by_termid":{"MONDO:0007485":null,"MONDO:0008030":null,"MONDO:0009053":null,"MONDO:0009910":null,"MONDO:0010196":null,"MONDO:0010457":null,"MONDO:0013755":null,"MONDO:0013878":null,"MONDO:0014157":null,"MONDO:0014612":null,"MONDO:0014690":null,"MONDO:0015026":null,"MONDO:0016368":null,"MONDO:0016369":null,"MONDO:0019569":null,"MONDO:0019570":null,"MONDO:0030690":null,"MONDO:0800029":null,"MONDO:0859147":null,"MONDO:0957261":null,"MONDO:0957263":null,"MONDO:0957264":null,"MONDO:0957294":null},"xrefs":{"Monarch":{"xref_id":"0019303"}}}


id: PBO:0068579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 30, pseudogene","termid":"PBO:0068579"}


id: GO:0060198
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A clathrin-sculpted lipid bilayer membrane-enclosed vesicle after clathrin release.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin-coated vesicle","termid":"GO:0030136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0031410"],"is_obsolete":false,"name":"clathrin-sculpted vesicle","synonyms":[{"name":"clathrin sculpted vesicle","type":"exact"}],"termid":"GO:0060198"}


id: PBO:0053564
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 575","termid":"PBO:0053564"}


id: GO:0009406
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete virulence (obsolete GO:0009406)","synonyms":[{"name":"virulence","type":"exact"}],"termid":"GO:0009406"}


id: MONDO:0005368
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete obsessive-compulsive disorder (obsolete MONDO:0005368)","termid":"MONDO:0005368","xrefs":{"Monarch":{"xref_id":"0005368"}}}


id: PBO:0089622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U5 snRNP-associated protein Prp18","termid":"PBO:0089622"}


id: GO:0000707
data:
  {"annotated_genes":["SJAG_03221","SJAG_01708","SJAG_02708"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96113],"is_not":false,"summary":null,"term":"GO:0000707"},{"annotations":[106821,109449],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010772"}]},"cv_name":"biological_process","definition":"During meiosis, the aggregation, arrangement and bonding together of strand exchange proteins (recombinases) to form higher order oligomers on single-stranded DNA.","definition_xrefs":["PMID:11459983","GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA recombinase assembly","termid":"GO:0000730"},{"relation_name":"is_a","term_name":"meiosis I cell cycle process","termid":"GO:0061982"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01708":null,"SJAG_02708":null,"SJAG_03221":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006281"},{"rel_name":"part_of","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0065003","GO:0006259","GO:0006281","GO:0007049","GO:0006310","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"meiotic DNA recombinase assembly","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0000707","terms_by_termid":{"GO:0000707":null,"GO:0010772":null}}


id: GO:1990072
data:
  {"annotated_genes":["SJAG_02525","SJAG_03467","SJAG_00820","SJAG_02655","SJAG_04021","SJAG_00850","SJAG_04837","SJAG_01415"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[87874,96505,98301,101710,102916,104056,104125,108976],"is_not":false,"summary":null,"term":"GO:1990072"}]},"cv_name":"cellular_component","definition":"A complex that functions in anterograde transport at the Golgi and also regulates autophagy. In yeast it includes at least the following subunits: Bet3 (as homodimer), Bet5, Trs20, Trs23, Trs31, Trs33, Trs85. TRAPPIII may include further, as yet undescribed, proteins.","definition_xrefs":["PMID:20375281","PMID:22669257","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"TRAPP complex","termid":"GO:0030008"},{"relation_name":"part_of","term_name":"Golgi apparatus","termid":"GO:0005794"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00820":null,"SJAG_00850":null,"SJAG_01415":null,"SJAG_02525":null,"SJAG_02655":null,"SJAG_03467":null,"SJAG_04021":null,"SJAG_04837":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005794"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005794","GO:0005737"],"is_obsolete":false,"name":"TRAPPIII protein complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990072","terms_by_termid":{"GO:1990072":null}}


id: PBO:0011958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase allele types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial_amino_acid_deletion","termid":"PBO:0011958"}


id: PBO:0066704
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 1","termid":"PBO:0066704"}


id: FYPO:0004888
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the telomere of a chromosome is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to chromosome","termid":"FYPO:0004996"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal protein localization to telomere","synonyms":[{"name":"abnormal protein localisation to chromosome, telomeric region","type":"exact"},{"name":"abnormal protein localisation to telomere","type":"exact"},{"name":"abnormal protein localization to chromosome, telomeric region","type":"exact"}],"termid":"FYPO:0004888"}


id: PBO:0087426
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit a of the vacuolar-ATPase V0 domain; encodes one of two isoforms, located in vacuolar V-ATPase complexes while STV1 encodes the second isoform and is located in Golgi and endosomal V-ATPase complexes; interaction with PI(3,5)P2 increases V-ATPase activity and contributes to hyperosmotic stress tolerance; relative distribution to the vacuolar membrane decreases upon DNA replication stress; human homolog ATP6V0A4 implicated in renal tubular acidosis, can complement yeast null mutant","termid":"PBO:0087426"}


id: FYPO:0009031
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 bleomycin than normal.","definition_xrefs":["PomBase:mlr"],"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:0000003","FYPO:0000139","FYPO:0001985","FYPO:0005447","FYPO:0002682"],"is_obsolete":false,"name":"resistance to bleomycin","synonyms":[{"name":"resistance to bleomycin during mitotic cell cycle","type":"related"},{"name":"resistance to bleomycin during vegetative growth","type":"exact"},{"name":"resistant to bleomycin","type":"exact"}],"termid":"FYPO:0009031"}


id: GO:0033154
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + oligogalacturonide(out) = ADP + phosphate + oligogalacturonide(in).","definition_xrefs":["PMID:11555291","GOC:mlg","PMID:17451747"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ABC-type oligosaccharide transporter activity","termid":"GO:0015422"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"ABC-type oligogalacturonide transporter activity","secondary_identifiers":["GO:0033155","TC:3.A.1.1.11"],"synonyms":[{"name":"ATP-dependent oligogalacturonide transmembrane transporter activity","type":"related"},{"name":"ATPase-coupled oligogalacturonide transmembrane transporter activity","type":"related"},{"name":"oligogalacturonide transmembrane transporter activity","type":"narrow"},{"name":"oligogalacturonide transporting ATPase activity","type":"related"},{"name":"oligogalacturonide-transporting ATPase activity","type":"exact"}],"termid":"GO:0033154"}


id: PBO:0043308
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chloride intracellular channel 1 pseudogene 1","termid":"PBO:0043308"}


id: MONDO:0006762
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition occurring in the female offspring of dizygotic twins (twin, dizygotic) in a mixed-sex pregnancy, usually in cattle. Freemartinism can occur in other mammals. When placental fusion between the male and the female fetuses permits the exchange of fetal cells and fetal hormones, testicular hormones from the male fetus can androgenize the female fetus producing a sterile xx/xy chimeric 'female'(chimerism).","definition_xrefs":["MESH:D005611"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cattle disease","termid":"MONDO:0024913"},{"relation_name":"is_a","term_name":"difference of sexual differentiation, non-human animal","termid":"MONDO:0700105"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"freemartinism","secondary_identifiers":["DOID:4671","EFO:1000939"],"termid":"MONDO:0006762","xrefs":{"Monarch":{"xref_id":"0006762"}}}


id: GO:0033132
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of glucokinase activity, the catalysis of the transfer of a phosphate group, usually from ATP, to a glucose molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glucokinase activity","termid":"GO:0033131"},{"relation_name":"is_a","term_name":"negative regulation of hexokinase activity","termid":"GO:1903300"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0005975"],"is_obsolete":false,"name":"negative regulation of glucokinase activity","synonyms":[{"name":"down regulation of glucokinase activity","type":"exact"},{"name":"down-regulation of glucokinase activity","type":"exact"},{"name":"downregulation of glucokinase activity","type":"exact"},{"name":"glucokinase inhibitor","type":"narrow"},{"name":"inhibition of glucokinase activity","type":"narrow"}],"termid":"GO:0033132"}


id: GO:2000038
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of stomatal complex development.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of post-embryonic development","termid":"GO:0048580"},{"relation_name":"regulates","term_name":"stomatal complex development","termid":"GO:0010374"}],"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 stomatal complex development","termid":"GO:2000038"}


id: PBO:0046931
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 47 member E","termid":"PBO:0046931"}


id: GO:0102366
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 7-beta-hydroxytaxusin + NADPH + O2 + H+ = 2alpha, 7-beta-dihydroxytaxusin + NADP + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 7-beta-hydroxytaxusin 2-alpha-hydroxylase activity (obsolete GO:0102366)","termid":"GO:0102366"}


id: MONDO:0015927
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"eosinophilic pneumonia","termid":"MONDO:0005749"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"idiopathic eosinophilic pneumonia","secondary_identifiers":["Orphanet:182101","SCTID:708031000","GARD:20246","MEDGEN:836928","UMLS:C3872845"],"termid":"MONDO:0015927","xrefs":{"Monarch":{"xref_id":"0015927"}}}


id: PBO:0067184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 242, pseudogene","termid":"PBO:0067184"}


id: MONDO:0859322
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":"myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis","secondary_identifiers":["MEDGEN:1824033","OMIM:620138","UMLS:C5774260"],"termid":"MONDO:0859322","xrefs":{"Monarch":{"xref_id":"0859322"}}}


id: PBO:0083092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor required for activating GAL genes; responds to galactose; repressed by Gal80p and activated by Gal3p","termid":"PBO:0083092"}


id: PBO:0030527
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_chromatin","termid":"PBO:0030527"}


id: PBO:0028507
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_RNA_splicing_at_cryptic_splice_sites","termid":"PBO:0028507"}


id: MONDO:0018738
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the metanephros.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney benign neoplasm","termid":"MONDO:0002513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"benign metanephric tumor","secondary_identifiers":["Orphanet:464359","UMLS:C5681098","MEDGEN:1830110"],"termid":"MONDO:0018738","xrefs":{"Monarch":{"xref_id":"0018738"}}}


id: GO:0061374
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the mammillothalamic axonal tract, from its formation to the mature structure. The mammillothalamic tract is the collection of axons that connects the two major subdivisions of the diencephalon (hypothalamus and thalamus) and closes the diencephalic circuit.","definition_xrefs":["GOC:dph","PMID:10662642","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"mammillary axonal complex development","termid":"GO:0061373"}],"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":"mammillothalamic axonal tract development","termid":"GO:0061374"}


id: PBO:0061130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NMD3 ribosome export adaptor","termid":"PBO:0061130"}


id: PR:P26306
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cell cycle checkpoint control protein RAD9B that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00700"],"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 protein rad9 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC664.07c","secondary_identifiers":["UniProtKB:P26306"],"synonyms":[{"name":"Spom972h-RAD9B","type":"exact"}],"termid":"PR:P26306"}


id: MONDO:0958274
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"atrophic papulosis","termid":"MONDO:0958110"}],"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":"benign atrophic papulosis","secondary_identifiers":["Orphanet:656085"],"termid":"MONDO:0958274","xrefs":{"Monarch":{"xref_id":"0958274"}}}


id: MOD:00923
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative","definition_xrefs":["Unimod:495"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"Cy5 CyDye DIGE Fluor saturation dye","synonyms":[{"name":"Cy5 CyDye DIGE Fluor saturation dye","type":"related"},{"name":"CyDye-Cy5","type":"related"}],"termid":"MOD:00923"}


id: PBO:0040469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase c subunit lysine N-methyltransferase","termid":"PBO:0040469"}


id: MONDO:0026185
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic respiratory or mediastinal malformation (obsolete MONDO:0026185)","secondary_identifiers":["Orphanet:183554"],"termid":"MONDO:0026185","xrefs":{"Monarch":{"xref_id":"0026185"}}}


id: PBO:0017882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uridine diphosphate-N-acetylglucosamine transmembrane transporter Hut1","termid":"PBO:0017882"}


id: PBO:0031877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol polyphosphate phosphatase Inp53 (predicted)","termid":"PBO:0031877"}


id: PBO:0027304
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_thioredoxin-disulfide_reductase_activity","termid":"PBO:0027304"}


id: PBO:0030502
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitotic_cell_cycle_checkpoint","termid":"PBO:0030502"}


id: GO:0002558
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An inflammatory response driven by antigen recognition by antibodies bound to Fc receptors on mast cells, occurring within minutes after exposure of a sensitized individual to the antigen, and leading to the release of a variety of inflammatory mediators such as histamines.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mast cell mediated immunity","termid":"GO:0002448"},{"relation_name":"is_a","term_name":"type I hypersensitivity","termid":"GO:0016068"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"type I hypersensitivity mediated by mast cells","termid":"GO:0002558"}


id: MONDO:0008420
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A common benign skin neoplasm usually affecting older individuals. The lesions usually are multiple and arise in the face, chest, and shoulders. They appear as black or brown, slightly elevated skin lesions.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"keratosis","termid":"MONDO:0006566"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"seborrheic keratosis","secondary_identifiers":["ICD9:702.1","EFO:0005584","UMLS:C0022603","ICD10CM:L82","MESH:D017492","MEDGEN:5957","OMIM:182000","DOID:6498","NCIT:C9006","SCTID:398838000","Wikipedia:Seborrheic_keratosis"],"synonyms":[{"name":"basal cell papilloma","type":"exact"},{"name":"keratosis Seborrheica","type":"exact"},{"name":"keratosis, seborrheic","type":"related"},{"name":"keratosis, seborrheic, somatic","type":"exact"}],"termid":"MONDO:0008420","xrefs":{"Monarch":{"xref_id":"0008420"}}}


id: GO:0018889
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 2-chloro-N-isopropylacetanilide, an acylanide herbicide widely used to protect corn, onion, cabbage, rose bushes, and ornamental plants.","definition_xrefs":["UM-BBD_pathwayID:ppc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"},{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"},{"relation_name":"is_a","term_name":"organohalogen metabolic process","termid":"GO:0090345"}],"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":"2-chloro-N-isopropylacetanilide metabolic process","synonyms":[{"name":"2-chloro-N-isopropylacetanilide metabolism","type":"exact"},{"name":"propachlor metabolic process","type":"exact"},{"name":"propachlor metabolism","type":"exact"}],"termid":"GO:0018889"}


id: PBO:0057887
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3191","termid":"PBO:0057887"}


id: GO:0031588
data:
  {"annotated_genes":["SJAG_02785","SJAG_03802","SJAG_03501"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[88416,115273,117348],"is_not":false,"summary":null,"term":"GO:0031588"}]},"cv_name":"cellular_component","definition":"A protein complex that possesses nucleotide-dependent protein kinase activity. The nucleotide can be AMP (in S. pombe and human) or ADP (in S. cerevisiae).","definition_xrefs":["GOC:vw","GOC:mah","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"is_a","term_name":"protein kinase complex","termid":"GO:1902911"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02785":null,"SJAG_03501":null,"SJAG_03802":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"nucleotide-activated protein kinase complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"5'-AMP-activated protein kinase complex","type":"narrow"},{"name":"ADP-activated protein kinase complex","type":"narrow"},{"name":"AMP-activated protein kinase complex","type":"narrow"},{"name":"AMPK complex","type":"related"},{"name":"SNF1/AMPK protein kinase complex","type":"narrow"},{"name":"Snf1 kinase complex","type":"narrow"},{"name":"Snf1 serine/threonine protein kinase complex","type":"narrow"}],"termid":"GO:0031588","terms_by_termid":{"GO:0031588":null}}


id: PBO:0040364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase peripheral stalk-membrane subunit b pseudogene 1","termid":"PBO:0040364"}


id: PBO:0043690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 4I2","termid":"PBO:0043690"}


id: MONDO:0017338
data:
  {"annotated_genes":["SJAG_02306","SJAG_04016","SJAG_03641","SJAG_03222","SJAG_03701","SJAG_01147","SJAG_02397"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84372],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011582"},{"annotations":[84898],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013675"},{"annotations":[85249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014132"},{"annotations":[84517],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014611"},{"annotations":[84584],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033282"},{"annotations":[85227],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054785"},{"annotations":[85572],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957382"}]},"cv_name":"mondo","definition":"Multiple mitochondrial dysfunctions syndrome describes a group of rare inborn errors of energy metabolism due to defects in mitochondrial [4Fe-4S] protein assembly. Patients present with a neonatal/infancy onset of metabolic lactic acidosis (that may be associated with hyperglycinemia and other abnormal metabolic testing results), muscular hypotonia, absence of psychomotor development or developmental regression, as well as abnormal neuroimaging findings (including leukodystrophy, brain developmental defects, white matter abnormalities, cerebral atrophy), and other variable clinical features (e.g., optic atrophy, cardiomyopathy, pulmonary hypertension, seizures, and dysmorphic features). Early fatal outcome is usual.","definition_xrefs":["Orphanet:289573"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited lipoic acid biosynthesis defect","termid":"MONDO:0018424"}],"gene_count":7,"genes_by_uniquename":{"SJAG_01147":null,"SJAG_02306":null,"SJAG_02397":null,"SJAG_03222":null,"SJAG_03641":null,"SJAG_03701":null,"SJAG_04016":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525","MONDO:0004069"],"is_obsolete":false,"name":"fatal multiple mitochondrial dysfunctions syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:12632","OMIMPS:605711","SCTID:720827002","MEDGEN:502474","MESH:C565304","UMLS:C3502075","DOID:0070330"],"synonyms":[{"name":"MMDS","type":"related"},{"name":"fatal multiple mitochondrial dysfunction syndrome","type":"related"},{"name":"multiple mitochondrial dysfunctions syndrome","type":"exact"}],"termid":"MONDO:0017338","terms_by_termid":{"MONDO:0011582":null,"MONDO:0013675":null,"MONDO:0014132":null,"MONDO:0014611":null,"MONDO:0033282":null,"MONDO:0054785":null,"MONDO:0957382":null},"xrefs":{"Monarch":{"xref_id":"0017338"}}}


id: MONDO:1011883
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":"dilute coat color with neurological defects, non-human animal","secondary_identifiers":["OMIA:001501"],"termid":"MONDO:1011883","xrefs":{"Monarch":{"xref_id":"1011883"}}}


id: MONDO:0013208
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypermanganesemia with dystonia","termid":"MONDO:0000214"},{"relation_name":"is_a","term_name":"disorder of manganese transport","termid":"MONDO:0017766"},{"relation_name":"is_a","term_name":"parkinsonian disorder","termid":"MONDO:0021095"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome","secondary_identifiers":["UMLS:C2750442","OMIM:613280","GARD:10706","MESH:C548016","Orphanet:309854","DOID:0080536","ICD9:277.89","SCTID:702377007","MEDGEN:412958"],"synonyms":[{"name":"HMDPC","type":"related"},{"name":"HMNDYT1","type":"related"},{"name":"cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome","type":"exact"},{"name":"hypermanganesemia with dystonia 1","type":"related"},{"name":"hypermanganesemia with dystonia polycythemia and cirrhosis","type":"related"},{"name":"hypermanganesemia with dystonia, polycythemia, and cirrhosis","type":"related"}],"termid":"MONDO:0013208","xrefs":{"Monarch":{"xref_id":"0013208"}}}


id: GO:0000096
data:
  {"annotated_genes":["SJAG_04459","SJAG_03671","SJAG_01880","SJAG_00419","SJAG_00832","SJAG_03881","SJAG_02293","SJAG_00309","SJAG_01466","SJAG_03556","SJAG_00234","SJAG_00582","SJAG_02689","SJAG_03659","SJAG_03102","SJAG_00988","SJAG_04305","SJAG_04953","SJAG_00881","SJAG_03712","SJAG_03141","SJAG_01404","SJAG_04042","SJAG_03614","SJAG_00283","SJAG_02972","SJAG_03152","SJAG_04425","SJAG_02290","SJAG_03494","SJAG_03856","SJAG_00395"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109648,64848,105151,110231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071266"},{"annotations":[101074],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019344"},{"annotations":[94689,101075,108608,96084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006535"},{"annotations":[109649],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019343"},{"annotations":[117302,92505,99855,102773,97723],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006534"},{"annotations":[110679,102803,110680],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052699"},{"annotations":[89230,101912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050667"},{"annotations":[109650],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071269"},{"annotations":[99856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019280"},{"annotations":[113066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019279"},{"annotations":[99190,94760],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990355"},{"annotations":[91859,88982,98211,99842,106165,111565],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019509"},{"annotations":[111110,95837,97606,97724,89231,110233,114918,101913],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009086"},{"annotations":[109810,111835,102568],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006555"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving amino acids containing sulfur, comprising cysteine, homocysteine, methionine and selenocysteine.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"}],"gene_count":32,"genes_by_uniquename":{"SJAG_00234":null,"SJAG_00283":null,"SJAG_00309":null,"SJAG_00395":null,"SJAG_00419":null,"SJAG_00582":null,"SJAG_00832":null,"SJAG_00881":null,"SJAG_00988":null,"SJAG_01404":null,"SJAG_01466":null,"SJAG_01880":null,"SJAG_02290":null,"SJAG_02293":null,"SJAG_02689":null,"SJAG_02972":null,"SJAG_03102":null,"SJAG_03141":null,"SJAG_03152":null,"SJAG_03494":null,"SJAG_03556":null,"SJAG_03614":null,"SJAG_03659":null,"SJAG_03671":null,"SJAG_03712":null,"SJAG_03856":null,"SJAG_03881":null,"SJAG_04042":null,"SJAG_04305":null,"SJAG_04425":null,"SJAG_04459":null,"SJAG_04953":null},"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:0006790"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006790"],"is_obsolete":false,"name":"sulfur amino acid metabolic process","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"sulfur amino acid metabolism","type":"exact"},{"name":"sulphur amino acid metabolic process","type":"exact"},{"name":"sulphur amino acid metabolism","type":"exact"}],"termid":"GO:0000096","terms_by_termid":{"GO:0006534":null,"GO:0006535":null,"GO:0006555":null,"GO:0009086":null,"GO:0019279":null,"GO:0019280":null,"GO:0019343":null,"GO:0019344":null,"GO:0019509":null,"GO:0050667":null,"GO:0052699":null,"GO:0071266":null,"GO:0071269":null,"GO:1990355":null}}


id: PBO:0071035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 37","termid":"PBO:0071035"}


id: PBO:0058157
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4452","termid":"PBO:0058157"}


id: PBO:0087685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the NuA3 histone acetyltransferase complex; this complex acetylates histone H3; contains PHD finger domain that interacts with methylated histone H3","termid":"PBO:0087685"}


id: MONDO:0006613
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Stromal pigmentation such as that in ochronosis results from chronic irritation. The melanin is in the superficial stroma and the basal layer of the corneal epithelium.","definition_xrefs":["EFO:1000770"],"direct_ancestors":[{"relation_name":"is_a","term_name":"corneal deposit","termid":"MONDO:0001308"}],"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":"stromal corneal pigmentation","secondary_identifiers":["DOID:12311","ICD9:371.12","MEDGEN:509791","SCTID:55031000","UMLS:C0155105"],"synonyms":[{"name":"stromal corneal pigmentations","type":"exact"}],"termid":"MONDO:0006613","xrefs":{"Monarch":{"xref_id":"0006613"}}}


id: PBO:0062527
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily U member 3","termid":"PBO:0062527"}


id: MONDO:0001522
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder characterized by a fascination with fire and recurrent episodes of fire setting during which the individual experiences a rising subjective sense of tension before the fire setting and a sense of gratification or relief when setting the fire. There is no ulterior motive (such as monetary gain or the expression of political ideology) to the fire setting.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"impulse control disorder","termid":"MONDO:0001162"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyromania","secondary_identifiers":["MEDGEN:42028","SCTID:600009","ICD10CM:F63.1","DOID:12402","icd11.foundation:1532500290","ICD9:312.33","MESH:D005391","NCIT:C94334","UMLS:C0016142"],"synonyms":[{"name":"firesetting behavior","type":"exact"},{"name":"firesetting behaviour","type":"exact"},{"name":"pathological firesetting","type":"exact"}],"termid":"MONDO:0001522","xrefs":{"Monarch":{"xref_id":"0001522"}}}


id: MONDO:0005277
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A common, severe type of vascular headache often associated with increased sympathetic activity, resulting in nausea, vomiting, and light sensitivity.","definition_xrefs":["NCIT:C89715"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"hypnic headache","termid":"MONDO:0017181"},{"relation_name":"is_a","term_name":"neurovascular disorder","termid":"MONDO:0043218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"migraine disorder","secondary_identifiers":["ICD9:346.9","UMLS:C0149931","MESH:D008881","DOID:6364","MEDGEN:57451","ICD9:346"],"synonyms":[{"name":"migraine","type":"exact"},{"name":"migraine disorder","type":"exact"},{"name":"migraine headache","type":"exact"},{"name":"migraine variant","type":"exact"},{"name":"migraine with or without aura","type":"exact"}],"termid":"MONDO:0005277","xrefs":{"Monarch":{"xref_id":"0005277"}}}


id: PBO:0086466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative mitochondrial aconitase isozyme; similarity to Aco1p, an aconitase required for the TCA cycle; expression induced during growth on glucose, by amino acid starvation via Gcn4p, and repressed on ethanol","termid":"PBO:0086466"}


id: PBO:0074469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermine synthase","termid":"PBO:0074469"}


id: GO:0042394
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The shedding of the old protein-based cuticular fragments during the molting cycle. Examples of this process are found in invertebrates.","definition_xrefs":["GOC:mtg_sensu","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete ecdysis, protein-based cuticle (obsolete GO:0042394)","synonyms":[{"name":"ecdysis, protein-based cuticle","type":"exact"}],"termid":"GO:0042394"}


id: PBO:0083363
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; overlaps the verified gene SIR2/YDL042C","termid":"PBO:0083363"}


id: PBO:0091082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"candidate Dms1 ortholog, syntenic position (possible gene prediction error)","termid":"PBO:0091082"}


id: MONDO:0007688
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Myhre syndrome is characterized by striking muscular build, short stature, reduced joint mobility, brachydactyly, mixed hearing loss and mental retardation of variable severity. Facial dysmorphism with short palpebral fissures, short philtrum, thin lips, maxillary hypoplasia and prognathism is present. Thick skin has been observed in six patients.","definition_xrefs":["Orphanet:2588"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"acromelic dysplasia","termid":"MONDO:0019695"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"Myhre syndrome","secondary_identifiers":["MESH:C537620","MEDGEN:167103","NCIT:C123815","ICD9:759.89","UMLS:C0796081","OMIM:139210","SCTID:699316006","NORD:1481","GARD:2572"],"synonyms":[{"name":"Growth mental deficiency syndrome of Myhre","type":"related"},{"name":"Growth-mental deficiency syndrome of Myhre","type":"related"},{"name":"LAPS syndrome","type":"related"},{"name":"MYHRE syndrome","type":"related"},{"name":"MYHRS","type":"related"},{"name":"Myhre syndrome","type":"exact"},{"name":"facial dysmorphism - intellectual deficit - short stature - hearing loss","type":"related"},{"name":"facial dysmorphism-intellectual disability-short stature-hearing loss syndrome","type":"exact"},{"name":"laryngotracheal stenosis, arthropathy, prognathism, and short stature","type":"related"}],"termid":"MONDO:0007688","xrefs":{"Monarch":{"xref_id":"0007688"}}}


id: PR:O13639
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An adenosylhomocysteinase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR23420:SF0","PRO:DNx","OMA:SCHPO02844"],"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":"adenosylhomocysteinase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC8D2.18c","secondary_identifiers":["UniProtKB:O13639"],"synonyms":[{"name":"AdoHcyase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"S-adenosyl-L-homocysteine hydrolase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-AHCY","type":"exact"}],"termid":"PR:O13639"}


id: MONDO:0016990
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of prothrombin deficiency that is acquired during the lifetime of the individual.","definition_xrefs":["MONDO:patterns/acquired"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"congenital prothrombin deficiency","termid":"MONDO:0013361"},{"relation_name":"is_a","term_name":"prothrombin deficiency","termid":"MONDO:0024307"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"acquired prothrombin deficiency","secondary_identifiers":["MEDGEN:140275","MESH:C538174","NCIT:C131622","UMLS:C0392610","Orphanet:26348","SCTID:4152002","GARD:475"],"synonyms":[{"name":"acquired factor II deficiency","type":"related"},{"name":"acquired hypoprothrombinemia","type":"exact"},{"name":"acquired prothrombin deficiency","type":"exact"},{"name":"hypoprothrombinemia, acquired","type":"related"}],"termid":"MONDO:0016990","xrefs":{"Monarch":{"xref_id":"0016990"}}}


id: PBO:0047969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FRAS1 related extracellular matrix 2","termid":"PBO:0047969"}


id: MONDO:0859171
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":"Luo-Schoch-Yamamoto syndrome","secondary_identifiers":["DOID:0070416","MEDGEN:1794156","UMLS:C5561946","OMIM:619460"],"termid":"MONDO:0859171","xrefs":{"Monarch":{"xref_id":"0859171"}}}


id: PBO:0063601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal biogenesis factor 13","termid":"PBO:0063601"}


id: PBO:0070371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY5 pseudogene 9","termid":"PBO:0070371"}


id: GO:1902976
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any DNA replication preinitiation complex assembly that is involved in meiotic cell cycle.","definition_xrefs":["GO_REF:0000060","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA replication preinitiation complex assembly","termid":"GO:0071163"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"},{"relation_name":"part_of","term_name":"premeiotic DNA replication","termid":"GO:0006279"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006260"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0007049","GO:0044085","GO:0065003","GO:0006260","GO:0006259","GO:0008150"],"is_obsolete":false,"name":"premeiotic DNA replication preinitiation complex assembly","synonyms":[{"name":"DNA replication preinitiation complex formation involved in meiotic cell cycle","type":"exact"},{"name":"pre-IC complex assembly involved in meiotic cell cycle","type":"exact"}],"termid":"GO:1902976"}


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: PBO:0054720
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 2129","termid":"PBO:0054720"}


id: PBO:0074944
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 109A","termid":"PBO:0074944"}


id: PATO:0000337
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color quality inhering in a bearer by virtue of the bearer's lacking color.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"color pattern","termid":"PATO:0000019"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"colorless","secondary_identifiers":["PATO:0000334"],"synonyms":[{"name":"unpigmented","type":"related"}],"termid":"PATO:0000337"}


id: GO:0035341
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the directed movement of inosine into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of purine nucleoside transport","termid":"GO:0032245"},{"relation_name":"regulates","term_name":"inosine transport","termid":"GO:0035340"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of inosine transport","synonyms":[{"name":"regulation of hypoxanthine riboside transport","type":"exact"}],"termid":"GO:0035341"}


id: CHEBI:17326
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoside triphosphate","termid":"CHEBI:17326"}


id: MONDO:0005769
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A viral ear infection caused by the spread of varicella-zoster virus to the facial nerves. It is characterized by intense otalgia and a cutaneous vesicular eruption.","definition_xrefs":["NCIT:C84763"],"direct_ancestors":[{"relation_name":"is_a","term_name":"herpes zoster","termid":"MONDO:0005609"},{"relation_name":"is_a","term_name":"Bell's palsy","termid":"MONDO:0005665"},{"relation_name":"is_a","term_name":"ear infection","termid":"MONDO:0021666"},{"relation_name":"is_a","term_name":"viral infection of central nervous system","termid":"MONDO:0024318"}],"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":"geniculate herpes zoster","secondary_identifiers":["ICD9:351.8","MEDGEN:6581","NORD:1647","UMLS:C0017409","GARD:7525","EFO:0007281","Orphanet:3020","ICD10EXP:B02.2+","ICD9:053.11","SCTID:95670000","ICD10EXP:G53.0*","DOID:9210"],"synonyms":[{"name":"Herpes Zoster Oticus","type":"exact"},{"name":"Herpes zoster auricularis","type":"exact"},{"name":"Hunt syndrome (formerly)","type":"related"},{"name":"Hunt's syndrome (formerly)","type":"related"},{"name":"Ramsay Hunt Syndrome","type":"exact"},{"name":"Ramsay Hunt syndrome","type":"exact"},{"name":"Ramsay Hunt syndrome type 2","type":"related"},{"name":"Ramsay Hunt syndrome type 2 (formerly)","type":"related"},{"name":"Ramsay Hunt syndrome type II","type":"related"},{"name":"Ramsey Hunt syndrome","type":"exact"},{"name":"facial nerve palsy due to VZV","type":"exact"},{"name":"facial nerve palsy due to herpes zoster infection","type":"exact"},{"name":"facial nerve paralysis due to VZV","type":"exact"},{"name":"geniculate neuralgia","type":"exact"},{"name":"herpetic geniculate ganglionitis","type":"exact"},{"name":"nervus intermedius neuralgia","type":"exact"}],"termid":"MONDO:0005769","xrefs":{"Monarch":{"xref_id":"0005769"}}}


id: PBO:0040905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMS1 pseudogene 9","termid":"PBO:0040905"}


id: MONDO:0019095
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Plague is a severe bacterial infection caused by the gram-negative bacterium Yersinia pestis.","definition_xrefs":["Orphanet:707"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary bacterial infectious disease","termid":"MONDO:0000314"},{"relation_name":"is_a","term_name":"Yersinia infectious disease","termid":"MONDO:0007023"},{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plague","secondary_identifiers":["MESH:D010930","DOID:3482","EFO:0009425","ICD9:020","NCIT:C85015","GARD:18702","icd11.foundation:1596449540","ICD9:020.9","NORD:1583","ICD10CM:A20","ICD9:136.8","MEDGEN:10785","MESH:D015009","UMLS:C0032064","MedDRA:10061416","SCTID:58750007","MedDRA:10035148"],"synonyms":[{"name":"Yersiniosis","type":"broad"},{"name":"black death","type":"related"},{"name":"infection by Yersinia pestis","type":"related"},{"name":"pest","type":"related"},{"name":"pestilential fever","type":"related"},{"name":"plague","type":"exact"}],"termid":"MONDO:0019095","xrefs":{"Monarch":{"xref_id":"0019095"}}}


id: PR:Q9P7W5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A serine/threonine-protein kinase RIO2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10593:SF1","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":"serine/threonine-protein kinase rio2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1703.05","secondary_identifiers":["UniProtKB:Q9P7W5"],"synonyms":[{"name":"SPBC1703.05","type":"related"},{"name":"Spom972h-RIOK2","type":"exact"}],"termid":"PR:Q9P7W5"}


id: MONDO:0019452
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This subgroup of myeloproliferative neoplasms includes cases which do not meet the morphologic criteria of any of the defined myeloproliferative neoplasms, or which have characteristics that overlap at least two of the myeloproliferative neoplasms.","definition_xrefs":["NCIT:C27350"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloproliferative neoplasm","termid":"MONDO:0020076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"myeloproliferative neoplasm, unclassifiable","secondary_identifiers":["GARD:16764","UMLS:C1333046","Orphanet:86830","MEDGEN:232365","ICDO:9975/3"],"synonyms":[{"name":"CMPD, U","type":"exact"},{"name":"CMPD-U","type":"exact"},{"name":"MPN, U","type":"exact"},{"name":"MPN-U","type":"exact"},{"name":"chronic myeloproliferative disease, unclassifiable","type":"exact"},{"name":"chronic myeloproliferative disorder, unclassifiable","type":"exact"},{"name":"myeloproliferative neoplasm, unclassifiable","type":"exact"},{"name":"unclassifiable chronic myeloproliferative disease","type":"exact"},{"name":"unclassifiable chronic myeloproliferative disorder","type":"exact"},{"name":"undifferentiated myeloproliferative disease","type":"exact"}],"termid":"MONDO:0019452","xrefs":{"Monarch":{"xref_id":"0019452"}}}


id: GO:0061797
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A gated channel activity that enables the transmembrane transfer of a chloride ion by a channel that opens in response to a change in pH.","definition_xrefs":["GOC:dph","PMID:27358471"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chloride channel activity","termid":"GO:0005254"},{"relation_name":"is_a","term_name":"ligand-gated monoatomic anion channel activity","termid":"GO:0099095"},{"relation_name":"is_a","term_name":"pH-gated monoatomic ion channel activity","termid":"GO:0160128"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"pH-gated chloride channel activity","termid":"GO:0061797"}


id: PBO:0052549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"killer cell lectin like receptor C2","termid":"PBO:0052549"}


id: PBO:0034794
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent helicase Slh1, human ASCC3 ortholog (predicted)","termid":"PBO:0034794"}


id: PBO:0018116
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved in eukarotes only","termid":"PBO:0018116"}


id: PBO:0087077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L38; homologous to mammalian ribosomal protein L38, no bacterial homolog","termid":"PBO:0087077"}


id: RO:HOM0000047
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Historical homology that involves the chromosomes able to pair (synapse) during meiosis.","definition_xrefs":["ISBN:0195307615"],"direct_ancestors":[{"relation_name":"is_a","term_name":"in_historical_homology_relationship_with","termid":"RO:HOM0000007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_chromosomal_homology_relationship_with","synonyms":[{"name":"chromosomal homologous to","type":"exact"}],"termid":"RO:HOM0000047"}


id: PBO:0089543
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HAD-superfamily hydrolase, subfamily IIA","termid":"PBO:0089543"}


id: GO:0010142
data:
  {"annotated_genes":["SJAG_03352","SJAG_00580","SJAG_04568","SJAG_04307","SJAG_00413","SJAG_01474","SJAG_03349","SJAG_04499","SJAG_04865","SJAG_03715"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87908,93642,95787,97234,98789,101063,105686,108631,112876,114035],"is_not":false,"summary":null,"term":"GO:0010142"}]},"cv_name":"biological_process","definition":"The pathway that converts acetate, in the form of acetyl-CoA, to farnesyl diphosphate (FPP) through a series of mevalonate intermediates. Farnesyl diphosphate is an important substrate for other essential pathways, such as biosynthesis of sterols.","definition_xrefs":["GOC:pz","MetaCyc:PWY-922"],"direct_ancestors":[{"relation_name":"is_a","term_name":"farnesyl diphosphate biosynthetic process","termid":"GO:0045337"},{"relation_name":"is_a","term_name":"isoprenoid biosynthetic process via mevalonate","termid":"GO:1902767"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00413":null,"SJAG_00580":null,"SJAG_01474":null,"SJAG_03349":null,"SJAG_03352":null,"SJAG_03715":null,"SJAG_04307":null,"SJAG_04499":null,"SJAG_04568":null,"SJAG_04865":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"farnesyl diphosphate biosynthetic process, mevalonate pathway","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Ac-MVA pathway","type":"narrow"},{"name":"acetate-mevalonate pathway","type":"narrow"},{"name":"farnesyl diphosphate anabolism, mevalonate pathway","type":"exact"},{"name":"farnesyl diphosphate formation, mevalonate pathway","type":"exact"},{"name":"farnesyl diphosphate synthesis, mevalonate pathway","type":"exact"},{"name":"isoprenoid pathway","type":"exact"}],"termid":"GO:0010142","terms_by_termid":{"GO:0010142":null}}


id: PBO:0063305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PCF11 antisense RNA 1","termid":"PBO:0063305"}


id: PBO:0078419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gly (anticodon GCC) 1-5","termid":"PBO:0078419"}


id: PBO:0110188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial poly(A) RNA polymerase Atp25","termid":"PBO:0110188"}


id: MOD:01912
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively substitutes one hydrogen atom of a residue with one bromine atom.","definition_xrefs":["Unimod:340"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brominated residue","termid":"MOD:00754"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monobrominated residue","synonyms":[{"name":"Br1Res","type":"exact"}],"termid":"MOD:01912"}


id: MONDO:0023045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"ectodermal dysplasia arthrogryposis diabetes mellitus","secondary_identifiers":["GARD:2042"],"termid":"MONDO:0023045","xrefs":{"Monarch":{"xref_id":"0023045"}}}


id: PBO:0002443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sm snRNP core protein Smd2","termid":"PBO:0002443"}


id: PBO:0076377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TAB3 antisense RNA 1","termid":"PBO:0076377"}


id: GO:0045030
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a nucleotide and transmitting the signal to a heterotrimeric G-protein complex to initiate a change in cell activity, activated by UTP.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled pyrimidinergic nucleotide receptor activity","termid":"GO:0071553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"G protein-coupled UTP receptor activity","secondary_identifiers":["GO:0015065"],"synonyms":[{"name":"UTP-activated nucleotide receptor activity","type":"broad"},{"name":"purinoceptor type U","type":"broad"},{"name":"uridine nucleotide receptor activity","type":"broad"}],"termid":"GO:0045030"}


id: GO:0035979
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: histone H2AX-serine (position 139) + ATP = histone H2AX-phosphoserine (position 139) + ADP. This reaction is the addition of a phosphate group to the serine residue at position 139 of histone variant H2AX.","definition_xrefs":["GOC:yaf","PMID:11893489","PMID:16061642"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine kinase activity","termid":"GO:0004674"},{"relation_name":"is_a","term_name":"histone H2AX kinase activity","termid":"GO:0141003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0003824","GO:0004672","GO:0140096","GO:0016740","GO:0016301","GO:0003674"],"is_obsolete":false,"name":"histone H2AXS139 kinase activity","synonyms":[{"name":"histone H2AS139 kinase activity","type":"related"},{"name":"histone kinase activity (H2A-S139 specific)","type":"related"},{"name":"histone kinase activity (H2A.x-S139 specific)","type":"narrow"}],"termid":"GO:0035979"}


id: GO:1902767
data:
  {"annotated_genes":["SJAG_03715","SJAG_03349","SJAG_03352","SJAG_04499","SJAG_02719","SJAG_00413","SJAG_04307","SJAG_00580","SJAG_04568","SJAG_04865","SJAG_01474"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110452],"is_not":false,"summary":null,"term":"GO:1902767"},{"annotations":[101063,105686,87908,108631,112876,95787,93642,97234,98789,114035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010142"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of isoprenoid via mevalonate.","definition_xrefs":["GO_REF:0000092","GOC:mengo_curators","GOC:TermGenie","PMID:11078528"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoprenoid biosynthetic process","termid":"GO:0008299"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00413":null,"SJAG_00580":null,"SJAG_01474":null,"SJAG_02719":null,"SJAG_03349":null,"SJAG_03352":null,"SJAG_03715":null,"SJAG_04307":null,"SJAG_04499":null,"SJAG_04568":null,"SJAG_04865":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"isoprenoid biosynthetic process via mevalonate","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"isoprenoid anabolism via mevalonate","type":"exact"},{"name":"isoprenoid biosynthesis via mevalonate","type":"exact"},{"name":"isoprenoid formation via mevalonate","type":"exact"},{"name":"isoprenoid synthesis via mevalonate","type":"exact"}],"termid":"GO:1902767","terms_by_termid":{"GO:0010142":null,"GO:1902767":null}}


id: PBO:0051495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IGSF11 antisense RNA 1","termid":"PBO:0051495"}


id: GO:0036016
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an interleukin-3 stimulus.","definition_xrefs":["GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to interleukin-3","termid":"GO:0036015"},{"relation_name":"is_a","term_name":"cellular response to cytokine stimulus","termid":"GO:0071345"}],"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 interleukin-3","synonyms":[{"name":"cellular response to IL-3","type":"exact"}],"termid":"GO:0036016"}


id: PBO:0053817
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 1078","termid":"PBO:0053817"}


id: PBO:0055406
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 2836","termid":"PBO:0055406"}


id: PBO:0028743
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_level_during_cellular_response_to_methyl_methanesulfonate","termid":"PBO:0028743"}


id: PBO:0043660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coenzyme Q5, methyltransferase","termid":"PBO:0043660"}


id: PBO:0075865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSX family pseudogene 5","termid":"PBO:0075865"}


id: MONDO:0700246
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any eye disorder in which the cause of the disease is a variant in the PAX6 gene itself or a variant within another locus that results in defective regulation of the PAX6 gene.","definition_xrefs":["PMID:26394807","PMID:24290376","PMID:17679951"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"}],"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":"ocular dysgenesis caused by defects in PAX6 regulation","termid":"MONDO:0700246","xrefs":{"Monarch":{"xref_id":"0700246"}}}


id: PBO:0039608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANTXR cell adhesion molecule 1","termid":"PBO:0039608"}


id: PBO:0066287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein Y-linked family 2 member M, pseudogene","termid":"PBO:0066287"}


id: PBO:0083768
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential non-ATPase regulatory subunit of the 26S proteasome; similar to another S. cerevisiae regulatory subunit, Rpn5p, as well as to mammalian proteasome subunits","termid":"PBO:0083768"}


id: RO:0002132
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"The relation between a neuron projection bundle and a neuron projection that is fasciculated with it.","direct_ancestors":[{"relation_name":"is_a","term_name":"overlaps","termid":"RO:0002131"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_fasciculating_neuron_projection","termid":"RO:0002132"}


id: GO:0047520
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 11-cis-retinyl palmitate + H2O = 11-cis-retinol + H+ + palmitate.","definition_xrefs":["RHEA:19697","EC:3.1.1.63"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"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:0016788"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787","GO:0016788"],"is_obsolete":false,"name":"11-cis-retinyl-palmitate hydrolase activity","secondary_identifiers":["KEGG_REACTION:R03049","Reactome:R-HSA-2465941","MetaCyc:11-CIS-RETINYL-PALMITATE-HYDROLASE-RXN"],"synonyms":[{"name":"11-cis-retinol palmitate esterase activity","type":"related"},{"name":"11-cis-retinyl-palmitate acylhydrolase activity","type":"related"},{"name":"RPH","type":"related"}],"termid":"GO:0047520"}


id: MONDO:0015720
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Moderately severe hemophilia A is a form of hemophilia A characterized by factor VIII deficiency leading to abnormal bleeding as a result of minor injuries, or following surgery or tooth extraction.","definition_xrefs":["Orphanet:169805"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemophilia A","termid":"MONDO:0010602"}],"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":"moderately severe hemophilia A","secondary_identifiers":["UMLS:C0272323","GARD:17060","MEDGEN:543974"],"synonyms":[{"name":"moderately severe factor VIII deficiency","type":"exact"},{"name":"moderately severe haemophilia type A","type":"exact"},{"name":"moderately severe hemophilia type A","type":"exact"}],"termid":"MONDO:0015720","xrefs":{"Monarch":{"xref_id":"0015720"}}}


id: GO:0060872
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the semicircular canal from its initial formation to the mature structure.","definition_xrefs":["GOC:tb","GOC:dph","GOC:sdb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tube development","termid":"GO:0035295"},{"relation_name":"part_of","term_name":"inner ear development","termid":"GO:0048839"}],"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":"semicircular canal development","termid":"GO:0060872"}


id: PBO:0091423
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"M-Factor precursor","termid":"PBO:0091423"}


id: PR:O74921
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC757.11c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74921"],"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 C757.11c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC757.11c","synonyms":[{"name":"Spom972h-SPCC757.11c","type":"exact"}],"termid":"PR:O74921"}


id: MONDO:0031002
data:
  {"annotated_genes":["SJAG_04002"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84803],"is_not":false,"summary":null,"term":"MONDO:0031002"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04002":null},"genotype_count":0,"is_obsolete":false,"name":"Baralle-Macken syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5543241","MEDGEN:1778777","OMIM:619255"],"synonyms":[{"name":"BARMACS","type":"exact"},{"name":"neurodevelopmental disorder with cataracts and variable microcephaly","type":"exact"}],"termid":"MONDO:0031002","terms_by_termid":{"MONDO:0031002":null},"xrefs":{"Monarch":{"xref_id":"0031002"}}}


id: PBO:0079744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBX domain protein 11","termid":"PBO:0079744"}


id: PBO:0002169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TLDc domain protein 1","termid":"PBO:0002169"}


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


id: MONDO:0017132
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hereditary ATTR amyloidosis (obsolete MONDO:0017132)","termid":"MONDO:0017132","xrefs":{"Monarch":{"xref_id":"0017132"}}}


id: PBO:0055625
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 3064","termid":"PBO:0055625"}


id: PBO:0088311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trehalose 6-phosphate synthase/phosphatase complex","termid":"PBO:0088311"}


id: GO:0103003
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: oleate + a lipid hydroperoxide = 9,10-epoxystearate + a lipid alcohol.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete oleate peroxygenase activity (obsolete GO:0103003)","termid":"GO:0103003"}


id: GO:0005746
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The protein complexes that form the mitochondrial electron transport system (the respiratory chain), associated with the inner mitochondrial membrane. The respiratory chain complexes transfer electrons from an electron donor to an electron acceptor and are associated with a proton pump to create a transmembrane electrochemical gradient.","definition_xrefs":["GOC:ecd","ISBN:0198547684","GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial respirasome (obsolete GO:0005746)","synonyms":[{"name":"mitochondrial electron transport chain","type":"exact"},{"name":"mitochondrial respiratory chain","type":"exact"},{"name":"mitochondrial respiratory chain supercomplex","type":"exact"},{"name":"mitochondrial respiratory supercomplex","type":"exact"}],"termid":"GO:0005746"}


id: PBO:0003443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial peptidase (predicted)","termid":"PBO:0003443"}


id: PBO:0058307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4680","termid":"PBO:0058307"}


id: PBO:0000584
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial leucine-tRNA ligase (predicted)","termid":"PBO:0000584"}


id: PBO:0077655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF receptor superfamily member 6b","termid":"PBO:0077655"}


id: GO:0046816
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A vesicle used to transport the partial or complete virion between cellular compartments.","definition_xrefs":["PMID:7933124","GOC:vesicles"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular vesicle","termid":"GO:0097708"}],"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":"virion transport vesicle","termid":"GO:0046816"}


id: MONDO:0016604
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":"dysraphism-cleft lip/palate-limb reduction defects syndrome","secondary_identifiers":["GARD:3438","MEDGEN:1809965","Orphanet:2476","UMLS:C5679624"],"synonyms":[{"name":"Medeira-Dennis-Donnai syndrome","type":"exact"},{"name":"dysraphism, cleft lip/palate, limb reduction defects","type":"related"}],"termid":"MONDO:0016604","xrefs":{"Monarch":{"xref_id":"0016604"}}}


id: GO:0043842
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reactions: (KDO)-lipid IVA + CMP-3-deoxy-D-manno-octulosonate = KDO2-lipid IVA + CMP, and lipid IVA + CMP-3-deoxy-D-manno-octulosonate = (KDO)-lipid IVA + CMP.","definition_xrefs":["PMID:9195966","PMID:1577828","PMID:2033061"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosyltransferase activity","termid":"GO:0016757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016757"],"is_obsolete":false,"name":"Kdo transferase activity","synonyms":[{"name":"3-deoxy-D-manno-octulosonic-acid transferase activity","type":"exact"},{"name":"WaaA","type":"related"},{"name":"kdtA","type":"related"}],"termid":"GO:0043842"}


id: PBO:0081602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 526","termid":"PBO:0081602"}


id: GO:0055039
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A crystalline exocytotic organelle composed of small, acidic proteins existing primarily as disulphide-linked dimers. The trichocyst is an organelle that releases long filamentous proteins that capture predators in net-like structures, to slow them down when the cell is disturbed. The protein is nontoxic and shaped like a long, striated, fibrous shaft.","definition_xrefs":["GOC:jid","GOC:rph","PMID:3667715"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular membraneless organelle","termid":"GO:0043264"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005576"}],"interesting_parent_ids":["GO:0005575","GO:0005576"],"is_obsolete":false,"name":"trichocyst","secondary_identifiers":["Wikipedia:Trichocyst"],"termid":"GO:0055039"}


id: MONDO:0017276
data:
  {"annotated_genes":["SJAG_04489","SJAG_03345"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84550],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010936"},{"annotations":[85947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008178"}]},"cv_name":"mondo","definition":"Frontotemporal dementia (FTD) comprises a group of neurodegenerative disorders, characterized by progressive changes in behavior, executive dysfunction and language impairment, as a result of degeneration of the medial prefrontal and frontoinsular cortices. Four clinical subtypes have been identified: semantic dementia, progressive non-fluent aphasia, behavioral variant FTD and right temporal lobar atrophy.","definition_xrefs":["Orphanet:282"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"basal ganglia disorder","termid":"MONDO:0003996"},{"relation_name":"is_a","term_name":"hereditary dementia","termid":"MONDO:0015547"},{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03345":null,"SJAG_04489":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0002039"],"is_obsolete":false,"name":"frontotemporal dementia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MedDRA:10068968","UMLS:C0338451","DOID:9255","GARD:8436","MEDGEN:83266","MESH:D057180","NANDO:1200548","icd11.foundation:831337417","NCIT:C84719"],"synonyms":[{"name":"FTD","type":"exact"},{"name":"MSTD","type":"related"},{"name":"Wilhemsen-Lynch disease","type":"exact"},{"name":"frontotemporal lobar degeneration","type":"exact"},{"name":"frontotemporal lobe dementia (FLDEM)","type":"related"},{"name":"multiple system tauopathy with presenile dementia","type":"exact"},{"name":"pallidopontonigral degeneration","type":"exact"}],"termid":"MONDO:0017276","terms_by_termid":{"MONDO:0008178":null,"MONDO:0010936":null},"xrefs":{"Monarch":{"xref_id":"0017276"}}}


id: PBO:0057925
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3650","termid":"PBO:0057925"}


id: PATO:0002149
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer exhibiting increased density resulting in exhibiting increased degree of radiopacity (in X-rays).","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased mass density","termid":"PATO:0001788"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ivory","termid":"PATO:0002149"}


id: PBO:0089580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II CTD small phosphatase Psr1","termid":"PBO:0089580"}


id: GO:0034907
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: acetanilide + O2 + 2 H+ + NADH = catechol + NAD+ + acetamide.","definition_xrefs":["UM-BBD_reactionID:r0723"],"gene_count":0,"genotype_count":0,"name":"obsolete acetanilide 1,2-dioxygenase activity (obsolete GO:0034907)","termid":"GO:0034907"}


id: MONDO:0010354
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome with neuromuscular involvement characterized by infantile hypotonia, muscular hypoplasia, spastic paraparesis with dystonic/athetoic movements, and severe cognitive deficiency.","definition_xrefs":["Orphanet:59"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"peripheral hypothyroidism","termid":"MONDO:0016412"},{"relation_name":"excluded_subClassOf","term_name":"Pelizaeus-Merzbacher-like disease","termid":"MONDO:0017226"},{"relation_name":"excluded_subClassOf","term_name":"obsolete pure or complex X-linked spastic paraplegia (obsolete MONDO:0017916)","termid":"MONDO:0017916"},{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Allan-Herndon-Dudley syndrome","secondary_identifiers":["NORD:1415","MEDGEN:208645","icd11.foundation:56813604","MESH:C537047","NANDO:1200580","NANDO:2201292","SCTID:702327009","NCIT:C118843","UMLS:C0795889","OMIM:300523","GARD:5617","DOID:0050631"],"synonyms":[{"name":"AHDS","type":"exact"},{"name":"ALLAN-Herndon syndrome","type":"exact"},{"name":"ALLAN-Herndon-DUDLEY syndrome","type":"related"},{"name":"Allan-Herndon syndrome","type":"related"},{"name":"Allan-Herndon-Dudley syndrome","type":"exact"},{"name":"MCT8 deficiency","type":"exact"},{"name":"MCT8-Specific Thyroid Hormone Cell Transporter Deficiency","type":"exact"},{"name":"MCT8-specific thyroid hormone cell Membrane transporter deficiency","type":"exact"},{"name":"T3 resisitence","type":"related"},{"name":"T3 resistance","type":"related"},{"name":"X-linked intellectual disability with hypotonia","type":"related"},{"name":"X-linked intellectual disability-hypotonia syndrome","type":"exact"},{"name":"intellectual disability and muscular atrophy","type":"related"},{"name":"intellectual disability, X-linked, with hypotonia","type":"related"},{"name":"mental retardation and muscular atrophy","type":"related"},{"name":"mental retardation, X-linked, with hypotonia","type":"related"},{"name":"monocarboxylate transporter 8 deficiency","type":"exact"},{"name":"monocarboxylate transporter-8 deficiency","type":"related"},{"name":"triiodothyronine resistance","type":"related"}],"termid":"MONDO:0010354","xrefs":{"Monarch":{"xref_id":"0010354"}}}


id: SO:0001405
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A post translationally modified tyrosine amino acid feature.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified_amino_acid_feature","termid":"SO:0001385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modified_L_tyrosine","secondary_identifiers":["MOD:00919"],"synonyms":[{"name":"ModTry","type":"exact"},{"name":"modified L tyrosine","type":"exact"},{"name":"modified L-tyrosine","type":"exact"}],"termid":"SO:0001405"}


id: GO:0001588
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with the neurotransmitter dopamine and activating adenylate cyclase via coupling to Gs to initiate a change in cell activity.","definition_xrefs":["IUPHAR_RECEPTOR:2252","GOC:mah","ISBN:0953351033","IUPHAR_RECEPTOR:2260"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dopamine neurotransmitter receptor activity","termid":"GO:0004952"}],"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:0038023","GO:0003674"],"is_obsolete":false,"name":"dopamine neurotransmitter receptor activity, coupled via Gs","secondary_identifiers":["GO:0001589","GO:0001590"],"synonyms":[{"name":"dopamine D1 receptor activity","type":"narrow"},{"name":"dopamine D5 receptor activity","type":"narrow"}],"termid":"GO:0001588"}


id: PR:P78965
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A glutathione reductase, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR22912:SF27","OMA:SCHPO02853"],"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":"glutathione reductase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC17A3.07","secondary_identifiers":["UniProtKB:P78965"],"synonyms":[{"name":"GR (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"GRase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-GSR","type":"exact"}],"termid":"PR:P78965"}


id: GO:0039555
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus stops, prevents, or reduces the activity of MDA-5 (also known as IFIH1) by binding to MDA-5 itself. For example, direct binding of viral proteins to the host MDA-5 protein can inhibit interaction of MDA-5 with MAVS, its downstream signaling effector.","definition_xrefs":["VZ:603","PMID:19019954"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host MDA-5 activity via MDA-5 binding (obsolete GO:0039555)","synonyms":[{"name":"suppression by virus of host MDA5 activity by MDA-5 binding","type":"exact"}],"termid":"GO:0039555"}


id: GO:0036115
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a fatty-acyl-CoA, any derivative of coenzyme A in which the sulfhydryl group is in thiolester linkage with a fatty-acyl group.","definition_xrefs":["PMID:10578051"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty-acyl-CoA metabolic process","termid":"GO:0035337"},{"relation_name":"is_a","term_name":"sulfur compound catabolic process","termid":"GO:0044273"},{"relation_name":"is_a","term_name":"purine-containing compound catabolic process","termid":"GO:0072523"},{"relation_name":"is_a","term_name":"nucleoside phosphate catabolic process","termid":"GO:1901292"},{"relation_name":"is_a","term_name":"fatty acid derivative catabolic process","termid":"GO:1901569"}],"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:0006790"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0006790","GO:0055086","GO:0044248","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"fatty-acyl-CoA catabolic process","synonyms":[{"name":"fatty-acyl-CoA breakdown","type":"exact"},{"name":"fatty-acyl-CoA catabolism","type":"exact"},{"name":"fatty-acyl-CoA degradation","type":"exact"}],"termid":"GO:0036115"}


id: FYPO:0000814
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 nucleolus organization is abnormal. Nucleolus organization results in the assembly, arrangement of constituent parts, or disassembly of the nucleolus.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nucleus organization","termid":"FYPO:0000810"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal nucleolus organization","synonyms":[{"name":"abnormal nucleolus organisation","type":"exact"},{"name":"abnormal nucleolus organization during mitotic cell cycle","type":"related"},{"name":"abnormal nucleolus organization during vegetative growth","type":"exact"}],"termid":"FYPO:0000814"}


id: MONDO:0015869
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any of the forms of breast benign neoplasm that have a rare incidence.","definition_xrefs":["MONDO:patterns/rare"],"gene_count":0,"genotype_count":0,"name":"obsolete rare benign breast tumor (obsolete MONDO:0015869)","secondary_identifiers":["Orphanet:180253"],"synonyms":[{"name":"rare breast benign neoplasm","type":"exact"}],"termid":"MONDO:0015869","xrefs":{"Monarch":{"xref_id":"0015869"}}}


id: PBO:0086178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for the spindle pole body (SPB) duplication; localizes at the cytoplasmic side of the central plaque periphery of the SPB; forms a complex with a nuclear envelope protein Mps2p and SPB components Spc29p and Kar1p; required for mitotic functions of Cdc5p","termid":"PBO:0086178"}


id: MONDO:0016509
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":"microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome","secondary_identifiers":["MEDGEN:1667341","Orphanet:231736","UMLS:C4751163","GARD:10938"],"synonyms":[{"name":"MPPC syndrome","type":"exact"},{"name":"microcornea posterior megalolenticonus persistent fetal vasculature coloboma","type":"related"},{"name":"microcornea posterior megalolenticonus persistent foetal vasculature coloboma","type":"related"}],"termid":"MONDO:0016509","xrefs":{"Monarch":{"xref_id":"0016509"}}}


id: PBO:0062437
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 101 pseudogene","termid":"PBO:0062437"}


id: GO:0001050
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a single subunit RNA polymerase enzyme, which is composed of a single catalytic subunit similar to the RNA polymerase enzymes from phages T3, T7, and SP6.","definition_xrefs":["GOC:txnOH","PMID:20701995"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase binding","termid":"GO:0070063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"single-subunit type RNA polymerase binding","synonyms":[{"name":"SP6-type RNA polymerase binding","type":"exact"},{"name":"T3-type RNA polymerase binding","type":"exact"},{"name":"T3/T7 type RNA polymerase binding","type":"exact"},{"name":"T7-type RNA polymerase binding","type":"exact"}],"termid":"GO:0001050"}


id: _global:occupancy
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD_extension_relations","definition":"A number representing what proportion of copies of the protein have the modification.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"occupancy","termid":"_global:occupancy"}


id: MONDO:1010665
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Evans syndrome that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Evans syndrome, non-human animal","termid":"MONDO:1010082"},{"relation_name":"is_a","term_name":"thrombocytopenia, horse","termid":"MONDO:1010661"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Evans syndrome, horse","secondary_identifiers":["OMIA:001286-9796"],"termid":"MONDO:1010665","xrefs":{"Monarch":{"xref_id":"1010665"}}}


id: PBO:0072415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27 pseudogene 20","termid":"PBO:0072415"}


id: FYPO:0002492
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which DNA 5'-adenosine monophosphate hydrolase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA 5'-adenosine monophosphate hydrolase activity","termid":"FYPO:0002491"},{"relation_name":"is_a","term_name":"abolished nuclease activity","termid":"FYPO:0003164"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000002","FYPO:0000661","FYPO:0001985","FYPO:0000707","FYPO:0000654","FYPO:0005447"],"is_obsolete":false,"name":"abolished DNA 5'-adenosine monophosphate hydrolase activity","synonyms":[{"name":"DNA 5'-adenosine monophosphate hydrolase activity abolished","type":"exact"}],"termid":"FYPO:0002492"}


id: PBO:0070563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 29","termid":"PBO:0070563"}


id: GO:0032932
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the depolymerization of astral microtubules.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of microtubule depolymerization","termid":"GO:0007026"},{"relation_name":"is_a","term_name":"negative regulation of cell cycle process","termid":"GO:0010948"},{"relation_name":"is_a","term_name":"regulation of spindle organization","termid":"GO:0090224"},{"relation_name":"negatively_regulates","term_name":"astral microtubule depolymerization","termid":"GO:0060172"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0000226"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0000226"},{"rel_name":"negatively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0000226","GO:0008150","GO:0007010","GO:0007049"],"is_obsolete":false,"name":"negative regulation of astral microtubule depolymerization","synonyms":[{"name":"astral microtubule stabilization","type":"exact"}],"termid":"GO:0032932"}


id: SO:1000159
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An intrachromosomal transposition whereby the segment between the first two breaks listed is removed and inserted at the third break; the insertion is in cytologically the same orientation as its flanking segments.","definition_xrefs":["FB:reference_manual"],"direct_ancestors":[{"relation_name":"has_part","term_name":"direct","termid":"SO:0001514"},{"relation_name":"is_a","term_name":"intrachromosomal_transposition","termid":"SO:1000041"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uninverted_intrachromosomal_transposition","synonyms":[{"name":"(Drosophila)eTp","type":"related"},{"name":"uninverted intrachromosomal transposition","type":"exact"}],"termid":"SO:1000159"}


id: PBO:0047526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibrinogen beta chain","termid":"PBO:0047526"}


id: FYPO:0006827
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 zinc ion measured in the cytosol is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular zinc level","termid":"FYPO:0001534"},{"relation_name":"is_a","term_name":"decreased level of substance in cytosol","termid":"FYPO:0001605"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"decreased cytosolic zinc level","synonyms":[{"name":"decreased cytosolic zinc ion level","type":"exact"},{"name":"decreased cytosolic zinc ion level during vegetative growth","type":"exact"},{"name":"decreased cytosolic zinc level during mitotic cell cycle","type":"related"},{"name":"decreased level of zinc ions in cytosol","type":"exact"},{"name":"decreased levels of free cytosolic zinc","type":"exact"},{"name":"reduced cytosolic zinc level","type":"exact"}],"termid":"FYPO:0006827"}


id: MONDO:0016371
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cranial neuralgia","termid":"MONDO:0016374"}],"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":"combined hyperactive dysfunction syndrome of the cranial nerves","secondary_identifiers":["GARD:20541","Orphanet:221078","UMLS:C5190851","MEDGEN:1677292","icd11.foundation:457686735"],"termid":"MONDO:0016371","xrefs":{"Monarch":{"xref_id":"0016371"}}}


id: MONDO:1010874
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lysosomal storage disease characterised by impaired unesterified cholesterol and sphingomyelin transport and metabolism, resulting in the accumulation of un-esterified cholesterol and glycosphingolipids within late endosomes and lysosomes that occurs in cats due to a mutation in the NPC1 gene. Affected animals present with hepatosplenomegaly, neurological degeneration and premature death.","definition_xrefs":["OMIA:000725-9685"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal storage disease, domestic cat","termid":"MONDO:1010861"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Niemann-Pick disease, NPC1-related, domestic cat","synonyms":[{"name":"Niemann-Pick disease, type C1, domestic cat","type":"related"}],"termid":"MONDO:1010874","xrefs":{"Monarch":{"xref_id":"1010874"}}}


id: GO:0002952
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (2S)-2-hydroxy-3,4-dioxopentyl phosphate = 3-hydroxy-2,4-dioxopentyl phosphate.","definition_xrefs":["RHEA:44360"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, interconverting aldoses and ketoses","termid":"GO:0016861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016853","GO:0003674"],"is_obsolete":false,"name":"(4S)-4-hydroxy-5-phosphonooxypentane-2,3-dione isomerase activity","secondary_identifiers":["MetaCyc:RXN-15216","EC:5.3.1.32"],"synonyms":[{"name":"phospho-AI-2 isomerase activity","type":"related"}],"termid":"GO:0002952"}


id: GO:0003127
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events by which an endogenous stimulus is received by a cilium on a cell and converted to a molecular signal contributing to left/right asymmetry.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to endogenous stimulus","termid":"GO:0071495"},{"relation_name":"part_of","term_name":"determination of left/right symmetry","termid":"GO:0007368"}],"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 nodal flow","termid":"GO:0003127"}


id: PBO:0059108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MORN repeat containing 4","termid":"PBO:0059108"}


id: PBO:0060089
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 36","termid":"PBO:0060089"}


id: PBO:0077829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TP53 target 3 family member H, pseudogene","termid":"PBO:0077829"}


id: GO:0071070
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alpha4-beta1 integrin complex bound to thrombospondin-2.","definition_xrefs":["PMID:11980922"],"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":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005886"],"is_obsolete":false,"name":"alpha4-beta1 integrin-thrombospondin-2 complex","synonyms":[{"name":"ITGA4-ITGB1-THBS2 complex","type":"narrow"}],"termid":"GO:0071070"}


id: PBO:0047587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroblast growth factor receptor 4","termid":"PBO:0047587"}


id: PBO:0057143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 222","termid":"PBO:0057143"}


id: PBO:0079564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin associated protein 2","termid":"PBO:0079564"}


id: GO:0033876
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3'-phospho-5'-adenylyl sulfate + glycochenodeoxycholate = adenosine 3',5'-diphosphate + glycochenodeoxycholate 7-sulfate + H+.","definition_xrefs":["RHEA:17689","EC:2.8.2.34"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016782","GO:0016740"],"is_obsolete":false,"name":"glycochenodeoxycholate sulfotransferase activity","secondary_identifiers":["KEGG_REACTION:R07289","MetaCyc:2.8.2.34-RXN"],"synonyms":[{"name":"3'-phosphoadenylyl-sulfate:glycochenodeoxycholate 7-sulfotransferase activity","type":"related"},{"name":"BAST","type":"related"},{"name":"bile acid:3'-phosphoadenosine-5'-phosphosulfate sulfotransferase activity","type":"broad"},{"name":"bile acid:PAPS:sulfotransferase activity","type":"related"}],"termid":"GO:0033876"}


id: PBO:0053830
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 1095","termid":"PBO:0053830"}


id: PBO:0059177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"muscle RAS oncogene homolog","termid":"PBO:0059177"}


id: GO:0034294
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a sexual spore wall, the specialized envelope lying outside the cell membrane of a spore derived from a product of meiosis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"spore wall assembly","termid":"GO:0042244"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"},{"relation_name":"part_of","term_name":"sexual sporulation","termid":"GO:0034293"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0071554"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0007049","GO:0071554","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"sexual spore wall assembly","synonyms":[{"name":"sexual spore wall formation","type":"exact"}],"termid":"GO:0034294"}


id: PBO:0002859
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin I light chain Cam2","termid":"PBO:0002859"}


id: GO:0002339
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process dependent upon B cell antigen receptor signaling in response to self or foreign antigen through which B cells are selected for survival.","definition_xrefs":["GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system process","termid":"GO:0002376"},{"relation_name":"part_of","term_name":"B cell differentiation","termid":"GO:0030183"}],"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 selection","synonyms":[{"name":"B lymphocyte selection","type":"exact"},{"name":"B-cell selection","type":"exact"},{"name":"B-lymphocyte selection","type":"exact"}],"termid":"GO:0002339"}


id: FYPO:0001317
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of RNA measured in a cell is normal (i.e. indistinguishable from wild type) when the cell is in the vegetative growth phase of the life cycle. Total RNA or a specific RNA, such as the mRNA transcribed from a gene of interest, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA level","termid":"FYPO:0000840"},{"relation_name":"is_a","term_name":"normal level of substance in cell during vegetative growth","termid":"FYPO:0001316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal RNA level during vegetative growth","secondary_identifiers":["FYPO:0002938"],"synonyms":[{"name":"normal RNA level during mitotic cell cycle","type":"related"},{"name":"normal cellular RNA level during vegetative growth","type":"exact"},{"name":"normal mRNA accumulation","type":"related"},{"name":"normal mRNA level during mitotic cell cycle","type":"related"},{"name":"normal mRNA level during vegetative growth","type":"narrow"},{"name":"normal mRNA transcript level during vegetative growth","type":"narrow"},{"name":"normal transcript level during vegetative growth","type":"exact"}],"termid":"FYPO:0001317"}


id: PBO:0081503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 407","termid":"PBO:0081503"}


id: GO:0070917
data:
  {"annotated_genes":["SJAG_03015"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[94338],"is_not":false,"summary":null,"term":"GO:0070917"}]},"cv_name":"molecular_function","definition":"Binds to and modulates the activity of inositol phosphoceramide synthase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme regulator activity","termid":"GO:0030234"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03015":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0030234"}],"interesting_parent_ids":["GO:0030234","GO:0003674","GO:0098772"],"is_obsolete":false,"name":"inositol phosphoceramide synthase regulator activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"IPC synthase regulator activity","type":"exact"}],"termid":"GO:0070917","terms_by_termid":{"GO:0070917":null}}


id: GO:0043836
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: xanthine + H2O = 4-ureido-5-imidazole carboxylate.","definition_xrefs":["PMID:13278326","MetaCyc:R127-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides","termid":"GO:0016812"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0016810","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"xanthine hydrolase activity","synonyms":[{"name":"xanthinase activity","type":"exact"}],"termid":"GO:0043836"}


id: FYPO:0003400
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 20S ribosomal RNA precursor measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal rRNA or precursor level","termid":"FYPO:0006000"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal 20S rRNA precursor level","synonyms":[{"name":"normal 20S rRNA precursor accumulation","type":"related"},{"name":"normal 20S rRNA precursor level during mitotic cell cycle","type":"related"},{"name":"normal 20S rRNA precursor level during vegetative growth","type":"exact"},{"name":"normal 20S rRNA precursor transcript level","type":"exact"}],"termid":"FYPO:0003400"}


id: PBO:0027101
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_antisense_RNA_level","termid":"PBO:0027101"}


id: RO:HOM0000033
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Convergence that results from co-evolution usually involving an evolutionary arms race.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_convergence_relationship_with","termid":"RO:HOM0000004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_mimicry_relationship_with","synonyms":[{"name":"mimicrous to","type":"exact"}],"termid":"RO:HOM0000033"}


id: PBO:0073672
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal regulatory protein beta 1","termid":"PBO:0073672"}


id: PBO:0050054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major histocompatibility complex, class I, U (pseudogene)","termid":"PBO:0050054"}


id: GO:0004591
data:
  {"annotated_genes":["SJAG_02464"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[109277],"is_not":false,"summary":null,"term":"GO:0004591"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-oxoglutarate + lipoamide + H+ = S-succinyldihydrolipoamide + CO2.","definition_xrefs":["EC:1.2.4.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor","termid":"GO:0016624"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02464":null},"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:0016491","GO:0003824"],"is_obsolete":false,"name":"oxoglutarate dehydrogenase (succinyl-transferring) activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:2OXOGLUTDECARB-RXN","RHEA:12188","Reactome:R-HSA-71401"],"synonyms":[{"name":"2-ketoglutarate dehydrogenase activity","type":"related"},{"name":"2-oxoglutarate dehydrogenase activity","type":"related"},{"name":"2-oxoglutarate: lipoate oxidoreductase activity","type":"related"},{"name":"2-oxoglutarate:dihydrolipoyllysine-residue succinyltransferase-lipoyllysine 2-oxidoreductase (decarboxylating, acceptor-succinylating)","type":"related"},{"name":"2-oxoglutarate:lipoamide 2-oxidoreductase (decarboxylating and acceptor-succinylating) activity","type":"related"},{"name":"AKGDH activity","type":"related"},{"name":"OGDC activity","type":"related"},{"name":"alpha-ketoglutarate dehydrogenase activity","type":"related"},{"name":"alpha-ketoglutaric acid dehydrogenase activity","type":"related"},{"name":"alpha-ketoglutaric dehydrogenase activity","type":"related"},{"name":"alpha-oxoglutarate dehydrogenase activity","type":"related"},{"name":"ketoglutaric dehydrogenase activity","type":"related"},{"name":"oxoglutarate decarboxylase activity","type":"related"},{"name":"oxoglutarate dehydrogenase (lipoamide) activity","type":"exact"},{"name":"oxoglutarate dehydrogenase activity","type":"related"}],"termid":"GO:0004591","terms_by_termid":{"GO:0004591":null}}


id: GO:0106001
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Uptake of hexoses, notably D-glucose, fructose, and galactose, into the blood by absorption from the small intestine.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal absorption","termid":"GO:0050892"}],"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":"intestinal hexose absorption","termid":"GO:0106001"}


id: MONDO:0008404
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Scalp-ear-nipple syndrome is characterized by the following triad: areas of hairless raw skin over the scalp (present at birth and healing during childhood), prominent, hypoplastic ears with almost absent pinnae, and bilateral amastia. Thirty cases have been described so far. Renal and urinary tract abnormalities, as well as cataract, have also been observed. Transmission is autosomal dominant.","definition_xrefs":["Orphanet:2036"],"direct_ancestors":[{"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":"mixed dermis disorder","termid":"MONDO:0019294"}],"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":"scalp-ear-nipple syndrome","secondary_identifiers":["OMIM:181270","GARD:159","icd11.foundation:88843032","MESH:C536623","SCTID:721888002","MEDGEN:357183","DOID:0111550","UMLS:C1867020"],"synonyms":[{"name":"Finlay-Marks syndrome","type":"exact"},{"name":"SENS","type":"related"},{"name":"Sen syndrome","type":"related"},{"name":"hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples","type":"related"},{"name":"scalp ear nipple syndrome","type":"related"},{"name":"scalp-EAR-nipple syndrome","type":"related"},{"name":"scalp-ear-nipple syndrome","type":"exact"}],"termid":"MONDO:0008404","xrefs":{"Monarch":{"xref_id":"0008404"}}}


id: PBO:0004772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S acidic ribosomal protein Rpp1-2","termid":"PBO:0004772"}


id: PBO:0028168
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_crossover_junction_endodeoxyribonuclease_activity","termid":"PBO:0028168"}


id: PBO:0065195
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pre-mRNA processing factor 6","termid":"PBO:0065195"}


id: FYPO:0006742
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 transcription from a promoter that contains one or more MluI cell cycle box factor elements (MCBs) is normal (i.e. indistinguishable from wild type) in extent, timing, start or termination site, etc.","definition_xrefs":["PMID:30134042","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal transcription during vegetative growth","termid":"FYPO:0001855"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000294"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000257","FYPO:0000294","FYPO:0001312"],"is_obsolete":false,"name":"normal transcription from MCB promoter","synonyms":[{"name":"normal expression of MBF target genes","type":"related"},{"name":"normal transcription from MCB promoter during mitotic cell cycle","type":"related"},{"name":"normal transcription from MCB promoter during vegetative growth","type":"exact"}],"termid":"FYPO:0006742"}


id: PBO:0051699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol polyphosphate-4-phosphatase type I A","termid":"PBO:0051699"}


id: GO:0043076
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The nucleus of a megasporocyte, a diploid cell that undergoes meiosis to produce four megaspores, and its descendents.","definition_xrefs":["GOC:jl","ISBN:0618254153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus","termid":"GO:0005634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005634"],"is_obsolete":false,"name":"megasporocyte nucleus","synonyms":[{"name":"megaspore mother cell nucleus","type":"exact"}],"termid":"GO:0043076"}


id: PBO:0113161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hsp90 chaperone; functionally redundant with Hsc82p; required for pheromone signaling; negative regulator of the Hsf1p-dependent heat shock response with Cpr7p; docks with Tom70p for mitochondrial preprotein delivery; promotes telomerase DNA binding, nucleotide addition; promotes solubility of chaperone-substrate complexes; DNA damage induced nuclear import is Aha1p dependent; protein abundance increases in response to DNA replication stress; human homolog, HSP90AB1, complements null mutant","termid":"PBO:0113161"}


id: PATO:0000554
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000554 cold sensitive (obsolete PATO:0000554)","termid":"PATO:0000554"}


id: MONDO:0033373
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 64","secondary_identifiers":["MEDGEN:1633501","DOID:0070375","OMIM:618004","UMLS:C4693899"],"synonyms":[{"name":"DEE64","type":"exact"},{"name":"EIEE64","type":"exact"},{"name":"developmental and epileptic encephalopathy 64","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 64","type":"exact"}],"termid":"MONDO:0033373","xrefs":{"Monarch":{"xref_id":"0033373"}}}


id: PBO:0055317
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 2745","termid":"PBO:0055317"}


id: RO:0002380
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x is a branching part of y if and only if x is part of y and x is connected directly or indirectly to the main stem of y","direct_ancestors":[{"relation_name":"is_a","term_name":"part_of","termid":"BFO:0000050"},{"relation_name":"is_a","term_name":"in_branching_relationship_with","termid":"RO:0002375"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"branching_part_of","termid":"RO:0002380"}


id: MONDO:0010512
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability, X-linked, syndromic, Bain type","secondary_identifiers":["UMLS:C4310814","MEDGEN:934781","GARD:13442","OMIM:300986","DOID:0070538","Orphanet:662198"],"synonyms":[{"name":"MRXSB","type":"exact"},{"name":"intellectual developmental disorder, X-linked, syndromic, Bain type, X-linked dominant","type":"exact"},{"name":"intellectual disability, X-linked, syndromic, Bain type","type":"exact"},{"name":"mental retardation, X-linked, syndromic, Bain type","type":"exact"}],"termid":"MONDO:0010512","xrefs":{"Monarch":{"xref_id":"0010512"}}}


id: PBO:0088792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA replication termination factor Rtf2","termid":"PBO:0088792"}


id: GO:0015653
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: glycine betaine(out) + H+(out) = glycine betaine(in) + H+(in).","definition_xrefs":["TC:2.A.15.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino-acid betaine transmembrane transporter activity","termid":"GO:0015199"},{"relation_name":"is_a","term_name":"quaternary ammonium group:proton symporter activity","termid":"GO:0015652"}],"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:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"glycine betaine:proton symporter activity","synonyms":[{"name":"glycine betaine:hydrogen symporter activity","type":"exact"}],"termid":"GO:0015653"}


id: PBO:0041619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium binding protein 5","termid":"PBO:0041619"}


id: MONDO:0019980
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bilateral renal hypoplasia is a form of renal hypoplasia, a renal developmental anomaly in which both kidneys are small and have a deficit in the number of nephrons present.","definition_xrefs":["Orphanet:97362"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal hypoplasia","termid":"MONDO:0019637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"renal hypoplasia, bilateral","secondary_identifiers":["SCTID:268232000","ICD10CM:Q60.4","MEDGEN:609099","GARD:19374","UMLS:C0431692"],"termid":"MONDO:0019980","xrefs":{"Monarch":{"xref_id":"0019980"}}}


id: PBO:0036168
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cytoplasmic_microtubule_nucleation_from_spindle_pole_body_during_mitotic_interphase","termid":"PBO:0036168"}


id: GO:0006695
data:
  {"annotated_genes":["SJAG_04018"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109004],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0045540"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of cholesterol, cholest-5-en-3 beta-ol, the principal sterol of vertebrates and the precursor of many steroids, including bile acids and steroid hormones.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cholesterol metabolic process","termid":"GO:0008203"},{"relation_name":"is_a","term_name":"sterol biosynthetic process","termid":"GO:0016126"},{"relation_name":"is_a","term_name":"secondary alcohol biosynthetic process","termid":"GO:1902653"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"cholesterol biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"cholesterol anabolism","type":"exact"},{"name":"cholesterol biosynthesis","type":"exact"},{"name":"cholesterol formation","type":"exact"},{"name":"cholesterol synthesis","type":"exact"}],"termid":"GO:0006695","terms_by_termid":{"GO:0045540":null}}


id: MONDO:1010575
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diabetes mellitus that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diabetes mellitus, non-human animal","termid":"MONDO:1010052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diabetes mellitus, domestic cat","secondary_identifiers":["OMIA:000279-9685"],"termid":"MONDO:1010575","xrefs":{"Monarch":{"xref_id":"1010575"}}}


id: FYPO:0000245
data:
  {"alleles_by_uniquename":{"SJAG_02527:allele-1":{"allele_type":"disruption","description":"RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage","gene_uniquename":"SJAG_02527","name":"lig4::KanMX6","uniquename":"SJAG_02527:allele-1"},"SJAG_04312:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04312","name":"pka1delta","uniquename":"SJAG_04312:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118617],"is_not":false,"summary":null,"term":"FYPO:0000245"},{"annotations":[118630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0005231"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a smaller than normal proportion of cells in the population remains viable after entering stationary phase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"},{"relation_name":"is_a","term_name":"cell population viability","termid":"FYPO:0002057"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02527":null,"SJAG_04312":null},"genotype_count":2,"genotypes_by_uniquename":{"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown":{"display_name":"lig4::KanMX6(RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage)[Knockdown]","display_uniquename":"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02527:allele-1","expression":"Knockdown"}]}]},"pka1delta":{"display_name":"pka1delta","display_uniquename":"pka1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04312:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"loss of viability in stationary phase","references_by_uniquename":{"PMID:27678009":null,"PMID:37233261":null},"single_locus_annotated_genes":["SJAG_04312","SJAG_02527"],"single_locus_genotype_uniquenames":["lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","pka1delta"],"synonyms":[{"name":"decreased chronological lifespan","type":"related"},{"name":"decreased viability in stationary phase","type":"exact"},{"name":"growth defect, required for stationary phase","type":"related"},{"name":"increased chronological cell aging","type":"related"},{"name":"loss of cell population viability in stationary phase","type":"exact"},{"name":"reduced viability in stationary phase","type":"exact"}],"termid":"FYPO:0000245","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0000245":null,"FYPO:0005231":null}}


id: PBO:0083115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA repair methyltransferase (6-O-methylguanine-DNA methylase); involved in protection against DNA alkylation damage","termid":"PBO:0083115"}


id: GO:0006555
data:
  {"annotated_genes":["SJAG_03659","SJAG_01404","SJAG_02689","SJAG_02293","SJAG_04953","SJAG_04459","SJAG_02972","SJAG_00309","SJAG_00234","SJAG_03141","SJAG_04425","SJAG_03671","SJAG_00395","SJAG_03556","SJAG_02290","SJAG_04042","SJAG_03712","SJAG_01466","SJAG_00419","SJAG_03152","SJAG_00881","SJAG_03881","SJAG_03614"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102568,109810,111835],"is_not":false,"summary":null,"term":"GO:0006555"},{"annotations":[105151,64848,109648,110231],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071266"},{"annotations":[99856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019280"},{"annotations":[113066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019279"},{"annotations":[94760,99190],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990355"},{"annotations":[111565,106165,91859,98211,88982,99842],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019509"},{"annotations":[89231,97606,95837,111110,97724,101913,110233,114918],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009086"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving methionine (2-amino-4-(methylthio)butanoic acid), a sulfur-containing, essential amino acid found in peptide linkage in proteins.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur amino acid metabolic process","termid":"GO:0000096"},{"relation_name":"is_a","term_name":"aspartate family amino acid metabolic process","termid":"GO:0009066"}],"gene_count":23,"genes_by_uniquename":{"SJAG_00234":null,"SJAG_00309":null,"SJAG_00395":null,"SJAG_00419":null,"SJAG_00881":null,"SJAG_01404":null,"SJAG_01466":null,"SJAG_02290":null,"SJAG_02293":null,"SJAG_02689":null,"SJAG_02972":null,"SJAG_03141":null,"SJAG_03152":null,"SJAG_03556":null,"SJAG_03614":null,"SJAG_03659":null,"SJAG_03671":null,"SJAG_03712":null,"SJAG_03881":null,"SJAG_04042":null,"SJAG_04425":null,"SJAG_04459":null,"SJAG_04953":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006520","GO:0006790"],"is_obsolete":false,"name":"methionine metabolic process","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["UM-BBD_pathwayID:met"],"synonyms":[{"name":"methionine and threonine metabolic process","type":"broad"},{"name":"methionine and threonine metabolism","type":"broad"},{"name":"methionine metabolism","type":"exact"}],"termid":"GO:0006555","terms_by_termid":{"GO:0006555":null,"GO:0009086":null,"GO:0019279":null,"GO:0019280":null,"GO:0019509":null,"GO:0071266":null,"GO:1990355":null}}


id: MOD:00028
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a source amino acid residue to L-tyrosine.","definition_xrefs":["PubMed:2190093","PubMed:6061414","PubMed:2542938","DeltaMass:0","PubMed:6692818","RESID:AA0019","PubMed:6120171","ChEBI:29975","PubMed:5550972"],"direct_ancestors":[{"relation_name":"is_a","term_name":"natural, standard, encoded residue","termid":"MOD:01441"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-tyrosine residue","synonyms":[{"name":"(2S)-2-amino-3-(4-hydoxyphenyl)propanoic acid","type":"exact"},{"name":"2-azanyl-3-(4-hydoxyphenyl)propanoic acid","type":"exact"},{"name":"L-tyrosine","type":"exact"},{"name":"Tyr","type":"exact"},{"name":"alpha-amino-beta-(para-hydroxyphenyl)propionic acid","type":"exact"},{"name":"p-tyrosine","type":"exact"},{"name":"para-hydroxyphenylalanine","type":"exact"}],"termid":"MOD:00028"}


id: PBO:0041214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1D nuclear receptor corepressor pseudogene 2","termid":"PBO:0041214"}


id: PBO:0059115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mov10 RISC complex RNA helicase","termid":"PBO:0059115"}


id: GO:0039524
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont inhibits or disrupts mRNA processing in its host. mRNA processing is the conversion of a primary mRNA transcript into one or more mature mRNA(s) prior to translation into polypeptide. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:bf","GOC:sp","PMID:16571812","VZ:903"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host gene expression","termid":"GO:0039656"}],"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 mRNA processing","synonyms":[{"name":"inhibition by virus of host mRNA processing","type":"narrow"},{"name":"inhibition of host mRNA processing","type":"exact"},{"name":"inhibition of host pre-mRNA processing by virus","type":"narrow"},{"name":"negative regulation of host mRNA processing","type":"broad"},{"name":"suppression by virus of host mRNA processing","type":"narrow"}],"termid":"GO:0039524"}


id: FYPO:0007219
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 acetylation of lysine at position 14 of histone H3 in regions containing protein-coding genes is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:31260531","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone H3-K14 acetylation during vegetative growth","termid":"FYPO:0003224"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0001320","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal histone H3-K14 acetylation at protein coding gene during vegetative growth","synonyms":[{"name":"normal histone H3-K14 acetylation at protein coding gene during mitotic cell cycle","type":"related"},{"name":"normal histone H3-K14 acetylation at protein-coding gene during vegetative growth","type":"exact"},{"name":"normal histone H3K14 acetylation at protein coding gene during vegetative growth","type":"exact"}],"termid":"FYPO:0007219"}


id: MONDO:0012763
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing child absence epilepsy or idiopathic generalized epilepsy, in which the cause of the disease is a mutation in the CACNA1H gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene","MONDO:patterns/inherited_susceptibility"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epilepsy, childhood absence, susceptibility to, 6","secondary_identifiers":["MEDGEN:440896","UMLS:C2749872","OMIM:611942"],"synonyms":[{"name":"CACNA1H childhood absence epilepsy","type":"related"},{"name":"ECA6","type":"exact"},{"name":"childhood absence epilepsy caused by mutation in CACNA1H","type":"related"},{"name":"epilepsy, childhood absence, susceptibility to, 6","type":"exact"},{"name":"epilepsy, childhood absence, susceptibility to, type 6","type":"exact"},{"name":"epilepsy, idiopathic generalized, susceptibility to, 6","type":"related"},{"name":"susceptibility to childhood absence epilepsy 6","type":"exact"}],"termid":"MONDO:0012763","xrefs":{"Monarch":{"xref_id":"0012763"}}}


id: PBO:0050336
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1pseudogene 38","termid":"PBO:0050336"}


id: PBO:0113408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Regulatory subunit of vacuolar transporter chaperone (VTC) complex; VTC complex is involved in membrane trafficking, vacuolar polyphosphate accumulation, microautophagy and non-autophagic vacuolar fusion; important regulator of substrate invagination from the vacuolar membrane; also binds mRNA; targeted to vacuole via AP-3 pathway; protein abundance increases in response to DNA replication stress","termid":"PBO:0113408"}


id: MONDO:0008097
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85110],"is_not":false,"summary":null,"term":"MONDO:0008097"}]},"cv_name":"mondo","definition":"Linear nevus sebaceous syndrome (LNSS) is characterized by the association of a large sebaceous nevus, usually appearing on the face or on the scalp, with a broad spectrum of abnormalities that may affect every organ system, including the central nervous system (brain neoplasms, hemimegalencephaly and lateral ventricle enlargement).","definition_xrefs":["Orphanet:2612"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hamartoma","termid":"MONDO:0006499"},{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"},{"relation_name":"is_a","term_name":"palpebral nevus","termid":"MONDO:0020179"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03453":null},"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":"linear nevus sebaceous syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NCIT:C4678","OMIM:163200","DOID:0111530","MEDGEN:1646345","NORD:1692","GARD:10291","UMLS:C4552097"],"synonyms":[{"name":"Epidermal Nevus syndrome, formerly","type":"related"},{"name":"JNP","type":"related"},{"name":"Jadassohn Nevus phakomatosis","type":"related"},{"name":"Jadassohn nevus phakomatosis","type":"related"},{"name":"Nevus Sebaceus Syndrome","type":"exact"},{"name":"Nevus sebaceous of Jadassohn","type":"exact"},{"name":"Nevus sebaceus of Jadassohn","type":"exact"},{"name":"Nevus sebaceus syndrome","type":"exact"},{"name":"SCHIMMELPENNING-FEUERSTEIN-MIMS syndrome","type":"related"},{"name":"SFM","type":"related"},{"name":"SFM syndrome","type":"related"},{"name":"Schimmelpenning Feuerstein Mims syndrome","type":"related"},{"name":"Schimmelpenning syndrome","type":"exact"},{"name":"Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic","type":"exact"},{"name":"Sfm syndrome","type":"related"},{"name":"Solomon syndrome","type":"exact"},{"name":"epidermal nevus syndrome","type":"related"},{"name":"linear sebaceous Nevus","type":"exact"},{"name":"linear sebaceous Nevus syndrome","type":"related"},{"name":"organoid Nevus","type":"exact"},{"name":"organoid Nevus phakomatosis","type":"related"},{"name":"organoid nevus phakomatosis","type":"related"},{"name":"organoid nevus syndrome","type":"exact"},{"name":"sebaceous Nevus syndrome, linear","type":"related"},{"name":"sebaceous nevus syndrome linear","type":"related"}],"termid":"MONDO:0008097","terms_by_termid":{"MONDO:0008097":null},"xrefs":{"Monarch":{"xref_id":"0008097"}}}


id: MONDO:0007693
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypertrichosis cubiti is a rare hair anomaly characterized by symmetrical, congenital or early-onset, bilateral hypertrychosis localized on the externsor surfaces of the upper extremities (especially the elbows). Short stature, or other abnormalities, such as developmental delay, facial anomalies and intellectual disability, may or may not be associated.","definition_xrefs":["Orphanet:2220"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertrichosis","termid":"MONDO:0019280"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"hypertrichosis cubiti-short stature syndrome","secondary_identifiers":["MedDRA:10068636","MEDGEN:870835","OMIM:139600","GARD:143","MESH:C535618","UMLS:C4025295"],"synonyms":[{"name":"MacDermot-Patton-Williams syndrome","type":"exact"},{"name":"hairy elbows","type":"exact"},{"name":"hairy elbows syndrome","type":"exact"},{"name":"hypertrichosis cubiti","type":"related"}],"termid":"MONDO:0007693","xrefs":{"Monarch":{"xref_id":"0007693"}}}


id: MONDO:0003740
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An overwhelming, irrational, and persistent fear of contracting Acquired Immune Deficiency Syndrome.","definition_xrefs":["NCIT:C35614"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nosophobia","termid":"MONDO:0000600"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AIDS phobia","secondary_identifiers":["UMLS:C0853870","MEDGEN:167692","DOID:603"],"synonyms":[{"name":"AIDS phobia","type":"exact"}],"termid":"MONDO:0003740","xrefs":{"Monarch":{"xref_id":"0003740"}}}


id: PBO:0058748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6872","termid":"PBO:0058748"}


id: PBO:0059780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 6","termid":"PBO:0059780"}


id: MONDO:0020543
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Malignant steroid cell tumor of the ovary, not otherwise specified is a rare malignant sex cord stromal tumor of ovary of unknown histological lineage, occurring in adult women, characterized, in most cases, by manifestations of androgen excess (hirsutism, hair loss, amenorrhea, or oligomenorrhea) and, occasionally, Cushing syndrome.","definition_xrefs":["Orphanet:99917"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant sex cord stromal tumor of ovary","termid":"MONDO:0018172"}],"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":"theca steroid-producing cell malignant tumor of ovary, not further specified","secondary_identifiers":["MEDGEN:904268","UMLS:C4274494","GARD:19708"],"synonyms":[{"name":"theca (steroid-producing) cell cancer, not further specified","type":"exact"}],"termid":"MONDO:0020543","xrefs":{"Monarch":{"xref_id":"0020543"}}}


id: GO:0080036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cytokinin signaling.","definition_xrefs":["GOC:dhl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"regulates","term_name":"cytokinin-activated signaling pathway","termid":"GO:0009736"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of cytokinin-activated signaling pathway","synonyms":[{"name":"regulation of cytokinin mediated signaling pathway","type":"related"},{"name":"regulation of cytokinin mediated signalling","type":"exact"}],"termid":"GO:0080036"}


id: MONDO:0001890
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tooth erosion, non-bacterial that involves the dental pulp.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tooth erosion, non-bacterial","termid":"MONDO:0002325"},{"relation_name":"is_a","term_name":"dental pulp disorder","termid":"MONDO:0003394"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulp erosion","secondary_identifiers":["DOID:14140","ICD9:521.33","UMLS:C1456163","MEDGEN:1843466"],"synonyms":[{"name":"dental pulp tooth erosion, non-bacterial","type":"exact"},{"name":"tooth erosion, non-bacterial of dental pulp","type":"exact"}],"termid":"MONDO:0001890","xrefs":{"Monarch":{"xref_id":"0001890"}}}


id: FYPO:0001097
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 amitrole. Cells stop growing (and may die) at a concentration of amitrole that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002683","FYPO:0005447","FYPO:0001985","FYPO:0000139","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to amitrole","synonyms":[{"name":"hypersensitive to amitrole","type":"exact"},{"name":"sensitive to 3-amino-1,2,4-triazole","type":"exact"},{"name":"sensitive to amitrole during mitotic cell cycle","type":"related"},{"name":"sensitive to amitrole during vegetative growth","type":"exact"}],"termid":"FYPO:0001097"}


id: GO:0045191
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of isotype switching.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA recombination","termid":"GO:0000018"},{"relation_name":"is_a","term_name":"regulation of immunoglobulin production","termid":"GO:0002637"},{"relation_name":"is_a","term_name":"regulation of immunoglobulin mediated immune response","termid":"GO:0002889"},{"relation_name":"is_a","term_name":"regulation of B cell activation","termid":"GO:0050864"},{"relation_name":"regulates","term_name":"isotype switching","termid":"GO:0045190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0006310","GO:0006259"],"is_obsolete":false,"name":"regulation of isotype switching","synonyms":[{"name":"regulation of class switch recombination","type":"exact"},{"name":"regulation of class switching","type":"exact"},{"name":"regulation of isotype switch recombination","type":"exact"}],"termid":"GO:0045191"}


id: MONDO:0014082
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"non-SCID combined immunodeficiency","termid":"MONDO:0018814"},{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"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":"cryptosporidiosis-chronic cholangitis-liver disease syndrome","secondary_identifiers":["UMLS:C3554687","MEDGEN:767601","OMIM:615207","Orphanet:357329","DOID:0111982","GARD:17550"],"synonyms":[{"name":"IL21R immunodeficiency","type":"related"},{"name":"IMD56","type":"related"},{"name":"cryptosporidiosis-chronic cholangitis-liver disease syndrome","type":"exact"},{"name":"immunodeficiency 56","type":"related"}],"termid":"MONDO:0014082","xrefs":{"Monarch":{"xref_id":"0014082"}}}


id: PBO:0029687
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_level_of_iron_ion_starvation-repressed_proteins","termid":"PBO:0029687"}


id: RO:0003305
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relationship between an entity (e.g. a genotype, genetic variation, chemical, or environmental exposure) and a condition (a phenotype or disease), where the entity influences the severity with which a condition manifests in an individual.","direct_ancestors":[{"relation_name":"is_a","term_name":"contributes_to_condition","termid":"RO:0003304"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"contributes_to_severity_of_condition","termid":"RO:0003305"}


id: FYPO:0000239
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 transcription from a promoter that contains one or more MluI cell cycle box factor elements (MCBs) occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased transcription during vegetative growth","termid":"FYPO:0000780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000294","FYPO:0006551","FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased transcription from MCB promoter","synonyms":[{"name":"expression of MBF target genes increased","type":"related"},{"name":"increased transcription from MCB promoter during mitotic cell cycle","type":"related"},{"name":"increased transcription from MCB promoter during vegetative growth","type":"exact"}],"termid":"FYPO:0000239"}


id: MONDO:1010530
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cleft palate that occurs in cattle.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cleft palate, non-human animal","termid":"MONDO:1010037"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cleft palate, cattle","secondary_identifiers":["OMIA:000197-9913"],"termid":"MONDO:1010530","xrefs":{"Monarch":{"xref_id":"1010530"}}}


id: PBO:0000274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pig-V, dolichyl-phosphate-mannose-glycolipid alpha-mannosyltransferase (predicted)","termid":"PBO:0000274"}


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


id: GO:0072433
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of events in which information about damage to DNA is received and converted into a molecular signal, contributing to a mitotic G2/M transition DNA damage checkpoint.","definition_xrefs":["GOC:mtg_cell_cycle"],"gene_count":0,"genotype_count":0,"name":"obsolete detection of DNA damage stimulus involved in mitotic G2 DNA damage checkpoint (obsolete GO:0072433)","synonyms":[{"name":"G2/M transition DNA damage checkpoint sensor mechanism","type":"related"},{"name":"detection of DNA damage stimulus involved in G2 DNA damage checkpoint","type":"related"},{"name":"detection of DNA damage stimulus involved in G2/M transition DNA damage checkpoint","type":"related"},{"name":"detection of DNA damage stimulus involved in mitotic G2/M transition DNA damage checkpoint","type":"exact"},{"name":"mitotic G2/M transition DNA damage checkpoint sensor mechanism","type":"related"},{"name":"mitotic G2/M transition DNA damage checkpoint sensor process","type":"related"},{"name":"sensing involved in G2/M transition DNA damage checkpoint","type":"related"},{"name":"sensing involved in mitotic G2/M transition DNA damage checkpoint","type":"related"}],"termid":"GO:0072433"}


id: MONDO:0017478
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"amelia of upper limb","termid":"MONDO:0017437"}],"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":"amelia of upper limb, unilateral","secondary_identifiers":["icd11.foundation:790781203","Orphanet:295053"],"termid":"MONDO:0017478","xrefs":{"Monarch":{"xref_id":"0017478"}}}


id: PATO:0002028
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An osmolality which is relatively low.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"osmolality","termid":"PATO:0002027"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased osmolality","synonyms":[{"name":"low osmolality","type":"exact"}],"termid":"PATO:0002028"}


id: MOD:01348
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue to an O-hexosyl-L-threonine.","definition_xrefs":["PubMed:8597590","PubMed:15279557","Unimod:41#T"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-glycosyl-L-threonine","termid":"MOD:00005"},{"relation_name":"is_a","term_name":"hexosylated residue","termid":"MOD:00434"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"O-hexosylated threonine","synonyms":[{"name":"Hex","type":"related"},{"name":"Hexose","type":"related"}],"termid":"MOD:01348"}


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


id: GO:0050563
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + CoA + trans-ferulate = (E)-feruloyl-CoA + ADP + phosphate. ADP + phosphate or AMP + diphosphate may be formed in this reaction.","definition_xrefs":["EC:6.2.1.34","PMID:22649270"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CoA-ligase activity","termid":"GO:0016405"}],"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:0016874"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016874"],"is_obsolete":false,"name":"trans-feruloyl-CoA synthase activity","secondary_identifiers":["GO:0106287","MetaCyc:6.2.1.34-RXN"],"synonyms":[{"name":"ferulate-CoA ligase activity","type":"related"},{"name":"trans-ferulate:CoASH ligase (ATP-hydrolysing)","type":"related"},{"name":"trans-feruloyl-CoA synthetase activity","type":"related"}],"termid":"GO:0050563"}


id: PBO:0088626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dubious, SPNCRNA.1420 syntenic position","termid":"PBO:0088626"}


id: FYPO:0001185
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of an alpha-glucosidase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal alpha-glucosidase activity","termid":"FYPO:0001183"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000654","FYPO:0000652","FYPO:0001985","FYPO:0000707"],"is_obsolete":false,"name":"decreased alpha-glucosidase activity","synonyms":[{"name":"reduced alpha-glucosidase activity","type":"exact"}],"termid":"FYPO:0001185"}


id: GO:0007495
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of cell-cell signaling between visceral mesoderm cells and endoderm cells that is involved in the differentiation of cells in the midgut.","definition_xrefs":["GOC:dph","GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell signaling","termid":"GO:0007267"},{"relation_name":"part_of","term_name":"midgut development","termid":"GO:0007494"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"visceral mesoderm-endoderm interaction involved in midgut development","synonyms":[{"name":"visceral mesoderm/endoderm interaction","type":"exact"}],"termid":"GO:0007495"}


id: FYECO:0000191
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which biotin 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":"+ biotin","termid":"FYECO:0000191"}


id: GO:0061595
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction 6-deoxy-6-sulfofructose-1-phosphate = 3-sulfolactaldehyde + dihydroxyacetone phosphate.","definition_xrefs":["PMID:24463506"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde-lyase activity","termid":"GO:0016832"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"6-deoxy-6-sulfofructose-1-phosphate aldolase activity","termid":"GO:0061595"}


id: PBO:0078048
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 38","termid":"PBO:0078048"}


id: MONDO:0800316
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete contiguous ABCD1/DXS1375E deletion syndrome (obsolete MONDO:0800316)","termid":"MONDO:0800316","xrefs":{"Monarch":{"xref_id":"0800316"}}}


id: PBO:0073836
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC7A11 antisense RNA 1","termid":"PBO:0073836"}


id: PATO:0005003
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's resembling the form of a paddle.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paddle shaped","termid":"PATO:0005003"}


id: MOD:01670
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to N6-methyl-L-lysine.","definition_xrefs":["PubMed:16091367","PubMed:17260957","PubMed:16195462","RESID:AA0524"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"},{"relation_name":"is_a","term_name":"halogenated lysine","termid":"MOD:01672"},{"relation_name":"is_a","term_name":"monochlorinated residue","termid":"MOD:01911"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N6-chloro-L-lysine","synonyms":[{"name":"(2S)-2-amino-6-(chloroamino)hexanoic acid","type":"exact"},{"name":"N(zeta)-chlorolysine","type":"exact"},{"name":"N6-chloro-L-lysine","type":"exact"},{"name":"N6ClLys","type":"exact"},{"name":"epsilon-chlorolysine","type":"exact"},{"name":"lysine chloramine","type":"exact"}],"termid":"MOD:01670"}


id: PBO:0030223
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-fragmented_spindle_pole_body","termid":"PBO:0030223"}


id: PBO:0110468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain 40 molecular ruler complex subunit","termid":"PBO:0110468"}


id: PBO:0015266
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glucosidase 2 Beta Subunit","termid":"PBO:0015266"}


id: GO:0097159
data:
  {"annotated_genes":["SJAG_00653","SJAG_03703","SJAG_03916","SJAG_02311","SJAG_03850","SJAG_02200","SJAG_03538","SJAG_03592","SJAG_03927","SJAG_03257","SJAG_02390","SJAG_02720","SJAG_04282","SJAG_00243","SJAG_02381","SJAG_00412","SJAG_01708","SJAG_01157","SJAG_04920","SJAG_05249","SJAG_02637","SJAG_02531","SJAG_04043","SJAG_02906","SJAG_01249","SJAG_04949","SJAG_04145","SJAG_00164","SJAG_03945","SJAG_02194","SJAG_03179","SJAG_01062","SJAG_00579","SJAG_03174","SJAG_06608","SJAG_04064","SJAG_02994","SJAG_03188","SJAG_04387","SJAG_03706","SJAG_04597","SJAG_04587","SJAG_00516","SJAG_03903","SJAG_02656","SJAG_03855","SJAG_03751","SJAG_04695","SJAG_01471","SJAG_00544","SJAG_02493","SJAG_04457","SJAG_00898","SJAG_04599","SJAG_01234","SJAG_01314","SJAG_03438","SJAG_01616","SJAG_02575","SJAG_02456","SJAG_00430","SJAG_00809","SJAG_03036","SJAG_02563","SJAG_03660","SJAG_02736","SJAG_04389","SJAG_02212","SJAG_03572","SJAG_00124","SJAG_02977","SJAG_04081","SJAG_03128","SJAG_03210","SJAG_01201","SJAG_05248","SJAG_04678","SJAG_00765","SJAG_03011","SJAG_03702","SJAG_01182","SJAG_01695","SJAG_01487","SJAG_02535","SJAG_03698","SJAG_04036","SJAG_04655","SJAG_01807","SJAG_01419","SJAG_05332","SJAG_01215","SJAG_04823","SJAG_00330","SJAG_03898","SJAG_01944","SJAG_02602","SJAG_01587","SJAG_02794","SJAG_03286","SJAG_02696","SJAG_02698","SJAG_04712","SJAG_00833","SJAG_00634","SJAG_03469","SJAG_03145","SJAG_16457","SJAG_00881","SJAG_02472","SJAG_00886","SJAG_04573","SJAG_04745","SJAG_01262","SJAG_01332","SJAG_03529","SJAG_01870","SJAG_03017","SJAG_02460","SJAG_01152","SJAG_03014","SJAG_02904","SJAG_03722","SJAG_04537","SJAG_00402","SJAG_00577","SJAG_03156","SJAG_01669","SJAG_03069","SJAG_03676","SJAG_01829","SJAG_02431","SJAG_00996","SJAG_00488","SJAG_02606","SJAG_01181","SJAG_03946","SJAG_04981","SJAG_03132","SJAG_00106","SJAG_01648","SJAG_02206","SJAG_04845","SJAG_02262","SJAG_04521","SJAG_00889","SJAG_02352","SJAG_03659","SJAG_00863","SJAG_06449","SJAG_04206","SJAG_03720","SJAG_02722","SJAG_05030","SJAG_05239","SJAG_00465","SJAG_03047","SJAG_02808","SJAG_00583","SJAG_01407","SJAG_00304","SJAG_03948","SJAG_01918","SJAG_00783","SJAG_01529","SJAG_03237","SJAG_05006","SJAG_01400","SJAG_02364","SJAG_02183","SJAG_00541","SJAG_00861","SJAG_03007","SJAG_03785","SJAG_04766","SJAG_00504","SJAG_03735","SJAG_01307","SJAG_02017","SJAG_01352","SJAG_02336","SJAG_00623","SJAG_01046","SJAG_01296","SJAG_03501","SJAG_01186","SJAG_03708","SJAG_06597","SJAG_01671","SJAG_04381","SJAG_03905","SJAG_02149","SJAG_05979","SJAG_04622","SJAG_01351","SJAG_03485","SJAG_01049","SJAG_00234","SJAG_00045","SJAG_05014","SJAG_04310","SJAG_00503","SJAG_04324","SJAG_04988","SJAG_00939","SJAG_05018","SJAG_02334","SJAG_01343","SJAG_00225","SJAG_02818","SJAG_04589","SJAG_02628","SJAG_03068","SJAG_04409","SJAG_03788","SJAG_04094","SJAG_00539","SJAG_00757","SJAG_03475","SJAG_02135","SJAG_01659","SJAG_04117","SJAG_06642","SJAG_03161","SJAG_03144","SJAG_04754","SJAG_06576","SJAG_03613","SJAG_05025","SJAG_02326","SJAG_05271","SJAG_01408","SJAG_03355","SJAG_02513","SJAG_01677","SJAG_01010","SJAG_02394","SJAG_01852","SJAG_03539","SJAG_05019","SJAG_04175","SJAG_00073","SJAG_02298","SJAG_03384","SJAG_01759","SJAG_04114","SJAG_03409","SJAG_00941","SJAG_01235","SJAG_00555","SJAG_04970","SJAG_00713","SJAG_01164","SJAG_00604","SJAG_02595","SJAG_02236","SJAG_00845","SJAG_03383","SJAG_03872","SJAG_02618","SJAG_02250","SJAG_04508","SJAG_03472","SJAG_00802","SJAG_04421","SJAG_03954","SJAG_01379","SJAG_03345","SJAG_01909","SJAG_01650","SJAG_01929","SJAG_00178","SJAG_03937","SJAG_01198","SJAG_03984","SJAG_05343","SJAG_04022","SJAG_01694","SJAG_00421","SJAG_00741","SJAG_03952","SJAG_01436","SJAG_01601","SJAG_00054","SJAG_04018","SJAG_03092","SJAG_04210","SJAG_00987","SJAG_04640","SJAG_16460","SJAG_01518","SJAG_04092","SJAG_04224","SJAG_00364","SJAG_00031","SJAG_04663","SJAG_03141","SJAG_03578","SJAG_00669","SJAG_01873","SJAG_00768","SJAG_02667","SJAG_01696","SJAG_03987","SJAG_03096","SJAG_04791","SJAG_02254","SJAG_03583","SJAG_04611","SJAG_00887","SJAG_03061","SJAG_01243","SJAG_05193","SJAG_05353","SJAG_01740","SJAG_01377","SJAG_04069","SJAG_04126","SJAG_02420","SJAG_03354","SJAG_03570","SJAG_02022","SJAG_00931","SJAG_02597","SJAG_03160","SJAG_03629","SJAG_02506","SJAG_02748","SJAG_00597","SJAG_03674","SJAG_03923","SJAG_02226","SJAG_05153","SJAG_02313","SJAG_01595","SJAG_02895","SJAG_16455","SJAG_02723","SJAG_02406","SJAG_03125","SJAG_01764","SJAG_01378","SJAG_03077","SJAG_02556","SJAG_04762","SJAG_00884","SJAG_00208","SJAG_01119","SJAG_02243","SJAG_02036","SJAG_02061","SJAG_03410","SJAG_02384","SJAG_02589","SJAG_03994","SJAG_04157","SJAG_01644","SJAG_03434","SJAG_03584","SJAG_01179","SJAG_02923","SJAG_00150","SJAG_00356","SJAG_00992","SJAG_00432","SJAG_03122","SJAG_01074","SJAG_01082","SJAG_03995","SJAG_03451","SJAG_03284","SJAG_00563","SJAG_02104","SJAG_00457","SJAG_00037","SJAG_00034","SJAG_04199","SJAG_02828","SJAG_04743","SJAG_00166","SJAG_01495","SJAG_04042","SJAG_01070","SJAG_02399","SJAG_00359","SJAG_00410","SJAG_02340","SJAG_00662","SJAG_00424","SJAG_01831","SJAG_02604","SJAG_04230","SJAG_04181","SJAG_01521","SJAG_04475","SJAG_04693","SJAG_01268","SJAG_04847","SJAG_03961","SJAG_02878","SJAG_00169","SJAG_00083","SJAG_04065","SJAG_03289","SJAG_03689","SJAG_00027","SJAG_02039","SJAG_03433","SJAG_03780","SJAG_03129","SJAG_01076","SJAG_01855","SJAG_02995","SJAG_01953","SJAG_00114","SJAG_03197","SJAG_00704","SJAG_02813","SJAG_05333","SJAG_01919","SJAG_03249","SJAG_05009","SJAG_04281","SJAG_05000","SJAG_01766","SJAG_00300","SJAG_00390","SJAG_04032","SJAG_02374","SJAG_01956","SJAG_02530","SJAG_04840","SJAG_04816","SJAG_01458","SJAG_00988","SJAG_16456","SJAG_03457","SJAG_04855","SJAG_04574","SJAG_01469","SJAG_03453","SJAG_02747","SJAG_04842","SJAG_02249","SJAG_00384","SJAG_04486","SJAG_04362","SJAG_02148","SJAG_04584","SJAG_01447","SJAG_01191","SJAG_01410","SJAG_01441","SJAG_00392","SJAG_00231","SJAG_01087","SJAG_03496","SJAG_03388","SJAG_03071","SJAG_01771","SJAG_00247","SJAG_03473","SJAG_01907","SJAG_01813","SJAG_04490","SJAG_03939","SJAG_04414","SJAG_01339","SJAG_04261","SJAG_04320","SJAG_04908","SJAG_05313","SJAG_04188","SJAG_02280","SJAG_00067","SJAG_01874","SJAG_03545","SJAG_01511","SJAG_00986","SJAG_01724","SJAG_00325","SJAG_02348","SJAG_05022","SJAG_03942","SJAG_04380","SJAG_04810","SJAG_02292","SJAG_02359","SJAG_01173","SJAG_03734","SJAG_01762","SJAG_04351","SJAG_03918","SJAG_02825","SJAG_00335","SJAG_04760","SJAG_01832","SJAG_03362","SJAG_02791","SJAG_00663","SJAG_00984","SJAG_02858","SJAG_04825","SJAG_04339","SJAG_01474","SJAG_02950","SJAG_01988","SJAG_00853","SJAG_01684","SJAG_00315","SJAG_01075","SJAG_03585","SJAG_00759","SJAG_00660","SJAG_00912","SJAG_03519","SJAG_00338","SJAG_03654","SJAG_04283","SJAG_02447","SJAG_02601","SJAG_03671","SJAG_02362","SJAG_04993","SJAG_02688","SJAG_01391","SJAG_02415","SJAG_04610","SJAG_02015","SJAG_02335","SJAG_02517","SJAG_01863","SJAG_01500","SJAG_04744","SJAG_04039","SJAG_00599","SJAG_00153","SJAG_01916","SJAG_02185","SJAG_03887","SJAG_04682","SJAG_02498","SJAG_04461","SJAG_02622","SJAG_04318","SJAG_04342","SJAG_04213","SJAG_02294","SJAG_00486","SJAG_00670","SJAG_02596","SJAG_01019","SJAG_04373","SJAG_02444","SJAG_01622","SJAG_04009","SJAG_01903","SJAG_01137","SJAG_01024","SJAG_04666","SJAG_03115","SJAG_01840","SJAG_03497","SJAG_01366","SJAG_03922","SJAG_00502","SJAG_02824","SJAG_02680","SJAG_01816","SJAG_01194","SJAG_02367","SJAG_04108","SJAG_00888","SJAG_02752","SJAG_01881","SJAG_02738","SJAG_03461","SJAG_01364","SJAG_00427","SJAG_04761","SJAG_02608","SJAG_04917","SJAG_00531","SJAG_00329","SJAG_01254","SJAG_01851","SJAG_01329","SJAG_01577","SJAG_00322","SJAG_02073","SJAG_00425","SJAG_02097","SJAG_00136","SJAG_01176","SJAG_01084","SJAG_04477","SJAG_02261","SJAG_04187","SJAG_00855","SJAG_02815","SJAG_04276","SJAG_01704","SJAG_03213","SJAG_03557","SJAG_04738","SJAG_02385","SJAG_01731","SJAG_02207","SJAG_03594","SJAG_02469","SJAG_05288","SJAG_02304","SJAG_00637","SJAG_02978","SJAG_04549","SJAG_01064","SJAG_03223","SJAG_03241","SJAG_01478","SJAG_00069","SJAG_00766","SJAG_02342","SJAG_01067","SJAG_04265","SJAG_04160","SJAG_04552","SJAG_04150","SJAG_01741","SJAG_00901","SJAG_02323","SJAG_01522","SJAG_00619","SJAG_04465","SJAG_05290","SJAG_02554","SJAG_02048","SJAG_04418","SJAG_03853","SJAG_01611","SJAG_05020","SJAG_00993","SJAG_03290","SJAG_04407","SJAG_04511","SJAG_04163","SJAG_01217","SJAG_04256","SJAG_02640","SJAG_04753","SJAG_02713","SJAG_04270","SJAG_02350","SJAG_00686","SJAG_02457","SJAG_00203","SJAG_05280","SJAG_05276","SJAG_04544","SJAG_00949","SJAG_05209","SJAG_01000","SJAG_02052","SJAG_00004","SJAG_03147","SJAG_04856","SJAG_03626","SJAG_04203","SJAG_01002","SJAG_00983","SJAG_01354","SJAG_01197","SJAG_03226","SJAG_03053","SJAG_04280","SJAG_03363","SJAG_04495","SJAG_04405","SJAG_04006","SJAG_04767","SJAG_03567","SJAG_00729","SJAG_00897","SJAG_03879","SJAG_00851","SJAG_02741","SJAG_02889","SJAG_02205","SJAG_05010","SJAG_01877","SJAG_01315","SJAG_04998","SJAG_02897","SJAG_03798","SJAG_01797","SJAG_04388","SJAG_01668","SJAG_02558","SJAG_01282","SJAG_01615","SJAG_02187","SJAG_03679","SJAG_03209","SJAG_04974","SJAG_00256","SJAG_01373","SJAG_00265","SJAG_01954","SJAG_00938","SJAG_02545","SJAG_04186","SJAG_01558","SJAG_02600","SJAG_02697","SJAG_02305","SJAG_05339","SJAG_03915","SJAG_02607","SJAG_00527","SJAG_01221","SJAG_05186","SJAG_00409","SJAG_00370","SJAG_03441","SJAG_04934","SJAG_01376","SJAG_02605","SJAG_03214","SJAG_01200","SJAG_02180","SJAG_03137","SJAG_03232","SJAG_03423","SJAG_03157","SJAG_04334","SJAG_00930","SJAG_03301","SJAG_05015","SJAG_04410","SJAG_04257","SJAG_00342","SJAG_01129","SJAG_05372","SJAG_02686","SJAG_02827","SJAG_03944","SJAG_04877","SJAG_01081","SJAG_04700","SJAG_04366","SJAG_04669","SJAG_02838","SJAG_00436","SJAG_00659","SJAG_00639","SJAG_00698","SJAG_05253","SJAG_04692","SJAG_06586","SJAG_03941","SJAG_00748","SJAG_02508","SJAG_02279","SJAG_02712","SJAG_04190","SJAG_02734","SJAG_04689","SJAG_00559","SJAG_00896","SJAG_02307","SJAG_03028","SJAG_04383","SJAG_02429","SJAG_04749","SJAG_02991","SJAG_01080","SJAG_02800","SJAG_01245","SJAG_00871","SJAG_00358","SJAG_05230","SJAG_01530","SJAG_04918","SJAG_01172","SJAG_02599","SJAG_03140","SJAG_00378","SJAG_01769","SJAG_05304","SJAG_01041","SJAG_00249","SJAG_05240","SJAG_05218","SJAG_02083","SJAG_04940","SJAG_04650","SJAG_00657","SJAG_02785","SJAG_01608","SJAG_00879","SJAG_00344","SJAG_04657","SJAG_02037","SJAG_04857","SJAG_01654","SJAG_04478","SJAG_02627","SJAG_00198","SJAG_03709","SJAG_03967","SJAG_04586","SJAG_00661","SJAG_04004","SJAG_04862","SJAG_02890","SJAG_02521","SJAG_01818","SJAG_02760","SJAG_06599","SJAG_03341","SJAG_02796","SJAG_02043","SJAG_02569","SJAG_02658","SJAG_03959","SJAG_04995","SJAG_04524","SJAG_05187","SJAG_05340","SJAG_04670","SJAG_01412","SJAG_MIT04","SJAG_02400","SJAG_01745","SJAG_01830","SJAG_00294","SJAG_01277","SJAG_02810","SJAG_04360","SJAG_03486","SJAG_01643","SJAG_00163","SJAG_04287","SJAG_04911","SJAG_02610","SJAG_00678","SJAG_04268","SJAG_04118","SJAG_02829","SJAG_02297","SJAG_01938","SJAG_04183","SJAG_04813","SJAG_00640","SJAG_02690","SJAG_00337","SJAG_01311","SJAG_02835","SJAG_00253","SJAG_00307","SJAG_00269","SJAG_02360","SJAG_01575","SJAG_03811","SJAG_02468","SJAG_02288","SJAG_04527","SJAG_05694","SJAG_00195","SJAG_00336","SJAG_01620","SJAG_03919","SJAG_03436","SJAG_00921","SJAG_00963","SJAG_04079","SJAG_03275","SJAG_00474","SJAG_05012","SJAG_02730","SJAG_05301","SJAG_04019","SJAG_04562","SJAG_03342","SJAG_04782","SJAG_01240","SJAG_01026","SJAG_01609","SJAG_00673","SJAG_02775","SJAG_00399","SJAG_03877","SJAG_05194","SJAG_04312","SJAG_04980","SJAG_02652","SJAG_00566","SJAG_03852","SJAG_03252","SJAG_01571","SJAG_05242","SJAG_04898","SJAG_04258","SJAG_01438","SJAG_02922","SJAG_03113","SJAG_01827","SJAG_04054","SJAG_02894","SJAG_04030","SJAG_01132","SJAG_02421","SJAG_03312","SJAG_05231","SJAG_04372","SJAG_02138","SJAG_04839","SJAG_04959","SJAG_04680","SJAG_03543","SJAG_01402","SJAG_00513","SJAG_03665","SJAG_00355","SJAG_01713","SJAG_03055","SJAG_01222","SJAG_01169","SJAG_00779","SJAG_03097","SJAG_02564","SJAG_03799","SJAG_04394","SJAG_01937","SJAG_02398","SJAG_00701","SJAG_02615","SJAG_01698","SJAG_00039","SJAG_00790","SJAG_03897","SJAG_00572","SJAG_04233","SJAG_03276","SJAG_02074","SJAG_01380","SJAG_00470","SJAG_04509","SJAG_00500","SJAG_03745","SJAG_03411","SJAG_02331","SJAG_05265","SJAG_02822","SJAG_02908","SJAG_03688","SJAG_01489","SJAG_03217","SJAG_02687","SJAG_03996","SJAG_04950","SJAG_03534","SJAG_00682","SJAG_00830","SJAG_01839","SJAG_03696","SJAG_02458","SJAG_04865","SJAG_00801","SJAG_00813","SJAG_05257","SJAG_04178","SJAG_00403","SJAG_04946","SJAG_02079","SJAG_03747","SJAG_00235","SJAG_04277","SJAG_00649","SJAG_00259","SJAG_04914","SJAG_02171","SJAG_02465","SJAG_01942","SJAG_01327","SJAG_02082","SJAG_02252","SJAG_03346","SJAG_00272","SJAG_06621","SJAG_00564","SJAG_00226","SJAG_02684","SJAG_03369","SJAG_02611","SJAG_04492","SJAG_00773","SJAG_02382","SJAG_04156","SJAG_03277","SJAG_04882","SJAG_03495","SJAG_00609","SJAG_05173","SJAG_01664","SJAG_MIT07","SJAG_04755","SJAG_02982","SJAG_01323","SJAG_04530","SJAG_01047","SJAG_01791","SJAG_00964","SJAG_03336","SJAG_04824","SJAG_01420","SJAG_03120","SJAG_03712","SJAG_00707","SJAG_00545","SJAG_00958","SJAG_04285","SJAG_00281","SJAG_03236","SJAG_04435","SJAG_00815","SJAG_04671","SJAG_01718","SJAG_00302","SJAG_00906","SJAG_00118","SJAG_01534","SJAG_00628","SJAG_00664","SJAG_03876","SJAG_02702","SJAG_03376","SJAG_02233","SJAG_02353","SJAG_03533","SJAG_01930","SJAG_04497","SJAG_02840","SJAG_03854","SJAG_00097","SJAG_01008","SJAG_01440","SJAG_04551","SJAG_01131","SJAG_02527","SJAG_04919","SJAG_02571","SJAG_00950","SJAG_04408","SJAG_00582","SJAG_04612","SJAG_01568","SJAG_03909","SJAG_03102","SJAG_04849","SJAG_02489","SJAG_03861","SJAG_01825","SJAG_00495","SJAG_01252","SJAG_02377","SJAG_02024","SJAG_03896","SJAG_04084","SJAG_01787","SJAG_01444","SJAG_02477","SJAG_02372","SJAG_00792","SJAG_02464","SJAG_04891","SJAG_03070","SJAG_04874","SJAG_02945","SJAG_00353","SJAG_04894","SJAG_05003","SJAG_03732","SJAG_02392","SJAG_04343","SJAG_02199","SJAG_03449","SJAG_01468","SJAG_00638","SJAG_04665","SJAG_02926","SJAG_01432","SJAG_03152","SJAG_00636","SJAG_04056","SJAG_00533","SJAG_00650","SJAG_03950","SJAG_03796","SJAG_00769","SJAG_00381","SJAG_00972","SJAG_03143","SJAG_00313","SJAG_04747","SJAG_01456","SJAG_01452","SJAG_01964","SJAG_02025","SJAG_04566","SJAG_01576","SJAG_03666","SJAG_00690","SJAG_02058","SJAG_03042","SJAG_04249","SJAG_00749","SJAG_00706","SJAG_00882","SJAG_01625","SJAG_03547","SJAG_01579","SJAG_03498","SJAG_02812","SJAG_03240","SJAG_02725","SJAG_01532","SJAG_05214","SJAG_01789","SJAG_02417","SJAG_04066","SJAG_02031","SJAG_01910","SJAG_04777","SJAG_01837","SJAG_03982","SJAG_00712","SJAG_00159","SJAG_00147","SJAG_04003","SJAG_03983","SJAG_00943","SJAG_00332","SJAG_02496","SJAG_05247","SJAG_00629","SJAG_00605","SJAG_03479","SJAG_02378","SJAG_01765","SJAG_03603","SJAG_01777","SJAG_04686","SJAG_01618","SJAG_04125","SJAG_04752","SJAG_00386","SJAG_02312","SJAG_02376","SJAG_02176","SJAG_00266","SJAG_01344","SJAG_01322","SJAG_01546","SJAG_01263","SJAG_01887","SJAG_02952","SJAG_04052","SJAG_01722","SJAG_01712","SJAG_02619","SJAG_05221","SJAG_03460","SJAG_03932","SJAG_02038","SJAG_02299","SJAG_04424","SJAG_02018","SJAG_02101","SJAG_02242","SJAG_03718","SJAG_03320","SJAG_03476","SJAG_03484","SJAG_02872","SJAG_03906","SJAG_02638","SJAG_01843","SJAG_02366","SJAG_03306","SJAG_02156","SJAG_00220","SJAG_02709","SJAG_04469","SJAG_02997","SJAG_03622","SJAG_03846","SJAG_00956","SJAG_03682","SJAG_00319","SJAG_00507","SJAG_02196","SJAG_01882","SJAG_03750","SJAG_00446","SJAG_05024","SJAG_00692","SJAG_00744","SJAG_04635","SJAG_03326","SJAG_01162","SJAG_03929","SJAG_02704","SJAG_01435","SJAG_04480","SJAG_01015","SJAG_00466","SJAG_04482","SJAG_02189","SJAG_00464","SJAG_02721","SJAG_04000","SJAG_04470","SJAG_01358","SJAG_04942","SJAG_04818","SJAG_03374","SJAG_03048","SJAG_02375","SJAG_02856","SJAG_00731","SJAG_04385","SJAG_03866","SJAG_03840","SJAG_00186","SJAG_01387","SJAG_01819","SJAG_02300","SJAG_00995","SJAG_04089","SJAG_05322","SJAG_02573","SJAG_03911","SJAG_03883","SJAG_00633","SJAG_00103","SJAG_MIT06","SJAG_04038","SJAG_04189","SJAG_00168","SJAG_02142","SJAG_02879","SJAG_02239","SJAG_02182","SJAG_00854","SJAG_02286","SJAG_00308","SJAG_02042","SJAG_03828","SJAG_02861","SJAG_03206","SJAG_02758","SJAG_02287","SJAG_04214","SJAG_02661","SJAG_04367","SJAG_03224","SJAG_01717","SJAG_03216","SJAG_00324","SJAG_03550","SJAG_04001","SJAG_01885","SJAG_05295","SJAG_03421","SJAG_03418","SJAG_03684","SJAG_03386","SJAG_00285","SJAG_02426","SJAG_02520","SJAG_05337","SJAG_04191","SJAG_04900","SJAG_03371","SJAG_02275","SJAG_04507","SJAG_03067","SJAG_02598","SJAG_03283","SJAG_03956","SJAG_02263","SJAG_02643","SJAG_03892","SJAG_01259","SJAG_04778","SJAG_01774","SJAG_01510","SJAG_00048","SJAG_04634","SJAG_00420","SJAG_04379","SJAG_03118","SJAG_01248","SJAG_00202","SJAG_02724","SJAG_03728","SJAG_01063","SJAG_02663","SJAG_MIT05","SJAG_03471","SJAG_02744","SJAG_02164","SJAG_05205","SJAG_03813","SJAG_05027","SJAG_01613","SJAG_04369","SJAG_04271","SJAG_00875","SJAG_04355","SJAG_03569","SJAG_02708","SJAG_04772","SJAG_03542","SJAG_04427","SJAG_02488","SJAG_00718","SJAG_01302","SJAG_02503","SJAG_04217","SJAG_04601","SJAG_03658","SJAG_02428","SJAG_00447","SJAG_03635","SJAG_02077","SJAG_00523","SJAG_04091","SJAG_04232","SJAG_02295","SJAG_01583","SJAG_00616","SJAG_03957","SJAG_00391","SJAG_01859","SJAG_04757","SJAG_04814","SJAG_00786","SJAG_03743","SJAG_01799","SJAG_00084","SJAG_00878","SJAG_00414","SJAG_00327","SJAG_03038","SJAG_02267","SJAG_01018","SJAG_01313","SJAG_02870","SJAG_01836","SJAG_02938","SJAG_01148","SJAG_05213","SJAG_02557","SJAG_03313","SJAG_00111","SJAG_03526","SJAG_01449","SJAG_02646","SJAG_00443","SJAG_01267","SJAG_03349","SJAG_00303","SJAG_00298","SJAG_04608","SJAG_03730","SJAG_01040","SJAG_04375","SJAG_03448","SJAG_03299","SJAG_02427","SJAG_04321","SJAG_03072","SJAG_02621","SJAG_00980","SJAG_01878","SJAG_00112","SJAG_03678","SJAG_03422","SJAG_00210","SJAG_03602","SJAG_04880","SJAG_01012","SJAG_04149","SJAG_03297","SJAG_04153","SJAG_02099","SJAG_04121","SJAG_01822","SJAG_04147","SJAG_03176","SJAG_02972","SJAG_03669","SJAG_16453","SJAG_02370","SJAG_05021","SJAG_04863","SJAG_00088","SJAG_00926","SJAG_00819","SJAG_02956","SJAG_00323","SJAG_04154","SJAG_00840","SJAG_04288","SJAG_03562","SJAG_03335","SJAG_00937","SJAG_00782","SJAG_04933","SJAG_00252","SJAG_01623","SJAG_05190","SJAG_04627","SJAG_01693","SJAG_04167","SJAG_04652","SJAG_03914","SJAG_00945","SJAG_02302","SJAG_04879","SJAG_01466","SJAG_02509","SJAG_05373","SJAG_06622","SJAG_01405","SJAG_02592","SJAG_02848","SJAG_00145","SJAG_02213","SJAG_02843","SJAG_02790","SJAG_02662","SJAG_00947","SJAG_01638","SJAG_00979","SJAG_01517","SJAG_01383","SJAG_01044","SJAG_04916","SJAG_01159","SJAG_02471","SJAG_00042","SJAG_01629","SJAG_04582","SJAG_03886","SJAG_00244","SJAG_00529","SJAG_02475","SJAG_03193","SJAG_00537","SJAG_04734","SJAG_02172","SJAG_04304","SJAG_02887","SJAG_06612","SJAG_01680","SJAG_01117","SJAG_01499","SJAG_00798","SJAG_01805","SJAG_00058","SJAG_00473","SJAG_04055","SJAG_04347","SJAG_00857","SJAG_00714","SJAG_01679","SJAG_01971","SJAG_02821","SJAG_02218","SJAG_00999","SJAG_01052","SJAG_00360","SJAG_03926","SJAG_00693","SJAG_01725","SJAG_04245","SJAG_03789","SJAG_00293","SJAG_01945","SJAG_04473","SJAG_04468","SJAG_03724","SJAG_03753","SJAG_00585","SJAG_00935","SJAG_05105","SJAG_00610","SJAG_02401","SJAG_00968","SJAG_01301","SJAG_04459","SJAG_01317","SJAG_01590","SJAG_02875","SJAG_04756","SJAG_01297","SJAG_03183","SJAG_00475","SJAG_00331","SJAG_00796","SJAG_04577","SJAG_01544","SJAG_02084","SJAG_04061","SJAG_00044","SJAG_03832","SJAG_00174","SJAG_04071","SJAG_03997","SJAG_03985","SJAG_03430","SJAG_03804","SJAG_01653","SJAG_00498"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[59379],"is_not":false,"summary":null,"term":"GO:0097159"},{"annotations":[98558],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070337"},{"annotations":[101670,96677,88131,92565,96678,101671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008097"},{"annotations":[90036,115066,114265,113499,115777,90830],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008312"},{"annotations":[92735],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002055"},{"annotations":[97372],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032136"},{"annotations":[94066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035485"},{"annotations":[88339,88424,92054,102563],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043531"},{"annotations":[100762,106227],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032131"},{"annotations":[88425,92737,115232,88095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016208"},{"annotations":[116554,113606,117140,90355,89820,104344,95269,111552,113904,88475,115976,109492,113185,92297,97559,112722,115623,117358,93474,94255,101295,88016,102928,103080,104686,108373,106380,111380,91937,111776,94633,90377,117407,112119,103839,117320,87959,92139,98205,92625,104855,91878,106496,117080,91163,88340,105590,103766,111146,90363,93028,116946,88859,88785,107525,92055,92826,95971,114220,109510,87159,114897,97192,91365,98151,115817,115828,105085,103247,94670,108447,112225,112985,86912,109909,57597,117166,106995,100990,117053,111179,99367,107419,99261,87591,92941,100065,106109,112218,94628,91291,93082,93796,100778,92762,89410,94651,96144,103922,116439,110123,107499,86739,102113,110136,95313,96351,98197,93466,87545,104106,90759,86990,95402,113025,61056,106275,91390,112903,101683,93624,90872,93865,91763,113193,113420,109143,88706,92899,95855,99419,109399,110813,111661,114865,98052,88503,105070,95866,89434,116958,111700,87071,117108,110434,95789,97763,109336,112154,108238,113952,103645,88382,96693,111911,114811,98263,114635,87806,96864,93949,95188,95055,114475,103809,115144,102307,93539,101579,114040,100572,102016,115829,117180,99896,104159,99378,87958,91703,101422,118147,102501,103746,93617,95895,88107,88182,104398,99769,109812,112292,114322,67553,103530,110709,114049,89023,96250,109676,98439,89469,100379,103388,107658,87225,92485,96135,94466,97449,90142,105385,109978,112553,112728,116262,96203,86998,63879,107730,112862,99581,117982,86913,104658,104523,91939,93729,95669,114416,93007,95723,101275,95812,113641,107011,101334,116138,92919,103338,115265,109746,112714,100289,93973,92860,103695,106348,92013,100815,107294,99281,104237,92469,101037,114243,93493,98669,87476,88484,91108,108187,109613,87026,112965,94767,62972,111843,114093,88167,115414,117684,113404,91341,96116,110986,110222,87844,98531,91558,117516,117636,102570,92508,112431,117152,115198,90934,91936,88059,96846,106952,91467,106437,92663,107700,99222,107330,117859,95003,57304,105553,98132,67978,86758,104444,91853,93810,87365,106144,89531,108355,102708,104370,100323,94242,109075,87195,98431,93162,91892,92414,95453,100643,101160,105615,115181,115233,114172,115441,114105,91325,97468,92264,91816,93644,117331,107857,101347,97122,98883,91540,91641,91047,100876,98537,99837,89979,105819,116747,115372,88331,88558,92064,110164,107019,112091,102577,115320,115500,116431,107821,91379,91591,95195,102564,87910,94440,116378,92446,109392,116064,116291,114714,87372,99821,97282,113396,98767,93578,115125,100185,98341,102029,105356,106269,111872,115156,116593,89277,107373,107566,87382,98722,87035,116360,114142,89008,100204,104023,95216,92170,95574,90091,90005,63910,98113,87125,113092,109373,116528,117735,96790,90446,94453,100132,100593,108829,90172,113254,91938,96283,102437,95100,102936,105546,102725,96213,96489,110091,95681,105154,105205,98036,99079,95254,86974,104627,103855,106409,100290,103459,87510,88729,107054,89053,97355,110305,110530,92617,58200,106235,96856,110445,110070,102459,99138,103651,88272,107101,112311,106673,105781,113972,101318,112093,96907,113246,117009,91806,99389,106444,105230,90310,103484,112090,104757,110113,100984,97633,112089,97258,99736,103413,117538,110276,101447,117311,95163,117744,105993,102353,104533,111965,114636,90367,106078,91717,104979,87007,103498,89497,100087,94422,95945,101854,102884,113652,114558,97993,118045,101454,104936,97325,95652,110497,108220,98228,114188,88426,112370,116086,114750,110387,97386,86959,94860,88285,96404,96587,104599,117796,93455,105679,106899,93673,91350,105439,112092,115576,98811,101931,90961,110207,99252,116718,89225,95643,111483,103681,103005,88262,101011,111631,112517,100560,114831,65803,109914,113635,97932,91570,89855,103754],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005524"},{"annotations":[116005,90133,106983,105465,115664,116196,115048,87028,88263,106901,102355,116721,111192,112519],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061776"},{"annotations":[94551,105452,89219,100351],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034513"},{"annotations":[92861,110624,98560,115940],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000405"},{"annotations":[99628],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030552"},{"annotations":[90554,104640,101249,115606],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019237"},{"annotations":[110269,94726,113529,106160,109101],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031490"},{"annotations":[108285,98774,106085,114501],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043035"},{"annotations":[115208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000987"},{"annotations":[89875],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001046"},{"annotations":[93933],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000402"},{"annotations":[90060,86950],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002135"},{"annotations":[97373],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035486"},{"annotations":[97374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035488"},{"annotations":[98561],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062037"},{"annotations":[93813,87501,102080,110566,113421,116453,91380,87388,92201,109966,100764,110879,116276,61698,95377,103168,107268,110698,97375,110390,116722,117892,115393,110092],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003684"},{"annotations":[96352,110418,95356,101593,105669,109118,118167,103272,116243,94434,101208,111760,112933,64195,110730,97673,114733,94468,103735,111761,112273,107176,112194,115834,118160,111874,114157,93050,104629,105119,93107,105795,115835,95217,95345,98330,111431,90323,90135,109106,88320,97450,91808,94257,89799,111936,113680,88132,111762,94939,87607,91583,90995,94673,111716,116893,109698,116468,92436,93165,118168,93282,114145,89555,104040,116850,91396,91236,87376,100163,93411,90325,101223,103407,113803,107671,93295,116842,113256,101209,86607,106228,109705,96286,112433,110619,115341,87029,89135,90744,87198,101868,66815,57672,101222,106147,111717,101224,106859,115494,96324,111324,104955,114583,101207,97347,98238,87838,100712,109823,96009,103801,111967,90480,60432,115463,105358,89470,89281,99664,88766,106845,111414,107595,116256,118159,88504,90324,103603,114805,108265,101685,88787,92447,98504,63511,60483,87085,87847,111715,113026],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003677"},{"annotations":[89303,114158],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008301"},{"annotations":[87016,95378,88384,87761,89499,115941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045027"},{"annotations":[96522,104644,106998,109374,112313,96628,110786,107207,110532,114245],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003688"},{"annotations":[106229],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140431"},{"annotations":[102357,112522,115049,115666,115942,111193],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106260"},{"annotations":[102358,111664,112523,115050],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990814"},{"annotations":[105233,99772,115943],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000406"},{"annotations":[113782,116007,101150,99741,106515,106902,112700,115944,91882,88883,107960,111194,104079,111195,95379,99838,93262,107672,116579,94277,115051,102359,114820,102136,115126,98270,102331,90556,98269,116991,107082,95443,90136,107135,113422,106918,70130,87694,108726,105796,92080,106827,91203,107306,91954,109634,110093,112524,98562,115667,118064,87030,88917],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003690"},{"annotations":[95196,114821,101358,108995,61060,117745,106468,107645,115127],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003725"},{"annotations":[88386,105304,88976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003691"},{"annotations":[110913,113885,100652,109972,97608,112146,108836,107588,95839,102417,117132,113915],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071949"},{"annotations":[102375,93935,111665,115946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070336"},{"annotations":[110950,103861,111931,86645,102968,88395,107631,108786,117543,100718,89233,87433,117902,104388,93312,106867,101915,112390,88665,116608],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050660"},{"annotations":[86923,87434,96184,100670,106221,86981,89234,112953,113226,110970,116609,89378,106868,88586,100719,86939,101916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010181"},{"annotations":[105234,94073,93936,91854,96120,99839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000400"},{"annotations":[88387,111666,98926,103141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051880"},{"annotations":[94287],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098505"},{"annotations":[90899,90062,91630,109684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019003"},{"annotations":[114822,88096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019002"},{"annotations":[116626,111540,92597,106359,108419,93704,94958,95472,88450,111539,117602,92800,105711,97092,106298,106597,110668,90063,94424,105172,107858,115219,100150,100426,116627,91186,92460,103776,103826,110586,117491,104069,99151,100037,111272,116458,97499,102672,92798,107886,98833,101836,102846,89511,112004,107624,87117,100953,103190,106337,98909,91910,88648,95703,101949,103098,108908,90290,97498,91221,99305,60807,106589,93045,97581,91127,99847,102064,100637,109984,109678,112665,92799,88097,96263,101812,115750,93431,90503,118081,109686,92070,111538,108480,96942,109685,116621,104223,93481,91998,117603,88943,118080,104580,100475,108007,115106,93528,115069,91631,92650,109417,117601],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005525"},{"annotations":[95259],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990605"},{"annotations":[105235,115579],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032137"},{"annotations":[114823],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905108"},{"annotations":[86982,115245,114368,91432,87686,115847,90699,112331,118154,117416,93835,107003,107119],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0020037"},{"annotations":[99773,105236,105107],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000404"},{"annotations":[96373,96374,111598,88234,114493,114494,115710,115711,113618,114853,113617],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070180"},{"annotations":[111002,103477,114559,92030,94354,117247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106222"},{"annotations":[102651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036042"},{"annotations":[92552],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990943"},{"annotations":[96428,104582],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990856"},{"annotations":[95260],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035939"},{"annotations":[97376,114824,87809,103749,90964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030983"},{"annotations":[94331,97377],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001018"},{"annotations":[104082,104432,78065,109087,112459,110213,113835,117434,103587,117441],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035925"},{"annotations":[117442,106880,87618,118040,110715,88694,72293,97336,88908,96308,73951,97712,99282,114280],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003730"},{"annotations":[99646],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048027"},{"annotations":[112678,105042,97284,99655,102208,106102,72934,92314,88655,88022,89403,90220,94574,98290,99068,107478,110428,111525,115907,96754,113084,102385,91571,110886,90771,99118,71336,99234,94535,112869,95732,117845,105429,99069,104485,112715,99233,108971,93146,89569,92818,116959,117443,114512,62597,87533,87967,98968,89821,104445,95782,101049,101894,111296,92817,111526,114751,107479,104741,70896,94379,114797,115006,115906,116132,90221,117248,97683,116778,95766,93201,105828,91397,90021,101932,103541,110016,112412,114448,109956,117797,103209,78653,113480,87780,97250,92785,111147,75305,111504,114382,102811,97333,98820,89087,115762,86935,116416],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003729"},{"annotations":[90762],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098808"},{"annotations":[118041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000900"},{"annotations":[108556,108106,108555,108105,104253,117903,105664,108557,108559,108109,108560,108107,116044,108104,117632,108558,98975,100218,104009,97357,93178,105346,108108,108110,95555,114921,108554],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051287"},{"annotations":[111113,113940,89266,113559,103375],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070403"},{"annotations":[104390,103636,108565,108113,113941,113196,110721,112148,96179,111114,64012,108114,108112,108111,108563,108561,87435,99351,106869,108116,108567,108562,106222,96090,108115,117573,108566,108117,108564,93313],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050661"},{"annotations":[97358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070401"},{"annotations":[102220,113836,113924],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070402"},{"annotations":[87389],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032132"},{"annotations":[94067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032357"},{"annotations":[93449,115359,108516,110473,107361,101796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008142"},{"annotations":[96738,88292,103478,97713,91134,73947,108357,88656,88695,106881,96309,72289],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008143"},{"annotations":[94355,95025,109088,114072,73948,106882,94823,72290,105509,97714,112024,88696,96310,115545],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008266"},{"annotations":[102386],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008187"},{"annotations":[102387,108704,100436],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030628"},{"annotations":[109798,112413],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030627"},{"annotations":[116351,88293,96038,117250],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036002"},{"annotations":[64624],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045131"},{"annotations":[97213,117251,100097],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097157"},{"annotations":[111025],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140585"},{"annotations":[104083],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062104"},{"annotations":[98580,66881,91981,109584,93687,87885,87056,97550,90908,100024,109653,65677,64096,68272,104701,110959,91420,101489,59863,98219,106042,102775,117512,90509,94974,102957,105934,113068,110379,92832],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030170"},{"annotations":[94601,101360,102093,102529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000182"},{"annotations":[114159,101465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043110"},{"annotations":[101466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110035"},{"annotations":[91955,107136],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010844"},{"annotations":[109525],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902444"},{"annotations":[103730,117721],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033204"},{"annotations":[112274,97348,93297],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032549"},{"annotations":[114513,89111,98969,103928,112610],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000340"},{"annotations":[109351,108654,86991,100866,104026,100859,101815,90730,116904,102196,106365,113186,95119,95629,108138,106625,61395,107093,94803,101661,101733,105969,103696,89834,106760,117314,107774,95530,110588,92574,94319,90415,102895,92134,93987,101653,103127,110625,113994,90007,95454,95408,96925,66987,113691,89523,95314,95706,97030,88997,94125,101654,114505,103142,89047,105670,94841,93298,89314,108321,110558,107045,100553,91592,110183,116568,101678,68051,104794,106781,109041,87731,112206,107922,113567,92251,111623,88684,104554,109773,94159,111586,112241,86881,100552,97769,108320,115024,90763,59302,99012,97989,99665,95823,67333,98813,101151,104937,107252,108383,114584,104769,96451,90605,89011,106954,88202,89139,103038,107775,116567,113690,95628,99593,107527,114912,116529,102711,112128,97316,112242,111924,102094,93682,93859,89449,98928,107032,56818,57072,88223,105633,90263,58632,69612,104909,102391,101272,98368,107150,110184,98357,110675,88039,74064,88697,67364,90264,92031,99779,114312,97419,92281,106481,101599,86882,116362,91204,117044,105053,117199,88363,103613,94543,104089,112747,105392,114913,99081,95261,114313,115677,87395,112592,100594,100860,90022,88243,87010,105163,106178,106943,117254,105298,107137,115785,111667,109220,111358,103341,111937,89448,103909,87293,91867,102339,110396,97157,104845,92829,116541,98369,111888,90875,114464,91887,112629,109657,101830,103122,92090,94320,104084,113046,89315,93929,102235,98332,95988,110557,112403,105968,66704,103967,113047,113429,91000,90093,94705,102547,117410,105923,91893,104846,90436,96986,98356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003723"},{"annotations":[102168],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000339"},{"annotations":[115585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001165"},{"annotations":[111076,108304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001164"},{"annotations":[108892,102530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001163"},{"annotations":[109870,110044,95240,97621,92498,96125,108202,95483,87174,103950,94891,87669,115744,96726,88674,77591,99313,101467,108343,79663,106738,108846,117478,91956,112816,112540,103625,96727,101414,107789,96729,99685,88250,103630,107138,101883,87245,110028,115608,91670,98698,99001,95777,105005,110011,110203,93941,111026,93266,107961,113221,106215,92912,101232,116618,97308,106161,111065,113717,89305,113968,92499,91116,86811,93925,96730,96728,103135,107378,102735,105416,108506,96255,96496,100675,108342,105273,87613,115211,117193,105533,96573,92441,105890,111066],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000978"},{"annotations":[107962,106216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044377"},{"annotations":[94777,93347,111027,88492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000979"},{"annotations":[106739],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001162"},{"annotations":[114769,117194,88004,88086,101415],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000977"},{"annotations":[87400,98775],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000992"},{"annotations":[98777],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001002"},{"annotations":[98778],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001003"},{"annotations":[94780,102249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001006"},{"annotations":[101362,109089],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035613"},{"annotations":[108697,104777,106469],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033592"},{"annotations":[108698,104778],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034057"},{"annotations":[107074,102259,114885,90890,101089,99656,101496,87563,116791,109880,107368,91682,105220,94552,90527,96050,111463,88144,101088,91298,116790,109879,109530,100507,111281,103425,89220,88143,105870,107075,101120,100352,95545,97412,99965,111464,103426,95767,104890,113336,95546,108699,89088,97413,105219,107367,113159,93761,93760,100508,91683,104891,99922,104593,104592,113160,113337,94595,94108,114726,99966,94109,105871],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019843"},{"annotations":[113038,97174,90723,95696,105822],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042134"},{"annotations":[78470,101468,114160,111028,93926,114390,94005,88005,68349,91957,92472,117195,117201,95579],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043565"},{"annotations":[106217],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044374"},{"annotations":[114161,87144],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990837"},{"annotations":[90302],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990825"},{"annotations":[105237],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032138"},{"annotations":[97379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032141"},{"annotations":[114825,95078],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990165"},{"annotations":[115394,115947,116723,109187,114661,89013,117893,96630,95381,100693,98271,98272,91883,88918,104495,102138,112701,114246,110699,95444,101379,114420,109967,113785,115668,100197,114826,112525,108241,110700,116277,117315,92474,89656,99742,105593,118065,109377,107707,87502,88264,94945,106412,102360,104122,106828,98617,109643,111196,111556,91165,110626,115052],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003697"},{"annotations":[105594,90764,91416,117226,90482,87781,106413,91459,109644,114421,100198],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003727"},{"annotations":[107277,95263,109518,113745,94288,110676,110701,88388],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043047"},{"annotations":[87990,111350,117227],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035197"},{"annotations":[114843,115150,95827,98851,98852],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070181"},{"annotations":[113039,106266,109713,109127,107758,90724,90521,93328,108875,109247,105379,97720,107194,91248,90891,102302,110199,110921,112673,99945,110491,92032,88446,91837,106127,100757,105141,111139],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030515"},{"annotations":[104654,107195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017069"},{"annotations":[93836],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005496"},{"annotations":[105492,89632,100850,109006],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032934"},{"annotations":[106087],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071443"},{"annotations":[100353,89850,107278,110702,112026,107096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070034"},{"annotations":[88978,114662,113423,110703,110094,96760,107097,104271,98919],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042162"},{"annotations":[98723],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030975"},{"annotations":[110977,96467,112392,109278,87720,96466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030976"},{"annotations":[97380],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035487"},{"annotations":[72220,95997,102296,107618,75708,71365,112768],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000976"},{"annotations":[99082,101469,106956],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001147"},{"annotations":[99647,98648,87782,97905,111805,101098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008494"},{"annotations":[111544,112006,117608,108323,117607,117609,118083,116088,94322,102066,92805,97504,118082,111545,111546,92804,113861,108322,72094,94539,111285,92806,97505,94321],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003746"},{"annotations":[86741,95861,96431,97007,95783,106470,104770,113111,109758,110484,96926,99292,97583,89571,95068,91972,96051,102392,96987,114753,106179,104751,104779,89149,103929,99691,101816,104583,109844,103234,89112,98126,93988,104486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003743"},{"annotations":[115170,116629,101254,90303,106339,95135,97851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003747"},{"annotations":[97852],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016150"},{"annotations":[90304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016149"},{"annotations":[94324,103877,108324,94323,108325],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008079"},{"annotations":[106433,117747,104944,115183,99638,86952,103314,117055,98602,104718,93912,100645,108640,97685,117168,92920,113542,114813,93467,89670,94630,102071,93679,111290,95283,101455,108831,111778,94662,87789,112007,96407,93867,105023,118113,91818,97686,93128,107568,112667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000049"},{"annotations":[112414,90772,97214,109786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030619"},{"annotations":[95026,97215,115008,100927,107696,111789,114074,112027,105510,104678,115546],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030620"},{"annotations":[114886,107860,93530,94922,114331],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034511"},{"annotations":[92154],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030621"},{"annotations":[97216,105713],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030623"},{"annotations":[92155,107697,97217,96039,116352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017070"},{"annotations":[90066,90877],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002134"},{"annotations":[115948,105797,98564,99774,105238,93937,87767,107673,78208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000403"}]},"cv_name":"molecular_function","definition":"Binding to an organic cyclic compound, any molecular entity that contains carbon arranged in a cyclic molecular structure.","definition_xrefs":["GOC:sjw","PMID:7583672"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding","termid":"GO:0005488"}],"gene_count":1525,"genes_by_uniquename":{"SJAG_00004":null,"SJAG_00027":null,"SJAG_00031":null,"SJAG_00034":null,"SJAG_00037":null,"SJAG_00039":null,"SJAG_00042":null,"SJAG_00044":null,"SJAG_00045":null,"SJAG_00048":null,"SJAG_00054":null,"SJAG_00058":null,"SJAG_00067":null,"SJAG_00069":null,"SJAG_00073":null,"SJAG_00083":null,"SJAG_00084":null,"SJAG_00088":null,"SJAG_00097":null,"SJAG_00103":null,"SJAG_00106":null,"SJAG_00111":null,"SJAG_00112":null,"SJAG_00114":null,"SJAG_00118":null,"SJAG_00124":null,"SJAG_00136":null,"SJAG_00145":null,"SJAG_00147":null,"SJAG_00150":null,"SJAG_00153":null,"SJAG_00159":null,"SJAG_00163":null,"SJAG_00164":null,"SJAG_00166":null,"SJAG_00168":null,"SJAG_00169":null,"SJAG_00174":null,"SJAG_00178":null,"SJAG_00186":null,"SJAG_00195":null,"SJAG_00198":null,"SJAG_00202":null,"SJAG_00203":null,"SJAG_00208":null,"SJAG_00210":null,"SJAG_00220":null,"SJAG_00225":null,"SJAG_00226":null,"SJAG_00231":null,"SJAG_00234":null,"SJAG_00235":null,"SJAG_00243":null,"SJAG_00244":null,"SJAG_00247":null,"SJAG_00249":null,"SJAG_00252":null,"SJAG_00253":null,"SJAG_00256":null,"SJAG_00259":null,"SJAG_00265":null,"SJAG_00266":null,"SJAG_00269":null,"SJAG_00272":null,"SJAG_00281":null,"SJAG_00285":null,"SJAG_00293":null,"SJAG_00294":null,"SJAG_00298":null,"SJAG_00300":null,"SJAG_00302":null,"SJAG_00303":null,"SJAG_00304":null,"SJAG_00307":null,"SJAG_00308":null,"SJAG_00313":null,"SJAG_00315":null,"SJAG_00319":null,"SJAG_00322":null,"SJAG_00323":null,"SJAG_00324":null,"SJAG_00325":null,"SJAG_00327":null,"SJAG_00329":null,"SJAG_00330":null,"SJAG_00331":null,"SJAG_00332":null,"SJAG_00335":null,"SJAG_00336":null,"SJAG_00337":null,"SJAG_00338":null,"SJAG_00342":null,"SJAG_00344":null,"SJAG_00353":null,"SJAG_00355":null,"SJAG_00356":null,"SJAG_00358":null,"SJAG_00359":null,"SJAG_00360":null,"SJAG_00364":null,"SJAG_00370":null,"SJAG_00378":null,"SJAG_00381":null,"SJAG_00384":null,"SJAG_00386":null,"SJAG_00390":null,"SJAG_00391":null,"SJAG_00392":null,"SJAG_00399":null,"SJAG_00402":null,"SJAG_00403":null,"SJAG_00409":null,"SJAG_00410":null,"SJAG_00412":null,"SJAG_00414":null,"SJAG_00420":null,"SJAG_00421":null,"SJAG_00424":null,"SJAG_00425":null,"SJAG_00427":null,"SJAG_00430":null,"SJAG_00432":null,"SJAG_00436":null,"SJAG_00443":null,"SJAG_00446":null,"SJAG_00447":null,"SJAG_00457":null,"SJAG_00464":null,"SJAG_00465":null,"SJAG_00466":null,"SJAG_00470":null,"SJAG_00473":null,"SJAG_00474":null,"SJAG_00475":null,"SJAG_00486":null,"SJAG_00488":null,"SJAG_00495":null,"SJAG_00498":null,"SJAG_00500":null,"SJAG_00502":null,"SJAG_00503":null,"SJAG_00504":null,"SJAG_00507":null,"SJAG_00513":null,"SJAG_00516":null,"SJAG_00523":null,"SJAG_00527":null,"SJAG_00529":null,"SJAG_00531":null,"SJAG_00533":null,"SJAG_00537":null,"SJAG_00539":null,"SJAG_00541":null,"SJAG_00544":null,"SJAG_00545":null,"SJAG_00555":null,"SJAG_00559":null,"SJAG_00563":null,"SJAG_00564":null,"SJAG_00566":null,"SJAG_00572":null,"SJAG_00577":null,"SJAG_00579":null,"SJAG_00582":null,"SJAG_00583":null,"SJAG_00585":null,"SJAG_00597":null,"SJAG_00599":null,"SJAG_00604":null,"SJAG_00605":null,"SJAG_00609":null,"SJAG_00610":null,"SJAG_00616":null,"SJAG_00619":null,"SJAG_00623":null,"SJAG_00628":null,"SJAG_00629":null,"SJAG_00633":null,"SJAG_00634":null,"SJAG_00636":null,"SJAG_00637":null,"SJAG_00638":null,"SJAG_00639":null,"SJAG_00640":null,"SJAG_00649":null,"SJAG_00650":null,"SJAG_00653":null,"SJAG_00657":null,"SJAG_00659":null,"SJAG_00660":null,"SJAG_00661":null,"SJAG_00662":null,"SJAG_00663":null,"SJAG_00664":null,"SJAG_00669":null,"SJAG_00670":null,"SJAG_00673":null,"SJAG_00678":null,"SJAG_00682":null,"SJAG_00686":null,"SJAG_00690":null,"SJAG_00692":null,"SJAG_00693":null,"SJAG_00698":null,"SJAG_00701":null,"SJAG_00704":null,"SJAG_00706":null,"SJAG_00707":null,"SJAG_00712":null,"SJAG_00713":null,"SJAG_00714":null,"SJAG_00718":null,"SJAG_00729":null,"SJAG_00731":null,"SJAG_00741":null,"SJAG_00744":null,"SJAG_00748":null,"SJAG_00749":null,"SJAG_00757":null,"SJAG_00759":null,"SJAG_00765":null,"SJAG_00766":null,"SJAG_00768":null,"SJAG_00769":null,"SJAG_00773":null,"SJAG_00779":null,"SJAG_00782":null,"SJAG_00783":null,"SJAG_00786":null,"SJAG_00790":null,"SJAG_00792":null,"SJAG_00796":null,"SJAG_00798":null,"SJAG_00801":null,"SJAG_00802":null,"SJAG_00809":null,"SJAG_00813":null,"SJAG_00815":null,"SJAG_00819":null,"SJAG_00830":null,"SJAG_00833":null,"SJAG_00840":null,"SJAG_00845":null,"SJAG_00851":null,"SJAG_00853":null,"SJAG_00854":null,"SJAG_00855":null,"SJAG_00857":null,"SJAG_00861":null,"SJAG_00863":null,"SJAG_00871":null,"SJAG_00875":null,"SJAG_00878":null,"SJAG_00879":null,"SJAG_00881":null,"SJAG_00882":null,"SJAG_00884":null,"SJAG_00886":null,"SJAG_00887":null,"SJAG_00888":null,"SJAG_00889":null,"SJAG_00896":null,"SJAG_00897":null,"SJAG_00898":null,"SJAG_00901":null,"SJAG_00906":null,"SJAG_00912":null,"SJAG_00921":null,"SJAG_00926":null,"SJAG_00930":null,"SJAG_00931":null,"SJAG_00935":null,"SJAG_00937":null,"SJAG_00938":null,"SJAG_00939":null,"SJAG_00941":null,"SJAG_00943":null,"SJAG_00945":null,"SJAG_00947":null,"SJAG_00949":null,"SJAG_00950":null,"SJAG_00956":null,"SJAG_00958":null,"SJAG_00963":null,"SJAG_00964":null,"SJAG_00968":null,"SJAG_00972":null,"SJAG_00979":null,"SJAG_00980":null,"SJAG_00983":null,"SJAG_00984":null,"SJAG_00986":null,"SJAG_00987":null,"SJAG_00988":null,"SJAG_00992":null,"SJAG_00993":null,"SJAG_00995":null,"SJAG_00996":null,"SJAG_00999":null,"SJAG_01000":null,"SJAG_01002":null,"SJAG_01008":null,"SJAG_01010":null,"SJAG_01012":null,"SJAG_01015":null,"SJAG_01018":null,"SJAG_01019":null,"SJAG_01024":null,"SJAG_01026":null,"SJAG_01040":null,"SJAG_01041":null,"SJAG_01044":null,"SJAG_01046":null,"SJAG_01047":null,"SJAG_01049":null,"SJAG_01052":null,"SJAG_01062":null,"SJAG_01063":null,"SJAG_01064":null,"SJAG_01067":null,"SJAG_01070":null,"SJAG_01074":null,"SJAG_01075":null,"SJAG_01076":null,"SJAG_01080":null,"SJAG_01081":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01087":null,"SJAG_01117":null,"SJAG_01119":null,"SJAG_01129":null,"SJAG_01131":null,"SJAG_01132":null,"SJAG_01137":null,"SJAG_01148":null,"SJAG_01152":null,"SJAG_01157":null,"SJAG_01159":null,"SJAG_01162":null,"SJAG_01164":null,"SJAG_01169":null,"SJAG_01172":null,"SJAG_01173":null,"SJAG_01176":null,"SJAG_01179":null,"SJAG_01181":null,"SJAG_01182":null,"SJAG_01186":null,"SJAG_01191":null,"SJAG_01194":null,"SJAG_01197":null,"SJAG_01198":null,"SJAG_01200":null,"SJAG_01201":null,"SJAG_01215":null,"SJAG_01217":null,"SJAG_01221":null,"SJAG_01222":null,"SJAG_01234":null,"SJAG_01235":null,"SJAG_01240":null,"SJAG_01243":null,"SJAG_01245":null,"SJAG_01248":null,"SJAG_01249":null,"SJAG_01252":null,"SJAG_01254":null,"SJAG_01259":null,"SJAG_01262":null,"SJAG_01263":null,"SJAG_01267":null,"SJAG_01268":null,"SJAG_01277":null,"SJAG_01282":null,"SJAG_01296":null,"SJAG_01297":null,"SJAG_01301":null,"SJAG_01302":null,"SJAG_01307":null,"SJAG_01311":null,"SJAG_01313":null,"SJAG_01314":null,"SJAG_01315":null,"SJAG_01317":null,"SJAG_01322":null,"SJAG_01323":null,"SJAG_01327":null,"SJAG_01329":null,"SJAG_01332":null,"SJAG_01339":null,"SJAG_01343":null,"SJAG_01344":null,"SJAG_01351":null,"SJAG_01352":null,"SJAG_01354":null,"SJAG_01358":null,"SJAG_01364":null,"SJAG_01366":null,"SJAG_01373":null,"SJAG_01376":null,"SJAG_01377":null,"SJAG_01378":null,"SJAG_01379":null,"SJAG_01380":null,"SJAG_01383":null,"SJAG_01387":null,"SJAG_01391":null,"SJAG_01400":null,"SJAG_01402":null,"SJAG_01405":null,"SJAG_01407":null,"SJAG_01408":null,"SJAG_01410":null,"SJAG_01412":null,"SJAG_01419":null,"SJAG_01420":null,"SJAG_01432":null,"SJAG_01435":null,"SJAG_01436":null,"SJAG_01438":null,"SJAG_01440":null,"SJAG_01441":null,"SJAG_01444":null,"SJAG_01447":null,"SJAG_01449":null,"SJAG_01452":null,"SJAG_01456":null,"SJAG_01458":null,"SJAG_01466":null,"SJAG_01468":null,"SJAG_01469":null,"SJAG_01471":null,"SJAG_01474":null,"SJAG_01478":null,"SJAG_01487":null,"SJAG_01489":null,"SJAG_01495":null,"SJAG_01499":null,"SJAG_01500":null,"SJAG_01510":null,"SJAG_01511":null,"SJAG_01517":null,"SJAG_01518":null,"SJAG_01521":null,"SJAG_01522":null,"SJAG_01529":null,"SJAG_01530":null,"SJAG_01532":null,"SJAG_01534":null,"SJAG_01544":null,"SJAG_01546":null,"SJAG_01558":null,"SJAG_01568":null,"SJAG_01571":null,"SJAG_01575":null,"SJAG_01576":null,"SJAG_01577":null,"SJAG_01579":null,"SJAG_01583":null,"SJAG_01587":null,"SJAG_01590":null,"SJAG_01595":null,"SJAG_01601":null,"SJAG_01608":null,"SJAG_01609":null,"SJAG_01611":null,"SJAG_01613":null,"SJAG_01615":null,"SJAG_01616":null,"SJAG_01618":null,"SJAG_01620":null,"SJAG_01622":null,"SJAG_01623":null,"SJAG_01625":null,"SJAG_01629":null,"SJAG_01638":null,"SJAG_01643":null,"SJAG_01644":null,"SJAG_01648":null,"SJAG_01650":null,"SJAG_01653":null,"SJAG_01654":null,"SJAG_01659":null,"SJAG_01664":null,"SJAG_01668":null,"SJAG_01669":null,"SJAG_01671":null,"SJAG_01677":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01684":null,"SJAG_01693":null,"SJAG_01694":null,"SJAG_01695":null,"SJAG_01696":null,"SJAG_01698":null,"SJAG_01704":null,"SJAG_01708":null,"SJAG_01712":null,"SJAG_01713":null,"SJAG_01717":null,"SJAG_01718":null,"SJAG_01722":null,"SJAG_01724":null,"SJAG_01725":null,"SJAG_01731":null,"SJAG_01740":null,"SJAG_01741":null,"SJAG_01745":null,"SJAG_01759":null,"SJAG_01762":null,"SJAG_01764":null,"SJAG_01765":null,"SJAG_01766":null,"SJAG_01769":null,"SJAG_01771":null,"SJAG_01774":null,"SJAG_01777":null,"SJAG_01787":null,"SJAG_01789":null,"SJAG_01791":null,"SJAG_01797":null,"SJAG_01799":null,"SJAG_01805":null,"SJAG_01807":null,"SJAG_01813":null,"SJAG_01816":null,"SJAG_01818":null,"SJAG_01819":null,"SJAG_01822":null,"SJAG_01825":null,"SJAG_01827":null,"SJAG_01829":null,"SJAG_01830":null,"SJAG_01831":null,"SJAG_01832":null,"SJAG_01836":null,"SJAG_01837":null,"SJAG_01839":null,"SJAG_01840":null,"SJAG_01843":null,"SJAG_01851":null,"SJAG_01852":null,"SJAG_01855":null,"SJAG_01859":null,"SJAG_01863":null,"SJAG_01870":null,"SJAG_01873":null,"SJAG_01874":null,"SJAG_01877":null,"SJAG_01878":null,"SJAG_01881":null,"SJAG_01882":null,"SJAG_01885":null,"SJAG_01887":null,"SJAG_01903":null,"SJAG_01907":null,"SJAG_01909":null,"SJAG_01910":null,"SJAG_01916":null,"SJAG_01918":null,"SJAG_01919":null,"SJAG_01929":null,"SJAG_01930":null,"SJAG_01937":null,"SJAG_01938":null,"SJAG_01942":null,"SJAG_01944":null,"SJAG_01945":null,"SJAG_01953":null,"SJAG_01954":null,"SJAG_01956":null,"SJAG_01964":null,"SJAG_01971":null,"SJAG_01988":null,"SJAG_02015":null,"SJAG_02017":null,"SJAG_02018":null,"SJAG_02022":null,"SJAG_02024":null,"SJAG_02025":null,"SJAG_02031":null,"SJAG_02036":null,"SJAG_02037":null,"SJAG_02038":null,"SJAG_02039":null,"SJAG_02042":null,"SJAG_02043":null,"SJAG_02048":null,"SJAG_02052":null,"SJAG_02058":null,"SJAG_02061":null,"SJAG_02073":null,"SJAG_02074":null,"SJAG_02077":null,"SJAG_02079":null,"SJAG_02082":null,"SJAG_02083":null,"SJAG_02084":null,"SJAG_02097":null,"SJAG_02099":null,"SJAG_02101":null,"SJAG_02104":null,"SJAG_02135":null,"SJAG_02138":null,"SJAG_02142":null,"SJAG_02148":null,"SJAG_02149":null,"SJAG_02156":null,"SJAG_02164":null,"SJAG_02171":null,"SJAG_02172":null,"SJAG_02176":null,"SJAG_02180":null,"SJAG_02182":null,"SJAG_02183":null,"SJAG_02185":null,"SJAG_02187":null,"SJAG_02189":null,"SJAG_02194":null,"SJAG_02196":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02205":null,"SJAG_02206":null,"SJAG_02207":null,"SJAG_02212":null,"SJAG_02213":null,"SJAG_02218":null,"SJAG_02226":null,"SJAG_02233":null,"SJAG_02236":null,"SJAG_02239":null,"SJAG_02242":null,"SJAG_02243":null,"SJAG_02249":null,"SJAG_02250":null,"SJAG_02252":null,"SJAG_02254":null,"SJAG_02261":null,"SJAG_02262":null,"SJAG_02263":null,"SJAG_02267":null,"SJAG_02275":null,"SJAG_02279":null,"SJAG_02280":null,"SJAG_02286":null,"SJAG_02287":null,"SJAG_02288":null,"SJAG_02292":null,"SJAG_02294":null,"SJAG_02295":null,"SJAG_02297":null,"SJAG_02298":null,"SJAG_02299":null,"SJAG_02300":null,"SJAG_02302":null,"SJAG_02304":null,"SJAG_02305":null,"SJAG_02307":null,"SJAG_02311":null,"SJAG_02312":null,"SJAG_02313":null,"SJAG_02323":null,"SJAG_02326":null,"SJAG_02331":null,"SJAG_02334":null,"SJAG_02335":null,"SJAG_02336":null,"SJAG_02340":null,"SJAG_02342":null,"SJAG_02348":null,"SJAG_02350":null,"SJAG_02352":null,"SJAG_02353":null,"SJAG_02359":null,"SJAG_02360":null,"SJAG_02362":null,"SJAG_02364":null,"SJAG_02366":null,"SJAG_02367":null,"SJAG_02370":null,"SJAG_02372":null,"SJAG_02374":null,"SJAG_02375":null,"SJAG_02376":null,"SJAG_02377":null,"SJAG_02378":null,"SJAG_02381":null,"SJAG_02382":null,"SJAG_02384":null,"SJAG_02385":null,"SJAG_02390":null,"SJAG_02392":null,"SJAG_02394":null,"SJAG_02398":null,"SJAG_02399":null,"SJAG_02400":null,"SJAG_02401":null,"SJAG_02406":null,"SJAG_02415":null,"SJAG_02417":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_02426":null,"SJAG_02427":null,"SJAG_02428":null,"SJAG_02429":null,"SJAG_02431":null,"SJAG_02444":null,"SJAG_02447":null,"SJAG_02456":null,"SJAG_02457":null,"SJAG_02458":null,"SJAG_02460":null,"SJAG_02464":null,"SJAG_02465":null,"SJAG_02468":null,"SJAG_02469":null,"SJAG_02471":null,"SJAG_02472":null,"SJAG_02475":null,"SJAG_02477":null,"SJAG_02488":null,"SJAG_02489":null,"SJAG_02493":null,"SJAG_02496":null,"SJAG_02498":null,"SJAG_02503":null,"SJAG_02506":null,"SJAG_02508":null,"SJAG_02509":null,"SJAG_02513":null,"SJAG_02517":null,"SJAG_02520":null,"SJAG_02521":null,"SJAG_02527":null,"SJAG_02530":null,"SJAG_02531":null,"SJAG_02535":null,"SJAG_02545":null,"SJAG_02554":null,"SJAG_02556":null,"SJAG_02557":null,"SJAG_02558":null,"SJAG_02563":null,"SJAG_02564":null,"SJAG_02569":null,"SJAG_02571":null,"SJAG_02573":null,"SJAG_02575":null,"SJAG_02589":null,"SJAG_02592":null,"SJAG_02595":null,"SJAG_02596":null,"SJAG_02597":null,"SJAG_02598":null,"SJAG_02599":null,"SJAG_02600":null,"SJAG_02601":null,"SJAG_02602":null,"SJAG_02604":null,"SJAG_02605":null,"SJAG_02606":null,"SJAG_02607":null,"SJAG_02608":null,"SJAG_02610":null,"SJAG_02611":null,"SJAG_02615":null,"SJAG_02618":null,"SJAG_02619":null,"SJAG_02621":null,"SJAG_02622":null,"SJAG_02627":null,"SJAG_02628":null,"SJAG_02637":null,"SJAG_02638":null,"SJAG_02640":null,"SJAG_02643":null,"SJAG_02646":null,"SJAG_02652":null,"SJAG_02656":null,"SJAG_02658":null,"SJAG_02661":null,"SJAG_02662":null,"SJAG_02663":null,"SJAG_02667":null,"SJAG_02680":null,"SJAG_02684":null,"SJAG_02686":null,"SJAG_02687":null,"SJAG_02688":null,"SJAG_02690":null,"SJAG_02696":null,"SJAG_02697":null,"SJAG_02698":null,"SJAG_02702":null,"SJAG_02704":null,"SJAG_02708":null,"SJAG_02709":null,"SJAG_02712":null,"SJAG_02713":null,"SJAG_02720":null,"SJAG_02721":null,"SJAG_02722":null,"SJAG_02723":null,"SJAG_02724":null,"SJAG_02725":null,"SJAG_02730":null,"SJAG_02734":null,"SJAG_02736":null,"SJAG_02738":null,"SJAG_02741":null,"SJAG_02744":null,"SJAG_02747":null,"SJAG_02748":null,"SJAG_02752":null,"SJAG_02758":null,"SJAG_02760":null,"SJAG_02775":null,"SJAG_02785":null,"SJAG_02790":null,"SJAG_02791":null,"SJAG_02794":null,"SJAG_02796":null,"SJAG_02800":null,"SJAG_02808":null,"SJAG_02810":null,"SJAG_02812":null,"SJAG_02813":null,"SJAG_02815":null,"SJAG_02818":null,"SJAG_02821":null,"SJAG_02822":null,"SJAG_02824":null,"SJAG_02825":null,"SJAG_02827":null,"SJAG_02828":null,"SJAG_02829":null,"SJAG_02835":null,"SJAG_02838":null,"SJAG_02840":null,"SJAG_02843":null,"SJAG_02848":null,"SJAG_02856":null,"SJAG_02858":null,"SJAG_02861":null,"SJAG_02870":null,"SJAG_02872":null,"SJAG_02875":null,"SJAG_02878":null,"SJAG_02879":null,"SJAG_02887":null,"SJAG_02889":null,"SJAG_02890":null,"SJAG_02894":null,"SJAG_02895":null,"SJAG_02897":null,"SJAG_02904":null,"SJAG_02906":null,"SJAG_02908":null,"SJAG_02922":null,"SJAG_02923":null,"SJAG_02926":null,"SJAG_02938":null,"SJAG_02945":null,"SJAG_02950":null,"SJAG_02952":null,"SJAG_02956":null,"SJAG_02972":null,"SJAG_02977":null,"SJAG_02978":null,"SJAG_02982":null,"SJAG_02991":null,"SJAG_02994":null,"SJAG_02995":null,"SJAG_02997":null,"SJAG_03007":null,"SJAG_03011":null,"SJAG_03014":null,"SJAG_03017":null,"SJAG_03028":null,"SJAG_03036":null,"SJAG_03038":null,"SJAG_03042":null,"SJAG_03047":null,"SJAG_03048":null,"SJAG_03053":null,"SJAG_03055":null,"SJAG_03061":null,"SJAG_03067":null,"SJAG_03068":null,"SJAG_03069":null,"SJAG_03070":null,"SJAG_03071":null,"SJAG_03072":null,"SJAG_03077":null,"SJAG_03092":null,"SJAG_03096":null,"SJAG_03097":null,"SJAG_03102":null,"SJAG_03113":null,"SJAG_03115":null,"SJAG_03118":null,"SJAG_03120":null,"SJAG_03122":null,"SJAG_03125":null,"SJAG_03128":null,"SJAG_03129":null,"SJAG_03132":null,"SJAG_03137":null,"SJAG_03140":null,"SJAG_03141":null,"SJAG_03143":null,"SJAG_03144":null,"SJAG_03145":null,"SJAG_03147":null,"SJAG_03152":null,"SJAG_03156":null,"SJAG_03157":null,"SJAG_03160":null,"SJAG_03161":null,"SJAG_03174":null,"SJAG_03176":null,"SJAG_03179":null,"SJAG_03183":null,"SJAG_03188":null,"SJAG_03193":null,"SJAG_03197":null,"SJAG_03206":null,"SJAG_03209":null,"SJAG_03210":null,"SJAG_03213":null,"SJAG_03214":null,"SJAG_03216":null,"SJAG_03217":null,"SJAG_03223":null,"SJAG_03224":null,"SJAG_03226":null,"SJAG_03232":null,"SJAG_03236":null,"SJAG_03237":null,"SJAG_03240":null,"SJAG_03241":null,"SJAG_03249":null,"SJAG_03252":null,"SJAG_03257":null,"SJAG_03275":null,"SJAG_03276":null,"SJAG_03277":null,"SJAG_03283":null,"SJAG_03284":null,"SJAG_03286":null,"SJAG_03289":null,"SJAG_03290":null,"SJAG_03297":null,"SJAG_03299":null,"SJAG_03301":null,"SJAG_03306":null,"SJAG_03312":null,"SJAG_03313":null,"SJAG_03320":null,"SJAG_03326":null,"SJAG_03335":null,"SJAG_03336":null,"SJAG_03341":null,"SJAG_03342":null,"SJAG_03345":null,"SJAG_03346":null,"SJAG_03349":null,"SJAG_03354":null,"SJAG_03355":null,"SJAG_03362":null,"SJAG_03363":null,"SJAG_03369":null,"SJAG_03371":null,"SJAG_03374":null,"SJAG_03376":null,"SJAG_03383":null,"SJAG_03384":null,"SJAG_03386":null,"SJAG_03388":null,"SJAG_03409":null,"SJAG_03410":null,"SJAG_03411":null,"SJAG_03418":null,"SJAG_03421":null,"SJAG_03422":null,"SJAG_03423":null,"SJAG_03430":null,"SJAG_03433":null,"SJAG_03434":null,"SJAG_03436":null,"SJAG_03438":null,"SJAG_03441":null,"SJAG_03448":null,"SJAG_03449":null,"SJAG_03451":null,"SJAG_03453":null,"SJAG_03457":null,"SJAG_03460":null,"SJAG_03461":null,"SJAG_03469":null,"SJAG_03471":null,"SJAG_03472":null,"SJAG_03473":null,"SJAG_03475":null,"SJAG_03476":null,"SJAG_03479":null,"SJAG_03484":null,"SJAG_03485":null,"SJAG_03486":null,"SJAG_03495":null,"SJAG_03496":null,"SJAG_03497":null,"SJAG_03498":null,"SJAG_03501":null,"SJAG_03519":null,"SJAG_03526":null,"SJAG_03529":null,"SJAG_03533":null,"SJAG_03534":null,"SJAG_03538":null,"SJAG_03539":null,"SJAG_03542":null,"SJAG_03543":null,"SJAG_03545":null,"SJAG_03547":null,"SJAG_03550":null,"SJAG_03557":null,"SJAG_03562":null,"SJAG_03567":null,"SJAG_03569":null,"SJAG_03570":null,"SJAG_03572":null,"SJAG_03578":null,"SJAG_03583":null,"SJAG_03584":null,"SJAG_03585":null,"SJAG_03592":null,"SJAG_03594":null,"SJAG_03602":null,"SJAG_03603":null,"SJAG_03613":null,"SJAG_03622":null,"SJAG_03626":null,"SJAG_03629":null,"SJAG_03635":null,"SJAG_03654":null,"SJAG_03658":null,"SJAG_03659":null,"SJAG_03660":null,"SJAG_03665":null,"SJAG_03666":null,"SJAG_03669":null,"SJAG_03671":null,"SJAG_03674":null,"SJAG_03676":null,"SJAG_03678":null,"SJAG_03679":null,"SJAG_03682":null,"SJAG_03684":null,"SJAG_03688":null,"SJAG_03689":null,"SJAG_03696":null,"SJAG_03698":null,"SJAG_03702":null,"SJAG_03703":null,"SJAG_03706":null,"SJAG_03708":null,"SJAG_03709":null,"SJAG_03712":null,"SJAG_03718":null,"SJAG_03720":null,"SJAG_03722":null,"SJAG_03724":null,"SJAG_03728":null,"SJAG_03730":null,"SJAG_03732":null,"SJAG_03734":null,"SJAG_03735":null,"SJAG_03743":null,"SJAG_03745":null,"SJAG_03747":null,"SJAG_03750":null,"SJAG_03751":null,"SJAG_03753":null,"SJAG_03780":null,"SJAG_03785":null,"SJAG_03788":null,"SJAG_03789":null,"SJAG_03796":null,"SJAG_03798":null,"SJAG_03799":null,"SJAG_03804":null,"SJAG_03811":null,"SJAG_03813":null,"SJAG_03828":null,"SJAG_03832":null,"SJAG_03840":null,"SJAG_03846":null,"SJAG_03850":null,"SJAG_03852":null,"SJAG_03853":null,"SJAG_03854":null,"SJAG_03855":null,"SJAG_03861":null,"SJAG_03866":null,"SJAG_03872":null,"SJAG_03876":null,"SJAG_03877":null,"SJAG_03879":null,"SJAG_03883":null,"SJAG_03886":null,"SJAG_03887":null,"SJAG_03892":null,"SJAG_03896":null,"SJAG_03897":null,"SJAG_03898":null,"SJAG_03903":null,"SJAG_03905":null,"SJAG_03906":null,"SJAG_03909":null,"SJAG_03911":null,"SJAG_03914":null,"SJAG_03915":null,"SJAG_03916":null,"SJAG_03918":null,"SJAG_03919":null,"SJAG_03922":null,"SJAG_03923":null,"SJAG_03926":null,"SJAG_03927":null,"SJAG_03929":null,"SJAG_03932":null,"SJAG_03937":null,"SJAG_03939":null,"SJAG_03941":null,"SJAG_03942":null,"SJAG_03944":null,"SJAG_03945":null,"SJAG_03946":null,"SJAG_03948":null,"SJAG_03950":null,"SJAG_03952":null,"SJAG_03954":null,"SJAG_03956":null,"SJAG_03957":null,"SJAG_03959":null,"SJAG_03961":null,"SJAG_03967":null,"SJAG_03982":null,"SJAG_03983":null,"SJAG_03984":null,"SJAG_03985":null,"SJAG_03987":null,"SJAG_03994":null,"SJAG_03995":null,"SJAG_03996":null,"SJAG_03997":null,"SJAG_04000":null,"SJAG_04001":null,"SJAG_04003":null,"SJAG_04004":null,"SJAG_04006":null,"SJAG_04009":null,"SJAG_04018":null,"SJAG_04019":null,"SJAG_04022":null,"SJAG_04030":null,"SJAG_04032":null,"SJAG_04036":null,"SJAG_04038":null,"SJAG_04039":null,"SJAG_04042":null,"SJAG_04043":null,"SJAG_04052":null,"SJAG_04054":null,"SJAG_04055":null,"SJAG_04056":null,"SJAG_04061":null,"SJAG_04064":null,"SJAG_04065":null,"SJAG_04066":null,"SJAG_04069":null,"SJAG_04071":null,"SJAG_04079":null,"SJAG_04081":null,"SJAG_04084":null,"SJAG_04089":null,"SJAG_04091":null,"SJAG_04092":null,"SJAG_04094":null,"SJAG_04108":null,"SJAG_04114":null,"SJAG_04117":null,"SJAG_04118":null,"SJAG_04121":null,"SJAG_04125":null,"SJAG_04126":null,"SJAG_04145":null,"SJAG_04147":null,"SJAG_04149":null,"SJAG_04150":null,"SJAG_04153":null,"SJAG_04154":null,"SJAG_04156":null,"SJAG_04157":null,"SJAG_04160":null,"SJAG_04163":null,"SJAG_04167":null,"SJAG_04175":null,"SJAG_04178":null,"SJAG_04181":null,"SJAG_04183":null,"SJAG_04186":null,"SJAG_04187":null,"SJAG_04188":null,"SJAG_04189":null,"SJAG_04190":null,"SJAG_04191":null,"SJAG_04199":null,"SJAG_04203":null,"SJAG_04206":null,"SJAG_04210":null,"SJAG_04213":null,"SJAG_04214":null,"SJAG_04217":null,"SJAG_04224":null,"SJAG_04230":null,"SJAG_04232":null,"SJAG_04233":null,"SJAG_04245":null,"SJAG_04249":null,"SJAG_04256":null,"SJAG_04257":null,"SJAG_04258":null,"SJAG_04261":null,"SJAG_04265":null,"SJAG_04268":null,"SJAG_04270":null,"SJAG_04271":null,"SJAG_04276":null,"SJAG_04277":null,"SJAG_04280":null,"SJAG_04281":null,"SJAG_04282":null,"SJAG_04283":null,"SJAG_04285":null,"SJAG_04287":null,"SJAG_04288":null,"SJAG_04304":null,"SJAG_04310":null,"SJAG_04312":null,"SJAG_04318":null,"SJAG_04320":null,"SJAG_04321":null,"SJAG_04324":null,"SJAG_04334":null,"SJAG_04339":null,"SJAG_04342":null,"SJAG_04343":null,"SJAG_04347":null,"SJAG_04351":null,"SJAG_04355":null,"SJAG_04360":null,"SJAG_04362":null,"SJAG_04366":null,"SJAG_04367":null,"SJAG_04369":null,"SJAG_04372":null,"SJAG_04373":null,"SJAG_04375":null,"SJAG_04379":null,"SJAG_04380":null,"SJAG_04381":null,"SJAG_04383":null,"SJAG_04385":null,"SJAG_04387":null,"SJAG_04388":null,"SJAG_04389":null,"SJAG_04394":null,"SJAG_04405":null,"SJAG_04407":null,"SJAG_04408":null,"SJAG_04409":null,"SJAG_04410":null,"SJAG_04414":null,"SJAG_04418":null,"SJAG_04421":null,"SJAG_04424":null,"SJAG_04427":null,"SJAG_04435":null,"SJAG_04457":null,"SJAG_04459":null,"SJAG_04461":null,"SJAG_04465":null,"SJAG_04468":null,"SJAG_04469":null,"SJAG_04470":null,"SJAG_04473":null,"SJAG_04475":null,"SJAG_04477":null,"SJAG_04478":null,"SJAG_04480":null,"SJAG_04482":null,"SJAG_04486":null,"SJAG_04490":null,"SJAG_04492":null,"SJAG_04495":null,"SJAG_04497":null,"SJAG_04507":null,"SJAG_04508":null,"SJAG_04509":null,"SJAG_04511":null,"SJAG_04521":null,"SJAG_04524":null,"SJAG_04527":null,"SJAG_04530":null,"SJAG_04537":null,"SJAG_04544":null,"SJAG_04549":null,"SJAG_04551":null,"SJAG_04552":null,"SJAG_04562":null,"SJAG_04566":null,"SJAG_04573":null,"SJAG_04574":null,"SJAG_04577":null,"SJAG_04582":null,"SJAG_04584":null,"SJAG_04586":null,"SJAG_04587":null,"SJAG_04589":null,"SJAG_04597":null,"SJAG_04599":null,"SJAG_04601":null,"SJAG_04608":null,"SJAG_04610":null,"SJAG_04611":null,"SJAG_04612":null,"SJAG_04622":null,"SJAG_04627":null,"SJAG_04634":null,"SJAG_04635":null,"SJAG_04640":null,"SJAG_04650":null,"SJAG_04652":null,"SJAG_04655":null,"SJAG_04657":null,"SJAG_04663":null,"SJAG_04665":null,"SJAG_04666":null,"SJAG_04669":null,"SJAG_04670":null,"SJAG_04671":null,"SJAG_04678":null,"SJAG_04680":null,"SJAG_04682":null,"SJAG_04686":null,"SJAG_04689":null,"SJAG_04692":null,"SJAG_04693":null,"SJAG_04695":null,"SJAG_04700":null,"SJAG_04712":null,"SJAG_04734":null,"SJAG_04738":null,"SJAG_04743":null,"SJAG_04744":null,"SJAG_04745":null,"SJAG_04747":null,"SJAG_04749":null,"SJAG_04752":null,"SJAG_04753":null,"SJAG_04754":null,"SJAG_04755":null,"SJAG_04756":null,"SJAG_04757":null,"SJAG_04760":null,"SJAG_04761":null,"SJAG_04762":null,"SJAG_04766":null,"SJAG_04767":null,"SJAG_04772":null,"SJAG_04777":null,"SJAG_04778":null,"SJAG_04782":null,"SJAG_04791":null,"SJAG_04810":null,"SJAG_04813":null,"SJAG_04814":null,"SJAG_04816":null,"SJAG_04818":null,"SJAG_04823":null,"SJAG_04824":null,"SJAG_04825":null,"SJAG_04839":null,"SJAG_04840":null,"SJAG_04842":null,"SJAG_04845":null,"SJAG_04847":null,"SJAG_04849":null,"SJAG_04855":null,"SJAG_04856":null,"SJAG_04857":null,"SJAG_04862":null,"SJAG_04863":null,"SJAG_04865":null,"SJAG_04874":null,"SJAG_04877":null,"SJAG_04879":null,"SJAG_04880":null,"SJAG_04882":null,"SJAG_04891":null,"SJAG_04894":null,"SJAG_04898":null,"SJAG_04900":null,"SJAG_04908":null,"SJAG_04911":null,"SJAG_04914":null,"SJAG_04916":null,"SJAG_04917":null,"SJAG_04918":null,"SJAG_04919":null,"SJAG_04920":null,"SJAG_04933":null,"SJAG_04934":null,"SJAG_04940":null,"SJAG_04942":null,"SJAG_04946":null,"SJAG_04949":null,"SJAG_04950":null,"SJAG_04959":null,"SJAG_04970":null,"SJAG_04974":null,"SJAG_04980":null,"SJAG_04981":null,"SJAG_04988":null,"SJAG_04993":null,"SJAG_04995":null,"SJAG_04998":null,"SJAG_05000":null,"SJAG_05003":null,"SJAG_05006":null,"SJAG_05009":null,"SJAG_05010":null,"SJAG_05012":null,"SJAG_05014":null,"SJAG_05015":null,"SJAG_05018":null,"SJAG_05019":null,"SJAG_05020":null,"SJAG_05021":null,"SJAG_05022":null,"SJAG_05024":null,"SJAG_05025":null,"SJAG_05027":null,"SJAG_05030":null,"SJAG_05105":null,"SJAG_05153":null,"SJAG_05173":null,"SJAG_05186":null,"SJAG_05187":null,"SJAG_05190":null,"SJAG_05193":null,"SJAG_05194":null,"SJAG_05205":null,"SJAG_05209":null,"SJAG_05213":null,"SJAG_05214":null,"SJAG_05218":null,"SJAG_05221":null,"SJAG_05230":null,"SJAG_05231":null,"SJAG_05239":null,"SJAG_05240":null,"SJAG_05242":null,"SJAG_05247":null,"SJAG_05248":null,"SJAG_05249":null,"SJAG_05253":null,"SJAG_05257":null,"SJAG_05265":null,"SJAG_05271":null,"SJAG_05276":null,"SJAG_05280":null,"SJAG_05288":null,"SJAG_05290":null,"SJAG_05295":null,"SJAG_05301":null,"SJAG_05304":null,"SJAG_05313":null,"SJAG_05322":null,"SJAG_05332":null,"SJAG_05333":null,"SJAG_05337":null,"SJAG_05339":null,"SJAG_05340":null,"SJAG_05343":null,"SJAG_05353":null,"SJAG_05372":null,"SJAG_05373":null,"SJAG_05694":null,"SJAG_05979":null,"SJAG_06449":null,"SJAG_06576":null,"SJAG_06586":null,"SJAG_06597":null,"SJAG_06599":null,"SJAG_06608":null,"SJAG_06612":null,"SJAG_06621":null,"SJAG_06622":null,"SJAG_06642":null,"SJAG_16453":null,"SJAG_16455":null,"SJAG_16456":null,"SJAG_16457":null,"SJAG_16460":null,"SJAG_MIT04":null,"SJAG_MIT05":null,"SJAG_MIT06":null,"SJAG_MIT07":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"organic cyclic compound binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-1497796"],"termid":"GO:0097159","terms_by_termid":{"GO:0000049":null,"GO:0000182":null,"GO:0000339":null,"GO:0000340":null,"GO:0000400":null,"GO:0000402":null,"GO:0000403":null,"GO:0000404":null,"GO:0000405":null,"GO:0000406":null,"GO:0000900":null,"GO:0000976":null,"GO:0000977":null,"GO:0000978":null,"GO:0000979":null,"GO:0000987":null,"GO:0000992":null,"GO:0001002":null,"GO:0001003":null,"GO:0001006":null,"GO:0001018":null,"GO:0001046":null,"GO:0001147":null,"GO:0001162":null,"GO:0001163":null,"GO:0001164":null,"GO:0001165":null,"GO:0002055":null,"GO:0002134":null,"GO:0002135":null,"GO:0003677":null,"GO:0003684":null,"GO:0003688":null,"GO:0003690":null,"GO:0003691":null,"GO:0003697":null,"GO:0003723":null,"GO:0003725":null,"GO:0003727":null,"GO:0003729":null,"GO:0003730":null,"GO:0003743":null,"GO:0003746":null,"GO:0003747":null,"GO:0005496":null,"GO:0005524":null,"GO:0005525":null,"GO:0008079":null,"GO:0008097":null,"GO:0008142":null,"GO:0008143":null,"GO:0008187":null,"GO:0008266":null,"GO:0008301":null,"GO:0008312":null,"GO:0008494":null,"GO:0010181":null,"GO:0010844":null,"GO:0016149":null,"GO:0016150":null,"GO:0016208":null,"GO:0017069":null,"GO:0017070":null,"GO:0019002":null,"GO:0019003":null,"GO:0019237":null,"GO:0019843":null,"GO:0020037":null,"GO:0030170":null,"GO:0030515":null,"GO:0030552":null,"GO:0030619":null,"GO:0030620":null,"GO:0030621":null,"GO:0030623":null,"GO:0030627":null,"GO:0030628":null,"GO:0030975":null,"GO:0030976":null,"GO:0030983":null,"GO:0031490":null,"GO:0032131":null,"GO:0032132":null,"GO:0032136":null,"GO:0032137":null,"GO:0032138":null,"GO:0032141":null,"GO:0032357":null,"GO:0032549":null,"GO:0032934":null,"GO:0033204":null,"GO:0033592":null,"GO:0034057":null,"GO:0034511":null,"GO:0034513":null,"GO:0035197":null,"GO:0035485":null,"GO:0035486":null,"GO:0035487":null,"GO:0035488":null,"GO:0035613":null,"GO:0035925":null,"GO:0035939":null,"GO:0036002":null,"GO:0036042":null,"GO:0042134":null,"GO:0042162":null,"GO:0043035":null,"GO:0043047":null,"GO:0043110":null,"GO:0043531":null,"GO:0043565":null,"GO:0044374":null,"GO:0044377":null,"GO:0045027":null,"GO:0045131":null,"GO:0048027":null,"GO:0050660":null,"GO:0050661":null,"GO:0051287":null,"GO:0051880":null,"GO:0061776":null,"GO:0062037":null,"GO:0062104":null,"GO:0070034":null,"GO:0070180":null,"GO:0070181":null,"GO:0070336":null,"GO:0070337":null,"GO:0070401":null,"GO:0070402":null,"GO:0070403":null,"GO:0071443":null,"GO:0071949":null,"GO:0097157":null,"GO:0097159":null,"GO:0098505":null,"GO:0098808":null,"GO:0106222":null,"GO:0106260":null,"GO:0110035":null,"GO:0140431":null,"GO:0140585":null,"GO:1902444":null,"GO:1905108":null,"GO:1990165":null,"GO:1990605":null,"GO:1990814":null,"GO:1990825":null,"GO:1990837":null,"GO:1990856":null,"GO:1990943":null}}


id: MONDO:1010016
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mitral valve stenosis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiovascular disorder, non-human animal","termid":"MONDO:1011306"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitral valve stenosis, non-human animal","secondary_identifiers":["OMIA:000655"],"termid":"MONDO:1010016","xrefs":{"Monarch":{"xref_id":"1010016"}}}


id: GO:0046739
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The transport of a virus between cells in a multicellular organism. The cells can be adjacent or spatially separated (e.g. in different tissues or organs).","definition_xrefs":["GOC:bf","GOC:jl","ISBN:0781718325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"migration in host","termid":"GO:0044001"},{"relation_name":"is_a","term_name":"transport of virus","termid":"GO:0046794"}],"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":"transport of virus in multicellular host","synonyms":[{"name":"spread of virus in multicellular host","type":"related"},{"name":"spread of virus within multicellular host","type":"exact"},{"name":"viral spread within multicellular host","type":"exact"}],"termid":"GO:0046739"}


id: FYECO:0000231
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which sodium sulfite (Na2SO3) 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":"+ Na2SO3","synonyms":[{"name":"sodium sulfite added","type":"exact"}],"termid":"FYECO:0000231"}


id: MONDO:1012232
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary adenomatosis, non-human animal","termid":"MONDO:1011927"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pulmonary adenomatosis, cattle","secondary_identifiers":["OMIA:000840-9913"],"termid":"MONDO:1012232","xrefs":{"Monarch":{"xref_id":"1012232"}}}


id: PBO:0047124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 168 member A","termid":"PBO:0047124"}


id: MONDO:0010756
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary von Willebrand disease","termid":"MONDO:0019565"}],"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":"Von Willebrand disease, X-linked form","secondary_identifiers":["UMLS:C1839113","OMIM:314560","MESH:C564041","MEDGEN:333255"],"synonyms":[{"name":"Von Willebrand disease, X-linked","type":"related"},{"name":"Von Willebrand disease, X-linked form","type":"exact"}],"termid":"MONDO:0010756","xrefs":{"Monarch":{"xref_id":"0010756"}}}


id: GO:0007133
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle phase during which chromosomes separate and migrate towards the poles of the spindle the as part of meiosis I.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiosis I cell cycle phase","termid":"GO:0098764"},{"relation_name":"part_of","term_name":"anaphase","termid":"GO:0051322"},{"relation_name":"part_of","term_name":"meiotic M phase","termid":"GO:0051327"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0051327"}],"interesting_parent_ids":["GO:0008150","GO:0051327"],"is_obsolete":false,"name":"meiotic anaphase I","termid":"GO:0007133"}


id: GO:1902406
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cellular process in which the mitotic contractile ring cytokinetic ring attains its fully functional state.","definition_xrefs":["PMID:25451933"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actomyosin contractile ring maturation","termid":"GO:0031566"},{"relation_name":"is_a","term_name":"mitotic cell cycle process","termid":"GO:1903047"},{"relation_name":"part_of","term_name":"mitotic cytokinesis","termid":"GO:0000281"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0030036"},{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0000281"}],"interesting_parent_ids":["GO:0007049","GO:0007010","GO:0030036","GO:0008150","GO:0000281"],"is_obsolete":false,"name":"mitotic actomyosin contractile ring maturation","synonyms":[{"name":"mitotic cytokinesis contractile ring maintenance","type":"related"}],"termid":"GO:1902406"}


id: PBO:0084744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial isoleucyl-tRNA synthetase; null mutant is deficient in respiratory growth; human homolog IARS2 implicated in mitochondrial diseases, can partially complement yeast null mutant","termid":"PBO:0084744"}


id: PBO:0070588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 54","termid":"PBO:0070588"}


id: PBO:0072562
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAS related 2","termid":"PBO:0072562"}


id: PBO:0073366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serpin family I member 1","termid":"PBO:0073366"}


id: PBO:0087888
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcriptional repressor involved in regulating multidrug resistance; negatively regulates expression of the PDR5 gene; member of the Gal4p family of zinc cluster proteins","termid":"PBO:0087888"}


id: GO:0075014
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The increase in size or mass of symbiont, or the progression of the symbiont from an initial condition to a later condition, occurring on or near its host rhizosphere. The host rhizosphere is defined as total below-ground surfaces of a plant as a habitat for its symbiont. 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 growth or development of symbiont on or near host rhizosphere (obsolete GO:0075014)","synonyms":[{"name":"growth or development of symbiont on or near host rhizosphere","type":"exact"}],"termid":"GO:0075014"}


id: GO:0003205
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of a cardiac chamber over time, from its formation to the mature structure. A cardiac chamber is an enclosed cavity within the heart.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"heart development","termid":"GO:0007507"}],"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 chamber development","termid":"GO:0003205"}


id: PBO:0028473
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_succinate_dehydrogenase_(ubiquinone)_activity","termid":"PBO:0028473"}


id: GO:0008625
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals in which a signal is conveyed from the cell surface to trigger the apoptotic death of a cell. The pathway starts with a ligand binding to a death domain receptor on the cell surface, and ends when the execution phase of apoptosis is triggered.","definition_xrefs":["GOC:mah","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrinsic apoptotic signaling pathway","termid":"GO:0097191"}],"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":"extrinsic apoptotic signaling pathway via death domain receptors","synonyms":[{"name":"death receptor-mediated apoptosis","type":"narrow"},{"name":"induction of apoptosis via death domain receptors","type":"related"},{"name":"induction of apoptosis via death receptors","type":"exact"}],"termid":"GO:0008625"}


id: GO:0035299
data:
  {"annotated_genes":["SJAG_01148"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[116139],"is_not":false,"summary":null,"term":"GO:0035299"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 1D-myo-inositol 1,3,4,5,6-pentakisphosphate + ATP = 1D-myo-inositol hexakisphosphate + ADP + H+.","definition_xrefs":["RHEA:20313"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol pentakisphosphate kinase activity","termid":"GO:0120517"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01148":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016301","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"inositol-1,3,4,5,6-pentakisphosphate 2-kinase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R05202","EC:2.7.1.158","MetaCyc:RXN-7163","Reactome:R-HSA-1855176","Reactome:R-HSA-1855179"],"synonyms":[{"name":"IP5 2-kinase activity","type":"related"},{"name":"Ins(1,3,4,5,6)P5 2-kinase activity","type":"related"},{"name":"inositol hexakisphosphate synthase","type":"related"},{"name":"inositol pentakisphosphate 2-kinase activity","type":"exact"},{"name":"inositol polyphosphate kinase activity","type":"related"},{"name":"inositol-pentakisphosphate 2-kinase activity","type":"related"}],"termid":"GO:0035299","terms_by_termid":{"GO:0035299":null}}


id: PBO:0047617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FGF1 intracellular binding protein","termid":"PBO:0047617"}


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


id: PBO:0030768
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_response_to_stress_during_vegetative_growth","termid":"PBO:0030768"}


id: PR:O59782
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An anion exchange transporter that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04211","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":"sulfate permease C320.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC320.05","secondary_identifiers":["UniProtKB:O59782"],"synonyms":[{"name":"Spom972h-SLC26A7","type":"exact"}],"termid":"PR:O59782"}


id: PBO:0045786
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epididymal protein 3A","termid":"PBO:0045786"}


id: SO:0002169
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that falls in the polypyrimidine tract at 3' end of intron between 17 and 3 bases from the end (acceptor -3 to acceptor -17).","direct_ancestors":[{"relation_name":"is_a","term_name":"splicing_variant","termid":"SO:0001568"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splice_polypyrimidine_tract_variant","synonyms":[{"name":"splice polypyrimidine tract variant","type":"exact"}],"termid":"SO:0002169"}


id: PBO:0045386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dipeptidyl peptidase 8","termid":"PBO:0045386"}


id: MONDO:0034962
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare ophthalmic disorder with cortical involvement (obsolete MONDO:0034962)","secondary_identifiers":["Orphanet:519343"],"termid":"MONDO:0034962","xrefs":{"Monarch":{"xref_id":"0034962"}}}


id: GO:0017006
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The covalent linking of a tetrapyrrole to a protein.","definition_xrefs":["GOC:ai"],"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":"protein-tetrapyrrole linkage","termid":"GO:0017006"}


id: PBO:0034809
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 MAGE family subunit Nse3","termid":"PBO:0034809"}


id: GO:0045352
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Blocks the binding of interleukin-1 to interleukin-1 type I receptors.","definition_xrefs":["GOC:ebc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interleukin-1 receptor antagonist activity","termid":"GO:0005152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140678"}],"interesting_parent_ids":["GO:0005488","GO:0098772","GO:0140678","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"interleukin-1 type I receptor antagonist activity","synonyms":[{"name":"IL-1ra type I","type":"exact"}],"termid":"GO:0045352"}


id: GO:0039682
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process of unidirectional viral DNA replication that takes place on a circular DNA to rapidly produce numerous copies of the viral genome. Involves creating a nick in one strand of the circular DNA molecule at the origin of replication. DNA is then synthesized by DNA polymerase. Using the non-nicked strand as a template, replication proceeds around the circular DNA molecule, displacing the nicked strand as single-stranded DNA.","definition_xrefs":["Wikipedia:Rolling_circle_replication","GOC:bf","GOC:jl","VZ:915"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral DNA strand displacement replication","termid":"GO:0039687"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"rolling circle viral DNA replication","termid":"GO:0039682"}


id: PBO:0064896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 2 regulatory subunit B'beta","termid":"PBO:0064896"}


id: GO:0019122
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of peptidyl-D-alanine, by either racemization or from peptidyl-L-serine.","definition_xrefs":["RESID:AA0191"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-L-amino acid racemization","termid":"GO:0018085"},{"relation_name":"is_a","term_name":"peptidyl-alanine modification","termid":"GO:0018194"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0008150"],"is_obsolete":false,"name":"peptidyl-D-alanine racemization","synonyms":[{"name":"alanine racemization","type":"broad"}],"termid":"GO:0019122"}


id: PBO:0075292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 31","termid":"PBO:0075292"}


id: GO:0051388
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the neurotrophin TRK receptor signaling pathway.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of signal transduction","termid":"GO:0009967"},{"relation_name":"is_a","term_name":"regulation of neurotrophin TRK receptor signaling pathway","termid":"GO:0051386"},{"relation_name":"positively_regulates","term_name":"neurotrophin TRK receptor signaling pathway","termid":"GO:0048011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of neurotrophin TRK receptor signaling pathway","synonyms":[{"name":"activation of nerve growth factor receptor signaling pathway","type":"narrow"},{"name":"positive regulation of NGF receptor signaling pathway","type":"exact"},{"name":"positive regulation of NGF receptor signalling pathway","type":"exact"},{"name":"positive regulation of nerve growth factor receptor signaling pathway","type":"related"},{"name":"positive regulation of nerve growth factor receptor signalling pathway","type":"exact"},{"name":"stimulation of nerve growth factor receptor signaling pathway","type":"narrow"},{"name":"up regulation of nerve growth factor receptor signaling pathway","type":"exact"},{"name":"up-regulation of nerve growth factor receptor signaling pathway","type":"exact"},{"name":"upregulation of nerve growth factor receptor signaling pathway","type":"exact"}],"termid":"GO:0051388"}


id: PBO:0049694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"huntingtin associated protein 1","termid":"PBO:0049694"}


id: PBO:0011485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human COMT catechol O-methyltransferase homolog 1","termid":"PBO:0011485"}


id: GO:0008797
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-aspartate = fumarate + NH3.","definition_xrefs":["EC:4.3.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ammonia-lyase activity","termid":"GO:0016841"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"aspartate ammonia-lyase activity","secondary_identifiers":["MetaCyc:ASPARTASE-RXN","RHEA:16601"],"synonyms":[{"name":"L-aspartase activity","type":"related"},{"name":"L-aspartate ammonia-lyase (fumarate-forming)","type":"related"},{"name":"L-aspartate ammonia-lyase activity","type":"related"},{"name":"aspartase activity","type":"related"},{"name":"fumaric aminase activity","type":"related"}],"termid":"GO:0008797"}


id: GO:0014070
data:
  {"annotated_genes":["SJAG_01584"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115552],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031990"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an organic cyclic compound stimulus.","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01584":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to organic cyclic compound","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"response to organic cyclic substance","type":"exact"}],"termid":"GO:0014070","terms_by_termid":{"GO:0031990":null}}


id: PBO:0052563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine methyltransferase 2C","termid":"PBO:0052563"}


id: SO:0002185
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A non-coding locus that originates from within the promoter region of a protein-coding gene, with transcription proceeding in the opposite direction on the other strand.","direct_ancestors":[{"relation_name":"is_a","term_name":"lncRNA_gene","termid":"SO:0002127"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bidirectional_promoter_lncRNA_gene","synonyms":[{"name":"bidirectional promoter lncRNA","type":"exact"},{"name":"bidirectional promoter lncRNA gene","type":"exact"},{"name":"bidirectional_promoter_lncRNA_gene","type":"exact"}],"termid":"SO:0002185"}


id: PBO:0045165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein axonemal intermediate chain 7","termid":"PBO:0045165"}


id: MONDO:0021373
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the parietal lobe.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm of cerebral hemisphere","termid":"MONDO:0021374"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neoplasm of parietal lobe","secondary_identifiers":["NCIT:C5573","SCTID:126956001","MEDGEN:266073","UMLS:C1263888"],"synonyms":[{"name":"neoplasm of parietal lobe","type":"exact"},{"name":"neoplasm of the parietal lobe","type":"exact"},{"name":"parietal lobe neoplasm","type":"exact"},{"name":"parietal lobe neoplasm (disease)","type":"exact"},{"name":"parietal lobe tumor","type":"exact"},{"name":"parietal lobe tumour","type":"exact"},{"name":"tumor of parietal lobe","type":"exact"},{"name":"tumor of the parietal lobe","type":"exact"},{"name":"tumour of parietal lobe","type":"exact"},{"name":"tumour of the parietal lobe","type":"exact"}],"termid":"MONDO:0021373","xrefs":{"Monarch":{"xref_id":"0021373"}}}


id: GO:0046888
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the regulated release of a hormone from a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell communication","termid":"GO:0010648"},{"relation_name":"is_a","term_name":"negative regulation of signaling","termid":"GO:0023057"},{"relation_name":"is_a","term_name":"regulation of hormone secretion","termid":"GO:0046883"},{"relation_name":"is_a","term_name":"negative regulation of secretion by cell","termid":"GO:1903531"},{"relation_name":"negatively_regulates","term_name":"hormone secretion","termid":"GO:0046879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of hormone secretion","synonyms":[{"name":"down regulation of hormone secretion","type":"exact"},{"name":"down-regulation of hormone secretion","type":"exact"},{"name":"downregulation of hormone secretion","type":"exact"},{"name":"inhibition of hormone secretion","type":"narrow"}],"termid":"GO:0046888"}


id: PBO:0083742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential component of the MIND kinetochore complex; joins kinetochore subunits contacting DNA to those contacting microtubules; required for accurate chromosome segregation; complex consists of Mtw1p Including Nnf1p-Nsl1p-Dsn1p (MIND)","termid":"PBO:0083742"}


id: PBO:0034639
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_H4-K16_acetylation_at_telomere","termid":"PBO:0034639"}


id: GO:0034545
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: fumarylpyruvate + H2O = fumarate + pyruvate + H+.","definition_xrefs":["UM-BBD_reactionID:r0811"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid carbon-carbon bonds, in ketonic substances","termid":"GO:0016823"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"fumarylpyruvate hydrolase activity","secondary_identifiers":["EC:3.7.1.20","RHEA:26168"],"termid":"GO:0034545"}


id: PBO:0057299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 513c","termid":"PBO:0057299"}


id: MONDO:0013037
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":"Giacheti syndrome","secondary_identifiers":["MESH:C567864","OMIM:612917","MEDGEN:414543","UMLS:C2752043"],"synonyms":[{"name":"Giacheti syndrome","type":"exact"},{"name":"Marfanoid habitus and specific language and learning disabilities","type":"related"}],"termid":"MONDO:0013037","xrefs":{"Monarch":{"xref_id":"0013037"}}}


id: MONDO:0004705
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A solitary fibrous tumor that arises from the liver. It affects females more frequently than males. Signs and symptoms include the presence of an abdominal mass and abdominal discomfort.","definition_xrefs":["NCIT:C5752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibroma","termid":"MONDO:0005167"},{"relation_name":"is_a","term_name":"solitary fibrous tumor","termid":"MONDO:0016238"},{"relation_name":"is_a","term_name":"liver and intrahepatic bile duct neoplasm","termid":"MONDO:0024477"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"liver solitary fibrous tumor","secondary_identifiers":["DOID:907","UMLS:C1333965","MEDGEN:232273"],"synonyms":[{"name":"fibroma of liver","type":"exact"},{"name":"fibroma of the liver","type":"exact"},{"name":"hepatic fibroma","type":"exact"},{"name":"liver fibroma","type":"exact"},{"name":"liver localised fibrous mesothelioma","type":"exact"},{"name":"liver localised fibrous tumour","type":"exact"},{"name":"liver localized fibrous mesothelioma","type":"exact"},{"name":"liver localized fibrous tumor","type":"exact"},{"name":"liver solitary fibrous tumor","type":"exact"}],"termid":"MONDO:0004705","xrefs":{"Monarch":{"xref_id":"0004705"}}}


id: GO:0042992
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of the movement of a transcription factor from the cytoplasm to the nucleus.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of transcription factor import into nucleus (obsolete GO:0042992)","synonyms":[{"name":"down regulation of transcription factor import into nucleus","type":"exact"},{"name":"down-regulation of transcription factor import into nucleus","type":"exact"},{"name":"downregulation of transcription factor import into nucleus","type":"exact"},{"name":"inhibition of transcription factor import into nucleus","type":"narrow"},{"name":"negative regulation of transcription factor import into cell nucleus","type":"exact"},{"name":"negative regulation of transcription factor transport from cytoplasm to nucleus","type":"exact"},{"name":"negative regulation of transcription factor-nucleus import","type":"exact"}],"termid":"GO:0042992"}


id: PBO:0087400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Stress-responsive transcriptional activator; activated in stochastic pulses of nuclear localization in response to various stress conditions; binds DNA at stress response elements of responsive genes, inducing gene expression; involved in diauxic shift","termid":"PBO:0087400"}


id: GO:0018044
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The formation of a C-terminal peptidyl-leucine amide by hydrolysis and oxidation of an interior Leu-Gly peptide in a secreted protein.","definition_xrefs":["RESID:AA0091"],"gene_count":0,"genotype_count":0,"name":"obsolete C-terminal peptidyl-leucine amidation (obsolete GO:0018044)","termid":"GO:0018044"}


id: PBO:0090086
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal ubiquitin-protein ligase E3 Pex12","termid":"PBO:0090086"}


id: PBO:0028320
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_nucleus_during_cellular_response_to_hydrogen_peroxide","termid":"PBO:0028320"}


id: PBO:0050134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 44","termid":"PBO:0050134"}


id: GO:0052880
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which a diphenol, or related compound, acts as a hydrogen or electron donor and reduces a copper protein.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on diphenols and related substances as donors","termid":"GO:0016679"}],"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:0016491","GO:0003674"],"is_obsolete":false,"name":"oxidoreductase activity, acting on diphenols and related substances as donors, with copper protein as acceptor","secondary_identifiers":["EC:1.10.9.-"],"termid":"GO:0052880"}


id: PBO:0091334
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphatase Z Homolog","termid":"PBO:0091334"}


id: PBO:0075902
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3","termid":"PBO:0075902"}


id: MONDO:0012892
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic disease, caused by lack of lysyl hydrohylase 3 (LH3) activity, characterized by multiple tissue and organ involvement, including skeletal abnormalities (club foot, progressive scoliosis, osteopenia, pathologic fractures), ocular involvement (flat retinae, myopia, cataracts) and hair, nail and skin anomalies (coarse, abnormally distributed hair, skin blistering, reduced palmar creases, hypoplastic nails). Patients also present intrauterine growth retardation, facial dysmorphism (flat facial profile, low-set ears, shallow orbits, short and upturned nose, downturned corners of mouth) and joint flexion contractures. Growth and developmental delay, bilateral sensorineural deafness, friable diaphragm and later-onset spontaneous vascular ruptures are additional reported features.","definition_xrefs":["Orphanet:300284"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bone fragility with contractures, arterial rupture, and deafness","secondary_identifiers":["GARD:17362","OMIM:612394","MEDGEN:382811","SCTID:763318007","UMLS:C2676285","MESH:C567320"],"synonyms":[{"name":"LH3 deficiency","type":"related"},{"name":"bone fragility with contractures, arterial rupture, and deafness","type":"exact"},{"name":"bone fragility-contractures-arterial rupture-deafness syndrome","type":"exact"},{"name":"connective tissue disorder due to LH3 deficiency","type":"exact"},{"name":"connective tissue disorder due to lysyl hydroxylase-3 deficiency","type":"exact"},{"name":"lysyl Hydroxylase 3 deficiency","type":"related"}],"termid":"MONDO:0012892","xrefs":{"Monarch":{"xref_id":"0012892"}}}


id: FYPO:0004971
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 one or more messenger RNAs that are normally expressed during a cellular response to stress measured in a cell is lower than normal (i.e. lower than observed in wild-type cells during vegetative growth) during a cellular response to phosphate starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of stress responsive gene mRNA during vegetative growth","termid":"FYPO:0005908"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0006551","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased level of stress responsive gene mRNA during cellular response to phosphate starvation","synonyms":[{"name":"decreased level of cellular response to stress gene mRNA during cellular response to phosphate starvation","type":"exact"},{"name":"decreased level of stress responsive gene RNA during cellular response to phosphate starvation","type":"exact"},{"name":"decreased level of stress responsive gene mRNA during cellular response to phosphate starvation during mitotic cell cycle","type":"related"},{"name":"decreased level of stress responsive gene mRNA during cellular response to phosphate starvation during vegetative growth","type":"exact"},{"name":"decreased level of stress responsive gene transcripts during cellular response to phosphate starvation","type":"exact"},{"name":"decreased mRNA level of stress responsive genes during cellular response to phosphate starvation","type":"exact"},{"name":"decreased stress responsive gene mRNA accumulation during cellular response to phosphate starvation","type":"related"},{"name":"reduced level of stress responsive gene mRNA during cellular response to phosphate starvation","type":"exact"}],"termid":"FYPO:0004971"}


id: MOD:01455
data:
  {"annotated_genes":["SJAG_02763","SJAG_00318","SJAG_01587","SJAG_02183","SJAG_00331","SJAG_03012","SJAG_02472","SJAG_02498","SJAG_02592"],"annotation_feature_type":"gene","cv_annotations":{"PSI-MOD":[{"annotations":[79982,79866,79906,79917,79812,79857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00042"},{"annotations":[79828,118683,118684,118569,118570,118685,118686,79827],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00046"}]},"cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue hydroxyl or carboxyl hydrogen with a phosphono group (H2PO3 or 'phosphate').","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphorylated residue","termid":"MOD:00696"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00318":null,"SJAG_00331":null,"SJAG_01587":null,"SJAG_02183":null,"SJAG_02472":null,"SJAG_02498":null,"SJAG_02592":null,"SJAG_02763":null,"SJAG_03012":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00696"}],"interesting_parent_ids":["MOD:00696"],"is_obsolete":false,"name":"O-phosphorylated residue","references_by_uniquename":{"PMID:26774782":null,"PMID:31150379":null,"PMID:36408920":null},"synonyms":[{"name":"OPhosRes","type":"exact"}],"termid":"MOD:01455","terms_by_termid":{"GO:0034599":null,"GO:0034605":null,"GO:0071475":null,"GO:1904547":null,"MOD:00042":null,"MOD:00046":null}}


id: FYPO:0008246
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 transcribed from cenH measured in a cell is normal. cenH is a region located between mat2-P and mat3-M that is homologous to centromeric repeats, and that produces non-coding RNAs and small interfering RNAs.","definition_xrefs":["PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA level during vegetative growth","termid":"FYPO:0001317"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0000257","FYPO:0001320"],"is_obsolete":false,"name":"normal cenH-derived RNA level","termid":"FYPO:0008246"}


id: MONDO:0001836
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The absence of menses in a woman who has achieved reproductive age.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"female reproductive system disorder","termid":"MONDO:0002263"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amenorrhea","secondary_identifiers":["MESH:D000568","UMLS:C0002453","MEDGEN:8016","NCIT:C61443","ICD9:626.0","HP:0000141","DOID:13938"],"synonyms":[{"name":"absence of menstruation","type":"exact"},{"name":"amenia","type":"exact"},{"name":"amenorrhea","type":"exact"},{"name":"amenorrhea (disease)","type":"exact"}],"termid":"MONDO:0001836","xrefs":{"Monarch":{"xref_id":"0001836"}}}


id: MONDO:0021465
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the vermiform appendix.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"appendiceal neoplasm","termid":"MONDO:0001236"},{"relation_name":"is_a","term_name":"benign neoplasm of cecum","termid":"MONDO:0021464"}],"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":"benign neoplasm of appendix","secondary_identifiers":["UMLS:C0496860","NCIT:C4773","SCTID:91981009","icd11.foundation:7146014","MEDGEN:99221","ICD10CM:D12.1"],"synonyms":[{"name":"benign appendix neoplasm","type":"exact"},{"name":"benign appendix tumor","type":"exact"},{"name":"benign appendix tumour","type":"exact"},{"name":"benign neoplasm of the appendix","type":"exact"},{"name":"benign tumor of appendix","type":"exact"},{"name":"benign tumor of the appendix","type":"exact"},{"name":"benign tumour of appendix","type":"exact"},{"name":"benign tumour of the appendix","type":"exact"},{"name":"vermiform appendix benign neoplasm","type":"exact"}],"termid":"MONDO:0021465","xrefs":{"Monarch":{"xref_id":"0021465"}}}


id: PBO:0068685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 66, pseudogene","termid":"PBO:0068685"}


id: PBO:0040834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"baculoviral IAP repeat containing 8","termid":"PBO:0040834"}


id: PBO:0070620
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 like 1 pseudogene 4","termid":"PBO:0070620"}


id: GO:0033678
data:
  {"annotated_genes":["SJAG_03780","SJAG_02242"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[99077,111660],"is_not":false,"summary":null,"term":"GO:0033678"}]},"cv_name":"molecular_function","definition":"Unwinding of a DNA/RNA duplex in the 5' to 3' direction, driven by ATP hydrolysis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA/RNA helicase activity","termid":"GO:0033677"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02242":null,"SJAG_03780":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0140097","GO:0140098"],"is_obsolete":false,"name":"5'-3' DNA/RNA helicase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0033682","Reactome:R-HSA-163120"],"synonyms":[{"name":"5' to 3' DNA/RNA helicase activity","type":"exact"},{"name":"ATP-dependent 5' to 3' DNA/RNA helicase activity","type":"exact"},{"name":"ATP-dependent 5'-3' DNA/RNA helicase activity","type":"exact"}],"termid":"GO:0033678","terms_by_termid":{"GO:0033678":null}}


id: _global:causal_relation_between_processes
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"p is causally related to q if and only if p or any part of p and q or any part of q are linked by a chain of events where each event pair is one where the execution of p influences the execution of q. p may be upstream, downstream, part of, or a container of q.","direct_ancestors":[{"relation_name":"is_a","term_name":"causally_related_to","termid":"_global:causally_related_to"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"causal_relation_between_processes","secondary_identifiers":["RO:0002501"],"termid":"_global:causal_relation_between_processes"}


id: PBO:0073048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small cysteine and glycine repeat containing 6","termid":"PBO:0073048"}


id: PBO:0089146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterol transfer protein Osh41","termid":"PBO:0089146"}


id: FYPO:0007266
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the endoplasmic reticulum (ER) colocalizes with eisosomes to a lower extent than normal.","definition_xrefs":["PMID:32023460","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cortical endoplasmic reticulum organization","termid":"FYPO:0007571"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased colocalization of cortical endoplasmic reticulum with eisosomes","synonyms":[{"name":"decreased colocalization of cortical ER with eisosomes","type":"exact"},{"name":"decreased colocalization of cortical endoplasmic reticulum with eisosomes during mitotic cell cycle","type":"related"},{"name":"decreased colocalization of cortical endoplasmic reticulum with eisosomes during vegetative growth","type":"exact"},{"name":"decreased colocalization of tubular cortical ER with eisosomes","type":"exact"},{"name":"decreased cortical ER-eisosome colocalization","type":"exact"},{"name":"reduced colocalization of cortical endoplasmic reticulum with eisosomes","type":"exact"}],"termid":"FYPO:0007266"}


id: GO:0052156
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont alters or subverts the T-cell mediated immune response of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host immune response","termid":"GO:0052553"}],"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 perturbation of host T-cell mediated immune response","secondary_identifiers":["GO:0052295"],"synonyms":[{"name":"modulation by organism of T-cell mediated immune response of other organism involved in symbiotic interaction","type":"broad"},{"name":"modulation by symbiont of host T-cell mediated immune response","type":"exact"},{"name":"perturbation of host T-cell mediated immune response","type":"exact"},{"name":"symbiont-mediated modulation of host cell-mediated immune response","type":"exact"},{"name":"symbiont-mediated perturbation of host cell-mediated immune response","type":"exact"}],"termid":"GO:0052156"}


id: PBO:0054232
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 1614","termid":"PBO:0054232"}


id: MONDO:0016439
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Elastoderma is a rare condition that affects the skin. People affected by elastoderma generally have increased laxity of skin covering a specific area of the body. Decreased recoil of the skin has also been reported. Although any part of the body can be affected, the skin of the neck and extremities (arms and legs, especially at the elbows and/or knees) are most commonly involved. The exact underlying cause is currently unknown; however, it generally occurs sporadically in people with no family history of the condition. There is no standard therapy available for elastoderma. Some cases have been treated with surgical excision (removal of affected skin), but hyperlaxity of skin often returns following the surgery.","direct_ancestors":[{"relation_name":"is_a","term_name":"dermis disorder","termid":"MONDO:0021154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"elastoderma","secondary_identifiers":["SCTID:238832003","UMLS:C0406555","icd11.foundation:1880397739","ICD9:701.8","GARD:12716","MEDGEN:590504","Orphanet:228240"],"termid":"MONDO:0016439","xrefs":{"Monarch":{"xref_id":"0016439"}}}


id: PBO:0001521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase type 2A (predicted)","termid":"PBO:0001521"}


id: PBO:0002745
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein, human ZNF593 ortholog","termid":"PBO:0002745"}


id: MONDO:0859312
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurodevelopmental disorder","termid":"MONDO:0700092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities","secondary_identifiers":["UMLS:C5774251","MEDGEN:1824024","OMIM:620113"],"termid":"MONDO:0859312","xrefs":{"Monarch":{"xref_id":"0859312"}}}


id: GO:0020002
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The plasma membrane surrounding a host cell.","definition_xrefs":["GOC:mb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell membrane","termid":"GO:0033644"}],"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 plasma membrane","termid":"GO:0020002"}


id: FYPO:0000546
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 protein modification begins later than normal. All modifications may be affected, or only modifications of a certain type, or on specific proteins, or even specific sites within specific proteins.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein modification during vegetative growth","termid":"FYPO:0000329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002494","FYPO:0005447","FYPO:0002274","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"delayed onset of protein modification during vegetative growth","synonyms":[{"name":"delayed onset of protein modification during mitotic cell cycle","type":"related"},{"name":"delayed onset of protein/peptide modification during vegetative growth","type":"exact"},{"name":"delayed protein modification during vegetative growth","type":"exact"},{"name":"protein/peptide modification: delayed","type":"related"}],"termid":"FYPO:0000546"}


id: PATO:0001987
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's having a three dimensional cavity with a narrow or no opening, and often containing an anatomical substance.","definition_xrefs":["PATOC:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure, cavities","termid":"PATO:0002014"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"saccular","synonyms":[{"name":"sacular","type":"exact"}],"termid":"PATO:0001987"}


id: MONDO:0002742
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually well to moderately differentiated cervical adenocarcinoma characterized by the presence of malignant glandular cells that contain significant amount of intracytoplasmic mucin.","definition_xrefs":["NCIT:C36095"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucinous adenocarcinoma","termid":"MONDO:0004957"},{"relation_name":"is_a","term_name":"cervical adenocarcinoma","termid":"MONDO:0005153"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"cervical mucinous adenocarcinoma","secondary_identifiers":["DOID:3701","MEDGEN:232048","UMLS:C1332919"],"synonyms":[{"name":"cervical mucinous adenocarcinoma","type":"exact"},{"name":"uterine cervix mucinous adenocarcinoma","type":"exact"}],"termid":"MONDO:0002742","xrefs":{"Monarch":{"xref_id":"0002742"}}}


id: MONDO:0000353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Saldino-Noonan syndrome (obsolete MONDO:0000353)","termid":"MONDO:0000353","xrefs":{"Monarch":{"xref_id":"0000353"}}}


id: GO:0048923
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a posterior lateral line neuromast hair cell. (N.B. This may be development of neuromast hair cell type or a set of cell of neuromast hair cell type. This will involve the change of a cell or set of cells from one cell identity to another). Hair cells are the sensory receptors of the neuromast and are located in a portion of the neuromast called the sensory strip. Each hair cell of the neuromast is morphologically polarized as a result of the relative position of the single kinocilium and the clusters of stereocilia on its apical surface. There are approximately seven hair cells within each neuromast, with each hair cell innervated by afferent and efferent neurons.","definition_xrefs":["ISBN:0125296509"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuromast hair cell differentiation","termid":"GO:0048886"},{"relation_name":"part_of","term_name":"posterior lateral line neuromast development","termid":"GO:0048919"}],"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":"posterior lateral line neuromast hair cell differentiation","termid":"GO:0048923"}


id: PBO:0085761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase of the bud neck involved in the septin checkpoint; associates with septin proteins, negatively regulates Swe1p by phosphorylation, shows structural homology to bud neck kinases Gin4p and Hsl1p; KCC4 has a paralog, GIN4, that arose from the whole genome duplication","termid":"PBO:0085761"}


id: PR:Q9UUD6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ubp11 gene.","definition_xrefs":["UniProtKB:Q9UUD6","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin carboxyl-terminal hydrolase 11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19C2.04c","synonyms":[{"name":"Spom972h-ubp11","type":"exact"},{"name":"deubiquitinating enzyme 11 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin thioesterase 11 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin-specific-processing protease 11 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UUD6"}


id: PBO:0076260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"supervillin family member 2, pseudogene","termid":"PBO:0076260"}


id: FYPO:0005814
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 plus ends of microtubules does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to microtubule during vegetative growth","termid":"FYPO:0003269"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"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:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0001320","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein localization to microtubule plus-end","synonyms":[{"name":"abolished protein localisation to microtubule plus-end","type":"exact"},{"name":"abolished protein localization to microtubule plus end","type":"exact"},{"name":"abolished protein localization to microtubule plus-end during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to microtubule plus-end during vegetative growth","type":"exact"},{"name":"protein localization to microtubule plus-end abolished","type":"exact"}],"termid":"FYPO:0005814"}


id: PBO:0091648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar heme ABC transmembrane exporter Abc3","termid":"PBO:0091648"}


id: FYPO:0005945
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 chromosomal truncation that would result in the loss of one of two different alleles of a gene occurs at a normal (i.e. indistinguishable from wild type) frequency.","definition_xrefs":["PomBase:mah","PMID:19798055"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal frequency of break-induced loss of heterozygosity","termid":"FYPO:0005945"}


id: PBO:0081395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 234","termid":"PBO:0081395"}


id: GO:0047541
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-furoate + ATP + CoA = 2-furoyl-CoA + AMP + diphosphate + H+.","definition_xrefs":["EC:6.2.1.31","RHEA:19269"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CoA-ligase activity","termid":"GO:0016405"},{"relation_name":"is_a","term_name":"acid-thiol ligase activity","termid":"GO:0016878"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016874","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"2-furoate-CoA ligase activity","secondary_identifiers":["KEGG_REACTION:R02986","MetaCyc:2-FUROATE--COA-LIGASE-RXN"],"synonyms":[{"name":"2-furoate:CoA ligase (AMP-forming)","type":"related"},{"name":"2-furoyl coenzyme A synthetase activity","type":"related"}],"termid":"GO:0047541"}


id: PBO:0040210
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ASXL transcriptional regulator 3","termid":"PBO:0040210"}


id: PBO:0083783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential protein involved in maturation of 18S rRNA; depletion leads to inhibited pre-rRNA processing and reduced polysome levels; localizes primarily to the nucleolus","termid":"PBO:0083783"}


id: GO:0051197
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways involving a coenzyme.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of coenzyme metabolic process (obsolete GO:0051197)","synonyms":[{"name":"activation of coenzyme metabolic process","type":"narrow"},{"name":"positive regulation of coenzyme and prosthetic group metabolic process","type":"broad"},{"name":"positive regulation of coenzyme and prosthetic group metabolism","type":"broad"},{"name":"positive regulation of coenzyme metabolism","type":"exact"},{"name":"stimulation of coenzyme metabolic process","type":"narrow"},{"name":"up regulation of coenzyme metabolic process","type":"exact"},{"name":"up-regulation of coenzyme metabolic process","type":"exact"},{"name":"upregulation of coenzyme metabolic process","type":"exact"}],"termid":"GO:0051197"}


