# terms

id: MONDO:0975751
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"intellectual disability, autosomal dominant 20","termid":"MONDO:0013266"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain abnormalities-severe developmental delay-facial dysmorphism-intellectual disability syndrome due to MEF2C mutation","secondary_identifiers":["Orphanet:664416"],"termid":"MONDO:0975751","xrefs":{"Monarch":{"xref_id":"0975751"}}}


id: GO:1902798
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of snoRNA processing.","definition_xrefs":["PMID:24210919","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of gene expression","termid":"GO:0010628"},{"relation_name":"is_a","term_name":"regulation of snoRNA processing","termid":"GO:1902796"},{"relation_name":"is_a","term_name":"positive regulation of snoRNA metabolic process","termid":"GO:1903325"},{"relation_name":"positively_regulates","term_name":"sno(s)RNA processing","termid":"GO:0043144"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0016074"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016074"}],"interesting_parent_ids":["GO:0010467","GO:0016074","GO:0008150"],"is_obsolete":false,"name":"positive regulation of snoRNA processing","synonyms":[{"name":"activation of snoRNA processing","type":"narrow"},{"name":"up regulation of snoRNA processing","type":"exact"},{"name":"up-regulation of snoRNA processing","type":"exact"},{"name":"upregulation of snoRNA processing","type":"exact"}],"termid":"GO:1902798"}


id: MONDO:0010948
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the CRYBA1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset non-syndromic cataract","termid":"MONDO:0011060"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"cataract 10 multiple types","secondary_identifiers":["MESH:C563435","OMIM:600881","UMLS:C1833229","DOID:0110258","MEDGEN:318817"],"synonyms":[{"name":"CCZS","type":"narrow"},{"name":"CRYBA1 early-onset non-syndromic cataract","type":"exact"},{"name":"CTRCT10","type":"exact"},{"name":"cataract 10, multiple types","type":"related"},{"name":"cataract, congenital zonular, with sutural opacities","type":"related"},{"name":"congenital zonular cataract with sutural opacities","type":"narrow"},{"name":"early-onset non-syndromic cataract caused by mutation in CRYBA1","type":"exact"}],"termid":"MONDO:0010948","xrefs":{"Monarch":{"xref_id":"0010948"}}}


id: GO:0004937
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with epinephrine or norepinephrine to initiate a change in cell activity via activation of a G protein, with pharmacological characteristics of alpha1-adrenergic receptors; the activity involves transmitting the signal to the Gq alpha subunit of a heterotrimeric G protein.","definition_xrefs":["GOC:cb","GOC:mah","IUPHAR_GPCR:1274"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-adrenergic receptor activity","termid":"GO:0004936"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"alpha1-adrenergic receptor activity","synonyms":[{"name":"alpha1 adrenoceptor","type":"exact"}],"termid":"GO:0004937"}


id: GO:0061129
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of directed movement of a motile cell or organism up a concentration gradient of 3',5'-cAMP by the action of DIF-2. DIF-2 is a chlorinated alkylphenone.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of positive chemotaxis to cAMP by DIF-2","termid":"GO:0061121"},{"relation_name":"is_a","term_name":"negative regulation of positive chemotaxis to cAMP by chlorinated alkylphenone","termid":"GO:0061125"}],"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 positive chemotaxis to cAMP by DIF-2","termid":"GO:0061129"}


id: MONDO:0009178
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"epidermolysis bullosa dystrophica","termid":"MONDO:0006543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"epidermolysis bullosa dystrophica Neurotrophica","secondary_identifiers":["OMIM:226500","MEDGEN:78666","UMLS:C0268368","MESH:C562637","ICD9:757.39","SCTID:254176007"],"synonyms":[{"name":"epidermolysis bullosa dystrophica Neurotrophica","type":"exact"},{"name":"epidermolysis bullosa progressiva, recessive","type":"related"},{"name":"epidermolysis bullosa with congenital deafness","type":"related"}],"termid":"MONDO:0009178","xrefs":{"Monarch":{"xref_id":"0009178"}}}


id: GO:0061578
data:
  {"annotated_genes":["SJAG_01528","SJAG_01281"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91124,96030],"is_not":false,"summary":null,"term":"GO:0061578"}]},"cv_name":"molecular_function","definition":"Hydrolysis of a ubiquitin unit from a ubiquitinated protein linked via the Lys63 residue of ubiquitin.","definition_xrefs":["GOC:pg","PMID:18313383","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deubiquitinase activity","termid":"GO:0101005"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01281":null,"SJAG_01528":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0008233","GO:0140096","GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"K63-linked deubiquitinase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-936381","Reactome:R-HSA-5357845","Reactome:R-HSA-5690856","Reactome:R-HSA-9711016","Reactome:R-HSA-5691411","Reactome:R-HSA-936390","Reactome:R-HSA-9685219","Reactome:R-HSA-741411","Reactome:R-HSA-9750942","Reactome:R-HSA-5696547","Reactome:R-HSA-8869506","Reactome:R-HSA-9817400","Reactome:R-HSA-5691439","Reactome:R-HSA-688136","Reactome:R-HSA-5691431"],"synonyms":[{"name":"K63-specific deubiquitinase activity","type":"exact"},{"name":"Lys63-specific deubiquitinase activity","type":"exact"}],"termid":"GO:0061578","terms_by_termid":{"GO:0061578":null}}


id: PBO:0063283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin gamma subfamily A, 9","termid":"PBO:0063283"}


id: MONDO:0007520
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An EEC syndrome characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 7q11.2-q21.3.","definition_xrefs":["PMID:1424230","DOID:0060784","PMID:5454938"],"direct_ancestors":[{"relation_name":"is_a","term_name":"EEC syndrome","termid":"MONDO:0010004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0000426"],"is_obsolete":false,"name":"ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1","secondary_identifiers":["OMIM:129900","MEDGEN:343663","MESH:C565062","GARD:15063","UMLS:C1851841"],"synonyms":[{"name":"EEC","type":"related"},{"name":"EEC syndrome 1","type":"exact"},{"name":"EEC syndrome-1","type":"exact"},{"name":"EEC1","type":"exact"},{"name":"ectrodactyly, ectodermal dysplasia, and cleft LIP/palate syndrome 1","type":"related"},{"name":"ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome type 1","type":"exact"}],"termid":"MONDO:0007520","xrefs":{"Monarch":{"xref_id":"0007520"}}}


id: PBO:0081373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 212","termid":"PBO:0081373"}


id: GO:0050908
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events involved in visual perception in which a light stimulus is received and converted into a molecular signal.","definition_xrefs":["GOC:dos","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of light stimulus involved in sensory perception","termid":"GO:0050962"},{"relation_name":"part_of","term_name":"visual perception","termid":"GO:0007601"}],"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 light stimulus involved in visual perception","synonyms":[{"name":"sensory detection of light during visual perception","type":"exact"},{"name":"sensory detection of light stimulus during visual perception","type":"exact"},{"name":"sensory transduction of light during visual perception","type":"exact"},{"name":"sensory transduction of light stimulus during visual perception","type":"exact"},{"name":"visual perception, detection of light stimulus","type":"exact"},{"name":"visual perception, sensory transduction during perception of light","type":"exact"},{"name":"visual perception, sensory transduction of light stimulus","type":"exact"}],"termid":"GO:0050908"}


id: PBO:0086648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the nucleolus and nucleus; predicted to be involved in ribosome biogenesis","termid":"PBO:0086648"}


id: GO:0070199
data:
  {"annotated_genes":["SJAG_01297","SJAG_02761","SJAG_03540","SJAG_02336"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103404,118164,99884,107752],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140210"}]},"cv_name":"biological_process","definition":"The directed movement of a protein to a specific location on a chromosome.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to chromosome","termid":"GO:0034502"},{"relation_name":"is_a","term_name":"establishment of protein localization to organelle","termid":"GO:0072594"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01297":null,"SJAG_02336":null,"SJAG_02761":null,"SJAG_03540":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"establishment of protein localization to chromosome","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"establishment of protein localisation to chromosome","type":"exact"}],"termid":"GO:0070199","terms_by_termid":{"GO:0140210":null}}


id: FYPO:0001566
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of L-citrulline measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cellular amino acid level","termid":"FYPO:0003986"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"increased cellular citrulline level","synonyms":[{"name":"increased cellular L-citrulline level","type":"exact"},{"name":"increased cellular citrulline level during mitotic cell cycle","type":"related"},{"name":"increased cellular citrulline level during vegetative growth","type":"exact"},{"name":"increased citrulline accumulation","type":"related"}],"termid":"FYPO:0001566"}


id: GO:0008802
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: betaine aldehyde + NAD+ + H2O = betaine + NADH + H+.","definition_xrefs":["EC:1.2.1.8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde dehydrogenase (NAD+) activity","termid":"GO:0004029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"betaine-aldehyde dehydrogenase (NAD+) activity","secondary_identifiers":["RHEA:15305","MetaCyc:BADH-RXN","Reactome:R-HSA-6797955"],"synonyms":[{"name":"BADH activity","type":"related"},{"name":"BetB","type":"related"},{"name":"betaine aldehyde dehydrogenase activity","type":"related"},{"name":"betaine aldehyde oxidase activity","type":"related"},{"name":"betaine-aldehyde:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0008802"}


id: PBO:0080072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 36","termid":"PBO:0080072"}


id: PBO:0075227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 3 pseudogene 1 X-linked","termid":"PBO:0075227"}


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


id: PBO:0000686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamine aminotransferease subunit (predicted)","termid":"PBO:0000686"}


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


id: GO:0005469
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: succinate(out) + fumarate(in) = succinate(in) + fumarate(out).","definition_xrefs":["TC:2.A.29.13.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fumarate transmembrane transporter activity","termid":"GO:0015138"},{"relation_name":"is_a","term_name":"succinate transmembrane transporter activity","termid":"GO:0015141"},{"relation_name":"is_a","term_name":"antiporter activity","termid":"GO:0015297"}],"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":"succinate:fumarate antiporter activity","secondary_identifiers":["RHEA:29323"],"termid":"GO:0005469"}


id: FYPO:0004156
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of protein measured in a cell during mitosis is lower than normal. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein level during vegetative growth","termid":"FYPO:0001324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0006551","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased protein level during mitosis","synonyms":[{"name":"decreased protein accumulation during mitosis","type":"related"},{"name":"decreased protein level during mitosis during vegetative growth","type":"exact"},{"name":"decreased protein level during mitotic M phase","type":"related"},{"name":"decreased protein level during mitotic nuclear division","type":"exact"},{"name":"reduced protein level during mitosis","type":"exact"}],"termid":"FYPO:0004156"}


id: GO:0047962
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: benzoyl-CoA + glycine = N-benzoylglycine + CoA + H+.","definition_xrefs":["EC:2.3.1.71","RHEA:18493"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016746","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"glycine N-benzoyltransferase activity","secondary_identifiers":["Reactome:R-HSA-159574","Reactome:R-HSA-9750001","MetaCyc:GLYCINE-N-BENZOYLTRANSFERASE-RXN","KEGG_REACTION:R02452","Reactome:R-HSA-159566"],"synonyms":[{"name":"benzoyl CoA-amino acid N-acyltransferase activity","type":"related"},{"name":"benzoyl-CoA:glycine N-acyltransferase activity","type":"related"},{"name":"benzoyl-CoA:glycine N-benzoyltransferase activity","type":"related"}],"termid":"GO:0047962"}


id: GO:1903546
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a photoreceptor outer segment.","definition_xrefs":["GO_REF:0000087","PMID:11481257","GOC:TermGenie","PMID:21867699"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to non-motile cilium","termid":"GO:0097499"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to photoreceptor outer segment","synonyms":[{"name":"protein localisation in photoreceptor outer segment","type":"exact"},{"name":"protein localisation to photoreceptor outer segment","type":"exact"},{"name":"protein localization in photoreceptor outer segment","type":"exact"}],"termid":"GO:1903546"}


id: PBO:0030397
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_level_during_cellular_response_to_pheromone","termid":"PBO:0030397"}


id: PBO:0089345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-oxoacyl-[acyl-carrier-protein]-synthase condensing enzyme Cem1","termid":"PBO:0089345"}


id: PBO:0047109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 157 member B","termid":"PBO:0047109"}


id: PBO:0077084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIFA inhibitor","termid":"PBO:0077084"}


id: GO:0070933
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H4 by the removal of one or more acetyl groups.","definition_xrefs":["GOC:BHF","GOC:rl"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H4 deacetylation (obsolete GO:0070933)","termid":"GO:0070933"}


id: PBO:0043185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondrogenesis-associated transcript","termid":"PBO:0043185"}


id: GO:0046926
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The post-translational cross-linking of a cysteine residue to an L-threonine residue to form 2-(S-L-cysteinyl)-D-allo-threonine.","definition_xrefs":["PMID:12696888","PMID:36302388","RESID:AA0342"],"gene_count":0,"genotype_count":0,"name":"obsolete peptide cross-linking via 2-(S-L-cysteinyl)-D-allo-threonine (obsolete GO:0046926)","termid":"GO:0046926"}


id: GO:0016188
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Steps required to form an initiated synaptic vesicle into a fully formed and transmissible synaptic vesicle.","definition_xrefs":["PMID:10099709","GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle organization","termid":"GO:0016050"},{"relation_name":"is_a","term_name":"developmental maturation","termid":"GO:0021700"}],"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":"synaptic vesicle maturation","termid":"GO:0016188"}


id: GO:0061452
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a neuron whose cell body resides in the retrotrapezoid nucleus.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system neuron differentiation","termid":"GO:0021953"},{"relation_name":"part_of","term_name":"retrotrapezoid nucleus development","termid":"GO:0061451"}],"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":"retrotrapezoid nucleus neuron differentiation","termid":"GO:0061452"}


id: PBO:0085035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Non-catalytic subunit of N-terminal acetyltransferase of the NatC type; required for replication of dsRNA virus; member of the Sm protein family","termid":"PBO:0085035"}


id: MONDO:0011156
data:
  {"annotated_genes":["SJAG_03363"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86399],"is_not":false,"summary":null,"term":"MONDO:0011156"}]},"cv_name":"mondo","definition":"Progressive familial intrahepatic cholestasis type 2 (PFIC2), a type of progressive familial intrahepatic cholestasis (PFIC), is a severe, neonatal, hereditary disorder in bile formation that is hepatocellular in origin and not associated with extrahepatic features. Initially, PFIC2 was reported under the name Byler syndrome.","definition_xrefs":["Orphanet:79304"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign recurrent intrahepatic cholestasis type 2","termid":"MONDO:0011559"},{"relation_name":"is_a","term_name":"progressive familial intrahepatic cholestasis","termid":"MONDO:0015762"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03363":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335","MONDO:0005066"],"is_obsolete":false,"name":"progressive familial intrahepatic cholestasis type 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3489789","GARD:1288","NANDO:1201044","OMIM:601847","DOID:0070222","icd11.foundation:1168921980","MEDGEN:483742"],"synonyms":[{"name":"ABCB11 progressive familial intrahepatic cholestasis","type":"exact"},{"name":"BSEP deficiency","type":"exact"},{"name":"PFIC2","type":"exact"},{"name":"cholestasis, progressive familial intrahepatic 2","type":"exact"},{"name":"cholestasis, progressive familial intrahepatic, 2","type":"related"},{"name":"cholestasis, progressive familial intrahepatic, type 2","type":"exact"},{"name":"progressive familial intrahepatic cholestasis caused by mutation in ABCB11","type":"exact"},{"name":"progressive familial intrahepatic cholestasis type 2","type":"exact"},{"name":"severe ABCB11 deficiency","type":"related"}],"termid":"MONDO:0011156","terms_by_termid":{"MONDO:0011156":null},"xrefs":{"Monarch":{"xref_id":"0011156"}}}


id: PBO:0027429
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_rate_of_DNA_strand_elongation_involved_in_mitotic_DNA_replication_at_highly_transcribed_RNA_polymerase_II_genes","termid":"PBO:0027429"}


id: GO:0044010
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which planktonically growing microorganisms of the same species grow at a liquid-air interface or on a solid substrate under the flow of a liquid and produce extracellular polymers that facilitate matrix formation, resulting in a change in the organisms' growth rate and gene transcription.","definition_xrefs":["GOC:cc","GOC:di","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biofilm formation","termid":"GO:0042710"},{"relation_name":"is_a","term_name":"biological process involved in intraspecies interaction between organisms","termid":"GO:0051703"}],"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":"single-species biofilm formation","secondary_identifiers":["GO:0052000"],"synonyms":[{"name":"auto-aggregation","type":"broad"},{"name":"bfp-dependent aggregation","type":"narrow"},{"name":"bundle-forming fimbriae-dependent aggregation","type":"narrow"},{"name":"bundle-forming pili-dependent aggregation","type":"narrow"},{"name":"tfp-dependent aggregation","type":"narrow"},{"name":"type IV pili-dependent aggregation","type":"narrow"}],"termid":"GO:0044010"}


id: PBO:0029481
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_sterol_ester_level","termid":"PBO:0029481"}


id: GO:2000266
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of blood coagulation, intrinsic pathway.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of blood coagulation","termid":"GO:0030193"},{"relation_name":"is_a","term_name":"regulation of protein activation cascade","termid":"GO:2000257"},{"relation_name":"regulates","term_name":"blood coagulation, intrinsic pathway","termid":"GO:0007597"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0051604"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0051604"],"is_obsolete":false,"name":"regulation of blood coagulation, intrinsic pathway","termid":"GO:2000266"}


id: PR:Q9UTG5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1805.10 gene.","definition_xrefs":["UniProtKB:Q9UTG5","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C1805.10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1805.10","synonyms":[{"name":"Spom972h-SPAC1805.10","type":"exact"}],"termid":"PR:Q9UTG5"}


id: MONDO:0006446
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant germ cell neoplasm arising from the testis. It is composed of primitive epithelial cells arranged in solid, papillary, and glandular configurations. Most patients present with a testicular mass, which may be associated with pain. More than half of the patients have metastatic disease at diagnosis. The form of treatment following radical orchiectomy is stage dependent.","definition_xrefs":["NCIT:C6341"],"direct_ancestors":[{"relation_name":"is_a","term_name":"testicular pure germ cell tumor","termid":"MONDO:0002874"},{"relation_name":"is_a","term_name":"testicular non-seminomatous germ cell cancer","termid":"MONDO:0003403"},{"relation_name":"is_a","term_name":"embryonal carcinoma","termid":"MONDO:0005440"},{"relation_name":"is_a","term_name":"embryonal neoplasm","termid":"MONDO:0005564"}],"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":"testicular embryonal carcinoma","secondary_identifiers":["DOID:5680","EFO:1000565","UMLS:C0238448","MEDGEN:66771"],"synonyms":[{"name":"embryonal carcinoma of testis","type":"exact"},{"name":"embryonal carcinoma of the testis","type":"exact"},{"name":"embryonal testis carcinoma","type":"exact"},{"name":"testicular embryonal carcinoma","type":"exact"},{"name":"testis embryonal carcinoma","type":"exact"}],"termid":"MONDO:0006446","xrefs":{"Monarch":{"xref_id":"0006446"}}}


id: FYPO:0004444
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the prospore membrane is decreased, and the protein is instead present in the plasma membrane, during the second meiotic nuclear division.","definition_xrefs":["PMID:21832151","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during meiosis","termid":"FYPO:0003549"},{"relation_name":"is_a","term_name":"decreased protein localization to prospore membrane","termid":"FYPO:0004442"}],"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to prospore membrane during meiosis II with protein mislocalized to plasma membrane","synonyms":[{"name":"decreased protein localisation to prospore membrane during meiosis II with protein mislocalized to plasma membrane","type":"exact"},{"name":"decreased protein localization to forespore membrane during meiosis II with protein mislocalized to plasma membrane","type":"exact"},{"name":"decreased protein localization to prospore membrane during second meiotic nuclear division with protein mislocalized to plasma membrane","type":"exact"},{"name":"decreased protein localization to prospore membrane with protein mislocalized to plasma membrane during meiosis II","type":"related"},{"name":"reduced protein localization to prospore membrane during meiosis II with protein mislocalized to plasma membrane","type":"exact"}],"termid":"FYPO:0004444"}


id: PBO:0070591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 57","termid":"PBO:0070591"}


id: GO:0052781
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of any chitobiose, a family of compounds derived from chitin and based on the structure of D-glucosaminyl-(1->4)-D-glucosamine.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chitobiose metabolic process","termid":"GO:0052780"},{"relation_name":"is_a","term_name":"amino disaccharide catabolic process","termid":"GO:0052782"}],"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":"chitobiose catabolic process","termid":"GO:0052781"}


id: PBO:0059200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAS related GPR family member X7, pseudogene","termid":"PBO:0059200"}


id: GO:0032481
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of type I interferon production. Type I interferons include the interferon-alpha, beta, delta, episilon, zeta, kappa, tau, and omega gene families.","definition_xrefs":["GOC:add","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cytokine production","termid":"GO:0001819"},{"relation_name":"is_a","term_name":"regulation of type I interferon production","termid":"GO:0032479"},{"relation_name":"positively_regulates","term_name":"type I interferon production","termid":"GO:0032606"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of type I interferon production","secondary_identifiers":["Reactome:R-HSA-1834949"],"synonyms":[{"name":"activation of type I interferon production","type":"narrow"},{"name":"positive regulation of type I IFN production","type":"exact"},{"name":"stimulation of type I interferon production","type":"narrow"},{"name":"up regulation of type I interferon production","type":"exact"},{"name":"up-regulation of type I interferon production","type":"exact"},{"name":"upregulation of type I interferon production","type":"exact"}],"termid":"GO:0032481"}


id: MOD:00795
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod","definition_xrefs":["Unimod:371","PubMed:11743741"],"direct_ancestors":[{"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":"Michael addition of hydroxymethylvinyl ketone to cysteine","synonyms":[{"name":"HMVK","type":"related"},{"name":"Michael addition of hydroxymethylvinyl ketone to cysteine","type":"related"}],"termid":"MOD:00795"}


id: PBO:0088717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aspartate kinase","termid":"PBO:0088717"}


id: GO:0051663
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of the nucleus to a specific location within a cell during the establishment and maintenance of the dorsal/ventral axis of the oocyte.","definition_xrefs":["GOC:dph","GOC:tb","GOC:mtg_sensu","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus localization","termid":"GO:0051647"},{"relation_name":"part_of","term_name":"oocyte dorsal/ventral axis specification","termid":"GO:0007310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"oocyte nucleus localization involved in oocyte dorsal/ventral axis specification","secondary_identifiers":["GO:0051662"],"synonyms":[{"name":"establishment and maintenance of oocyte nucleus localization during oocyte axis determination","type":"exact"},{"name":"oocyte axis determination, oocyte nucleus localization","type":"exact"},{"name":"oocyte nucleus localisation involved in oocyte dorsal/ventral axis specification","type":"exact"},{"name":"oocyte nucleus localization during oocyte axis determination","type":"related"},{"name":"oocyte nucleus localization involved in oocyte dorsal-ventral axis specification","type":"exact"},{"name":"oocyte nucleus localization involved in oocyte dorsal/ventral axis determination","type":"exact"},{"name":"oocyte nucleus localization involved in oocyte dorsoventral axis specification","type":"exact"}],"termid":"GO:0051663"}


id: PBO:0076864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed 13B","termid":"PBO:0076864"}


id: GO:0045753
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways resulting in the breakdown of acetate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of catabolic process","termid":"GO:0009895"},{"relation_name":"is_a","term_name":"regulation of acetate catabolic process","termid":"GO:0045734"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"negatively_regulates","term_name":"acetate catabolic process","termid":"GO:0045733"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0044248"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0044248"}],"interesting_parent_ids":["GO:0044248","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"negative regulation of acetate catabolic process","synonyms":[{"name":"down regulation of acetate catabolic process","type":"exact"},{"name":"down-regulation of acetate catabolic process","type":"exact"},{"name":"downregulation of acetate catabolic process","type":"exact"},{"name":"inhibition of acetate catabolic process","type":"narrow"},{"name":"negative regulation of acetate breakdown","type":"exact"},{"name":"negative regulation of acetate catabolism","type":"exact"},{"name":"negative regulation of acetate degradation","type":"exact"}],"termid":"GO:0045753"}


id: PBO:0028382
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_chromatin_organization_during_G0","termid":"PBO:0028382"}


id: GO:0034522
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: cis-1,2-dihydroxy-1,2-dihydro-8-carboxynaphthalene = 1,2-dihydroxy-8-carboxynaphthalene + 2 H+ + 2 e-.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete cis-1,2-dihydroxy-1,2-dihydro-8-carboxynaphthalene dehydrogenase activity (obsolete GO:0034522)","termid":"GO:0034522"}


id: PBO:0073822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 7 member 2","termid":"PBO:0073822"}


id: PBO:0067399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 505, pseudogene","termid":"PBO:0067399"}


id: GO:0007567
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The reproductive process in which the parent is separated from its offspring either by giving birth to live young or by laying eggs.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multi-organism reproductive process","termid":"GO:0044703"},{"relation_name":"is_a","term_name":"multi-multicellular organism process","termid":"GO:0044706"}],"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":"parturition","synonyms":[{"name":"egg laying","type":"narrow"},{"name":"giving birth","type":"exact"}],"termid":"GO:0007567"}


id: PBO:0040229
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"activating transcription factor 4 pseudogene 1","termid":"PBO:0040229"}


id: MONDO:0015044
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mu-heavy chain disease (mu-HCD) is a type of HCD characterized by the production of incomplete monoclonal mu-heavy chains without associated light chains. The clinical presentation resembles that of patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL).","definition_xrefs":["Orphanet:100024"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heavy chain disease","termid":"MONDO:0019464"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"mu-heavy chain disease","secondary_identifiers":["SCTID:61493004","NCIT:C3892","DOID:0060128","ICD9:273.2","UMLS:C0242310","MEDGEN:66875","GARD:19741","icd11.foundation:963887455"],"synonyms":[{"name":"mu chain disease","type":"exact"},{"name":"mu heavy chain disease","type":"exact"},{"name":"mu-HCD","type":"exact"}],"termid":"MONDO:0015044","xrefs":{"Monarch":{"xref_id":"0015044"}}}


id: MONDO:0009002
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coloboma","termid":"MONDO:0001476"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"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":"coloboma, ocular, autosomal recessive","secondary_identifiers":["OMIM:216820","UMLS:C4011974","MEDGEN:860411"],"synonyms":[{"name":"coloboma, ocular, autosomal recessive","type":"exact"}],"termid":"MONDO:0009002","xrefs":{"Monarch":{"xref_id":"0009002"}}}


id: PBO:0074088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC26A4 antisense RNA 1","termid":"PBO:0074088"}


id: FYPO:0005861
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which CCR4-NOT complex binding by a gene product (usually a protein) in a mutant does not occur. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah","PMID:26942678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein-protein interaction","termid":"FYPO:0000705"},{"relation_name":"is_a","term_name":"abnormal protein complex binding","termid":"FYPO:0003591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000702","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"abolished CCR4-NOT complex binding","synonyms":[{"name":"CCR4-NOT complex binding abolished","type":"exact"}],"termid":"FYPO:0005861"}


id: GO:0042723
data:
  {"annotated_genes":["SJAG_02406","SJAG_04866","SJAG_02047","SJAG_00381","SJAG_04067","SJAG_03538","SJAG_01970","SJAG_03362","SJAG_00827","SJAG_02420","SJAG_02421","SJAG_04282","SJAG_01742"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[113177,88514],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090180"},{"annotations":[99024,113084,106867,93777,113090,113501,115517],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009228"},{"annotations":[113085,113091,113502,115518,99025,93778],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009229"},{"annotations":[58605,65695,99026],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006772"},{"annotations":[109939,109940,99027],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036172"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving thiamine (vitamin B1), and compounds derived from it.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"water-soluble vitamin metabolic process","termid":"GO:0006767"},{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"relation_name":"is_a","term_name":"pyrimidine-containing compound metabolic process","termid":"GO:0072527"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00381":null,"SJAG_00827":null,"SJAG_01742":null,"SJAG_01970":null,"SJAG_02047":null,"SJAG_02406":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_03362":null,"SJAG_03538":null,"SJAG_04067":null,"SJAG_04282":null,"SJAG_04866":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006790","GO:0006766"],"is_obsolete":false,"name":"thiamine-containing compound metabolic process","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-196819"],"synonyms":[{"name":"thiamin and derivative metabolic process","type":"exact"},{"name":"thiamin and derivative metabolism","type":"exact"},{"name":"thiamin-containing compound metabolic process","type":"exact"},{"name":"thiamine and derivative metabolic process","type":"exact"},{"name":"thiamine and derivative metabolism","type":"exact"},{"name":"thiamine-containing compound metabolism","type":"exact"},{"name":"vitamin B1 and derivative metabolic process","type":"exact"},{"name":"vitamin B1 and derivative metabolism","type":"exact"}],"termid":"GO:0042723","terms_by_termid":{"GO:0006772":null,"GO:0009228":null,"GO:0009229":null,"GO:0036172":null,"GO:0090180":null}}


id: PBO:0058484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5591","termid":"PBO:0058484"}


id: PBO:0081160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger RNA binding protein","termid":"PBO:0081160"}


id: GO:1903108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of transcription occurring in the mitochondrion.","definition_xrefs":["PMID:21357609","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA-templated transcription","termid":"GO:0006355"},{"relation_name":"is_a","term_name":"regulation of mitochondrial gene expression","termid":"GO:0062125"},{"relation_name":"regulates","term_name":"mitochondrial transcription","termid":"GO:0006390"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0140053"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0140053","GO:0006355","GO:0008150","GO:0006351"],"is_obsolete":false,"name":"regulation of mitochondrial transcription","synonyms":[{"name":"regulation of transcription from mitochondrial promoter","type":"exact"}],"termid":"GO:1903108"}


id: GO:0048814
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of dendrite morphogenesis.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of anatomical structure morphogenesis","termid":"GO:0022603"},{"relation_name":"is_a","term_name":"regulation of dendrite development","termid":"GO:0050773"},{"relation_name":"regulates","term_name":"dendrite morphogenesis","termid":"GO:0048813"}],"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 dendrite morphogenesis","termid":"GO:0048814"}


id: PBO:0081020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger C2HC-type containing 1B","termid":"PBO:0081020"}


id: MONDO:0018387
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare male infertility due to adrenal disorder (obsolete MONDO:0018387)","secondary_identifiers":["Orphanet:399584"],"termid":"MONDO:0018387","xrefs":{"Monarch":{"xref_id":"0018387"}}}


id: MONDO:0008214
data:
  {"annotated_genes":["SJAG_04810"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85718],"is_not":false,"summary":null,"term":"MONDO:0008214"}]},"cv_name":"mondo","definition":"An autosomal dominant inherited condition caused by mutations in the lamin B receptor gene. It is characterized by defects in the neutrophil lobulation, resulting in the presence of dumbbell-shaped neutrophils with bilobed nuclei in the peripheral blood smear.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"leukocyte disorder","termid":"MONDO:0004805"},{"relation_name":"is_a","term_name":"laminopathy","termid":"MONDO:0021106"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04810":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0000426","MONDO:0005046"],"is_obsolete":false,"name":"Pelger-Huet anomaly","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:10617","MESH:D010381","DOID:9631","NCIT:C85002","OMIM:169400","icd11.foundation:1210390183","GARD:9148","SCTID:85559002","EFO:1001093","UMLS:C0030779","MedDRA:10029377"],"synonyms":[{"name":"PHA","type":"related"},{"name":"Pelger Huet anomaly","type":"related"},{"name":"Pelger-Huet anomaly","type":"exact"},{"name":"Pelger-Huet nuclear anomaly","type":"related"},{"name":"ovoid neutrophil nuclei, developmental delay, epilepsy and skeletal abnormalities","type":"related"}],"termid":"MONDO:0008214","terms_by_termid":{"MONDO:0008214":null},"xrefs":{"Monarch":{"xref_id":"0008214"}}}


id: GO:0102297
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: selenic acid + ATP + 2 H+ = adenylyl selenate + diphosphoric acid.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete selenate adenylyltransferase activity (obsolete GO:0102297)","termid":"GO:0102297"}


id: PBO:0086432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative integral membrane protein; member of DUP240 gene family; green fluorescent protein (GFP)-fusion protein localizes to the plasma membrane in a punctate pattern","termid":"PBO:0086432"}


id: GO:1905315
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any cell proliferation that is involved in endocardial cushion morphogenesis.","definition_xrefs":["GOC:TermGenie","GOC:BHF","GO_REF:0000060","PMID:20652948","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell proliferation involved in heart morphogenesis","termid":"GO:0061323"},{"relation_name":"part_of","term_name":"endocardial cushion morphogenesis","termid":"GO:0003203"}],"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 endocardial cushion morphogenesis","termid":"GO:1905315"}


id: GO:0042834
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Interacting selectively and non-covalently, in a non-covalent manner, with peptidoglycan, any of a class of glycoconjugates found in bacterial cell walls.","definition_xrefs":["GOC:go_curators","PMID:14698226"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosaminoglycan binding","termid":"GO:0005539"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"peptidoglycan binding","termid":"GO:0042834"}


id: MONDO:0007589
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"FZD4-related exudative vitreoretinopathy","termid":"MONDO:1040041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005559"],"is_obsolete":false,"name":"exudative vitreoretinopathy 1","secondary_identifiers":["NCIT:C175048","OMIM:133780","UMLS:C1851402","DOID:0111412","MESH:C536382","GARD:15068","MEDGEN:343561"],"synonyms":[{"name":"Criswick-Schepens syndrome","type":"related"},{"name":"EVR1","type":"related"},{"name":"FEVR, autosomal dominant","type":"related"},{"name":"exudative vitreoretinopathy 1","type":"exact"},{"name":"exudative vitreoretinopathy type 1","type":"exact"},{"name":"exudative vitreoretinopathy, familial, autosomal dominant","type":"related"},{"name":"retinopathy of prematurity","type":"related"}],"termid":"MONDO:0007589","xrefs":{"Monarch":{"xref_id":"0007589"}}}


id: MONDO:0018335
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete deep dermatophytosis (obsolete MONDO:0018335)","termid":"MONDO:0018335","xrefs":{"Monarch":{"xref_id":"0018335"}}}


id: PBO:0050265
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosomal binding domain 2 pseudogene 43","termid":"PBO:0050265"}


id: GO:1900260
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of RNA-directed 5'-3' RNA polymerase activity.","definition_xrefs":["GOC:pf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transferase activity","termid":"GO:0051348"}],"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 RNA-dependent RNA polymerase activity","synonyms":[{"name":"down regulation of PB1 proteins","type":"related"},{"name":"down regulation of PB2 proteins","type":"related"},{"name":"down regulation of RDRP","type":"related"},{"name":"down regulation of RNA nucleotidyltransferase (RNA-directed) activity","type":"exact"},{"name":"down regulation of RNA replicase activity","type":"exact"},{"name":"down regulation of RNA synthetase activity","type":"related"},{"name":"down regulation of RNA-dependent RNA polymerase activity","type":"exact"},{"name":"down regulation of RNA-dependent RNA replicase activity","type":"exact"},{"name":"down regulation of RNA-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"down regulation of RNA-directed RNA polymerase activity","type":"exact"},{"name":"down regulation of phage f2 replicase","type":"narrow"},{"name":"down regulation of polymerase L","type":"related"},{"name":"down regulation of ribonucleic acid replicase activity","type":"exact"},{"name":"down regulation of ribonucleic acid-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"down regulation of ribonucleic acid-dependent ribonucleic acid polymerase activity","type":"exact"},{"name":"down regulation of ribonucleic replicase activity","type":"exact"},{"name":"down regulation of ribonucleic synthetase activity","type":"related"},{"name":"down regulation of transcriptase","type":"broad"},{"name":"down-regulation of PB1 proteins","type":"related"},{"name":"down-regulation of PB2 proteins","type":"related"},{"name":"down-regulation of RDRP","type":"related"},{"name":"down-regulation of RNA nucleotidyltransferase (RNA-directed) activity","type":"exact"},{"name":"down-regulation of RNA replicase activity","type":"exact"},{"name":"down-regulation of RNA synthetase activity","type":"related"},{"name":"down-regulation of RNA-dependent RNA polymerase activity","type":"exact"},{"name":"down-regulation of RNA-dependent RNA replicase activity","type":"exact"},{"name":"down-regulation of RNA-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"down-regulation of RNA-directed RNA polymerase activity","type":"exact"},{"name":"down-regulation of phage f2 replicase","type":"narrow"},{"name":"down-regulation of polymerase L","type":"related"},{"name":"down-regulation of ribonucleic acid replicase activity","type":"exact"},{"name":"down-regulation of ribonucleic synthetase activity","type":"related"},{"name":"down-regulation of transcriptase","type":"broad"},{"name":"downregulation of PB1 proteins","type":"related"},{"name":"downregulation of PB2 proteins","type":"related"},{"name":"downregulation of RDRP","type":"related"},{"name":"downregulation of RNA nucleotidyltransferase (RNA-directed) activity","type":"exact"},{"name":"downregulation of RNA replicase activity","type":"exact"},{"name":"downregulation of RNA synthetase activity","type":"related"},{"name":"downregulation of RNA-dependent RNA polymerase activity","type":"exact"},{"name":"downregulation of RNA-dependent RNA replicase activity","type":"exact"},{"name":"downregulation of RNA-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"downregulation of RNA-directed RNA polymerase activity","type":"exact"},{"name":"downregulation of nucleoside-triphosphate:RNA nucleotidyltransferase (RNA-directed)","type":"exact"},{"name":"downregulation of phage f2 replicase","type":"narrow"},{"name":"downregulation of polymerase L","type":"related"},{"name":"downregulation of ribonucleic acid replicase activity","type":"exact"},{"name":"downregulation of ribonucleic acid-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"downregulation of ribonucleic acid-dependent ribonucleic acid polymerase activity","type":"exact"},{"name":"downregulation of ribonucleic replicase activity","type":"exact"},{"name":"downregulation of ribonucleic synthetase activity","type":"related"},{"name":"downregulation of transcriptase","type":"broad"},{"name":"inhibition of PB1 proteins","type":"related"},{"name":"inhibition of PB2 proteins","type":"related"},{"name":"inhibition of RDRP","type":"related"},{"name":"inhibition of RNA nucleotidyltransferase (RNA-directed) activity","type":"exact"},{"name":"inhibition of RNA replicase activity","type":"exact"},{"name":"inhibition of RNA synthetase activity","type":"related"},{"name":"inhibition of RNA-dependent RNA polymerase activity","type":"exact"},{"name":"inhibition of RNA-dependent RNA replicase activity","type":"exact"},{"name":"inhibition of RNA-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"inhibition of RNA-directed RNA polymerase activity","type":"narrow"},{"name":"inhibition of nucleoside-triphosphate:RNA nucleotidyltransferase (RNA-directed)","type":"exact"},{"name":"inhibition of phage f2 replicase","type":"narrow"},{"name":"inhibition of polymerase L","type":"related"},{"name":"inhibition of ribonucleic acid replicase activity","type":"exact"},{"name":"inhibition of ribonucleic acid-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"inhibition of ribonucleic acid-dependent ribonucleic acid polymerase activity","type":"exact"},{"name":"inhibition of ribonucleic replicase activity","type":"exact"},{"name":"inhibition of ribonucleic synthetase activity","type":"related"},{"name":"inhibition of transcriptase","type":"broad"},{"name":"negative regulation of 3D polymerase activity","type":"exact"},{"name":"negative regulation of PB1 proteins","type":"related"},{"name":"negative regulation of PB2 proteins","type":"related"},{"name":"negative regulation of RDRP","type":"related"},{"name":"negative regulation of RNA nucleotidyltransferase (RNA-directed) activity","type":"exact"},{"name":"negative regulation of RNA replicase activity","type":"exact"},{"name":"negative regulation of RNA synthetase activity","type":"related"},{"name":"negative regulation of RNA-dependent RNA replicase activity","type":"exact"},{"name":"negative regulation of RNA-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"negative regulation of RNA-directed 5'-3' RNA polymerase activity","type":"exact"},{"name":"negative regulation of RNA-directed RNA polymerase activity","type":"broad"},{"name":"negative regulation of nucleoside-triphosphate:RNA nucleotidyltransferase (RNA-directed)","type":"exact"},{"name":"negative regulation of phage f2 replicase","type":"narrow"},{"name":"negative regulation of polymerase L","type":"related"},{"name":"negative regulation of ribonucleic acid replicase activity","type":"exact"},{"name":"negative regulation of ribonucleic acid-dependent ribonucleate nucleotidyltransferase activity","type":"exact"},{"name":"negative regulation of ribonucleic acid-dependent ribonucleic acid polymerase activity","type":"exact"},{"name":"negative regulation of ribonucleic replicase activity","type":"exact"},{"name":"negative regulation of ribonucleic synthetase activity","type":"related"},{"name":"negative regulation of transcriptase","type":"broad"}],"termid":"GO:1900260"}


id: PBO:0091368
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased frequency of long tract gene conversion in the rad57delta single mutant was suppressed in the swi5delta rad57delta double mutant, to a level similar to that observed in the rad51 mutant","termid":"PBO:0091368"}


id: GO:0019164
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: pyruvate + CoA + 2 oxidized ferredoxin = acetyl-CoA + CO2 + 2 reduced ferredoxin + 2 H+.","definition_xrefs":["KEGG_REACTION:R01196"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, iron-sulfur protein as acceptor","termid":"GO:0016625"}],"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":"pyruvate synthase activity","secondary_identifiers":["MetaCyc:PYRUFLAVREDUCT-RXN","EC:1.2.7.1","GO:0018696","RHEA:12765"],"synonyms":[{"name":"PFOR","type":"exact"},{"name":"pyruvate oxidoreductase activity","type":"related"},{"name":"pyruvate synthetase activity","type":"related"},{"name":"pyruvate-ferredoxin reductase activity","type":"exact"},{"name":"pyruvate:ferredoxin 2-oxidoreductase (CoA-acetylating)","type":"related"},{"name":"pyruvate:ferredoxin oxidoreductase activity","type":"related"},{"name":"pyruvic-ferredoxin oxidoreductase activity","type":"related"}],"termid":"GO:0019164"}


id: GO:1904593
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to prostaglandin.","definition_xrefs":["GO_REF:0000067","PMID:21445266","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid derivative binding","termid":"GO:1901567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0008289","GO:0003674"],"is_obsolete":false,"name":"prostaglandin binding","termid":"GO:1904593"}


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


id: MONDO:0008976
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":"chondroitin-6-sulfaturia, defective cellular immunity, nephrotic syndrome","secondary_identifiers":["OMIM:215250","MEDGEN:349095","MESH:C565852","UMLS:C1859104"],"synonyms":[{"name":"chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome","type":"exact"}],"termid":"MONDO:0008976","xrefs":{"Monarch":{"xref_id":"0008976"}}}


id: PBO:0109016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSX family member 17, pseudogene","termid":"PBO:0109016"}


id: PBO:0015260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CLRC ubiquitin E3 ligase complex specificiy factor Raf1/Dos1","termid":"PBO:0015260"}


id: PBO:0113438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Stalled-ribosome rescue factor srRF1; similar to human peptidyl-tRNA hydrolase ICT1; associates with mitochondrial large subunit; not an essential gene","termid":"PBO:0113438"}


id: FYPO:0003460
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 trehalose measured in a cell is lower than normal when the cell is subject to oxidative stress.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"},{"relation_name":"is_a","term_name":"decreased cellular trehalose level","termid":"FYPO:0001447"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"decreased cellular trehalose level during cellular response to oxidative stress","synonyms":[{"name":"decreased cellular trehalose level during cellular response to oxidative stress during mitotic cell cycle","type":"related"},{"name":"decreased cellular trehalose level during oxidative stress response","type":"exact"},{"name":"decreased cellular trehalose level during vegetative growth and during cellular response to oxidative stress","type":"exact"},{"name":"decreased cellular trehalose level in response to oxidative stress","type":"exact"},{"name":"decreased trehalose accumulation during cellular response to oxidative stress","type":"related"},{"name":"reduced cellular trehalose level during cellular response to oxidative stress","type":"exact"}],"termid":"FYPO:0003460"}


id: GO:0014846
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which force is generated within smooth muscle tissue, resulting in a change in muscle geometry. This process occurs in the esophagus. Force generation involves a chemo-mechanical energy conversion step that is carried out by the actin/myosin complex activity, which generates force through ATP hydrolysis. The esophagus is the muscular membranous segment between the pharynx and the stomach in the upper gastrointestinal tract.","definition_xrefs":["GOC:mtg_muscle","GOC:ef","MA:0001573","MSH:D041742"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastro-intestinal system smooth muscle contraction","termid":"GO:0014831"}],"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":"esophagus smooth muscle contraction","synonyms":[{"name":"oesophagus smooth muscle contraction","type":"related"}],"termid":"GO:0014846"}


id: PBO:0003732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAR adaptor protein","termid":"PBO:0003732"}


id: PBO:0088368
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein","termid":"PBO:0088368"}


id: GO:1905961
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of protein-cysteine S-palmitoyltransferase activity.","definition_xrefs":["GO_REF:0000088","GOC:TermGenie","GOC:bhm","PMID:20851885"],"direct_ancestors":[{"relation_name":"is_a","term_name":"palmitoyltransferase complex","termid":"GO:0002178"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"protein-cysteine S-palmitoyltransferase complex","synonyms":[{"name":"Palmitoyltransferase ERF2-SHR5 complex","type":"narrow"},{"name":"Palmitoyltransferase ERF2/SHR5 complex","type":"narrow"}],"termid":"GO:1905961"}


id: GO:0048265
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a pain stimulus. Pain stimuli cause activation of nociceptors, peripheral receptors for pain, include receptors which are sensitive to painful mechanical stimuli, extreme heat or cold, and chemical stimuli.","definition_xrefs":["GOC:jid","PMID:12723742","PMID:10203867","Wikipedia:Pain","PMID:12843304"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal response to stress","termid":"GO:0033555"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to pain","secondary_identifiers":["GO:0048267"],"synonyms":[{"name":"physiological response to pain","type":"exact"}],"termid":"GO:0048265"}


id: GO:1902291
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any DNA ligation that is involved in cell cycle DNA replication.","definition_xrefs":["GOC:mtg_cell_cycle","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete cell cycle DNA replication DNA ligation (obsolete GO:1902291)","synonyms":[{"name":"DNA ligation involved in cell cycle DNA replication","type":"exact"}],"termid":"GO:1902291"}


id: GO:0004769
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 3-oxo-delta(5)-steroid = a 3-oxo-delta(4)-steroid.","definition_xrefs":["RHEA:14709"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, transposing C=C bonds","termid":"GO:0016863"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016853","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"steroid Delta-isomerase activity","secondary_identifiers":["Reactome:R-HSA-193073","EC:5.3.3.1","Reactome:R-HSA-195690","Reactome:R-HSA-193961","Reactome:R-HSA-6807052","MetaCyc:STEROID-DELTA-ISOMERASE-RXN","Reactome:R-HSA-193052"],"synonyms":[{"name":"3-oxosteroid delta5-delta4-isomerase activity","type":"related"},{"name":"3-oxosteroid isomerase activity","type":"related"},{"name":"delta(5)-3-keto steroid isomerase activity","type":"related"},{"name":"delta(5)-3-ketosteroid isomerase activity","type":"related"},{"name":"delta(5)-3-oxosteroid isomerase activity","type":"related"},{"name":"delta(5)-steroid isomerase activity","type":"related"},{"name":"delta5(or delta4)-3-keto steroid isomerase activity","type":"related"},{"name":"delta5-3-keto steroid isomerase activity","type":"related"},{"name":"delta5-3-ketosteroid isomerase activity","type":"related"},{"name":"delta5-3-oxosteroid isomerase activity","type":"related"},{"name":"delta5-ketosteroid isomerase activity","type":"related"},{"name":"delta5-steroid isomerase activity","type":"related"},{"name":"hydroxysteroid isomerase activity","type":"related"},{"name":"steroid D-isomerase activity","type":"exact"},{"name":"steroid isomerase activity","type":"related"}],"termid":"GO:0004769"}


id: PBO:0091695
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Latrunculin Sensitive Knockout","termid":"PBO:0091695"}


id: MONDO:0016846
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal 22q11.2 microduplication syndrome is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the long arm of chromosome 22, with a highly variable phenotype principally characterized by developmental delay, intellectual disability, hypotonia, growth retardation, velopharyngeal insufficiency, mild craniofacial dysmorphism (microcephaly, tall/broad forehead, small downslating palpebral fissures, hooded eyelids, flat nasal bridge, low posterior hairline) and digital anomalies. Congenital heart malformations, visual and hearing impairment, urogenital abnormalities, behavourial problems and seizures have also been reported.","definition_xrefs":["Orphanet:261337"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 22q11.2 microduplication syndrome","termid":"MONDO:0012020"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal 22q11.2 microduplication syndrome","secondary_identifiers":["SCTID:764524005","MEDGEN:1637660","GARD:20780","UMLS:C4706942"],"synonyms":[{"name":"distal dup(22)(q11.2)","type":"exact"},{"name":"distal trisomy 22q11.2","type":"exact"}],"termid":"MONDO:0016846","xrefs":{"Monarch":{"xref_id":"0016846"}}}


id: PBO:0038427
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-2-macroglobulin pseudogene 1","termid":"PBO:0038427"}


id: FYPO:0002960
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 RNAs that are normally expressed during the meiotic cell cycle, and that contain determinant of selective removal (DSR) sequences, measured in a cell is higher than normal (i.e. higher than observed in wild-type cells during vegetative growth).","definition_xrefs":["PomBase:mah","PMID:23980030"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of meiotic gene mRNA during vegetative growth","termid":"FYPO:0002173"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0006551","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased level of DSR-containing meiotic gene mRNA during vegetative growth","synonyms":[{"name":"increased DSR-containing meiotic gene mRNA accumulation during vegetative growth","type":"related"},{"name":"increased level of DSR-containing meiosis gene mRNA during vegetative growth","type":"exact"},{"name":"increased level of DSR-containing meiotic cell cycle gene mRNA during vegetative growth","type":"related"},{"name":"increased level of DSR-containing meiotic gene RNA during vegetative growth","type":"exact"},{"name":"increased level of DSR-containing meiotic gene mRNA during mitotic cell cycle","type":"related"},{"name":"increased level of DSR-containing meiotic gene transcripts during vegetative growth","type":"exact"},{"name":"increased level of DSR-containing meiotic nuclear division gene mRNA during vegetative growth","type":"exact"}],"termid":"FYPO:0002960"}


id: MONDO:0019339
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"47, XYY syndrome is a sex chromosome aneuploidy where males receive an additional Y chromosome, and is characterized clinically by tall stature evident from childhood, macrocephaly, facial features (mild hypertelorism, low set ears, a mildly flat malar region), speech delay and an increased risk for social and emotional difficulties, attention deficit hyperactive disorder and autistic spectrum disorder.","definition_xrefs":["Orphanet:8"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"chromosome Y disorder","termid":"MONDO:0700028"},{"relation_name":"is_a","term_name":"trisomy","termid":"MONDO:0700065"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"47,XYY syndrome","secondary_identifiers":["GARD:5674","MESH:C535317","MEDGEN:473794","NCIT:C85237","UMLS:C3266843","NORD:1871","MedDRA:10056894","SCTID:50749006"],"synonyms":[{"name":"47, XYY syndrome","type":"related"},{"name":"47,XYY","type":"exact"},{"name":"47,XYY syndrome","type":"exact"},{"name":"Double Y","type":"exact"},{"name":"Double Y syndrome","type":"exact"},{"name":"XYY Syndrome","type":"exact"},{"name":"XYY karyotype","type":"exact"},{"name":"XYY syndrome","type":"exact"},{"name":"Y disomy","type":"exact"},{"name":"YY syndrome","type":"related"},{"name":"disomy Y","type":"exact"}],"termid":"MONDO:0019339","xrefs":{"Monarch":{"xref_id":"0019339"}}}


id: GO:0080007
data:
  {"annotated_genes":["SJAG_01457"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[102982],"is_not":false,"summary":null,"term":"GO:0080007"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: S-nitrosoglutathione + NADH + H+ = S-(hydroxysulfenamide)glutathione + NAD+.","definition_xrefs":["PMID:27094420","PMID:30795534","PMID:11260719"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01457":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"S-nitrosoglutathione reductase (NADH) activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:78371","MetaCyc:RXN-17884"],"termid":"GO:0080007","terms_by_termid":{"GO:0080007":null}}


id: PBO:0090749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DENN domain-like containing protein, implicated in vesicle formation/trafficking","termid":"PBO:0090749"}


id: GO:0015227
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of O-acyl-L-carnitine from one side of a membrane to the other. O-acyl-L-carnitine is the condensation product of a carboxylic acid and carnitine and is the transport form for a fatty acid crossing the mitochondrial membrane.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"quaternary ammonium group transmembrane transporter activity","termid":"GO:0015651"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"O-acyl-L-carnitine transmembrane transporter activity","synonyms":[{"name":"acylcarnitine transporter activity","type":"broad"}],"termid":"GO:0015227"}


id: MONDO:0700123
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Variants in SMARCC1 cause a novel human syndrome characterized by developmental delay, cerebral ventriculomegaly and aqueductal stenosis, and other associated structural brain and cardiac defects.","direct_ancestors":[{"relation_name":"is_a","term_name":"BAFopathy","termid":"MONDO:0700120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMARCC1-associated developmental dysgenesis syndrome","synonyms":[{"name":"SMARCC1-related BAFopathy","type":"exact"}],"termid":"MONDO:0700123","xrefs":{"Monarch":{"xref_id":"0700123"}}}


id: MONDO:0016872
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal deletion","termid":"MONDO:0000761"},{"relation_name":"is_a","term_name":"chromosome 7 disorder","termid":"MONDO:0700014"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of chromosome 7","secondary_identifiers":["GARD:20795","UMLS:C5679655","Orphanet:261796","MEDGEN:1825962"],"synonyms":[{"name":"partial deletion of chromosome type 7","type":"exact"},{"name":"partial monosomy of chromosome 7","type":"exact"}],"termid":"MONDO:0016872","xrefs":{"Monarch":{"xref_id":"0016872"}}}


id: GO:0098845
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An endosomal compartment that is part of the post-synapse. Only early and recycling endosomes are typically present in the postsynapse.","definition_xrefs":["PMID:20820847"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endosome","termid":"GO:0005768"},{"relation_name":"part_of","term_name":"postsynapse","termid":"GO:0098794"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005768"}],"interesting_parent_ids":["GO:0031410","GO:0005737","GO:0005768","GO:0005575"],"is_obsolete":false,"name":"postsynaptic endosome","termid":"GO:0098845"}


id: FYPO:0007046
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which alkaline phosphatase activity is absent during a cellular response to zinc ion starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished alkaline phosphatase activity","termid":"FYPO:0007043"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000707","FYPO:0000652","FYPO:0001985","FYPO:0000661"],"is_obsolete":false,"name":"abolished alkaline phosphatase activity during cellular response to zinc ion starvation","synonyms":[{"name":"abolished alkaline phosphatase activity during cellular response to zinc ion depletion","type":"exact"},{"name":"abolished alkaline phosphatase activity during cellular response to zinc ion deprivation","type":"exact"},{"name":"abolished alkaline phosphatase activity during cellular response to zinc ion limitation","type":"exact"},{"name":"abolished alkaline phosphatase activity during cellular response to zinc starvation","type":"exact"},{"name":"alkaline phosphatase activity abolished during cellular response to zinc ion starvation","type":"exact"}],"termid":"FYPO:0007046"}


id: PBO:0069194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 448, pseudogene","termid":"PBO:0069194"}


id: PBO:0077789
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA topoisomerase III beta pseudogene 1","termid":"PBO:0077789"}


id: MONDO:0009930
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Pulmonary arteriovenous malformation (PAVM) describes an anatomic communication between a pulmonary artery and a pulmonary vein leading to a right to left extracardiac shunt that can be asymptomatic or can lead to varying manifestations such as dyspnea, hemoptysis, and neurological symptoms.","definition_xrefs":["Orphanet:2038"],"gene_count":0,"genotype_count":0,"name":"obsolete pulmonary arteriovenous malformation (obsolete MONDO:0009930)","secondary_identifiers":["MESH:C562404","NCIT:C99029","HP:0006548","MedDRA:10037332","OMIM:265140","NANDO:2200295","icd11.foundation:913404991","SCTID:303070000"],"synonyms":[{"name":"PAVM","type":"exact"},{"name":"arteriovenous fistula of pulmonary vessels","type":"exact"},{"name":"pulmonar arteriovenous aneurysm","type":"related"},{"name":"pulmonary AV fistula","type":"exact"},{"name":"pulmonary arterio-veinous fistula","type":"related"},{"name":"pulmonary arteriovenous fistula","type":"exact"},{"name":"pulmonary arteriovenous fistulas","type":"related"},{"name":"pulmonary arteriovenous malformation","type":"exact"},{"name":"pulmonary arteriovenous malformation (disease)","type":"exact"}],"termid":"MONDO:0009930","xrefs":{"Monarch":{"xref_id":"0009930"}}}


id: GO:0008810
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the endohydrolysis of (1->4)-beta-D-glucosidic linkages in cellulose, lichenin and cereal beta-D-glucans.","definition_xrefs":["EC:3.2.1.4"],"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:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016798","GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"cellulase activity","secondary_identifiers":["MetaCyc:RXN-2043"],"synonyms":[{"name":"1,4-(1,3;1,4)-beta-D-glucan 4-glucanohydrolase activity","type":"related"},{"name":"9.5 cellulase activity","type":"related"},{"name":"alkali cellulase activity","type":"narrow"},{"name":"avicelase activity","type":"related"},{"name":"beta-1,4-endoglucan hydrolase activity","type":"broad"},{"name":"beta-1,4-glucanase activity","type":"broad"},{"name":"carboxymethyl cellulase activity","type":"narrow"},{"name":"celluase A","type":"related"},{"name":"celludextrinase activity","type":"related"},{"name":"cellulase A 3","type":"related"},{"name":"cellulosin AP","type":"related"},{"name":"endo-1,4-beta-D-glucanase activity","type":"broad"},{"name":"endo-1,4-beta-D-glucanohydrolase activity","type":"broad"},{"name":"endo-1,4-beta-glucanase activity","type":"broad"},{"name":"endoglucanase D","type":"related"},{"name":"endoglucanase activity","type":"broad"},{"name":"pancellase SS","type":"related"}],"termid":"GO:0008810"}


id: PBO:0077429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 167A","termid":"PBO:0077429"}


id: PBO:0034492
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_biological_process","termid":"PBO:0034492"}


id: GO:0010931
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process involving any mechanism for tolerance induction in macrophages.","definition_xrefs":["GOC:BHF","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tolerance induction","termid":"GO:0002507"}],"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":"macrophage tolerance induction","termid":"GO:0010931"}


id: MONDO:0000621
data:
  {"annotated_genes":["SJAG_02527","SJAG_03453","SJAG_05979","SJAG_01013","SJAG_03905","SJAG_01349","SJAG_01748"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86847,86848,86692,86693,86695,86694],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018874"},{"annotations":[86814],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009693"}]},"cv_name":"mondo","definition":"A malignant neoplasm involving the immune system","direct_ancestors":[{"relation_name":"is_a","term_name":"cancer","termid":"MONDO:0004992"},{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"}],"gene_count":7,"genes_by_uniquename":{"SJAG_01013":null,"SJAG_01349":null,"SJAG_01748":null,"SJAG_02527":null,"SJAG_03453":null,"SJAG_03905":null,"SJAG_05979":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004992"],"is_obsolete":false,"name":"immune system cancer","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0060083"],"synonyms":[{"name":"cancer of immune system","type":"exact"},{"name":"immune system cancer","type":"exact"},{"name":"malignant immune system neoplasm","type":"exact"},{"name":"malignant neoplasm of immune system","type":"exact"}],"termid":"MONDO:0000621","terms_by_termid":{"MONDO:0009693":null,"MONDO:0018874":null},"xrefs":{"Monarch":{"xref_id":"0000621"}}}


id: PBO:0072705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RWD domain containing 1 pseudogene 1","termid":"PBO:0072705"}


id: MONDO:0859286
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures","secondary_identifiers":["UMLS:C5774213","OMIM:620029","DOID:0070536","MEDGEN:1823986"],"termid":"MONDO:0859286","xrefs":{"Monarch":{"xref_id":"0859286"}}}


id: PBO:0078626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 75","termid":"PBO:0078626"}


id: GO:0015851
data:
  {"annotated_genes":["SJAG_00760","SJAG_04714","SJAG_03777","SJAG_03970","SJAG_02147","SJAG_04717"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77584],"is_not":false,"summary":null,"term":"GO:0015851"},{"annotations":[112034],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098702"},{"annotations":[112035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098710"},{"annotations":[114646],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140140"},{"annotations":[87566],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905530"},{"annotations":[87910],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904082"},{"annotations":[87921,95023],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098721"},{"annotations":[87911],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042906"}]},"cv_name":"biological_process","definition":"The directed movement of a nucleobase, any nitrogenous base that is a constituent of a nucleoside, nucleotide, or nucleic acid, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrogen compound transport","termid":"GO:0071705"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00760":null,"SJAG_02147":null,"SJAG_03777":null,"SJAG_03970":null,"SJAG_04714":null,"SJAG_04717":null},"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:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"nucleobase transport","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"nucleobase transmembrane transport","type":"exact"}],"termid":"GO:0015851","terms_by_termid":{"GO:0015851":null,"GO:0042906":null,"GO:0098702":null,"GO:0098710":null,"GO:0098721":null,"GO:0140140":null,"GO:1904082":null,"GO:1905530":null}}


id: PBO:0045719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"E2F transcription factor 4","termid":"PBO:0045719"}


id: PBO:0039179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"A-kinase anchoring protein 9","termid":"PBO:0039179"}


id: GO:0015431
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + H2O + glutathione S-conjugate(in) -> ADP + phosphate + glutathione S-conjugate(out).","definition_xrefs":["RHEA:19121","GOC:jl","PMID:1455517"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"},{"relation_name":"is_a","term_name":"sulfur compound transmembrane transporter activity","termid":"GO:1901682"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"ABC-type glutathione S-conjugate transporter activity","secondary_identifiers":["GO:0071997","MetaCyc:TRANS-RXN-358","EC:7.6.2.3"],"synonyms":[{"name":"ATP-dependent glutathione S-conjugate export pump","type":"exact"},{"name":"ATPase-coupled glutathione S-conjugate transmembrane transporter activity","type":"related"},{"name":"GS-X pump","type":"exact"},{"name":"MRP1/GS-X pump","type":"exact"},{"name":"conjugate transporter activity","type":"broad"},{"name":"glutathione S-conjugate-exporting ATPase activity","type":"narrow"},{"name":"glutathione S-conjugate-transporting ATPase activity","type":"related"}],"termid":"GO:0015431"}


id: PBO:0057985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3911","termid":"PBO:0057985"}


id: MONDO:0008335
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Short stature-craniofacial anomalies-genital hypoplasia syndrome is characterized by the association of short stature, craniofacial anomalies and genital hypoplasia. Intellectual deficit is also found in the majority of cases, sometimes together with pterygia. Less than 20 cases have been described so far. The mode of transmission is likely to be autosomal dominant with incomplete penetrance. The syndrome is caused by unbalanced reciprocal translocations of the distal parts of chromosomes 6q and 9p, leading to partial trisomy of the distal region of chromosome 6q and partial monosomy of the distal region of chromosome 9p.","definition_xrefs":["Orphanet:2994"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"short stature-craniofacial anomalies-genital hypoplasia syndrome","secondary_identifiers":["MEDGEN:357988","MESH:C535844","OMIM:177980","SCTID:716090004","UMLS:C1867443","GARD:2605"],"synonyms":[{"name":"Haspeslagh syndrome","type":"related"},{"name":"Haspeslagh-Fryns-Muelenaere syndrome","type":"exact"},{"name":"pterygia intellectual disability facial dysmorphism","type":"related"},{"name":"pterygia mental retardation facial dysmorphism","type":"related"},{"name":"pterygia, intellectual disability and distinctive craniofacial features","type":"related"},{"name":"pterygia, intellectual disability, and distinctive craniofacial features","type":"related"},{"name":"pterygia, mental retardation and distinctive craniofacial features","type":"related"},{"name":"pterygia, mental retardation, and distinctive craniofacial features","type":"related"}],"termid":"MONDO:0008335","xrefs":{"Monarch":{"xref_id":"0008335"}}}


id: GO:0004342
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glucosamine 6-phosphate + H2O = beta-D-fructose 6-phosphate + NH4.","definition_xrefs":["EC:3.5.99.6","RHEA:12172"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deaminase activity","termid":"GO:0019239"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0016810","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"glucosamine-6-phosphate deaminase activity","secondary_identifiers":["Reactome:R-HSA-6799604","MetaCyc:GLUCOSAMINE-6-P-DEAMIN-RXN","KEGG_REACTION:R00765"],"synonyms":[{"name":"2-amino-2-deoxy-D-glucose-6-phosphate aminohydrolase (ketol isomerizing)","type":"related"},{"name":"GlcN6P deaminase activity","type":"related"},{"name":"aminodeoxyglucosephosphate isomerase activity","type":"related"},{"name":"glucosamine phosphate deaminase activity","type":"related"},{"name":"glucosamine-6-phosphate isomerase activity","type":"related"},{"name":"glucosaminephosphate isomerase","type":"broad"},{"name":"phosphoglucosamine isomerase activity","type":"related"},{"name":"phosphoglucosaminisomerase activity","type":"related"}],"termid":"GO:0004342"}


id: MONDO:0020383
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fundus pulverulentus is a rare form of patterned dystrophy of the retinal pigment epithelium characterized by a granular appearance in the macula, with coarse and punctiform mottling of the retinal pigment epithelium within the macular region. Association with choroidal neovascularization has been reported.","definition_xrefs":["Orphanet:99004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"patterned dystrophy of the retinal pigment epithelium","termid":"MONDO:0018973"}],"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":"fundus pulverulentus","secondary_identifiers":["MEDGEN:1669231","UMLS:C4749286","GARD:19613","icd11.foundation:871251875","ICD10CM:H35.5"],"termid":"MONDO:0020383","xrefs":{"Monarch":{"xref_id":"0020383"}}}


id: GO:0034993
data:
  {"annotated_genes":["SJAG_04558","SJAG_01538","SJAG_05196"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[96200,102308,112331],"is_not":false,"summary":null,"term":"GO:0034993"},{"annotations":[96203,102316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990612"}]},"cv_name":"cellular_component","definition":"A nuclear membrane protein complex which connects the nuclear outer and inner membranes together, and links links the nuclear lumen to cytoplasmic microtubules during meiosis.","definition_xrefs":["PMID:18692466","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear membrane microtubule tethering complex","termid":"GO:0106094"},{"relation_name":"part_of","term_name":"microtubule organizing center attachment site","termid":"GO:0034992"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01538":null,"SJAG_04558":null,"SJAG_05196":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"meiotic nuclear membrane microtubule tethering complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"LINC complex","type":"exact"},{"name":"LInker of Nucleoskeleton and Cytoskeleton complex","type":"exact"},{"name":"SUN-KASH complex","type":"exact"}],"termid":"GO:0034993","terms_by_termid":{"GO:0034993":null,"GO:1990612":null}}


id: PBO:0026997
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_DNA_binding_at_PCB","termid":"PBO:0026997"}


id: GO:0018220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The covalent attachment of a palmitoyl group to an oxygen (O) atom in a threonine residue to form peptidyl-O-palmitoyl-L-threonine.","definition_xrefs":["RESID:AA0079"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-threonine palmitoylation (obsolete GO:0018220)","synonyms":[{"name":"peptidyl-threonine O-palmitoylation","type":"exact"}],"termid":"GO:0018220"}


id: MONDO:1012252
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spastic paresis, non-human animal","termid":"MONDO:1011859"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spastic paresis, pig","secondary_identifiers":["OMIA:000928-9823"],"termid":"MONDO:1012252","xrefs":{"Monarch":{"xref_id":"1012252"}}}


id: GO:0042006
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The determination of male sex and sexual phenotype in the germ-line of the hermaphrodite. An example of this is found in Caenorhabditis elegans.","definition_xrefs":["GOC:ems"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hermaphrodite germ-line sex determination","termid":"GO:0040021"}],"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":"masculinization of hermaphroditic germ-line","termid":"GO:0042006"}


id: PR:P17610
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ypt3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P17610"],"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":"GTP-binding protein ypt3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC18G6.03","synonyms":[{"name":"RAB (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ypt3","type":"exact"}],"termid":"PR:P17610"}


id: GO:2000950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of xyloglucan metabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of macromolecule metabolic process","termid":"GO:0010604"},{"relation_name":"is_a","term_name":"positive regulation of carbohydrate metabolic process","termid":"GO:0045913"},{"relation_name":"is_a","term_name":"regulation of xyloglucan metabolic process","termid":"GO:2000948"},{"relation_name":"positively_regulates","term_name":"xyloglucan metabolic process","termid":"GO:0010411"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"positive regulation of xyloglucan metabolic process","synonyms":[{"name":"positive regulation of xyloglucan metabolism","type":"exact"}],"termid":"GO:2000950"}


id: PBO:0060087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 34","termid":"PBO:0060087"}


id: PR:P87114
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- fft1 gene.","definition_xrefs":["UniProtKB:P87114","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":"ATP-dependent helicase fft1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC20G8.08c","synonyms":[{"name":"Fun thirty-related protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-fft1","type":"exact"}],"termid":"PR:P87114"}


id: PR:O74840
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cue2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74840"],"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":"Smr domain-containing protein C1235.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1235.03","synonyms":[{"name":"Spom972h-cue2","type":"exact"}],"termid":"PR:O74840"}


id: MONDO:1011250
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Leber congenital amaurosis that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Leber congenital amaurosis, non-human animal","termid":"MONDO:1010329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leber congenital amaurosis, dog","secondary_identifiers":["OMIA:001222-9615"],"termid":"MONDO:1011250","xrefs":{"Monarch":{"xref_id":"1011250"}}}


id: GO:0048801
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the antennal joint are generated and organized.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"antennal joint development","termid":"GO:0048098"},{"relation_name":"part_of","term_name":"antennal morphogenesis","termid":"GO:0048800"}],"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":"antennal joint morphogenesis","termid":"GO:0048801"}


id: GO:0001306
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of oxidative stress, a state often resulting from exposure to high levels of reactive oxygen species, where the change varies according to the age of the cell or organism.","definition_xrefs":["PMID:12044938","GOC:jh"],"gene_count":0,"genotype_count":0,"name":"obsolete age-dependent response to oxidative stress (obsolete GO:0001306)","termid":"GO:0001306"}


id: GO:0045035
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of four asymmetric divisions undergone by the sensory organ precursor cells to generate cells that have distinct cell fates. For example, in the external sensory organ, the precursor cells give rise to one multidendritic neuron and four additional cells (the socket, shaft, sheath cells and the external sense neuron).","definition_xrefs":["GOC:mah","PMID:18295597","PMID:11171389"],"direct_ancestors":[{"relation_name":"is_a","term_name":"asymmetric cell division","termid":"GO:0008356"},{"relation_name":"part_of","term_name":"sensory organ development","termid":"GO:0007423"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"sensory organ precursor cell division","synonyms":[{"name":"sense organ precursor cell division","type":"exact"}],"termid":"GO:0045035"}


id: GO:0060817
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Compensating for the two-fold variation in X-chromosome:autosome ratios between sexes by a global inactivation of all, or most of, the genes specifically on the paternal X-chromosome in the XX sex.","definition_xrefs":["GOC:dph","GOC:sdb_2009","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete inactivation of paternal X chromosome (obsolete GO:0060817)","termid":"GO:0060817"}


id: MONDO:0013462
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":"fucosyltransferase 6 deficiency","secondary_identifiers":["OMIM:613852","MEDGEN:462569","UMLS:C3151219"],"synonyms":[{"name":"fucosyltransferase 6 deficiency","type":"exact"}],"termid":"MONDO:0013462","xrefs":{"Monarch":{"xref_id":"0013462"}}}


id: PBO:0080886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"yrdC N(6)-threonylcarbamoyltransferase domain containing pseudogene 2","termid":"PBO:0080886"}


id: GO:0141088
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process in which a symbiont initiates, promotes, or enhances the activation of autophagy in the host cell. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pg"],"gene_count":0,"genotype_count":0,"name":"obsolete symbiont-mediated activation of host autophagy (obsolete GO:0141088)","synonyms":[{"name":"induction of host autophagy","type":"exact"},{"name":"positive regulation by symbiont of host autophagy","type":"exact"}],"termid":"GO:0141088"}


id: GO:0106114
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of mitotic cohesin dsDNA (leading strand) loading.","definition_xrefs":["PMID:29358048"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of mitotic cohesin dsDNA (leading strand) loading (obsolete GO:0106114)","termid":"GO:0106114"}


id: MONDO:1012122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"primary hypothyroidism, non-human animal","termid":"MONDO:1011678"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary hypothyroidism, domestic cat","secondary_identifiers":["OMIA:000538-9685"],"termid":"MONDO:1012122","xrefs":{"Monarch":{"xref_id":"1012122"}}}


id: PBO:0057385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548b","termid":"PBO:0057385"}


id: GO:0072249
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a metanephric glomerular visceral epithelial cell over time, from its formation to the mature structure. A metanephric glomerular visceral epithelial cell is a specialized epithelial cell that contains 'feet' that interdigitate with the 'feet' of other glomerular epithelial cells in the metanephros.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"podocyte development","termid":"GO:0072015"},{"relation_name":"is_a","term_name":"metanephric glomerular epithelial cell development","termid":"GO:0072313"},{"relation_name":"part_of","term_name":"metanephric podocyte differentiation","termid":"GO:0072248"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric podocyte development","synonyms":[{"name":"metanephric glomerular visceral epithelial cell development","type":"exact"}],"termid":"GO:0072249"}


id: MOD:00388
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively attaches an L-alanine residue to murein peptidoglycan by a pentaglycine linker peptide.","definition_xrefs":["PubMed:8163519","RESID:AA0383"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-alanine residue","termid":"MOD:00901"},{"relation_name":"is_a","term_name":"peptidoglycanated residue","termid":"MOD:01159"}],"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":"L-alanyl-pentaglycyl-murein peptidoglycan","synonyms":[{"name":"(2R,6S)-2-(N-mureinyl-(R)-alanyl-(S)-isoglutamyl)amino-6-(alanyl-pentaglycyl)amino-pimeloyl-(S)-alanyl-(S)-alanine","type":"exact"},{"name":"L-alanyl-pentaglycyl-murein peptidoglycan","type":"exact"},{"name":"MOD_RES Pentaglycyl murein peptidoglycan amidated alanine","type":"exact"}],"termid":"MOD:00388"}


id: PBO:0067760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 60","termid":"PBO:0067760"}


id: FYPO:0003505
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which glutathione gamma-glutamylcysteinyltransferase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished catalytic activity","termid":"FYPO:0000664"},{"relation_name":"is_a","term_name":"abnormal glutathione gamma-glutamylcysteinyltransferase activity","termid":"FYPO:0000754"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000661","FYPO:0000654","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"abolished glutathione gamma-glutamylcysteinyltransferase activity","synonyms":[{"name":"glutathione gamma-glutamylcysteinyltransferase activity abolished","type":"exact"}],"termid":"FYPO:0003505"}


id: GO:0018789
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cyclohexylsulfamate + H2O = cyclohexylamine + sulfate.","definition_xrefs":["RHEA:18481","EC:3.10.1.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid sulfur-nitrogen bonds","termid":"GO:0016826"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"cyclamate sulfohydrolase activity","secondary_identifiers":["KEGG_REACTION:R02564","MetaCyc:CYCLAMATE-SULFOHYDROLASE-RXN","UM-BBD_reactionID:r0755"],"synonyms":[{"name":"cyclamate sulfamatase activity","type":"exact"},{"name":"cyclamate sulfamidase activity","type":"related"},{"name":"cyclamate sulphohydrolase activity","type":"exact"},{"name":"cyclohexylsulfamate sulfamidase activity","type":"related"},{"name":"cyclohexylsulfamate sulfohydrolase activity","type":"related"}],"termid":"GO:0018789"}


id: GO:0042144
data:
  {"annotated_genes":["SJAG_00380","SJAG_04966","SJAG_01080","SJAG_03072","SJAG_02433","SJAG_03386","SJAG_00330","SJAG_01598","SJAG_01072","SJAG_03137","SJAG_01299","SJAG_04909","SJAG_03915","SJAG_05194","SJAG_02384","SJAG_00029"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90655,90781,99459,99750,99810,100251,100620,104134,107766,108917,109761,114013,116324],"is_not":false,"summary":null,"term":"GO:0042144"},{"annotations":[100950],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0061192"},{"annotations":[97115,109759],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0061191"},{"annotations":[96882],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032889"}]},"cv_name":"biological_process","definition":"The fusion of two vacuole membranes to form a single vacuole.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vacuole fusion","termid":"GO:0097576"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00029":null,"SJAG_00330":null,"SJAG_00380":null,"SJAG_01072":null,"SJAG_01080":null,"SJAG_01299":null,"SJAG_01598":null,"SJAG_02384":null,"SJAG_02433":null,"SJAG_03072":null,"SJAG_03137":null,"SJAG_03386":null,"SJAG_03915":null,"SJAG_04909":null,"SJAG_04966":null,"SJAG_05194":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"vacuole fusion, non-autophagic","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0042145"],"synonyms":[{"name":"homotypic vacuole fusion","type":"exact"},{"name":"homotypic vacuole fusion (non-autophagic)","type":"exact"},{"name":"homotypic vacuole fusion, non-autophagic","type":"exact"},{"name":"vacuole fusion (non-autophagic)","type":"exact"}],"termid":"GO:0042144","terms_by_termid":{"GO:0032889":null,"GO:0042144":null,"GO:0061191":null,"GO:0061192":null}}


id: PBO:0111301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U1 snRNP-associated protein Prp39","termid":"PBO:0111301"}


id: GO:2000487
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of glutamine transport.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of organic acid transport","termid":"GO:0032892"},{"relation_name":"is_a","term_name":"positive regulation of amino acid transport","termid":"GO:0051957"},{"relation_name":"is_a","term_name":"regulation of glutamine transport","termid":"GO:2000485"},{"relation_name":"positively_regulates","term_name":"glutamine transport","termid":"GO:0006868"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of glutamine transport","synonyms":[{"name":"positive regulation of L-glutamine transport","type":"related"}],"termid":"GO:2000487"}


id: MONDO:0016095
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mesenchymal neoplasm with skeletal muscle differentiation arising from the vagina.","definition_xrefs":["NCIT:C128080"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vagina sarcoma","termid":"MONDO:0002140"},{"relation_name":"is_a","term_name":"rhabdomyosarcoma","termid":"MONDO:0005212"}],"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":"vaginal rhabdomyosarcoma","secondary_identifiers":["UMLS:C4288035","Orphanet:206492","MEDGEN:925567","SCTID:766759009","GARD:20348"],"synonyms":[{"name":"rhabdomyosarcoma (disease) of vagina","type":"exact"},{"name":"vagina rhabdomyosarcoma","type":"exact"},{"name":"vagina rhabdomyosarcoma (disease)","type":"exact"},{"name":"vaginal rhabdomyosarcoma","type":"exact"},{"name":"vulvovaginal rhabdomyosarcoma","type":"related"}],"termid":"MONDO:0016095","xrefs":{"Monarch":{"xref_id":"0016095"}}}


id: PBO:0071737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L39 pseudogene 35","termid":"PBO:0071737"}


id: GO:0047039
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADP+ + scytalone = NADPH + H+ + 1,3,6,8-naphthalenetetrol.","definition_xrefs":["MetaCyc:1.1.1.252-RXN","EC:1.1.1.252"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"tetrahydroxynaphthalene reductase activity","secondary_identifiers":["RHEA:21908"],"synonyms":[{"name":"T4HN reductase activity","type":"related"},{"name":"scytalone:NADP+ delta5-oxidoreductase activity","type":"related"}],"termid":"GO:0047039"}


id: FYPO:0006045
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 mitotic sister chromatid biorientation begins later than normal.","definition_xrefs":["PomBase:mah","PMID:27146110"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid biorientation","termid":"FYPO:0000326"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000138","FYPO:0000631","FYPO:0005447","FYPO:0000337","FYPO:0000002","FYPO:0000641"],"is_obsolete":false,"name":"delayed onset of mitotic sister chromatid biorientation","synonyms":[{"name":"delayed mitotic sister chromatid biorientation","type":"exact"},{"name":"delayed onset of mitotic sister chromatid biorientation during vegetative growth","type":"exact"},{"name":"delayed onset of sister chromatid biorientation during mitotic cell cycle","type":"related"},{"name":"mitotic sister chromatid biorientation delayed","type":"exact"}],"termid":"FYPO:0006045"}


id: GO:1901452
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of response to benzene.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of response to benzene","termid":"GO:1901451"},{"relation_name":"negatively_regulates","term_name":"response to benzene","termid":"GO:1901423"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of response to benzene","synonyms":[{"name":"down regulation of response to benzene","type":"exact"},{"name":"down-regulation of response to benzene","type":"exact"},{"name":"downregulation of response to benzene","type":"exact"},{"name":"inhibition of response to benzene","type":"narrow"}],"termid":"GO:1901452"}


id: GO:0052365
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism resulting in the breakdown of xylan within the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete catabolism by host of symbiont xylan (obsolete GO:0052365)","termid":"GO:0052365"}


id: PBO:0088452
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PWWP domain protein Pdp2","termid":"PBO:0088452"}


id: PBO:0070106
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 20 pseudogene","termid":"PBO:0070106"}


id: PBO:0088940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial [2Fe-2S] cluster assembly and type II fatty acid synthase component","termid":"PBO:0088940"}


id: MONDO:0002053
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hypoglycemic coma (obsolete MONDO:0002053)","secondary_identifiers":["ICD9:251.0","SCTID:267384006","HP:0001325","DOID:1607"],"termid":"MONDO:0002053","xrefs":{"Monarch":{"xref_id":"0002053"}}}


id: GO:1901172
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving phytoene.","definition_xrefs":["GOC:TermGenie","UniPathway:UPA00799","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carotene metabolic process","termid":"GO:0016119"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"phytoene metabolic process","synonyms":[{"name":"phytoene metabolism","type":"exact"}],"termid":"GO:1901172"}


id: GO:0009498
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete bacterial-type ferredoxin (obsolete GO:0009498)","synonyms":[{"name":"bacterial-type ferredoxin","type":"exact"}],"termid":"GO:0009498"}


id: PBO:0084847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial ribosomal protein of the large subunit; homologous to bacterial L16 ribosomal protein; synthetic lethality with hac1 mutation suggests a possible role in synthesis of precursors for protein glycosylation","termid":"PBO:0084847"}


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


id: GO:1990204
data:
  {"annotated_genes":["SJAG_03337","SJAG_01671","SJAG_00755","SJAG_MIT13","SJAG_01763","SJAG_MIT03","SJAG_01190","SJAG_MIT20","SJAG_03163","SJAG_07007","SJAG_02006","SJAG_03920","SJAG_07006","SJAG_01355","SJAG_03861","SJAG_03641","SJAG_00866","SJAG_02504","SJAG_02901","SJAG_05629","SJAG_01077","SJAG_00260","SJAG_03290","SJAG_00976","SJAG_01490","SJAG_02464","SJAG_04665","SJAG_02158","SJAG_04675","SJAG_02398","SJAG_04677","SJAG_MIT04","SJAG_02646","SJAG_00885","SJAG_03064","SJAG_03490","SJAG_00080","SJAG_00601"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[88144,95889,86898,112518],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005960"},{"annotations":[91935,91931],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033573"},{"annotations":[109618,111560,86901],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045252"},{"annotations":[86902,94487,113731,117955,108079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045254"},{"annotations":[116250,112687,88660,88290],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045273"},{"annotations":[103991,112894,89450,117184,118552,117661,114593,107449,103578],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045275"},{"annotations":[118547,87672,114953,114151,88699,118574,113720,116313,107769,118525,91435],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045277"},{"annotations":[91919,106747],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005971"}]},"cv_name":"cellular_component","definition":"Any protein complex that possesses oxidoreductase activity.","definition_xrefs":["GOC:bhm","PMID:18982432"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":38,"genes_by_uniquename":{"SJAG_00080":null,"SJAG_00260":null,"SJAG_00601":null,"SJAG_00755":null,"SJAG_00866":null,"SJAG_00885":null,"SJAG_00976":null,"SJAG_01077":null,"SJAG_01190":null,"SJAG_01355":null,"SJAG_01490":null,"SJAG_01671":null,"SJAG_01763":null,"SJAG_02006":null,"SJAG_02158":null,"SJAG_02398":null,"SJAG_02464":null,"SJAG_02504":null,"SJAG_02646":null,"SJAG_02901":null,"SJAG_03064":null,"SJAG_03163":null,"SJAG_03290":null,"SJAG_03337":null,"SJAG_03490":null,"SJAG_03641":null,"SJAG_03861":null,"SJAG_03920":null,"SJAG_04665":null,"SJAG_04675":null,"SJAG_04677":null,"SJAG_05629":null,"SJAG_07006":null,"SJAG_07007":null,"SJAG_MIT03":null,"SJAG_MIT04":null,"SJAG_MIT13":null,"SJAG_MIT20":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"oxidoreductase complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"oxidation-reduction complex","type":"exact"},{"name":"redox complex","type":"exact"}],"termid":"GO:1990204","terms_by_termid":{"GO:0005960":null,"GO:0005971":null,"GO:0033573":null,"GO:0045252":null,"GO:0045254":null,"GO:0045273":null,"GO:0045275":null,"GO:0045277":null}}


id: MONDO:0000551
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neuroblastoma that involves the retroperitoneal space.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroblastoma","termid":"MONDO:0005072"},{"relation_name":"is_a","term_name":"retroperitoneal neoplasm","termid":"MONDO:0024645"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retroperitoneal neuroblastoma","secondary_identifiers":["MEDGEN:1843500","DOID:0050937","UMLS:C2211613"],"synonyms":[{"name":"neuroblastoma of retroperitoneal space","type":"exact"},{"name":"retroperitoneal space neuroblastoma","type":"exact"}],"termid":"MONDO:0000551","xrefs":{"Monarch":{"xref_id":"0000551"}}}


id: FYPO:0000193
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A stress response phenotype observed in the vegetative growth phase of the life cycle in which a cellular response to osmotic stress is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular response to stress during vegetative growth","termid":"FYPO:0001341"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000298","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal cellular response to osmotic stress","synonyms":[{"name":"abnormal cellular response to osmotic stress during mitotic cell cycle","type":"related"},{"name":"abnormal cellular response to osmotic stress during vegetative growth","type":"exact"}],"termid":"FYPO:0000193"}


id: PBO:0049200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GRIK1 antisense RNA 1","termid":"PBO:0049200"}


id: MONDO:0017860
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Methanol poisoning is a rare poisoning resulting in elevated anion gap metabolic acidosis, due to the alcohol dehydrogenase (ADH)-mediated production of formic acid (which is poisonous to the central nervous system), and characterized by dizziness, nausea, vomiting, confusion, metabolic acidosis, visual disturbances (which if left untreated can lead to blindness), coma, and death (due to respiratory failure).","definition_xrefs":["Orphanet:31825"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methanol poisoning","secondary_identifiers":["GARD:18804"],"termid":"MONDO:0017860","xrefs":{"Monarch":{"xref_id":"0017860"}}}


id: MONDO:0011869
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Epidermolysis bullosa simplex superficialis (EBSS) is a suprabasal subtype of epidermolysis bullosa simplex (EBS) characterized by generalized or acral superficial erosions in the absence of blisters.","definition_xrefs":["Orphanet:89839"],"direct_ancestors":[{"relation_name":"is_a","term_name":"suprabasal epidermolysis bullosa simplex","termid":"MONDO:0015550"}],"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":"epidermolysis bullosa simplex superficialis","secondary_identifiers":["MESH:C564368","OMIM:607600","UMLS:C1843477","icd11.foundation:1738578678","MEDGEN:334412"],"synonyms":[{"name":"EBSS","type":"exact"},{"name":"epidermolysis bullosa simplex superficialis","type":"exact"}],"termid":"MONDO:0011869","xrefs":{"Monarch":{"xref_id":"0011869"}}}


id: GO:0047993
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: hydroxymalonate + NAD+ = H+ + NADH + oxomalonate.","definition_xrefs":["EC:1.1.1.167","RHEA:11284"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"hydroxymalonate dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R02969","MetaCyc:HYDROXYMALONATE-DEHYDROGENASE-RXN"],"synonyms":[{"name":"hydroxymalonate:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0047993"}


id: PBO:0030710
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_chromatin_binding","termid":"PBO:0030710"}


id: GO:0031298
data:
  {"annotated_genes":["SJAG_02724","SJAG_03097","SJAG_04671"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[98857,106120,108000],"is_not":false,"summary":null,"term":"GO:0031298"}]},"cv_name":"cellular_component","definition":"A protein complex conserved in eukaryotes and associated with the replication fork; the complex stabilizes stalled replication forks and is thought to be involved in coordinating leading- and lagging-strand synthesis and in replication checkpoint signaling.","definition_xrefs":["PMID:15367656"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear replication fork","termid":"GO:0043596"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02724":null,"SJAG_03097":null,"SJAG_04671":null},"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:0005694"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005694","GO:0005634"],"is_obsolete":false,"name":"replication fork protection complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Swi1-Swi3 complex","type":"narrow"},{"name":"TIMELESS-TIPIN complex","type":"narrow"},{"name":"replisome progression complex","type":"exact"}],"termid":"GO:0031298","terms_by_termid":{"GO:0031298":null}}


id: PBO:0073779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 5 member 1","termid":"PBO:0073779"}


id: PBO:0029223
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_trichostatin_A","termid":"PBO:0029223"}


id: MONDO:0025598
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An pneumonia caused by infection with Chlamydia.","definition_xrefs":["MONDO:patterns/specific_infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chlamydia trachomatis infectious disease","termid":"MONDO:0005701"},{"relation_name":"is_a","term_name":"pneumonia caused by gram negative bacteria","termid":"MONDO:0041850"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pneumonia caused by chlamydia","secondary_identifiers":["MESH:D061387","ICD9:483.1","SCTID:233609002","UMLS:C0339959","MEDGEN:452440","DOID:0040083"],"synonyms":[{"name":"Chlamydia caused pneumonia","type":"exact"},{"name":"Chlamydia pneumonia","type":"exact"},{"name":"chlamydia pneumonia","type":"exact"},{"name":"chlamydial pneumonia","type":"exact"}],"termid":"MONDO:0025598","xrefs":{"Monarch":{"xref_id":"0025598"}}}


id: GO:0090709
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of plant organ formation at a consistent predetermined time point during development.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of development, heterochronic","termid":"GO:0040034"},{"relation_name":"is_a","term_name":"regulation of plant organ formation","termid":"GO:1905428"}],"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 timing of plant organ formation","termid":"GO:0090709"}


id: _global:partial_evidence_for_feature
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"B is partial_evidence_for_feature A if the extent of B supports part_of but not all of A.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"evidence_for_feature","termid":"_global:evidence_for_feature"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial_evidence_for_feature","termid":"_global:partial_evidence_for_feature"}


id: GO:0075247
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a dikaryotic spore of typically a rust fungus is produced in an aecium; in heteroecious rusts, the aeciospore is a spore stage that infects the alternate host.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"asexual sporulation resulting in formation of a cellular spore","termid":"GO:0043936"}],"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":"aeciospore formation","termid":"GO:0075247"}


id: PBO:0027938
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_glucose_consumption","termid":"PBO:0027938"}


id: FYPO:0000900
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which linear element assembly is abnormal. Linear element assembly includes the assembly of LinE complexes and their close association with chromatin to form a proteinaceous scaffold (related to the synaptonemal complex) on chromosomes during meiotic prophase.","definition_xrefs":["PomBase:mah","PMID:30640914"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular component assembly","termid":"FYPO:0000336"},{"relation_name":"is_a","term_name":"abnormal homologous chromosome pairing","termid":"FYPO:0003024"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0000631","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abnormal linear element assembly","synonyms":[{"name":"abnormal linear element formation","type":"exact"}],"termid":"FYPO:0000900"}


id: GO:0140544
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of cytoskeletal structures comprising the septin collar.","definition_xrefs":["PMID:21736496","PMID:32386534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"septin cytoskeleton organization","termid":"GO:0032185"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0007010","GO:0008150"],"is_obsolete":false,"name":"septin collar organization","synonyms":[{"name":"cellular bud neck septin hourglass organization","type":"exact"}],"termid":"GO:0140544"}


id: GO:0140904
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process which results in the assembly, arrangement of constituent parts, or disassembly of a cytoophidium. Cytoophidia are mesoscale, intracellular, filamentous structures that contain metabolic enzymes.","definition_xrefs":["PMID:25223282","PMID:27362644"],"direct_ancestors":[{"relation_name":"is_a","term_name":"supramolecular fiber organization","termid":"GO:0097435"}],"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":"cytoophidium organization","termid":"GO:0140904"}


id: GO:2000137
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of cell proliferation involved in heart morphogenesis.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell population proliferation","termid":"GO:0008285"},{"relation_name":"is_a","term_name":"regulation of cell proliferation involved in heart morphogenesis","termid":"GO:2000136"},{"relation_name":"negatively_regulates","term_name":"cell proliferation involved in heart morphogenesis","termid":"GO:0061323"}],"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 cell proliferation involved in heart morphogenesis","termid":"GO:2000137"}


id: PBO:0076471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAF family member associated NFKB activator","termid":"PBO:0076471"}


id: PBO:0062689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 51 subfamily A member 10 pseudogene","termid":"PBO:0062689"}


id: MONDO:0009111
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dihydropyrimidinase (DPD) deficiency is a very rare pyrimidine metabolism disorder with a variable clinical presentation including gastrointestinal manifestations (feeding problems, cyclic vomiting, gastroesophageal reflux, malabsorption with villous atrophy), hypotonia, intellectual deficit, seizures, and less frequently growth retardation, failure to thrive, microcephaly and autism. Asymptomatic cases are also reported. DPD deficiency increases the risk of 5-FU toxicity.","definition_xrefs":["Orphanet:38874"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of pyrimidine metabolism","termid":"MONDO:0019238"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019254"}],"interesting_parent_ids":["MONDO:0019254","MONDO:0005066"],"is_obsolete":false,"name":"dihydropyrimidinuria","secondary_identifiers":["GARD:12347","ICD9:277.2","MEDGEN:83353","DOID:0111629","OMIM:222748","SCTID:238014002","UMLS:C0342803"],"synonyms":[{"name":"DPYSD","type":"related"},{"name":"Dph deficiency","type":"related"},{"name":"Dpys deficiency","type":"related"},{"name":"dihydropyrimidinase deficiency","type":"exact"},{"name":"dihydropyrimidinuria","type":"exact"}],"termid":"MONDO:0009111","xrefs":{"Monarch":{"xref_id":"0009111"}}}


id: GO:0042865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of the siderochrome pyochelin (2-(2-o-hydroxyphenyl-2-thiazolin-4-yl)-3-methylthiazolidine-4-carboxylic acid).","definition_xrefs":["PMID:6794030","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound catabolic process","termid":"GO:0019336"},{"relation_name":"is_a","term_name":"pyochelin metabolic process","termid":"GO:0042863"},{"relation_name":"is_a","term_name":"sulfur compound catabolic process","termid":"GO:0044273"},{"relation_name":"is_a","term_name":"siderophore catabolic process","termid":"GO:0046215"},{"relation_name":"is_a","term_name":"carboxylic acid catabolic process","termid":"GO:0046395"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0019748","GO:0044248","GO:0006790","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"pyochelin catabolic process","synonyms":[{"name":"pyochelin breakdown","type":"exact"},{"name":"pyochelin catabolism","type":"exact"},{"name":"pyochelin degradation","type":"exact"}],"termid":"GO:0042865"}


id: MONDO:0033821
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"fungal infection of eye","termid":"MONDO:0020944"},{"relation_name":"is_a","term_name":"corneal infection","termid":"MONDO:0023865"}],"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":"fungal keratitis","secondary_identifiers":["MEDGEN:687913","GARD:22134","NCIT:C128370","UMLS:C1262117","Orphanet:519930","icd11.foundation:712798367"],"termid":"MONDO:0033821","xrefs":{"Monarch":{"xref_id":"0033821"}}}


id: MONDO:0014327
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete nonepidermolytic palmoplantar keratoderma (obsolete MONDO:0006588)","termid":"MONDO:0006588"},{"relation_name":"excluded_subClassOf","term_name":"obsolete isolated focal palmoplantar keratoderma (obsolete MONDO:0017673)","termid":"MONDO:0017673"},{"relation_name":"is_a","term_name":"hereditary palmoplantar keratoderma","termid":"MONDO:0019272"}],"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":"palmoplantar keratoderma, nonepidermolytic, focal or diffuse","secondary_identifiers":["DOID:0111710","MEDGEN:816724","Orphanet:402003","GARD:17669","OMIM:615735","UMLS:C3810394"],"synonyms":[{"name":"PPKNEFD","type":"related"},{"name":"autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering","type":"exact"},{"name":"palmoplantar keratoderma, nonepidermolytic, focal or diffuse","type":"exact"}],"termid":"MONDO:0014327","xrefs":{"Monarch":{"xref_id":"0014327"}}}


id: MONDO:0023186
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":"Fraser Jequier Chen syndrome","secondary_identifiers":["UMLS:C2930912","MEDGEN:419665","MESH:C535481"],"synonyms":[{"name":"chondrodysplasia, situs inversus totalis, cleft epiglottis and larynx, hexadactyly of hands and feet, pancreatic cystic dysplasia, renal dysplasia/abs","type":"related"}],"termid":"MONDO:0023186","xrefs":{"Monarch":{"xref_id":"0023186"}}}


id: PBO:0087775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of UAF (upstream activation factor) complex; UAF is an RNA polymerase I specific transcription stimulatory factor composed of Uaf30p, Rrn5p, Rrn9p, Rrn10p, histones H3 and H4; targeting factor for the UAF that facilitates activation of many rDNA genes; deletion decreases cellular growth rate; UAF30 has a paralog, TRI1, that arose from the whole genome duplication","termid":"PBO:0087775"}


id: GO:0061744
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specific neuromuscular movement of a single organism in response to external or internal stimuli.","definition_xrefs":["GOC:PARL","GOC:bf","PMID:25318560"],"direct_ancestors":[{"relation_name":"is_a","term_name":"behavior","termid":"GO:0007610"}],"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":"motor behavior","termid":"GO:0061744"}


id: MONDO:0014688
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An asphyxiating thoracic dystrophy that has material basis in homozygous mutation in the KIAA0586 gene on chromosome 14q23.","definition_xrefs":["PMID:26166481","DOID:0110096"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome with Jeune asphyxiating thoracic dystrophy","termid":"MONDO:0018342"},{"relation_name":"is_a","term_name":"Jeune syndrome","termid":"MONDO:0018770"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0006025"],"is_obsolete":false,"name":"short-rib thoracic dysplasia 14 with polydactyly","secondary_identifiers":["GARD:18467","OMIM:616546","UMLS:C4225286","MEDGEN:901479"],"synonyms":[{"name":"SRTD14","type":"exact"},{"name":"short-rib thoracic dysplasia 14 with polydactyly","type":"exact"}],"termid":"MONDO:0014688","xrefs":{"Monarch":{"xref_id":"0014688"}}}


id: PBO:0070465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L5","termid":"PBO:0070465"}


id: PBO:0087515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of heterotrimeric Replication Protein A (RPA); RPA is a highly conserved single-stranded DNA binding protein complex involved in DNA replication, repair, recombination; RPA protects against inappropriate telomere recombination, and upon telomere uncapping, prevents cell proliferation by a checkpoint-independent pathway; with Sgs1p-Top2p-Rmi1p, stimulates DNA catenation/decatenation activity of Top3p; protein abundance increases in response to DNA replication stress","termid":"PBO:0087515"}


id: GO:1901472
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of Golgi calcium ion export.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of release of sequestered calcium ion into cytosol","termid":"GO:0051279"},{"relation_name":"regulates","term_name":"release of sequestered calcium ion into cytosol by Golgi","termid":"GO:0061454"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"regulation of Golgi calcium ion export","termid":"GO:1901472"}


id: GO:0005507
data:
  {"annotated_genes":["SJAG_04677","SJAG_00802","SJAG_04553","SJAG_00449","SJAG_02399","SJAG_MIT04","SJAG_00668","SJAG_01996","SJAG_01140","SJAG_01694","SJAG_MIT20","SJAG_05398","SJAG_03322"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[88339,91139,91938,95773,99655,101626,106351,106977,107344,114531,116551,116986,118527,118576],"is_not":false,"summary":null,"term":"GO:0005507"}]},"cv_name":"molecular_function","definition":"Binding to a copper (Cu) ion.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transition metal ion binding","termid":"GO:0046914"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00449":null,"SJAG_00668":null,"SJAG_00802":null,"SJAG_01140":null,"SJAG_01694":null,"SJAG_01996":null,"SJAG_02399":null,"SJAG_03322":null,"SJAG_04553":null,"SJAG_04677":null,"SJAG_05398":null,"SJAG_MIT04":null,"SJAG_MIT20":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0046872"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0046872","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"copper ion binding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"copper binding","type":"exact"},{"name":"copper/cadmium binding","type":"broad"}],"termid":"GO:0005507","terms_by_termid":{"GO:0005507":null}}


id: GO:0090333
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of stomatal closure. Stomatal closure is the process of closing of stomata, pores in the epidermis of leaves and stems bordered by two guard cells and serving in gas exchange.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of stomatal movement","termid":"GO:0010119"},{"relation_name":"regulates","term_name":"stomatal closure","termid":"GO:0090332"}],"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 closure","termid":"GO:0090333"}


id: PBO:0003751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EST1 family protein (predicted)","termid":"PBO:0003751"}


id: PBO:0064458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein O-glucosyltransferase 3","termid":"PBO:0064458"}


id: GO:2000855
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mineralocorticoid secretion.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of corticosteroid hormone secretion","termid":"GO:2000846"},{"relation_name":"regulates","term_name":"mineralocorticoid secretion","termid":"GO:0035931"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0006810"],"is_obsolete":false,"name":"regulation of mineralocorticoid secretion","termid":"GO:2000855"}


id: PBO:0031378
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_meiosis","termid":"PBO:0031378"}


id: PBO:0000214
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gene structure may be incorrect","termid":"PBO:0000214"}


id: MONDO:0018499
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"double outlet right ventricle","termid":"MONDO:0018089"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy","secondary_identifiers":["Orphanet:423712","GARD:21756","UMLS:C5680071","MEDGEN:1842277"],"synonyms":[{"name":"DORV with atrioventricular septal defect, pulmonary stenosis, heterotaxy","type":"exact"}],"termid":"MONDO:0018499","xrefs":{"Monarch":{"xref_id":"0018499"}}}


id: GO:0045734
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 breakdown of acetate, the anion of acetic acid.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of catabolic process","termid":"GO:0009894"},{"relation_name":"is_a","term_name":"regulation of ketone metabolic process","termid":"GO:0010565"},{"relation_name":"is_a","term_name":"regulation of small molecule metabolic process","termid":"GO:0062012"},{"relation_name":"regulates","term_name":"acetate catabolic process","termid":"GO:0045733"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0044248","GO:0008150"],"is_obsolete":false,"name":"regulation of acetate catabolic process","synonyms":[{"name":"regulation of acetate breakdown","type":"exact"},{"name":"regulation of acetate catabolism","type":"exact"},{"name":"regulation of acetate degradation","type":"exact"}],"termid":"GO:0045734"}


id: PBO:0053763
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 1005","termid":"PBO:0053763"}


id: MOD:01715
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom of a residue with a Proteome Sciences TMT6plex reporter+balance group.","definition_xrefs":["Unimod:214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isotope tagged reagent derivatized residue","termid":"MOD:01426"},{"relation_name":"is_a","term_name":"(13)C isotope tagged reagent","termid":"MOD:01428"},{"relation_name":"is_a","term_name":"(15)N isotope tagged reagent","termid":"MOD:01429"},{"relation_name":"is_a","term_name":"isotope tagged reagent acylated residue","termid":"MOD:01705"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMT6plex reporter+balance reagent acylated residue","synonyms":[{"name":"3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl","type":"exact"},{"name":"Sixplex Tandem Mass Tag(TM)","type":"related"},{"name":"TMT6plex","type":"related"}],"termid":"MOD:01715"}


id: PBO:0064124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase domain containing, cytoplasmic","termid":"PBO:0064124"}


id: SO:0001440
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A non-polar, hydorophobic amino acid encoded by the codon TGG.","direct_ancestors":[{"relation_name":"is_a","term_name":"amino_acid","termid":"SO:0001237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tryptophan","synonyms":[{"name":"Trp","type":"exact"},{"name":"W","type":"exact"}],"termid":"SO:0001440"}


id: PBO:0080557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WBP2 N-terminal like","termid":"PBO:0080557"}


id: GO:0008633
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The conversion of proteins that induce or sustain apoptosis to an active form.","definition_xrefs":["GOC:mtg_apoptosis","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of pro-apoptotic gene products (obsolete GO:0008633)","synonyms":[{"name":"activation of pro-apoptotic gene products","type":"exact"},{"name":"induction of pro-apoptotic gene products","type":"related"}],"termid":"GO:0008633"}


id: PBO:0051884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ITCH antisense RNA 1","termid":"PBO:0051884"}


id: MONDO:0006905
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, small and slightly elevated brown or black skin lesion with usually well-demarcated borders. It is characterized by the presence of a melanocytic proliferation resulting in the formation of uniform cellular nests. Sometimes the clinical and morphologic features may be difficult to distinguish from melanoma.","definition_xrefs":["NCIT:C4751"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanocytic nevus","termid":"MONDO:0005073"}],"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":"pigmented spindle cell nevus","secondary_identifiers":["MEDGEN:105378","MESH:D018331","SCTID:254812004","UMLS:C0474967"],"synonyms":[{"name":"spindle cell Nevus of Reed","type":"exact"}],"termid":"MONDO:0006905","xrefs":{"Monarch":{"xref_id":"0006905"}}}


id: MONDO:0018986
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete leiomyosarcoma (obsolete MONDO:0018986)","termid":"MONDO:0018986","xrefs":{"Monarch":{"xref_id":"0018986"}}}


id: MONDO:0022893
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"craniosynostosis","termid":"MONDO:0015469"}],"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":"craniosynostosis arthrogryposis cleft palate","secondary_identifiers":["GARD:1587"],"termid":"MONDO:0022893","xrefs":{"Monarch":{"xref_id":"0022893"}}}


id: GO:0016202
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of striated muscle development.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle organ development","termid":"GO:0048634"},{"relation_name":"is_a","term_name":"regulation of muscle tissue development","termid":"GO:1901861"},{"relation_name":"regulates","term_name":"striated muscle tissue development","termid":"GO:0014706"}],"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 striated muscle tissue development","termid":"GO:0016202"}


id: PBO:0066895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 195","termid":"PBO:0066895"}


id: PBO:0078014
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 4","termid":"PBO:0078014"}


id: GO:0035696
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The migration of a monocyte from the blood vessels into the surrounding tissue.","definition_xrefs":["PMID:10657654","CL:0000576","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular extravasation","termid":"GO:0045123"},{"relation_name":"is_a","term_name":"mononuclear cell migration","termid":"GO:0071674"},{"relation_name":"is_a","term_name":"myeloid leukocyte migration","termid":"GO:0097529"}],"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":"monocyte extravasation","termid":"GO:0035696"}


id: PBO:0064471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase epsilon 2, accessory subunit","termid":"PBO:0064471"}


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


id: PBO:0049994
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeodomain interacting protein kinase 1","termid":"PBO:0049994"}


id: MONDO:0003822
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A papillary neoplasm of the urinary bladder in which the transitional cells form papillae. The papillary structures exhibit minimal architectural distortion and minimal atypia. Mitoses are infrequent. Patients are at an increased risk of developing new papillary lesions. Occasionally, the new lesions are urothelial carcinomas.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bladder papillary urothelial neoplasm","termid":"MONDO:0003442"},{"relation_name":"is_a","term_name":"urinary tract non-invasive transitional cell neoplasm","termid":"MONDO:0003755"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-invasive bladder papillary urothelial neoplasm","secondary_identifiers":["UMLS:C1518358","DOID:6239","MEDGEN:309424","NCIT:C39831"],"synonyms":[{"name":"bladder PUNLMP","type":"exact"},{"name":"bladder papillary neoplasm of low malignant potential","type":"exact"},{"name":"non-invasive bladder papillary urothelial neoplasm","type":"exact"},{"name":"papillary urothelial neoplasm of low malignant potential","type":"exact"}],"termid":"MONDO:0003822","xrefs":{"Monarch":{"xref_id":"0003822"}}}


id: GO:0006891
data:
  {"annotated_genes":["SJAG_03054","SJAG_03663","SJAG_04474","SJAG_03158","SJAG_03467","SJAG_01600","SJAG_04837","SJAG_04739","SJAG_02655","SJAG_04569","SJAG_02211","SJAG_03842","SJAG_04021","SJAG_04358","SJAG_00192","SJAG_00330","SJAG_00041","SJAG_01415","SJAG_00578","SJAG_02316","SJAG_00804","SJAG_02234","SJAG_04023","SJAG_04002","SJAG_01459","SJAG_01071","SJAG_05030","SJAG_04070","SJAG_02750","SJAG_02525","SJAG_00332","SJAG_01508"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88141,90652,95786,96802,97235,97955,98046,98609,99263,99835,101810,102031,102771,102875,102969,103623,104387,105638,106615,109055,109299,109320,111504,113248,115924,116387,116902],"is_not":false,"summary":null,"term":"GO:0006891"},{"annotations":[97590],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048219"},{"annotations":[90632,108987,88440,116331],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000301"}]},"cv_name":"biological_process","definition":"The directed movement of substances within the Golgi, mediated by small transport vesicles. These either fuse with the cis-Golgi or with each other to form the membrane stacks known as the cis-Golgi reticulum (network).","definition_xrefs":["ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Golgi vesicle transport","termid":"GO:0048193"}],"gene_count":32,"genes_by_uniquename":{"SJAG_00041":null,"SJAG_00192":null,"SJAG_00330":null,"SJAG_00332":null,"SJAG_00578":null,"SJAG_00804":null,"SJAG_01071":null,"SJAG_01415":null,"SJAG_01459":null,"SJAG_01508":null,"SJAG_01600":null,"SJAG_02211":null,"SJAG_02234":null,"SJAG_02316":null,"SJAG_02525":null,"SJAG_02655":null,"SJAG_02750":null,"SJAG_03054":null,"SJAG_03158":null,"SJAG_03467":null,"SJAG_03663":null,"SJAG_03842":null,"SJAG_04002":null,"SJAG_04021":null,"SJAG_04023":null,"SJAG_04070":null,"SJAG_04358":null,"SJAG_04474":null,"SJAG_04569":null,"SJAG_04739":null,"SJAG_04837":null,"SJAG_05030":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150","GO:0016192"],"is_obsolete":false,"name":"intra-Golgi vesicle-mediated transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"intra-Golgi transport","type":"exact"}],"termid":"GO:0006891","terms_by_termid":{"GO:0000301":null,"GO:0006891":null,"GO:0048219":null}}


id: MONDO:0014705
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any craniosynostosis in which the cause of the disease is a mutation in the ZIC1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated oxycephaly","termid":"MONDO:0018971"}],"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":"craniosynostosis 6","secondary_identifiers":["OMIM:616602","Orphanet:672985","GARD:18048","MEDGEN:904675","UMLS:C4225269"],"synonyms":[{"name":"CRS6","type":"related"},{"name":"ZIC1 craniosynostosis","type":"exact"},{"name":"craniosynostosis 6","type":"exact"},{"name":"craniosynostosis caused by mutation in ZIC1","type":"exact"},{"name":"craniosynostosis type 6","type":"exact"}],"termid":"MONDO:0014705","xrefs":{"Monarch":{"xref_id":"0014705"}}}


id: MONDO:0007232
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant brachyolmia is a relatively severe form of brachyolmia, a group of rare genetic skeletal disorders, characterized by short-trunked short stature, platyspondyly and kyphoscoliosis. Degenerative joint disease (osteoarthropathy) in the spine, large joints and interphalangeal joints becomes manifest in adulthood.","definition_xrefs":["Orphanet:93304"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"brachyolmia","termid":"MONDO:0015262"},{"relation_name":"is_a","term_name":"TRPV4-related bone disorder","termid":"MONDO:0018240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant brachyolmia","secondary_identifiers":["OMIM:113500","MEDGEN:96583","SCTID:717264003","GARD:10429","UMLS:C0432227"],"synonyms":[{"name":"BCYM3","type":"related"},{"name":"brachyolmia autosomal dominant","type":"related"},{"name":"brachyolmia type 3","type":"exact"},{"name":"brachyolmia, autosomal dominant","type":"exact"},{"name":"brachyrachia","type":"related"}],"termid":"MONDO:0007232","xrefs":{"Monarch":{"xref_id":"0007232"}}}


id: PBO:0071233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 74","termid":"PBO:0071233"}


id: GO:0170003
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of heme B from one side of a membrane to the other.","definition_xrefs":["PMID:20610401","PMID:32121449","PMID:15369674","PMID:9657107"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heme transmembrane transporter activity","termid":"GO:0015232"}],"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:0022857","GO:0003674"],"is_obsolete":false,"name":"heme B transmembrane transporter activity","termid":"GO:0170003"}


id: SO:0000397
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"U6atac_snRNA is an snRNA required for the splicing of the minor U12-dependent class of eukaryotic nuclear introns. It forms a base paired complex with U4atac_snRNA (SO:0000394).","direct_ancestors":[{"relation_name":"is_a","term_name":"snRNA","termid":"SO:0000274"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U6atac_snRNA","synonyms":[{"name":"U6atac small nuclear RNA","type":"exact"},{"name":"U6atac snRNA","type":"exact"},{"name":"snRNA U6atac","type":"exact"}],"termid":"SO:0000397"}


id: GO:0008334
data:
  {"annotated_genes":["SJAG_03745"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91728],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071044"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving an mRNA encoding a histone.","definition_xrefs":["GOC:mah","PMID:17855393","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA metabolic process","termid":"GO:0016071"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03745":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016071"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016071","GO:0008150"],"is_obsolete":false,"name":"histone mRNA metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"histone mRNA metabolism","type":"exact"},{"name":"stem-loop-containing histone mRNA 3'-end processing","type":"narrow"}],"termid":"GO:0008334","terms_by_termid":{"GO:0071044":null}}


id: PR:P08092
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ran1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P08092"],"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":"negative regulator of sexual conjugation and meiosis (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19C2.05","synonyms":[{"name":"Spom972h-ran1","type":"exact"}],"termid":"PR:P08092"}


id: PBO:0047218
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 224 member B","termid":"PBO:0047218"}


id: MONDO:0012882
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bipolar disorder","termid":"MONDO:0004985"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major affective disorder 9","secondary_identifiers":["MEDGEN:398108","OMIM:612372","MESH:C567531","UMLS:C2700440"],"synonyms":[{"name":"MAFD9","type":"exact"},{"name":"MAJOR affective disorder 9","type":"related"},{"name":"bipolar affective disorder","type":"related"},{"name":"major affective disorder 9","type":"exact"},{"name":"major affective disorder-9, susceptibility to","type":"exact"}],"termid":"MONDO:0012882","xrefs":{"Monarch":{"xref_id":"0012882"}}}


id: MONDO:0012585
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any coronary artery disease in which the cause of the disease is a mutation in the CD36 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coronary heart disease, susceptibility to, 7","secondary_identifiers":["MEDGEN:370260","OMIM:610938","UMLS:C1970441"],"synonyms":[{"name":"CD36 coronary artery disease","type":"exact"},{"name":"CHDS7","type":"related"},{"name":"coronary artery disease caused by mutation in CD36","type":"exact"},{"name":"coronary heart disease, susceptibility to, 7","type":"exact"},{"name":"coronary heart disease, susceptibility to, type 7","type":"exact"},{"name":"susceptibility to coronary heart disease 7","type":"related"}],"termid":"MONDO:0012585","xrefs":{"Monarch":{"xref_id":"0012585"}}}


id: PBO:0038446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AAR2 splicing factor","termid":"PBO:0038446"}


id: GO:0045442
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-oxoglutarate + deacetoxycephalosporin C + O2 = CO2 + deacetylcephalosporin C + succinate.","definition_xrefs":["RHEA:16805","EC:1.14.11.26"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"deacetoxycephalosporin-C hydroxylase activity","secondary_identifiers":["MetaCyc:1.14.11.26-RXN","KEGG_REACTION:R05229"],"synonyms":[{"name":"3'-methylcephem hydroxylase activity","type":"related"},{"name":"DACS","type":"related"},{"name":"DAOC hydroxylase activity","type":"related"},{"name":"beta-lactam hydroxylase activity","type":"exact"},{"name":"deacetoxycephalosporin C hydroxylase activity","type":"related"},{"name":"deacetoxycephalosporin-C,2-oxoglutarate:oxygen oxidoreductase (3-hydroxylating) activity","type":"related"},{"name":"deacetylcephalosporin C synthase activity","type":"related"}],"termid":"GO:0045442"}


id: FYPO:0001291
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of CDP-diacylglycerol-serine O-phosphatidyltransferase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0001985","FYPO:0000707","FYPO:0000654","FYPO:0000661"],"is_obsolete":false,"name":"abnormal CDP-diacylglycerol-serine O-phosphatidyltransferase activity","termid":"FYPO:0001291"}


id: PBO:0062208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily AC member 4 pseudogene","termid":"PBO:0062208"}


id: PBO:0069080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 327, pseudogene","termid":"PBO:0069080"}


id: FYPO:0005947
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing potassium chloride.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0002060","FYPO:0000003","FYPO:0000139","FYPO:0002058","FYPO:0000257","FYPO:0002057"],"is_obsolete":false,"name":"normal growth on potassium chloride","synonyms":[{"name":"normal cell population growth in presence of potassium chloride","type":"exact"},{"name":"normal cell population growth on KCl","type":"exact"},{"name":"normal cell population growth on potassium chloride","type":"exact"},{"name":"normal cellular response to potassium chloride","type":"related"},{"name":"normal vegetative cell population growth on potassium chloride","type":"exact"}],"termid":"FYPO:0005947"}


id: PBO:0062941
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prolyl 4-hydroxylase, transmembrane","termid":"PBO:0062941"}


id: MONDO:0013815
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial bent bone dysplasia syndrome","termid":"MONDO:0031615"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bent bone dysplasia syndrome 1","secondary_identifiers":["Orphanet:313855","GARD:10965","OMIM:614592","UMLS:C3281247","MEDGEN:482877"],"synonyms":[{"name":"BBDS","type":"related"},{"name":"FGFR2-related bent bone dysplasia","type":"exact"},{"name":"bent bone dysplasia (BBD)-FGFR2 type","type":"related"},{"name":"bent bone dysplasia syndrome","type":"related"},{"name":"perinatal lethal bent bone dysplasia","type":"exact"}],"termid":"MONDO:0013815","xrefs":{"Monarch":{"xref_id":"0013815"}}}


id: PR:O74869
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nic1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74869"],"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":"high-affinity nickel transport protein nic1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1884.02","synonyms":[{"name":"Spom972h-nic1","type":"exact"}],"termid":"PR:O74869"}


id: PBO:0052933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 21-1","termid":"PBO:0052933"}


id: PBO:0001777
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by P. carnii Brl1","termid":"PBO:0001777"}


id: PBO:0072154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 31","termid":"PBO:0072154"}


id: PBO:0075395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sp8 transcription factor","termid":"PBO:0075395"}


id: MONDO:0012173
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) is a mitochondrial disorder of long chain fatty acid oxidation characterized in most patients by onset in infancy/ early childhood with hypoketotic hypoglycemia, metabolic acidosis, liver disease, hypotonia and frequently cardiac involvement with arrhythmias and/or cardiomyopathy.","definition_xrefs":["Orphanet:5"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"3-hydroxyacyl-CoA dehydrogenase deficiency","termid":"MONDO:0017715"},{"relation_name":"is_a","term_name":"disorder of fatty acid oxidation and ketogenesis","termid":"MONDO:0017713"},{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"},{"relation_name":"is_a","term_name":"familial hypertrophic cardiomyopathy","termid":"MONDO:0024573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0002525","MONDO:0005244","MONDO:0005267","MONDO:0005066"],"is_obsolete":false,"name":"long chain 3-hydroxyacyl-CoA dehydrogenase deficiency","secondary_identifiers":["NCIT:C129929","UMLS:C3711645","GARD:6867","OMIM:609016","SCTID:726021008","icd11.foundation:760613381","MEDGEN:778253"],"synonyms":[{"name":"3-hydroxyacyl-CoA dehydrogenase long chain deficiency","type":"related"},{"name":"HELLP syndrome, maternal, of pregnancy","type":"exact"},{"name":"LCHAD deficiency","type":"exact"},{"name":"LCHADD","type":"exact"},{"name":"fatty liver, acute, of pregnancy","type":"exact"},{"name":"long chain 3-hydroxyacyl-CoA dehydrogenase deficiency","type":"exact"},{"name":"long-chain 3-OH acyl-CoA dehydrogenase deficiency","type":"related"},{"name":"long-chain 3-hydroxy acyl CoA dehydrogenase deficiency","type":"related"},{"name":"long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency","type":"related"},{"name":"long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency","type":"exact"},{"name":"trifunctional protein deficiency type 1","type":"related"}],"termid":"MONDO:0012173","xrefs":{"Monarch":{"xref_id":"0012173"}}}


id: MONDO:0001547
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tympanic membrane disorder","termid":"MONDO:0003648"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atrophic nonflaccid tympanic membrane","secondary_identifiers":["SCTID:72052003","MEDGEN:509983","DOID:12546","ICD9:384.82","UMLS:C0155471"],"termid":"MONDO:0001547","xrefs":{"Monarch":{"xref_id":"0001547"}}}


id: PBO:0050892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immediate early response 3 interacting protein 1","termid":"PBO:0050892"}


id: PBO:0038448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alanyl-tRNA synthetase 1","termid":"PBO:0038448"}


id: PBO:0063710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoglucomutase 5","termid":"PBO:0063710"}


id: FYPO:0003287
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through the meiotic cell cycle is arrested during the first meiotic interphase, before premeiotic DNA replication has taken place.","definition_xrefs":["PomBase:mah","GO:0051328"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormally arrested meiotic cell cycle","termid":"FYPO:0002224"}],"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:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000631"],"is_obsolete":false,"name":"abnormal cell cycle arrest in meiotic interphase before premeiotic DNA replication","synonyms":[{"name":"abnormal cell cycle arrest in meiotic interphase preceding premeiotic DNA replication","type":"exact"},{"name":"abnormal meiotic cell cycle arrest in interphase before premeiotic DNA replication","type":"exact"}],"termid":"FYPO:0003287"}


id: GO:0030323
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the respiratory tube over time, from its formation to the mature structure. The respiratory tube is assumed to mean any tube in the respiratory tract.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tube development","termid":"GO:0035295"},{"relation_name":"is_a","term_name":"animal organ development","termid":"GO:0048513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"respiratory tube development","termid":"GO:0030323"}


id: PBO:0040456
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase phospholipid transporting 11C","termid":"PBO:0040456"}


id: PBO:0027900
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_calcium_import","termid":"PBO:0027900"}


id: PATO:0002478
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's being marked by narrow lines or grooves, usually parallel, that are oriented transversely relative to the long axis of the bearer.","definition_xrefs":["PATOC:DS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"striated","termid":"PATO:0001410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transversely striated","termid":"PATO:0002478"}


id: PBO:0111818
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"haloacid dehalogenase-like hydrolase","termid":"PBO:0111818"}


id: MOD:01657
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that is produced by reaction with 4-(4-dimethylaminophenylazo)benzenesulfonyl chloride, dabsyl chloride, to form N6-Dabsyl-lysine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"},{"relation_name":"is_a","term_name":"Dabsyl chloride derivatized residue","termid":"MOD:01656"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N6-Dabsyl derivatized lysine","synonyms":[{"name":"N6-[4-([4-(dimethylamino)phenyl]diazenyl)benzenesulfonyl]lysine","type":"exact"},{"name":"N6DabsylLys","type":"exact"}],"termid":"MOD:01657"}


id: PBO:0067983
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 285","termid":"PBO:0067983"}


id: GO:0031237
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of a plasma membrane consisting of gene products and protein complexes that penetrate the periplasmic side of the plasma membrane only, either directly or via some covalently attached hydrophobic anchor.","definition_xrefs":["GOC:mah","GOC:mtg_sensu"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of periplasmic side of plasma membrane (obsolete GO:0031237)","synonyms":[{"name":"intrinsic to external leaflet of plasma membrane, in periplasmic space","type":"exact"},{"name":"intrinsic to periplasmic side of plasma membrane","type":"exact"}],"termid":"GO:0031237"}


id: GO:0071398
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a fatty acid stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to fatty acid","termid":"GO:0070542"},{"relation_name":"is_a","term_name":"cellular response to lipid","termid":"GO:0071396"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to fatty acid","termid":"GO:0071398"}


id: GO:1900266
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of substance P receptor binding.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of substance P receptor binding (obsolete GO:1900266)","synonyms":[{"name":"down regulation of neurokinin-1 receptor binding","type":"exact"},{"name":"down regulation of substance P receptor binding","type":"exact"},{"name":"down regulation of substance P receptor ligand","type":"narrow"},{"name":"down-regulation of neurokinin-1 receptor binding","type":"exact"},{"name":"down-regulation of substance P receptor binding","type":"exact"},{"name":"down-regulation of substance P receptor ligand","type":"narrow"},{"name":"downregulation of neurokinin-1 receptor binding","type":"exact"},{"name":"downregulation of substance P receptor binding","type":"exact"},{"name":"downregulation of substance P receptor ligand","type":"narrow"},{"name":"inhibition of neurokinin-1 receptor binding","type":"exact"},{"name":"inhibition of substance P receptor binding","type":"narrow"},{"name":"inhibition of substance P receptor ligand","type":"narrow"},{"name":"negative regulation of neurokinin-1 receptor binding","type":"exact"},{"name":"negative regulation of substance P receptor ligand","type":"narrow"}],"termid":"GO:1900266"}


id: PR:O94306
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpp21 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94306"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C16C4.19 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC16C4.19","synonyms":[{"name":"Spom972h-rpp21","type":"exact"}],"termid":"PR:O94306"}


id: MONDO:0019742
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nephronophthisis","termid":"MONDO:0019005"},{"relation_name":"is_a","term_name":"inborn disorder of peptide metabolism","termid":"MONDO:0019232"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"late-onset nephronophthisis","secondary_identifiers":["MEDGEN:1842314","UMLS:C5681620","GARD:16824","Orphanet:93589"],"termid":"MONDO:0019742","xrefs":{"Monarch":{"xref_id":"0019742"}}}


id: PBO:0051989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"JAKMIP1 divergent transcript","termid":"PBO:0051989"}


id: PBO:0038976
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADPGK antisense RNA 1","termid":"PBO:0038976"}


id: PBO:0089142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBX domain Sre1 cleavage protein","termid":"PBO:0089142"}


id: PBO:0081047
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger CCHC-type containing 3","termid":"PBO:0081047"}


id: _global:disconnected_from
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"X is disconnected_from Y iff it is not the case that X overlaps Y.","definition_xrefs":["PMID:20226267"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disconnected_from","termid":"_global:disconnected_from"}


id: MONDO:0019101
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Retinal cavernous hemangioma is a rare, benign, usually unilateral retinal vascular hamartoma that in most cases is asymptomatic but in some patients may present with blurred vision or floaters and that is characterized by the presence of grape-like vacuoles.","definition_xrefs":["Orphanet:71213"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital vitreoretinal dysplasia","termid":"MONDO:0020247"},{"relation_name":"is_a","term_name":"retina neoplasm","termid":"MONDO:0021231"},{"relation_name":"is_a","term_name":"vascular neoplasm","termid":"MONDO:0024296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005328"],"is_obsolete":false,"name":"retinal capillary malformation","secondary_identifiers":["GARD:18908"],"termid":"MONDO:0019101","xrefs":{"Monarch":{"xref_id":"0019101"}}}


id: PBO:0027370
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_cellular_amino_acid_level_during_vegetative_growth","termid":"PBO:0027370"}


id: PBO:0058079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4297","termid":"PBO:0058079"}


id: MOD:01222
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to O-formyl-L-serine.","definition_xrefs":["PubMed:15799070","PubMed:15627961","Unimod:122#S"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-formylated residue","termid":"MOD:01483"},{"relation_name":"is_a","term_name":"O3-acylated L-serine","termid":"MOD:02003"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-formyl-L-serine","synonyms":[{"name":"Formyl","type":"related"},{"name":"Formylation","type":"related"}],"termid":"MOD:01222"}


id: PBO:0063829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphohistidine phosphatase 1","termid":"PBO:0063829"}


id: GO:2000451
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of CD8-positive, alpha-beta T cell extravasation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of T cell extravasation","termid":"GO:2000409"},{"relation_name":"is_a","term_name":"regulation of CD8-positive, alpha-beta T cell extravasation","termid":"GO:2000449"},{"relation_name":"positively_regulates","term_name":"CD8-positive, alpha-beta T cell extravasation","termid":"GO:0035697"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of CD8-positive, alpha-beta T cell extravasation","termid":"GO:2000451"}


id: PR:Q8TFH7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A tRNA-splicing endonuclease subunit Sen2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR21227:SF0"],"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":"tRNA-splicing endonuclease subunit sen2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB17E12.07c","secondary_identifiers":["UniProtKB:Q8TFH7"],"synonyms":[{"name":"SPAPB17E12.07c","type":"related"},{"name":"Spom972h-TSEN2","type":"exact"},{"name":"tRNA-intron endonuclease sen2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q8TFH7"}


id: MONDO:0850107
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"infectious disorder of the nervous system","termid":"MONDO:0020010"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"postinfectious cerebellitis","secondary_identifiers":["Orphanet:624244","GARD:22502","MEDGEN:1843009","UMLS:C5575321"],"termid":"MONDO:0850107","xrefs":{"Monarch":{"xref_id":"0850107"}}}


id: PBO:0001997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJ domain protein Erj5 (predicted)","termid":"PBO:0001997"}


id: GO:0120053
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-D-xylose + D-ribitol 5-phosphate-R = UDP + beta1,4-xylosyl-D-ribitol 5-phosphate-R.","definition_xrefs":["PMID:27733679"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-xylosyltransferase activity","termid":"GO:0035252"}],"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:0016740"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016757","GO:0003824"],"is_obsolete":false,"name":"ribitol beta-1,4-xylosyltransferase activity","termid":"GO:0120053"}


id: MONDO:0015507
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Rare genetic liver disease.","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic hepatic disease (obsolete MONDO:0015507)","secondary_identifiers":["Orphanet:156601"],"synonyms":[{"name":"rare genetic liver disease","type":"exact"}],"termid":"MONDO:0015507","xrefs":{"Monarch":{"xref_id":"0015507"}}}


id: MONDO:0003626
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare serous adenocarcinoma that arises from the uterine ligament.","definition_xrefs":["NCIT:C40136"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uterine ligament adenocarcinoma","termid":"MONDO:0002741"},{"relation_name":"is_a","term_name":"cervical serous adenocarcinoma","termid":"MONDO:0003631"}],"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":"uterine ligament serous adenocarcinoma","secondary_identifiers":["DOID:5747","UMLS:C1519872","MEDGEN:275561"],"synonyms":[{"name":"uterine ligament serous adenocarcinoma","type":"exact"}],"termid":"MONDO:0003626","xrefs":{"Monarch":{"xref_id":"0003626"}}}


id: GO:0071600
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the otic vesicle are generated and organized. The otic vesicle is a transient embryonic structure formed during development of the vertebrate inner ear.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inner ear morphogenesis","termid":"GO:0042472"},{"relation_name":"is_a","term_name":"embryonic organ morphogenesis","termid":"GO:0048562"},{"relation_name":"is_a","term_name":"epithelial tube morphogenesis","termid":"GO:0060562"},{"relation_name":"part_of","term_name":"otic vesicle development","termid":"GO:0071599"}],"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":"otic vesicle morphogenesis","termid":"GO:0071600"}


id: MONDO:0010429
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the SYP gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic X-linked intellectual disability","termid":"MONDO:0019181"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability, X-linked 96","secondary_identifiers":["DOID:0112035","GARD:22685","MEDGEN:477039","UMLS:C3275408","OMIM:300802"],"synonyms":[{"name":"MRX96","type":"related"},{"name":"SYP non-syndromic X-linked intellectual disability","type":"exact"},{"name":"intellectual developmental disorder, X-linked 96, X-linked recessive","type":"exact"},{"name":"intellectual disability, X-linked 96","type":"exact"},{"name":"intellectual disability, X-linked type 96","type":"exact"},{"name":"mental retardation, X-linked 96","type":"related"},{"name":"mental retardation, X-linked type 96","type":"exact"},{"name":"non-syndromic X-linked intellectual disability caused by mutation in SYP","type":"exact"}],"termid":"MONDO:0010429","xrefs":{"Monarch":{"xref_id":"0010429"}}}


id: FYPO:0008340
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the activation of a ubiquitin ligase activator does not occur. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PMID:22437499"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal molecular function","termid":"FYPO:0000707"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"abolished ubiquitin ligase activator activity","termid":"FYPO:0008340"}


id: PBO:0089881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell wall alpha-1,3-glucan synthase Ags1","termid":"PBO:0089881"}


id: PBO:0055693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIX1 and RIOK2 antisense RNA 1","termid":"PBO:0055693"}


id: MONDO:0000009
data:
  {"annotated_genes":["SJAG_02091","SJAG_02093","SJAG_03204","SJAG_04887","SJAG_04621","SJAG_03703","SJAG_04312","SJAG_02431"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957580"},{"annotations":[85604,85605,85606],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018794"},{"annotations":[85845,85844],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015912"},{"annotations":[84642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014078"},{"annotations":[86212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014518"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hemorrhagic disease","termid":"MONDO:0002243"},{"relation_name":"is_a","term_name":"blood platelet disease","termid":"MONDO:0002245"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":8,"genes_by_uniquename":{"SJAG_02091":null,"SJAG_02093":null,"SJAG_02431":null,"SJAG_03204":null,"SJAG_03703":null,"SJAG_04312":null,"SJAG_04621":null,"SJAG_04887":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"inherited bleeding disorder, platelet-type","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0005818","DOID:2218","OMIMPS:231200","MEDGEN:610"],"synonyms":[{"name":"bleeding disorder, platelet-type","type":"exact"},{"name":"blood platelet disease","type":"broad"},{"name":"platelet disorder","type":"broad"},{"name":"thrombocytopathy","type":"related"}],"termid":"MONDO:0000009","terms_by_termid":{"MONDO:0014078":null,"MONDO:0014518":null,"MONDO:0015912":null,"MONDO:0018794":null,"MONDO:0957580":null},"xrefs":{"Monarch":{"xref_id":"0000009"}}}


id: PBO:0048812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase","termid":"PBO:0048812"}


id: PBO:0065552
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostaglandin E receptor 4 pseudogene 2","termid":"PBO:0065552"}


id: PBO:0055832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat and fibronectin type III domain containing 2","termid":"PBO:0055832"}


id: PBO:0064518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II subunit M","termid":"PBO:0064518"}


id: PBO:0060366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myogenin promoter associated myogenic regulatory antisense long non coding RNA","termid":"PBO:0060366"}


id: PBO:0068575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 26, pseudogene","termid":"PBO:0068575"}


id: PBO:0035702
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_H4-K16_acetylation_during_vegetative_growth","termid":"PBO:0035702"}


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


id: GO:0052887
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 7,9,9'-tri-cis-neurosporene + a quinone = 7,9,7',9'-tetra-cis-lycopene + a quinol.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 7,9,9'-tricis-neurosporene:quinone oxidoreductase activity (obsolete GO:0052887)","termid":"GO:0052887"}


id: PBO:0004186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-ZnF type","termid":"PBO:0004186"}


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: GO:0043598
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cytoplasmic complex of two polypeptides that loads the DNA polymerase processivity factor proliferating cell nuclear antigen (PCNA) onto DNA, thereby permitting processive DNA synthesis catalyzed by DNA polymerase. Examples of this component are found in prokaryotic species.","definition_xrefs":["PMID:16172520","GOC:mtg_sensu","PMID:14646196"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA replication factor C complex","termid":"GO:0005663"},{"relation_name":"part_of","term_name":"cytoplasmic replisome","termid":"GO:0043600"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005737","GO:0005694","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"cytoplasmic DNA replication factor C complex","synonyms":[{"name":"cytoplasmic RFC","type":"exact"},{"name":"cytoplasmic clamp loader","type":"exact"}],"termid":"GO:0043598"}


id: PBO:0053910
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 1204","termid":"PBO:0053910"}


id: MONDO:0016602
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Citrin deficiency is a rare autosomal recessive urea cycle defect characterized clinically by recurring episodes of hyperammonemia and associated neuropsychiatric symptoms in the adult-onset form (citrullinemia type II), and by transient cholestasis and variable hepatic dysfunction in the neonatal form (neonatal intrahepatic cholestasis due to citrin deficiency).","definition_xrefs":["Orphanet:247582"],"direct_ancestors":[{"relation_name":"is_a","term_name":"citrullinemia","termid":"MONDO:0015991"},{"relation_name":"is_a","term_name":"urea cycle disorder or inherited hyperammonemia","termid":"MONDO:0800153"}],"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:0005066","MONDO:0004736"],"is_obsolete":false,"name":"citrin deficiency","secondary_identifiers":["SCTID:429735007","MEDGEN:372684","GARD:20661","NANDO:2200483","UMLS:C1997910","NANDO:1200978","icd11.foundation:348535193"],"synonyms":[{"name":"citrin deficiency","type":"exact"}],"termid":"MONDO:0016602","xrefs":{"Monarch":{"xref_id":"0016602"}}}


id: PBO:0053427
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 370","termid":"PBO:0053427"}


id: PBO:0072408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27 pseudogene 13","termid":"PBO:0072408"}


id: MOD:01625
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a glycine residue to 1-thioglycine.","definition_xrefs":["PubMed:11463785","RESID:AA0265","PubMed:9367957"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur substitution for oxygen","termid":"MOD:00749"},{"relation_name":"is_a","term_name":"modified glycine residue","termid":"MOD:00908"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1-thioglycine","synonyms":[{"name":"1-thioglycine","type":"exact"},{"name":"2-amino-1-sulfanylethanone","type":"exact"},{"name":"Carboxy->Thiocarboxy","type":"related"},{"name":"MOD_RES 1-thioglycine","type":"exact"},{"name":"S(O)Gly","type":"exact"},{"name":"aminoethanethioic acid","type":"exact"},{"name":"aminothioacetic acid","type":"exact"},{"name":"thiocarboxylic acid","type":"related"}],"termid":"MOD:01625"}


id: PBO:0071837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S2 pseudogene 32","termid":"PBO:0071837"}


id: GO:0034720
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by the removal of a methyl group from lysine at position 4 of the histone.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-K4 demethylation (obsolete GO:0034720)","synonyms":[{"name":"H3K4 demethylation (me1 me2 and me3)","type":"related"}],"termid":"GO:0034720"}


id: MONDO:0004768
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of both the cornea and the conjunctiva.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"keratitis","termid":"MONDO:0003085"},{"relation_name":"is_a","term_name":"conjunctivitis","termid":"MONDO:0003799"}],"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":"keratoconjunctivitis","secondary_identifiers":["DOID:9368","HP:0001096","ICD9:370.49","ICD9:370.40","MEDGEN:44014","MESH:D007637","UMLS:C0022573","ICD9:370.8","NCIT:C34744","ICD10CM:H16.2","SCTID:88151007"],"termid":"MONDO:0004768","xrefs":{"Monarch":{"xref_id":"0004768"}}}


id: GO:1905949
data:
  {"annotated_genes":["SJAG_00296","SJAG_03631"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90701,112854],"is_not":false,"summary":null,"term":"GO:1905949"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of calcium ion import across plasma membrane.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","GOC:bhm","PMID:17640527"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of calcium ion import","termid":"GO:0090281"},{"relation_name":"is_a","term_name":"negative regulation of calcium ion transmembrane transport","termid":"GO:1903170"},{"relation_name":"is_a","term_name":"regulation of calcium ion import across plasma membrane","termid":"GO:1905664"},{"relation_name":"negatively_regulates","term_name":"calcium ion import across plasma membrane","termid":"GO:0098703"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00296":null,"SJAG_03631":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"negative regulation of calcium ion import across plasma membrane","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of calcium ion import across plasma membrane","type":"exact"},{"name":"down-regulation of calcium ion import across plasma membrane","type":"exact"},{"name":"downregulation of calcium ion import across plasma membrane","type":"exact"},{"name":"inhibition of calcium ion import across plasma membrane","type":"narrow"}],"termid":"GO:1905949","terms_by_termid":{"GO:1905949":null}}


id: MONDO:0007518
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"edema, familial idiopathic, prepubertal","secondary_identifiers":["UMLS:C1851847","OMIM:129840","MESH:C565063","MEDGEN:377535"],"synonyms":[{"name":"edema, familial idiopathic, prepubertal","type":"exact"}],"termid":"MONDO:0007518","xrefs":{"Monarch":{"xref_id":"0007518"}}}


id: PBO:0084372
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lipoate-protein ligase; octanoyl-CoA: protein transferase required along with Lip2 and Lip5 for lipoylation of Lat1p and Kgd2p; similar to E. coli LplA; null mutant displays reduced frequency of mitochondrial genome loss","termid":"PBO:0084372"}


id: PBO:0066519
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ral guanine nucleotide dissociation stimulator like 4","termid":"PBO:0066519"}


id: GO:0033243
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways leading to the breakdown of amines.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catabolic process","termid":"GO:0009896"},{"relation_name":"is_a","term_name":"positive regulation of amine metabolic process","termid":"GO:0033240"},{"relation_name":"is_a","term_name":"regulation of amine catabolic process","termid":"GO:0033241"},{"relation_name":"positively_regulates","term_name":"amine catabolic process","termid":"GO:0009310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of amine catabolic process","synonyms":[{"name":"positive regulation of amine breakdown","type":"exact"},{"name":"positive regulation of amine catabolism","type":"exact"},{"name":"positive regulation of amine degradation","type":"exact"}],"termid":"GO:0033243"}


id: GO:0031205
data:
  {"annotated_genes":["SJAG_02588","SJAG_02354","SJAG_00175","SJAG_03955"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[90063,109120,109896,95221],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031207"}]},"cv_name":"cellular_component","definition":"An endoplasmic reticulum membrane-associated complex involved in the translocation of proteins that are targeted to the ER. In yeast, this complex consists of two subcomplexes, namely, the Sec61 complex and the Sec62/Sec63 complex.","definition_xrefs":["PMID:14617809","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"is_a","term_name":"endoplasmic reticulum protein-containing complex","termid":"GO:0140534"},{"relation_name":"part_of","term_name":"rough endoplasmic reticulum membrane","termid":"GO:0030867"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00175":null,"SJAG_02354":null,"SJAG_02588":null,"SJAG_03955":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"part_of","termid":"GO:0005789"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005789","GO:0032991","GO:0005783"],"is_obsolete":false,"name":"endoplasmic reticulum Sec complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0031205","terms_by_termid":{"GO:0031207":null}}


id: FYPO:0007641
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the methylation of lysine at position 9 of histone H3 occurs to a lower extent than normal during G0 phase.","definition_xrefs":["PMID:27738016","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone modification during G0","termid":"FYPO:0007470"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0002494","FYPO:0002274","FYPO:0001985"],"is_obsolete":false,"name":"decreased histone H3-K9 methylation during G0","synonyms":[{"name":"decreased histone H3 K9 methylation during G0","type":"exact"},{"name":"decreased histone H3-K9 methylation during cell quiescence","type":"exact"},{"name":"decreased histone H3-K9 methylation during quiescence","type":"exact"},{"name":"decreased histone H3K9 methylation during G0","type":"exact"},{"name":"decreased histone H3K9me2 methylation during G0","type":"exact"},{"name":"reduced histone H3-K9 methylation during G0","type":"exact"}],"termid":"FYPO:0007641"}


id: PBO:0036103
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_H3-K9_trimethylation_at_silent_mating-type_cassette_during_vegetative_growth","termid":"PBO:0036103"}


id: GO:1901224
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the non-canonical NF-kappaB cascade.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of non-canonical NF-kappaB signal transduction","termid":"GO:1901222"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"non-canonical NF-kappaB signal transduction","termid":"GO:0038061"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of non-canonical NF-kappaB signal transduction","secondary_identifiers":["GO:0042346","GO:0008588"],"synonyms":[{"name":"activation of NIK/NF-kappaB cascade","type":"narrow"},{"name":"activation of non-canonical NF-KB signaling","type":"exact"},{"name":"activation of noncanonical NF-kappaB signaling","type":"exact"},{"name":"activation of noncanonical nuclear factor kappaB (NF-kappaB) pathway","type":"exact"},{"name":"activation of p52-dependent NF-kappaB signaling","type":"narrow"},{"name":"positive regulation of NF-kappaB import into nucleus","type":"narrow"},{"name":"positive regulation of NIK/NF-kappaB cascade","type":"exact"},{"name":"positive regulation of NIK/NF-kappaB signaling","type":"exact"},{"name":"positive regulation of non-canonical NF-KB signaling","type":"exact"},{"name":"positive regulation of noncanonical NF-kappaB signaling","type":"exact"},{"name":"positive regulation of noncanonical nuclear factor kappaB (NF-kappaB) pathway","type":"exact"},{"name":"positive regulation of p52-dependent NF-kappaB signaling","type":"narrow"},{"name":"up regulation of NIK/NF-kappaB cascade","type":"exact"},{"name":"up regulation of non-canonical NF-KB signaling","type":"exact"},{"name":"up regulation of noncanonical NF-kappaB signaling","type":"exact"},{"name":"up regulation of noncanonical nuclear factor kappaB (NF-kappaB) pathway","type":"exact"},{"name":"up regulation of p52-dependent NF-kappaB signaling","type":"narrow"},{"name":"up-regulation of NIK/NF-kappaB cascade","type":"related"},{"name":"up-regulation of non-canonical NF-KB signaling","type":"exact"},{"name":"up-regulation of noncanonical NF-kappaB signaling","type":"broad"},{"name":"up-regulation of noncanonical nuclear factor kappaB (NF-kappaB) pathway","type":"exact"},{"name":"up-regulation of p52-dependent NF-kappaB signaling","type":"narrow"},{"name":"upregulation of NIK/NF-kappaB cascade","type":"exact"},{"name":"upregulation of non-canonical NF-KB signaling","type":"exact"},{"name":"upregulation of noncanonical NF-kappaB signaling","type":"broad"},{"name":"upregulation of noncanonical nuclear factor kappaB (NF-kappaB) pathway","type":"exact"},{"name":"upregulation of p52-dependent NF-kappaB signaling","type":"narrow"}],"termid":"GO:1901224"}


id: GO:0016787
data:
  {"annotated_genes":["SJAG_06636","SJAG_01281","SJAG_05272","SJAG_03121","SJAG_04355","SJAG_00199","SJAG_01597","SJAG_04153","SJAG_03684","SJAG_00823","SJAG_01795","SJAG_02336","SJAG_03316","SJAG_00667","SJAG_01528","SJAG_01612","SJAG_04850","SJAG_00670","SJAG_04435","SJAG_02131","SJAG_00485","SJAG_03420","SJAG_04487","SJAG_04306","SJAG_02061","SJAG_01036","SJAG_04426","SJAG_01029","SJAG_04488","SJAG_03374","SJAG_00599","SJAG_00947","SJAG_04067","SJAG_00443","SJAG_02084","SJAG_02602","SJAG_01180","SJAG_01400","SJAG_04767","SJAG_02601","SJAG_05313","SJAG_04975","SJAG_03227","SJAG_02289","SJAG_01832","SJAG_02400","SJAG_02580","SJAG_03063","SJAG_00244","SJAG_01824","SJAG_01595","SJAG_02658","SJAG_01344","SJAG_03732","SJAG_00923","SJAG_01542","SJAG_02908","SJAG_02268","SJAG_00853","SJAG_02563","SJAG_03948","SJAG_02394","SJAG_02502","SJAG_05001","SJAG_04157","SJAG_00096","SJAG_02430","SJAG_05316","SJAG_05030","SJAG_04258","SJAG_01817","SJAG_00863","SJAG_04994","SJAG_03398","SJAG_04311","SJAG_04103","SJAG_02267","SJAG_00938","SJAG_04824","SJAG_00685","SJAG_03909","SJAG_02082","SJAG_02382","SJAG_03896","SJAG_03204","SJAG_01179","SJAG_02715","SJAG_04846","SJAG_02943","SJAG_02598","SJAG_01501","SJAG_01558","SJAG_04084","SJAG_02582","SJAG_02748","SJAG_03745","SJAG_04064","SJAG_01259","SJAG_00774","SJAG_04380","SJAG_04785","SJAG_03832","SJAG_04916","SJAG_00814","SJAG_02487","SJAG_04928","SJAG_04323","SJAG_03868","SJAG_04596","SJAG_00623","SJAG_01997","SJAG_02356","SJAG_00573","SJAG_02528","SJAG_02825","SJAG_00650","SJAG_00541","SJAG_03482","SJAG_03258","SJAG_04189","SJAG_02984","SJAG_MIT07","SJAG_01860","SJAG_00457","SJAG_01231","SJAG_02068","SJAG_01653","SJAG_03495","SJAG_02656","SJAG_02384","SJAG_03022","SJAG_02203","SJAG_03927","SJAG_05351","SJAG_02444","SJAG_03137","SJAG_02298","SJAG_02618","SJAG_04332","SJAG_01677","SJAG_02738","SJAG_00902","SJAG_MIT06","SJAG_03310","SJAG_05019","SJAG_01544","SJAG_02985","SJAG_02593","SJAG_01381","SJAG_01044","SJAG_01731","SJAG_01971","SJAG_04167","SJAG_02621","SJAG_04003","SJAG_03739","SJAG_02433","SJAG_02000","SJAG_03009","SJAG_01749","SJAG_04264","SJAG_04198","SJAG_00382","SJAG_00310","SJAG_00851","SJAG_03108","SJAG_04007","SJAG_03032","SJAG_00321","SJAG_00754","SJAG_01879","SJAG_02199","SJAG_04015","SJAG_02373","SJAG_01297","SJAG_03570","SJAG_03425","SJAG_03892","SJAG_00772","SJAG_02331","SJAG_04888","SJAG_05286","SJAG_02114","SJAG_00181","SJAG_04582","SJAG_03780","SJAG_00920","SJAG_00806","SJAG_02690","SJAG_02056","SJAG_03429","SJAG_01519","SJAG_01419","SJAG_04277","SJAG_02708","SJAG_03759","SJAG_00378","SJAG_00106","SJAG_01836","SJAG_02261","SJAG_01002","SJAG_00330","SJAG_02478","SJAG_00620","SJAG_02419","SJAG_01936","SJAG_00063","SJAG_02302","SJAG_04579","SJAG_04019","SJAG_04285","SJAG_00766","SJAG_01581","SJAG_01260","SJAG_02822","SJAG_02895","SJAG_00808","SJAG_00272","SJAG_02763","SJAG_04150","SJAG_01569","SJAG_00790","SJAG_03686","SJAG_00784","SJAG_02545","SJAG_00587","SJAG_03072","SJAG_04203","SJAG_04541","SJAG_01768","SJAG_02957","SJAG_02900","SJAG_04851","SJAG_02460","SJAG_00659","SJAG_02556","SJAG_02766","SJAG_02575","SJAG_02997","SJAG_05287","SJAG_03962","SJAG_04527","SJAG_00158","SJAG_01906","SJAG_01868","SJAG_00645","SJAG_01831","SJAG_00212","SJAG_00475","SJAG_01404","SJAG_03724","SJAG_03161","SJAG_00128","SJAG_01438","SJAG_02171","SJAG_03627","SJAG_02991","SJAG_00762","SJAG_04467","SJAG_04343","SJAG_03844","SJAG_04533","SJAG_05029","SJAG_01623","SJAG_MIT05","SJAG_02093","SJAG_04641","SJAG_03785","SJAG_04215","SJAG_04262","SJAG_01797","SJAG_03977","SJAG_04870","SJAG_02649","SJAG_00401","SJAG_01088","SJAG_02366","SJAG_02711","SJAG_04292","SJAG_00857","SJAG_00516","SJAG_03994","SJAG_00390","SJAG_04004","SJAG_01129","SJAG_01551","SJAG_02540","SJAG_02295","SJAG_01131","SJAG_01449","SJAG_00811","SJAG_04327","SJAG_03915","SJAG_04128","SJAG_16455","SJAG_04398","SJAG_02405","SJAG_02446","SJAG_01613","SJAG_02713","SJAG_01198","SJAG_04166","SJAG_04681","SJAG_00742","SJAG_03375","SJAG_04927","SJAG_02431","SJAG_01769","SJAG_04924","SJAG_01696","SJAG_04055","SJAG_01667","SJAG_01277","SJAG_02993","SJAG_02100","SJAG_03377","SJAG_02848","SJAG_02680","SJAG_00450","SJAG_01286","SJAG_03798","SJAG_03415","SJAG_03185","SJAG_04819","SJAG_02595","SJAG_02809","SJAG_01186","SJAG_02553","SJAG_01014","SJAG_02856","SJAG_03665","SJAG_02561","SJAG_03866","SJAG_03295","SJAG_04509","SJAG_03950","SJAG_03237","SJAG_01489","SJAG_01673","SJAG_00729","SJAG_04242","SJAG_02619","SJAG_01570","SJAG_02339","SJAG_02074","SJAG_00773","SJAG_03886","SJAG_01913","SJAG_02818","SJAG_03132","SJAG_02244","SJAG_03586","SJAG_00463","SJAG_01152","SJAG_01354","SJAG_00930","SJAG_02516","SJAG_02562","SJAG_03797","SJAG_02399","SJAG_03363","SJAG_03444","SJAG_02180","SJAG_04545","SJAG_02179","SJAG_02547","SJAG_04818","SJAG_00955","SJAG_04692","SJAG_01702","SJAG_00500","SJAG_00493","SJAG_04410","SJAG_01321","SJAG_01987","SJAG_04369","SJAG_02542","SJAG_01974","SJAG_04123","SJAG_02265","SJAG_03131","SJAG_01476","SJAG_02790","SJAG_02907","SJAG_00444","SJAG_00609","SJAG_03982","SJAG_03556","SJAG_03675","SJAG_03396","SJAG_01945","SJAG_02774","SJAG_02590","SJAG_01433","SJAG_02432","SJAG_00253","SJAG_02949","SJAG_02959","SJAG_03744","SJAG_00352","SJAG_03453","SJAG_02897","SJAG_00226","SJAG_03393","SJAG_04895","SJAG_02397","SJAG_02706","SJAG_00377","SJAG_04121","SJAG_02782","SJAG_00776","SJAG_02718","SJAG_00430","SJAG_02192","SJAG_00983","SJAG_04210","SJAG_00308","SJAG_00065","SJAG_01283","SJAG_04864","SJAG_02679","SJAG_03682","SJAG_00081","SJAG_00712","SJAG_01968","SJAG_01874","SJAG_03893","SJAG_01430","SJAG_04156","SJAG_02276","SJAG_04651","SJAG_03299","SJAG_03275","SJAG_00082","SJAG_01285","SJAG_02353","SJAG_01989","SJAG_01173","SJAG_00018","SJAG_01095","SJAG_02341","SJAG_03151","SJAG_01822","SJAG_03703","SJAG_00250","SJAG_04407","SJAG_02247","SJAG_00107","SJAG_01405","SJAG_00957","SJAG_04986","SJAG_04755","SJAG_01424","SJAG_03320","SJAG_04301","SJAG_01481","SJAG_00546","SJAG_01929","SJAG_01136","SJAG_03534","SJAG_03261","SJAG_04587","SJAG_03292","SJAG_03496","SJAG_05213","SJAG_00975","SJAG_03897","SJAG_04154","SJAG_00447","SJAG_01004","SJAG_04757","SJAG_04501","SJAG_01655","SJAG_02275","SJAG_04238","SJAG_01807","SJAG_02481","SJAG_01402","SJAG_02117","SJAG_01979","SJAG_05214","SJAG_00795","SJAG_00400","SJAG_03206","SJAG_01119","SJAG_00344","SJAG_04110","SJAG_04583","SJAG_03567","SJAG_02610","SJAG_01620","SJAG_04679","SJAG_03539","SJAG_04790","SJAG_02161","SJAG_01862","SJAG_04874","SJAG_02704","SJAG_03560","SJAG_05008","SJAG_02091","SJAG_00969","SJAG_00306","SJAG_00589","SJAG_04885","SJAG_04538","SJAG_01396","SJAG_04171","SJAG_00570","SJAG_01379","SJAG_04038","SJAG_01163","SJAG_00231","SJAG_00878","SJAG_01646","SJAG_01240","SJAG_01995","SJAG_01664","SJAG_00414","SJAG_01896","SJAG_02854","SJAG_02374","SJAG_00898","SJAG_04300","SJAG_02543","SJAG_01628","SJAG_03714","SJAG_02031","SJAG_04006","SJAG_02647","SJAG_03451","SJAG_03497","SJAG_02214","SJAG_04187","SJAG_02872","SJAG_04118","SJAG_02926","SJAG_01410","SJAG_04752","SJAG_02292","SJAG_01546","SJAG_01816","SJAG_03013","SJAG_02824","SJAG_02132","SJAG_01774","SJAG_03096","SJAG_01219","SJAG_02015","SJAG_04964","SJAG_00087","SJAG_01838","SJAG_00997","SJAG_00373","SJAG_01651","SJAG_03631","SJAG_00479","SJAG_03091","SJAG_05032","SJAG_03706","SJAG_00880","SJAG_00332","SJAG_03672","SJAG_05197","SJAG_01883","SJAG_00884","SJAG_03850","SJAG_02565","SJAG_05237","SJAG_00466","SJAG_02640","SJAG_01024","SJAG_05209","SJAG_00109","SJAG_01648","SJAG_00871","SJAG_03658","SJAG_00662","SJAG_01447","SJAG_01948","SJAG_04449","SJAG_04519","SJAG_01672","SJAG_04470","SJAG_01397","SJAG_03648","SJAG_16454","SJAG_03624","SJAG_00691","SJAG_01888","SJAG_01781","SJAG_00764","SJAG_00944","SJAG_00964","SJAG_04351","SJAG_01416","SJAG_02994","SJAG_03689","SJAG_03952","SJAG_06022","SJAG_03760","SJAG_00031","SJAG_02076","SJAG_03126","SJAG_02558","SJAG_01884","SJAG_05280","SJAG_03407","SJAG_00669","SJAG_04738","SJAG_01248","SJAG_03234","SJAG_01944","SJAG_02420","SJAG_03604","SJAG_04859","SJAG_00841","SJAG_04147","SJAG_03846","SJAG_01970","SJAG_01499","SJAG_04955","SJAG_03471","SJAG_02604","SJAG_06586","SJAG_01154","SJAG_00392","SJAG_05257","SJAG_03036","SJAG_01669","SJAG_03263","SJAG_03775","SJAG_02156","SJAG_03502","SJAG_03358","SJAG_04599","SJAG_02606","SJAG_00135","SJAG_01790","SJAG_02378","SJAG_01428","SJAG_05010","SJAG_00644","SJAG_04939","SJAG_00757","SJAG_00778","SJAG_04107","SJAG_01644","SJAG_00966","SJAG_01339","SJAG_00248","SJAG_00581","SJAG_01221","SJAG_01055","SJAG_02571","SJAG_05314","SJAG_01530","SJAG_05332","SJAG_03280","SJAG_03011","SJAG_04907","SJAG_04497","SJAG_03876","SJAG_02077","SJAG_00136","SJAG_04511","SJAG_00376","SJAG_04418","SJAG_00705","SJAG_01851","SJAG_01798","SJAG_00476","SJAG_03345","SJAG_03461","SJAG_01017","SJAG_02457","SJAG_01635","SJAG_02242","SJAG_02260","SJAG_03771","SJAG_00768","SJAG_02769","SJAG_04666","SJAG_04940","SJAG_03688","SJAG_04858","SJAG_02389","SJAG_02581","SJAG_04001","SJAG_01010","SJAG_03050","SJAG_01471","SJAG_03147","SJAG_04183","SJAG_03515","SJAG_03342","SJAG_02799","SJAG_03910","SJAG_02089","SJAG_02033","SJAG_03328","SJAG_04514","SJAG_02187","SJAG_03708","SJAG_00406","SJAG_00936","SJAG_00451","SJAG_00906","SJAG_04789","SJAG_03752","SJAG_00734","SJAG_01431","SJAG_01615","SJAG_00984","SJAG_03646","SJAG_03362","SJAG_02828","SJAG_01187","SJAG_03734","SJAG_02286","SJAG_00039","SJAG_00995","SJAG_04969","SJAG_03545","SJAG_01262","SJAG_03923","SJAG_01510","SJAG_02428","SJAG_01312","SJAG_04229","SJAG_02605","SJAG_03824","SJAG_01596","SJAG_01875","SJAG_01858","SJAG_04973","SJAG_01171","SJAG_02536","SJAG_04105","SJAG_04357","SJAG_02906","SJAG_01662","SJAG_00604","SJAG_04745","SJAG_02798","SJAG_01391","SJAG_04531","SJAG_02039","SJAG_03700","SJAG_00737","SJAG_06613","SJAG_02503","SJAG_00424","SJAG_02226","SJAG_00720","SJAG_03763","SJAG_02521","SJAG_01435","SJAG_00564","SJAG_04363","SJAG_03676","SJAG_00622","SJAG_01500","SJAG_00663","SJAG_00730","SJAG_03248","SJAG_00035","SJAG_04862","SJAG_00600","SJAG_01161","SJAG_01463","SJAG_03276","SJAG_01762","SJAG_02013","SJAG_01054","SJAG_00956","SJAG_01625","SJAG_04566","SJAG_05294","SJAG_03964","SJAG_00074","SJAG_03613","SJAG_03796","SJAG_05295","SJAG_04091","SJAG_03406","SJAG_03443","SJAG_02435","SJAG_01456","SJAG_00214","SJAG_02684","SJAG_04114","SJAG_04477","SJAG_05977","SJAG_00711","SJAG_00111","SJAG_02853","SJAG_00132","SJAG_00254","SJAG_05221","SJAG_04711","SJAG_04169","SJAG_00125","SJAG_04375","SJAG_04317","SJAG_02182","SJAG_02023","SJAG_02233","SJAG_05373","SJAG_03371"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[89742,92138,92526,92527,93194,97148,97752,98371,98850,99208,100110,100321,104936,108086,108576,117870],"is_not":false,"summary":null,"term":"GO:0016787"},{"annotations":[101358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003847"},{"annotations":[90126,100554],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004113"},{"annotations":[98519],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043716"},{"annotations":[118266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990599"},{"annotations":[115039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008441"},{"annotations":[115880],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004119"},{"annotations":[115881],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004118"},{"annotations":[115882],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004115"},{"annotations":[115883],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047555"},{"annotations":[71400,102329,104427,115855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008408"},{"annotations":[104725,108600],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008296"},{"annotations":[103174,95112,110743,103913,89456,107272,91741,101590,107980,106955,102443,115156,117807,104762,98444,114826,116101],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000175"},{"annotations":[116605],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048257"},{"annotations":[91641,109395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042781"},{"annotations":[118438],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017005"},{"annotations":[107573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003860"},{"annotations":[105435],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990043"},{"annotations":[103662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990601"},{"annotations":[112972,91037],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140932"},{"annotations":[96616,87870,92481],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035312"},{"annotations":[102698],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008409"},{"annotations":[94447,89792,90105],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004534"},{"annotations":[116674],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002953"},{"annotations":[102699,96617,103663,100671,87871,107247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017108"},{"annotations":[91183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140432"},{"annotations":[87063,87064,93843,113203,113202,90028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008253"},{"annotations":[95632],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034042"},{"annotations":[115600],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070694"},{"annotations":[95633],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034043"},{"annotations":[87454],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017168"},{"annotations":[114831,105028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017057"},{"annotations":[118100,96593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106379"},{"annotations":[94353,73627,95634],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034039"},{"annotations":[99028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044715"},{"annotations":[87332],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004741"},{"annotations":[76317,90927],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003986"},{"annotations":[106268],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0018773"},{"annotations":[113184,106401,87190,106402,112836,109941,109730,109942,112835],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003993"},{"annotations":[98520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043874"},{"annotations":[106269],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047621"},{"annotations":[114187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043530"},{"annotations":[103451],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004000"},{"annotations":[112197],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004013"},{"annotations":[113452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043262"},{"annotations":[112809],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047631"},{"annotations":[102937,103121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004035"},{"annotations":[101077],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003905"},{"annotations":[91944],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004037"},{"annotations":[111005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004555"},{"annotations":[101098,101099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004558"},{"annotations":[113491,117836,103503,93535,94701,117284,94324],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004556"},{"annotations":[99846],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004557"},{"annotations":[95598,95597,87101,87102],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090599"},{"annotations":[87782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004559"},{"annotations":[112133,97161,93205,104165,115543,97580,94529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002161"},{"annotations":[107630,101572,98153,91056],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004045"},{"annotations":[87975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004177"},{"annotations":[101313],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003876"},{"annotations":[113453],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004050"},{"annotations":[96841,112700],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004053"},{"annotations":[94207],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042500"},{"annotations":[97900,94340,59876,94342,115100,94341,79410],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004190"},{"annotations":[116923,104960,106740,101191,107059,112016,97145,102901,103371,102337,112325,110556,95546,99512,89055,111768,94712,91450,98845,116807,110879,117090,107284,99043,88225,112814,103260,90011,114552,87176,90635,88374,110894,98977,116193,88072,96240,107080,98419,88745,101093,112271,102785,103049,96545,91986,95480,112917,94756,94544,105090,110736,113455,90006,97738,88601,102827,102763,113268,114780,98535,90014,116025,117383,67055,115261,110327,114686,102174,94942,115939,114412,118010,105687,94084,87459,101840,104352,106566,107231,97421,93449,111986,89682,112232,96105,114584,105921,90013,87513,98746,115000,88652,89324,94262,88226,96374,103032,107387,98738,99389,108158,90007,95455,109248,109738,95936,91247,96411,91610,100134,102679,104681,87389,100209,95974,100636,87423,103715,118226,107343,87636,95800,116449,75419,107626,90012,98438,96578,110025,114607,114506,116192,99119,118109,92161,104074,87810,98485,111188,101701,101130,115804,97249,106475,95695,100379,115430,94961,87290,88435,90657,103786,102633,96266,111736,89706,95561,90008,95962,117706,99815,99442,112880,107754,101595,103412,104575,104183,113348,89769,117695,105716,87177,118233,98065,91393,96015,116727,104009,109367,106440,87238,90009,88325,96439,100082,103252,110846,112793,117455,117686,88754,90280,110485,115410,106679,100226,92755,108713,110044,101326,89279,115001,90010,89549,100049,98512,103406,111542,103979,88110,111838,101137,99533,115683,90378,100517,112579,93911,95140,91197,92337,102003,89641,98839,106829,99689,91537,103574,107327,92580,105561,98570,112673,118421,111291],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016887"},{"annotations":[110486,92756,118234],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004176"},{"annotations":[115621],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004564"},{"annotations":[107884,115122,86928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008422"},{"annotations":[88191],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034431"},{"annotations":[88192],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034432"},{"annotations":[110941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047710"},{"annotations":[116585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004081"},{"annotations":[88193],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008796"},{"annotations":[112860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004723"},{"annotations":[112861],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033192"},{"annotations":[100436,99248,92998,100058],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052689"},{"annotations":[108865,87683],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004180"},{"annotations":[113456],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036384"},{"annotations":[91256],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004099"},{"annotations":[101012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004568"},{"annotations":[99347,110479,88575],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010945"},{"annotations":[59415,94222,96413,100672,101025,116606],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008821"},{"annotations":[105416],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043907"},{"annotations":[115450,92890,111252,87840,104113,109827,87968,105295,113119,93982,90888,97510,113802,110628,94782,99370,93624,111193,114309,96029,105131,114664,114737],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004843"},{"annotations":[115332,91107,117078],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004197"},{"annotations":[108483,104786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008234"},{"annotations":[88673],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004126"},{"annotations":[99947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051500"},{"annotations":[107868],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004132"},{"annotations":[87094,107803],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019239"},{"annotations":[109828,89116,94783,104787,108484,89115],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019784"},{"annotations":[105621,89747],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016929"},{"annotations":[99600,101282,114665,110190,111253],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0101005"},{"annotations":[109888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000810"},{"annotations":[116668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008835"},{"annotations":[88930],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004151"},{"annotations":[111328],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004551"},{"annotations":[88614],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008239"},{"annotations":[88194],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008486"},{"annotations":[115222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061685"},{"annotations":[118101,98493],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035870"},{"annotations":[115181],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033699"},{"annotations":[89860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004520"},{"annotations":[89861],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004536"},{"annotations":[101079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052820"},{"annotations":[115182],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120108"},{"annotations":[74067,101080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008725"},{"annotations":[74065,101081],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043916"},{"annotations":[110398],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047874"},{"annotations":[88027,109450],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008311"},{"annotations":[96619,107248],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051908"},{"annotations":[100673],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990238"},{"annotations":[101678,107982],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032296"},{"annotations":[100674],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106332"},{"annotations":[96594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036218"},{"annotations":[98494],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004170"},{"annotations":[93508,99646],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052861"},{"annotations":[99792,113603,118544,103618,105436,118545,66901,87606,118536,109451,118537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004519"},{"annotations":[110646,110888,92834,101387,95951,114139,111254,117079,97128,117338,87990,115451,95720,115070,92663,99255],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004175"},{"annotations":[111280,115350,88195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000298"},{"annotations":[117597],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070551"},{"annotations":[113948],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004301"},{"annotations":[94883],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004527"},{"annotations":[95278,111281,104688],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004309"},{"annotations":[113928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008859"},{"annotations":[100245],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016297"},{"annotations":[108201,106964,96307,101141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047617"},{"annotations":[99553,114099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0103026"},{"annotations":[99449,75552,89169,88450],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004331"},{"annotations":[68862,90336],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003925"},{"annotations":[113457,99828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004382"},{"annotations":[86857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106407"},{"annotations":[99286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004573"},{"annotations":[102805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004339"},{"annotations":[88572,110808],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051118"},{"annotations":[99647,94588,93509],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042973"},{"annotations":[101450,107558,101449],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046557"},{"annotations":[87757,101451,101452,107559,94589],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004338"},{"annotations":[93703,90080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015926"},{"annotations":[109906,92302,92905,110572,116799],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004359"},{"annotations":[97871,98704],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036374"},{"annotations":[99761],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000121"},{"annotations":[101016],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047389"},{"annotations":[116675],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050484"},{"annotations":[113435,86916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003923"},{"annotations":[93014],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062050"},{"annotations":[89783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003934"},{"annotations":[86950,100646],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003935"},{"annotations":[91914,97883,92281,102156,104913,108223,108759,110333,100160,106668,110936,97391,104399,111895,93815,116998,105503,92193,106043,93333,91508,108195,100789,104104,99217,89213,101702,106629,108820,110036,97801,117978,103075,87381,93086,97321,111017,117980,102132,90339,102996,92352,88389,99616,103424,106921,90783,115470,116113,111897,117979,93087,117866,113458,109763,116827,88720,100740,93088,109250,110035,112364,115433,102386,106690,91473,96558,93718,111896,100952,97241,99141,106929,100351,100463,118494,95583,92746,88918,97802,93992],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003924"},{"annotations":[104154],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061791"},{"annotations":[114527],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008892"},{"annotations":[114513],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004401"},{"annotations":[108960,111604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031078"},{"annotations":[108961],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032129"},{"annotations":[108962],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140937"},{"annotations":[108963,96711],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034739"},{"annotations":[108964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180032"},{"annotations":[108965],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180033"},{"annotations":[98457,88775],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016817"},{"annotations":[96648,91665],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016818"},{"annotations":[88005,99839,110942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016811"},{"annotations":[98833,99724,113839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016788"},{"annotations":[97742,106184,88170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004553"},{"annotations":[99822],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004416"},{"annotations":[115867],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033971"},{"annotations":[107995],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050483"},{"annotations":[118481],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003937"},{"annotations":[102789,109535],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004239"},{"annotations":[99554,93191,96270,104689,114100],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004427"},{"annotations":[104690],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052840"},{"annotations":[76762],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008934"},{"annotations":[106404,88196,106403],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052745"},{"annotations":[108307],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052712"},{"annotations":[107782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990651"},{"annotations":[107783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990649"},{"annotations":[107784],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052659"},{"annotations":[115040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052829"},{"annotations":[110658,107785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052658"},{"annotations":[115041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004441"},{"annotations":[114555,104691,88197],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052846"},{"annotations":[88198,104692],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052847"},{"annotations":[114556,88199,104693],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052843"},{"annotations":[107786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990650"},{"annotations":[107787],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990640"},{"annotations":[107788],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990648"},{"annotations":[107789],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030487"},{"annotations":[104694,88200],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052845"},{"annotations":[118102],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036220"},{"annotations":[111194,87841],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990380"},{"annotations":[91124,96030],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061578"},{"annotations":[99762,109633],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036424"},{"annotations":[98317],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016298"},{"annotations":[91374,100313,89599,91366,93405,114254,116473,113557,102478],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004622"},{"annotations":[101759,118272,101747,101758,96422],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008496"},{"annotations":[108308],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052714"},{"annotations":[66284,95197],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004571"},{"annotations":[97119],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033549"},{"annotations":[116576,95461],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990439"},{"annotations":[103304,91147,94520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033550"},{"annotations":[103305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017017"},{"annotations":[102270,99462],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990606"},{"annotations":[99371,104114,105296,109829,94784,105132,114310,115452,111255,87969,91125,95887,114666,96031,93625,113120,114738],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140492"},{"annotations":[87722,97335,87977,109536,102791,113949,105251,92876],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070006"},{"annotations":[73772,93954],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004181"},{"annotations":[96232,101763],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070573"},{"annotations":[89043,105078,116151,118235,100586,96831,101713,89727,91793,100545,96821,108687,112685,97813,110487,107564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004222"},{"annotations":[113704,115694],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008235"},{"annotations":[106462,97511,99601,114654,110191,89117,98312,114145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008237"},{"annotations":[107836,111908],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004477"},{"annotations":[77872,97171,70472,117084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047372"},{"annotations":[91185],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034353"},{"annotations":[98486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140818"},{"annotations":[101105],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000225"},{"annotations":[104609],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000210"},{"annotations":[104610],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035529"},{"annotations":[109112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008936"},{"annotations":[90137],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070635"},{"annotations":[90138],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070636"},{"annotations":[87191],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004726"},{"annotations":[105519,93774,117416,87884,103666,88029,118210],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004518"},{"annotations":[111329,113459],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047429"},{"annotations":[94439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050152"},{"annotations":[95637],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008534"},{"annotations":[95638],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000703"},{"annotations":[92999,100059,100437,108487,110399],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008474"},{"annotations":[98917,88489,94344,97129,94343,97130,94345,86955,86956],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008233"},{"annotations":[104233],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000224"},{"annotations":[94173,109943,103122,109944,114102,106022,99556,97809,113190,114497,99487,98225,98033],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016791"},{"annotations":[90948,107487,109889],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008195"},{"annotations":[97260],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034479"},{"annotations":[117352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008962"},{"annotations":[99790],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050185"},{"annotations":[92867],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004435"},{"annotations":[110749],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016314"},{"annotations":[107790],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034485"},{"annotations":[110659,87208,107791],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043813"},{"annotations":[90974],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004438"},{"annotations":[110660,100452,107792],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004439"},{"annotations":[96393,105479],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043812"},{"annotations":[91186],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990174"},{"annotations":[102701,109452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004528"},{"annotations":[103123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008967"},{"annotations":[102479,114255,89600,91375,91367,99250,100314],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004623"},{"annotations":[113341,92051],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004620"},{"annotations":[95421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004630"},{"annotations":[112862,111844,102076,94032,89482,113302,114978,92941,104004,99771],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004721"},{"annotations":[107351],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004635"},{"annotations":[107352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004636"},{"annotations":[117268],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008081"},{"annotations":[112416,92891,115161,116102,107273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004535"},{"annotations":[93211],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990838"},{"annotations":[93188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046403"},{"annotations":[98487],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004651"},{"annotations":[112960],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051722"},{"annotations":[104005,98034,114979,116083,116578,113573,99772,113574,88668,109226,95462,116577,97120,95463,96683,106899,109574,92942,111458,89483],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004722"},{"annotations":[89484,87525,87192,94033,94521,111845,91148,104711],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004725"},{"annotations":[103306],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008330"},{"annotations":[67021,106449],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008418"},{"annotations":[77984,106450],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070773"},{"annotations":[91108],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019786"},{"annotations":[113311,97230],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990738"},{"annotations":[90139,111665],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008477"},{"annotations":[94356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000701"},{"annotations":[98091,98090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106432"},{"annotations":[99764],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110130"},{"annotations":[73207,115492,102943,109338,101680],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004525"},{"annotations":[96280,105156,95987,114894,118092,112987,114807,98995,105155,94197,104055,104273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000171"},{"annotations":[112988,104056,96281,101559,94198,104274,118093,114808,98996],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004526"},{"annotations":[111330,99829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017111"},{"annotations":[89001,106957,117574,115829,90107,87824,89863,112417,88511,95321,108493],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004521"},{"annotations":[117599,91699],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016891"},{"annotations":[99121,91742,100538,106958],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004532"},{"annotations":[89710],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008419"},{"annotations":[91187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110152"},{"annotations":[104611],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110153"},{"annotations":[115205,95553,106959,115162,89795,89864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004540"},{"annotations":[91090,93129],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008420"},{"annotations":[95325,96684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180007"},{"annotations":[111459],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180005"},{"annotations":[87780,97617,102449,108617],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004523"},{"annotations":[73712],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050278"},{"annotations":[92513],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017171"},{"annotations":[91306,103896,87684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004185"},{"annotations":[117941,91094,92664,104331,108688,100793,102578,97131,107565,93648,103317,112908,86957,103324,92758],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004252"},{"annotations":[88615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008236"},{"annotations":[100642,88030,106848],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008310"},{"annotations":[111080,96621],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045145"},{"annotations":[88031,109530,89865,110316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000014"},{"annotations":[99765],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050286"},{"annotations":[108309],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004767"},{"annotations":[99741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042392"},{"annotations":[114571,102857,103500],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004771"},{"annotations":[115622],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004575"},{"annotations":[89748,105622],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070139"},{"annotations":[57055],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050334"},{"annotations":[109945,109946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042131"},{"annotations":[99733,110209,97198,93481],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004298"},{"annotations":[96631,91338],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004805"},{"annotations":[91380,89593,93519,114289,93406,97969],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004806"},{"annotations":[100794],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008240"},{"annotations":[117181,100299,105420,100839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000213"},{"annotations":[100610,103741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052717"},{"annotations":[103453],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043829"},{"annotations":[99830,113460],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045134"},{"annotations":[113396],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004844"},{"annotations":[90935],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009039"},{"annotations":[91261],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004848"},{"annotations":[90140],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045437"},{"annotations":[96595],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036221"},{"annotations":[118103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036222"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of various bonds, e.g. C-O, C-N, C-C, phosphoric anhydride bonds, etc.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity","termid":"GO:0003824"}],"gene_count":810,"genes_by_uniquename":{"SJAG_00018":null,"SJAG_00031":null,"SJAG_00035":null,"SJAG_00039":null,"SJAG_00063":null,"SJAG_00065":null,"SJAG_00074":null,"SJAG_00081":null,"SJAG_00082":null,"SJAG_00087":null,"SJAG_00096":null,"SJAG_00106":null,"SJAG_00107":null,"SJAG_00109":null,"SJAG_00111":null,"SJAG_00125":null,"SJAG_00128":null,"SJAG_00132":null,"SJAG_00135":null,"SJAG_00136":null,"SJAG_00158":null,"SJAG_00181":null,"SJAG_00199":null,"SJAG_00212":null,"SJAG_00214":null,"SJAG_00226":null,"SJAG_00231":null,"SJAG_00244":null,"SJAG_00248":null,"SJAG_00250":null,"SJAG_00253":null,"SJAG_00254":null,"SJAG_00272":null,"SJAG_00306":null,"SJAG_00308":null,"SJAG_00310":null,"SJAG_00321":null,"SJAG_00330":null,"SJAG_00332":null,"SJAG_00344":null,"SJAG_00352":null,"SJAG_00373":null,"SJAG_00376":null,"SJAG_00377":null,"SJAG_00378":null,"SJAG_00382":null,"SJAG_00390":null,"SJAG_00392":null,"SJAG_00400":null,"SJAG_00401":null,"SJAG_00406":null,"SJAG_00414":null,"SJAG_00424":null,"SJAG_00430":null,"SJAG_00443":null,"SJAG_00444":null,"SJAG_00447":null,"SJAG_00450":null,"SJAG_00451":null,"SJAG_00457":null,"SJAG_00463":null,"SJAG_00466":null,"SJAG_00475":null,"SJAG_00476":null,"SJAG_00479":null,"SJAG_00485":null,"SJAG_00493":null,"SJAG_00500":null,"SJAG_00516":null,"SJAG_00541":null,"SJAG_00546":null,"SJAG_00564":null,"SJAG_00570":null,"SJAG_00573":null,"SJAG_00581":null,"SJAG_00587":null,"SJAG_00589":null,"SJAG_00599":null,"SJAG_00600":null,"SJAG_00604":null,"SJAG_00609":null,"SJAG_00620":null,"SJAG_00622":null,"SJAG_00623":null,"SJAG_00644":null,"SJAG_00645":null,"SJAG_00650":null,"SJAG_00659":null,"SJAG_00662":null,"SJAG_00663":null,"SJAG_00667":null,"SJAG_00669":null,"SJAG_00670":null,"SJAG_00685":null,"SJAG_00691":null,"SJAG_00705":null,"SJAG_00711":null,"SJAG_00712":null,"SJAG_00720":null,"SJAG_00729":null,"SJAG_00730":null,"SJAG_00734":null,"SJAG_00737":null,"SJAG_00742":null,"SJAG_00754":null,"SJAG_00757":null,"SJAG_00762":null,"SJAG_00764":null,"SJAG_00766":null,"SJAG_00768":null,"SJAG_00772":null,"SJAG_00773":null,"SJAG_00774":null,"SJAG_00776":null,"SJAG_00778":null,"SJAG_00784":null,"SJAG_00790":null,"SJAG_00795":null,"SJAG_00806":null,"SJAG_00808":null,"SJAG_00811":null,"SJAG_00814":null,"SJAG_00823":null,"SJAG_00841":null,"SJAG_00851":null,"SJAG_00853":null,"SJAG_00857":null,"SJAG_00863":null,"SJAG_00871":null,"SJAG_00878":null,"SJAG_00880":null,"SJAG_00884":null,"SJAG_00898":null,"SJAG_00902":null,"SJAG_00906":null,"SJAG_00920":null,"SJAG_00923":null,"SJAG_00930":null,"SJAG_00936":null,"SJAG_00938":null,"SJAG_00944":null,"SJAG_00947":null,"SJAG_00955":null,"SJAG_00956":null,"SJAG_00957":null,"SJAG_00964":null,"SJAG_00966":null,"SJAG_00969":null,"SJAG_00975":null,"SJAG_00983":null,"SJAG_00984":null,"SJAG_00995":null,"SJAG_00997":null,"SJAG_01002":null,"SJAG_01004":null,"SJAG_01010":null,"SJAG_01014":null,"SJAG_01017":null,"SJAG_01024":null,"SJAG_01029":null,"SJAG_01036":null,"SJAG_01044":null,"SJAG_01054":null,"SJAG_01055":null,"SJAG_01088":null,"SJAG_01095":null,"SJAG_01119":null,"SJAG_01129":null,"SJAG_01131":null,"SJAG_01136":null,"SJAG_01152":null,"SJAG_01154":null,"SJAG_01161":null,"SJAG_01163":null,"SJAG_01171":null,"SJAG_01173":null,"SJAG_01179":null,"SJAG_01180":null,"SJAG_01186":null,"SJAG_01187":null,"SJAG_01198":null,"SJAG_01219":null,"SJAG_01221":null,"SJAG_01231":null,"SJAG_01240":null,"SJAG_01248":null,"SJAG_01259":null,"SJAG_01260":null,"SJAG_01262":null,"SJAG_01277":null,"SJAG_01281":null,"SJAG_01283":null,"SJAG_01285":null,"SJAG_01286":null,"SJAG_01297":null,"SJAG_01312":null,"SJAG_01321":null,"SJAG_01339":null,"SJAG_01344":null,"SJAG_01354":null,"SJAG_01379":null,"SJAG_01381":null,"SJAG_01391":null,"SJAG_01396":null,"SJAG_01397":null,"SJAG_01400":null,"SJAG_01402":null,"SJAG_01404":null,"SJAG_01405":null,"SJAG_01410":null,"SJAG_01416":null,"SJAG_01419":null,"SJAG_01424":null,"SJAG_01428":null,"SJAG_01430":null,"SJAG_01431":null,"SJAG_01433":null,"SJAG_01435":null,"SJAG_01438":null,"SJAG_01447":null,"SJAG_01449":null,"SJAG_01456":null,"SJAG_01463":null,"SJAG_01471":null,"SJAG_01476":null,"SJAG_01481":null,"SJAG_01489":null,"SJAG_01499":null,"SJAG_01500":null,"SJAG_01501":null,"SJAG_01510":null,"SJAG_01519":null,"SJAG_01528":null,"SJAG_01530":null,"SJAG_01542":null,"SJAG_01544":null,"SJAG_01546":null,"SJAG_01551":null,"SJAG_01558":null,"SJAG_01569":null,"SJAG_01570":null,"SJAG_01581":null,"SJAG_01595":null,"SJAG_01596":null,"SJAG_01597":null,"SJAG_01612":null,"SJAG_01613":null,"SJAG_01615":null,"SJAG_01620":null,"SJAG_01623":null,"SJAG_01625":null,"SJAG_01628":null,"SJAG_01635":null,"SJAG_01644":null,"SJAG_01646":null,"SJAG_01648":null,"SJAG_01651":null,"SJAG_01653":null,"SJAG_01655":null,"SJAG_01662":null,"SJAG_01664":null,"SJAG_01667":null,"SJAG_01669":null,"SJAG_01672":null,"SJAG_01673":null,"SJAG_01677":null,"SJAG_01696":null,"SJAG_01702":null,"SJAG_01731":null,"SJAG_01749":null,"SJAG_01762":null,"SJAG_01768":null,"SJAG_01769":null,"SJAG_01774":null,"SJAG_01781":null,"SJAG_01790":null,"SJAG_01795":null,"SJAG_01797":null,"SJAG_01798":null,"SJAG_01807":null,"SJAG_01816":null,"SJAG_01817":null,"SJAG_01822":null,"SJAG_01824":null,"SJAG_01831":null,"SJAG_01832":null,"SJAG_01836":null,"SJAG_01838":null,"SJAG_01851":null,"SJAG_01858":null,"SJAG_01860":null,"SJAG_01862":null,"SJAG_01868":null,"SJAG_01874":null,"SJAG_01875":null,"SJAG_01879":null,"SJAG_01883":null,"SJAG_01884":null,"SJAG_01888":null,"SJAG_01896":null,"SJAG_01906":null,"SJAG_01913":null,"SJAG_01929":null,"SJAG_01936":null,"SJAG_01944":null,"SJAG_01945":null,"SJAG_01948":null,"SJAG_01968":null,"SJAG_01970":null,"SJAG_01971":null,"SJAG_01974":null,"SJAG_01979":null,"SJAG_01987":null,"SJAG_01989":null,"SJAG_01995":null,"SJAG_01997":null,"SJAG_02000":null,"SJAG_02013":null,"SJAG_02015":null,"SJAG_02023":null,"SJAG_02031":null,"SJAG_02033":null,"SJAG_02039":null,"SJAG_02056":null,"SJAG_02061":null,"SJAG_02068":null,"SJAG_02074":null,"SJAG_02076":null,"SJAG_02077":null,"SJAG_02082":null,"SJAG_02084":null,"SJAG_02089":null,"SJAG_02091":null,"SJAG_02093":null,"SJAG_02100":null,"SJAG_02114":null,"SJAG_02117":null,"SJAG_02131":null,"SJAG_02132":null,"SJAG_02156":null,"SJAG_02161":null,"SJAG_02171":null,"SJAG_02179":null,"SJAG_02180":null,"SJAG_02182":null,"SJAG_02187":null,"SJAG_02192":null,"SJAG_02199":null,"SJAG_02203":null,"SJAG_02214":null,"SJAG_02226":null,"SJAG_02233":null,"SJAG_02242":null,"SJAG_02244":null,"SJAG_02247":null,"SJAG_02260":null,"SJAG_02261":null,"SJAG_02265":null,"SJAG_02267":null,"SJAG_02268":null,"SJAG_02275":null,"SJAG_02276":null,"SJAG_02286":null,"SJAG_02289":null,"SJAG_02292":null,"SJAG_02295":null,"SJAG_02298":null,"SJAG_02302":null,"SJAG_02331":null,"SJAG_02336":null,"SJAG_02339":null,"SJAG_02341":null,"SJAG_02353":null,"SJAG_02356":null,"SJAG_02366":null,"SJAG_02373":null,"SJAG_02374":null,"SJAG_02378":null,"SJAG_02382":null,"SJAG_02384":null,"SJAG_02389":null,"SJAG_02394":null,"SJAG_02397":null,"SJAG_02399":null,"SJAG_02400":null,"SJAG_02405":null,"SJAG_02419":null,"SJAG_02420":null,"SJAG_02428":null,"SJAG_02430":null,"SJAG_02431":null,"SJAG_02432":null,"SJAG_02433":null,"SJAG_02435":null,"SJAG_02444":null,"SJAG_02446":null,"SJAG_02457":null,"SJAG_02460":null,"SJAG_02478":null,"SJAG_02481":null,"SJAG_02487":null,"SJAG_02502":null,"SJAG_02503":null,"SJAG_02516":null,"SJAG_02521":null,"SJAG_02528":null,"SJAG_02536":null,"SJAG_02540":null,"SJAG_02542":null,"SJAG_02543":null,"SJAG_02545":null,"SJAG_02547":null,"SJAG_02553":null,"SJAG_02556":null,"SJAG_02558":null,"SJAG_02561":null,"SJAG_02562":null,"SJAG_02563":null,"SJAG_02565":null,"SJAG_02571":null,"SJAG_02575":null,"SJAG_02580":null,"SJAG_02581":null,"SJAG_02582":null,"SJAG_02590":null,"SJAG_02593":null,"SJAG_02595":null,"SJAG_02598":null,"SJAG_02601":null,"SJAG_02602":null,"SJAG_02604":null,"SJAG_02605":null,"SJAG_02606":null,"SJAG_02610":null,"SJAG_02618":null,"SJAG_02619":null,"SJAG_02621":null,"SJAG_02640":null,"SJAG_02647":null,"SJAG_02649":null,"SJAG_02656":null,"SJAG_02658":null,"SJAG_02679":null,"SJAG_02680":null,"SJAG_02684":null,"SJAG_02690":null,"SJAG_02704":null,"SJAG_02706":null,"SJAG_02708":null,"SJAG_02711":null,"SJAG_02713":null,"SJAG_02715":null,"SJAG_02718":null,"SJAG_02738":null,"SJAG_02748":null,"SJAG_02763":null,"SJAG_02766":null,"SJAG_02769":null,"SJAG_02774":null,"SJAG_02782":null,"SJAG_02790":null,"SJAG_02798":null,"SJAG_02799":null,"SJAG_02809":null,"SJAG_02818":null,"SJAG_02822":null,"SJAG_02824":null,"SJAG_02825":null,"SJAG_02828":null,"SJAG_02848":null,"SJAG_02853":null,"SJAG_02854":null,"SJAG_02856":null,"SJAG_02872":null,"SJAG_02895":null,"SJAG_02897":null,"SJAG_02900":null,"SJAG_02906":null,"SJAG_02907":null,"SJAG_02908":null,"SJAG_02926":null,"SJAG_02943":null,"SJAG_02949":null,"SJAG_02957":null,"SJAG_02959":null,"SJAG_02984":null,"SJAG_02985":null,"SJAG_02991":null,"SJAG_02993":null,"SJAG_02994":null,"SJAG_02997":null,"SJAG_03009":null,"SJAG_03011":null,"SJAG_03013":null,"SJAG_03022":null,"SJAG_03032":null,"SJAG_03036":null,"SJAG_03050":null,"SJAG_03063":null,"SJAG_03072":null,"SJAG_03091":null,"SJAG_03096":null,"SJAG_03108":null,"SJAG_03121":null,"SJAG_03126":null,"SJAG_03131":null,"SJAG_03132":null,"SJAG_03137":null,"SJAG_03147":null,"SJAG_03151":null,"SJAG_03161":null,"SJAG_03185":null,"SJAG_03204":null,"SJAG_03206":null,"SJAG_03227":null,"SJAG_03234":null,"SJAG_03237":null,"SJAG_03248":null,"SJAG_03258":null,"SJAG_03261":null,"SJAG_03263":null,"SJAG_03275":null,"SJAG_03276":null,"SJAG_03280":null,"SJAG_03292":null,"SJAG_03295":null,"SJAG_03299":null,"SJAG_03310":null,"SJAG_03316":null,"SJAG_03320":null,"SJAG_03328":null,"SJAG_03342":null,"SJAG_03345":null,"SJAG_03358":null,"SJAG_03362":null,"SJAG_03363":null,"SJAG_03371":null,"SJAG_03374":null,"SJAG_03375":null,"SJAG_03377":null,"SJAG_03393":null,"SJAG_03396":null,"SJAG_03398":null,"SJAG_03406":null,"SJAG_03407":null,"SJAG_03415":null,"SJAG_03420":null,"SJAG_03425":null,"SJAG_03429":null,"SJAG_03443":null,"SJAG_03444":null,"SJAG_03451":null,"SJAG_03453":null,"SJAG_03461":null,"SJAG_03471":null,"SJAG_03482":null,"SJAG_03495":null,"SJAG_03496":null,"SJAG_03497":null,"SJAG_03502":null,"SJAG_03515":null,"SJAG_03534":null,"SJAG_03539":null,"SJAG_03545":null,"SJAG_03556":null,"SJAG_03560":null,"SJAG_03567":null,"SJAG_03570":null,"SJAG_03586":null,"SJAG_03604":null,"SJAG_03613":null,"SJAG_03624":null,"SJAG_03627":null,"SJAG_03631":null,"SJAG_03646":null,"SJAG_03648":null,"SJAG_03658":null,"SJAG_03665":null,"SJAG_03672":null,"SJAG_03675":null,"SJAG_03676":null,"SJAG_03682":null,"SJAG_03684":null,"SJAG_03686":null,"SJAG_03688":null,"SJAG_03689":null,"SJAG_03700":null,"SJAG_03703":null,"SJAG_03706":null,"SJAG_03708":null,"SJAG_03714":null,"SJAG_03724":null,"SJAG_03732":null,"SJAG_03734":null,"SJAG_03739":null,"SJAG_03744":null,"SJAG_03745":null,"SJAG_03752":null,"SJAG_03759":null,"SJAG_03760":null,"SJAG_03763":null,"SJAG_03771":null,"SJAG_03775":null,"SJAG_03780":null,"SJAG_03785":null,"SJAG_03796":null,"SJAG_03797":null,"SJAG_03798":null,"SJAG_03824":null,"SJAG_03832":null,"SJAG_03844":null,"SJAG_03846":null,"SJAG_03850":null,"SJAG_03866":null,"SJAG_03868":null,"SJAG_03876":null,"SJAG_03886":null,"SJAG_03892":null,"SJAG_03893":null,"SJAG_03896":null,"SJAG_03897":null,"SJAG_03909":null,"SJAG_03910":null,"SJAG_03915":null,"SJAG_03923":null,"SJAG_03927":null,"SJAG_03948":null,"SJAG_03950":null,"SJAG_03952":null,"SJAG_03962":null,"SJAG_03964":null,"SJAG_03977":null,"SJAG_03982":null,"SJAG_03994":null,"SJAG_04001":null,"SJAG_04003":null,"SJAG_04004":null,"SJAG_04006":null,"SJAG_04007":null,"SJAG_04015":null,"SJAG_04019":null,"SJAG_04038":null,"SJAG_04055":null,"SJAG_04064":null,"SJAG_04067":null,"SJAG_04084":null,"SJAG_04091":null,"SJAG_04103":null,"SJAG_04105":null,"SJAG_04107":null,"SJAG_04110":null,"SJAG_04114":null,"SJAG_04118":null,"SJAG_04121":null,"SJAG_04123":null,"SJAG_04128":null,"SJAG_04147":null,"SJAG_04150":null,"SJAG_04153":null,"SJAG_04154":null,"SJAG_04156":null,"SJAG_04157":null,"SJAG_04166":null,"SJAG_04167":null,"SJAG_04169":null,"SJAG_04171":null,"SJAG_04183":null,"SJAG_04187":null,"SJAG_04189":null,"SJAG_04198":null,"SJAG_04203":null,"SJAG_04210":null,"SJAG_04215":null,"SJAG_04229":null,"SJAG_04238":null,"SJAG_04242":null,"SJAG_04258":null,"SJAG_04262":null,"SJAG_04264":null,"SJAG_04277":null,"SJAG_04285":null,"SJAG_04292":null,"SJAG_04300":null,"SJAG_04301":null,"SJAG_04306":null,"SJAG_04311":null,"SJAG_04317":null,"SJAG_04323":null,"SJAG_04327":null,"SJAG_04332":null,"SJAG_04343":null,"SJAG_04351":null,"SJAG_04355":null,"SJAG_04357":null,"SJAG_04363":null,"SJAG_04369":null,"SJAG_04375":null,"SJAG_04380":null,"SJAG_04398":null,"SJAG_04407":null,"SJAG_04410":null,"SJAG_04418":null,"SJAG_04426":null,"SJAG_04435":null,"SJAG_04449":null,"SJAG_04467":null,"SJAG_04470":null,"SJAG_04477":null,"SJAG_04487":null,"SJAG_04488":null,"SJAG_04497":null,"SJAG_04501":null,"SJAG_04509":null,"SJAG_04511":null,"SJAG_04514":null,"SJAG_04519":null,"SJAG_04527":null,"SJAG_04531":null,"SJAG_04533":null,"SJAG_04538":null,"SJAG_04541":null,"SJAG_04545":null,"SJAG_04566":null,"SJAG_04579":null,"SJAG_04582":null,"SJAG_04583":null,"SJAG_04587":null,"SJAG_04596":null,"SJAG_04599":null,"SJAG_04641":null,"SJAG_04651":null,"SJAG_04666":null,"SJAG_04679":null,"SJAG_04681":null,"SJAG_04692":null,"SJAG_04711":null,"SJAG_04738":null,"SJAG_04745":null,"SJAG_04752":null,"SJAG_04755":null,"SJAG_04757":null,"SJAG_04767":null,"SJAG_04785":null,"SJAG_04789":null,"SJAG_04790":null,"SJAG_04818":null,"SJAG_04819":null,"SJAG_04824":null,"SJAG_04846":null,"SJAG_04850":null,"SJAG_04851":null,"SJAG_04858":null,"SJAG_04859":null,"SJAG_04862":null,"SJAG_04864":null,"SJAG_04870":null,"SJAG_04874":null,"SJAG_04885":null,"SJAG_04888":null,"SJAG_04895":null,"SJAG_04907":null,"SJAG_04916":null,"SJAG_04924":null,"SJAG_04927":null,"SJAG_04928":null,"SJAG_04939":null,"SJAG_04940":null,"SJAG_04955":null,"SJAG_04964":null,"SJAG_04969":null,"SJAG_04973":null,"SJAG_04975":null,"SJAG_04986":null,"SJAG_04994":null,"SJAG_05001":null,"SJAG_05008":null,"SJAG_05010":null,"SJAG_05019":null,"SJAG_05029":null,"SJAG_05030":null,"SJAG_05032":null,"SJAG_05197":null,"SJAG_05209":null,"SJAG_05213":null,"SJAG_05214":null,"SJAG_05221":null,"SJAG_05237":null,"SJAG_05257":null,"SJAG_05272":null,"SJAG_05280":null,"SJAG_05286":null,"SJAG_05287":null,"SJAG_05294":null,"SJAG_05295":null,"SJAG_05313":null,"SJAG_05314":null,"SJAG_05316":null,"SJAG_05332":null,"SJAG_05351":null,"SJAG_05373":null,"SJAG_05977":null,"SJAG_06022":null,"SJAG_06586":null,"SJAG_06613":null,"SJAG_06636":null,"SJAG_16454":null,"SJAG_16455":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:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674"],"is_obsolete":false,"name":"hydrolase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-2029475","Reactome:R-HSA-8938314","Reactome:R-HSA-6788295","EC:3.-.-.-","Reactome:R-HSA-5695964","Reactome:R-HSA-1236938","Reactome:R-HSA-8952137","Reactome:R-HSA-6786190","Reactome:R-HSA-5694583"],"termid":"GO:0016787","terms_by_termid":{"GO:0000014":null,"GO:0000121":null,"GO:0000171":null,"GO:0000175":null,"GO:0000210":null,"GO:0000213":null,"GO:0000224":null,"GO:0000225":null,"GO:0000298":null,"GO:0000701":null,"GO:0000703":null,"GO:0000810":null,"GO:0002161":null,"GO:0002953":null,"GO:0003847":null,"GO:0003860":null,"GO:0003876":null,"GO:0003905":null,"GO:0003923":null,"GO:0003924":null,"GO:0003925":null,"GO:0003934":null,"GO:0003935":null,"GO:0003937":null,"GO:0003986":null,"GO:0003993":null,"GO:0004000":null,"GO:0004013":null,"GO:0004035":null,"GO:0004037":null,"GO:0004045":null,"GO:0004050":null,"GO:0004053":null,"GO:0004081":null,"GO:0004099":null,"GO:0004113":null,"GO:0004115":null,"GO:0004118":null,"GO:0004119":null,"GO:0004126":null,"GO:0004132":null,"GO:0004151":null,"GO:0004170":null,"GO:0004175":null,"GO:0004176":null,"GO:0004177":null,"GO:0004180":null,"GO:0004181":null,"GO:0004185":null,"GO:0004190":null,"GO:0004197":null,"GO:0004222":null,"GO:0004239":null,"GO:0004252":null,"GO:0004298":null,"GO:0004301":null,"GO:0004309":null,"GO:0004331":null,"GO:0004338":null,"GO:0004339":null,"GO:0004359":null,"GO:0004382":null,"GO:0004401":null,"GO:0004416":null,"GO:0004427":null,"GO:0004435":null,"GO:0004438":null,"GO:0004439":null,"GO:0004441":null,"GO:0004477":null,"GO:0004518":null,"GO:0004519":null,"GO:0004520":null,"GO:0004521":null,"GO:0004523":null,"GO:0004525":null,"GO:0004526":null,"GO:0004527":null,"GO:0004528":null,"GO:0004532":null,"GO:0004534":null,"GO:0004535":null,"GO:0004536":null,"GO:0004540":null,"GO:0004551":null,"GO:0004553":null,"GO:0004555":null,"GO:0004556":null,"GO:0004557":null,"GO:0004558":null,"GO:0004559":null,"GO:0004564":null,"GO:0004568":null,"GO:0004571":null,"GO:0004573":null,"GO:0004575":null,"GO:0004620":null,"GO:0004622":null,"GO:0004623":null,"GO:0004630":null,"GO:0004635":null,"GO:0004636":null,"GO:0004651":null,"GO:0004721":null,"GO:0004722":null,"GO:0004723":null,"GO:0004725":null,"GO:0004726":null,"GO:0004741":null,"GO:0004767":null,"GO:0004771":null,"GO:0004805":null,"GO:0004806":null,"GO:0004843":null,"GO:0004844":null,"GO:0004848":null,"GO:0008081":null,"GO:0008195":null,"GO:0008233":null,"GO:0008234":null,"GO:0008235":null,"GO:0008236":null,"GO:0008237":null,"GO:0008239":null,"GO:0008240":null,"GO:0008253":null,"GO:0008296":null,"GO:0008310":null,"GO:0008311":null,"GO:0008330":null,"GO:0008408":null,"GO:0008409":null,"GO:0008418":null,"GO:0008419":null,"GO:0008420":null,"GO:0008422":null,"GO:0008441":null,"GO:0008474":null,"GO:0008477":null,"GO:0008486":null,"GO:0008496":null,"GO:0008534":null,"GO:0008725":null,"GO:0008796":null,"GO:0008821":null,"GO:0008835":null,"GO:0008859":null,"GO:0008892":null,"GO:0008934":null,"GO:0008936":null,"GO:0008962":null,"GO:0008967":null,"GO:0009039":null,"GO:0010945":null,"GO:0015926":null,"GO:0016297":null,"GO:0016298":null,"GO:0016314":null,"GO:0016787":null,"GO:0016788":null,"GO:0016791":null,"GO:0016811":null,"GO:0016817":null,"GO:0016818":null,"GO:0016887":null,"GO:0016891":null,"GO:0016929":null,"GO:0017005":null,"GO:0017017":null,"GO:0017057":null,"GO:0017108":null,"GO:0017111":null,"GO:0017168":null,"GO:0017171":null,"GO:0018773":null,"GO:0019239":null,"GO:0019784":null,"GO:0019786":null,"GO:0030487":null,"GO:0031078":null,"GO:0032129":null,"GO:0032296":null,"GO:0033192":null,"GO:0033549":null,"GO:0033550":null,"GO:0033699":null,"GO:0033971":null,"GO:0034039":null,"GO:0034042":null,"GO:0034043":null,"GO:0034353":null,"GO:0034431":null,"GO:0034432":null,"GO:0034479":null,"GO:0034485":null,"GO:0034739":null,"GO:0035312":null,"GO:0035529":null,"GO:0035870":null,"GO:0036218":null,"GO:0036220":null,"GO:0036221":null,"GO:0036222":null,"GO:0036374":null,"GO:0036384":null,"GO:0036424":null,"GO:0042131":null,"GO:0042392":null,"GO:0042500":null,"GO:0042781":null,"GO:0042973":null,"GO:0043262":null,"GO:0043530":null,"GO:0043716":null,"GO:0043812":null,"GO:0043813":null,"GO:0043829":null,"GO:0043874":null,"GO:0043907":null,"GO:0043916":null,"GO:0044715":null,"GO:0045134":null,"GO:0045145":null,"GO:0045437":null,"GO:0046403":null,"GO:0046557":null,"GO:0047372":null,"GO:0047389":null,"GO:0047429":null,"GO:0047555":null,"GO:0047617":null,"GO:0047621":null,"GO:0047631":null,"GO:0047710":null,"GO:0047874":null,"GO:0048257":null,"GO:0050152":null,"GO:0050185":null,"GO:0050278":null,"GO:0050286":null,"GO:0050334":null,"GO:0050483":null,"GO:0050484":null,"GO:0051118":null,"GO:0051500":null,"GO:0051722":null,"GO:0051908":null,"GO:0052658":null,"GO:0052659":null,"GO:0052689":null,"GO:0052712":null,"GO:0052714":null,"GO:0052717":null,"GO:0052745":null,"GO:0052820":null,"GO:0052829":null,"GO:0052840":null,"GO:0052843":null,"GO:0052845":null,"GO:0052846":null,"GO:0052847":null,"GO:0052861":null,"GO:0061578":null,"GO:0061685":null,"GO:0061791":null,"GO:0062050":null,"GO:0070006":null,"GO:0070139":null,"GO:0070551":null,"GO:0070573":null,"GO:0070635":null,"GO:0070636":null,"GO:0070694":null,"GO:0070773":null,"GO:0090599":null,"GO:0101005":null,"GO:0103026":null,"GO:0106332":null,"GO:0106379":null,"GO:0106407":null,"GO:0106432":null,"GO:0110130":null,"GO:0110152":null,"GO:0110153":null,"GO:0120108":null,"GO:0140432":null,"GO:0140492":null,"GO:0140818":null,"GO:0140932":null,"GO:0140937":null,"GO:0180005":null,"GO:0180007":null,"GO:0180032":null,"GO:0180033":null,"GO:1990043":null,"GO:1990174":null,"GO:1990238":null,"GO:1990380":null,"GO:1990439":null,"GO:1990599":null,"GO:1990601":null,"GO:1990606":null,"GO:1990640":null,"GO:1990648":null,"GO:1990649":null,"GO:1990650":null,"GO:1990651":null,"GO:1990738":null,"GO:1990838":null}}


id: GO:0034093
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the extent to which the association between sister chromatids of a replicated chromosome is maintained.","definition_xrefs":["GOC:vw","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of maintenance of sister chromatid cohesion","termid":"GO:0034091"},{"relation_name":"is_a","term_name":"positive regulation of sister chromatid cohesion","termid":"GO:0045876"},{"relation_name":"positively_regulates","term_name":"maintenance of sister chromatid cohesion","termid":"GO:0034086"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"positive regulation of maintenance of sister chromatid cohesion","termid":"GO:0034093"}


id: GO:0030118
data:
  {"annotated_genes":["SJAG_02805","SJAG_02282","SJAG_04517","SJAG_04609","SJAG_00379","SJAG_04931","SJAG_01809","SJAG_04565","SJAG_00104","SJAG_01167","SJAG_04644","SJAG_02177","SJAG_00800"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[112273,100622,118379,112488],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030121"},{"annotations":[95752,107816,111082,111141],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030122"},{"annotations":[110986],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030131"},{"annotations":[94375,112397],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030130"},{"annotations":[94376],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071439"},{"annotations":[114374,117989],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030125"}]},"cv_name":"cellular_component","definition":"A membrane coat found on coated pits and some coated vesicles; consists of polymerized clathrin triskelions, each comprising three clathrin heavy chains and three clathrin light chains, linked to the membrane via one of the AP adaptor complexes.","definition_xrefs":["PMID:9531549","PMID:11252894","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane coat","termid":"GO:0030117"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00104":null,"SJAG_00379":null,"SJAG_00800":null,"SJAG_01167":null,"SJAG_01809":null,"SJAG_02177":null,"SJAG_02282":null,"SJAG_02805":null,"SJAG_04517":null,"SJAG_04565":null,"SJAG_04609":null,"SJAG_04644":null,"SJAG_04931":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"clathrin coat","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["NIF_Subcellular:sao879919129","GO:0016190","Wikipedia:Clathrin"],"synonyms":[{"name":"clathrin cage","type":"exact"}],"termid":"GO:0030118","terms_by_termid":{"GO:0030121":null,"GO:0030122":null,"GO:0030125":null,"GO:0030130":null,"GO:0030131":null,"GO:0071439":null}}


id: FYPO:0005685
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to cadmium ions is lower than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during vegetative growth","termid":"FYPO:0001117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0006551","FYPO:0001985"],"is_obsolete":false,"name":"decreased RNA level during cellular response to cadmium ion","synonyms":[{"name":"decreased RNA accumulation during cellular response to cadmium ion","type":"related"},{"name":"decreased RNA level during cellular response to cadmium","type":"exact"},{"name":"decreased RNA level during cellular response to cadmium ion during mitotic cell cycle","type":"related"},{"name":"decreased RNA level during cellular response to cadmium ion during vegetative growth","type":"exact"},{"name":"decreased transcript level during cellular response to cadmium ion","type":"exact"},{"name":"reduced RNA level during cellular response to cadmium ion","type":"exact"}],"termid":"FYPO:0005685"}


id: MONDO:0008453
data:
  {"annotated_genes":["SJAG_03170","SJAG_00053"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86202,86203],"is_not":false,"summary":null,"term":"MONDO:0008453"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spinal muscular atrophy","termid":"MONDO:0001516"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_03170":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"adult-onset proximal spinal muscular atrophy, autosomal dominant","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C1854058","GARD:17102","OMIM:182980","DOID:0111194","Orphanet:209335","MEDGEN:340120"],"synonyms":[{"name":"Finkel disease","type":"exact"},{"name":"Finkel late-adult type Sma","type":"related"},{"name":"SMAFK","type":"related"},{"name":"autosomal dominant adult-onset proximal SMA","type":"exact"},{"name":"autosomal dominant adult-onset proximal spinal muscular atrophy","type":"related"},{"name":"autosomal dominant late-onset spinal muscular atrophy, Finkel type","type":"exact"},{"name":"spinal muscular atrophy, late-onset, FINKEL type","type":"related"},{"name":"spinal muscular atrophy, proximal, adult, autosomal dominant","type":"related"}],"termid":"MONDO:0008453","terms_by_termid":{"MONDO:0008453":null},"xrefs":{"Monarch":{"xref_id":"0008453"}}}


id: GO:0080122
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of AMP, adenosine monophosphate, from one side of a membrane to the other.","definition_xrefs":["PMID:18923018"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenine nucleotide transmembrane transporter activity","termid":"GO:0000295"},{"relation_name":"is_a","term_name":"purine ribonucleotide transmembrane transporter activity","termid":"GO:0005346"},{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"},{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"AMP transmembrane transporter activity","synonyms":[{"name":"adenosine monophosphate transmembrane transporter activity","type":"exact"}],"termid":"GO:0080122"}


id: MONDO:0010651
data:
  {"annotated_genes":["SJAG_02399"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84940],"is_not":false,"summary":null,"term":"MONDO:0010651"}]},"cv_name":"mondo","definition":"A usually severe multisystemic disorder of copper metabolism, characterized by progressive neurodegeneration and marked connective tissue anomalies as well as typical sparse abnormal steely hair.","definition_xrefs":["Orphanet:565"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"disorder of pilosebaceous unit","termid":"MONDO:0002917"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic hair shaft abnormality (obsolete MONDO:0019282)","termid":"MONDO:0019282"},{"relation_name":"excluded_subClassOf","term_name":"obsolete eyebrow/eyelashes structural anomaly (obsolete MONDO:0020189)","termid":"MONDO:0020189"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"inborn metal metabolism disorder","termid":"MONDO:0004689"},{"relation_name":"is_a","term_name":"disorder of copper metabolism","termid":"MONDO:0017762"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02399":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"Menkes disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NORD:1440","NCIT:C75486","DOID:1838","OMIM:309400","ICD9:759.89","MedDRA:10027294","icd11.foundation:986728180","MEDGEN:44030","GARD:1521","MESH:D007706","NANDO:1200653","NANDO:2200580","SCTID:59178007","UMLS:C0022716"],"synonyms":[{"name":"MD","type":"exact"},{"name":"MNK","type":"exact"},{"name":"Menkea syndrome","type":"related"},{"name":"Menkes disease","type":"exact"},{"name":"Menkes kinky hair syndrome","type":"exact"},{"name":"Menkes kinky-hair syndrome","type":"exact"},{"name":"Menkes syndrome","type":"exact"},{"name":"Mk","type":"exact"},{"name":"Trichopoliodystrophy","type":"exact"},{"name":"X-linked copper deficiency","type":"exact"},{"name":"copper transport disease","type":"broad"},{"name":"kinky hair disease","type":"exact"},{"name":"kinky hair syndrome","type":"exact"},{"name":"menkes disease, X-linked recessive","type":"exact"},{"name":"steely hair disease","type":"exact"},{"name":"steely hair syndrome","type":"exact"}],"termid":"MONDO:0010651","terms_by_termid":{"MONDO:0010651":null},"xrefs":{"Monarch":{"xref_id":"0010651"}}}


id: PATO:0005004
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape that is almost an ellipse.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"superelliptic","termid":"PATO:0002318"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subelliptical","termid":"PATO:0005004"}


id: PR:O94271
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A RING finger protein 10 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03807"],"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 RING finger protein P8B7.23 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP8B7.23","secondary_identifiers":["UniProtKB:O94271"],"synonyms":[{"name":"Spom972h-RNF10","type":"exact"}],"termid":"PR:O94271"}


id: GO:0010678
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any cellular process that decreases the rate, extent or frequency of the chemical reactions and pathways involving carbohydrates carried out by repression of transcription.","definition_xrefs":["GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of cellular carbohydrate metabolic process by negative regulation of transcription, DNA-templated (obsolete GO:0010678)","synonyms":[{"name":"negative regulation of cellular carbohydrate metabolic process by negative regulation of transcription, DNA-dependent","type":"exact"},{"name":"negative regulation of cellular carbohydrate metabolic process by repression of transcription","type":"exact"},{"name":"negative regulation of cellular carbohydrate metabolic process by transcriptional repression","type":"exact"}],"termid":"GO:0010678"}


id: PBO:0068056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 361","termid":"PBO:0068056"}


id: PBO:0078553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 43","termid":"PBO:0078553"}


id: PBO:0068731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U5A small nuclear 2, pseudogene","termid":"PBO:0068731"}


id: GO:0000276
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. All non-F1 subunits of the mitochondrial hydrogen-transporting ATP synthase, including integral and peripheral mitochondrial inner membrane proteins.","definition_xrefs":["GOC:mtg_sensu","PMID:10838056"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial proton-transporting ATP synthase complex, coupling factor F(o) (obsolete GO:0000276)","termid":"GO:0000276"}


id: MONDO:0009752
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":"neuropathy, painful","secondary_identifiers":["OMIM:256870","MEDGEN:342490","UMLS:C1850383","MESH:C564945"],"synonyms":[{"name":"neuropathy, painful","type":"exact"}],"termid":"MONDO:0009752","xrefs":{"Monarch":{"xref_id":"0009752"}}}


id: PR:O59779
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC1235.01 gene.","definition_xrefs":["UniProtKB:O59779","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C1235.01 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1235.01","synonyms":[{"name":"Spom972h-SPCC1235.01","type":"exact"}],"termid":"PR:O59779"}


id: PR:O94676
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A nucleolar protein 6 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR17972:SF0","OMA:SCHPO03600","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":"U3 small nucleolar RNA-associated protein 22 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC776.08c","secondary_identifiers":["UniProtKB:O94676"],"synonyms":[{"name":"Spom972h-NOL6","type":"exact"},{"name":"U3 snoRNA-associated protein 22 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94676"}


id: PBO:0030333
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_phosphoinositide_level","termid":"PBO:0030333"}


id: GO:0046714
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to borate, the anion (BO3)3-.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"borate binding","synonyms":[{"name":"boron binding","type":"related"}],"termid":"GO:0046714"}


id: GO:0042214
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving terpenes, any of a large group of hydrocarbons that are made up of isoprene (C5H8) units which may be cyclic, acyclic or multicyclic, saturated or unsaturated, and may contain various functional groups.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoprenoid metabolic process","termid":"GO:0006720"},{"relation_name":"is_a","term_name":"hydrocarbon metabolic process","termid":"GO:0120252"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"terpene metabolic process","synonyms":[{"name":"terpene metabolism","type":"exact"}],"termid":"GO:0042214"}


id: GO:0019099
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The determination of sex and sexual phenotype in a female organism's germ line.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary sex determination, germ-line","termid":"GO:0007542"},{"relation_name":"is_a","term_name":"germ-line sex determination","termid":"GO:0018992"},{"relation_name":"is_a","term_name":"female sex determination","termid":"GO:0030237"}],"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":"female germ-line sex determination","secondary_identifiers":["GO:0007544"],"synonyms":[{"name":"sex determination, female germ-line determination","type":"exact"}],"termid":"GO:0019099"}


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


id: FYPO:0003814
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which a mitotic cell cycle arrest that normally occurs in response to the S phase DNA damage checkpoint (also known as the intra-S phase DNA damage checkpoint) does not occur. The S phase DNA damage checkpoint slows progression through S phase in response to DNA damage. In a mutant, the checkpoint may fail to arrest or delay cell cycle progression under appropriate conditions, or the incidence or duration of arrest or delay may differ from wild type under any specified set of conditions.","definition_xrefs":["PomBase:mah","GO:0072429"],"direct_ancestors":[{"relation_name":"has_output","term_name":"decreased rate of DNA replication during cellular response to DNA damage","termid":"FYPO:0004241"},{"relation_name":"is_a","term_name":"abnormal S-phase DNA damage checkpoint","termid":"FYPO:0000007"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000298"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0001320","FYPO:0000631","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abolished response to S-phase DNA damage checkpoint signaling","synonyms":[{"name":"abolished response to S-phase DNA damage checkpoint signaling abolished","type":"exact"},{"name":"abolished response to S-phase DNA damage checkpoint signaling during mitotic cell cycle","type":"related"},{"name":"abolished response to S-phase DNA damage checkpoint signaling during vegetative growth","type":"exact"},{"name":"abolished response to intra-S DNA damage checkpoint signaling","type":"exact"},{"name":"abolished response to mitotic S-phase DNA damage checkpoint signaling","type":"exact"}],"termid":"FYPO:0003814"}


id: MONDO:0005285
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete kidney stone (obsolete MONDO:0005285)","termid":"MONDO:0005285","xrefs":{"Monarch":{"xref_id":"0005285"}}}


id: PBO:0060111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND6 pseudogene 12","termid":"PBO:0060111"}


id: PBO:0051533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 3 receptor subunit alpha","termid":"PBO:0051533"}


id: GO:1905608
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of presynapse assembly.","definition_xrefs":["GOC:bc","GO_REF:0000058","GOC:PARL","GOC:TermGenie","PMID:25533483"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"is_a","term_name":"regulation of presynapse assembly","termid":"GO:1905606"},{"relation_name":"positively_regulates","term_name":"presynapse assembly","termid":"GO:0099054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"positive regulation of presynapse assembly","synonyms":[{"name":"activation of presynapse assembly","type":"narrow"},{"name":"activation of presynapse biogenesis","type":"narrow"},{"name":"activation of presynaptic terminal assembly","type":"narrow"},{"name":"positive regulation of presynapse biogenesis","type":"exact"},{"name":"positive regulation of presynaptic terminal assembly","type":"exact"},{"name":"up regulation of presynapse assembly","type":"exact"},{"name":"up regulation of presynapse biogenesis","type":"exact"},{"name":"up regulation of presynaptic terminal assembly","type":"exact"},{"name":"up-regulation of presynapse assembly","type":"exact"},{"name":"up-regulation of presynapse biogenesis","type":"exact"},{"name":"up-regulation of presynaptic terminal assembly","type":"exact"},{"name":"upregulation of presynapse assembly","type":"exact"},{"name":"upregulation of presynapse biogenesis","type":"exact"},{"name":"upregulation of presynaptic terminal assembly","type":"exact"}],"termid":"GO:1905608"}


id: FYPO:0006363
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the spindle forms with microtubules emanating from only one pole during the first meiotic nuclear division.","definition_xrefs":["PomBase:mah","PMID:24954111"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle morphology during meiosis I","termid":"FYPO:0005652"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0002399","FYPO:0000054","FYPO:0000120"],"is_obsolete":false,"name":"monopolar spindle during meiosis I","synonyms":[{"name":"V-shaped spindle during meiosis I","type":"related"},{"name":"fan-shaped spindle during meiosis I","type":"exact"},{"name":"monopolar spindle during first meiotic nuclear division","type":"exact"}],"termid":"FYPO:0006363"}


id: PBO:0086608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; gene expression regulated by copper levels","termid":"PBO:0086608"}


id: MONDO:0017190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sporadic pheochromocytoma/secreting paraganglioma are isolated, non-familial, catecholamin-producing tumors arising from neuroendocrine chromaffin cells in the adrenal medulla or in extra-adrenal chromaffin tissue, respectively. The majority of these tumors are benign and the presenting symptoms are typically caused by the increased catecholamine production of the tumor, including hypertension (often paroxysmal), tachycardia, anxiety and/or excessive sweating.","definition_xrefs":["Orphanet:276621"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paraganglioma","termid":"MONDO:0000448"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sporadic pheochromocytoma/secreting paraganglioma","secondary_identifiers":["MEDGEN:1636854","GARD:7385","UMLS:C4707333"],"termid":"MONDO:0017190","xrefs":{"Monarch":{"xref_id":"0017190"}}}


id: PBO:0079581
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 C pseudogene 2","termid":"PBO:0079581"}


id: GO:0098582
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A vocalisation behavior that is innate, i.e. that does not need to be learned in order to occur.","definition_xrefs":["GOC:dos","GOC:rl","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vocalization behavior","termid":"GO:0071625"}],"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":"innate vocalization behavior","termid":"GO:0098582"}


id: MONDO:1010796
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Darier disease that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Darier disease, non-human animal","termid":"MONDO:1010153"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Darier disease, dog","secondary_identifiers":["OMIA:002265-9615"],"termid":"MONDO:1010796","xrefs":{"Monarch":{"xref_id":"1010796"}}}


id: GO:0070504
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a prosthetic group that contains selenium, as in the selenium-dependent molybdenum hydroxylases. The selenium atom in the prosthetic group is required for enzymatic function but is labile to a variety of treatments.","definition_xrefs":["GOC:dh","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prosthetic group biosynthetic process","termid":"GO:0051191"},{"relation_name":"is_a","term_name":"selenium-containing prosthetic group metabolic process","termid":"GO:0070503"}],"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":"selenium-containing prosthetic group biosynthetic process","synonyms":[{"name":"selenium-containing prosthetic group anabolism","type":"exact"},{"name":"selenium-containing prosthetic group biosynthesis","type":"exact"},{"name":"selenium-containing prosthetic group formation","type":"exact"},{"name":"selenium-containing prosthetic group synthesis","type":"exact"}],"termid":"GO:0070504"}


id: GO:2000386
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ovarian follicle development.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"regulation of ovarian follicle development","termid":"GO:2000354"},{"relation_name":"positively_regulates","term_name":"ovarian follicle development","termid":"GO:0001541"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of ovarian follicle development","synonyms":[{"name":"positive regulation of follicular phase","type":"related"}],"termid":"GO:2000386"}


id: MONDO:0011866
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any non-syndromic pontocerebellar hypoplasia in which the cause of the disease is a mutation in the VRK1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pontocerebellar hypoplasia type 1","termid":"MONDO:0016396"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0020022","MONDO:0005066","MONDO:0037792","MONDO:0006025","MONDO:0005559"],"is_obsolete":false,"name":"pontocerebellar hypoplasia type 1A","secondary_identifiers":["MEDGEN:335969","OMIM:607596","UMLS:C1843504","GARD:15416","DOID:0060265"],"synonyms":[{"name":"PCH1A","type":"related"},{"name":"Pch1","type":"related"},{"name":"VRK1 non-syndromic pontocerebellar hypoplasia","type":"exact"},{"name":"non-syndromic pontocerebellar hypoplasia caused by mutation in VRK1","type":"exact"},{"name":"pontocerebellar hypoplasia with anterior horn cell disease","type":"related"},{"name":"pontocerebellar hypoplasia with infantile spinal muscular atrophy","type":"related"},{"name":"pontocerebellar hypoplasia, type 1A","type":"related"}],"termid":"MONDO:0011866","xrefs":{"Monarch":{"xref_id":"0011866"}}}


id: MONDO:0014971
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"amelogenesis imperfecta type 2","termid":"MONDO:0015048"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amelogenesis imperfecta, hypomaturation type, IIa6","secondary_identifiers":["OMIM:617217","MEDGEN:934632","UMLS:C4310665","DOID:0080960","GARD:16211"],"synonyms":[{"name":"AI2A6","type":"exact"},{"name":"amelogenesis imperfecta, hypomaturation type, IIa6","type":"exact"},{"name":"amelogenesis imperfecta, hypomaturation type, IIa6; AI2A6","type":"exact"}],"termid":"MONDO:0014971","xrefs":{"Monarch":{"xref_id":"0014971"}}}


id: GO:0052586
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of an oxidation-reduction (redox) reaction in which a nitrogenous group, excluding NH and NH2 groups, acts as a hydrogen or electron donor and reduces a quinone or similar compound.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete oxidoreductase activity, acting on other nitrogenous compounds as donors, with a quinone or similar compound as acceptor (obsolete GO:0052586)","termid":"GO:0052586"}


id: FYPO:0000637
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which a cell population in the vegetative growth phase of the life cycle grows at a faster rate than normal in a medium containing glucose as the carbon source.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cell population growth rate","termid":"FYPO:0000636"},{"relation_name":"is_a","term_name":"increased vegetative cell population growth","termid":"FYPO:0004557"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000139","FYPO:0000003","FYPO:0002058","FYPO:0002057","FYPO:0001985"],"is_obsolete":false,"name":"increased cell population growth rate on glucose carbon source","synonyms":[{"name":"enhanced growth on glucose","type":"related"},{"name":"fast cell population growth on glucose carbon source","type":"exact"},{"name":"increased cell population proliferation on glucose carbon source","type":"related"},{"name":"increased cell proliferation on glucose carbon source","type":"related"},{"name":"increased vegetative cell population growth rate on glucose carbon source","type":"exact"}],"termid":"FYPO:0000637"}


id: GO:1904851
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of establishment of protein localization to telomere.","definition_xrefs":["GOC:BHF_telomere","PMID:25467444","GOC:BHF","GO_REF:0000058","GOC:nc","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of establishment of protein localization to telomere","termid":"GO:0070203"},{"relation_name":"is_a","term_name":"positive regulation of protein localization to chromosome, telomeric region","termid":"GO:1904816"},{"relation_name":"is_a","term_name":"positive regulation of establishment of protein localization","termid":"GO:1904951"},{"relation_name":"positively_regulates","term_name":"establishment of protein localization to telomere","termid":"GO:0070200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of establishment of protein localization to telomere","synonyms":[{"name":"activation of establishment of protein localisation to telomere","type":"narrow"},{"name":"activation of establishment of protein localization to chromosome, telomeric region","type":"narrow"},{"name":"activation of establishment of protein localization to telomere","type":"narrow"},{"name":"positive regulation of establishment of protein localisation to telomere","type":"exact"},{"name":"positive regulation of establishment of protein localization to chromosome, telomeric region","type":"exact"},{"name":"up regulation of establishment of protein localisation to telomere","type":"exact"},{"name":"up regulation of establishment of protein localization to chromosome, telomeric region","type":"exact"},{"name":"up regulation of establishment of protein localization to telomere","type":"exact"},{"name":"up-regulation of establishment of protein localisation to telomere","type":"exact"},{"name":"up-regulation of establishment of protein localization to chromosome, telomeric region","type":"exact"},{"name":"up-regulation of establishment of protein localization to telomere","type":"exact"},{"name":"upregulation of establishment of protein localisation to telomere","type":"exact"},{"name":"upregulation of establishment of protein localization to chromosome, telomeric region","type":"exact"},{"name":"upregulation of establishment of protein localization to telomere","type":"exact"}],"termid":"GO:1904851"}


id: GO:0039677
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of the viral genome or a viral particle out of the host cell nucleus that involves disruption of the nuclear membrane envelope by the virus.","definition_xrefs":["VZ:2176"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exit of virus from host cell nucleus","termid":"GO:0039674"}],"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":"exit of virus from host cell nucleus via nuclear envelope disassembly","synonyms":[{"name":"exit of virus from host cell nucleus via nuclear envelope breakdown","type":"exact"}],"termid":"GO:0039677"}


id: FYECO:0000454
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which tetracycline was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ tetracycline","termid":"FYECO:0000454"}


id: GO:0071514
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The establishment of epigenetic modifications (imprints) during gametogenesis, and propagation of these imprints during the organism's life. Genomic imprinting leads to an asymmetry between the maternal and paternal alleles and differential expression of the corresponding alleles. This can happen through heterochromatin formation or differential chromatin loop formation.","definition_xrefs":["PMID:24492710","PMID:31896690","PMID:31965998"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epigenetic programming of gene expression","termid":"GO:0043045"},{"relation_name":"part_of","term_name":"germ cell development","termid":"GO:0007281"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0006325","GO:0010467"],"is_obsolete":false,"name":"genomic imprinting","synonyms":[{"name":"DNA imprinting","type":"exact"},{"name":"establishment of genomic imprinting","type":"exact"},{"name":"genetic imprinting","type":"exact"}],"termid":"GO:0071514"}


id: PBO:0041253
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 1 open reading frame 174","termid":"PBO:0041253"}


id: PR:Q9HGL0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC800.12c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9HGL0"],"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 ubiquitin-like protein C800.12c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC800.12c","synonyms":[{"name":"Spom972h-SPBC800.12c","type":"exact"}],"termid":"PR:Q9HGL0"}


id: GO:0022804
data:
  {"annotated_genes":["SJAG_00276","SJAG_04673","SJAG_03960","SJAG_00547","SJAG_03406","SJAG_04698","SJAG_01541","SJAG_01490","SJAG_04167","SJAG_01033","SJAG_MIT13","SJAG_05294","SJAG_03497","SJAG_03785","SJAG_03363","SJAG_01400","SJAG_04955","SJAG_04028","SJAG_02463","SJAG_04152","SJAG_04258","SJAG_03608","SJAG_02782","SJAG_00057","SJAG_01471","SJAG_04015","SJAG_01435","SJAG_04905","SJAG_01817","SJAG_01145","SJAG_02504","SJAG_03502","SJAG_04241","SJAG_01183","SJAG_04506","SJAG_03515","SJAG_02077","SJAG_04616","SJAG_01597","SJAG_00373","SJAG_03951","SJAG_01913","SJAG_00233","SJAG_00136","SJAG_02646","SJAG_07006","SJAG_04406","SJAG_01960","SJAG_02050","SJAG_01397","SJAG_02457","SJAG_01129","SJAG_04068","SJAG_03850","SJAG_04714","SJAG_00612","SJAG_03560","SJAG_03358","SJAG_01059","SJAG_04096","SJAG_03820","SJAG_02399","SJAG_00275","SJAG_MIT03","SJAG_01872","SJAG_00976","SJAG_00601","SJAG_04757","SJAG_00516","SJAG_05629","SJAG_01406","SJAG_03337","SJAG_05213","SJAG_07007","SJAG_MIT04","SJAG_01077","SJAG_03595","SJAG_01669","SJAG_03415","SJAG_01447","SJAG_02780","SJAG_02779","SJAG_02602","SJAG_04277","SJAG_MIT20","SJAG_03606","SJAG_01190","SJAG_00212","SJAG_01344","SJAG_02958","SJAG_01355","SJAG_03866","SJAG_03490","SJAG_03401","SJAG_00339","SJAG_02023","SJAG_00755","SJAG_01879"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[88752],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140481"},{"annotations":[108156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015410"},{"annotations":[106677],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015421"},{"annotations":[117704,96543],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044604"},{"annotations":[100377,101091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140359"},{"annotations":[95559,117453],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008559"},{"annotations":[110455],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046715"},{"annotations":[111751,92822,95979,88454,116518,92591],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015297"},{"annotations":[110388],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005471"},{"annotations":[102357],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140987"},{"annotations":[114585,100518,94943],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019829"},{"annotations":[117707],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042626"},{"annotations":[90185,90686,115061,97829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015369"},{"annotations":[113665,110138,72659,102484,116703,91974,75801,113671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005351"},{"annotations":[91266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071913"},{"annotations":[118578,113722,114955,107771,114153,118550,118528,87674,88701,91437,116315,118549,118577],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004129"},{"annotations":[116707],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005358"},{"annotations":[100176],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034216"},{"annotations":[101157],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015366"},{"annotations":[95257],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005364"},{"annotations":[90687],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010486"},{"annotations":[97539,92056],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005366"},{"annotations":[112351],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008137"},{"annotations":[101132,108160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005388"},{"annotations":[107345],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043682"},{"annotations":[114586,100520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015662"},{"annotations":[107346],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140581"},{"annotations":[111839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008556"},{"annotations":[111840],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008900"},{"annotations":[87179,87178,113269],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008553"},{"annotations":[111841],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008554"},{"annotations":[94944],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140358"},{"annotations":[103285,112220,109196,93526,115289,116005,104120],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005315"},{"annotations":[105195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015379"},{"annotations":[88795],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015386"},{"annotations":[104682,107081,102786,111292,90379,99045,96375,99817,107060],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015450"},{"annotations":[101138,91538,96106,109368,118227,89325,95141,87514,89642,99443,99513,102175,103413,98420],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046961"},{"annotations":[109614],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008271"},{"annotations":[88796,96230],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015385"},{"annotations":[110457],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005452"},{"annotations":[91548,91542],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015295"},{"annotations":[101160],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097434"},{"annotations":[95258],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008506"},{"annotations":[111758],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005371"},{"annotations":[118554,107452,117188,103994,103580,117663,112896],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008121"},{"annotations":[87923,95024],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015505"}]},"cv_name":"molecular_function","definition":"Enables the transfer of a specific substance or related group of substances from one side of a membrane to the other, up the solute's concentration gradient. The transporter binds the solute and undergoes a series of conformational changes. Transport works equally well in either direction.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":98,"genes_by_uniquename":{"SJAG_00057":null,"SJAG_00136":null,"SJAG_00212":null,"SJAG_00233":null,"SJAG_00275":null,"SJAG_00276":null,"SJAG_00339":null,"SJAG_00373":null,"SJAG_00516":null,"SJAG_00547":null,"SJAG_00601":null,"SJAG_00612":null,"SJAG_00755":null,"SJAG_00976":null,"SJAG_01033":null,"SJAG_01059":null,"SJAG_01077":null,"SJAG_01129":null,"SJAG_01145":null,"SJAG_01183":null,"SJAG_01190":null,"SJAG_01344":null,"SJAG_01355":null,"SJAG_01397":null,"SJAG_01400":null,"SJAG_01406":null,"SJAG_01435":null,"SJAG_01447":null,"SJAG_01471":null,"SJAG_01490":null,"SJAG_01541":null,"SJAG_01597":null,"SJAG_01669":null,"SJAG_01817":null,"SJAG_01872":null,"SJAG_01879":null,"SJAG_01913":null,"SJAG_01960":null,"SJAG_02023":null,"SJAG_02050":null,"SJAG_02077":null,"SJAG_02399":null,"SJAG_02457":null,"SJAG_02463":null,"SJAG_02504":null,"SJAG_02602":null,"SJAG_02646":null,"SJAG_02779":null,"SJAG_02780":null,"SJAG_02782":null,"SJAG_02958":null,"SJAG_03337":null,"SJAG_03358":null,"SJAG_03363":null,"SJAG_03401":null,"SJAG_03406":null,"SJAG_03415":null,"SJAG_03490":null,"SJAG_03497":null,"SJAG_03502":null,"SJAG_03515":null,"SJAG_03560":null,"SJAG_03595":null,"SJAG_03606":null,"SJAG_03608":null,"SJAG_03785":null,"SJAG_03820":null,"SJAG_03850":null,"SJAG_03866":null,"SJAG_03951":null,"SJAG_03960":null,"SJAG_04015":null,"SJAG_04028":null,"SJAG_04068":null,"SJAG_04096":null,"SJAG_04152":null,"SJAG_04167":null,"SJAG_04241":null,"SJAG_04258":null,"SJAG_04277":null,"SJAG_04406":null,"SJAG_04506":null,"SJAG_04616":null,"SJAG_04673":null,"SJAG_04698":null,"SJAG_04714":null,"SJAG_04757":null,"SJAG_04905":null,"SJAG_04955":null,"SJAG_05213":null,"SJAG_05294":null,"SJAG_05629":null,"SJAG_07006":null,"SJAG_07007":null,"SJAG_MIT03":null,"SJAG_MIT04":null,"SJAG_MIT13":null,"SJAG_MIT20":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"active transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"active carrier activity","type":"exact"},{"name":"carrier activity","type":"exact"},{"name":"permease activity","type":"exact"},{"name":"pump activity","type":"exact"}],"termid":"GO:0022804","terms_by_termid":{"GO:0004129":null,"GO:0005315":null,"GO:0005351":null,"GO:0005358":null,"GO:0005364":null,"GO:0005366":null,"GO:0005371":null,"GO:0005388":null,"GO:0005452":null,"GO:0005471":null,"GO:0008121":null,"GO:0008137":null,"GO:0008271":null,"GO:0008506":null,"GO:0008553":null,"GO:0008554":null,"GO:0008556":null,"GO:0008559":null,"GO:0008900":null,"GO:0010486":null,"GO:0015295":null,"GO:0015297":null,"GO:0015366":null,"GO:0015369":null,"GO:0015379":null,"GO:0015385":null,"GO:0015386":null,"GO:0015410":null,"GO:0015421":null,"GO:0015450":null,"GO:0015505":null,"GO:0015662":null,"GO:0019829":null,"GO:0034216":null,"GO:0042626":null,"GO:0043682":null,"GO:0044604":null,"GO:0046715":null,"GO:0046961":null,"GO:0071913":null,"GO:0097434":null,"GO:0140358":null,"GO:0140359":null,"GO:0140481":null,"GO:0140581":null,"GO:0140987":null}}


id: GO:0009563
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an uncellularized nucleus cellularizes and acquires the specialized features of a synergid cell.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"megagametogenesis","termid":"GO:0009561"}],"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":"synergid differentiation","synonyms":[{"name":"synergid cell differentiation","type":"exact"}],"termid":"GO:0009563"}


id: PATO:0000488
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A response quality inhering in a bearer by virtue of the bearer's lack of reaction to a stimulus or an agent.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to","termid":"PATO:0000077"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unresponsive to","synonyms":[{"name":"unresponsive","type":"exact"}],"termid":"PATO:0000488"}


id: PBO:0035804
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_H3-K9_trimethylation_during_vegetative_growth","termid":"PBO:0035804"}


id: PBO:0041541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 17 open reading frame 99","termid":"PBO:0041541"}


id: GO:1903153
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any ferrous iron transmembrane transporter activity that is involved in ferrous iron import into cell.","definition_xrefs":["ISBN:0-8249-3695-6","GOC:TermGenie","GO_REF:0000061","GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete ferrous iron transmembrane transporter activity involved in ferrous iron import into cell (obsolete GO:1903153)","synonyms":[{"name":"ferrous iron transmembrane transporter activity involved in ferrous ion import into cell","type":"exact"},{"name":"ferrous iron transmembrane transporter activity involved in ferrous iron import into cell","type":"exact"}],"termid":"GO:1903153"}


id: PBO:0068190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 497","termid":"PBO:0068190"}


id: GO:0072353
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of reactive oxygen species, where the change varies according to the age of the cell or organism.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete cellular age-dependent response to reactive oxygen species (obsolete GO:0072353)","termid":"GO:0072353"}


id: GO:0030221
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized myeloid precursor cell acquires specialized features of a basophil cell.","definition_xrefs":["GOC:jid","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"granulocyte differentiation","termid":"GO:0030851"}],"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":"basophil differentiation","synonyms":[{"name":"basophil cell differentiation","type":"exact"}],"termid":"GO:0030221"}


id: GO:0003718
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any activity that brings about termination of transcription by RNA polymerase III.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete RNA polymerase III transcription termination factor activity (obsolete GO:0003718)","synonyms":[{"name":"Pol III transcription termination factor activity","type":"exact"},{"name":"RNA polymerase III transcription termination factor activity","type":"exact"}],"termid":"GO:0003718"}


id: GO:0100047
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that negatively regulates inositol biosynthetic process.","definition_xrefs":["GOC:cjm","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of inositol biosynthetic process by transcription from RNA polymerase II promoter (obsolete GO:0100047)","termid":"GO:0100047"}


id: PBO:0004356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IMP 5'-nucleotidase (predicted)","termid":"PBO:0004356"}


id: GO:0021595
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to the act of creating the structural organization of the rhombomere structure. Rhombomeres are transverse segments of the developing rhombencephalon. Rhombomeres are lineage restricted, express different genes from one another, and adopt different developmental fates.","definition_xrefs":["GOC:dph","GOC:jid","ISBN:0838580343","GO_REF:0000021","GOC:cls","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure arrangement","termid":"GO:0048532"},{"relation_name":"part_of","term_name":"rhombomere morphogenesis","termid":"GO:0021593"}],"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":"rhombomere structural organization","synonyms":[{"name":"rhombomere structural organisation","type":"exact"}],"termid":"GO:0021595"}


id: MONDO:0017631
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare tumor of gallbladder and extrahepatic biliary tract (obsolete MONDO:0017631)","secondary_identifiers":["Orphanet:306633"],"synonyms":[{"name":"rare tumor of gallbladder and EBT","type":"exact"}],"termid":"MONDO:0017631","xrefs":{"Monarch":{"xref_id":"0017631"}}}


id: FYPO:0006939
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 actomyosin contractile ring contraction progresses in a radially asymmetric fashion.","definition_xrefs":["PomBase:mah","PMID:30709916"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actomyosin contractile ring contraction","termid":"FYPO:0001364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000032","FYPO:0000002","FYPO:0005447","FYPO:0000631","FYPO:0001985","FYPO:0001320","FYPO:0004803"],"is_obsolete":false,"name":"asymmetric actomyosin contractile ring contraction","synonyms":[{"name":"asymmetric actomyosin contractile ring contraction during mitotic cell cycle","type":"related"},{"name":"asymmetric actomyosin contractile ring contraction during vegetative growth","type":"exact"},{"name":"non-concentric actomyosin contractile ring contraction","type":"exact"}],"termid":"FYPO:0006939"}


id: PBO:0089748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Gpl1-Gih35-Wdr83 complex RNA helicase subunit, Gih35","termid":"PBO:0089748"}


id: MOD:01929
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an either an L-asparagine residue or an L-aspartic acid residue with an L-lysine residue by an isopeptide bond with the formation of N6-(L-isoaspartyl)-L-lysine.","definition_xrefs":["PubMed:11000116","RESID:AA0294","DeltaMass:0","ChEBI:21862","PubMed:6503713"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isopeptide crosslinked residues","termid":"MOD:00688"},{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"}],"interesting_parent_ids":["MOD:01875"],"is_obsolete":false,"name":"N6-(L-isoaspartyl)-L-lysine","synonyms":[{"name":"(2S)-2-amino-6-([(3S)-3-amino-3-carboxypropanoyl]amino)hexanoic acid","type":"exact"},{"name":"CROSSLNK Isoaspartyl lysine isopeptide (Lys-Asn)","type":"exact"},{"name":"N(epsilon)-(beta-aspartyl)lysine","type":"exact"},{"name":"N-(beta-Aspartyl)-Lysine (Crosslink)","type":"exact"},{"name":"N6-(L-isoaspartyl)-L-lysine","type":"exact"},{"name":"XLNK-4Asp-N6Lys","type":"exact"},{"name":"beta-(N6-lysyl)aspartyl acid","type":"exact"},{"name":"isoaspartyl N6-lysine","type":"exact"}],"termid":"MOD:01929"}


id: GO:0098659
data:
  {"annotated_genes":["SJAG_03631","SJAG_01493","SJAG_04551","SJAG_00296","SJAG_02883","SJAG_04246","SJAG_05229","SJAG_04830","SJAG_01353","SJAG_02968","SJAG_04668","SJAG_02877","SJAG_01090","SJAG_04185"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99129,91883,91832,113933],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098703"},{"annotations":[87415,114085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098705"},{"annotations":[90701,112854],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1905949"},{"annotations":[115495],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098716"},{"annotations":[101647],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905665"},{"annotations":[88990,96485],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990573"},{"annotations":[103677,112707],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071578"}]},"cv_name":"biological_process","definition":"The directed movement of inorganic cations from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inorganic cation transmembrane transport","termid":"GO:0098662"},{"relation_name":"is_a","term_name":"inorganic ion import across plasma membrane","termid":"GO:0099587"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00296":null,"SJAG_01090":null,"SJAG_01353":null,"SJAG_01493":null,"SJAG_02877":null,"SJAG_02883":null,"SJAG_02968":null,"SJAG_03631":null,"SJAG_04185":null,"SJAG_04246":null,"SJAG_04551":null,"SJAG_04668":null,"SJAG_04830":null,"SJAG_05229":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"inorganic cation import across plasma membrane","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"inorganic cation import into cell","type":"exact"}],"termid":"GO:0098659","terms_by_termid":{"GO:0071578":null,"GO:0098703":null,"GO:0098705":null,"GO:0098716":null,"GO:1905665":null,"GO:1905949":null,"GO:1990573":null}}


id: GO:0017188
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-aspartate + acetyl-CoA = N-acetyl-L-aspartate + CoA + H+.","definition_xrefs":["RHEA:14165"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acetyltransferase activity","termid":"GO:0008080"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0016746","GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"aspartate N-acetyltransferase activity","secondary_identifiers":["Reactome:R-HSA-8954468","MetaCyc:ASPARTATE-N-ACETYLTRANSFERASE-RXN","EC:2.3.1.17","KEGG_REACTION:R00487"],"synonyms":[{"name":"L-aspartate N-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:L-aspartate N-acetyltransferase activity","type":"related"},{"name":"aspartate acetyltransferase activity","type":"related"}],"termid":"GO:0017188"}


id: PBO:0052294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KH domain containing 3 like, subcortical maternal complex member","termid":"PBO:0052294"}


id: GO:0044336
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell, followed by propagation of the signal via beta-catenin, and ending with a change in transcription of target genes involved in the negative regulation of apoptotic process.","definition_xrefs":["GOC:jl","GOC:mtg_apoptosis","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"canonical Wnt signaling pathway","termid":"GO:0060070"},{"relation_name":"part_of","term_name":"negative regulation of apoptotic process","termid":"GO:0043066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"canonical Wnt signaling pathway involved in negative regulation of apoptotic process","synonyms":[{"name":"canonical Wnt receptor signaling pathway involved in negative regulation of apoptosis","type":"narrow"},{"name":"canonical Wnt receptor signaling pathway involved in negative regulation of apoptotic process","type":"exact"},{"name":"canonical Wnt receptor signalling pathway involved in negative regulation of apoptosis","type":"exact"}],"termid":"GO:0044336"}


id: FYPO:0008287
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 1-chloro-2,4-dinitrobenzene (CDNB). Cells stop growing (and may die) at a concentration of 1-chloro-2,4-dinitrobenzene that allows wild type cells to grow.","definition_xrefs":["PomBase:pc"],"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0002683","FYPO:0000003","FYPO:0001985","FYPO:0000139","FYPO:0005447"],"is_obsolete":false,"name":"sensitive to 1-chloro-2,4-dinitrobenzene","termid":"FYPO:0008287"}


id: PBO:0079622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 M","termid":"PBO:0079622"}


id: GO:0006186
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of introducing a phosphate group into dGDP, deoxyguanosine diphosphate, to produce dGTP.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete dGDP phosphorylation (obsolete GO:0006186)","termid":"GO:0006186"}


id: GO:0140976
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cellular processes and signaling pathways by which a cell responds to disruption of the integrity of its plasma membrane by another organism. Some toxins produced by other organisms can form pores in membranes, or affect the membrane permeability.","definition_xrefs":["PMID:21518219","PMID:17234446"],"direct_ancestors":[{"relation_name":"is_a","term_name":"defense response to symbiont","termid":"GO:0140546"}],"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":"host defense response against symbiont-mediated perturbation of plasma membrane integrity","synonyms":[{"name":"defense response against disruption of plasma membrane integrity","type":"exact"},{"name":"defense response against perturbation of plasma membrane integrity","type":"related"}],"termid":"GO:0140976"}


id: FYPO:0004974
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which telomere localization, a process in which a telomere is transported to, and/or maintained in, a specific location, is normal (i.e. indistinguishable from wild type) during interphase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal telomere localization","termid":"FYPO:0004973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal telomere localization during mitotic interphase","synonyms":[{"name":"normal telomere localisation during mitotic interphase","type":"exact"},{"name":"normal telomere localization during interphase of mitotic cell cycle","type":"exact"},{"name":"normal telomere localization during mitotic interphase during vegetative growth","type":"exact"},{"name":"normal telomere tethering to nuclear periphery during mitotic interphase","type":"exact"}],"termid":"FYPO:0004974"}


id: PBO:0043461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCR4-NOT transcription complex subunit 2","termid":"PBO:0043461"}


id: MONDO:0005409
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete variant Creutzfeld Jacob disease (obsolete MONDO:0005409)","termid":"MONDO:0005409","xrefs":{"Monarch":{"xref_id":"0005409"}}}


id: PBO:0024858
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MCM4/6/7 helicase complex translocates along double-stranded DNA","termid":"PBO:0024858"}


id: PBO:0039489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 20 family member A12, pseudogene","termid":"PBO:0039489"}


id: PATO:0000563
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000563 relative size value (obsolete PATO:0000563)","termid":"PATO:0000563"}


id: RO:0008504
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of kleptoparasite of","direct_ancestors":[{"relation_name":"is_a","term_name":"parasitized_by","termid":"RO:0002445"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kleptoparasitized_by","termid":"RO:0008504"}


id: PBO:0073221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"semaphorin 6B","termid":"PBO:0073221"}


id: GO:0047548
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-methyleneglutarate = 2-methylene-3-methylsuccinate.","definition_xrefs":["EC:5.4.99.4","RHEA:13793"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular transferase activity","termid":"GO:0016866"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"2-methyleneglutarate mutase activity","secondary_identifiers":["MetaCyc:2-METHYLENEGLUTARATE-MUTASE-RXN","KEGG_REACTION:R03908"],"synonyms":[{"name":"2-methyleneglutarate carboxy-methylenemethylmutase activity","type":"related"},{"name":"alpha-methyleneglutarate mutase activity","type":"related"}],"termid":"GO:0047548"}


id: PBO:0077595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane serine protease 6","termid":"PBO:0077595"}


id: PBO:0052209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium voltage-gated channel subfamily Q member 5","termid":"PBO:0052209"}


id: GO:1904414
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cardiac ventricle development.","definition_xrefs":["PMID:19590510","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of cardiac ventricle development","termid":"GO:1904412"},{"relation_name":"positively_regulates","term_name":"cardiac ventricle development","termid":"GO:0003231"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of cardiac ventricle development","synonyms":[{"name":"activation of cardiac ventricle development","type":"narrow"},{"name":"up regulation of cardiac ventricle development","type":"exact"},{"name":"up-regulation of cardiac ventricle development","type":"exact"},{"name":"upregulation of cardiac ventricle development","type":"exact"}],"termid":"GO:1904414"}


id: PBO:0017951
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cation diffusion family zinc transmembrane transporter Zrg17","termid":"PBO:0017951"}


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:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002683","FYPO:0001985","FYPO:0000139","FYPO:0005447"],"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: PR:O13881
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- clr2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13881"],"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":"cryptic loci regulator 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1B3.17","synonyms":[{"name":"Spom972h-clr2","type":"exact"}],"termid":"PR:O13881"}


id: MONDO:0800145
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any non-severe combined immunodeficiency in which the cause of the disease is variation in the POLD1/POLD2 gene.","definition_xrefs":["PMID:31449058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-SCID combined immunodeficiency","termid":"MONDO:0018814"}],"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":"non-severe combined immunodeficiency due to polymerase delta deficiency","termid":"MONDO:0800145","xrefs":{"Monarch":{"xref_id":"0800145"}}}


id: GO:0046892
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The dehydration of peptidyl-S-carbamoyl-L-cysteine to form peptidyl-S-cyano-L-cysteine.","definition_xrefs":["PMID:12586941","RESID:AA0333"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-S-carbamoyl-L-cysteine dehydration (obsolete GO:0046892)","synonyms":[{"name":"formation of peptidyl-S-cyanocysteine","type":"exact"},{"name":"formation of peptidyl-serine thiocyanate ester","type":"exact"}],"termid":"GO:0046892"}


id: PBO:0077788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA topoisomerase III beta","termid":"PBO:0077788"}


id: GO:0034957
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 3-nitrophenol + 2 NADH + 2 H+ = 3-hydroxyaminophenol + 2 NAD+ + H2O.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-nitrophenol nitroreductase activity (obsolete GO:0034957)","termid":"GO:0034957"}


id: PR:O43083
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- hip4 gene.","definition_xrefs":["UniProtKB:O43083","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":"histone promoter control protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC947.08c","synonyms":[{"name":"Spom972h-hip4","type":"exact"}],"termid":"PR:O43083"}


id: PBO:0065019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxiredoxin 2 pseudogene 3","termid":"PBO:0065019"}


id: GO:0086103
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An G protein-coupled receptor signaling pathway which contributes to a circulatory system process carried out by the heart.","definition_xrefs":["PMID:17376402","GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway","termid":"GO:0007186"},{"relation_name":"part_of","term_name":"heart process","termid":"GO:0003015"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"G protein-coupled receptor signaling pathway involved in heart process","synonyms":[{"name":"G-protein coupled receptor signaling pathway involved in heart process","type":"exact"},{"name":"G-protein coupled receptor signalling pathway involved in heart process","type":"exact"},{"name":"GPCR signaling pathway involved in cardiac process","type":"exact"},{"name":"GPCR signaling pathway involved in heart process","type":"exact"}],"termid":"GO:0086103"}


id: MONDO:0040679
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm derived from the transitional epithelium of the urinary tract (urinary bladder, ureter, urethra, or renal pelvis). It is frequently papillary.","definition_xrefs":["NCIT:C4030"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant urinary system neoplasm","termid":"MONDO:0006295"},{"relation_name":"is_a","term_name":"transitional cell carcinoma","termid":"MONDO:0006474"},{"relation_name":"is_a","term_name":"urothelial neoplasm","termid":"MONDO:0024337"}],"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":"urothelial carcinoma","secondary_identifiers":["EFO:0008528","MEDGEN:760495","UMLS:C2145472"],"synonyms":[{"name":"Uroepithelial carcinoma","type":"exact"},{"name":"transitional cell car. -uroth.","type":"exact"},{"name":"transitional cell carcinoma of the urinary tract","type":"exact"},{"name":"transitional cell carcinoma of the urothelial tract","type":"exact"},{"name":"urothelial carcinoma","type":"exact"}],"termid":"MONDO:0040679","xrefs":{"Monarch":{"xref_id":"0040679"}}}


id: MONDO:0015357
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypoparathyroidism","termid":"MONDO:0001220"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secondary hypoparathyroidism due to impaired parathormon secretion","secondary_identifiers":["Orphanet:140286","UMLS:C4305428","GARD:19922","MEDGEN:931097","icd11.foundation:1229357339"],"termid":"MONDO:0015357","xrefs":{"Monarch":{"xref_id":"0015357"}}}


id: GO:0072123
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of intraglomerular glomerular mesangium cells by cell division, resulting in the expansion of their population. Intraglomerular mesangial cells are specialized pericytes located among the glomerular capillaries within a renal corpuscle of a kidney. They are required for filtration, structural support and phagocytosis.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerular mesangial cell proliferation","termid":"GO:0072110"}],"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":"intraglomerular mesangial cell proliferation","termid":"GO:0072123"}


id: PBO:0058296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4670","termid":"PBO:0058296"}


id: GO:0006886
data:
  {"annotated_genes":["SJAG_03781","SJAG_02103","SJAG_00971","SJAG_02588","SJAG_02524","SJAG_03540","SJAG_00800","SJAG_01748","SJAG_00490","SJAG_01281","SJAG_03959","SJAG_01027","SJAG_04857","SJAG_01297","SJAG_01328","SJAG_01013","SJAG_00850","SJAG_05220","SJAG_01546","SJAG_03783","SJAG_01697","SJAG_01584","SJAG_04936","SJAG_04044","SJAG_04643","SJAG_00687","SJAG_00826","SJAG_02640","SJAG_03889","SJAG_03499","SJAG_01360","SJAG_02398","SJAG_04552","SJAG_02264","SJAG_00840","SJAG_04070","SJAG_02117","SJAG_04931","SJAG_00208","SJAG_04343","SJAG_00702","SJAG_03593","SJAG_00360","SJAG_03453","SJAG_02592","SJAG_01621","SJAG_01120","SJAG_03299","SJAG_04740","SJAG_04996","SJAG_02811","SJAG_04275","SJAG_00753","SJAG_01083","SJAG_03838","SJAG_01167","SJAG_00181","SJAG_04474","SJAG_03250","SJAG_03396","SJAG_02525","SJAG_02211","SJAG_00851","SJAG_01374","SJAG_03684","SJAG_03385","SJAG_00284","SJAG_00137","SJAG_03552","SJAG_02241","SJAG_04645","SJAG_00326","SJAG_00104","SJAG_01598","SJAG_00578","SJAG_03976","SJAG_04349","SJAG_02368","SJAG_01780","SJAG_03502","SJAG_04513","SJAG_01242","SJAG_05030","SJAG_02034","SJAG_03137","SJAG_01534","SJAG_02208","SJAG_03662","SJAG_00216","SJAG_00968","SJAG_02418","SJAG_05303","SJAG_02693","SJAG_00586","SJAG_04912","SJAG_01025","SJAG_04023","SJAG_04464","SJAG_03907","SJAG_00380","SJAG_01409","SJAG_03002","SJAG_00569","SJAG_01415","SJAG_03915","SJAG_04428","SJAG_02004","SJAG_02422","SJAG_03347","SJAG_04411","SJAG_01586","SJAG_01282","SJAG_00204","SJAG_01772","SJAG_00530","SJAG_00192","SJAG_00065","SJAG_05266","SJAG_04598","SJAG_02757","SJAG_01065","SJAG_05950","SJAG_04956","SJAG_03072","SJAG_01442","SJAG_00375","SJAG_03244","SJAG_03470","SJAG_03515","SJAG_04402","SJAG_01488","SJAG_03048","SJAG_04312","SJAG_02234","SJAG_05319","SJAG_00064","SJAG_04902","SJAG_04837","SJAG_00959","SJAG_01809","SJAG_00357","SJAG_02824","SJAG_04472","SJAG_02361","SJAG_03892","SJAG_03005","SJAG_04358","SJAG_01311","SJAG_00404","SJAG_05345","SJAG_03324","SJAG_02839","SJAG_01834","SJAG_01642","SJAG_01185","SJAG_00918","SJAG_02520","SJAG_03729","SJAG_01030","SJAG_01456","SJAG_01558","SJAG_04565","SJAG_01949","SJAG_01088","SJAG_04517","SJAG_00108","SJAG_04112","SJAG_01211","SJAG_03864","SJAG_01759","SJAG_04909","SJAG_01324","SJAG_01229","SJAG_04489","SJAG_00821","SJAG_16459","SJAG_03933","SJAG_01367","SJAG_01633","SJAG_02330","SJAG_05207","SJAG_01165","SJAG_04763","SJAG_00907","SJAG_03536","SJAG_00330","SJAG_02797","SJAG_00430","SJAG_02355","SJAG_01655","SJAG_03153","SJAG_04739","SJAG_04218","SJAG_02204","SJAG_02750","SJAG_02655","SJAG_01039","SJAG_03970","SJAG_02425","SJAG_02761","SJAG_04886","SJAG_01358","SJAG_04021","SJAG_00416","SJAG_02997","SJAG_00383","SJAG_01775","SJAG_02912","SJAG_01789","SJAG_00379","SJAG_01879","SJAG_04366","SJAG_00804","SJAG_03270","SJAG_02453","SJAG_00919","SJAG_01449","SJAG_04509","SJAG_03560","SJAG_02277","SJAG_03986","SJAG_00471","SJAG_04024","SJAG_03345","SJAG_03848","SJAG_03437","SJAG_00332","SJAG_04966","SJAG_02210","SJAG_00093","SJAG_03440","SJAG_04391","SJAG_03467","SJAG_00314","SJAG_00144","SJAG_02482","SJAG_00072","SJAG_01951","SJAG_04592","SJAG_02160","SJAG_02998","SJAG_05344","SJAG_04002","SJAG_03504","SJAG_02274","SJAG_05315","SJAG_02584","SJAG_04960","SJAG_04569","SJAG_02349","SJAG_02320","SJAG_02315","SJAG_02456","SJAG_04196","SJAG_01071","SJAG_01379","SJAG_02731","SJAG_00899","SJAG_03416","SJAG_05210","SJAG_00171","SJAG_02511","SJAG_04129","SJAG_01981","SJAG_04978","SJAG_03158","SJAG_02282","SJAG_04148","SJAG_01640","SJAG_00906","SJAG_02619","SJAG_03054","SJAG_03693","SJAG_00557","SJAG_03726","SJAG_03358","SJAG_01459","SJAG_01805","SJAG_02354","SJAG_01909","SJAG_00891","SJAG_01224","SJAG_01626","SJAG_02586","SJAG_03756","SJAG_00143","SJAG_02805","SJAG_03044","SJAG_01925","SJAG_04609","SJAG_01245","SJAG_02336","SJAG_00632","SJAG_02539","SJAG_03415","SJAG_04208","SJAG_01371","SJAG_04629","SJAG_03963","SJAG_04400","SJAG_03300","SJAG_05013","SJAG_01508","SJAG_05184","SJAG_03836","SJAG_03246","SJAG_05194","SJAG_00820"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[58687,62995,87531,88099,88142,88628,88867,89194,89755,90051,90376,90631,90653,90677,90962,91015,91112,92625,92711,92844,92981,93122,93346,93377,93531,93674,93749,93764,93804,93875,94285,94429,94479,94632,95002,95039,95101,95271,95435,95540,95579,95619,95760,95787,96368,96372,96803,97236,97254,97591,97693,97956,98047,98412,98549,98610,99014,99040,99215,99264,99403,99517,99710,99748,99808,100249,100329,100348,100579,100948,101209,101420,101811,102032,102196,102639,102772,102970,102991,103230,103240,103624,103781,104102,104133,104388,104456,104679,105513,105639,106279,106616,106798,106877,106982,107047,107515,107823,107912,108172,108220,108230,108669,108986,109077,109149,109246,109300,109321,109701,109758,110238,110331,110992,111087,111149,111472,111505,111660,111683,111946,112175,112406,112964,113124,113249,113359,113651,113859,114370,114626,114725,115841,115872,115925,116091,116330,116394,116463,116903,117006,117050,117711,117907,117928,118033,118336,118514],"is_not":false,"summary":null,"term":"GO:0006886"},{"annotations":[87598,87485,90985,91120,87563,112802,90550,113945,105247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120113"},{"annotations":[112277,112497,94380,90775,118383,100627],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099638"},{"annotations":[105304],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0042308"},{"annotations":[100650,105646,115915,118198,103166,91204],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006607"},{"annotations":[110501,99937,93289,101350],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0046827"},{"annotations":[93857,90331,101887],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0042307"},{"annotations":[105659,107795,108824,97543,109897,96829,90064],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031204"},{"annotations":[106062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032527"},{"annotations":[100651,116889,92648,90563,95993,109083,107957,117176],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006611"},{"annotations":[92934,97320,107958,93771,113956,99908,116759,102498,88388,115325,91411,65834,93471,102153,115011,90435,112740,92881,88904,94463,114486,106421,118199,115299,103167,102880,109921,114388,95247,104065,107259,104877,104551,102056,105826,106063,88484,95610],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006606"},{"annotations":[89703,101765,95958,89915,110882,97731,104734,109539],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016558"},{"annotations":[102593,111342,96446],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016560"},{"annotations":[98073,114798,100806,116804],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016562"},{"annotations":[110883,94912,89907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045046"},{"annotations":[88133,106786,92267,107057,115765,89870,107079,112690,98928,102423,107000],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045039"},{"annotations":[97732,109901,109540,111284,89849,98083,107058,90387,109891],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045040"},{"annotations":[90486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044395"},{"annotations":[103567,88383,96890,91601,106230,89658,100619,101634,103548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006623"},{"annotations":[103250],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099117"},{"annotations":[118164,99884,103404,107752],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140210"},{"annotations":[90464,108372,116412,98127,106994,113592,89223,96264,109387,88619,100018],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990976"},{"annotations":[100390,87432,115886,90988,97452,104467,110126,110958,87601,91486,95452,106052,114205,91772,106861,109286,90037,91123,108864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043328"},{"annotations":[87377,91503],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0033157"},{"annotations":[88740,92430],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030970"},{"annotations":[102084,107797,115428,105661,97545,108826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006616"}]},"cv_name":"biological_process","definition":"The directed movement of proteins in a cell, including the movement of proteins between specific compartments or structures within a cell, such as organelles of a eukaryotic cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein transport","termid":"GO:0015031"},{"relation_name":"is_a","term_name":"intracellular transport","termid":"GO:0046907"},{"relation_name":"part_of","term_name":"protein localization","termid":"GO:0008104"}],"gene_count":308,"genes_by_uniquename":{"SJAG_00064":null,"SJAG_00065":null,"SJAG_00072":null,"SJAG_00093":null,"SJAG_00104":null,"SJAG_00108":null,"SJAG_00137":null,"SJAG_00143":null,"SJAG_00144":null,"SJAG_00171":null,"SJAG_00181":null,"SJAG_00192":null,"SJAG_00204":null,"SJAG_00208":null,"SJAG_00216":null,"SJAG_00284":null,"SJAG_00314":null,"SJAG_00326":null,"SJAG_00330":null,"SJAG_00332":null,"SJAG_00357":null,"SJAG_00360":null,"SJAG_00375":null,"SJAG_00379":null,"SJAG_00380":null,"SJAG_00383":null,"SJAG_00404":null,"SJAG_00416":null,"SJAG_00430":null,"SJAG_00471":null,"SJAG_00490":null,"SJAG_00530":null,"SJAG_00557":null,"SJAG_00569":null,"SJAG_00578":null,"SJAG_00586":null,"SJAG_00632":null,"SJAG_00687":null,"SJAG_00702":null,"SJAG_00753":null,"SJAG_00800":null,"SJAG_00804":null,"SJAG_00820":null,"SJAG_00821":null,"SJAG_00826":null,"SJAG_00840":null,"SJAG_00850":null,"SJAG_00851":null,"SJAG_00891":null,"SJAG_00899":null,"SJAG_00906":null,"SJAG_00907":null,"SJAG_00918":null,"SJAG_00919":null,"SJAG_00959":null,"SJAG_00968":null,"SJAG_00971":null,"SJAG_01013":null,"SJAG_01025":null,"SJAG_01027":null,"SJAG_01030":null,"SJAG_01039":null,"SJAG_01065":null,"SJAG_01071":null,"SJAG_01083":null,"SJAG_01088":null,"SJAG_01120":null,"SJAG_01165":null,"SJAG_01167":null,"SJAG_01185":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01229":null,"SJAG_01242":null,"SJAG_01245":null,"SJAG_01281":null,"SJAG_01282":null,"SJAG_01297":null,"SJAG_01311":null,"SJAG_01324":null,"SJAG_01328":null,"SJAG_01358":null,"SJAG_01360":null,"SJAG_01367":null,"SJAG_01371":null,"SJAG_01374":null,"SJAG_01379":null,"SJAG_01409":null,"SJAG_01415":null,"SJAG_01442":null,"SJAG_01449":null,"SJAG_01456":null,"SJAG_01459":null,"SJAG_01488":null,"SJAG_01508":null,"SJAG_01534":null,"SJAG_01546":null,"SJAG_01558":null,"SJAG_01584":null,"SJAG_01586":null,"SJAG_01598":null,"SJAG_01621":null,"SJAG_01626":null,"SJAG_01633":null,"SJAG_01640":null,"SJAG_01642":null,"SJAG_01655":null,"SJAG_01697":null,"SJAG_01748":null,"SJAG_01759":null,"SJAG_01772":null,"SJAG_01775":null,"SJAG_01780":null,"SJAG_01789":null,"SJAG_01805":null,"SJAG_01809":null,"SJAG_01834":null,"SJAG_01879":null,"SJAG_01909":null,"SJAG_01925":null,"SJAG_01949":null,"SJAG_01951":null,"SJAG_01981":null,"SJAG_02004":null,"SJAG_02034":null,"SJAG_02103":null,"SJAG_02117":null,"SJAG_02160":null,"SJAG_02204":null,"SJAG_02208":null,"SJAG_02210":null,"SJAG_02211":null,"SJAG_02234":null,"SJAG_02241":null,"SJAG_02264":null,"SJAG_02274":null,"SJAG_02277":null,"SJAG_02282":null,"SJAG_02315":null,"SJAG_02320":null,"SJAG_02330":null,"SJAG_02336":null,"SJAG_02349":null,"SJAG_02354":null,"SJAG_02355":null,"SJAG_02361":null,"SJAG_02368":null,"SJAG_02398":null,"SJAG_02418":null,"SJAG_02422":null,"SJAG_02425":null,"SJAG_02453":null,"SJAG_02456":null,"SJAG_02482":null,"SJAG_02511":null,"SJAG_02520":null,"SJAG_02524":null,"SJAG_02525":null,"SJAG_02539":null,"SJAG_02584":null,"SJAG_02586":null,"SJAG_02588":null,"SJAG_02592":null,"SJAG_02619":null,"SJAG_02640":null,"SJAG_02655":null,"SJAG_02693":null,"SJAG_02731":null,"SJAG_02750":null,"SJAG_02757":null,"SJAG_02761":null,"SJAG_02797":null,"SJAG_02805":null,"SJAG_02811":null,"SJAG_02824":null,"SJAG_02839":null,"SJAG_02912":null,"SJAG_02997":null,"SJAG_02998":null,"SJAG_03002":null,"SJAG_03005":null,"SJAG_03044":null,"SJAG_03048":null,"SJAG_03054":null,"SJAG_03072":null,"SJAG_03137":null,"SJAG_03153":null,"SJAG_03158":null,"SJAG_03244":null,"SJAG_03246":null,"SJAG_03250":null,"SJAG_03270":null,"SJAG_03299":null,"SJAG_03300":null,"SJAG_03324":null,"SJAG_03345":null,"SJAG_03347":null,"SJAG_03358":null,"SJAG_03385":null,"SJAG_03396":null,"SJAG_03415":null,"SJAG_03416":null,"SJAG_03437":null,"SJAG_03440":null,"SJAG_03453":null,"SJAG_03467":null,"SJAG_03470":null,"SJAG_03499":null,"SJAG_03502":null,"SJAG_03504":null,"SJAG_03515":null,"SJAG_03536":null,"SJAG_03540":null,"SJAG_03552":null,"SJAG_03560":null,"SJAG_03593":null,"SJAG_03662":null,"SJAG_03684":null,"SJAG_03693":null,"SJAG_03726":null,"SJAG_03729":null,"SJAG_03756":null,"SJAG_03781":null,"SJAG_03783":null,"SJAG_03836":null,"SJAG_03838":null,"SJAG_03848":null,"SJAG_03864":null,"SJAG_03889":null,"SJAG_03892":null,"SJAG_03907":null,"SJAG_03915":null,"SJAG_03933":null,"SJAG_03959":null,"SJAG_03963":null,"SJAG_03970":null,"SJAG_03976":null,"SJAG_03986":null,"SJAG_04002":null,"SJAG_04021":null,"SJAG_04023":null,"SJAG_04024":null,"SJAG_04044":null,"SJAG_04070":null,"SJAG_04112":null,"SJAG_04129":null,"SJAG_04148":null,"SJAG_04196":null,"SJAG_04208":null,"SJAG_04218":null,"SJAG_04275":null,"SJAG_04312":null,"SJAG_04343":null,"SJAG_04349":null,"SJAG_04358":null,"SJAG_04366":null,"SJAG_04391":null,"SJAG_04400":null,"SJAG_04402":null,"SJAG_04411":null,"SJAG_04428":null,"SJAG_04464":null,"SJAG_04472":null,"SJAG_04474":null,"SJAG_04489":null,"SJAG_04509":null,"SJAG_04513":null,"SJAG_04517":null,"SJAG_04552":null,"SJAG_04565":null,"SJAG_04569":null,"SJAG_04592":null,"SJAG_04598":null,"SJAG_04609":null,"SJAG_04629":null,"SJAG_04643":null,"SJAG_04645":null,"SJAG_04739":null,"SJAG_04740":null,"SJAG_04763":null,"SJAG_04837":null,"SJAG_04857":null,"SJAG_04886":null,"SJAG_04902":null,"SJAG_04909":null,"SJAG_04912":null,"SJAG_04931":null,"SJAG_04936":null,"SJAG_04956":null,"SJAG_04960":null,"SJAG_04966":null,"SJAG_04978":null,"SJAG_04996":null,"SJAG_05013":null,"SJAG_05030":null,"SJAG_05184":null,"SJAG_05194":null,"SJAG_05207":null,"SJAG_05210":null,"SJAG_05220":null,"SJAG_05266":null,"SJAG_05303":null,"SJAG_05315":null,"SJAG_05319":null,"SJAG_05344":null,"SJAG_05345":null,"SJAG_05950":null,"SJAG_16459":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"intracellular protein transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0032779"],"synonyms":[{"name":"copper-induced intracellular protein transport","type":"related"}],"termid":"GO:0006886","terms_by_termid":{"GO:0006606":null,"GO:0006607":null,"GO:0006611":null,"GO:0006616":null,"GO:0006623":null,"GO:0006886":null,"GO:0016558":null,"GO:0016560":null,"GO:0016562":null,"GO:0030970":null,"GO:0031204":null,"GO:0032527":null,"GO:0033157":null,"GO:0042307":null,"GO:0042308":null,"GO:0043328":null,"GO:0044395":null,"GO:0045039":null,"GO:0045040":null,"GO:0045046":null,"GO:0046827":null,"GO:0099117":null,"GO:0099638":null,"GO:0120113":null,"GO:0140210":null,"GO:1990976":null}}


