# terms

id: PBO:0069038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 283, pseudogene","termid":"PBO:0069038"}


id: MOD:01905
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a source amino acid residue to 5-hydroxy-3-methyl-L-proline.","definition_xrefs":["PubMed:7592021","RESID:AA0473","PubMed:8557573"],"direct_ancestors":[{"relation_name":"has_functional_parent","term_name":"monohydroxylated proline","termid":"MOD:01024"},{"relation_name":"is_a","term_name":"modified residue that can arise from different natural residues","termid":"MOD:00859"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-hydroxy-3-methyl-L-proline","synonyms":[{"name":"(2S,3S,5Xi)-5-hydroxy-3-methylpyrrolidine-2-carboxylic acid","type":"exact"},{"name":"5-hydroxy-3-methyl-L-proline","type":"exact"},{"name":"5-hydroxy-3-methylproline","type":"exact"},{"name":"5Hy3MePro","type":"exact"},{"name":"MOD_RES 5-hydroxy-3-methylproline (Ile)","type":"exact"},{"name":"beta-methyl-delta-hydroxyproline","type":"exact"}],"termid":"MOD:01905"}


id: PBO:0001957
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulates rgf3","termid":"PBO:0001957"}


id: PBO:0064026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 60","termid":"PBO:0064026"}


id: PBO:0049803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypocretin receptor 2","termid":"PBO:0049803"}


id: PBO:0055145
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 2564","termid":"PBO:0055145"}


id: PBO:0087627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the cytosolic chaperonin Cct ring complex; related to Tcp1p, required for the assembly of actin and tubulins in vivo; mutant has increased aneuploidy tolerance","termid":"PBO:0087627"}


id: GO:1904956
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of midbrain dopaminergic neuron differentiation.","definition_xrefs":["GO_REF:0000058","GOC:bf","GOC:TermGenie","PMID:21347250","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of dopaminergic neuron differentiation","termid":"GO:1904338"},{"relation_name":"regulates","term_name":"midbrain dopaminergic neuron differentiation","termid":"GO:1904948"}],"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 midbrain dopaminergic neuron differentiation","synonyms":[{"name":"regulation of DA neurogenesis from midbrain floor plate","type":"exact"},{"name":"regulation of mDA neuron differentiation","type":"exact"},{"name":"regulation of midbrain DA neurogenesis","type":"exact"},{"name":"regulation of midbrain dopaminergic neuron production","type":"exact"}],"termid":"GO:1904956"}


id: FYPO:0000647
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An inviable phenotype in which a vegetative cell lyses, i.e. the plasma membrane ruptures and cytoplasm is lost. Note that in fission yeast cell lysis, the integrity of the cell wall is also compromised.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"inviable vegetative cell","termid":"FYPO:0001489"},{"relation_name":"is_a","term_name":"inviable vegetative cell","termid":"FYPO:0001489"},{"relation_name":"is_a","term_name":"cell lysis","termid":"FYPO:0002488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000004","FYPO:0000002"],"is_obsolete":false,"name":"vegetative cell lysis","synonyms":[{"name":"cell lysis during vegetative growth","type":"exact"},{"name":"cytolysis during vegetative growth","type":"exact"},{"name":"inviable, lysed vegetative cell","type":"exact"},{"name":"vegetative cell lysis during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000647"}


id: MONDO:0013379
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Noonan syndrome in which the cause of the disease is a mutation in the BRAF gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Noonan syndrome","termid":"MONDO:0018997"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005267"],"is_obsolete":false,"name":"Noonan syndrome 7","secondary_identifiers":["OMIM:613706","UMLS:C3150970","NCIT:C176935","DOID:0060585","MEDGEN:462320","GARD:15693"],"synonyms":[{"name":"BRAF Noonan syndrome","type":"exact"},{"name":"NS7","type":"exact"},{"name":"Noonan syndrome 7","type":"exact"},{"name":"Noonan syndrome caused by mutation in BRAF","type":"exact"},{"name":"Noonan syndrome type 7","type":"exact"}],"termid":"MONDO:0013379","xrefs":{"Monarch":{"xref_id":"0013379"}}}


id: GO:0070544
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 36 of the histone.","definition_xrefs":["PMID:19061644","GOC:sart"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-K36 demethylation (obsolete GO:0070544)","synonyms":[{"name":"H3K36 demethylation","type":"related"}],"termid":"GO:0070544"}


id: GO:0070845
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of misfolded polyubiquitinated proteins in a cell, including the movement of proteins between specific compartments or structures within a cell.","definition_xrefs":["GOC:BHF","GOC:mah","PMID:14675537"],"direct_ancestors":[{"relation_name":"is_a","term_name":"misfolded protein transport","termid":"GO:0070843"},{"relation_name":"is_a","term_name":"polyubiquitinated protein transport","termid":"GO:0070844"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"polyubiquitinated misfolded protein transport","synonyms":[{"name":"misfolded polyubiquitinated protein transport","type":"related"},{"name":"polyubiquitylated misfolded protein transport","type":"exact"}],"termid":"GO:0070845"}


id: PBO:0043244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"claudin 4","termid":"PBO:0043244"}


id: MONDO:0000133
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The Immunodeficiency, Centromeric region instability, Facial anomalies syndrome (ICF) is a rare autosomal recessive disease characterized by immunodeficiency, although B cells are present, and by characteristic rearrangements in the vicinity of the centromeres (the juxtacentromeric heterochromatin) of chromosomes 1 and 16 and sometimes 9.","definition_xrefs":["Orphanet:2268"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"telomere syndrome","termid":"MONDO:0100137"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019303"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019303"],"is_obsolete":false,"name":"immunodeficiency-centromeric instability-facial anomalies syndrome","secondary_identifiers":["DOID:0090007","GARD:2945","SCTID:234633000","UMLS:C0398788","NANDO:2200708","MESH:C537362","OMIMPS:242860","NANDO:1200334","MEDGEN:140770"],"synonyms":[{"name":"CIID","type":"related"},{"name":"ICF syndrome","type":"related"},{"name":"immunodeficiency-centromeric instability-facial anomalies","type":"exact"},{"name":"immunodeficiency-centromeric instability-facial anomalies syndrome","type":"exact"}],"termid":"MONDO:0000133","xrefs":{"Monarch":{"xref_id":"0000133"}}}


id: PBO:0056597
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MDH1 pseudogene 2","termid":"PBO:0056597"}


id: PBO:0027112
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cell_wall_organization","termid":"PBO:0027112"}


id: GO:0034703
data:
  {"annotated_genes":["SJAG_MIT09","SJAG_05229","SJAG_00836","SJAG_00985","SJAG_00133","SJAG_MIT37","SJAG_03925","SJAG_03114","SJAG_04122","SJAG_02598","SJAG_00438","SJAG_07003","SJAG_MIT15","SJAG_05204","SJAG_02105","SJAG_00915","SJAG_02564","SJAG_00542"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[104475,107274,115288,102519,108246,103166,118503,107366,118492,101307,93369,94346,118498,88641,92783,103137,92357],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045259"},{"annotations":[77290,57635,69579,63517,72175],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045261"},{"annotations":[63953,66446,59642,66860],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045263"},{"annotations":[99127],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005891"}]},"cv_name":"cellular_component","definition":"An ion channel complex through which cations pass.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoatomic ion channel complex","termid":"GO:0034702"}],"gene_count":18,"genes_by_uniquename":{"SJAG_00133":null,"SJAG_00438":null,"SJAG_00542":null,"SJAG_00836":null,"SJAG_00915":null,"SJAG_00985":null,"SJAG_02105":null,"SJAG_02564":null,"SJAG_02598":null,"SJAG_03114":null,"SJAG_03925":null,"SJAG_04122":null,"SJAG_05204":null,"SJAG_05229":null,"SJAG_07003":null,"SJAG_MIT09":null,"SJAG_MIT15":null,"SJAG_MIT37":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":"cation channel complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"termid":"GO:0034703","terms_by_termid":{"GO:0005891":null,"GO:0045259":null,"GO:0045261":null,"GO:0045263":null}}


id: FYPO:0000806
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 Golgi organization is abnormal. Golgi organization results in the assembly, arrangement of constituent parts, or disassembly of the Golgi apparatus.","definition_xrefs":["GO:0007030","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal endomembrane system organization","termid":"FYPO:0000804"}],"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"abnormal Golgi organization","synonyms":[{"name":"abnormal Golgi organisation","type":"exact"},{"name":"abnormal Golgi organization during mitotic cell cycle","type":"related"},{"name":"abnormal Golgi organization during vegetative growth","type":"exact"}],"termid":"FYPO:0000806"}


id: MONDO:0016865
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Kleefstra syndrome","termid":"MONDO:0012455"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Kleefstra syndrome due to a point mutation","secondary_identifiers":["Orphanet:261652","GARD:17253","UMLS:C5680724","MEDGEN:1826146"],"termid":"MONDO:0016865","xrefs":{"Monarch":{"xref_id":"0016865"}}}


id: MONDO:0006788
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hydrophthalmos (obsolete MONDO:0006788)","termid":"MONDO:0006788","xrefs":{"Monarch":{"xref_id":"0006788"}}}


id: MONDO:0010950
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing type 1 diabetes mellituss that has material basis in mutation of the locus at chromosome 6q25-q27.","definition_xrefs":["DOID:0110747","MONDO:patterns/inherited_susceptibility","PMID:7573053"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"type 1 diabetes mellitus","termid":"MONDO:0005147"},{"relation_name":"is_a","term_name":"diabetes mellitus, insulin-dependent, X-linked, susceptibility to","termid":"MONDO:0010255"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"type 1 diabetes mellitus 8","secondary_identifiers":["MEDGEN:331462","UMLS:C1833218","OMIM:600883","MESH:C563433"],"synonyms":[{"name":"IDDM8","type":"exact"},{"name":"diabetes mellitus, insulin-dependent, 8","type":"related"},{"name":"insulin-dependent diabetes mellitus 8","type":"exact"}],"termid":"MONDO:0010950","xrefs":{"Monarch":{"xref_id":"0010950"}}}


id: MONDO:0011337
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the PRF1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hemophagocytic lymphohistiocytosis","termid":"MONDO:0015541"}],"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":"familial hemophagocytic lymphohistiocytosis 2","secondary_identifiers":["GARD:9922","OMIM:603553","MEDGEN:400366","MESH:C537250","DOID:0110922","NANDO:2200728","UMLS:C1863727"],"synonyms":[{"name":"FHL2","type":"exact"},{"name":"HLH2","type":"exact"},{"name":"HPLH2","type":"exact"},{"name":"Hlh2","type":"related"},{"name":"Hplh2","type":"related"},{"name":"PRF1 genetic hemophagocytic lymphohistiocytosis","type":"exact"},{"name":"familial hemophagocytic lymphohistiocytosis type 2","type":"exact"},{"name":"genetic hemophagocytic lymphohistiocytosis caused by mutation in PRF1","type":"exact"},{"name":"hemophagocytic lymphohistiocytosis, familial, 2","type":"related"},{"name":"hemophagocytic lymphohistiocytosis, familial, type 2","type":"exact"}],"termid":"MONDO:0011337","xrefs":{"Monarch":{"xref_id":"0011337"}}}


id: PBO:0050903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IFI30 lysosomal thiol reductase","termid":"PBO:0050903"}


id: PBO:0057999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3923","termid":"PBO:0057999"}


id: PBO:0031856
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-haploinsufficient","termid":"PBO:0031856"}


id: GO:0045584
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of cytotoxic T cell differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of T cell differentiation","termid":"GO:0045581"},{"relation_name":"is_a","term_name":"regulation of cytotoxic T cell differentiation","termid":"GO:0045583"},{"relation_name":"negatively_regulates","term_name":"cytotoxic T cell differentiation","termid":"GO:0045065"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of cytotoxic T cell differentiation","synonyms":[{"name":"down regulation of cytotoxic T cell differentiation","type":"exact"},{"name":"down-regulation of cytotoxic T cell differentiation","type":"exact"},{"name":"downregulation of cytotoxic T cell differentiation","type":"exact"},{"name":"inhibition of cytotoxic T cell differentiation","type":"narrow"},{"name":"negative regulation of cytotoxic T cell development","type":"related"},{"name":"negative regulation of cytotoxic T lymphocyte differentiation","type":"exact"},{"name":"negative regulation of cytotoxic T-cell differentiation","type":"exact"},{"name":"negative regulation of cytotoxic T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0045584"}


id: MOD:00589
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-phenylalanine residue to (13)C,(15)N labeled L-phenylalanine.","definition_xrefs":["Unimod:269","PubMed:12771378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(13)C labeled residue","termid":"MOD:00842"},{"relation_name":"is_a","term_name":"(15)N labeled residue","termid":"MOD:00843"},{"relation_name":"is_a","term_name":"modified L-phenylalanine residue","termid":"MOD:00914"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1x(13)C,1x(15)N labeled L-phenylalanine","synonyms":[{"name":"13C(9) 15N(1) Silac label","type":"related"},{"name":"Label:13C(9)15N(1)","type":"related"}],"termid":"MOD:00589"}


id: GO:0045805
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of eclosion.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of eclosion","termid":"GO:0007563"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"eclosion","termid":"GO:0007562"}],"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 eclosion","synonyms":[{"name":"activation of eclosion","type":"narrow"},{"name":"stimulation of eclosion","type":"narrow"},{"name":"up regulation of eclosion","type":"exact"},{"name":"up-regulation of eclosion","type":"exact"},{"name":"upregulation of eclosion","type":"exact"}],"termid":"GO:0045805"}


id: PBO:0043364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"clathrin light chain B","termid":"PBO:0043364"}


id: PBO:0062989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"parkin coregulated like","termid":"PBO:0062989"}


id: MONDO:0020490
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mosaic trisomy 9 is a chromosomal abnormality that can affect may parts of the body. In people affected by this condition, some of the body's cells have three copies of chromosome 9 (trisomy), while other cells have the usual two copies of this chromosome. The signs and symptoms vary but may include mild to severe intellectual disability, developmental delay, growth problems (both before and after birth), congenital heart defects, and/or abnormalities of the craniofacial (skull and face) region. Most cases are not inherited; it often occurs sporadically as a random event during the formation of the reproductive cells (egg and sperm) or as the fertilized egg divides. Treatment is based on the signs and symptoms present in each person.","direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 9 disorder","termid":"MONDO:0700016"},{"relation_name":"is_a","term_name":"trisomy","termid":"MONDO:0700065"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mosaic trisomy 9","secondary_identifiers":["MESH:C535454","NORD:966","SCTID:764989007","UMLS:C2930908","MEDGEN:419661","Orphanet:99776","GARD:43"],"synonyms":[{"name":"Mosaic trisomy chromosome 9","type":"related"},{"name":"Mosaic trisomy type 9","type":"exact"},{"name":"trisomy 9 mosaicism","type":"related"}],"termid":"MONDO:0020490","xrefs":{"Monarch":{"xref_id":"0020490"}}}


id: PR:P78854
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- plb1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P78854"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysophospholipase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1A6.04c","synonyms":[{"name":"Spom972h-plb1","type":"exact"},{"name":"phospholipase B 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P78854"}


id: PBO:0077535
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 248","termid":"PBO:0077535"}


id: GO:1900175
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of a nodal signaling pathway, where the nodal signaling pathway is involved in determination of left/right asymmetry in the lateral mesoderm.","definition_xrefs":["GOC:TermGenie","GOC:vk","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of nodal signaling pathway involved in determination of lateral mesoderm left/right asymmetry (obsolete GO:1900175)","synonyms":[{"name":"regulation of nodal signalling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"}],"termid":"GO:1900175"}


id: PBO:0065154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRMT5 divergent transcript","termid":"PBO:0065154"}


id: MONDO:0000541
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A adenocarcinoma that involves the jejunum.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small intestine adenocarcinoma","termid":"MONDO:0003198"},{"relation_name":"is_a","term_name":"jejunal cancer","termid":"MONDO:0006815"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"jejunal adenocarcinoma","secondary_identifiers":["DOID:0050926","HP:0030411","NCIT:C181158","MEDGEN:893029","UMLS:C4072935"],"synonyms":[{"name":"jejunal adenocarcinoma","type":"exact"},{"name":"jejunal adenocarcinoma (disease)","type":"exact"},{"name":"jejunum adenocarcinoma","type":"exact"}],"termid":"MONDO:0000541","xrefs":{"Monarch":{"xref_id":"0000541"}}}


id: GO:0045655
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of monocyte differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of myeloid leukocyte differentiation","termid":"GO:0002761"},{"relation_name":"regulates","term_name":"monocyte differentiation","termid":"GO:0030224"}],"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 monocyte differentiation","termid":"GO:0045655"}


id: GO:0062211
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The the regeneration process by which a damaged or lost root regrows or re-differentiates. This process may occur via de-differentiation and subsequent reprogramming of somatic cells or activation of existing undifferentiated (meristematic) cells to form a new root meristem and subsequently new root.","definition_xrefs":["PMID:27143753"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regeneration","termid":"GO:0031099"},{"relation_name":"is_a","term_name":"root development","termid":"GO:0048364"}],"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":"root regeneration","termid":"GO:0062211"}


id: PBO:0088604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEL1 repeat protein","termid":"PBO:0088604"}


id: PBO:0091914
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RING Finger Protein","termid":"PBO:0091914"}


id: PBO:0076923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor CP2 like 1","termid":"PBO:0076923"}


id: GO:0030971
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a receptor that possesses protein tyrosine kinase activity.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"},{"relation_name":"is_a","term_name":"protein tyrosine kinase binding","termid":"GO:1990782"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"receptor tyrosine kinase binding","synonyms":[{"name":"transmembrane receptor protein tyrosine kinase ligand binding","type":"related"}],"termid":"GO:0030971"}


id: GO:0070483
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a stimulus indicating lowered oxygen tension is received by a cell and converted into a molecular signal. Hypoxia, defined as a decline in O2 levels below normoxic levels of 20.8 - 20.95%, results in metabolic adaptation at both the cellular and organismal level.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to hypoxia","termid":"GO:0001666"},{"relation_name":"is_a","term_name":"detection of oxygen","termid":"GO:0003032"}],"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 hypoxia","synonyms":[{"name":"detection of reduced oxygen levels","type":"exact"}],"termid":"GO:0070483"}


id: PBO:0055507
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 2941","termid":"PBO:0055507"}


id: PBO:0082072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-phosphoglycerate kinase; catalyzes transfer of high-energy phosphoryl groups from the acyl phosphate of 1,3-bisphosphoglycerate to ADP to produce ATP; key enzyme in glycolysis and gluconeogenesis","termid":"PBO:0082072"}


id: PBO:0052248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium channel tetramerization domain containing 17","termid":"PBO:0052248"}


id: MONDO:0014744
data:
  {"annotated_genes":["SJAG_04622"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85418],"is_not":false,"summary":null,"term":"MONDO:0014744"}]},"cv_name":"mondo","definition":"An autosomal recessive cerebellar ataxia that has material basis in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13.","definition_xrefs":["DOID:0111155"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"autosomal recessive syndromic cerebellar ataxia","termid":"MONDO:0020047"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04622":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:616719","GARD:17833","MEDGEN:1800507","Orphanet:466794","UMLS:C5569084"],"synonyms":[{"name":"SCAR21","type":"exact"},{"name":"acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome","type":"exact"},{"name":"autosomal recessive spinocerebellar ataxia 21","type":"related"},{"name":"autosomal recessive spinocerebellar ataxia 21 with hepatopathy","type":"exact"},{"name":"autosomal recessive spinocerebellar ataxia type 21","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 21","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 21, with hepatopathy","type":"related"},{"name":"spinocerebellar ataxia, autosomal recessive type 21","type":"exact"}],"termid":"MONDO:0014744","terms_by_termid":{"MONDO:0014744":null},"xrefs":{"Monarch":{"xref_id":"0014744"}}}


id: PBO:0049107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 162","termid":"PBO:0049107"}


id: MONDO:0012002
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 22q11.21-q12.1.","definition_xrefs":["DOID:0110499","PMID:14512974"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 40","secondary_identifiers":["GARD:22607","OMIM:608264","MEDGEN:334053","UMLS:C1842345","MESH:C564266"],"synonyms":[{"name":"DFNB40","type":"narrow"},{"name":"autosomal recessive deafness 40","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 40","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 40","type":"narrow"},{"name":"deafness, autosomal recessive 40","type":"narrow"}],"termid":"MONDO:0012002","xrefs":{"Monarch":{"xref_id":"0012002"}}}


id: GO:0005532
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 mannose binding lectin (obsolete GO:0005532)","synonyms":[{"name":"mannose binding lectin","type":"exact"},{"name":"mannose receptor","type":"related"}],"termid":"GO:0005532"}


id: PBO:0090687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-directed RNA polymerase III complex subunit Rpc53","termid":"PBO:0090687"}


id: MONDO:0018580
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome (obsolete MONDO:0018580)","secondary_identifiers":["Orphanet:438213"],"termid":"MONDO:0018580","xrefs":{"Monarch":{"xref_id":"0018580"}}}


id: GO:1905907
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of amyloid fibril formation.","definition_xrefs":["GO_REF:0000058","GOC:aruk","GOC:TermGenie","GOC:bc","PMID:23106396"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein metabolic process","termid":"GO:0051248"},{"relation_name":"is_a","term_name":"negative regulation of supramolecular fiber organization","termid":"GO:1902904"},{"relation_name":"is_a","term_name":"regulation of amyloid fibril formation","termid":"GO:1905906"},{"relation_name":"negatively_regulates","term_name":"amyloid fibril formation","termid":"GO:1990000"}],"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 amyloid fibril formation","synonyms":[{"name":"down regulation of amyloid fibril assembly","type":"related"},{"name":"down regulation of amyloid fibril formation","type":"exact"},{"name":"down regulation of amyloid structure assembly","type":"related"},{"name":"down regulation of amyloid structure formation","type":"related"},{"name":"down-regulation of amyloid fibril assembly","type":"related"},{"name":"down-regulation of amyloid fibril formation","type":"exact"},{"name":"down-regulation of amyloid structure assembly","type":"related"},{"name":"down-regulation of amyloid structure formation","type":"related"},{"name":"downregulation of amyloid fibril assembly","type":"related"},{"name":"downregulation of amyloid fibril formation","type":"exact"},{"name":"downregulation of amyloid structure assembly","type":"related"},{"name":"downregulation of amyloid structure formation","type":"related"},{"name":"inhibition of amyloid fibril assembly","type":"related"},{"name":"inhibition of amyloid fibril formation","type":"narrow"},{"name":"inhibition of amyloid structure assembly","type":"related"},{"name":"inhibition of amyloid structure formation","type":"related"},{"name":"negative regulation of amyloid fibril assembly","type":"related"},{"name":"negative regulation of amyloid structure assembly","type":"related"},{"name":"negative regulation of amyloid structure formation","type":"related"}],"termid":"GO:1905907"}


id: GO:0090378
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a seed trichome irreversibly increases in size in one [spatial] dimension or along one axis, resulting in the morphogenesis of the cell.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"unidimensional cell growth","termid":"GO:0009826"},{"relation_name":"is_a","term_name":"cellular process involved in reproduction in multicellular organism","termid":"GO:0022412"},{"relation_name":"part_of","term_name":"seed trichome differentiation","termid":"GO:0090376"}],"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":"seed trichome elongation","termid":"GO:0090378"}


id: MOD:00771
data:
  {"annotated_genes":["SJAG_02592","SJAG_02763","SJAG_03012"],"annotation_feature_type":"gene","cv_annotations":{"PSI-MOD":[{"annotations":[80043,119025,118661,119026,80042,119027,119028,118662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00046"}]},"cv_name":"PSI-MOD","definition":"Natural or modified residues with a mass of 166.98-167.00 Da.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"residues isobaric at a resolution below 0.01 Da","termid":"MOD:00770"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02592":null,"SJAG_02763":null,"SJAG_03012":null},"genotype_count":0,"is_obsolete":false,"name":"residues isobaric at 166.98-167.00 Da","references_by_uniquename":{"PMID:26774782":null,"PMID:31150379":null,"PMID:36408920":null},"termid":"MOD:00771","terms_by_termid":{"GO:0034599":null,"GO:0034605":null,"GO:0071475":null,"GO:1904547":null,"MOD:00046":null}}


id: GO:0047020
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADP+ + (5Z,13E)-(15S)-9-alpha,15-dihydroxy-11-oxoprosta-5,13-dienoate = NADPH + H+ + (5Z,13E)-9-alpha-hydroxy-11,15-dioxoprosta-5,13-dienoate.","definition_xrefs":["MetaCyc:1.1.1.196-RXN","EC:1.1.1.196"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"15-hydroxyprostaglandin-D dehydrogenase (NADP+) activity","secondary_identifiers":["RHEA:20744"],"synonyms":[{"name":"(5Z,13E)-(15S)-9alpha,15-dihydroxy-11-oxoprosta-5,13-dienoate:NADP+ 15-oxidoreductase activity","type":"related"},{"name":"15-hydroxy PGD2 dehydrogenase activity","type":"related"},{"name":"15-hydroxyprostaglandin dehydrogenase (NADP)","type":"related"},{"name":"NADP-PGD2 dehydrogenase activity","type":"related"},{"name":"NADP-dependent 15-hydroxyprostaglandin dehydrogenase","type":"broad"},{"name":"NADP-linked 15-hydroxyprostaglandin dehydrogenase","type":"broad"},{"name":"NADP-linked prostaglandin D2 dehydrogenase activity","type":"related"},{"name":"NADP-specific 15-hydroxyprostaglandin dehydrogenase","type":"broad"},{"name":"dehydrogenase, 15-hydroxyprostaglandin (nicotinamide adenine dinucleotide phosphate)","type":"related"},{"name":"dehydrogenase, prostaglandin D2","type":"related"},{"name":"prostaglandin D2 dehydrogenase activity","type":"related"},{"name":"prostaglandin-D 15-dehydrogenase (NADP(+)) activity","type":"related"},{"name":"prostaglandin-D 15-dehydrogenase (NADP)","type":"related"},{"name":"prostaglandin-D 15-dehydrogenase (NADP+) activity","type":"related"}],"termid":"GO:0047020"}


id: PBO:0074991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 115-2","termid":"PBO:0074991"}


id: MONDO:0019277
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete epidermal appendage anomaly (obsolete MONDO:0019277)","secondary_identifiers":["Orphanet:79362"],"termid":"MONDO:0019277","xrefs":{"Monarch":{"xref_id":"0019277"}}}


id: PBO:0075098
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 147","termid":"PBO:0075098"}


id: GO:0052454
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism modulates the frequency, rate or extent of the jasmonic acid-mediated defense response of the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by organism of symbiont jasmonic acid-mediated defense response (obsolete GO:0052454)","synonyms":[{"name":"modulation by organism of symbiont JA-mediated defense response","type":"exact"},{"name":"modulation by organism of symbiont jasmonic acid-mediated defense response","type":"exact"}],"termid":"GO:0052454"}


id: GO:0005160
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a transforming growth factor beta receptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor binding","termid":"GO:0005126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"transforming growth factor beta receptor binding","synonyms":[{"name":"TGF-beta receptor binding","type":"exact"},{"name":"TGFbeta receptor binding","type":"exact"},{"name":"activin","type":"related"},{"name":"inhibin","type":"related"},{"name":"transforming growth factor beta","type":"narrow"},{"name":"transforming growth factor beta ligand binding to type I receptor","type":"related"},{"name":"transforming growth factor beta ligand binding to type II receptor","type":"related"},{"name":"transforming growth factor beta receptor anchoring activity","type":"related"},{"name":"transforming growth factor beta receptor ligand","type":"narrow"}],"termid":"GO:0005160"}


id: PR:Q9C113
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1F8.08 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9C113"],"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 C1F8.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1F8.08","synonyms":[{"name":"Spom972h-SPAC1F8.08","type":"exact"}],"termid":"PR:Q9C113"}


id: GO:1903642
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of recombination hotspot binding.","definition_xrefs":["GO_REF:0000059","PMID:19436749","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of recombination hotspot binding (obsolete GO:1903642)","synonyms":[{"name":"regulation of DNA binding, recombination hotspot","type":"exact"}],"termid":"GO:1903642"}


id: PBO:0085952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; null mutant is resistant to 2-deoxy-D-glucose and displays abnormally elongated buds; DGR2 has a paralog, YMR102C, that arose from the whole genome duplication","termid":"PBO:0085952"}


id: PBO:0091600
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cor-C? is nse6","termid":"PBO:0091600"}


id: PBO:0069894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1184, pseudogene","termid":"PBO:0069894"}


id: PBO:0072133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 10","termid":"PBO:0072133"}


id: MONDO:0011462
data:
  {"annotated_genes":["SJAG_03596","SJAG_04077"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84656,84657],"is_not":false,"summary":null,"term":"MONDO:0011462"}]},"cv_name":"mondo","definition":"A rare pleiotropic autoinflammatory disorder of childhood, primarily affecting the joints and skin.","definition_xrefs":["Orphanet:69126"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"},{"relation_name":"is_a","term_name":"autoinflammatory syndrome","termid":"MONDO:0019751"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03596":null,"SJAG_04077":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"pyogenic arthritis-pyoderma gangrenosum-acne syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:346801","NANDO:1200868","NCIT:C119055","SCTID:724015007","DOID:0080519","MESH:C536253","NANDO:2200437","UMLS:C1858361","GARD:9176","OMIM:604416"],"synonyms":[{"name":"FRA","type":"exact"},{"name":"PAPA","type":"exact"},{"name":"Papas","type":"related"},{"name":"familial recurrent arthritis","type":"exact"},{"name":"fra","type":"exact"},{"name":"papa","type":"exact"},{"name":"papa syndrome","type":"exact"},{"name":"pyogenic STERILE arthritis, pyoderma gangrenosum, and acne","type":"related"},{"name":"pyogenic arthritis, pyoderma gangrenosum and acne","type":"related"},{"name":"pyogenic arthritis, pyoderma gangrenosum, and severe cystic acne","type":"related"}],"termid":"MONDO:0011462","terms_by_termid":{"MONDO:0011462":null},"xrefs":{"Monarch":{"xref_id":"0011462"}}}


id: PBO:0064890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 2 regulatory subunit Bdelta","termid":"PBO:0064890"}


id: GO:0046783
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any viral process that interferes with and inhibits the assembly and function of polysomes.","definition_xrefs":["PMID:10438802"],"gene_count":0,"genotype_count":0,"name":"obsolete modification by virus of host polysomes (obsolete GO:0046783)","synonyms":[{"name":"viral perturbation of polysomes","type":"exact"}],"termid":"GO:0046783"}


id: GO:0034068
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: nucleoside triphosphate + aminoglycoside = diphosphate + nucleotidylaminoglycoside.","definition_xrefs":["GOC:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotidyltransferase activity","termid":"GO:0016779"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016779"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016779"],"is_obsolete":false,"name":"aminoglycoside nucleotidyltransferase activity","synonyms":[{"name":"aminoglycoside adenylyltransferase activity","type":"narrow"},{"name":"streptomycin adenylate synthetase activity","type":"narrow"},{"name":"streptomycin adenyltransferase activity","type":"narrow"},{"name":"streptomycin adenylylase activity","type":"narrow"},{"name":"streptomycin adenylyltransferase activity","type":"narrow"},{"name":"streptomycin-spectinomycin adenylyltransferase activity","type":"narrow"}],"termid":"GO:0034068"}


id: PBO:0081759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 689","termid":"PBO:0081759"}


id: MONDO:0020261
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete neurological disease with abnormal eye movements (obsolete MONDO:0020261)","secondary_identifiers":["Orphanet:98691"],"synonyms":[{"name":"abnormal eye movements","type":"exact"}],"termid":"MONDO:0020261","xrefs":{"Monarch":{"xref_id":"0020261"}}}


id: PBO:0085768
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase related to mammalian GSK-3 glycogen synthase kinases; GSK-3 homologs (Mck1p, Rim11p, Mrk1p, Ygk3p) are involved in control of Msn2p-dependent transcription of stress responsive genes and in protein degradation; YGK3 has a paralog, MCK1, that arose from the whole genome duplication","termid":"PBO:0085768"}


id: MONDO:0859188
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurodevelopmental disorder","termid":"MONDO:0700092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with seizures and brain abnormalities","secondary_identifiers":["MEDGEN:1794189","OMIM:619517","UMLS:C5561979"],"termid":"MONDO:0859188","xrefs":{"Monarch":{"xref_id":"0859188"}}}


id: PBO:0060544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NAV2 antisense RNA 4","termid":"PBO:0060544"}


id: MONDO:0005416
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Noninflammatory degenerative disease of the knee joint consisting of three large categories: conditions that block normal synchronous movement, conditions that produce abnormal pathways of motion, and conditions that cause stress concentration resulting in changes to articular cartilage. (Crenshaw, Campbell's Operative Orthopaedics, 8th ed, p2019)","definition_xrefs":["MESH:D020370"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteoarthritis","termid":"MONDO:0005178"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoarthritis, knee","secondary_identifiers":["UMLS:C0409959","EFO:0004616","MEDGEN:98371"],"termid":"MONDO:0005416","xrefs":{"Monarch":{"xref_id":"0005416"}}}


id: MONDO:0002904
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A symptom of neurologic or psychiatric dysfunction in which the individual involuntarily and meaninglessly repeats a recently heard word, series of words, or a song.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"speech disorder","termid":"MONDO:0004730"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"echolalia","secondary_identifiers":["HP:0010529","icd11.foundation:928818606","MEDGEN:8532","UMLS:C0013528","MESH:D004454","DOID:4188"],"synonyms":[{"name":"echolalia","type":"exact"},{"name":"echolalia (disease)","type":"exact"}],"termid":"MONDO:0002904","xrefs":{"Monarch":{"xref_id":"0002904"}}}


id: PBO:0091538
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"not functionally complemented by human TPM1 skeletal muscle isoform","termid":"PBO:0091538"}


id: GO:1902880
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of BMP signaling pathway involved in spinal cord association neuron specification.","definition_xrefs":["GO_REF:0000058","GOC:mr","GOC:TermGenie","PMID:21730158"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of BMP signaling pathway involved in spinal cord association neuron specification (obsolete GO:1902880)","synonyms":[{"name":"activation of BMP signaling pathway involved in spinal cord association neuron specification","type":"narrow"},{"name":"activation of BMP signalling pathway involved in spinal cord association neuron specification","type":"narrow"},{"name":"activation of bone morphogenetic protein signaling pathway involved in spinal cord association neuron specification","type":"narrow"},{"name":"activation of bone morphogenetic protein signalling pathway involved in spinal cord association neuron specification","type":"narrow"},{"name":"positive regulation of BMP signalling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"positive regulation of bone morphogenetic protein signaling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"positive regulation of bone morphogenetic protein signalling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"up regulation of BMP signaling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"up regulation of BMP signalling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"up regulation of bone morphogenetic protein signaling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"up regulation of bone morphogenetic protein signalling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"up-regulation of BMP signaling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"up-regulation of BMP signalling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"up-regulation of bone morphogenetic protein signaling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"up-regulation of bone morphogenetic protein signalling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"upregulation of BMP signaling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"upregulation of BMP signalling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"upregulation of bone morphogenetic protein signaling pathway involved in spinal cord association neuron specification","type":"exact"},{"name":"upregulation of bone morphogenetic protein signalling pathway involved in spinal cord association neuron specification","type":"exact"}],"termid":"GO:1902880"}


id: PATO:0000119
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A 1-D extent quality inhering in a bearer by virtue of the bearer's vertical dimension of extension.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"1-D extent","termid":"PATO:0001708"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"height","termid":"PATO:0000119"}


id: PBO:0069266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 522, pseudogene","termid":"PBO:0069266"}


id: PBO:0057015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 103b-2","termid":"PBO:0057015"}


id: PBO:0072892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"suprabasin","termid":"PBO:0072892"}


id: FYPO:0008207
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate or other property of a microfilament motor activity is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal molecular function","termid":"FYPO:0000706"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000652"],"is_obsolete":false,"name":"normal microfilament motor activity","termid":"FYPO:0008207"}


id: MONDO:0009101
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Wolfram syndrome in which the cause of the disease is a mutation in the WFS1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"Wolfram syndrome","termid":"MONDO:0018105"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Wolfram syndrome 1","secondary_identifiers":["OMIM:222300","UMLS:C4551693","DOID:0110629","MEDGEN:1641635"],"synonyms":[{"name":"WFS1","type":"exact"},{"name":"WFS1 Wolfram syndrome","type":"exact"},{"name":"WOLFRAM syndrome 1","type":"related"},{"name":"Wfs","type":"related"},{"name":"Wolfram syndrome 1","type":"exact"},{"name":"Wolfram syndrome caused by mutation in WFS1","type":"exact"},{"name":"Wolfram syndrome type 1","type":"exact"},{"name":"diabetes insipidus and mellitus with optic atrophy and deafness","type":"related"}],"termid":"MONDO:0009101","xrefs":{"Monarch":{"xref_id":"0009101"}}}


id: GO:1904812
data:
  {"annotated_genes":["SJAG_01877"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92120],"is_not":false,"summary":null,"term":"GO:1904812"}]},"cv_name":"biological_process","definition":"Any rRNA acetylation that is involved in maturation of SSU-rRNA.","definition_xrefs":["GOC:TermGenie","GO_REF:0000060","PMID:25402480"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA acetylation","termid":"GO:1990882"},{"relation_name":"part_of","term_name":"maturation of SSU-rRNA","termid":"GO:0030490"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01877":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0042254"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0010467","GO:0042254","GO:0008150"],"is_obsolete":false,"name":"rRNA acetylation involved in maturation of SSU-rRNA","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"rRNA acetylation involved in SSU-rRNA maturation","type":"exact"},{"name":"rRNA acetylation involved in processing of 20S pre-rRNA","type":"narrow"}],"termid":"GO:1904812","terms_by_termid":{"GO:1904812":null}}


id: GO:1990574
data:
  {"annotated_genes":["SJAG_02286"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[87267],"is_not":false,"summary":null,"term":"GO:1990574"}]},"cv_name":"cellular_component","definition":"Any of the meiotic spindle microtubules that radiate in all directions from the spindle poles and are thought to contribute to the forces that separate the poles and position them in relation to the rest of the cell.","definition_xrefs":["PMID:10366596"],"direct_ancestors":[{"relation_name":"is_a","term_name":"astral microtubule","termid":"GO:0000235"},{"relation_name":"part_of","term_name":"meiotic spindle","termid":"GO:0072687"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02286":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0015630"}],"interesting_parent_ids":["GO:0015630","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"meiotic spindle astral microtubule","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990574","terms_by_termid":{"GO:1990574":null}}


id: GO:0061599
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction adenylyl-molybdopterin + molybdate = molybdenum cofactor + AMP.","definition_xrefs":["EC:2.10.1.1","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity","termid":"GO:0016740"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"molybdopterin molybdotransferase activity","secondary_identifiers":["Reactome:R-HSA-947531","RHEA:35047"],"termid":"GO:0061599"}


id: FYPO:0003770
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A transcription regulation phenotype in which pheromone-responsive positive regulation of transcription from an RNA polymerase II promoter is decreased.","definition_xrefs":["GO:0007329","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal positive regulation of transcription","termid":"FYPO:0000623"},{"relation_name":"is_a","term_name":"abnormal transcriptional response to pheromone","termid":"FYPO:0000984"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0006551","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"decreased transcriptional response to pheromone","synonyms":[{"name":"decreased positive regulation of transcription from RNA polymerase II promoter by pheromones","type":"exact"},{"name":"reduced positive regulation of transcription from RNA polymerase II promoter by pheromones","type":"exact"}],"termid":"FYPO:0003770"}


id: GO:0038133
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by binding of a ligand to a ERBB3 receptor on the surface of a cell, followed by transmission of the signal by a heterodimeric complex of ERBB2 and ERBB3. ERBB2, which does not bind any known ligand, is activated through formation of a heterodimer with another ligand-activated ERBB family member such as ERBB3. ERBB3 also has impaired kinase activity and relies on ERBB2 for activation and signal transmission.","definition_xrefs":["GOC:signaling","PMID:16460914"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ERBB2 signaling pathway","termid":"GO:0038128"},{"relation_name":"is_a","term_name":"ERBB3 signaling pathway","termid":"GO:0038129"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"ERBB2-ERBB3 signaling pathway","synonyms":[{"name":"ERBB2-ERBB3 signalling pathway","type":"exact"},{"name":"HER2-HER3 signaling pathway","type":"exact"}],"termid":"GO:0038133"}


id: PBO:0059438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane spanning 4-domains A7","termid":"PBO:0059438"}


id: PBO:0044991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DExH-box helicase 58","termid":"PBO:0044991"}


id: PBO:0062522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily R member 1 pseudogene","termid":"PBO:0062522"}


id: FYPO:0006184
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of one or more messenger RNAs that are normally expressed during a cellular response to osmotic stress measured in a cell differs from normal (i.e. is higher or lower than observed in wild-type cells during vegetative growth).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered level of stress responsive gene mRNA during vegetative growth","termid":"FYPO:0004363"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0006551","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"altered level of osmotic stress responsive gene mRNA during vegetative growth","synonyms":[{"name":"abnormal level of osmotic stress responsive gene mRNA during vegetative growth","type":"exact"},{"name":"altered level of cellular response to osmotic stress responsive gene mRNA","type":"exact"},{"name":"altered level of osmotic stress responsive gene RNA during vegetative growth","type":"exact"},{"name":"altered level of osmotic stress responsive gene mRNA during mitotic cell cycle","type":"related"},{"name":"altered level of osmotic stress responsive gene transcripts during vegetative growth","type":"exact"},{"name":"altered mRNA level of osmotic stress responsive genes during vegetative growth","type":"exact"},{"name":"altered osmotic stress responsive gene mRNA accumulation during vegetative growth","type":"related"}],"termid":"FYPO:0006184"}


id: PBO:0034556
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_microtubule-based_movement","termid":"PBO:0034556"}


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


id: PBO:0068878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 118, pseudogene","termid":"PBO:0068878"}


id: MONDO:0019483
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Methotrexate-associated lymphoproliferative disorders are rare immunodeficiency-associated lymphoproliferative diseases characterized by lymphoid proliferation or lymphomas (large B-cell lymphoma, T-cell lymphoma, Hodgkin lymphoma, reactive lymphadenitis and a polymorphic post-transplant lymphoproliferative disorder) that develop in patients with different autoimmune diseases treated with methotrexate. Swelling is the predominant manifestation of the disease and regression after methotrexate withdrawal is observed in a significant proportion of patients.","definition_xrefs":["Orphanet:86904"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoma","termid":"MONDO:0005062"},{"relation_name":"is_a","term_name":"immunodeficiency-associated lymphoproliferative disease","termid":"MONDO:0020083"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"methotrexate-associated lymphoproliferative disorders","secondary_identifiers":["UMLS:C1334749","GARD:19083","icd11.foundation:1520483526","MEDGEN:233702","DOID:5821","NCIT:C7184"],"synonyms":[{"name":"MTX-LPD","type":"exact"},{"name":"MTX-associated lymphoproliferative disorders","type":"exact"},{"name":"methotrexate-associated lymphoproliferation","type":"exact"},{"name":"methotrexate-associated lymphoproliferative disorder","type":"exact"}],"termid":"MONDO:0019483","xrefs":{"Monarch":{"xref_id":"0019483"}}}


id: GO:0016402
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: pristanoyl-CoA + O2 = trans-2,3-dehydropristanoyl-CoA + hydrogen peroxide.","definition_xrefs":["RHEA:40459","GOC:jsg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyl-CoA oxidase activity","termid":"GO:0003997"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"pristanoyl-CoA oxidase activity","secondary_identifiers":["Reactome:R-HSA-389891","Reactome:R-HSA-389889"],"termid":"GO:0016402"}


id: SO:0001166
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A non directional promoter motif with consensus sequence GAGAGCG.","definition_xrefs":["PMID:16827941"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA_motif","termid":"SO:0000713"},{"relation_name":"part_of","term_name":"RNApol_II_promoter","termid":"SO:0000170"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GAGA_motif","synonyms":[{"name":"GAGA","type":"exact"},{"name":"GAGA motif","type":"exact"},{"name":"NDM1","type":"exact"}],"termid":"SO:0001166"}


id: GO:0002128
data:
  {"annotated_genes":["SJAG_04649","SJAG_01269","SJAG_02352"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[114268],"is_not":false,"summary":null,"term":"GO:0002128"},{"annotations":[97349,102377],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002130"}]},"cv_name":"biological_process","definition":"The process that results in the modification of the sugar of a nucleoside in tRNA at the 2'O position.","definition_xrefs":["ISBN:155581073X","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA methylation","termid":"GO:0030488"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01269":null,"SJAG_02352":null,"SJAG_04649":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006399"],"is_obsolete":false,"name":"tRNA nucleoside ribose methylation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0002128","terms_by_termid":{"GO:0002128":null,"GO:0002130":null}}


id: PBO:0009178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sir antagonist","termid":"PBO:0009178"}


id: PBO:0072712
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RWD domain containing 4 pseudogene 1","termid":"PBO:0072712"}


id: GO:0140951
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-lysyl27-[histone H3] + 3 S-adenosyl-L-methionine = 3 H+ + N6,N6,N6-trimethyl-L-lysyl27-[histone H3] + 3 S-adenosyl-L-homocysteine. This reaction is the successive addition of three methyl groups to the unmethylated lysine residue at position 27 of histone H3, producing histone H3K27me3.","definition_xrefs":["RHEA:60292"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3K27 methyltransferase activity","termid":"GO:0046976"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016741","GO:0008276","GO:0140096","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"histone H3K27 trimethyltransferase activity","synonyms":[{"name":"histone H3-K27 trimethylase activity","type":"exact"},{"name":"histone H3-K27 trimethylation","type":"broad"},{"name":"histone H3K27 mono/di/trimethylase activity","type":"exact"},{"name":"histone H3K27 trimethylase activity","type":"exact"},{"name":"histone H3K27 trimethylation","type":"broad"},{"name":"histone lysine N-trimethyltransferase activity (H3-K27 specific)","type":"exact"}],"termid":"GO:0140951"}


id: PBO:0031613
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_vacuolar_transport","termid":"PBO:0031613"}


id: PBO:0049370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIIA","termid":"PBO:0049370"}


id: GO:0047216
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: myo-inositol + UDP-galactose = O-alpha-D-galactosyl-(1,3)-1D-myo-inositol + UDP.","definition_xrefs":["MetaCyc:2.4.1.123-RXN","EC:2.4.1.123"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-galactosyltransferase activity","termid":"GO:0035250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016757"],"is_obsolete":false,"name":"inositol 3-alpha-galactosyltransferase activity","secondary_identifiers":["RHEA:12464"],"synonyms":[{"name":"UDP-D-galactose:inositol galactosyltransferase activity","type":"related"},{"name":"UDP-galactose:myo-inositol 1-alpha-D-galactosyltransferase activity","type":"related"},{"name":"UDP-galactose:myo-inositol 3-alpha-D-galactosyltransferase activity","type":"related"},{"name":"UDPgalactose:myo-inositol 1-alpha-D-galactosyltransferase activity","type":"related"},{"name":"galactinol synthase activity","type":"related"},{"name":"inositol 1-alpha-galactosyltransferase activity","type":"exact"},{"name":"uridine diphosphogalactose-inositol galactosyltransferase activity","type":"related"}],"termid":"GO:0047216"}


id: MOD:00245
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks a glycine residue and an L-serine residue to form glycine oxazole-4-carboxylic acid.","definition_xrefs":["PubMed:8895467","PubMed:8183941","RESID:AA0240"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxazole/oxazoline ring crosslinked residues (Ser)","termid":"MOD:01421"},{"relation_name":"is_a","term_name":"didehydrogenated residue","termid":"MOD:01888"},{"relation_name":"is_a","term_name":"crosslinked glycine residue","termid":"MOD:02047"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycine oxazole-4-carboxylic acid","synonyms":[{"name":"2-aminomethyl-1,3-oxazole-4-carboxylic acid","type":"exact"},{"name":"2-azanylmethyl-1,3-oxazole-4-carboxylic acid","type":"exact"},{"name":"CROSSLNK Oxazole-4-carboxylic acid (Gly-Ser)","type":"exact"},{"name":"glycine oxazole-4-carboxylic acid","type":"exact"}],"termid":"MOD:00245"}


id: PBO:0051424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 3-1","termid":"PBO:0051424"}


id: PBO:0072686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RUNDC3A antisense RNA 1","termid":"PBO:0072686"}


id: FYPO:0002598
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which histone H2A phosphorylation occurs to a lower extent than normal. All histone H2A phosphorylation may be affected, or phosphorylation of specific sites on histone H2A may be decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone phosphorylation during vegetative growth","termid":"FYPO:0002591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"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:0002494"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0002274","FYPO:0005447","FYPO:0002494","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased histone H2A phosphorylation during vegetative growth","synonyms":[{"name":"decreased histone H2A phosphorylation during mitotic cell cycle","type":"related"},{"name":"reduced histone H2A phosphorylation","type":"exact"}],"termid":"FYPO:0002598"}


id: MONDO:0008559
data:
  {"annotated_genes":["SJAG_03712","SJAG_01466"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86805,86806],"is_not":false,"summary":null,"term":"MONDO:0008559"}]},"cv_name":"mondo","definition":"The formation of a blood clot (thrombus) in the lumen of a vein.","definition_xrefs":["NCIT:C99107"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited thrombophilia","termid":"MONDO:0100240"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01466":null,"SJAG_03712":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"thrombophilia due to thrombin defect","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:463623","ICD9:453.9","SCTID:111293003","DOID:0111907","OMIM:188050","UMLS:C3160733","GARD:10815","DOID:0080701"],"synonyms":[{"name":"THPH1","type":"related"},{"name":"Venous thromboembolism","type":"broad"},{"name":"factor II-related thrombophilia","type":"related"},{"name":"hyperprothrombinemia","type":"related"},{"name":"prothrombin 20210G>A thrombophilia","type":"related"},{"name":"prothrombin G20210A thrombophilia","type":"related"},{"name":"prothrombin thrombophilia","type":"exact"},{"name":"prothrombin-related thrombophilia","type":"exact"},{"name":"thromboembolism, susceptibility to","type":"related"},{"name":"thrombophilia 1 due to thrombin defect","type":"exact"},{"name":"thrombophilia due to factor 2 defect","type":"related"},{"name":"thrombophilia due to thrombin defect","type":"exact"},{"name":"thrombosis, protection against","type":"related"},{"name":"venous thromboembolism, susceptibility to","type":"exact"},{"name":"venous thrombosis","type":"related"},{"name":"venous thrombosis, protection against","type":"exact"}],"termid":"MONDO:0008559","terms_by_termid":{"MONDO:0008559":null},"xrefs":{"Monarch":{"xref_id":"0008559"}}}


id: GO:0010675
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the rate, extent or frequency of the chemical reactions and pathways involving carbohydrates, any of a group of organic compounds based of the general formula Cx(H2O)y, as carried out by individual cells.","definition_xrefs":["GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cellular carbohydrate metabolic process (obsolete GO:0010675)","termid":"GO:0010675"}


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":["PMID:27146110","PomBase:mah"],"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":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000337","FYPO:0000631","FYPO:0001320","FYPO:0000138","FYPO:0005447","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: PBO:0085171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Oligomeric mitochondrial matrix chaperone; cooperates with Ssc1p in mitochondrial thermotolerance after heat shock; able to prevent the aggregation of misfolded proteins as well as resolubilize protein aggregates","termid":"PBO:0085171"}


id: GO:0004715
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + protein L-tyrosine = ADP + protein L-tyrosine phosphate by a non-membrane spanning protein.","definition_xrefs":["EC:2.7.10.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein tyrosine kinase activity","termid":"GO:0004713"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0140096"},{"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:0016740","GO:0016301","GO:0004672","GO:0140096","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"non-membrane spanning protein tyrosine kinase activity","secondary_identifiers":["Reactome:R-HSA-1168767","Reactome:R-HSA-1369115","Reactome:R-HSA-1112602","Reactome:R-HSA-1168423","Reactome:R-HSA-1168459","Reactome:R-HSA-8871373","Reactome:R-HSA-6786095","Reactome:R-HSA-6786096","Reactome:R-HSA-453200","Reactome:R-HSA-1295519","Reactome:R-HSA-437936","Reactome:R-HSA-432148","Reactome:R-HSA-6788582","Reactome:R-HSA-1112703","Reactome:R-HSA-879910"],"synonyms":[{"name":"ATP:protein-L-tyrosine O-phosphotransferase (non-specific) activity","type":"related"},{"name":"ATP:protein-tyrosine O-phosphotransferase activity","type":"broad"},{"name":"Bruton's tyrosine kinase activity","type":"narrow"},{"name":"cytoplasmic protein tyrosine kinase activity","type":"narrow"},{"name":"focal adhesion kinase activity","type":"narrow"},{"name":"janus kinase 1 activity","type":"narrow"},{"name":"janus kinase 2 activity","type":"narrow"},{"name":"janus kinase 3 activity","type":"narrow"},{"name":"non-specific protein-tyrosine kinase activity","type":"related"},{"name":"p60c-src protein tyrosine kinase activity","type":"narrow"}],"termid":"GO:0004715"}


id: PBO:0065538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylserine synthase 2","termid":"PBO:0065538"}


id: PBO:0068171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 478","termid":"PBO:0068171"}


id: PBO:0086303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein with carboxyl methyl esterase activity; may have a role in demethylation of the phosphoprotein phosphatase catalytic subunit; also identified as a small subunit mitochondrial ribosomal protein","termid":"PBO:0086303"}


id: PBO:0075724
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermidine synthase","termid":"PBO:0075724"}


id: PBO:0065099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase cAMP-dependent type I regulatory subunit beta","termid":"PBO:0065099"}


id: GO:0033637
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism modulates a change in state or activity of a host cell or organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a cold stimulus, a temperature stimulus below the optimal temperature for that organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by symbiont of host response to cold (obsolete GO:0033637)","synonyms":[{"name":"freezing tolerance","type":"related"}],"termid":"GO:0033637"}


id: MONDO:0005242
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An accumulation of pus in a body cavity, usually the pleural space.","definition_xrefs":["NCIT:C34572"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial infectious disease","termid":"MONDO:0005113"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"empyema","secondary_identifiers":["MESH:D004653","ICD9:510","UMLS:C0014009","SCTID:312682007","EFO:0003097","MEDGEN:8597"],"synonyms":[{"name":"collection of pus","type":"related"}],"termid":"MONDO:0005242","xrefs":{"Monarch":{"xref_id":"0005242"}}}


id: PR:Q9Y7Z6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1539.02 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y7Z6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic chromosome segregation protein C1539.02 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1539.02","synonyms":[{"name":"Spom972h-SPBC1539.02","type":"exact"}],"termid":"PR:Q9Y7Z6"}


id: GO:0047761
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + butanoate = ADP + butanoyl phosphate + H+.","definition_xrefs":["EC:2.7.2.7","RHEA:13585"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, carboxyl group as acceptor","termid":"GO:0016774"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"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:0016301","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"butyrate kinase activity","secondary_identifiers":["MetaCyc:BUTYRATE-KINASE-RXN","KEGG_REACTION:R01688"],"synonyms":[{"name":"ATP:butanoate 1-phosphotransferase activity","type":"related"}],"termid":"GO:0047761"}


id: GO:0047481
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: alanyl-poly(glycerolphosphate) + D-alanine + ATP = D-alanyl-alanyl-poly(glycerolphosphate) + phosphate + ADP.","definition_xrefs":["MetaCyc:6.3.2.16-RXN","EC:6.3.2.16"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-amino acid ligase activity","termid":"GO:0016881"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016874","GO:0003674"],"is_obsolete":false,"name":"D-alanine-alanyl-poly(glycerolphosphate) ligase activity","synonyms":[{"name":"D-alanine-membrane acceptor-ligase activity","type":"related"},{"name":"D-alanine:alanyl-poly(glycerolphosphate) ligase (ADP-forming)","type":"related"},{"name":"D-alanine:membrane-acceptor ligase activity","type":"related"},{"name":"D-alanyl-alanyl-poly(glycerolphosphate) synthetase activity","type":"related"},{"name":"D-alanyl-poly(phosphoglycerol) synthetase activity","type":"related"},{"name":"D-alanylalanylpoly(phosphoglycerol) synthetase activity","type":"related"}],"termid":"GO:0047481"}


id: PBO:0075694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRD5A3 antisense RNA 1","termid":"PBO:0075694"}


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


id: PBO:0055996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long stress-induced non-coding transcript 5","termid":"PBO:0055996"}


id: SO:0002138
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript feature that has been predicted but is not yet validated.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript","termid":"SO:0000673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"predicted_transcript","synonyms":[{"name":"predicted transcript","type":"exact"}],"termid":"SO:0002138"}


id: PBO:0038587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetyl-CoA carboxylase alpha","termid":"PBO:0038587"}


id: PBO:0087555
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of SAGA and NuA4 histone acetyltransferase complexes; interacts with acidic activators (e.g., Gal4p) which leads to transcription activation; similar to human TRRAP, which is a cofactor for c-Myc mediated oncogenic transformation","termid":"PBO:0087555"}


id: PBO:0047683
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"flotillin 2","termid":"PBO:0047683"}


id: GO:2000273
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of signaling receptor activity.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signaling receptor activity","termid":"GO:0010469"},{"relation_name":"is_a","term_name":"positive regulation of molecular function","termid":"GO:0044093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of signaling receptor activity","synonyms":[{"name":"positive regulation of signalling receptor activity","type":"exact"}],"termid":"GO:2000273"}


id: MONDO:0006328
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cyst in the jaw that arises from tissues of tooth development.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neoplasm","termid":"MONDO:0005070"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"odontogenic cyst","secondary_identifiers":["NCIT:C54220","UMLS:C0028879","SCTID:235110008","ICD9:526.89","MESH:D009807","MEDGEN:14461","EFO:1000406","Wikipedia:Odontogenic_cyst"],"termid":"MONDO:0006328","xrefs":{"Monarch":{"xref_id":"0006328"}}}


id: PBO:0090205
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spindle pole body half bridge protein Sfi1","termid":"PBO:0090205"}


id: GO:0062095
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of an endoplasmic reticulum membrane to a peroxisome via molecular tethers that physically bridge the two membranes and attach them to each other.","definition_xrefs":["PMID:28463579"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxisome localization","termid":"GO:0060151"},{"relation_name":"is_a","term_name":"organelle localization by membrane tethering","termid":"GO:0140056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140056"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0140056"],"is_obsolete":false,"name":"endoplasmic reticulum-peroxisome tethering","termid":"GO:0062095"}


id: MONDO:0017505
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"apodia","termid":"MONDO:0017446"}],"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":"apodia, bilateral","secondary_identifiers":["Orphanet:295107","icd11.foundation:1292290082","MEDGEN:672391","UMLS:C0685440"],"synonyms":[{"name":"congenital absence of foot, bilateral","type":"exact"}],"termid":"MONDO:0017505","xrefs":{"Monarch":{"xref_id":"0017505"}}}


id: PBO:0041675
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CADM2 antisense RNA 1","termid":"PBO:0041675"}


id: PBO:0044472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 11 subfamily B member 1","termid":"PBO:0044472"}


id: PBO:0042946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil-helix-coiled-coil-helix domain containing 2","termid":"PBO:0042946"}


id: PBO:0082543
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cell wall protein related to glucanases localized in birth scars; possibly involved in cell wall septation; member of the SUN family; SUN4 has a paralog, SIM1, that arose from the whole genome duplication","termid":"PBO:0082543"}


id: PBO:0016943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Clp1-interacting, microtubule plus-end binding Nsk1","termid":"PBO:0016943"}


id: MONDO:0019563
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"CREST syndrome is a subtype of limited cutaneous systemic sclerosis (lcSSc) whose name is an acronym for the cardinal clinical features of the syndrome: calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly and telangiectasia.","definition_xrefs":["Orphanet:90290"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"limited cutaneous systemic sclerosis","termid":"MONDO:0016358"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005046"],"is_obsolete":false,"name":"CREST syndrome","secondary_identifiers":["SCTID:31848007","DOID:0060218","MedDRA:10011380","NANDO:1201011","UMLS:C0206138","MEDGEN:60083","MESH:D017675","NCIT:C70646"],"synonyms":[{"name":"CRST syndrome","type":"narrow"},{"name":"CRST syndromes","type":"narrow"},{"name":"calcinosis - Raynaud phenomenon - esophageal involvement - sclerodactyly - telangiectasia","type":"related"},{"name":"calcinosis Raynaud phenomenon sclerodactyly telangiectasia","type":"related"},{"name":"calcinosis, Raynaud's phenomenon, esophageal dismobility, sclerodactyly, telangiectasia syndrome","type":"related"},{"name":"calcinosis-Raynaud phenomenon-esophageal involvement-sclerodactyly-telangiectasia syndrome","type":"exact"},{"name":"calcinosis-Raynaud phenomenon-sclerodactyly-telangiectasia","type":"related"},{"name":"lcSSc","type":"broad"},{"name":"limited cutaneous Systemic Scleroderma","type":"exact"},{"name":"limited cutaneous Systemic sclerosis","type":"exact"},{"name":"phenomenon-sclerodactyly-telangiectasia, calcinosis-Raynaud","type":"related"},{"name":"syndrome, CREST","type":"related"}],"termid":"MONDO:0019563","xrefs":{"Monarch":{"xref_id":"0019563"}}}


id: PBO:0069985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1280, pseudogene","termid":"PBO:0069985"}


id: PBO:0069647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 924, pseudogene","termid":"PBO:0069647"}


id: FYPO:0003417
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 microtubule plus ends remain in contact with the cell cortex at cell tips for a longer time than normal.","definition_xrefs":["PMID:24530531","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule cytoskeleton organization during vegetative growth","termid":"FYPO:0001350"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000054","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"increased microtubule dwell time at cell tip","synonyms":[{"name":"increased microtubule dwell time at cell end","type":"exact"},{"name":"increased microtubule dwell time at cell tip during mitotic cell cycle","type":"related"},{"name":"increased microtubule dwell time at cell tip during vegetative growth","type":"exact"},{"name":"increased microtubule plus end dwell time at cell tip","type":"exact"}],"termid":"FYPO:0003417"}


id: MONDO:0017080
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"isolated encephalocele","termid":"MONDO:0016057"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"occipital encephalocele","secondary_identifiers":["UMLS:C0014067","ICD10CM:Q01.2","icd11.foundation:1075031814","GARD:20969","MEDGEN:4935","Orphanet:268823","SCTID:42376006"],"termid":"MONDO:0017080","xrefs":{"Monarch":{"xref_id":"0017080"}}}


id: MONDO:0015132
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete immunodeficiency predominantly affecting antibody production (obsolete MONDO:0015132)","secondary_identifiers":["Orphanet:101977","icd11.foundation:85074116"],"termid":"MONDO:0015132","xrefs":{"Monarch":{"xref_id":"0015132"}}}


id: PBO:0057982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3909","termid":"PBO:0057982"}


id: FYPO:0006376
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular metabolism phenotype in which the observed occurrence of protein processing is decreased when the cell is subject to nitrogen starvation.","definition_xrefs":["PMID:25803873","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein processing","termid":"FYPO:0006374"},{"relation_name":"is_a","term_name":"decreased proteolysis","termid":"FYPO:0006527"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0002494","FYPO:0000002","FYPO:0002274","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"decreased protein processing during nitrogen starvation","synonyms":[{"name":"decreased protein cleavage during nitrogen starvation","type":"related"},{"name":"decreased protein maturation by peptide bond cleavage during nitrogen starvation","type":"exact"},{"name":"decreased protein maturation by peptide bond hydrolysis during nitrogen starvation","type":"exact"},{"name":"decreased protein processing during nitrogen depletion","type":"exact"},{"name":"decreased protein processing during nitrogen deprivation","type":"exact"},{"name":"reduced protein processing during nitrogen starvation","type":"exact"}],"termid":"FYPO:0006376"}


id: GO:0102612
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 9beta-pimara-7,15-diene + NADPH + O2 + H+ = 6beta-hydroxy-syn-pimaradiene + NADP + H2O.","definition_xrefs":["PMID:22215681","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"syn-pimaradiene 6beta-hydroxylase activity","secondary_identifiers":["MetaCyc:RXN-15452"],"termid":"GO:0102612"}


id: PBO:0054392
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 1788","termid":"PBO:0054392"}


id: GO:1902461
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of mesenchymal stem cell proliferation.","definition_xrefs":["PMID:18672106","GOC:TermGenie","GOC:pm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mesenchymal stem cell proliferation","termid":"GO:1902460"},{"relation_name":"is_a","term_name":"negative regulation of stem cell proliferation","termid":"GO:2000647"},{"relation_name":"negatively_regulates","term_name":"mesenchymal stem cell proliferation","termid":"GO:0097168"}],"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 mesenchymal stem cell proliferation","synonyms":[{"name":"down regulation of MSC proliferation","type":"exact"},{"name":"down regulation of mesenchymal stem cell proliferation","type":"exact"},{"name":"down-regulation of MSC proliferation","type":"exact"},{"name":"down-regulation of mesenchymal stem cell proliferation","type":"exact"},{"name":"downregulation of MSC proliferation","type":"exact"},{"name":"downregulation of mesenchymal stem cell proliferation","type":"exact"},{"name":"inhibition of MSC proliferation","type":"narrow"},{"name":"inhibition of mesenchymal stem cell proliferation","type":"narrow"},{"name":"negative regulation of MSC proliferation","type":"exact"}],"termid":"GO:1902461"}


id: MONDO:0007635
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Frasier syndrome is characterized by the association of male pseudohermaphrodism and glomerular nephropathy. This syndrome is associated with a high risk of developing gonadoblastoma.","definition_xrefs":["Orphanet:347"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"46,XY disorder of sex development","termid":"MONDO:0020040"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"Frasier syndrome","secondary_identifiers":["MEDGEN:215533","MESH:D052159","UMLS:C0950122","GARD:2375","NCIT:C122805","OMIM:136680","ICD9:759.89","DOID:0050438","icd11.foundation:1659542949","SCTID:445431000"],"synonyms":[{"name":"Frasier syndrome","type":"exact"},{"name":"Frasier syndrome, autosomal dominant, somatic mutation","type":"exact"}],"termid":"MONDO:0007635","xrefs":{"Monarch":{"xref_id":"0007635"}}}


id: GO:0048854
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the brain are generated and organized. The brain is one of the two components of the central nervous system and is the center of thought and emotion. It is responsible for the coordination and control of bodily activities and the interpretation of information from the senses (sight, hearing, smell, etc.).","definition_xrefs":["GOC:jid","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ morphogenesis","termid":"GO:0009887"},{"relation_name":"part_of","term_name":"brain development","termid":"GO:0007420"}],"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":"brain morphogenesis","termid":"GO:0048854"}


id: MONDO:0017932
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"muscular hypertrophy-hepatomegaly-polyhydramnios syndrome","secondary_identifiers":["MEDGEN:1665387","Orphanet:324416","UMLS:C4751007","GARD:21441"],"termid":"MONDO:0017932","xrefs":{"Monarch":{"xref_id":"0017932"}}}


id: PBO:0071463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L32 pseudogene 4","termid":"PBO:0071463"}


id: GO:0030908
data:
  {"annotated_genes":["SJAG_01471"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[66912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016539"}]},"cv_name":"biological_process","definition":"The post-translational removal of peptide sequences from within a protein sequence.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein processing","termid":"GO:0016485"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01471":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051604"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051604","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"protein splicing","references_by_uniquename":{"GO_REF:0000002":null},"secondary_identifiers":["Wikipedia:Protein_splicing"],"termid":"GO:0030908","terms_by_termid":{"GO:0016539":null}}


id: PBO:0029095
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cysteine_synthase_activity","termid":"PBO:0029095"}


id: PR:P87015
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC186.03 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P87015"],"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":"L-asparaginase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC186.03","synonyms":[{"name":"L-asparagine amidohydrolase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPAC186.03","type":"exact"}],"termid":"PR:P87015"}


id: GO:1901572
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving chemical substance.","definition_xrefs":["GOC:pr","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete chemical substance metabolic process (obsolete GO:1901572)","synonyms":[{"name":"chemical substance metabolic process","type":"exact"},{"name":"chemical substance metabolism","type":"exact"}],"termid":"GO:1901572"}


id: PBO:0077746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TOG array regulator of axonemal microtubules 1","termid":"PBO:0077746"}


id: FYECO:0000344
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which manganese sulfate was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ MnSO4","synonyms":[{"name":"+ manganese sulfate","type":"exact"}],"termid":"FYECO:0000344"}


id: MONDO:0005425
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease of the lymphatic vessels of the lower extremities that is caused by chronic exposure to irritant soils.","definition_xrefs":["Wikipedia:Podoconiosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"elephantiasis","termid":"MONDO:0005424"}],"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":"podoconiosis","secondary_identifiers":["DOID:0050138","ICD9:457.1","UMLS:C1280469","SCTID:47595008","MEDGEN:473377","EFO:0004712"],"synonyms":[{"name":"elephantiasis from soil","type":"exact"},{"name":"non-filarial elephantiasis","type":"exact"},{"name":"nonfilarial elephantiasis","type":"exact"},{"name":"soil elephantiasis","type":"exact"}],"termid":"MONDO:0005425","xrefs":{"Monarch":{"xref_id":"0005425"}}}


id: MONDO:0012075
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":"oligodontia-cancer predisposition syndrome","secondary_identifiers":["MESH:C563898","Orphanet:300576","UMLS:C1837750","GARD:17376","MEDGEN:324868","OMIM:608615"],"synonyms":[{"name":"ODCRCS","type":"exact"},{"name":"autosomal dominant ectodermal dysplasia-cancer predisposition syndrome","type":"exact"},{"name":"oligodontia-cancer predisposition syndrome","type":"exact"},{"name":"oligodontia-colorectal cancer syndrome","type":"exact"},{"name":"tooth agenesis-colorectal cancer syndrome","type":"exact"}],"termid":"MONDO:0012075","xrefs":{"Monarch":{"xref_id":"0012075"}}}


id: PBO:0050730
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family D (Hsp60) member 1 pseudogene 16","termid":"PBO:0050730"}


id: PBO:0002523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldehyde dehydrogenase (predicted)","termid":"PBO:0002523"}


id: PBO:0004417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear distribution protein NUDC homolog","termid":"PBO:0004417"}


id: PBO:0034169
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-existence_ends_during","termid":"PBO:0034169"}


id: GO:0006972
data:
  {"annotated_genes":["SJAG_04668"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91910],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071474"}]},"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 detection of, or exposure to, a hyperosmotic environment, i.e. an environment with a higher concentration of solutes than the organism or cell.","definition_xrefs":["GOC:jl","PMID:12142009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to osmotic stress","termid":"GO:0006970"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04668":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"hyperosmotic response","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"HOG response","type":"exact"},{"name":"hypertonic response","type":"exact"},{"name":"response to hypertonicity","type":"exact"}],"termid":"GO:0006972","terms_by_termid":{"GO:0071474":null}}


id: PBO:0059017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"matrix metallopeptidase 3","termid":"PBO:0059017"}


id: GO:2000952
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of xyloglucan catabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of xyloglucan metabolic process","termid":"GO:2000949"},{"relation_name":"is_a","term_name":"regulation of xyloglucan catabolic process","termid":"GO:2000951"},{"relation_name":"is_a","term_name":"negative regulation of hemicellulose catabolic process","termid":"GO:2000989"},{"relation_name":"negatively_regulates","term_name":"xyloglucan catabolic process","termid":"GO:2000899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"negatively_regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"negative regulation of xyloglucan catabolic process","synonyms":[{"name":"negative regulation of xyloglucan catabolism","type":"exact"}],"termid":"GO:2000952"}


id: PBO:0069070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 317, pseudogene","termid":"PBO:0069070"}


id: PBO:0067470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 600, pseudogene","termid":"PBO:0067470"}


id: PBO:0061812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OFD1 pseudogene 2 Y-linked","termid":"PBO:0061812"}


id: FYPO:0001988
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population growth phenotype in which vegetative cells grow normally (i.e. indistinguishably from wild type) at a pH higher than that of standard S. pombe growth medium (abut 5.8).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002060"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0000257","FYPO:0002058","FYPO:0002057","FYPO:0002060","FYPO:0000003"],"is_obsolete":false,"name":"normal cell population growth at high pH","synonyms":[{"name":"normal growth at high pH","type":"broad"},{"name":"normal vegetative cell population growth at high pH","type":"exact"}],"termid":"FYPO:0001988"}


id: GO:0033207
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the transfer of an N-acetylgalactosaminyl residue from UDP-N-acetyl-galactosamine to an acceptor molecule, forming a beta-1,4 linkage.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete beta-1,4-N-acetylgalactosaminyltransferase activity (obsolete GO:0033207)","synonyms":[{"name":"beta-1,4-GalNAc transferase activity","type":"exact"}],"termid":"GO:0033207"}


id: GO:0032771
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the activity of a tyrosinase enzyme.","definition_xrefs":["GOC:dph","GOC:tb","GOC:mah","PMID:2494997"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of tyrosinase activity (obsolete GO:0032771)","synonyms":[{"name":"regulation of monophenol monooxygenase activity","type":"related"},{"name":"regulation of monophenol oxygenase activity","type":"exact"}],"termid":"GO:0032771"}


id: PBO:0053753
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 993","termid":"PBO:0053753"}


id: MONDO:0030014
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive limb-girdle muscular dystrophy","termid":"MONDO:0015152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0006025"],"is_obsolete":false,"name":"muscular dystrophy, limb-girdle, autosomal recessive 26","secondary_identifiers":["OMIM:618848","UMLS:C5394268","MEDGEN:1718449"],"synonyms":[{"name":"LGMDR26","type":"exact"},{"name":"MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 26","type":"exact"},{"name":"muscular dystrophy, limb-girdle, autosomal recessive 26","type":"exact"}],"termid":"MONDO:0030014","xrefs":{"Monarch":{"xref_id":"0030014"}}}


id: GO:2000374
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of oxygen metabolic process.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of metabolic process","termid":"GO:0019222"},{"relation_name":"regulates","term_name":"oxygen metabolic process","termid":"GO:0072592"}],"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 oxygen metabolic process","synonyms":[{"name":"regulation of diatomic oxygen metabolic process","type":"exact"},{"name":"regulation of oxygen metabolism","type":"exact"}],"termid":"GO:2000374"}


id: MOD:01341
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Isotopic label -","definition_xrefs":["Unimod:90#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ESP-Tag light d0","termid":"MOD:00468"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ESP-Tag light d0 - site K","synonyms":[{"name":"ESP","type":"related"},{"name":"ESP-Tag light d0","type":"related"}],"termid":"MOD:01341"}


id: PBO:0058259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4637","termid":"PBO:0058259"}


id: PBO:0029381
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_4'-phosphopantothenate_level","termid":"PBO:0029381"}


id: PBO:0052627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 6A","termid":"PBO:0052627"}


id: MONDO:0010838
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital disorder characterized by the complete absence of gonadal tissue.","definition_xrefs":["NCIT:C27228"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gonadal agenesis","secondary_identifiers":["MEDGEN:181797","UMLS:C0949331","OMIM:600171"],"synonyms":[{"name":"gonadal agenesis","type":"exact"}],"termid":"MONDO:0010838","xrefs":{"Monarch":{"xref_id":"0010838"}}}


id: PBO:0016960
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chitin DeAcetylase","termid":"PBO:0016960"}


id: PBO:0043282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-type lectin domain family 4 member F","termid":"PBO:0043282"}


id: PBO:0088017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Type I transmembrane sorting receptor for multiple vacuolar hydrolases; cycles between the late-Golgi and prevacuolar endosome-like compartments","termid":"PBO:0088017"}


id: MONDO:0033262
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial nephrotic syndrome","termid":"MONDO:0002350"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"nephrotic syndrome 15","secondary_identifiers":["DOID:0080271","MEDGEN:1620414","OMIM:617609","UMLS:C4539896"],"synonyms":[{"name":"NPHS15","type":"related"},{"name":"nephrotic syndrome 15","type":"exact"},{"name":"nephrotic syndrome, type 15","type":"exact"}],"termid":"MONDO:0033262","xrefs":{"Monarch":{"xref_id":"0033262"}}}


id: FYPO:0000214
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 chromosome condensation is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid segregation","termid":"FYPO:0000141"},{"relation_name":"is_a","term_name":"abnormal chromosome condensation","termid":"FYPO:0000159"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0000631","FYPO:0005447","FYPO:0000337","FYPO:0000641"],"is_obsolete":false,"name":"abnormal mitotic chromosome condensation","synonyms":[{"name":"abnormal chromosome condensation during mitotic cell cycle","type":"related"},{"name":"abnormal mitotic chromosome condensation during vegetative growth","type":"exact"}],"termid":"FYPO:0000214"}


id: GO:0032223
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of cholinergic synaptic transmission, the process of communication from a neuron to another neuron across a synapse using the neurotransmitter acetylcholine.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synaptic transmission, cholinergic","termid":"GO:0032222"},{"relation_name":"is_a","term_name":"negative regulation of synaptic transmission","termid":"GO:0050805"},{"relation_name":"negatively_regulates","term_name":"synaptic transmission, cholinergic","termid":"GO:0007271"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of synaptic transmission, cholinergic","synonyms":[{"name":"down regulation of synaptic transmission, cholinergic","type":"exact"},{"name":"down-regulation of synaptic transmission, cholinergic","type":"exact"},{"name":"downregulation of synaptic transmission, cholinergic","type":"exact"},{"name":"inhibition of synaptic transmission, cholinergic","type":"narrow"}],"termid":"GO:0032223"}


id: MONDO:0000380
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant epithelial neoplasm arising in the paranasal sinus.","definition_xrefs":["NCIT:C6014"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone carcinoma","termid":"MONDO:0002415"},{"relation_name":"is_a","term_name":"paranasal sinus cancer","termid":"MONDO:0020669"},{"relation_name":"is_a","term_name":"nasal cavity and paranasal sinus carcinoma","termid":"MONDO:0056819"}],"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":"paranasal sinus carcinoma","secondary_identifiers":["DOID:0050619","UMLS:C0854995","NCIT:C6019","MEDGEN:167751"],"synonyms":[{"name":"accessory sinus cancer","type":"exact"},{"name":"accessory sinus carcinoma","type":"exact"},{"name":"adenoid cystic carcinoma of accessory sinus","type":"related"},{"name":"adenoid cystic carcinoma of paranasal sinus","type":"related"},{"name":"cancer of paranasal sinus","type":"exact"},{"name":"carcinoma of accessory sinus","type":"exact"},{"name":"carcinoma of paranasal sinus","type":"exact"},{"name":"carcinoma of the accessory sinus","type":"exact"},{"name":"carcinoma of the paranasal sinus","type":"exact"},{"name":"epidermoid carcinoma of the paranasal sinus","type":"related"},{"name":"malignant neoplasm of paranasal sinus","type":"broad"},{"name":"malignant paranasal sinus neoplasm","type":"broad"},{"name":"mucoepidermoid carcinoma of accessory sinus","type":"related"},{"name":"paranasal sinus adenocarcinoma","type":"related"},{"name":"paranasal sinus adenoid cystic carcinoma","type":"related"},{"name":"paranasal sinus cancer","type":"broad"},{"name":"paranasal sinus carcinoma","type":"exact"},{"name":"paranasal sinus mucoepidermoid carcinoma","type":"related"},{"name":"paranasal sinus squamous cell carcinoma","type":"related"},{"name":"squamous cell carcinoma of paranasal sinus","type":"related"}],"termid":"MONDO:0000380","xrefs":{"Monarch":{"xref_id":"0000380"}}}


id: GO:0098739
data:
  {"annotated_genes":["SJAG_02780","SJAG_01493","SJAG_05175","SJAG_02779","SJAG_03631","SJAG_01983","SJAG_00991","SJAG_02877","SJAG_02883","SJAG_00922","SJAG_00296","SJAG_03608","SJAG_01406","SJAG_01660","SJAG_03595","SJAG_04551","SJAG_04246","SJAG_02605","SJAG_04714","SJAG_04905","SJAG_02968","SJAG_05229","SJAG_03960","SJAG_02463","SJAG_01353","SJAG_04718","SJAG_04637","SJAG_04673","SJAG_00057","SJAG_03970","SJAG_03591","SJAG_04506","SJAG_04668","SJAG_05346","SJAG_01090","SJAG_04185","SJAG_04830","SJAG_03777"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111989],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098702"},{"annotations":[91568,71342],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905135"},{"annotations":[91908,113881,99128,91857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098703"},{"annotations":[87455,114033],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098705"},{"annotations":[113618,116652],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098708"},{"annotations":[91569],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905136"},{"annotations":[102495],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140206"},{"annotations":[110098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140425"},{"annotations":[91997],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140270"},{"annotations":[95027],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098709"},{"annotations":[111990],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098710"},{"annotations":[99852],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097638"},{"annotations":[99853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097639"},{"annotations":[101145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098714"},{"annotations":[101146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098715"},{"annotations":[95271],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106081"},{"annotations":[97545,92079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904679"},{"annotations":[112802,90727],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905949"},{"annotations":[87605],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905533"},{"annotations":[87606],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1905530"},{"annotations":[115442],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098716"},{"annotations":[107748],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098717"},{"annotations":[101634],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905665"},{"annotations":[92833,109991,91250,98380],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905589"},{"annotations":[92834,91251,98381],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1905534"},{"annotations":[92835],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905626"},{"annotations":[96498,89025],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990573"},{"annotations":[100705,99846],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905647"},{"annotations":[101147],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098720"},{"annotations":[95273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106082"},{"annotations":[109578,99838],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902434"},{"annotations":[107449],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901583"},{"annotations":[100169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140125"},{"annotations":[102497],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140207"},{"annotations":[95040,87961],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098721"},{"annotations":[103659,112656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071578"}]},"cv_name":"biological_process","definition":"The directed movement of some substance 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":"transmembrane transport","termid":"GO:0055085"},{"relation_name":"is_a","term_name":"import into cell","termid":"GO:0098657"}],"gene_count":38,"genes_by_uniquename":{"SJAG_00057":null,"SJAG_00296":null,"SJAG_00922":null,"SJAG_00991":null,"SJAG_01090":null,"SJAG_01353":null,"SJAG_01406":null,"SJAG_01493":null,"SJAG_01660":null,"SJAG_01983":null,"SJAG_02463":null,"SJAG_02605":null,"SJAG_02779":null,"SJAG_02780":null,"SJAG_02877":null,"SJAG_02883":null,"SJAG_02968":null,"SJAG_03591":null,"SJAG_03595":null,"SJAG_03608":null,"SJAG_03631":null,"SJAG_03777":null,"SJAG_03960":null,"SJAG_03970":null,"SJAG_04185":null,"SJAG_04246":null,"SJAG_04506":null,"SJAG_04551":null,"SJAG_04637":null,"SJAG_04668":null,"SJAG_04673":null,"SJAG_04714":null,"SJAG_04718":null,"SJAG_04830":null,"SJAG_04905":null,"SJAG_05175":null,"SJAG_05229":null,"SJAG_05346":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"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"import across plasma membrane","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"uptake","type":"broad"}],"termid":"GO:0098739","terms_by_termid":{"GO:0071578":null,"GO:0097638":null,"GO:0097639":null,"GO:0098702":null,"GO:0098703":null,"GO:0098705":null,"GO:0098708":null,"GO:0098709":null,"GO:0098710":null,"GO:0098714":null,"GO:0098715":null,"GO:0098716":null,"GO:0098717":null,"GO:0098720":null,"GO:0098721":null,"GO:0106081":null,"GO:0106082":null,"GO:0140125":null,"GO:0140206":null,"GO:0140207":null,"GO:0140270":null,"GO:0140425":null,"GO:1901583":null,"GO:1902434":null,"GO:1904679":null,"GO:1905135":null,"GO:1905136":null,"GO:1905530":null,"GO:1905533":null,"GO:1905534":null,"GO:1905589":null,"GO:1905626":null,"GO:1905647":null,"GO:1905665":null,"GO:1905949":null,"GO:1990573":null}}


id: GO:0016430
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + tRNA = S-adenosyl-L-homocysteine + tRNA containing N6-methyladenine.","definition_xrefs":["EC:2.1.1.55"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-methyltransferase activity","termid":"GO:0008170"},{"relation_name":"is_a","term_name":"tRNA (adenine) methyltransferase activity","termid":"GO:0016426"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0140101"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0140098","GO:0016740","GO:0140101","GO:0016741"],"is_obsolete":false,"name":"tRNA (adenine-N6)-methyltransferase activity","secondary_identifiers":["MetaCyc:TRNA-ADENINE-N6--METHYLTRANSFERASE-RXN","RHEA:16785"],"synonyms":[{"name":"S-adenosyl-L-methionine:tRNA (adenine-6-N-)-methyltransferase activity","type":"related"},{"name":"S-adenosyl-L-methionine:tRNA (adenine-N6-)-methyltransferase activity","type":"related"},{"name":"tRNA (adenine-N6-)-methyltransferase activity","type":"exact"}],"termid":"GO:0016430"}


id: PBO:0089559
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial translation elongation factor G Mef1","termid":"PBO:0089559"}


id: MONDO:0015097
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital aortic valve stenosis","termid":"MONDO:0017735"}],"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":"aortic valve dysplasia","secondary_identifiers":["UMLS:C0344993","ICD9:746.89","GARD:19776","MEDGEN:576679","Orphanet:101043","SCTID:253604004"],"termid":"MONDO:0015097","xrefs":{"Monarch":{"xref_id":"0015097"}}}


id: MONDO:0971058
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare bacterial infectious disease characterized by development of endothelial cell-derived, blood-filled tumors on the surface of the skin during the chronic phase of infection with Bartonella bacilliformis. The lesions can persist for months to years and may cause pain and scarring due to ulceration. They are classified as miliary (multiple red papules of <3 mm in diameter), mular (blood-filled nodules), and diffuse (groups of subdermal nodules >5 mm in diameter). Eruptions may be accompanied by fever and malaise, lymphadenopathy, acute bone and joint pains, and headache. Fatality rates during this phase are low.","definition_xrefs":["Orphanet:659759"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Oroya fever","termid":"MONDO:0018984"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"verruga peruana","termid":"MONDO:0971058","xrefs":{"Monarch":{"xref_id":"0971058"}}}


id: MONDO:0013547
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any mitochondrial proton-transporting ATP synthase complex deficiency in which the cause of the disease is a mutation in the ATP5F1E gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex deficiency","termid":"MONDO:0000066"},{"relation_name":"is_a","term_name":"mitochondrial proton-transporting ATP synthase complex deficiency","termid":"MONDO:0014471"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"mitochondrial complex V (ATP synthase) deficiency nuclear type 3","secondary_identifiers":["MEDGEN:481338","OMIM:614053","DOID:0060332","GARD:18666","UMLS:C3279708"],"synonyms":[{"name":"ATP5F1E mitochondrial proton-transporting ATP synthase complex deficiency","type":"exact"},{"name":"MC5DN3","type":"exact"},{"name":"mitochondrial Complex 5 (ATP synthase) deficiency, Atp5E type","type":"related"},{"name":"mitochondrial Complex 5 (ATP synthase) deficiency, nuclear type 3","type":"related"},{"name":"mitochondrial complex V (ATP synthase) deficiency, nuclear type 3","type":"related"},{"name":"mitochondrial proton-transporting ATP synthase complex deficiency caused by mutation in ATP5F1E","type":"exact"}],"termid":"MONDO:0013547","xrefs":{"Monarch":{"xref_id":"0013547"}}}


id: PR:O14050
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- msy2 gene.","definition_xrefs":["UniProtKB:O14050","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 MscS family protein C2C4.17c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2C4.17c","synonyms":[{"name":"Spom972h-msy2","type":"exact"}],"termid":"PR:O14050"}


id: GO:0047589
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-oxoglutarate + 5-aminopentanoate = 5-oxopentanoate + L-glutamate.","definition_xrefs":["EC:2.6.1.48","RHEA:10212"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016769"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824","GO:0016769"],"is_obsolete":false,"name":"5-aminovalerate transaminase activity","secondary_identifiers":["KEGG_REACTION:R02274","MetaCyc:VAGL-RXN"],"synonyms":[{"name":"5-aminopentanoate:2-oxoglutarate aminotransferase activity","type":"related"},{"name":"5-aminovalerate aminotransferase activity","type":"exact"},{"name":"delta-aminovalerate aminotransferase activity","type":"related"},{"name":"delta-aminovalerate transaminase activity","type":"related"}],"termid":"GO:0047589"}


id: RO:0002441
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"An interaction relationship between two organisms living together in more or less intimate association in a relationship in which one benefits and the other is unaffected (GO).","direct_ancestors":[{"relation_name":"is_a","term_name":"symbiotically_interacts_with","termid":"RO:0002440"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"commensually_interacts_with","termid":"RO:0002441"}


id: PBO:0064838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPP1R12A antisense RNA 1","termid":"PBO:0064838"}


id: PBO:0029929
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_IMP_binding","termid":"PBO:0029929"}


id: PBO:0069036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 281, pseudogene","termid":"PBO:0069036"}


id: PR:Q9UTE2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An oxygen-dependent coproporphyrinogen-III oxidase, mitochondrial that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00382","PANTHER:PTHR10755: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":"oxygen-dependent coproporphyrinogen-III oxidase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC222.11","secondary_identifiers":["UniProtKB:Q9UTE2"],"synonyms":[{"name":"COX (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Coproporphyrinogenase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-CPOX","type":"exact"},{"name":"coprogen oxidase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UTE2"}


id: PBO:0058008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3935","termid":"PBO:0058008"}


id: PBO:0108539
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 202","termid":"PBO:0108539"}


id: PBO:0079149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetraspanin 10","termid":"PBO:0079149"}


id: MONDO:0015513
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A form of endocrine system disease that is both rare and inborn.","definition_xrefs":["MONDO:patterns/rare_genetic"],"gene_count":0,"genotype_count":0,"name":"obsolete rare genetic endocrine disease (obsolete MONDO:0015513)","secondary_identifiers":["Orphanet:156638"],"synonyms":[{"name":"rare genetic endocrine system disease","type":"exact"}],"termid":"MONDO:0015513","xrefs":{"Monarch":{"xref_id":"0015513"}}}


id: SO:0000745
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"DNA belonging to the genome of a chloroplast, a green plastid for photosynthesis.","direct_ancestors":[{"relation_name":"is_a","term_name":"plastid_sequence","termid":"SO:0000740"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chloroplast_sequence","synonyms":[{"name":"chloroplast sequence","type":"exact"}],"termid":"SO:0000745"}


id: GO:0110072
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The actin-mediated process that results in contraction of the apical end of a polarized columnar epithelial cell, contributing to formation of a ventral indentation (furrow) from the blastoderm epithelium, which is internalized to form a tube in the interior of the embryo, marking the start of gastrulation.","definition_xrefs":["GOC:ha","PMID:28495958"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apical constriction involved in gastrulation","termid":"GO:0003384"},{"relation_name":"part_of","term_name":"ventral furrow formation","termid":"GO:0007370"}],"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":"apical constriction involved in ventral furrow formation","termid":"GO:0110072"}


id: PR:P87176
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- slx8 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P87176"],"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":"E3 ubiquitin-protein ligase complex slx8-rfp subunit slx8 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3D6.11c","synonyms":[{"name":"RING finger protein slx8 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RING-dependent E3 ubiquitin-protein ligase slx8 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-slx8","type":"exact"},{"name":"synthetic lethal of unknown function protein 8 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P87176"}


id: PBO:0055723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lamin B2","termid":"PBO:0055723"}


id: PBO:0026732
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_kinetochore_during_mitotic_metaphase","termid":"PBO:0026732"}


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


id: PBO:0084416
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Major apurinic/apyrimidinic endonuclease; 3'-repair diesterase; involved in repair of DNA damage by oxidation and alkylating agents; also functions as a 3'-5' exonuclease to repair 7,8-dihydro-8-oxodeoxyguanosine; genetically interacts with NTG1 to maintain mitochondrial genome integrity","termid":"PBO:0084416"}


id: PBO:0072834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sin3A associated protein 25","termid":"PBO:0072834"}


id: PBO:0038391
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-assayed_transcript","termid":"PBO:0038391"}


id: GO:1990073
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cell wall part that is the part of a wall of a vessel member and bears one or more openings (perforations).","definition_xrefs":["ISBN:0471245194","GOC:PO_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cell wall","termid":"GO:0005618"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005618"}],"interesting_parent_ids":["GO:0005618","GO:0005575"],"is_obsolete":false,"name":"perforation plate","termid":"GO:1990073"}


id: FYPO:0004968
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell growth phenotype in which vegetative cell population growth is decreased relative to normal under conditions of phosphate starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased vegetative cell population growth","termid":"FYPO:0001355"}],"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0002058","FYPO:0001985","FYPO:0002060","FYPO:0005447","FYPO:0000003","FYPO:0000139"],"is_obsolete":false,"name":"decreased vegetative cell population growth during phosphate starvation","synonyms":[{"name":"decreased vegetative cell population growth during phosphate depletion","type":"exact"},{"name":"decreased vegetative cell population growth during phosphate deprivation","type":"exact"},{"name":"decreased vegetative cell population growth during phosphate limitation","type":"exact"},{"name":"decreased vegetative cell population growth in response to phosphate starvation","type":"exact"},{"name":"reduced vegetative cell population growth during phosphate starvation","type":"exact"},{"name":"sensitive to phosphate starvation","type":"related"},{"name":"slow vegetative cell population growth during phosphate starvation","type":"narrow"}],"termid":"FYPO:0004968"}


id: MONDO:0001278
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A syndrome characterized by progressive life-threatening RESPIRATORY INSUFFICIENCY in the absence of known LUNG DISEASES, usually following a systemic insult such as surgery or major TRAUMA.","definition_xrefs":["MESH:D012128"],"gene_count":0,"genotype_count":0,"name":"obsolete adult respiratory distress syndrome (obsolete MONDO:0001278)","termid":"MONDO:0001278","xrefs":{"Monarch":{"xref_id":"0001278"}}}


id: PBO:0074945
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 109B","termid":"PBO:0074945"}


id: GO:0031784
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a melatonin receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"melatonin receptor binding","synonyms":[{"name":"melatonin receptor ligand","type":"narrow"}],"termid":"GO:0031784"}


id: PBO:0056899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIER1 transcriptional regulator","termid":"PBO:0056899"}


id: FYPO:0006821
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cells elongate more slowly than normal in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell growth rate","termid":"FYPO:0006820"}],"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:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"slow vegetative cell growth","termid":"FYPO:0006821"}


id: GO:1901646
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of synoviocyte proliferation.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of epithelial cell proliferation","termid":"GO:0050680"},{"relation_name":"is_a","term_name":"regulation of synoviocyte proliferation","termid":"GO:1901645"},{"relation_name":"negatively_regulates","term_name":"synoviocyte proliferation","termid":"GO:0002941"}],"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 synoviocyte proliferation","synonyms":[{"name":"down regulation of synoviocyte proliferation","type":"exact"},{"name":"down-regulation of synoviocyte proliferation","type":"exact"},{"name":"downregulation of synoviocyte proliferation","type":"exact"},{"name":"inhibition of synoviocyte proliferation","type":"narrow"}],"termid":"GO:1901646"}


id: GO:0061441
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of a renal artery is generated and organized. Renal arteries supply the kidneys with blood.","definition_xrefs":["GOC:mtg_kidney_jan10","PMID:11891195"],"direct_ancestors":[{"relation_name":"is_a","term_name":"artery morphogenesis","termid":"GO:0048844"},{"relation_name":"part_of","term_name":"kidney vasculature morphogenesis","termid":"GO:0061439"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"renal artery morphogenesis","termid":"GO:0061441"}


id: FYPO:0005046
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the rate, or speed, of mitotic spindle elongation is decreased, and sister chromatids do not move towards the spindle poles at the same time during mitosis prior to completion of chromosome segregation. Although one or more chromosomes remain distant from the spindle pole after the bulk of the DNA has separated, mitotic sister chromatid segregation does eventually go on to complete separation of chromosomes.","definition_xrefs":["PomBase:mah","PMID:20935472"],"direct_ancestors":[{"relation_name":"has_part","term_name":"decreased rate of mitotic spindle elongation","termid":"FYPO:0003268"},{"relation_name":"is_a","term_name":"decreased rate of mitotic spindle elongation","termid":"FYPO:0003268"},{"relation_name":"is_a","term_name":"lagging mitotic chromosomes, with complete sister chromatid separation","termid":"FYPO:0004101"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000641"},{"rel_name":"has_part","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0000337"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000054","FYPO:0000337","FYPO:0000631","FYPO:0000641","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal mitotic sister chromatid segregation with lagging chromosomes, complete sister chromatid separation, and decreased rate of mitotic spindle elongation","synonyms":[{"name":"abnormal mitotic sister chromatid segregation with lagging chromosomes, complete sister chromatid separation, and decreased rate of mitotic spindle elongation during vegetative growth","type":"exact"},{"name":"abnormal sister chromatid segregation with lagging chromosomes, complete sister chromatid separation, and decreased rate of spindle elongation during mitotic cell cycle","type":"related"},{"name":"lagging mitotic chromosomes, with complete sister chromatid separation and decreased spindle elongation rate","type":"exact"},{"name":"lagging mitotic chromosomes, with complete sister chromatid separation, and decreased rate of mitotic spindle elongation","type":"exact"},{"name":"lagging mitotic sister chromatids, with complete sister chromatid separation, and decreased rate of mitotic spindle elongation","type":"exact"}],"termid":"FYPO:0005046"}


id: PBO:0027763
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_prospore_membrane_during_meiosis_II_with_protein_mislocalized_to_plasma_membrane","termid":"PBO:0027763"}


id: PBO:0024843
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"West syndrome","termid":"PBO:0024843"}


id: PBO:0028736
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-L-selenoneine_absent_from_cell","termid":"PBO:0028736"}


id: PBO:0064050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 84","termid":"PBO:0064050"}


id: PBO:0068272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease A family member 9 (inactive)","termid":"PBO:0068272"}


id: PBO:0036271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved fungal protein, possibly DNA J domain Hua1","termid":"PBO:0036271"}


id: FYPO:0001647
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the import of L-glutamate into the cell is abnormal when the cell is subject to nitrogen starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal glutamate import","termid":"FYPO:0001646"},{"relation_name":"is_a","term_name":"abnormal amino acid import during nitrogen starvation","termid":"FYPO:0001648"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"abnormal glutamate import during nitrogen starvation","synonyms":[{"name":"abnormal L-glutamate import across plasma membrane during nitrogen starvation","type":"exact"},{"name":"abnormal L-glutamate import during nitrogen starvation","type":"exact"},{"name":"abnormal glutamate import during nitrogen depletion","type":"exact"},{"name":"abnormal glutamate import during nitrogen deprivation","type":"exact"},{"name":"abnormal glutamate import into cell during nitrogen starvation","type":"exact"},{"name":"abnormal glutamate uptake during nitrogen starvation","type":"exact"}],"termid":"FYPO:0001647"}


id: FYPO:0002609
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which histone H2A phosphorylation occurs to a lower extent than normal at centromeric outer repeat regions. All histone H2A phosphorylation may be affected, or phosphorylation of specific sites on histone H2A may be decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased histone H2A phosphorylation during vegetative growth","termid":"FYPO:0002598"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0002274","FYPO:0002494","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased histone H2A phosphorylation at centromere outer repeat during vegetative growth","synonyms":[{"name":"decreased histone H2A phosphorylation at centromere otr during vegetative growth","type":"exact"},{"name":"decreased histone H2A phosphorylation at centromere outer repeat during mitotic cell cycle","type":"related"},{"name":"decreased histone H2A phosphorylation at centromeric outer repeat region during vegetative growth","type":"exact"},{"name":"decreased histone H2A phosphorylation at pericentric region during vegetative growth","type":"related"},{"name":"decreased histone H2A phosphorylation at pericentromeric region during vegetative growth","type":"related"},{"name":"reduced histone H2A phosphorylation at centromere outer repeat during vegetative growth","type":"exact"}],"termid":"FYPO:0002609"}


id: GO:0003743
data:
  {"annotated_genes":["SJAG_00662","SJAG_03788","SJAG_03223","SJAG_04772","SJAG_00507","SJAG_01576","SJAG_03678","SJAG_01643","SJAG_04981","SJAG_03629","SJAG_03732","SJAG_01487","SJAG_04744","SJAG_02628","SJAG_02471","SJAG_02376","SJAG_01117","SJAG_03147","SJAG_01954","SJAG_05003","SJAG_00466","SJAG_03996","SJAG_01659","SJAG_04635","SJAG_02390","SJAG_04891","SJAG_00786","SJAG_04900","SJAG_03433","SJAG_03472","SJAG_02164","SJAG_02995","SJAG_02856","SJAG_02307"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[87044,89417,89454,89876,92279,94295,95375,96089,96167,96358,96738,97232,97293,97313,97889,98432,99598,99997,102122,102700,103542,104237,104794,104891,105059,105078,105087,106487,106778,110067,110153,110793,113421,115063],"is_not":false,"summary":null,"term":"GO:0003743"}]},"cv_name":"molecular_function","definition":"Functions in the initiation of ribosome-mediated translation of mRNA into a polypeptide.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translation factor activity, RNA binding","termid":"GO:0008135"}],"gene_count":34,"genes_by_uniquename":{"SJAG_00466":null,"SJAG_00507":null,"SJAG_00662":null,"SJAG_00786":null,"SJAG_01117":null,"SJAG_01487":null,"SJAG_01576":null,"SJAG_01643":null,"SJAG_01659":null,"SJAG_01954":null,"SJAG_02164":null,"SJAG_02307":null,"SJAG_02376":null,"SJAG_02390":null,"SJAG_02471":null,"SJAG_02628":null,"SJAG_02856":null,"SJAG_02995":null,"SJAG_03147":null,"SJAG_03223":null,"SJAG_03433":null,"SJAG_03472":null,"SJAG_03629":null,"SJAG_03678":null,"SJAG_03732":null,"SJAG_03788":null,"SJAG_03996":null,"SJAG_04635":null,"SJAG_04744":null,"SJAG_04772":null,"SJAG_04891":null,"SJAG_04900":null,"SJAG_04981":null,"SJAG_05003":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0045182"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0045182","GO:0003674"],"is_obsolete":false,"name":"translation initiation factor activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-72621","Reactome:R-HSA-72697","Reactome:R-HSA-72722","GO:0003744","GO:0003745"],"termid":"GO:0003743","terms_by_termid":{"GO:0003743":null}}


id: GO:1903812
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of L-serine into a cell.","definition_xrefs":["GOC:TermGenie","PMID:23895341","GO_REF:0000075"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-serine transport","termid":"GO:0015825"},{"relation_name":"is_a","term_name":"serine import across plasma membrane","termid":"GO:0098718"},{"relation_name":"is_a","term_name":"L-alpha-amino acid transmembrane transport","termid":"GO:1902475"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"L-serine import across plasma membrane","synonyms":[{"name":"L-serine import into cell","type":"exact"}],"termid":"GO:1903812"}


id: PBO:0066786
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 85","termid":"PBO:0066786"}


id: MONDO:0008696
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This syndrome is characterized by the association of acanthosis nigricans, insulin resistance, severe muscle cramps and acral hypertrophy.","definition_xrefs":["Orphanet:90301"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"diabetes mellitus","termid":"MONDO:0005015"},{"relation_name":"is_a","term_name":"acanthosis nigricans","termid":"MONDO:0007035"},{"relation_name":"is_a","term_name":"epidermal disease","termid":"MONDO:0019268"}],"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":"acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome","secondary_identifiers":["GARD:453","OMIM:200170","UMLS:C1860215","MEDGEN:348051","MESH:C536000"],"synonyms":[{"name":"acanthosis nigricans muscle cramps acral enlargement","type":"related"},{"name":"acanthosis nigricans with muscle cramps and acral enlargement","type":"related"},{"name":"familial insulin resistance with acanthosis nigricans, acral hypertrophy and muscle cramps","type":"related"}],"termid":"MONDO:0008696","xrefs":{"Monarch":{"xref_id":"0008696"}}}


id: PBO:0058916
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 12135","termid":"PBO:0058916"}


id: PBO:0040635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BARX1 divergent transcript","termid":"PBO:0040635"}


id: GO:0000159
data:
  {"annotated_genes":["SJAG_00526","SJAG_03353","SJAG_00600","SJAG_00229","SJAG_03681","SJAG_01270","SJAG_00078"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[89472,92429,97356,99087,100762,103980,115343],"is_not":false,"summary":null,"term":"GO:0000159"}]},"cv_name":"cellular_component","definition":"A protein complex that has protein serine/threonine phosphatase activity that is polycation-stimulated (PCS), being directly stimulated by protamine, polylysine, or histone H1; it constitutes a subclass of several enzymes activated by different histones and polylysine, and consists of catalytic, scaffolding, and regulatory subunits. The catalytic and scaffolding subunits form the core enzyme, and the holoenzyme also includes the regulatory subunit.","definition_xrefs":["ISBN:0198547684","GOC:mah","PMID:17245430"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine phosphatase complex","termid":"GO:0008287"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00078":null,"SJAG_00229":null,"SJAG_00526":null,"SJAG_00600":null,"SJAG_01270":null,"SJAG_03353":null,"SJAG_03681":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"protein phosphatase type 2A complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"PP2A complex","type":"exact"},{"name":"PP2A-pi","type":"narrow"},{"name":"PP2a-protector","type":"narrow"},{"name":"protein phosphatase 2 complex","type":"related"}],"termid":"GO:0000159","terms_by_termid":{"GO:0000159":null}}


id: GO:0018235
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of peptidyl-lysine to form peptidyl-N6-carboxy-L-lysine.","definition_xrefs":["RESID:AA0114"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-lysine carboxylation (obsolete GO:0018235)","termid":"GO:0018235"}


id: PBO:0031031
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_plasma_membrane_organization","termid":"PBO:0031031"}


id: PATO:0000110
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000110 drought sensitivity (obsolete PATO:0000110)","termid":"PATO:0000110"}


id: PBO:0001370
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulates sdh41","termid":"PBO:0001370"}


id: GO:0140459
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 stimulus from a Gram-positive bacterium.","definition_xrefs":["PMID:23664307"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to bacterium","termid":"GO:0009617"}],"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 Gram-positive bacterium","termid":"GO:0140459"}


id: PBO:0071259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23 pseudogene 4","termid":"PBO:0071259"}


id: PBO:0073120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine dehydratase like","termid":"PBO:0073120"}


id: FYPO:0001684
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 purvalanol A 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:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased RNA level during cellular response to purvalanol A","synonyms":[{"name":"decreased RNA accumulation during cellular response to purvalanol A","type":"related"},{"name":"decreased RNA level during cellular response to purvalanol A during mitotic cell cycle","type":"related"},{"name":"decreased RNA level during cellular response to purvalanol A during vegetative growth","type":"exact"},{"name":"decreased mRNA level during cellular response to purvalanol A","type":"narrow"},{"name":"decreased transcript level during cellular response to purvalanol A","type":"exact"},{"name":"reduced RNA level during cellular response to purvalanol A","type":"exact"}],"termid":"FYPO:0001684"}


id: MONDO:0015427
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Paroxysmal dyskinesia (PD) is a rare heterogenous group of movement disorders manifesting as abnormal involuntary movements that recur episodically and last only a brief time. PD includes paroxysmal kinesigenic dyskinesia (PKD), paroxysmal non-kinesigenic dyskinesia (PNKD), paroxysmal exertion-induced dyskinesia (PED) and a variant form of PKD, infantile convulsion and choreoathetosis (ICCA syndrome).","definition_xrefs":["Orphanet:1431"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paroxysmal dystonia","termid":"MONDO:0016058"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0003441"}],"interesting_parent_ids":["MONDO:0003441"],"is_obsolete":false,"name":"paroxysmal dyskinesia","secondary_identifiers":["MESH:D002819","SCTID:49949003","UMLS:C0752210","GARD:18721","ICD9:333.5","MEDGEN:156242"],"synonyms":[{"name":"paroxysmal choreoathetosis","type":"exact"},{"name":"paroxysmal dystonic choreoathetosis","type":"exact"}],"termid":"MONDO:0015427","xrefs":{"Monarch":{"xref_id":"0015427"}}}


id: PBO:0044081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centriolar satellite-associated tubulin polyglutamylase complex regulator 1","termid":"PBO:0044081"}


id: PBO:0110364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exosomal polycystin 1 interacting protein","termid":"PBO:0110364"}


id: PBO:0003259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S17 (predicted)","termid":"PBO:0003259"}


id: MONDO:0021523
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the pharynx.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign neoplasm","termid":"MONDO:0005165"},{"relation_name":"is_a","term_name":"pharynx neoplasm","termid":"MONDO:0021246"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of pharynx","secondary_identifiers":["MEDGEN:102296","SCTID:92293007","ICD9:210.9","NCIT:C3597","UMLS:C0153940"],"synonyms":[{"name":"benign neoplasm of the pharynx","type":"exact"},{"name":"benign pharyngeal neoplasm","type":"exact"},{"name":"benign pharyngeal tumor","type":"exact"},{"name":"benign pharyngeal tumour","type":"exact"},{"name":"benign pharynx neoplasm","type":"exact"},{"name":"benign pharynx tumor","type":"exact"},{"name":"benign pharynx tumour","type":"exact"},{"name":"benign tumor of pharynx","type":"exact"},{"name":"benign tumor of the pharynx","type":"exact"},{"name":"benign tumour of pharynx","type":"exact"},{"name":"benign tumour of the pharynx","type":"exact"},{"name":"pharyngeal neoplasm benign","type":"exact"},{"name":"pharynx benign neoplasm","type":"exact"}],"termid":"MONDO:0021523","xrefs":{"Monarch":{"xref_id":"0021523"}}}


id: GO:0006384
data:
  {"annotated_genes":["SJAG_03007","SJAG_00585","SJAG_00421","SJAG_03120","SJAG_03035","SJAG_00067","SJAG_05339","SJAG_03354","SJAG_02600","SJAG_01827","SJAG_02815"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87702,88435,95082,99079,101037,102555,106392,107902,108592,114810],"is_not":false,"summary":null,"term":"GO:0006384"},{"annotations":[115650,102554],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070898"}]},"cv_name":"biological_process","definition":"A transcription initiation process that takes place at a RNA polymerase III gene promoter. Transfer RNAs (tRNA) genes, as well as some other non-coding RNAs, are transcribed by RNA polymerase III.","definition_xrefs":["GOC:txnOH","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-templated transcription initiation","termid":"GO:0006352"},{"relation_name":"part_of","term_name":"transcription by RNA polymerase III","termid":"GO:0006383"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00067":null,"SJAG_00421":null,"SJAG_00585":null,"SJAG_01827":null,"SJAG_02600":null,"SJAG_02815":null,"SJAG_03007":null,"SJAG_03035":null,"SJAG_03120":null,"SJAG_03354":null,"SJAG_05339":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006351"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006351"],"is_obsolete":false,"name":"transcription initiation at RNA polymerase III promoter","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0001024","GO:0001036","GO:0001022","GO:0001023"],"synonyms":[{"name":"transcription initiation from Pol III promoter","type":"exact"},{"name":"transcription initiation from RNA polymerase III hybrid type promoter","type":"narrow"},{"name":"transcription initiation from RNA polymerase III promoter","type":"exact"},{"name":"transcription initiation from RNA polymerase III type 1 promoter","type":"narrow"},{"name":"transcription initiation from RNA polymerase III type 2 promoter","type":"narrow"},{"name":"transcription initiation from RNA polymerase III type 3 promoter","type":"narrow"}],"termid":"GO:0006384","terms_by_termid":{"GO:0006384":null,"GO:0070898":null}}


id: PBO:0057249
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 450b","termid":"PBO:0057249"}


id: GO:0035969
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of sterol import by activating or increasing the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:dgf","PMID:11533229"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of sterol import by positive regulation of transcription from RNA polymerase II promoter (obsolete GO:0035969)","synonyms":[{"name":"positive regulation of sterol import by activation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol import by positive regulation of transcription from Pol II promoter","type":"exact"},{"name":"positive regulation of sterol import by stimulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol import by up regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol import by up-regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol import by upregulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol influx by activation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol influx by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol influx by stimulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol influx by up regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol influx by up-regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol influx by upregulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol uptake by activation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol uptake by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol uptake by stimulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol uptake by up regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol uptake by up-regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of sterol uptake by upregulation of transcription from RNA polymerase II promoter","type":"exact"}],"termid":"GO:0035969"}


id: GO:0002327
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of an immature B cell.","definition_xrefs":["GOC:jal","ISBN:0781735149","PMID:16551251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B cell differentiation","termid":"GO:0030183"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"immature B cell differentiation","synonyms":[{"name":"immature B cell development","type":"related"},{"name":"immature B lymphocyte differentiation","type":"exact"},{"name":"immature B-cell differentiation","type":"exact"},{"name":"immature B-lymphocyte differentiation","type":"exact"}],"termid":"GO:0002327"}


id: PBO:0050547
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HPS5 biogenesis of lysosomal organelles complex 2 subunit 2","termid":"PBO:0050547"}


id: _global:sequence_of
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sequence_of","termid":"_global:sequence_of"}


id: FYPO:0002286
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 osmotic stress 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"},{"relation_name":"is_a","term_name":"altered RNA level during cellular response to osmotic stress","termid":"FYPO:0003198"}],"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":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0006551"],"is_obsolete":false,"name":"decreased RNA level during cellular response to osmotic stress","synonyms":[{"name":"decreased RNA level during cellular response to osmotic stress during mitotic cell cycle","type":"related"},{"name":"decreased RNA level during cellular response to osmotic stress during vegetative growth","type":"exact"},{"name":"decreased mRNA level during cellular response to osmotic stress","type":"narrow"},{"name":"decreased transcript level during cellular response to osmotic stress","type":"exact"},{"name":"reduced RNA level during cellular response to osmotic stress","type":"exact"}],"termid":"FYPO:0002286"}


id: GO:0019136
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + 2'-deoxynucleoside = ADP + 2'-deoxynucleoside 5'-phosphate.","definition_xrefs":["EC:2.7.1.145"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside kinase activity","termid":"GO:0019206"}],"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:0016301"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0016301","GO:0003674"],"is_obsolete":false,"name":"deoxynucleoside kinase activity","secondary_identifiers":["MetaCyc:2.7.1.145-RXN","RHEA:12140","Reactome:R-HSA-74207"],"synonyms":[{"name":"ATP:deoxynucleoside 5'-phosphotransferase activity","type":"related"},{"name":"D. melanogaster deoxynucleoside kinase activity","type":"related"},{"name":"Dm-dNK","type":"related"},{"name":"Ms-dNK activity","type":"related"},{"name":"ms-dNK","type":"related"},{"name":"multifunctional deoxynucleoside kinase activity","type":"related"},{"name":"multispecific deoxynucleoside kinase activity","type":"related"},{"name":"multisubstrate deoxyribonucleoside kinase activity","type":"related"}],"termid":"GO:0019136"}


id: PBO:0018020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor TFIIK complex complex ubiquitin-protein ligase E3 subunit, Pmh1","termid":"PBO:0018020"}


id: FYPO:0006383
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A sporulation phenotype that results in the formation of an ascus that contains spores of non-uniform size and DNA content, as well as DNA that is not contained within any of the spores. There may also be fewer than four spores.","definition_xrefs":["PomBase:vw","PomBase:mah","PMID:17632059"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal sporulation resulting in formation of ascus containing non-uniform spores","termid":"FYPO:0000913"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000121"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000121","FYPO:0000631","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abnormal sporulation resulting in formation of ascus containing non-uniform spores and unencapsulated DNA","synonyms":[{"name":"abnormal ascospore formation resulting in formation ascus containing non-uniform spores and unencapsulated DNA","type":"exact"},{"name":"abnormal sporulation resulting in formation of asci containing non-uniform spores and unencapsulated DNA","type":"related"},{"name":"abnormal sporulation resulting in formation of ascus containing non-uniform spores and DNA excluded from spores","type":"exact"}],"termid":"FYPO:0006383"}


id: SO:0002060
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A translocation where the regions involved are from different chromosomes.","definition_xrefs":["NCBI:th"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosomal_translocation","termid":"SO:1000044"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interchromosomal_translocation","termid":"SO:0002060"}


id: PBO:0068774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 11, pseudogene","termid":"PBO:0068774"}


id: PBO:0072271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S23","termid":"PBO:0072271"}


id: MOD:00916
data:
  {"annotated_genes":["SJAG_02763","SJAG_03012","SJAG_04972","SJAG_02592"],"annotation_feature_type":"gene","cv_annotations":{"PSI-MOD":[{"annotations":[118661,118662,119025,80043,80042,119026,119028,119027],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00046"},{"annotations":[79996],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00159"}]},"cv_name":"PSI-MOD","definition":"A protein modification that modifies an L-serine residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by amino acid modified","termid":"MOD:01157"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02592":null,"SJAG_02763":null,"SJAG_03012":null,"SJAG_04972":null},"genotype_count":0,"is_obsolete":false,"name":"modified L-serine residue","references_by_uniquename":{"PMID:26774782":null,"PMID:31150379":null,"PMID:36408920":null},"synonyms":[{"name":"ModSer","type":"exact"}],"termid":"MOD:00916","terms_by_termid":{"GO:0034599":null,"GO:0034605":null,"GO:0071475":null,"GO:1904547":null,"MOD:00046":null,"MOD:00159":null}}


id: GO:2001119
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a methanofuran.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"}],"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":"methanofuran metabolic process","synonyms":[{"name":"methanofuran metabolism","type":"exact"}],"termid":"GO:2001119"}


id: PBO:0080586
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat domain 11","termid":"PBO:0080586"}


id: MOD:01313
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a lysine N6-hydrogen with a quaternary amine reagent heavy (+9amu) form group.","definition_xrefs":["PubMed:11857757","Unimod:63#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"},{"relation_name":"is_a","term_name":"isotope tagged reagent derivatized residue","termid":"MOD:01426"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"quaternary amine labeling reagent heavy form (+9amu) N6-L-lysine","synonyms":[{"name":"GIST-Quat:2H(9)","type":"related"},{"name":"Quaternary amine labeling reagent heavy form (+9amu), N-term & K","type":"related"}],"termid":"MOD:01313"}


id: GO:1904974
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of heparanase activity.","definition_xrefs":["GO_REF:0000088","PMID:12927802","GOC:TermGenie","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"heparanase complex","synonyms":[{"name":"HEPS complex","type":"exact"}],"termid":"GO:1904974"}


id: PBO:0005241
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.1.1.31","termid":"PBO:0005241"}


id: PBO:0042399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell division cycle 5 like","termid":"PBO:0042399"}


id: GO:1903767
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of sweet taste receptor activity.","definition_xrefs":["GOC:TermGenie","PMID:16720576","GOC:BHF","GOC:rl","GO_REF:0000088"],"direct_ancestors":[{"relation_name":"is_a","term_name":"taste receptor complex","termid":"GO:1903768"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"sweet taste receptor complex","termid":"GO:1903767"}


id: GO:0061259
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells acquire specialized structural and/or functional features that characterize the glomerular mesangial cells of the mesonephros as it progresses from its formation to the mature state.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesonephric mesangial cell differentiation","termid":"GO:0061260"},{"relation_name":"is_a","term_name":"glomerular mesangial cell differentiation","termid":"GO:0072008"},{"relation_name":"part_of","term_name":"mesonephric glomerular mesangium development","termid":"GO:0061247"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mesonephric glomerular mesangial cell differentiation","termid":"GO:0061259"}


id: GO:0046046
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving TTP, ribosylthymine triphosphate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine ribonucleoside triphosphate metabolic process","termid":"GO:0009208"},{"relation_name":"is_a","term_name":"pyrimidine ribonucleotide metabolic process","termid":"GO:0009218"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"TTP metabolic process","synonyms":[{"name":"TTP metabolism","type":"exact"}],"termid":"GO:0046046"}


id: GO:0099620
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-4-amino-4-deoxy-beta-L-arabinopyranose + 2-oxoglutarate = UDP-beta-L-threo-pentapyranos-4-ulose + L-glutamate.","definition_xrefs":["GOC:dos","GOC:al","PMID:12429098","PMID:12704196"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016769","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"UDP-4-amino-4-deoxy-L-arabinose aminotransferase","secondary_identifiers":["EC:2.6.1.87","RHEA:24710"],"synonyms":[{"name":"UDP-(beta-L-threo-pentapyranosyl-4''-ulose diphosphate) aminotransferase","type":"exact"},{"name":"UDP-4-amino-4-deoxy-L-arabinose---oxoglutarate aminotransferase","type":"exact"},{"name":"UDP-4-amino-4-deoxy-beta-L-arabinose:2-oxoglutarate aminotransferase","type":"exact"},{"name":"UDP-Ara4O aminotransferase","type":"exact"},{"name":"UDP-L-Ara4N transaminase","type":"exact"}],"termid":"GO:0099620"}


id: PBO:0077027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thymocyte selection associated family member 2","termid":"PBO:0077027"}


id: PBO:0110471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COA1 pseudogene 1","termid":"PBO:0110471"}


id: MONDO:0002707
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An invasive adenocarcinoma of the breast characterized by the presence of islands of small and uniform cells, surrounded by large amounts of mucin. Pure mucinous breast carcinomas generally have a favorable prognosis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"invasive ductal breast carcinoma","termid":"MONDO:0004953"},{"relation_name":"is_a","term_name":"mucinous adenocarcinoma","termid":"MONDO:0004957"}],"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":"breast mucinous carcinoma","secondary_identifiers":["UMLS:C1334807","MEDGEN:235337","ONCOTREE:IMMC","SCTID:444712000","DOID:3610","NCIT:C9131"],"synonyms":[{"name":"breast invasive mixed mucinous carcinoma","type":"related"},{"name":"breast mucinous carcinoma","type":"exact"},{"name":"colloid breast carcinoma","type":"exact"},{"name":"colloid carcinoma of breast","type":"exact"},{"name":"colloid carcinoma of the breast","type":"exact"},{"name":"infiltrating colloid breast carcinoma","type":"exact"},{"name":"infiltrating mucinous breast carcinoma","type":"exact"},{"name":"invasive colloid breast carcinoma","type":"exact"},{"name":"invasive mucinous breast carcinoma","type":"exact"},{"name":"mucinous breast cancer","type":"exact"},{"name":"mucinous breast carcinoma","type":"exact"},{"name":"mucinous carcinoma of breast","type":"exact"},{"name":"mucinous carcinoma of the breast","type":"exact"}],"termid":"MONDO:0002707","xrefs":{"Monarch":{"xref_id":"0002707"}}}


id: FYECO:0000376
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed in defined medium containing pyruvate, salts and water. May be supplemented with a set of amino acids as per the auxotrophic requirements of the strain.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping defined medium","termid":"FYECO:0000013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate MM","synonyms":[{"name":"pyruvate minimal medium","type":"exact"}],"termid":"FYECO:0000376"}


id: PBO:0090219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"candidate S. pombe SPBC1A4.04 ortholog, syntenic position, intrinsically disordered protein","termid":"PBO:0090219"}


id: PBO:0031704
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_nuclear_export","termid":"PBO:0031704"}


id: MONDO:0100162
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any recessive immunodeficiency (ID), with or without ectodermal dysplasia (EDA), in which the cause of the disease is mutation in the IKBKG gene. ID/EDA-ID patients, always males, are hemizygous for an IKBKG (NEMO) mutation that preserves residual NF-κB activation (hypomorphic mutations) and may also present with osteopetrosis and lymphoedema (OL-EDA-ID).","definition_xrefs":["PMID:35163099","PMID:11047757"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"IKBKG-related immunodeficiency with or without ectodermal dysplasia","synonyms":[{"name":"NEMO related ID/EDA-ID","type":"exact"}],"termid":"MONDO:0100162","xrefs":{"Monarch":{"xref_id":"0100162"}}}


id: GO:0021877
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into a neuron that resides in the forebrain.","definition_xrefs":["GOC:dgh","GOC:dph","GOC:jid","GO_REF:0000021","PMID:16226447","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron fate commitment","termid":"GO:0048663"},{"relation_name":"part_of","term_name":"forebrain neuron differentiation","termid":"GO:0021879"}],"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":"forebrain neuron fate commitment","termid":"GO:0021877"}


id: MONDO:0043135
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"blindness (disorder)","termid":"MONDO:0001941"},{"relation_name":"is_a","term_name":"microphthalmia","termid":"MONDO:0021129"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"microcephaly microphthalmos blindness","secondary_identifiers":["MESH:C537541","MEDGEN:419434","UMLS:C2931526"],"termid":"MONDO:0043135","xrefs":{"Monarch":{"xref_id":"0043135"}}}


id: PBO:0075676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spexin hormone","termid":"PBO:0075676"}


id: PBO:0083184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps the Ty1 long terminal repeat, YPRWdelta12","termid":"PBO:0083184"}


id: PBO:0002051
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin-like protein Pkl1","termid":"PBO:0002051"}


id: GO:0051437
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates, maintains or increases the rate of ubiquitin ligase activity that contributes to the regulation of the mitotic cell cycle phase transition.","definition_xrefs":["GOC:ai","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of ubiquitin-protein ligase activity involved in regulation of mitotic cell cycle transition (obsolete GO:0051437)","synonyms":[{"name":"activation of ubiquitin ligase activity during mitotic cell cycle","type":"narrow"},{"name":"mitotic SCF complex activator","type":"narrow"},{"name":"mitotic ubiquitin ligase activator","type":"narrow"},{"name":"positive regulation of ubiquitin ligase activity during mitotic cell cycle","type":"related"},{"name":"positive regulation of ubiquitin-protein ligase activity during mitotic cell cycle","type":"related"},{"name":"stimulation of ubiquitin ligase activity during mitotic cell cycle","type":"narrow"},{"name":"up regulation of ubiquitin ligase activity during mitotic cell cycle","type":"related"},{"name":"up-regulation of ubiquitin ligase activity during mitotic cell cycle","type":"related"},{"name":"upregulation of ubiquitin ligase activity during mitotic cell cycle","type":"related"}],"termid":"GO:0051437"}


id: MONDO:0044273
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hypertension, diastolic, resistance to (obsolete MONDO:0044273)","secondary_identifiers":["OMIM:608622"],"synonyms":[{"name":"hypertension, diastolic, resistance to","type":"related"}],"termid":"MONDO:0044273","xrefs":{"Monarch":{"xref_id":"0044273"}}}


id: MONDO:0030987
data:
  {"annotated_genes":["SJAG_00363"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85091],"is_not":false,"summary":null,"term":"MONDO:0030987"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00363":null},"genotype_count":0,"is_obsolete":false,"name":"vertebral, cardiac, tracheoesophageal, renal, and limb defects","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619227","MEDGEN:1788069","UMLS:C5543189"],"synonyms":[{"name":"VCTERL","type":"exact"},{"name":"VCTERL syndrome","type":"exact"}],"termid":"MONDO:0030987","terms_by_termid":{"MONDO:0030987":null},"xrefs":{"Monarch":{"xref_id":"0030987"}}}


id: PBO:0085903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; may be involved in responding to conditions of stress; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies; protein abundance increases in response to DNA replication stress","termid":"PBO:0085903"}


id: GO:0120268
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a paraflagellar rod, a large lattice-like axial structure found in some flagellated protists which extends alongside the axoneme.","definition_xrefs":["PMID:23787017","GOC:krc","PMID:32295845","GOC:ach"],"direct_ancestors":[{"relation_name":"is_a","term_name":"motile cilium assembly","termid":"GO:0044458"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"paraflagellar rod assembly","synonyms":[{"name":"PFR assembly","type":"related"},{"name":"paraflagellar rod biogenesis","type":"exact"},{"name":"paraflagellar rod formation","type":"exact"}],"termid":"GO:0120268"}


id: FYPO:0001435
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 erythromycin.","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:0002057"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0002058","FYPO:0000003","FYPO:0000257","FYPO:0000139","FYPO:0002060","FYPO:0002057"],"is_obsolete":false,"name":"normal growth on erythromycin","synonyms":[{"name":"normal cell population growth in presence of erythromycin","type":"exact"},{"name":"normal cell population growth on erythromycin","type":"exact"},{"name":"normal cellular response to erythromycin","type":"related"},{"name":"normal vegetative cell population growth on erythromycin","type":"exact"}],"termid":"FYPO:0001435"}


id: MONDO:0003647
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 flaccid tympanic membrane","secondary_identifiers":["UMLS:C0155470","MEDGEN:509982","ICD9:384.81","DOID:5781","SCTID:38645004"],"termid":"MONDO:0003647","xrefs":{"Monarch":{"xref_id":"0003647"}}}


id: PBO:0090620
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER membrane protein complex subunit Emc6","termid":"PBO:0090620"}


id: SO:0000611
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A pyrimidine rich sequence near the 3' end of an intron to which the 5'end becomes covalently bound during nuclear splicing. The resulting structure resembles a lariat.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal_intron_region","termid":"SO:0000841"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"branch_site","synonyms":[{"name":"branch point","type":"exact"},{"name":"branch site","type":"exact"},{"name":"branch_point","type":"exact"}],"termid":"SO:0000611"}


id: MONDO:0002833
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare transitional cell carcinoma that arises from the fallopian tube.","definition_xrefs":["NCIT:C40104"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fallopian tube carcinoma","termid":"MONDO:0006206"},{"relation_name":"is_a","term_name":"transitional cell carcinoma","termid":"MONDO:0006474"}],"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":"fallopian tube transitional cell carcinoma","secondary_identifiers":["DOID:4008","MEDGEN:274492","UMLS:C1517128"],"synonyms":[{"name":"fallopian tube transitional cell cancer","type":"exact"},{"name":"fallopian tube transitional cell carcinoma","type":"exact"}],"termid":"MONDO:0002833","xrefs":{"Monarch":{"xref_id":"0002833"}}}


id: MONDO:0018174
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary glaucoma is a clinically diverse group of rare eye disorders with genetic predisposition characterized by elevated intraocular pressure (IOP) and glaucomatous changes of the optic nerve head, leading to field defects, visual loss and blindness. Hereditary glaucoma can be sub-classified as primary (congenital glaucoma, juvenile glaucoma) or secondary according to the presence or absence of systemic or other ocular anomalies (iridogoniodysgenesis, Stickler syndrome, Coats syndrome). The clinical presentation is variable and is based on age, severity of glaucoma, presence of ocular abnormalities and development of secondary IOP related abnormalities.","definition_xrefs":["Orphanet:359"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete non-syndromic developmental defect of the eye (obsolete MONDO:0015217)","termid":"MONDO:0015217"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"glaucoma","termid":"MONDO:0005041"}],"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":"hereditary glaucoma","secondary_identifiers":["GARD:2486","UMLS:C3711383","MEDGEN:777991","MESH:C580055"],"synonyms":[{"name":"glaucoma, hereditary","type":"related"},{"name":"hereditary glaucoma (disease)","type":"exact"}],"termid":"MONDO:0018174","xrefs":{"Monarch":{"xref_id":"0018174"}}}


id: MONDO:0850115
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":"early-onset obesity-hyperphagia-severe developmental delay syndrome","secondary_identifiers":["Orphanet:99704","GARD:19685"],"termid":"MONDO:0850115","xrefs":{"Monarch":{"xref_id":"0850115"}}}


id: GO:0035717
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to chemokine (C-C motif) ligand 7.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-C chemokine binding","termid":"GO:0019957"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"chemokine (C-C motif) ligand 7 binding","synonyms":[{"name":"CCL7 binding","type":"exact"}],"termid":"GO:0035717"}


id: PBO:0072207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S18 pseudogene 6","termid":"PBO:0072207"}


id: MONDO:0008981
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This syndrome is characterized by intellectual deficit, calcification of the choroid plexus, and elevated levels of cerebrospinal fluid (CSF) protein. It has been described in two sibships from two unrelated families. The seven children of one of the sibships were born to consanguineous parents. Some patients also had strabismus, hyperactive deep tendon reflexes and foot deformities.","definition_xrefs":["Orphanet:1313"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infantile choroidocerebral calcification syndrome","secondary_identifiers":["OMIM:215480","SCTID:724228005","UMLS:C1859092","MESH:C535357","GARD:1313","MEDGEN:395174"],"synonyms":[{"name":"Choroido-cerebral calcification syndrome with retardation","type":"related"},{"name":"choroid plexus calcification and intellectual disability","type":"related"},{"name":"choroid plexus calcification and mental retardation","type":"related"},{"name":"choroid plexus calcification with intellectual disability","type":"related"},{"name":"choroid plexus calcification with mental retardation","type":"related"}],"termid":"MONDO:0008981","xrefs":{"Monarch":{"xref_id":"0008981"}}}


id: PBO:0009639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudouridine-metabolizing bifunctional protein (predicted)","termid":"PBO:0009639"}


id: GO:0071113
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alphaIIb-beta3 integrin complex bound to the cell adhesion molecule ICAM-4.","definition_xrefs":["PMID:12477717"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005886"],"is_obsolete":false,"name":"alphaIIb-beta3 integrin-ICAM-4 complex","synonyms":[{"name":"ITGAIIb-ITGB3-ICAM4 complex","type":"narrow"}],"termid":"GO:0071113"}


id: FYPO:0000615
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of progression through S phase of the mitotic cell cycle is shorter than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic S phase progression","termid":"FYPO:0000610"},{"relation_name":"is_a","term_name":"decreased duration of mitotic cell cycle phase","termid":"FYPO:0001070"}],"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:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000631","FYPO:0001320","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased duration of mitotic S phase","synonyms":[{"name":"decreased duration of S phase during mitotic cell cycle","type":"exact"},{"name":"decreased duration of mitotic S phase during vegetative growth","type":"exact"},{"name":"mitotic cell cycle progression in S phase: increased rate","type":"related"},{"name":"reduced duration of mitotic S phase","type":"exact"}],"termid":"FYPO:0000615"}


id: FYPO:0004206
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of mature snRNA measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered snRNA or precursor level","termid":"FYPO:0005997"},{"relation_name":"is_a","term_name":"increased ncRNA level during vegetative growth","termid":"FYPO:0008146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"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:0001320","FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0006551"],"is_obsolete":false,"name":"increased mature snRNA level","synonyms":[{"name":"increased mature small nuclear RNA level","type":"exact"},{"name":"increased mature snRNA accumulation","type":"related"},{"name":"increased mature snRNA level during mitotic cell cycle","type":"related"},{"name":"increased mature snRNA level during vegetative growth","type":"exact"},{"name":"increased mature snRNA transcript level","type":"broad"},{"name":"increased snRNA level","type":"broad"}],"termid":"FYPO:0004206"}


id: MONDO:0030439
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 57","secondary_identifiers":["DOID:0112338","MEDGEN:1794198","UMLS:C5561988","OMIM:619528"],"synonyms":[{"name":"SPGF57","type":"exact"}],"termid":"MONDO:0030439","xrefs":{"Monarch":{"xref_id":"0030439"}}}


id: PBO:0053166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"liver enriched antimicrobial peptide 2","termid":"PBO:0053166"}


id: SO:0001315
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"N6_acetyladenosine is a modified adenosine.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_adenosine","termid":"SO:0001273"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N6_acetyladenosine","secondary_identifiers":["RNAMOD:102"],"synonyms":[{"name":"N6 acetyladenosine","type":"exact"},{"name":"N6-acetyladenosine","type":"exact"},{"name":"ac6A","type":"exact"}],"termid":"SO:0001315"}


id: PBO:0017903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rad18 homolog ubiquitin protein ligase E3, Rhp18","termid":"PBO:0017903"}


id: PBO:0074935
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 102","termid":"PBO:0074935"}


id: FYPO:0009089
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of higher concentrations of sodium chloride and sodium dodecyl sulfate than normal.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002682"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0005447","FYPO:0002682","FYPO:0000139","FYPO:0001985"],"is_obsolete":false,"name":"resistance to sodium chloride and sodium dodecyl sulfate","synonyms":[{"name":"resistance to sodium chloride and SDS","type":"exact"},{"name":"resistance to sodium chloride and SDS during vegetative growth","type":"exact"},{"name":"resistance to sodium chloride and SDS in combination","type":"exact"},{"name":"resistance to sodium chloride and sodium dodecyl sulfate during mitotic cell cycle","type":"related"},{"name":"resistance to sodium chloride and sodium dodecyl sulfate during vegetative growth","type":"exact"},{"name":"resistance to sodium chloride and sodium dodecyl sulfate in combination","type":"exact"},{"name":"resistant to sodium chloride and SDS","type":"exact"},{"name":"resistant to sodium chloride and sodium dodecyl sulfate","type":"exact"}],"termid":"FYPO:0009089"}


id: MONDO:0018189
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome is a rare, genetic, slowly progressive neurodegenerative disease characterized by delayed psychomotor development beginning in infancy, mild to profound intellectual disability, gait and stance ataxia, pyramidal signs (hyperreflexia, extensor plantar responses), dysarthria, and ocular abnormalities (e.g. nystagmus, oculomotor apraxia, abduction deficits, esotropia, ptosis). Brain imaging reveals progressive, generalized cerebellar atrophy, mild ventriculomegaly and, in some, retrocerebellar cysts.","definition_xrefs":["Orphanet:363429"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of amino acid transport","termid":"MONDO:0019216"},{"relation_name":"is_a","term_name":"autosomal recessive metabolic cerebellar ataxia","termid":"MONDO:0020044"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome","secondary_identifiers":["MEDGEN:1644588","GARD:17556","UMLS:C4706388"],"termid":"MONDO:0018189","xrefs":{"Monarch":{"xref_id":"0018189"}}}


id: PBO:0078324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"triadin","termid":"PBO:0078324"}


id: GO:0051126
data:
  {"annotated_genes":["SJAG_03455"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90387],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034316"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of actin nucleation, the initial step in the formation of an actin filament in which actin monomers combine to form a new filament.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin nucleation","termid":"GO:0051125"},{"relation_name":"is_a","term_name":"negative regulation of cytoskeleton organization","termid":"GO:0051494"},{"relation_name":"is_a","term_name":"negative regulation of supramolecular fiber organization","termid":"GO:1902904"},{"relation_name":"negatively_regulates","term_name":"actin nucleation","termid":"GO:0045010"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03455":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0008150","GO:0030036","GO:0007010"],"is_obsolete":false,"name":"negative regulation of actin nucleation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of actin nucleation","type":"exact"},{"name":"down-regulation of actin nucleation","type":"exact"},{"name":"downregulation of actin nucleation","type":"exact"},{"name":"inhibition of actin nucleation","type":"narrow"}],"termid":"GO:0051126","terms_by_termid":{"GO:0034316":null}}


id: PBO:0028289
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cadmium_ion_import_into_vacuole","termid":"PBO:0028289"}


id: MONDO:0013787
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":"psychomotor retardation, epilepsy, and craniofacial dysmorphism","secondary_identifiers":["MEDGEN:482685","OMIM:614501","UMLS:C3281055"],"synonyms":[{"name":"PMRED","type":"related"},{"name":"neurodevelopmental disorder with hypotonia, craniofacial abnormalities, and seizures","type":"exact"},{"name":"psychomotor retardation, epilepsy, and craniofacial dysmorphism","type":"exact"}],"termid":"MONDO:0013787","xrefs":{"Monarch":{"xref_id":"0013787"}}}


id: SO:0000681
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript that has been processed \\\"incorrectly\\\", for example by the failure of splicing of one or more exons.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript","termid":"SO:0000673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aberrant_processed_transcript","synonyms":[{"name":"aberrant processed transcript","type":"exact"}],"termid":"SO:0000681"}


id: PBO:0047998
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fyn related Src family tyrosine kinase","termid":"PBO:0047998"}


id: PATO:0000804
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000804 motor performance value (obsolete PATO:0000804)","termid":"PATO:0000804"}


id: PBO:0043593
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collagen type XXIII alpha 1 chain","termid":"PBO:0043593"}


id: PBO:0068515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 107, pseudogene","termid":"PBO:0068515"}


id: PBO:0053535
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 537","termid":"PBO:0053535"}


id: PBO:0045977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EH domain containing 3","termid":"PBO:0045977"}


id: PBO:0052532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kallikrein related peptidase 5","termid":"PBO:0052532"}


id: MONDO:0017506
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Congenital absence/hypoplasia of thumb, unilateral is a rare developmental defect during embryogenesis characterized by the unilateral underdevelopment of the thumb, ranging from a slight decrease in thumb size to complete absence of the thumb.","definition_xrefs":["Orphanet:295110"],"gene_count":0,"genotype_count":0,"name":"obsolete congenital absence/hypoplasia of thumb, unilateral (obsolete MONDO:0017506)","synonyms":[{"name":"thumb hypodactyly, unilateral","type":"exact"},{"name":"thumb oligodactyly, unilateral","type":"exact"}],"termid":"MONDO:0017506","xrefs":{"Monarch":{"xref_id":"0017506"}}}


id: PATO:0000239
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000239 blinking reflex (obsolete PATO:0000239)","termid":"PATO:0000239"}


id: PBO:0075016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 115-27","termid":"PBO:0075016"}


id: GO:0071024
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A ribonucleoprotein complex that contains spliced leader (SL) RNA and associated proteins.","definition_xrefs":["ISBN:0879697393","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal snRNP complex","termid":"GO:0097525"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005634"],"is_obsolete":false,"name":"SL snRNP","termid":"GO:0071024"}


id: MONDO:0018478
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete primary hyperoxaluria (obsolete MONDO:0018478)","termid":"MONDO:0018478","xrefs":{"Monarch":{"xref_id":"0018478"}}}


id: GO:1990039
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Specialized part of the smooth endoplasmic reticulum that closely underlies the plasma membrane, usually within 60 nm or closer.","definition_xrefs":["ISBN:0195065719","NIF_Subcellular:sao1634374950"],"direct_ancestors":[{"relation_name":"is_a","term_name":"smooth endoplasmic reticulum cisterna","termid":"GO:0120082"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005783","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"hypolemmal cisterna","synonyms":[{"name":"hypolemmal cisternae","type":"exact"}],"termid":"GO:1990039"}


id: PBO:0042933
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell growth regulator with ring finger domain 1","termid":"PBO:0042933"}


id: PBO:0044389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 2 subfamily B member 6","termid":"PBO:0044389"}


id: MONDO:0007930
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A Bernard-Soulier syndrome characterized by autosomal dominant inheritance of mild to moderate bleeding tendency, thrombocytopenia, and an increased mean platelet size that has material basis in heterozygous mutations in the GP1BA gene on chromosome 17p.","definition_xrefs":["PMID:1730088","PMID:11222377","DOID:0111059"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Bernard-Soulier syndrome","termid":"MONDO:0009276"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"Bernard-Soulier syndrome, type A2, autosomal dominant","secondary_identifiers":["OMIM:153670","MEDGEN:478706","GARD:15082","UMLS:C3277076"],"synonyms":[{"name":"BSSA2","type":"exact"},{"name":"Bernard-Soulier syndrome type A2","type":"related"},{"name":"Bernard-Soulier syndrome, type A2 (dominant)","type":"exact"},{"name":"Bernard-Soulier syndrome, type A2, autosomal dominant","type":"exact"}],"termid":"MONDO:0007930","xrefs":{"Monarch":{"xref_id":"0007930"}}}


id: PBO:0055339
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 2767","termid":"PBO:0055339"}


id: PBO:0047699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FLYWCH family member 2","termid":"PBO:0047699"}


id: PBO:0053682
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 869","termid":"PBO:0053682"}


id: PR:Q10221
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rng8 gene.","definition_xrefs":["UniProtKB:Q10221","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 C4H3.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4H3.14c","synonyms":[{"name":"Spom972h-rng8","type":"exact"}],"termid":"PR:Q10221"}


id: GO:0140894
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by a ligand binding to an endolysosomal pattern recognition receptor (PRR) of the toll-like family. PRRs bind pathogen-associated molecular pattern (PAMPs), structures conserved among microbial species.","definition_xrefs":["PMID:29679565"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic pattern recognition receptor signaling pathway","termid":"GO:0002753"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"endolysosomal toll-like receptor signaling pathway","synonyms":[{"name":"endolysosomal pattern recognition receptor signaling pathway","type":"exact"}],"termid":"GO:0140894"}


id: PBO:0085517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein component of the small (40S) ribosomal subunit; homologous to mammalian ribosomal protein S18 and bacterial S13; RPS18A has a paralog, RPS18B, that arose from the whole genome duplication; protein increases in abundance and relocalizes from cytoplasm to nuclear foci upon DNA replication stress","termid":"PBO:0085517"}


id: PBO:0085354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phospholipid translocase (flippase); involved in generating phospholipid asymmetry in the plasma membrane; involved in endocytosis, vacuolar biogenesis and Golgi-to-ER vesicle-mediated transport; localizes to endosomes and the Golgi apparatus","termid":"PBO:0085354"}


id: MONDO:0011425
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dilated cardiomyopathy that has material basis in variation in the chromosome region 2q14-q22.","definition_xrefs":["PMID:10486326","DOID:0110429"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial dilated cardiomyopathy","termid":"MONDO:0016333"}],"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":"dilated cardiomyopathy 1H","secondary_identifiers":["OMIM:604288","GARD:15365","MESH:C536277","UMLS:C1858591","MEDGEN:348980"],"synonyms":[{"name":"CMD1H","type":"exact"},{"name":"cardiomyopathy, dilated, 1H","type":"related"},{"name":"cardiomyopathy, dilated, with conduction defect","type":"related"},{"name":"dilated cardiomyopathy type 1H","type":"exact"},{"name":"dilated cardiomyopathy with conduction defect","type":"exact"}],"termid":"MONDO:0011425","xrefs":{"Monarch":{"xref_id":"0011425"}}}


id: PR:P32834
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sxa1 gene.","definition_xrefs":["UniProtKB:P32834","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":"aspartic proteinase sxa1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC26A3.01","synonyms":[{"name":"Spom972h-sxa1","type":"exact"}],"termid":"PR:P32834"}


id: PBO:0066986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 289","termid":"PBO:0066986"}


id: MONDO:0022559
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A central nervous system vasculitis that has a benign course, with acute onset of neurologic symptoms, usually in the form of severe headache and/or a focal neurologic event.","definition_xrefs":["PMID:17043471"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system vasculitis","termid":"MONDO:0003346"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign angiitis of the central nervous system","secondary_identifiers":["GARD:8704"],"synonyms":[{"name":"BACNS","type":"related"}],"termid":"MONDO:0022559","xrefs":{"Monarch":{"xref_id":"0022559"}}}


id: PR:O43071
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A pre-mRNA-processing factor 17 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03361","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":"pre-mRNA-processing factor 17 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC6B1.10","secondary_identifiers":["UniProtKB:O43071"],"synonyms":[{"name":"Spom972h-CDC40","type":"exact"}],"termid":"PR:O43071"}


id: PBO:0000131
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4.1.1.1","termid":"PBO:0000131"}


id: GO:0031806
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a G protein-coupled (metabotropic) histamine receptor.","definition_xrefs":["GOC:nln","PMID:12679144","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"G protein-coupled histamine receptor binding","synonyms":[{"name":"G-protein coupled histamine receptor binding","type":"exact"},{"name":"metabotropic histamine receptor binding","type":"exact"},{"name":"metabotropic histamine receptor ligand","type":"narrow"}],"termid":"GO:0031806"}


id: PBO:0075260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 18 pseudogene 13","termid":"PBO:0075260"}


id: GO:0010529
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that decreases the frequency, rate or extent of transposition. Transposition results in the movement of discrete segments of DNA between nonhomologous sites.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of transposition (obsolete GO:0010529)","termid":"GO:0010529"}


id: GO:0005829
data:
  {"annotated_genes":["SJAG_03797","SJAG_01789","SJAG_04953","SJAG_05033","SJAG_03575","SJAG_04751","SJAG_04960","SJAG_03528","SJAG_01740","SJAG_03722","SJAG_02905","SJAG_01784","SJAG_02275","SJAG_02647","SJAG_01667","SJAG_02769","SJAG_00972","SJAG_02041","SJAG_01545","SJAG_03732","SJAG_02570","SJAG_01737","SJAG_03556","SJAG_01635","SJAG_01186","SJAG_04334","SJAG_04352","SJAG_01974","SJAG_01580","SJAG_01590","SJAG_02058","SJAG_02549","SJAG_00822","SJAG_04274","SJAG_01182","SJAG_02342","SJAG_00476","SJAG_03950","SJAG_03955","SJAG_04175","SJAG_01291","SJAG_00117","SJAG_04845","SJAG_07013","SJAG_00208","SJAG_02833","SJAG_01528","SJAG_01652","SJAG_03352","SJAG_04357","SJAG_01083","SJAG_04404","SJAG_04427","SJAG_05240","SJAG_02304","SJAG_04726","SJAG_01666","SJAG_00586","SJAG_04651","SJAG_02876","SJAG_03012","SJAG_02558","SJAG_01317","SJAG_00938","SJAG_03082","SJAG_00702","SJAG_01822","SJAG_00840","SJAG_03098","SJAG_01858","SJAG_01198","SJAG_02803","SJAG_01733","SJAG_04276","SJAG_03847","SJAG_04977","SJAG_00331","SJAG_04452","SJAG_04177","SJAG_02026","SJAG_00686","SJAG_00095","SJAG_02082","SJAG_05179","SJAG_03431","SJAG_02885","SJAG_01500","SJAG_00321","SJAG_03937","SJAG_01370","SJAG_00674","SJAG_02763","SJAG_00245","SJAG_01900","SJAG_02794","SJAG_02770","SJAG_04747","SJAG_01599","SJAG_03262","SJAG_04168","SJAG_03540","SJAG_05228","SJAG_00364","SJAG_02121","SJAG_02671","SJAG_00382","SJAG_05256","SJAG_05024","SJAG_01489","SJAG_02811","SJAG_02786","SJAG_02426","SJAG_02098","SJAG_01270","SJAG_02753","SJAG_01995","SJAG_01841","SJAG_00704","SJAG_03364","SJAG_03802","SJAG_04554","SJAG_04198","SJAG_02323","SJAG_01436","SJAG_02189","SJAG_03959","SJAG_00414","SJAG_04563","SJAG_00508","SJAG_03971","SJAG_04107","SJAG_03074","SJAG_04549","SJAG_04332","SJAG_02186","SJAG_00988","SJAG_04366","SJAG_04595","SJAG_00958","SJAG_05011","SJAG_04534","SJAG_02562","SJAG_03313","SJAG_02245","SJAG_00461","SJAG_00226","SJAG_04626","SJAG_01341","SJAG_04938","SJAG_01284","SJAG_00164","SJAG_01850","SJAG_01799","SJAG_02419","SJAG_00229","SJAG_00067","SJAG_04634","SJAG_04461","SJAG_05223","SJAG_01487","SJAG_02681","SJAG_04890","SJAG_00532","SJAG_04495","SJAG_04577","SJAG_05195","SJAG_03346","SJAG_00037","SJAG_02973","SJAG_01768","SJAG_01360","SJAG_04763","SJAG_01430","SJAG_01269","SJAG_00937","SJAG_01502","SJAG_04539","SJAG_04083","SJAG_00173","SJAG_01622","SJAG_03486","SJAG_04051","SJAG_00692","SJAG_00678","SJAG_04062","SJAG_05023","SJAG_02166","SJAG_01662","SJAG_05332","SJAG_04306","SJAG_03845","SJAG_00441","SJAG_03883","SJAG_02627","SJAG_03631","SJAG_04972","SJAG_03246","SJAG_00890","SJAG_01630","SJAG_02718","SJAG_02851","SJAG_01333","SJAG_03915","SJAG_00806","SJAG_00289","SJAG_02180","SJAG_03630","SJAG_01000","SJAG_02233","SJAG_01786","SJAG_04400","SJAG_04878","SJAG_00176","SJAG_02663","SJAG_00125","SJAG_02474","SJAG_01646","SJAG_03087","SJAG_01680","SJAG_04033","SJAG_03340","SJAG_02783","SJAG_04285","SJAG_00150","SJAG_03717","SJAG_02203","SJAG_00778","SJAG_01565","SJAG_01762","SJAG_04016","SJAG_02096","SJAG_03624","SJAG_00758","SJAG_02755","SJAG_00491","SJAG_04204","SJAG_00251","SJAG_02191","SJAG_03264","SJAG_00397","SJAG_03638","SJAG_00469","SJAG_04249","SJAG_04476","SJAG_00326","SJAG_04270","SJAG_00561","SJAG_02214","SJAG_03067","SJAG_02347","SJAG_03977","SJAG_02414","SJAG_02481","SJAG_04324","SJAG_00707","SJAG_00401","SJAG_01721","SJAG_02268","SJAG_00464","SJAG_00337","SJAG_03376","SJAG_04082","SJAG_00457","SJAG_02376","SJAG_00234","SJAG_01540","SJAG_00102","SJAG_02840","SJAG_01501","SJAG_02465","SJAG_00749","SJAG_00788","SJAG_03548","SJAG_02878","SJAG_00567","SJAG_03588","SJAG_02604","SJAG_04029","SJAG_04161","SJAG_04449","SJAG_03409","SJAG_02695","SJAG_01187","SJAG_01054","SJAG_02995","SJAG_01231","SJAG_02235","SJAG_04724","SJAG_03852","SJAG_02069","SJAG_00423","SJAG_01817","SJAG_04535","SJAG_03660","SJAG_02288","SJAG_04653","SJAG_03219","SJAG_04901","SJAG_03306","SJAG_01338","SJAG_04266","SJAG_02482","SJAG_02093","SJAG_02022","SJAG_03197","SJAG_02270","SJAG_01274","SJAG_02785","SJAG_02070","SJAG_02335","SJAG_06592","SJAG_03487","SJAG_03210","SJAG_02467","SJAG_01610","SJAG_05018","SJAG_02582","SJAG_03062","SJAG_02043","SJAG_03627","SJAG_04112","SJAG_02490","SJAG_02992","SJAG_02421","SJAG_01533","SJAG_01277","SJAG_01621","SJAG_00490","SJAG_00504","SJAG_00823","SJAG_01535","SJAG_01055","SJAG_02664","SJAG_02042","SJAG_02336","SJAG_00114","SJAG_00376","SJAG_03634","SJAG_01228","SJAG_03380","SJAG_01122","SJAG_02182","SJAG_03857","SJAG_02009","SJAG_02684","SJAG_01248","SJAG_00903","SJAG_04465","SJAG_02503","SJAG_02726","SJAG_04458","SJAG_04927","SJAG_03383","SJAG_02226","SJAG_04344","SJAG_01386","SJAG_01897","SJAG_01266","SJAG_03886","SJAG_01942","SJAG_03374","SJAG_03762","SJAG_04190","SJAG_04150","SJAG_04242","SJAG_01199","SJAG_00474","SJAG_03921","SJAG_02315","SJAG_02700","SJAG_04548","SJAG_00729","SJAG_02358","SJAG_00178","SJAG_04335","SJAG_04771","SJAG_01449","SJAG_02750","SJAG_04842","SJAG_00126","SJAG_01447","SJAG_01151","SJAG_04536","SJAG_02309","SJAG_00430","SJAG_04704","SJAG_00120","SJAG_03107","SJAG_00033","SJAG_00128","SJAG_03263","SJAG_00574","SJAG_04181","SJAG_00803","SJAG_04188","SJAG_01372","SJAG_02184","SJAG_01774","SJAG_04091","SJAG_01477","SJAG_00632","SJAG_00696","SJAG_01366","SJAG_04487","SJAG_03041","SJAG_01694","SJAG_00572","SJAG_00931","SJAG_02038","SJAG_03623","SJAG_05007","SJAG_05283","SJAG_00487","SJAG_04157","SJAG_04990","SJAG_04863","SJAG_04848","SJAG_02366","SJAG_00805","SJAG_07017","SJAG_00768","SJAG_01020","SJAG_02016","SJAG_05211","SJAG_03665","SJAG_02524","SJAG_01575","SJAG_02197","SJAG_03159","SJAG_05214","SJAG_03475","SJAG_02181","SJAG_01058","SJAG_01191","SJAG_05008","SJAG_02871","SJAG_04774","SJAG_04007","SJAG_02364","SJAG_00341","SJAG_03407","SJAG_04130","SJAG_02988","SJAG_02210","SJAG_03127","SJAG_03457","SJAG_00447","SJAG_02950","SJAG_04030","SJAG_03890","SJAG_05926","SJAG_02075","SJAG_04921","SJAG_04511","SJAG_04383","SJAG_03345","SJAG_01434","SJAG_01759","SJAG_00661","SJAG_00223","SJAG_02017","SJAG_01663","SJAG_02551","SJAG_00596","SJAG_00214","SJAG_02198","SJAG_02285","SJAG_01313","SJAG_04126","SJAG_05290","SJAG_01012","SJAG_02546","SJAG_00682","SJAG_03432","SJAG_01375","SJAG_00219","SJAG_04036","SJAG_04077","SJAG_03924","SJAG_02801","SJAG_00971","SJAG_02178","SJAG_01018","SJAG_04936","SJAG_03632","SJAG_02655","SJAG_04182","SJAG_06599","SJAG_03743","SJAG_00325","SJAG_00045","SJAG_03668","SJAG_01704","SJAG_03614","SJAG_04093","SJAG_02251","SJAG_02822","SJAG_00786","SJAG_02682","SJAG_01870","SJAG_02605","SJAG_01251","SJAG_02572","SJAG_01361","SJAG_04744","SJAG_03601","SJAG_01385","SJAG_04311","SJAG_03045","SJAG_00443","SJAG_02044","SJAG_04275","SJAG_04618","SJAG_04579","SJAG_00317","SJAG_01240","SJAG_00983","SJAG_00801","SJAG_03658","SJAG_02107","SJAG_01839","SJAG_02808","SJAG_02619","SJAG_01698","SJAG_02256","SJAG_01167","SJAG_04011","SJAG_01625","SJAG_00435","SJAG_00843","SJAG_02339","SJAG_01146","SJAG_00656","SJAG_00092","SJAG_03049","SJAG_02164","SJAG_00041","SJAG_04176","SJAG_02442","SJAG_01901","SJAG_04544","SJAG_02321","SJAG_05019","SJAG_03373","SJAG_02998","SJAG_04470","SJAG_00526","SJAG_03113","SJAG_04516","SJAG_04681","SJAG_03357","SJAG_00512","SJAG_03781","SJAG_01467","SJAG_02282","SJAG_00605","SJAG_04453","SJAG_00777","SJAG_03258","SJAG_02725","SJAG_01808","SJAG_03423","SJAG_00622","SJAG_01997","SJAG_05185","SJAG_04197","SJAG_03371","SJAG_01697","SJAG_00827","SJAG_02594","SJAG_03998","SJAG_03856","SJAG_05337","SJAG_03238","SJAG_03760","SJAG_01562","SJAG_01760","SJAG_00742","SJAG_02854","SJAG_04935","SJAG_02540","SJAG_02814","SJAG_02485","SJAG_01070","SJAG_01864","SJAG_02861","SJAG_03678","SJAG_00629","SJAG_03055","SJAG_02870","SJAG_00728","SJAG_01775","SJAG_02712","SJAG_01783","SJAG_04155","SJAG_03356","SJAG_04944","SJAG_00482","SJAG_03872","SJAG_04100","SJAG_01024","SJAG_00720","SJAG_05329","SJAG_02894","SJAG_03576","SJAG_00871","SJAG_02307","SJAG_02470","SJAG_01261","SJAG_03884","SJAG_04021","SJAG_02819","SJAG_01184","SJAG_01497","SJAG_00320","SJAG_04253","SJAG_03863","SJAG_04403","SJAG_04629","SJAG_00800","SJAG_01825","SJAG_02748","SJAG_01561","SJAG_03086","SJAG_00355","SJAG_02491","SJAG_04347","SJAG_01587","SJAG_03901","SJAG_00103","SJAG_00040","SJAG_05260","SJAG_01039","SJAG_00384","SJAG_03323","SJAG_02505","SJAG_00203","SJAG_03495","SJAG_03501","SJAG_04192","SJAG_03811","SJAG_03320","SJAG_03017","SJAG_00718","SJAG_00467","SJAG_03485","SJAG_02300","SJAG_03403","SJAG_01833","SJAG_01628","SJAG_02237","SJAG_00468","SJAG_05346","SJAG_02994","SJAG_00736","SJAG_02747","SJAG_01510","SJAG_03603","SJAG_03753","SJAG_03554","SJAG_02462","SJAG_03108","SJAG_05694","SJAG_05978","SJAG_01213","SJAG_03005","SJAG_00898","SJAG_01259","SJAG_03791","SJAG_02857","SJAG_04652","SJAG_02145","SJAG_03276","SJAG_02891","SJAG_04638","SJAG_00986","SJAG_00044","SJAG_01908","SJAG_01788","SJAG_00859","SJAG_03794","SJAG_03229","SJAG_02213","SJAG_02224","SJAG_04148","SJAG_00533","SJAG_03694","SJAG_00237","SJAG_02479","SJAG_04459","SJAG_03404","SJAG_00432","SJAG_02522","SJAG_00748","SJAG_01346","SJAG_00738","SJAG_00739","SJAG_01617","SJAG_02890","SJAG_00471","SJAG_01748","SJAG_04611","SJAG_05216","SJAG_00039","SJAG_03096","SJAG_04159","SJAG_00424","SJAG_05413","SJAG_04682","SJAG_01722","SJAG_00314","SJAG_00756","SJAG_03225","SJAG_00115","SJAG_01641","SJAG_04628","SJAG_02066","SJAG_05000","SJAG_01665","SJAG_01064","SJAG_01544","SJAG_03051","SJAG_03350","SJAG_00038","SJAG_02477","SJAG_04129","SJAG_03186","SJAG_03293","SJAG_03690","SJAG_00207","SJAG_01869","SJAG_00074","SJAG_00290","SJAG_00338","SJAG_02313","SJAG_00224","SJAG_03257","SJAG_03693","SJAG_01117","SJAG_03616","SJAG_00808","SJAG_02294","SJAG_02768","SJAG_05343","SJAG_01714","SJAG_03211","SJAG_03990","SJAG_01418","SJAG_03321","SJAG_02790","SJAG_04032","SJAG_02921","SJAG_02791","SJAG_04693","SJAG_02428","SJAG_04042","SJAG_01632","SJAG_04674","SJAG_02379","SJAG_01175","SJAG_02869","SJAG_04454","SJAG_01655","SJAG_02886","SJAG_03653","SJAG_01142","SJAG_00298","SJAG_01650","SJAG_03726","SJAG_03367","SJAG_03188","SJAG_03035","SJAG_16457","SJAG_01944","SJAG_04666","SJAG_01690","SJAG_01810","SJAG_00509","SJAG_03821","SJAG_01609","SJAG_01425","SJAG_02498","SJAG_03888","SJAG_00505","SJAG_02193","SJAG_01135","SJAG_05184","SJAG_02959","SJAG_00129","SJAG_02380","SJAG_02535","SJAG_00188","SJAG_04201","SJAG_03789","SJAG_02327","SJAG_00243","SJAG_00272","SJAG_00053","SJAG_02699","SJAG_01342","SJAG_02864","SJAG_03922","SJAG_05303","SJAG_00719","SJAG_00301","SJAG_01287","SJAG_02541","SJAG_02405","SJAG_02589","SJAG_04144","SJAG_00248","SJAG_00352","SJAG_04338","SJAG_04399","SJAG_03835","SJAG_03166","SJAG_03500","SJAG_02597","SJAG_03525","SJAG_02230","SJAG_03659","SJAG_04617","SJAG_01958","SJAG_00036","SJAG_04871","SJAG_02954","SJAG_02349","SJAG_03868","SJAG_00455","SJAG_02091","SJAG_04586","SJAG_00995","SJAG_04519","SJAG_00004","SJAG_01658","SJAG_04978","SJAG_00306","SJAG_00427","SJAG_03009","SJAG_02874","SJAG_00524","SJAG_01475","SJAG_02756","SJAG_04824","SJAG_03179","SJAG_01702","SJAG_04108","SJAG_03131","SJAG_00137","SJAG_03128","SJAG_04089","SJAG_03529","SJAG_04609","SJAG_03507","SJAG_03142","SJAG_02040","SJAG_02517","SJAG_00529","SJAG_02630","SJAG_04477","SJAG_04289","SJAG_01202","SJAG_00147","SJAG_00489","SJAG_01943","SJAG_04002","SJAG_01003","SJAG_02736","SJAG_00991","SJAG_04660","SJAG_01598","SJAG_02154","SJAG_03558","SJAG_03335","SJAG_04499","SJAG_02573","SJAG_03132","SJAG_04943","SJAG_02314","SJAG_02715","SJAG_00645","SJAG_02741","SJAG_03799","SJAG_02065","SJAG_02752","SJAG_03010","SJAG_01081","SJAG_02211","SJAG_02225","SJAG_01364","SJAG_03224","SJAG_04282","SJAG_01153","SJAG_02215","SJAG_00585","SJAG_02799","SJAG_01596","SJAG_04858","SJAG_01521","SJAG_05277","SJAG_03786","SJAG_01126","SJAG_02408","SJAG_00309","SJAG_00978","SJAG_02608","SJAG_03214","SJAG_03673","SJAG_04312","SJAG_01181","SJAG_04219","SJAG_04463","SJAG_01328","SJAG_04912","SJAG_01027","SJAG_02926","SJAG_01708","SJAG_01679","SJAG_02518","SJAG_04877","SJAG_00947","SJAG_02788","SJAG_00987","SJAG_01529","SJAG_04170","SJAG_04118","SJAG_02172","SJAG_03798","SJAG_03144","SJAG_02673","SJAG_02618","SJAG_02266","SJAG_04735","SJAG_03629","SJAG_00591","SJAG_00614","SJAG_03243","SJAG_04172","SJAG_02945","SJAG_03839","SJAG_00256","SJAG_00374","SJAG_04290","SJAG_04573","SJAG_00762","SJAG_02370","SJAG_02277","SJAG_02004","SJAG_04084","SJAG_01618","SJAG_02745","SJAG_00333","SJAG_02720","SJAG_02868","SJAG_02267","SJAG_04072","SJAG_00615","SJAG_04163","SJAG_04475","SJAG_01376","SJAG_03124","SJAG_02771","SJAG_02923","SJAG_04429","SJAG_03508","SJAG_00964","SJAG_02951","SJAG_03893","SJAG_04079","SJAG_02046","SJAG_00221","SJAG_00283","SJAG_04408","SJAG_02843","SJAG_02194","SJAG_04484","SJAG_00366","SJAG_00864","SJAG_05232","SJAG_04390","SJAG_02024","SJAG_00908","SJAG_02367","SJAG_01519","SJAG_01512","SJAG_03164","SJAG_02461","SJAG_02439","SJAG_04656","SJAG_00820","SJAG_00113","SJAG_03470","SJAG_01917","SJAG_04939","SJAG_00440","SJAG_02887","SJAG_01675","SJAG_01608","SJAG_01443","SJAG_03278","SJAG_02292","SJAG_02337","SJAG_06621","SJAG_01827","SJAG_01218","SJAG_00112","SJAG_04663","SJAG_00712","SJAG_02828","SJAG_02283","SJAG_00246","SJAG_02218","SJAG_00746","SJAG_02400","SJAG_03771","SJAG_05029","SJAG_03544","SJAG_03136","SJAG_02585","SJAG_04394","SJAG_05266","SJAG_01296","SJAG_02845","SJAG_04480","SJAG_03492","SJAG_04183","SJAG_00594","SJAG_00726","SJAG_04728","SJAG_03250","SJAG_02422","SJAG_05334","SJAG_07000","SJAG_02687","SJAG_04505","SJAG_01163","SJAG_02057","SJAG_03681","SJAG_01676","SJAG_04541","SJAG_00296","SJAG_02766","SJAG_01255","SJAG_00390","SJAG_03193","SJAG_01222","SJAG_05276","SJAG_03561","SJAG_04232","SJAG_03408","SJAG_00724","SJAG_03562","SJAG_01216","SJAG_04261","SJAG_05243","SJAG_02436","SJAG_01387","SJAG_00343","SJAG_04501","SJAG_02013","SJAG_00577","SJAG_00963","SJAG_01488","SJAG_04567","SJAG_00179","SJAG_00069","SJAG_00287","SJAG_00189","SJAG_01673","SJAG_16460","SJAG_00921","SJAG_00166","SJAG_00791","SJAG_03122","SJAG_00324","SJAG_02425","SJAG_02138","SJAG_03482","SJAG_00765","SJAG_03469","SJAG_00400","SJAG_01992","SJAG_05252","SJAG_04764","SJAG_03375","SJAG_04482","SJAG_04474","SJAG_01508","SJAG_02151","SJAG_03626","SJAG_00206","SJAG_00381","SJAG_02593","SJAG_04837","SJAG_03580","SJAG_02813","SJAG_00169","SJAG_00181","SJAG_02279","SJAG_04160","SJAG_00172","SJAG_01362","SJAG_00479","SJAG_01134","SJAG_01605","SJAG_04679","SJAG_01809","SJAG_02858","SJAG_04650","SJAG_01428","SJAG_03793","SJAG_00694","SJAG_05304","SJAG_04894","SJAG_01302","SJAG_07014","SJAG_00059","SJAG_01397","SJAG_00573","SJAG_01132","SJAG_01320","SJAG_04491","SJAG_00925","SJAG_03384","SJAG_00230","SJAG_00578","SJAG_01209","SJAG_04174","SJAG_00881","SJAG_00795","SJAG_01787","SJAG_06576","SJAG_06270","SJAG_01812","SJAG_02450","SJAG_03137","SJAG_02760","SJAG_02234","SJAG_03312","SJAG_01166","SJAG_02515","SJAG_02997","SJAG_02863","SJAG_00663","SJAG_00072","SJAG_05193","SJAG_01014","SJAG_03879","SJAG_04472","SJAG_03545","SJAG_01047","SJAG_04817","SJAG_01664","SJAG_04263","SJAG_04631","SJAG_03172","SJAG_04847","SJAG_01325","SJAG_02512","SJAG_00660","SJAG_04202","SJAG_04762","SJAG_04587","SJAG_03723","SJAG_00365","SJAG_04902","SJAG_02596","SJAG_05248","SJAG_02850","SJAG_00420","SJAG_06588","SJAG_02591","SJAG_00644","SJAG_03537","SJAG_01840","SJAG_03498","SJAG_01918","SJAG_03697","SJAG_04131","SJAG_04932","SJAG_03081","SJAG_03036","SJAG_03688","SJAG_01547","SJAG_00942","SJAG_00503","SJAG_00571","SJAG_01457","SJAG_02005","SJAG_00537","SJAG_00967","SJAG_03185","SJAG_01955","SJAG_00242","SJAG_00480","SJAG_00190","SJAG_05312","SJAG_02253","SJAG_01643","SJAG_01720","SJAG_02798","SJAG_03663","SJAG_00463","SJAG_03907","SJAG_03130","SJAG_03810","SJAG_00637","SJAG_05331","SJAG_02061","SJAG_00027","SJAG_00683","SJAG_02978","SJAG_01987","SJAG_01481","SJAG_02207","SJAG_00422","SJAG_04128","SJAG_01154","SJAG_02352","SJAG_02034","SJAG_03896","SJAG_04784","SJAG_04380","SJAG_05287","SJAG_03936","SJAG_03158","SJAG_02289","SJAG_01824","SJAG_01053","SJAG_04776","SJAG_04009","SJAG_02731","SJAG_01016","SJAG_00144","SJAG_02938","SJAG_03963","SJAG_01479","SJAG_00135","SJAG_04227","SJAG_03425","SJAG_02542","SJAG_03949","SJAG_01161","SJAG_02764","SJAG_02374","SJAG_04672","SJAG_01087","SJAG_04897","SJAG_03021","SJAG_00743","SJAG_03597","SJAG_00498","SJAG_04758","SJAG_01310","SJAG_02486","SJAG_00850","SJAG_02702","SJAG_04486","SJAG_03532","SJAG_04015","SJAG_04213","SJAG_04417","SJAG_04106","SJAG_04220","SJAG_04342","SJAG_03551","SJAG_04031","SJAG_03881","SJAG_03254","SJAG_04397","SJAG_02020","SJAG_04069","SJAG_01131","SJAG_02243","SJAG_02904","SJAG_03718","SJAG_04309","SJAG_00280","SJAG_01852","SJAG_03620","SJAG_04988","SJAG_04114","SJAG_02176","SJAG_01744","SJAG_00990","SJAG_00449","SJAG_01149","SJAG_00145","SJAG_04320","SJAG_04027","SJAG_01734","SJAG_04020","SJAG_04859","SJAG_02679","SJAG_01079","SJAG_00662","SJAG_02667","SJAG_01938","SJAG_01844","SJAG_05003","SJAG_01383","SJAG_02146","SJAG_02510","SJAG_01089","SJAG_02030","SJAG_01548","SJAG_02520","SJAG_01805","SJAG_04473","SJAG_00359","SJAG_04518","SJAG_03983","SJAG_02659","SJAG_01461","SJAG_03761","SJAG_04778","SJAG_03095","SJAG_00960","SJAG_01172","SJAG_03519","SJAG_03547","SJAG_03714","SJAG_03424","SJAG_00228","SJAG_01624","SJAG_01496","SJAG_03223","SJAG_01686","SJAG_05210","SJAG_01455","SJAG_02895","SJAG_03230","SJAG_03488","SJAG_02713","SJAG_04581","SJAG_01531","SJAG_02774","SJAG_03102","SJAG_01411","SJAG_03248","SJAG_02206","SJAG_00167","SJAG_02866","SJAG_04466","SJAG_03013","SJAG_03472","SJAG_00052","SJAG_04843","SJAG_04457","SJAG_03592","SJAG_02600","SJAG_03533","SJAG_03571","SJAG_03026","SJAG_03319","SJAG_03089","SJAG_04070","SJAG_03019","SJAG_00035","SJAG_01074","SJAG_01522","SJAG_01444","SJAG_04665","SJAG_05009","SJAG_00327","SJAG_00902","SJAG_04987","SJAG_03309","SJAG_03085","SJAG_00560","SJAG_01772","SJAG_04580","SJAG_02453","SJAG_02531","SJAG_01776","SJAG_04187","SJAG_01885","SJAG_00916","SJAG_04123","SJAG_03245","SJAG_03140","SJAG_02456","SJAG_04612","SJAG_03433","SJAG_01002","SJAG_04410","SJAG_04264","SJAG_01339","SJAG_00293","SJAG_03682","SJAG_01629","SJAG_02789","SJAG_00956","SJAG_06636","SJAG_04891","SJAG_04431","SJAG_04303","SJAG_04003","SJAG_03570","SJAG_00689","SJAG_02696","SJAG_03336","SJAG_04559","SJAG_01367","SJAG_00413","SJAG_01293","SJAG_03204","SJAG_04125","SJAG_02508","SJAG_01979","SJAG_04414","SJAG_00940","SJAG_02817","SJAG_04658","SJAG_02306","SJAG_02434","SJAG_01581","SJAG_03072","SJAG_00155","SJAG_01986","SJAG_00550","SJAG_04092","SJAG_01128","SJAG_02723","SJAG_04695","SJAG_02280","SJAG_04649","SJAG_01214","SJAG_00957","SJAG_00969","SJAG_04248","SJAG_03891","SJAG_01185","SJAG_04974","SJAG_05015","SJAG_02704","SJAG_03775","SJAG_04436","SJAG_04156","SJAG_04710","SJAG_00379","SJAG_05027","SJAG_00141","SJAG_04946","SJAG_00541","SJAG_04013","SJAG_04846","SJAG_02733","SJAG_00483","SJAG_01283","SJAG_00143","SJAG_03581","SJAG_01351","SJAG_02509","SJAG_02977","SJAG_04980","SJAG_04970","SJAG_00894","SJAG_04287","SJAG_02692","SJAG_02320","SJAG_00162","SJAG_03703","SJAG_00821","SJAG_04765","SJAG_00579","SJAG_04948","SJAG_07011","SJAG_03034","SJAG_04818","SJAG_02116","SJAG_03473","SJAG_01472","SJAG_04055","SJAG_00377","SJAG_00980","SJAG_04907","SJAG_00281","SJAG_04354","SJAG_04520","SJAG_03291","SJAG_01088","SJAG_04235","SJAG_04478","SJAG_01382","SJAG_00244","SJAG_03605","SJAG_03679","SJAG_02902","SJAG_01235","SJAG_01482","SJAG_03958","SJAG_03708","SJAG_02269","SJAG_03684","SJAG_00592","SJAG_02386","SJAG_03758","SJAG_01127","SJAG_03002","SJAG_03499","SJAG_01474","SJAG_03463","SJAG_01644","SJAG_00885","SJAG_02444","SJAG_00034","SJAG_00531","SJAG_04760","SJAG_02329","SJAG_02015","SJAG_02611","SJAG_02340","SJAG_00609","SJAG_03091","SJAG_03818","SJAG_04337","SJAG_03859","SJAG_00832","SJAG_00954","SJAG_00733","SJAG_00436","SJAG_04434","SJAG_04841","SJAG_03231","SJAG_00584","SJAG_04214","SJAG_04551","SJAG_04999","SJAG_04268","SJAG_04292","SJAG_05032","SJAG_04300","SJAG_00091","SJAG_04097","SJAG_03825","SJAG_04211","SJAG_00486","SJAG_03677","SJAG_00779","SJAG_02170","SJAG_03106","SJAG_04044","SJAG_01193","SJAG_02281","SJAG_02048","SJAG_04633","SJAG_01061","SJAG_01556","SJAG_04381","SJAG_06612","SJAG_03689","SJAG_01322","SJAG_01797","SJAG_01292","SJAG_04928","SJAG_01693","SJAG_01853","SJAG_03720","SJAG_00378","SJAG_03090","SJAG_04169","SJAG_04825","SJAG_01794","SJAG_00856","SJAG_02148","SJAG_03285","SJAG_02738","SJAG_03889","SJAG_04849","SJAG_04844","SJAG_04023","SJAG_00107","SJAG_01515","SJAG_01137","SJAG_01914","SJAG_00563","SJAG_00757","SJAG_03876","SJAG_03662","SJAG_02569","SJAG_03865","SJAG_01830","SJAG_04043","SJAG_02493","SJAG_00084","SJAG_02689","SJAG_04299","SJAG_02553","SJAG_03523","SJAG_04711","SJAG_04865","SJAG_02672","SJAG_04713","SJAG_01801","SJAG_00118","SJAG_04968","SJAG_01631","SJAG_03454","SJAG_00527","SJAG_01651","SJAG_01656","SJAG_01148","SJAG_01886","SJAG_02697","SJAG_02404","SJAG_02174","SJAG_03174","SJAG_03504","SJAG_04963","SJAG_04460","SJAG_01432","SJAG_02177","SJAG_04969","SJAG_03704","SJAG_02010","SJAG_04998","SJAG_02734","SJAG_00955","SJAG_01408","SJAG_03029","SJAG_00534","SJAG_00690","SJAG_03651","SJAG_04699","SJAG_02375","SJAG_00521","SJAG_01566","SJAG_02171","SJAG_02106","SJAG_05197","SJAG_05222","SJAG_01453","SJAG_02852","SJAG_04012","SJAG_02424","SJAG_04496","SJAG_00252","SJAG_04350","SJAG_01949","SJAG_02592","SJAG_03233","SJAG_00917","SJAG_04920","SJAG_01118","SJAG_01114","SJAG_04657","SJAG_01022","SJAG_04273","SJAG_00989","SJAG_00854","SJAG_03277","SJAG_04355","SJAG_00858","SJAG_03326","SJAG_04655","SJAG_00501","SJAG_02081","SJAG_03541","SJAG_00910","SJAG_04861","SJAG_00485","SJAG_00599","SJAG_02499","SJAG_00764","SJAG_01588","SJAG_03730","SJAG_03964","SJAG_01440","SJAG_01203","SJAG_03756","SJAG_04531","SJAG_03815","SJAG_02609","SJAG_00948","SJAG_00993","SJAG_00495","SJAG_03272","SJAG_03849","SJAG_01197","SJAG_01404","SJAG_04870","SJAG_01703","SJAG_02740","SJAG_03022","SJAG_01874","SJAG_03153","SJAG_01859","SJAG_04060","SJAG_02796","SJAG_04271","SJAG_01194","SJAG_04166","SJAG_02576","SJAG_03617","SJAG_02912","SJAG_04866","SJAG_01010","SJAG_02393","SJAG_05230","SJAG_04343","SJAG_01207","SJAG_04385","SJAG_02047","SJAG_04874","SJAG_02471","SJAG_01826","SJAG_02369","SJAG_00202","SJAG_00798","SJAG_03411","SJAG_01312","SJAG_03568","SJAG_03934","SJAG_00807","SJAG_04085","SJAG_04212","SJAG_00514","SJAG_04407","SJAG_00766","SJAG_04066","SJAG_04304","SJAG_04814","SJAG_03189","SJAG_03862","SJAG_01121","SJAG_00546","SJAG_02357","SJAG_03237","SJAG_04700","SJAG_02802","SJAG_02645","SJAG_01298","SJAG_04950","SJAG_00409","SJAG_05333","SJAG_00814","SJAG_00249","SJAG_03279","SJAG_01042","SJAG_01238","SJAG_01311","SJAG_02561","SJAG_00316","SJAG_03696","SJAG_00450","SJAG_01365","SJAG_03014","SJAG_05225","SJAG_01791","SJAG_00706","SJAG_04772","SJAG_03398","SJAG_02956","SJAG_00518","SJAG_02297","SJAG_03438","SJAG_03854","SJAG_01072","SJAG_00049","SJAG_01267","SJAG_00975","SJAG_01746","SJAG_01458","SJAG_00670","SJAG_00869","SJAG_00093","SJAG_02879","SJAG_02497","SJAG_03828","SJAG_01543","SJAG_01710","SJAG_00419","SJAG_04815","SJAG_03377","SJAG_02911","SJAG_01252","SJAG_01480","SJAG_01354","SJAG_03751","SJAG_00796","SJAG_02035","SJAG_03453","SJAG_03422","SJAG_04375","SJAG_02640","SJAG_04121","SJAG_03434","SJAG_03882","SJAG_01742","SJAG_01245","SJAG_00065","SJAG_04256","SJAG_02401","SJAG_00968","SJAG_00581","SJAG_04602","SJAG_00918","SJAG_04326","SJAG_04746","SJAG_00685","SJAG_05208","SJAG_04885","SJAG_03855","SJAG_03070","SJAG_00356","SJAG_03043","SJAG_02000","SJAG_04234","SJAG_01358","SJAG_00161","SJAG_04022","SJAG_02610","SJAG_03094","SJAG_01030","SJAG_04233","SJAG_04371","SJAG_03151","SJAG_03919","SJAG_04917","SJAG_00853","SJAG_04565","SJAG_00439","SJAG_03063","SJAG_01637","SJAG_02583","SJAG_00668","SJAG_01162","SJAG_00611","SJAG_02390","SJAG_04481","SJAG_02415","SJAG_01919","SJAG_03325","SJAG_05316","SJAG_02179","SJAG_04360","SJAG_01659","SJAG_01492","SJAG_01765","SJAG_05314","SJAG_04153","SJAG_00815","SJAG_01898","SJAG_01308","SJAG_00941","SJAG_01075","SJAG_00100","SJAG_02063","SJAG_04756","SJAG_03182","SJAG_04754","SJAG_03266","SJAG_02805","SJAG_01611","SJAG_04455","SJAG_02730","SJAG_00809","SJAG_03298","SJAG_03892","SJAG_05206","SJAG_05205","SJAG_00032","SJAG_04286","SJAG_06355","SJAG_01576","SJAG_05261","SJAG_03119","SJAG_00063","SJAG_04283","SJAG_03701","SJAG_01781","SJAG_03227","SJAG_01233","SJAG_06440","SJAG_05351","SJAG_02265","SJAG_01715","SJAG_00580","SJAG_02797","SJAG_01926","SJAG_01268","SJAG_01620","SJAG_00119","SJAG_03805","SJAG_00220","SJAG_03706","SJAG_04388","SJAG_03494","SJAG_00839","SJAG_04627","SJAG_04896","SJAG_03476","SJAG_01438","SJAG_03534","SJAG_01226","SJAG_04540","SJAG_02012","SJAG_03669","SJAG_00191","SJAG_00472","SJAG_00466","SJAG_03838","SJAG_00270","SJAG_01427","SJAG_02601","SJAG_05030","SJAG_04709","SJAG_02378","SJAG_03037","SJAG_04827","SJAG_04590","SJAG_03126","SJAG_03986","SJAG_03133","SJAG_03288","SJAG_04368","SJAG_03618","SJAG_02575","SJAG_02387","SJAG_01229","SJAG_01937","SJAG_00523","SJAG_05004","SJAG_03589","SJAG_01136","SJAG_00350","SJAG_03215","SJAG_02101","SJAG_02135","SJAG_00507","SJAG_03549","SJAG_02746","SJAG_01220","SJAG_01389","SJAG_02918","SJAG_03267","SJAG_04074","SJAG_01026","SJAG_03241","SJAG_02239","SJAG_04521","SJAG_04025","SJAG_01279","SJAG_00857","SJAG_04879","SJAG_04147","SJAG_00653","SJAG_02240","SJAG_02169","SJAG_03479","SJAG_03692","SJAG_03996","SJAG_02728","SJAG_04467","SJAG_04981","SJAG_04741","SJAG_04688","SJAG_03686","SJAG_01516","SJAG_04297","SJAG_04372","SJAG_00624","SJAG_04973","SJAG_00353","SJAG_00888","SJAG_01910","SJAG_04781","SJAG_05010","SJAG_02688","SJAG_03209","SJAG_02312","SJAG_02648","SJAG_01150","SJAG_02547","SJAG_03782","SJAG_02033","SJAG_03655","SJAG_02621","SJAG_04369","SJAG_01352","SJAG_00106","SJAG_04888","SJAG_00395","SJAG_05014","SJAG_00913","SJAG_02165","SJAG_04379","SJAG_00837","SJAG_02295","SJAG_04088","SJAG_04783","SJAG_02889","SJAG_01851","SJAG_00600","SJAG_01558","SJAG_02202","SJAG_02686","SJAG_02708","SJAG_04384","SJAG_05192","SJAG_03191","SJAG_02972","SJAG_03349","SJAG_00104","SJAG_01371","SJAG_03733","SJAG_00225","SJAG_02420","SJAG_04109","SJAG_03283","SJAG_01696","SJAG_01645","SJAG_02506","SJAG_01551","SJAG_01954","SJAG_00184","SJAG_03354","SJAG_02580","SJAG_06309","SJAG_04966","SJAG_03150","SJAG_00874","SJAG_02812","SJAG_00982","SJAG_04229","SJAG_01139","SJAG_00892","SJAG_01379","SJAG_03932","SJAG_03222","SJAG_04307","SJAG_02231","SJAG_01818","SJAG_03582","SJAG_01314","SJAG_04607","SJAG_03752","SJAG_02287","SJAG_03666","SJAG_00691","SJAG_01159","SJAG_03842","SJAG_02290","SJAG_04964","SJAG_00544","SJAG_03784","SJAG_00878","SJAG_01568","SJAG_03362","SJAG_03643","SJAG_04359","SJAG_06622","SJAG_02661","SJAG_05021","SJAG_00134","SJAG_04191","SJAG_01063","SJAG_01384","SJAG_03275","SJAG_01301","SJAG_00043","SJAG_04291","SJAG_00465","SJAG_03234","SJAG_03181","SJAG_03903","SJAG_04086","SJAG_01884","SJAG_04456","SJAG_00186","SJAG_03788","SJAG_01359","SJAG_03167","SJAG_02749","SJAG_03646","SJAG_00633","SJAG_05245","SJAG_02502","SJAG_00642","SJAG_01499","SJAG_00269","SJAG_02984","SJAG_04179","SJAG_04061","SJAG_02595","SJAG_01582","SJAG_02271","SJAG_03147","SJAG_01415","SJAG_00448","SJAG_02705","SJAG_01048","SJAG_01534","SJAG_03228","SJAG_04054","SJAG_03527","SJAG_05253","SJAG_02832","SJAG_02625","SJAG_00845","SJAG_05198","SJAG_03361","SJAG_01335","SJAG_03455","SJAG_02441","SJAG_00811","SJAG_04880","SJAG_02765"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[56864,57612,58245,58682,58838,58870,59148,59228,59284,59768,60293,60294,60811,60812,61208,61230,61854,62227,63598,63985,64028,65093,65456,65550,65645,65920,65962,65963,65964,66094,66095,66515,67131,68165,68473,68474,68652,70154,72516,74190,74841,75137,75448,75584,75684,76645,78022,78543,78758,79007,79107,79211,79851,86900,86923,86949,86958,86980,86985,86988,86999,87031,87039,87049,87098,87099,87116,87132,87147,87155,87165,87170,87188,87189,87228,87244,87249,87257,87280,87298,87303,87312,87321,87334,87354,87361,87424,87431,87435,87458,87478,87486,87491,87505,87512,87523,87561,87587,87591,87642,87687,87693,87705,87715,87733,87740,87751,87753,87807,87812,87816,87824,87835,87853,87865,87872,87874,87878,87900,87920,87935,87964,87994,88001,88018,88026,88031,88043,88046,88073,88082,88089,88095,88101,88115,88135,88141,88155,88156,88170,88191,88192,88204,88211,88222,88241,88245,88251,88252,88286,88292,88297,88312,88317,88324,88347,88355,88367,88384,88392,88404,88425,88432,88475,88479,88483,88530,88570,88666,88705,88714,88720,88745,88766,88812,88817,88833,88855,88882,88886,88895,88899,88905,88920,88925,88935,88943,88974,88981,88993,89013,89037,89052,89055,89082,89097,89114,89121,89148,89155,89160,89181,89189,89202,89207,89225,89240,89251,89261,89285,89290,89297,89304,89309,89334,89345,89368,89396,89404,89408,89412,89429,89436,89447,89458,89526,89533,89590,89603,89628,89677,89680,89696,89702,89711,89722,89734,89745,89746,89763,89790,89811,89821,89831,89839,89845,89861,89869,89900,89912,89917,89938,89943,89945,89952,89968,90057,90062,90071,90072,90098,90114,90120,90134,90142,90156,90163,90175,90184,90204,90221,90228,90257,90264,90276,90315,90336,90350,90373,90384,90393,90442,90449,90480,90486,90497,90511,90517,90518,90529,90530,90531,90556,90557,90572,90577,90582,90587,90602,90610,90642,90666,90700,90714,90722,90742,90757,90763,90768,90792,90815,90827,90833,90863,90873,90912,90936,90945,90947,90957,90963,90966,90979,90986,90997,91005,91030,91051,91057,91071,91078,91083,91087,91108,91121,91123,91156,91168,91177,91201,91212,91234,91258,91276,91281,91319,91341,91375,91384,91392,91425,91438,91461,91475,91486,91499,91502,91509,91521,91531,91589,91593,91607,91614,91620,91630,91641,91677,91693,91706,91711,91714,91719,91725,91729,91737,91771,91791,91803,91839,91849,91859,91870,91919,91943,91950,91965,91970,91973,91979,91983,91984,92006,92014,92020,92028,92100,92139,92164,92169,92175,92192,92195,92210,92265,92273,92307,92315,92323,92342,92351,92365,92372,92380,92389,92411,92418,92426,92435,92441,92457,92472,92480,92495,92510,92516,92517,92526,92535,92567,92592,92606,92623,92624,92635,92668,92675,92714,92736,92748,92756,92761,92788,92795,92806,92817,92824,92848,92851,92861,92882,92889,92894,92898,92905,92917,92929,92948,92950,92952,92964,92975,92985,92988,92994,93001,93005,93021,93022,93036,93045,93075,93076,93087,93095,93096,93097,93113,93114,93127,93146,93154,93193,93208,93219,93233,93250,93285,93326,93341,93353,93402,93437,93460,93479,93497,93509,93548,93576,93594,93607,93615,93623,93637,93643,93656,93662,93670,93675,93686,93692,93708,93730,93743,93746,93759,93777,93793,93797,93805,93818,93839,93853,93861,93868,93904,93947,93958,93960,93999,94015,94026,94028,94043,94059,94060,94071,94078,94091,94100,94125,94162,94168,94181,94186,94190,94194,94198,94204,94254,94259,94287,94314,94326,94337,94381,94382,94402,94407,94408,94420,94447,94468,94486,94490,94495,94500,94515,94519,94527,94534,94545,94551,94568,94576,94587,94614,94615,94633,94647,94652,94671,94687,94694,94716,94727,94733,94750,94765,94796,94843,94853,94865,94888,94914,94919,94926,94932,94938,94945,94963,94988,94994,95030,95035,95042,95064,95071,95088,95091,95095,95111,95125,95137,95144,95160,95172,95173,95192,95219,95236,95253,95259,95290,95369,95376,95404,95411,95431,95443,95446,95452,95457,95463,95472,95489,95537,95543,95549,95558,95563,95579,95596,95605,95632,95694,95695,95704,95716,95730,95736,95770,95777,95791,95807,95812,95818,95827,95832,95842,95843,95863,95872,95877,95887,95911,95929,95930,95939,95962,95978,95985,96004,96014,96022,96032,96040,96068,96076,96084,96090,96106,96135,96163,96168,96202,96225,96245,96248,96254,96297,96309,96321,96326,96327,96362,96393,96412,96437,96444,96449,96453,96473,96482,96487,96503,96513,96528,96540,96563,96565,96567,96572,96577,96596,96602,96610,96635,96641,96645,96652,96663,96685,96707,96716,96730,96741,96759,96760,96776,96808,96848,96868,96901,96907,96908,96960,96961,96972,97007,97013,97014,97015,97016,97017,97056,97063,97073,97081,97099,97116,97165,97176,97180,97193,97201,97207,97225,97233,97239,97252,97283,97294,97308,97315,97326,97338,97340,97345,97354,97371,97390,97407,97409,97436,97442,97448,97465,97492,97503,97535,97566,97606,97624,97644,97650,97687,97694,97708,97709,97735,97738,97744,97748,97758,97771,97786,97790,97798,97799,97812,97820,97821,97822,97823,97824,97835,97836,97849,97858,97884,97944,97965,97968,97976,98013,98046,98064,98089,98090,98102,98194,98212,98224,98235,98296,98305,98311,98315,98336,98343,98349,98356,98374,98386,98393,98410,98427,98433,98446,98488,98498,98514,98522,98537,98580,98581,98603,98639,98649,98654,98655,98666,98667,98686,98763,98769,98787,98830,98836,98840,98846,98850,98876,98880,98892,98930,98935,98982,98987,98997,99022,99031,99046,99054,99076,99092,99105,99141,99149,99150,99162,99170,99179,99186,99192,99208,99250,99265,99268,99287,99288,99307,99356,99402,99412,99421,99431,99440,99460,99481,99490,99522,99531,99532,99543,99555,99561,99569,99584,99591,99599,99645,99653,99660,99690,99702,99711,99721,99727,99739,99754,99762,99769,99790,99799,99814,99834,99843,99884,99910,99916,99917,99928,99939,99956,99973,99992,99998,100004,100020,100033,100050,100054,100056,100062,100096,100105,100118,100130,100150,100159,100171,100183,100186,100195,100206,100211,100214,100221,100229,100265,100266,100275,100276,100289,100294,100300,100313,100316,100327,100332,100351,100360,100374,100384,100390,100397,100412,100427,100432,100443,100448,100459,100483,100494,100515,100518,100533,100545,100550,100553,100593,100600,100617,100625,100633,100637,100648,100670,100683,100692,100697,100708,100722,100726,100735,100743,100750,100757,100769,100785,100792,100802,100807,100808,100850,100851,100862,100872,100907,100933,101006,101019,101034,101039,101040,101074,101075,101125,101157,101158,101173,101194,101210,101211,101212,101243,101254,101261,101270,101273,101282,101292,101302,101314,101323,101333,101346,101357,101366,101373,101384,101385,101407,101416,101449,101469,101542,101562,101583,101584,101595,101607,101628,101648,101686,101701,101714,101723,101747,101791,101815,101829,101901,101909,101931,101946,101951,101952,101968,101969,102025,102040,102050,102059,102064,102069,102073,102097,102127,102137,102156,102166,102178,102197,102214,102218,102224,102235,102241,102270,102277,102310,102320,102353,102359,102374,102424,102429,102448,102454,102459,102471,102513,102545,102569,102580,102588,102611,102642,102658,102696,102719,102752,102770,102794,102818,102830,102833,102847,102856,102861,102868,102874,102880,102903,102909,102912,102931,102956,102960,102984,102995,103004,103014,103046,103062,103079,103093,103097,103103,103109,103125,103142,103170,103179,103199,103204,103222,103240,103286,103292,103306,103310,103336,103342,103348,103361,103366,103399,103422,103431,103438,103445,103451,103515,103522,103539,103551,103581,103582,103602,103617,103623,103630,103686,103700,103725,103726,103739,103754,103788,103794,103801,103808,103824,103830,103835,103871,103879,103897,103913,103917,103934,103948,103978,103987,104009,104021,104026,104039,104044,104048,104058,104065,104076,104091,104103,104143,104151,104156,104176,104186,104192,104201,104203,104207,104218,104224,104232,104245,104259,104262,104271,104277,104282,104290,104299,104309,104312,104320,104359,104379,104398,104409,104432,104437,104454,104460,104480,104488,104493,104508,104517,104522,104526,104538,104541,104554,104562,104580,104589,104597,104622,104629,104638,104644,104662,104674,104684,104689,104699,104714,104717,104723,104741,104748,104771,104797,104804,104820,104835,104843,104863,104867,104868,104879,104885,104892,104893,104904,104910,104915,104916,104917,104953,104970,104979,104988,105002,105012,105018,105022,105027,105035,105037,105070,105080,105090,105095,105176,105183,105188,105189,105208,105218,105235,105247,105253,105270,105276,105290,105291,105300,105335,105357,105382,105390,105399,105435,105458,105472,105489,105506,105521,105522,105531,105547,105552,105576,105587,105593,105602,105613,105618,105647,105650,105690,105709,105711,105718,105750,105761,105764,105802,105821,105833,105843,105867,105877,105885,105903,105908,105926,105943,105949,105957,105965,105991,105996,106000,106001,106006,106033,106065,106068,106077,106108,106133,106145,106162,106170,106171,106203,106225,106236,106249,106254,106259,106264,106265,106282,106287,106296,106303,106308,106318,106331,106333,106362,106389,106396,106401,106406,106423,106436,106441,106457,106471,106478,106482,106504,106527,106538,106552,106553,106568,106585,106591,106599,106612,106620,106640,106674,106683,106723,106748,106764,106774,106801,106829,106841,106867,106877,106887,106936,106947,106949,106961,106972,106977,106999,107008,107018,107039,107062,107065,107089,107097,107101,107118,107139,107169,107180,107228,107266,107324,107330,107342,107359,107374,107375,107417,107451,107464,107504,107507,107516,107522,107528,107564,107569,107588,107635,107646,107647,107648,107658,107730,107752,107773,107778,107779,107793,107802,107812,107824,107828,107836,107847,107887,107899,107913,107927,107940,107948,107955,107960,107982,107987,108029,108056,108067,108076,108077,108090,108134,108149,108169,108174,108204,108212,108232,108252,108258,108281,108287,108318,108329,108354,108363,108364,108365,108366,108367,108368,108369,108436,108447,108468,108475,108480,108535,108557,108575,108597,108605,108614,108615,108658,108673,108679,108704,108718,108752,108763,108800,108805,108818,108836,108841,108842,108843,108844,108845,108846,108847,108920,108936,108944,108949,108957,108975,108981,108989,108990,109022,109035,109041,109051,109056,109075,109080,109098,109106,109127,109155,109165,109177,109194,109201,109210,109226,109236,109243,109273,109280,109289,109290,109328,109341,109356,109390,109399,109430,109441,109456,109457,109490,109499,109503,109506,109517,109536,109544,109559,109588,109596,109607,109612,109616,109623,109630,109633,109663,109688,109696,109704,109716,109729,109738,109739,109773,109794,109814,109841,109844,109864,109869,109874,109916,109955,109963,109968,109983,109988,110015,110024,110052,110064,110069,110083,110108,110123,110128,110143,110160,110166,110237,110241,110266,110296,110304,110316,110326,110327,110332,110363,110371,110390,110393,110404,110425,110455,110469,110475,110484,110485,110497,110514,110539,110553,110554,110565,110568,110573,110592,110599,110603,110610,110679,110693,110701,110707,110712,110715,110746,110764,110776,110785,110803,110812,110821,110845,110852,110856,110857,110898,110903,110911,110922,110936,110961,110970,110979,110985,110994,111012,111024,111043,111052,111053,111054,111073,111074,111085,111095,111105,111125,111138,111148,111160,111207,111222,111231,111246,111269,111275,111280,111290,111297,111345,111359,111376,111387,111399,111425,111459,111464,111465,111522,111528,111539,111563,111564,111572,111584,111618,111622,111641,111642,111661,111673,111680,111715,111731,111735,111755,111760,111764,111765,111776,111777,111797,111808,111821,111826,111827,111838,111856,111866,111872,111896,111909,111914,112006,112076,112082,112093,112101,112110,112116,112135,112144,112157,112172,112178,112202,112267,112289,112360,112364,112423,112431,112443,112466,112478,112506,112531,112545,112546,112567,112571,112594,112625,112644,112659,112684,112716,112753,112765,112785,112795,112811,112886,112888,112899,112903,112915,112921,112949,112950,112962,112968,112985,112989,113001,113017,113028,113035,113061,113074,113082,113116,113128,113140,113141,113150,113156,113157,113169,113174,113233,113251,113255,113265,113271,113285,113290,113309,113350,113351,113385,113409,113415,113436,113442,113447,113452,113461,113462,113491,113497,113507,113517,113532,113552,113559,113584,113606,113636,113637,113653,113688,113698,113708,113716,113765,113791,113795,113804,113848,113856,113883,113888,113899,113948,113964,113965,114009,114020,114029,114041,114064,114071,114083,114088,114103,114108,114117,114133,114143,114149,114164,114168,114198,114205,114211,114219,114244,114249,114256,114260,114265,114285,114290,114294,114306,114309,114353,114366,114391,114398,114418,114428,114435,114457,114472,114479,114484,114505,114534,114543,114562,114571,114578,114595,114608,114614,114615,114626,114642,114686,114693,114703,114705,114737,114747,114770,114775,114780,114787,114793,114794,114807,114817,114824,114826,114835,114842,114856,114863,114872,114880,114895,114919,114929,114930,114951,114962,114982,114989,114995,115013,115018,115056,115074,115084,115098,115111,115124,115138,115144,115154,115159,115165,115170,115178,115183,115202,115213,115225,115238,115243,115268,115276,115280,115321,115338,115354,115371,115394,115409,115421,115462,115469,115486,115494,115501,115513,115526,115531,115534,115537,115544,115556,115561,115570,115582,115592,115596,115602,115634,115639,115660,115675,115692,115706,115737,115738,115755,115761,115774,115778,115795,115806,115812,115817,115822,115842,115869,115874,115881,115890,115897,115902,115924,115938,115943,115967,116012,116013,116045,116067,116077,116083,116090,116158,116164,116185,116205,116210,116211,116225,116264,116268,116280,116324,116325,116337,116345,116352,116356,116363,116365,116393,116422,116426,116435,116446,116457,116484,116491,116519,116527,116529,116534,116570,116577,116606,116610,116617,116636,116665,116700,116707,116724,116729,116740,116747,116759,116767,116775,116782,116799,116807,116827,116835,116844,116849,116855,116862,116884,116896,116917,116924,116935,116944,116952,116957,116961,116982,117001,117009,117050,117056,117084,117092,117093,117131,117172,117178,117201,117209,117234,117237,117239,117246,117273,117282,117307,117326,117351,117361,117376,117381,117405,117413,117422,117434,117447,117454,117459,117468,117493,117499,117508,117520,117611,117617,117646,117652,117658,117704,117705,117715,117721,117730,117747,117786,117795,117806,117815,117825,117840,117862,117880,117904,117905,117906,117922,117938,117945,117977,118005,118012,118033,118042,118050,118078,118084,118104,118106,118150,118159,118175,118223,118224,118253,118264,118298,118323,118336,118337,118346,118353,118378,118387,118388,118414,118425,118432,118445,118454,119018],"is_not":false,"summary":null,"term":"GO:0005829"},{"annotations":[103945],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005945"},{"annotations":[108677,101312,91628,105688,110801,102318,106799,88360],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005832"},{"annotations":[98434,99523],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904564"},{"annotations":[99524,87156,88480,114206],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097361"},{"annotations":[117036,107452,116327,109740,110555,98668,90559,100278,100698,101970,100277,100398,107671,96664,98583,101971,107781,108991,93115,89612,96963,110182,97710,96962,109291,87694,111829,114616,87611,100853,116213,118395,108078,89748,87610,101386,89747,103584,110486,96329,98582,90558,111566,117707,110183,118225,118338,114796,94383,104272,95696,118396,109741,105019,96328,107649,111565,106554,113922,100810,112936,117085,96978,99918,90534,89115,116870,117094,101954,101953,111466,109292,112951,100852,96979,101159,91985,99369,107672,111767,114795,87190,113353,111644,108992,105191,100809,107336,94384,116212,105190,116326,113463,99919,113352,90532,110487,111643,91986,116869,88883,117095,101160,97711,96941,99370,93077,95697,111828,111076,113921,111467,117394,90533,96673,115160,89611,117210,118226,113967,111075,116015,112952,98669,96672,93116,107650,87612,96578,96940,108079,118339,87592,111388,116014,113464,117037,101387,103583,114617,111766,113966,117706,93078,87191,106555,107780,110556],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0022625"},{"annotations":[107360],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0022626"},{"annotations":[92518,94062,95932,92519,94409,101213,103293,95931,88158,90874,88194,96069,97838,103343,103918,100267,95844,104870,105028,104869,105135,103728,101215,90073,99151,105136,96909,105148,99152,94260,105523,95174,98139,98657,107376,93175,95175,93177,97837,88157,101214,104894,106172,111055,90519,111057,112548,113639,105524,112547,113992,115739,94410,116856,95845,111056,109442,103727,104895,110858,118140,112868,98656,105147,106173,112866,113638,87177,110859,88442,87176,93024,103337,88193,90520,93176,115875,98851,93023,113993,91109,101042,74301,111779,106266,88443,115740,111778,116850,112867,101041,94061,99957,98138,107377,90074,100268,105553,99289,96910,99290,99533,98166,106267,99534,98165],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0022627"},{"annotations":[105326,107871],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0002144"},{"annotations":[117987,91202,103594,94458],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090730"},{"annotations":[92690,102589,106343,109140,92462,97764,113313],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099128"},{"annotations":[117292,104238,92280,109321],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120510"},{"annotations":[104922,104923,104921],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000015"},{"annotations":[91944,106725],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005971"},{"annotations":[87437,114536],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0072380"},{"annotations":[92830,98376,90770],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033596"}]},"cv_name":"cellular_component","definition":"The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.","definition_xrefs":["GOC:jl","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":2109,"genes_by_uniquename":{"SJAG_00004":null,"SJAG_00027":null,"SJAG_00032":null,"SJAG_00033":null,"SJAG_00034":null,"SJAG_00035":null,"SJAG_00036":null,"SJAG_00037":null,"SJAG_00038":null,"SJAG_00039":null,"SJAG_00040":null,"SJAG_00041":null,"SJAG_00043":null,"SJAG_00044":null,"SJAG_00045":null,"SJAG_00049":null,"SJAG_00052":null,"SJAG_00053":null,"SJAG_00059":null,"SJAG_00063":null,"SJAG_00065":null,"SJAG_00067":null,"SJAG_00069":null,"SJAG_00072":null,"SJAG_00074":null,"SJAG_00084":null,"SJAG_00091":null,"SJAG_00092":null,"SJAG_00093":null,"SJAG_00095":null,"SJAG_00100":null,"SJAG_00102":null,"SJAG_00103":null,"SJAG_00104":null,"SJAG_00106":null,"SJAG_00107":null,"SJAG_00112":null,"SJAG_00113":null,"SJAG_00114":null,"SJAG_00115":null,"SJAG_00117":null,"SJAG_00118":null,"SJAG_00119":null,"SJAG_00120":null,"SJAG_00125":null,"SJAG_00126":null,"SJAG_00128":null,"SJAG_00129":null,"SJAG_00134":null,"SJAG_00135":null,"SJAG_00137":null,"SJAG_00141":null,"SJAG_00143":null,"SJAG_00144":null,"SJAG_00145":null,"SJAG_00147":null,"SJAG_00150":null,"SJAG_00155":null,"SJAG_00161":null,"SJAG_00162":null,"SJAG_00164":null,"SJAG_00166":null,"SJAG_00167":null,"SJAG_00169":null,"SJAG_00172":null,"SJAG_00173":null,"SJAG_00176":null,"SJAG_00178":null,"SJAG_00179":null,"SJAG_00181":null,"SJAG_00184":null,"SJAG_00186":null,"SJAG_00188":null,"SJAG_00189":null,"SJAG_00190":null,"SJAG_00191":null,"SJAG_00202":null,"SJAG_00203":null,"SJAG_00206":null,"SJAG_00207":null,"SJAG_00208":null,"SJAG_00214":null,"SJAG_00219":null,"SJAG_00220":null,"SJAG_00221":null,"SJAG_00223":null,"SJAG_00224":null,"SJAG_00225":null,"SJAG_00226":null,"SJAG_00228":null,"SJAG_00229":null,"SJAG_00230":null,"SJAG_00234":null,"SJAG_00237":null,"SJAG_00242":null,"SJAG_00243":null,"SJAG_00244":null,"SJAG_00245":null,"SJAG_00246":null,"SJAG_00248":null,"SJAG_00249":null,"SJAG_00251":null,"SJAG_00252":null,"SJAG_00256":null,"SJAG_00269":null,"SJAG_00270":null,"SJAG_00272":null,"SJAG_00280":null,"SJAG_00281":null,"SJAG_00283":null,"SJAG_00287":null,"SJAG_00289":null,"SJAG_00290":null,"SJAG_00293":null,"SJAG_00296":null,"SJAG_00298":null,"SJAG_00301":null,"SJAG_00306":null,"SJAG_00309":null,"SJAG_00314":null,"SJAG_00316":null,"SJAG_00317":null,"SJAG_00320":null,"SJAG_00321":null,"SJAG_00324":null,"SJAG_00325":null,"SJAG_00326":null,"SJAG_00327":null,"SJAG_00331":null,"SJAG_00333":null,"SJAG_00337":null,"SJAG_00338":null,"SJAG_00341":null,"SJAG_00343":null,"SJAG_00350":null,"SJAG_00352":null,"SJAG_00353":null,"SJAG_00355":null,"SJAG_00356":null,"SJAG_00359":null,"SJAG_00364":null,"SJAG_00365":null,"SJAG_00366":null,"SJAG_00374":null,"SJAG_00376":null,"SJAG_00377":null,"SJAG_00378":null,"SJAG_00379":null,"SJAG_00381":null,"SJAG_00382":null,"SJAG_00384":null,"SJAG_00390":null,"SJAG_00395":null,"SJAG_00397":null,"SJAG_00400":null,"SJAG_00401":null,"SJAG_00409":null,"SJAG_00413":null,"SJAG_00414":null,"SJAG_00419":null,"SJAG_00420":null,"SJAG_00422":null,"SJAG_00423":null,"SJAG_00424":null,"SJAG_00427":null,"SJAG_00430":null,"SJAG_00432":null,"SJAG_00435":null,"SJAG_00436":null,"SJAG_00439":null,"SJAG_00440":null,"SJAG_00441":null,"SJAG_00443":null,"SJAG_00447":null,"SJAG_00448":null,"SJAG_00449":null,"SJAG_00450":null,"SJAG_00455":null,"SJAG_00457":null,"SJAG_00461":null,"SJAG_00463":null,"SJAG_00464":null,"SJAG_00465":null,"SJAG_00466":null,"SJAG_00467":null,"SJAG_00468":null,"SJAG_00469":null,"SJAG_00471":null,"SJAG_00472":null,"SJAG_00474":null,"SJAG_00476":null,"SJAG_00479":null,"SJAG_00480":null,"SJAG_00482":null,"SJAG_00483":null,"SJAG_00485":null,"SJAG_00486":null,"SJAG_00487":null,"SJAG_00489":null,"SJAG_00490":null,"SJAG_00491":null,"SJAG_00495":null,"SJAG_00498":null,"SJAG_00501":null,"SJAG_00503":null,"SJAG_00504":null,"SJAG_00505":null,"SJAG_00507":null,"SJAG_00508":null,"SJAG_00509":null,"SJAG_00512":null,"SJAG_00514":null,"SJAG_00518":null,"SJAG_00521":null,"SJAG_00523":null,"SJAG_00524":null,"SJAG_00526":null,"SJAG_00527":null,"SJAG_00529":null,"SJAG_00531":null,"SJAG_00532":null,"SJAG_00533":null,"SJAG_00534":null,"SJAG_00537":null,"SJAG_00541":null,"SJAG_00544":null,"SJAG_00546":null,"SJAG_00550":null,"SJAG_00560":null,"SJAG_00561":null,"SJAG_00563":null,"SJAG_00567":null,"SJAG_00571":null,"SJAG_00572":null,"SJAG_00573":null,"SJAG_00574":null,"SJAG_00577":null,"SJAG_00578":null,"SJAG_00579":null,"SJAG_00580":null,"SJAG_00581":null,"SJAG_00584":null,"SJAG_00585":null,"SJAG_00586":null,"SJAG_00591":null,"SJAG_00592":null,"SJAG_00594":null,"SJAG_00596":null,"SJAG_00599":null,"SJAG_00600":null,"SJAG_00605":null,"SJAG_00609":null,"SJAG_00611":null,"SJAG_00614":null,"SJAG_00615":null,"SJAG_00622":null,"SJAG_00624":null,"SJAG_00629":null,"SJAG_00632":null,"SJAG_00633":null,"SJAG_00637":null,"SJAG_00642":null,"SJAG_00644":null,"SJAG_00645":null,"SJAG_00653":null,"SJAG_00656":null,"SJAG_00660":null,"SJAG_00661":null,"SJAG_00662":null,"SJAG_00663":null,"SJAG_00668":null,"SJAG_00670":null,"SJAG_00674":null,"SJAG_00678":null,"SJAG_00682":null,"SJAG_00683":null,"SJAG_00685":null,"SJAG_00686":null,"SJAG_00689":null,"SJAG_00690":null,"SJAG_00691":null,"SJAG_00692":null,"SJAG_00694":null,"SJAG_00696":null,"SJAG_00702":null,"SJAG_00704":null,"SJAG_00706":null,"SJAG_00707":null,"SJAG_00712":null,"SJAG_00718":null,"SJAG_00719":null,"SJAG_00720":null,"SJAG_00724":null,"SJAG_00726":null,"SJAG_00728":null,"SJAG_00729":null,"SJAG_00733":null,"SJAG_00736":null,"SJAG_00738":null,"SJAG_00739":null,"SJAG_00742":null,"SJAG_00743":null,"SJAG_00746":null,"SJAG_00748":null,"SJAG_00749":null,"SJAG_00756":null,"SJAG_00757":null,"SJAG_00758":null,"SJAG_00762":null,"SJAG_00764":null,"SJAG_00765":null,"SJAG_00766":null,"SJAG_00768":null,"SJAG_00777":null,"SJAG_00778":null,"SJAG_00779":null,"SJAG_00786":null,"SJAG_00788":null,"SJAG_00791":null,"SJAG_00795":null,"SJAG_00796":null,"SJAG_00798":null,"SJAG_00800":null,"SJAG_00801":null,"SJAG_00803":null,"SJAG_00805":null,"SJAG_00806":null,"SJAG_00807":null,"SJAG_00808":null,"SJAG_00809":null,"SJAG_00811":null,"SJAG_00814":null,"SJAG_00815":null,"SJAG_00820":null,"SJAG_00821":null,"SJAG_00822":null,"SJAG_00823":null,"SJAG_00827":null,"SJAG_00832":null,"SJAG_00837":null,"SJAG_00839":null,"SJAG_00840":null,"SJAG_00843":null,"SJAG_00845":null,"SJAG_00850":null,"SJAG_00853":null,"SJAG_00854":null,"SJAG_00856":null,"SJAG_00857":null,"SJAG_00858":null,"SJAG_00859":null,"SJAG_00864":null,"SJAG_00869":null,"SJAG_00871":null,"SJAG_00874":null,"SJAG_00878":null,"SJAG_00881":null,"SJAG_00885":null,"SJAG_00888":null,"SJAG_00890":null,"SJAG_00892":null,"SJAG_00894":null,"SJAG_00898":null,"SJAG_00902":null,"SJAG_00903":null,"SJAG_00908":null,"SJAG_00910":null,"SJAG_00913":null,"SJAG_00916":null,"SJAG_00917":null,"SJAG_00918":null,"SJAG_00921":null,"SJAG_00925":null,"SJAG_00931":null,"SJAG_00937":null,"SJAG_00938":null,"SJAG_00940":null,"SJAG_00941":null,"SJAG_00942":null,"SJAG_00947":null,"SJAG_00948":null,"SJAG_00954":null,"SJAG_00955":null,"SJAG_00956":null,"SJAG_00957":null,"SJAG_00958":null,"SJAG_00960":null,"SJAG_00963":null,"SJAG_00964":null,"SJAG_00967":null,"SJAG_00968":null,"SJAG_00969":null,"SJAG_00971":null,"SJAG_00972":null,"SJAG_00975":null,"SJAG_00978":null,"SJAG_00980":null,"SJAG_00982":null,"SJAG_00983":null,"SJAG_00986":null,"SJAG_00987":null,"SJAG_00988":null,"SJAG_00989":null,"SJAG_00990":null,"SJAG_00991":null,"SJAG_00993":null,"SJAG_00995":null,"SJAG_01000":null,"SJAG_01002":null,"SJAG_01003":null,"SJAG_01010":null,"SJAG_01012":null,"SJAG_01014":null,"SJAG_01016":null,"SJAG_01018":null,"SJAG_01020":null,"SJAG_01022":null,"SJAG_01024":null,"SJAG_01026":null,"SJAG_01027":null,"SJAG_01030":null,"SJAG_01039":null,"SJAG_01042":null,"SJAG_01047":null,"SJAG_01048":null,"SJAG_01053":null,"SJAG_01054":null,"SJAG_01055":null,"SJAG_01058":null,"SJAG_01061":null,"SJAG_01063":null,"SJAG_01064":null,"SJAG_01070":null,"SJAG_01072":null,"SJAG_01074":null,"SJAG_01075":null,"SJAG_01079":null,"SJAG_01081":null,"SJAG_01083":null,"SJAG_01087":null,"SJAG_01088":null,"SJAG_01089":null,"SJAG_01114":null,"SJAG_01117":null,"SJAG_01118":null,"SJAG_01121":null,"SJAG_01122":null,"SJAG_01126":null,"SJAG_01127":null,"SJAG_01128":null,"SJAG_01131":null,"SJAG_01132":null,"SJAG_01134":null,"SJAG_01135":null,"SJAG_01136":null,"SJAG_01137":null,"SJAG_01139":null,"SJAG_01142":null,"SJAG_01146":null,"SJAG_01148":null,"SJAG_01149":null,"SJAG_01150":null,"SJAG_01151":null,"SJAG_01153":null,"SJAG_01154":null,"SJAG_01159":null,"SJAG_01161":null,"SJAG_01162":null,"SJAG_01163":null,"SJAG_01166":null,"SJAG_01167":null,"SJAG_01172":null,"SJAG_01175":null,"SJAG_01181":null,"SJAG_01182":null,"SJAG_01184":null,"SJAG_01185":null,"SJAG_01186":null,"SJAG_01187":null,"SJAG_01191":null,"SJAG_01193":null,"SJAG_01194":null,"SJAG_01197":null,"SJAG_01198":null,"SJAG_01199":null,"SJAG_01202":null,"SJAG_01203":null,"SJAG_01207":null,"SJAG_01209":null,"SJAG_01213":null,"SJAG_01214":null,"SJAG_01216":null,"SJAG_01218":null,"SJAG_01220":null,"SJAG_01222":null,"SJAG_01226":null,"SJAG_01228":null,"SJAG_01229":null,"SJAG_01231":null,"SJAG_01233":null,"SJAG_01235":null,"SJAG_01238":null,"SJAG_01240":null,"SJAG_01245":null,"SJAG_01248":null,"SJAG_01251":null,"SJAG_01252":null,"SJAG_01255":null,"SJAG_01259":null,"SJAG_01261":null,"SJAG_01266":null,"SJAG_01267":null,"SJAG_01268":null,"SJAG_01269":null,"SJAG_01270":null,"SJAG_01274":null,"SJAG_01277":null,"SJAG_01279":null,"SJAG_01283":null,"SJAG_01284":null,"SJAG_01287":null,"SJAG_01291":null,"SJAG_01292":null,"SJAG_01293":null,"SJAG_01296":null,"SJAG_01298":null,"SJAG_01301":null,"SJAG_01302":null,"SJAG_01308":null,"SJAG_01310":null,"SJAG_01311":null,"SJAG_01312":null,"SJAG_01313":null,"SJAG_01314":null,"SJAG_01317":null,"SJAG_01320":null,"SJAG_01322":null,"SJAG_01325":null,"SJAG_01328":null,"SJAG_01333":null,"SJAG_01335":null,"SJAG_01338":null,"SJAG_01339":null,"SJAG_01341":null,"SJAG_01342":null,"SJAG_01346":null,"SJAG_01351":null,"SJAG_01352":null,"SJAG_01354":null,"SJAG_01358":null,"SJAG_01359":null,"SJAG_01360":null,"SJAG_01361":null,"SJAG_01362":null,"SJAG_01364":null,"SJAG_01365":null,"SJAG_01366":null,"SJAG_01367":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01372":null,"SJAG_01375":null,"SJAG_01376":null,"SJAG_01379":null,"SJAG_01382":null,"SJAG_01383":null,"SJAG_01384":null,"SJAG_01385":null,"SJAG_01386":null,"SJAG_01387":null,"SJAG_01389":null,"SJAG_01397":null,"SJAG_01404":null,"SJAG_01408":null,"SJAG_01411":null,"SJAG_01415":null,"SJAG_01418":null,"SJAG_01425":null,"SJAG_01427":null,"SJAG_01428":null,"SJAG_01430":null,"SJAG_01432":null,"SJAG_01434":null,"SJAG_01436":null,"SJAG_01438":null,"SJAG_01440":null,"SJAG_01443":null,"SJAG_01444":null,"SJAG_01447":null,"SJAG_01449":null,"SJAG_01453":null,"SJAG_01455":null,"SJAG_01457":null,"SJAG_01458":null,"SJAG_01461":null,"SJAG_01467":null,"SJAG_01472":null,"SJAG_01474":null,"SJAG_01475":null,"SJAG_01477":null,"SJAG_01479":null,"SJAG_01480":null,"SJAG_01481":null,"SJAG_01482":null,"SJAG_01487":null,"SJAG_01488":null,"SJAG_01489":null,"SJAG_01492":null,"SJAG_01496":null,"SJAG_01497":null,"SJAG_01499":null,"SJAG_01500":null,"SJAG_01501":null,"SJAG_01502":null,"SJAG_01508":null,"SJAG_01510":null,"SJAG_01512":null,"SJAG_01515":null,"SJAG_01516":null,"SJAG_01519":null,"SJAG_01521":null,"SJAG_01522":null,"SJAG_01528":null,"SJAG_01529":null,"SJAG_01531":null,"SJAG_01533":null,"SJAG_01534":null,"SJAG_01535":null,"SJAG_01540":null,"SJAG_01543":null,"SJAG_01544":null,"SJAG_01545":null,"SJAG_01547":null,"SJAG_01548":null,"SJAG_01551":null,"SJAG_01556":null,"SJAG_01558":null,"SJAG_01561":null,"SJAG_01562":null,"SJAG_01565":null,"SJAG_01566":null,"SJAG_01568":null,"SJAG_01575":null,"SJAG_01576":null,"SJAG_01580":null,"SJAG_01581":null,"SJAG_01582":null,"SJAG_01587":null,"SJAG_01588":null,"SJAG_01590":null,"SJAG_01596":null,"SJAG_01598":null,"SJAG_01599":null,"SJAG_01605":null,"SJAG_01608":null,"SJAG_01609":null,"SJAG_01610":null,"SJAG_01611":null,"SJAG_01617":null,"SJAG_01618":null,"SJAG_01620":null,"SJAG_01621":null,"SJAG_01622":null,"SJAG_01624":null,"SJAG_01625":null,"SJAG_01628":null,"SJAG_01629":null,"SJAG_01630":null,"SJAG_01631":null,"SJAG_01632":null,"SJAG_01635":null,"SJAG_01637":null,"SJAG_01641":null,"SJAG_01643":null,"SJAG_01644":null,"SJAG_01645":null,"SJAG_01646":null,"SJAG_01650":null,"SJAG_01651":null,"SJAG_01652":null,"SJAG_01655":null,"SJAG_01656":null,"SJAG_01658":null,"SJAG_01659":null,"SJAG_01662":null,"SJAG_01663":null,"SJAG_01664":null,"SJAG_01665":null,"SJAG_01666":null,"SJAG_01667":null,"SJAG_01673":null,"SJAG_01675":null,"SJAG_01676":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01686":null,"SJAG_01690":null,"SJAG_01693":null,"SJAG_01694":null,"SJAG_01696":null,"SJAG_01697":null,"SJAG_01698":null,"SJAG_01702":null,"SJAG_01703":null,"SJAG_01704":null,"SJAG_01708":null,"SJAG_01710":null,"SJAG_01714":null,"SJAG_01715":null,"SJAG_01720":null,"SJAG_01721":null,"SJAG_01722":null,"SJAG_01733":null,"SJAG_01734":null,"SJAG_01737":null,"SJAG_01740":null,"SJAG_01742":null,"SJAG_01744":null,"SJAG_01746":null,"SJAG_01748":null,"SJAG_01759":null,"SJAG_01760":null,"SJAG_01762":null,"SJAG_01765":null,"SJAG_01768":null,"SJAG_01772":null,"SJAG_01774":null,"SJAG_01775":null,"SJAG_01776":null,"SJAG_01781":null,"SJAG_01783":null,"SJAG_01784":null,"SJAG_01786":null,"SJAG_01787":null,"SJAG_01788":null,"SJAG_01789":null,"SJAG_01791":null,"SJAG_01794":null,"SJAG_01797":null,"SJAG_01799":null,"SJAG_01801":null,"SJAG_01805":null,"SJAG_01808":null,"SJAG_01809":null,"SJAG_01810":null,"SJAG_01812":null,"SJAG_01817":null,"SJAG_01818":null,"SJAG_01822":null,"SJAG_01824":null,"SJAG_01825":null,"SJAG_01826":null,"SJAG_01827":null,"SJAG_01830":null,"SJAG_01833":null,"SJAG_01839":null,"SJAG_01840":null,"SJAG_01841":null,"SJAG_01844":null,"SJAG_01850":null,"SJAG_01851":null,"SJAG_01852":null,"SJAG_01853":null,"SJAG_01858":null,"SJAG_01859":null,"SJAG_01864":null,"SJAG_01869":null,"SJAG_01870":null,"SJAG_01874":null,"SJAG_01884":null,"SJAG_01885":null,"SJAG_01886":null,"SJAG_01897":null,"SJAG_01898":null,"SJAG_01900":null,"SJAG_01901":null,"SJAG_01908":null,"SJAG_01910":null,"SJAG_01914":null,"SJAG_01917":null,"SJAG_01918":null,"SJAG_01919":null,"SJAG_01926":null,"SJAG_01937":null,"SJAG_01938":null,"SJAG_01942":null,"SJAG_01943":null,"SJAG_01944":null,"SJAG_01949":null,"SJAG_01954":null,"SJAG_01955":null,"SJAG_01958":null,"SJAG_01974":null,"SJAG_01979":null,"SJAG_01986":null,"SJAG_01987":null,"SJAG_01992":null,"SJAG_01995":null,"SJAG_01997":null,"SJAG_02000":null,"SJAG_02004":null,"SJAG_02005":null,"SJAG_02009":null,"SJAG_02010":null,"SJAG_02012":null,"SJAG_02013":null,"SJAG_02015":null,"SJAG_02016":null,"SJAG_02017":null,"SJAG_02020":null,"SJAG_02022":null,"SJAG_02024":null,"SJAG_02026":null,"SJAG_02030":null,"SJAG_02033":null,"SJAG_02034":null,"SJAG_02035":null,"SJAG_02038":null,"SJAG_02040":null,"SJAG_02041":null,"SJAG_02042":null,"SJAG_02043":null,"SJAG_02044":null,"SJAG_02046":null,"SJAG_02047":null,"SJAG_02048":null,"SJAG_02057":null,"SJAG_02058":null,"SJAG_02061":null,"SJAG_02063":null,"SJAG_02065":null,"SJAG_02066":null,"SJAG_02069":null,"SJAG_02070":null,"SJAG_02075":null,"SJAG_02081":null,"SJAG_02082":null,"SJAG_02091":null,"SJAG_02093":null,"SJAG_02096":null,"SJAG_02098":null,"SJAG_02101":null,"SJAG_02106":null,"SJAG_02107":null,"SJAG_02116":null,"SJAG_02121":null,"SJAG_02135":null,"SJAG_02138":null,"SJAG_02145":null,"SJAG_02146":null,"SJAG_02148":null,"SJAG_02151":null,"SJAG_02154":null,"SJAG_02164":null,"SJAG_02165":null,"SJAG_02166":null,"SJAG_02169":null,"SJAG_02170":null,"SJAG_02171":null,"SJAG_02172":null,"SJAG_02174":null,"SJAG_02176":null,"SJAG_02177":null,"SJAG_02178":null,"SJAG_02179":null,"SJAG_02180":null,"SJAG_02181":null,"SJAG_02182":null,"SJAG_02184":null,"SJAG_02186":null,"SJAG_02189":null,"SJAG_02191":null,"SJAG_02193":null,"SJAG_02194":null,"SJAG_02197":null,"SJAG_02198":null,"SJAG_02202":null,"SJAG_02203":null,"SJAG_02206":null,"SJAG_02207":null,"SJAG_02210":null,"SJAG_02211":null,"SJAG_02213":null,"SJAG_02214":null,"SJAG_02215":null,"SJAG_02218":null,"SJAG_02224":null,"SJAG_02225":null,"SJAG_02226":null,"SJAG_02230":null,"SJAG_02231":null,"SJAG_02233":null,"SJAG_02234":null,"SJAG_02235":null,"SJAG_02237":null,"SJAG_02239":null,"SJAG_02240":null,"SJAG_02243":null,"SJAG_02245":null,"SJAG_02251":null,"SJAG_02253":null,"SJAG_02256":null,"SJAG_02265":null,"SJAG_02266":null,"SJAG_02267":null,"SJAG_02268":null,"SJAG_02269":null,"SJAG_02270":null,"SJAG_02271":null,"SJAG_02275":null,"SJAG_02277":null,"SJAG_02279":null,"SJAG_02280":null,"SJAG_02281":null,"SJAG_02282":null,"SJAG_02283":null,"SJAG_02285":null,"SJAG_02287":null,"SJAG_02288":null,"SJAG_02289":null,"SJAG_02290":null,"SJAG_02292":null,"SJAG_02294":null,"SJAG_02295":null,"SJAG_02297":null,"SJAG_02300":null,"SJAG_02304":null,"SJAG_02306":null,"SJAG_02307":null,"SJAG_02309":null,"SJAG_02312":null,"SJAG_02313":null,"SJAG_02314":null,"SJAG_02315":null,"SJAG_02320":null,"SJAG_02321":null,"SJAG_02323":null,"SJAG_02327":null,"SJAG_02329":null,"SJAG_02335":null,"SJAG_02336":null,"SJAG_02337":null,"SJAG_02339":null,"SJAG_02340":null,"SJAG_02342":null,"SJAG_02347":null,"SJAG_02349":null,"SJAG_02352":null,"SJAG_02357":null,"SJAG_02358":null,"SJAG_02364":null,"SJAG_02366":null,"SJAG_02367":null,"SJAG_02369":null,"SJAG_02370":null,"SJAG_02374":null,"SJAG_02375":null,"SJAG_02376":null,"SJAG_02378":null,"SJAG_02379":null,"SJAG_02380":null,"SJAG_02386":null,"SJAG_02387":null,"SJAG_02390":null,"SJAG_02393":null,"SJAG_02400":null,"SJAG_02401":null,"SJAG_02404":null,"SJAG_02405":null,"SJAG_02408":null,"SJAG_02414":null,"SJAG_02415":null,"SJAG_02419":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_02422":null,"SJAG_02424":null,"SJAG_02425":null,"SJAG_02426":null,"SJAG_02428":null,"SJAG_02434":null,"SJAG_02436":null,"SJAG_02439":null,"SJAG_02441":null,"SJAG_02442":null,"SJAG_02444":null,"SJAG_02450":null,"SJAG_02453":null,"SJAG_02456":null,"SJAG_02461":null,"SJAG_02462":null,"SJAG_02465":null,"SJAG_02467":null,"SJAG_02470":null,"SJAG_02471":null,"SJAG_02474":null,"SJAG_02477":null,"SJAG_02479":null,"SJAG_02481":null,"SJAG_02482":null,"SJAG_02485":null,"SJAG_02486":null,"SJAG_02490":null,"SJAG_02491":null,"SJAG_02493":null,"SJAG_02497":null,"SJAG_02498":null,"SJAG_02499":null,"SJAG_02502":null,"SJAG_02503":null,"SJAG_02505":null,"SJAG_02506":null,"SJAG_02508":null,"SJAG_02509":null,"SJAG_02510":null,"SJAG_02512":null,"SJAG_02515":null,"SJAG_02517":null,"SJAG_02518":null,"SJAG_02520":null,"SJAG_02522":null,"SJAG_02524":null,"SJAG_02531":null,"SJAG_02535":null,"SJAG_02540":null,"SJAG_02541":null,"SJAG_02542":null,"SJAG_02546":null,"SJAG_02547":null,"SJAG_02549":null,"SJAG_02551":null,"SJAG_02553":null,"SJAG_02558":null,"SJAG_02561":null,"SJAG_02562":null,"SJAG_02569":null,"SJAG_02570":null,"SJAG_02572":null,"SJAG_02573":null,"SJAG_02575":null,"SJAG_02576":null,"SJAG_02580":null,"SJAG_02582":null,"SJAG_02583":null,"SJAG_02585":null,"SJAG_02589":null,"SJAG_02591":null,"SJAG_02592":null,"SJAG_02593":null,"SJAG_02594":null,"SJAG_02595":null,"SJAG_02596":null,"SJAG_02597":null,"SJAG_02600":null,"SJAG_02601":null,"SJAG_02604":null,"SJAG_02605":null,"SJAG_02608":null,"SJAG_02609":null,"SJAG_02610":null,"SJAG_02611":null,"SJAG_02618":null,"SJAG_02619":null,"SJAG_02621":null,"SJAG_02625":null,"SJAG_02627":null,"SJAG_02630":null,"SJAG_02640":null,"SJAG_02645":null,"SJAG_02647":null,"SJAG_02648":null,"SJAG_02655":null,"SJAG_02659":null,"SJAG_02661":null,"SJAG_02663":null,"SJAG_02664":null,"SJAG_02667":null,"SJAG_02671":null,"SJAG_02672":null,"SJAG_02673":null,"SJAG_02679":null,"SJAG_02681":null,"SJAG_02682":null,"SJAG_02684":null,"SJAG_02686":null,"SJAG_02687":null,"SJAG_02688":null,"SJAG_02689":null,"SJAG_02692":null,"SJAG_02695":null,"SJAG_02696":null,"SJAG_02697":null,"SJAG_02699":null,"SJAG_02700":null,"SJAG_02702":null,"SJAG_02704":null,"SJAG_02705":null,"SJAG_02708":null,"SJAG_02712":null,"SJAG_02713":null,"SJAG_02715":null,"SJAG_02718":null,"SJAG_02720":null,"SJAG_02723":null,"SJAG_02725":null,"SJAG_02726":null,"SJAG_02728":null,"SJAG_02730":null,"SJAG_02731":null,"SJAG_02733":null,"SJAG_02734":null,"SJAG_02736":null,"SJAG_02738":null,"SJAG_02740":null,"SJAG_02741":null,"SJAG_02745":null,"SJAG_02746":null,"SJAG_02747":null,"SJAG_02748":null,"SJAG_02749":null,"SJAG_02750":null,"SJAG_02752":null,"SJAG_02753":null,"SJAG_02755":null,"SJAG_02756":null,"SJAG_02760":null,"SJAG_02763":null,"SJAG_02764":null,"SJAG_02765":null,"SJAG_02766":null,"SJAG_02768":null,"SJAG_02769":null,"SJAG_02770":null,"SJAG_02771":null,"SJAG_02774":null,"SJAG_02783":null,"SJAG_02785":null,"SJAG_02786":null,"SJAG_02788":null,"SJAG_02789":null,"SJAG_02790":null,"SJAG_02791":null,"SJAG_02794":null,"SJAG_02796":null,"SJAG_02797":null,"SJAG_02798":null,"SJAG_02799":null,"SJAG_02801":null,"SJAG_02802":null,"SJAG_02803":null,"SJAG_02805":null,"SJAG_02808":null,"SJAG_02811":null,"SJAG_02812":null,"SJAG_02813":null,"SJAG_02814":null,"SJAG_02817":null,"SJAG_02819":null,"SJAG_02822":null,"SJAG_02828":null,"SJAG_02832":null,"SJAG_02833":null,"SJAG_02840":null,"SJAG_02843":null,"SJAG_02845":null,"SJAG_02850":null,"SJAG_02851":null,"SJAG_02852":null,"SJAG_02854":null,"SJAG_02857":null,"SJAG_02858":null,"SJAG_02861":null,"SJAG_02863":null,"SJAG_02864":null,"SJAG_02866":null,"SJAG_02868":null,"SJAG_02869":null,"SJAG_02870":null,"SJAG_02871":null,"SJAG_02874":null,"SJAG_02876":null,"SJAG_02878":null,"SJAG_02879":null,"SJAG_02885":null,"SJAG_02886":null,"SJAG_02887":null,"SJAG_02889":null,"SJAG_02890":null,"SJAG_02891":null,"SJAG_02894":null,"SJAG_02895":null,"SJAG_02902":null,"SJAG_02904":null,"SJAG_02905":null,"SJAG_02911":null,"SJAG_02912":null,"SJAG_02918":null,"SJAG_02921":null,"SJAG_02923":null,"SJAG_02926":null,"SJAG_02938":null,"SJAG_02945":null,"SJAG_02950":null,"SJAG_02951":null,"SJAG_02954":null,"SJAG_02956":null,"SJAG_02959":null,"SJAG_02972":null,"SJAG_02973":null,"SJAG_02977":null,"SJAG_02978":null,"SJAG_02984":null,"SJAG_02988":null,"SJAG_02992":null,"SJAG_02994":null,"SJAG_02995":null,"SJAG_02997":null,"SJAG_02998":null,"SJAG_03002":null,"SJAG_03005":null,"SJAG_03009":null,"SJAG_03010":null,"SJAG_03012":null,"SJAG_03013":null,"SJAG_03014":null,"SJAG_03017":null,"SJAG_03019":null,"SJAG_03021":null,"SJAG_03022":null,"SJAG_03026":null,"SJAG_03029":null,"SJAG_03034":null,"SJAG_03035":null,"SJAG_03036":null,"SJAG_03037":null,"SJAG_03041":null,"SJAG_03043":null,"SJAG_03045":null,"SJAG_03049":null,"SJAG_03051":null,"SJAG_03055":null,"SJAG_03062":null,"SJAG_03063":null,"SJAG_03067":null,"SJAG_03070":null,"SJAG_03072":null,"SJAG_03074":null,"SJAG_03081":null,"SJAG_03082":null,"SJAG_03085":null,"SJAG_03086":null,"SJAG_03087":null,"SJAG_03089":null,"SJAG_03090":null,"SJAG_03091":null,"SJAG_03094":null,"SJAG_03095":null,"SJAG_03096":null,"SJAG_03098":null,"SJAG_03102":null,"SJAG_03106":null,"SJAG_03107":null,"SJAG_03108":null,"SJAG_03113":null,"SJAG_03119":null,"SJAG_03122":null,"SJAG_03124":null,"SJAG_03126":null,"SJAG_03127":null,"SJAG_03128":null,"SJAG_03130":null,"SJAG_03131":null,"SJAG_03132":null,"SJAG_03133":null,"SJAG_03136":null,"SJAG_03137":null,"SJAG_03140":null,"SJAG_03142":null,"SJAG_03144":null,"SJAG_03147":null,"SJAG_03150":null,"SJAG_03151":null,"SJAG_03153":null,"SJAG_03158":null,"SJAG_03159":null,"SJAG_03164":null,"SJAG_03166":null,"SJAG_03167":null,"SJAG_03172":null,"SJAG_03174":null,"SJAG_03179":null,"SJAG_03181":null,"SJAG_03182":null,"SJAG_03185":null,"SJAG_03186":null,"SJAG_03188":null,"SJAG_03189":null,"SJAG_03191":null,"SJAG_03193":null,"SJAG_03197":null,"SJAG_03204":null,"SJAG_03209":null,"SJAG_03210":null,"SJAG_03211":null,"SJAG_03214":null,"SJAG_03215":null,"SJAG_03219":null,"SJAG_03222":null,"SJAG_03223":null,"SJAG_03224":null,"SJAG_03225":null,"SJAG_03227":null,"SJAG_03228":null,"SJAG_03229":null,"SJAG_03230":null,"SJAG_03231":null,"SJAG_03233":null,"SJAG_03234":null,"SJAG_03237":null,"SJAG_03238":null,"SJAG_03241":null,"SJAG_03243":null,"SJAG_03245":null,"SJAG_03246":null,"SJAG_03248":null,"SJAG_03250":null,"SJAG_03254":null,"SJAG_03257":null,"SJAG_03258":null,"SJAG_03262":null,"SJAG_03263":null,"SJAG_03264":null,"SJAG_03266":null,"SJAG_03267":null,"SJAG_03272":null,"SJAG_03275":null,"SJAG_03276":null,"SJAG_03277":null,"SJAG_03278":null,"SJAG_03279":null,"SJAG_03283":null,"SJAG_03285":null,"SJAG_03288":null,"SJAG_03291":null,"SJAG_03293":null,"SJAG_03298":null,"SJAG_03306":null,"SJAG_03309":null,"SJAG_03312":null,"SJAG_03313":null,"SJAG_03319":null,"SJAG_03320":null,"SJAG_03321":null,"SJAG_03323":null,"SJAG_03325":null,"SJAG_03326":null,"SJAG_03335":null,"SJAG_03336":null,"SJAG_03340":null,"SJAG_03345":null,"SJAG_03346":null,"SJAG_03349":null,"SJAG_03350":null,"SJAG_03352":null,"SJAG_03354":null,"SJAG_03356":null,"SJAG_03357":null,"SJAG_03361":null,"SJAG_03362":null,"SJAG_03364":null,"SJAG_03367":null,"SJAG_03371":null,"SJAG_03373":null,"SJAG_03374":null,"SJAG_03375":null,"SJAG_03376":null,"SJAG_03377":null,"SJAG_03380":null,"SJAG_03383":null,"SJAG_03384":null,"SJAG_03398":null,"SJAG_03403":null,"SJAG_03404":null,"SJAG_03407":null,"SJAG_03408":null,"SJAG_03409":null,"SJAG_03411":null,"SJAG_03422":null,"SJAG_03423":null,"SJAG_03424":null,"SJAG_03425":null,"SJAG_03431":null,"SJAG_03432":null,"SJAG_03433":null,"SJAG_03434":null,"SJAG_03438":null,"SJAG_03453":null,"SJAG_03454":null,"SJAG_03455":null,"SJAG_03457":null,"SJAG_03463":null,"SJAG_03469":null,"SJAG_03470":null,"SJAG_03472":null,"SJAG_03473":null,"SJAG_03475":null,"SJAG_03476":null,"SJAG_03479":null,"SJAG_03482":null,"SJAG_03485":null,"SJAG_03486":null,"SJAG_03487":null,"SJAG_03488":null,"SJAG_03492":null,"SJAG_03494":null,"SJAG_03495":null,"SJAG_03498":null,"SJAG_03499":null,"SJAG_03500":null,"SJAG_03501":null,"SJAG_03504":null,"SJAG_03507":null,"SJAG_03508":null,"SJAG_03519":null,"SJAG_03523":null,"SJAG_03525":null,"SJAG_03527":null,"SJAG_03528":null,"SJAG_03529":null,"SJAG_03532":null,"SJAG_03533":null,"SJAG_03534":null,"SJAG_03537":null,"SJAG_03540":null,"SJAG_03541":null,"SJAG_03544":null,"SJAG_03545":null,"SJAG_03547":null,"SJAG_03548":null,"SJAG_03549":null,"SJAG_03551":null,"SJAG_03554":null,"SJAG_03556":null,"SJAG_03558":null,"SJAG_03561":null,"SJAG_03562":null,"SJAG_03568":null,"SJAG_03570":null,"SJAG_03571":null,"SJAG_03575":null,"SJAG_03576":null,"SJAG_03580":null,"SJAG_03581":null,"SJAG_03582":null,"SJAG_03588":null,"SJAG_03589":null,"SJAG_03592":null,"SJAG_03597":null,"SJAG_03601":null,"SJAG_03603":null,"SJAG_03605":null,"SJAG_03614":null,"SJAG_03616":null,"SJAG_03617":null,"SJAG_03618":null,"SJAG_03620":null,"SJAG_03623":null,"SJAG_03624":null,"SJAG_03626":null,"SJAG_03627":null,"SJAG_03629":null,"SJAG_03630":null,"SJAG_03631":null,"SJAG_03632":null,"SJAG_03634":null,"SJAG_03638":null,"SJAG_03643":null,"SJAG_03646":null,"SJAG_03651":null,"SJAG_03653":null,"SJAG_03655":null,"SJAG_03658":null,"SJAG_03659":null,"SJAG_03660":null,"SJAG_03662":null,"SJAG_03663":null,"SJAG_03665":null,"SJAG_03666":null,"SJAG_03668":null,"SJAG_03669":null,"SJAG_03673":null,"SJAG_03677":null,"SJAG_03678":null,"SJAG_03679":null,"SJAG_03681":null,"SJAG_03682":null,"SJAG_03684":null,"SJAG_03686":null,"SJAG_03688":null,"SJAG_03689":null,"SJAG_03690":null,"SJAG_03692":null,"SJAG_03693":null,"SJAG_03694":null,"SJAG_03696":null,"SJAG_03697":null,"SJAG_03701":null,"SJAG_03703":null,"SJAG_03704":null,"SJAG_03706":null,"SJAG_03708":null,"SJAG_03714":null,"SJAG_03717":null,"SJAG_03718":null,"SJAG_03720":null,"SJAG_03722":null,"SJAG_03723":null,"SJAG_03726":null,"SJAG_03730":null,"SJAG_03732":null,"SJAG_03733":null,"SJAG_03743":null,"SJAG_03751":null,"SJAG_03752":null,"SJAG_03753":null,"SJAG_03756":null,"SJAG_03758":null,"SJAG_03760":null,"SJAG_03761":null,"SJAG_03762":null,"SJAG_03771":null,"SJAG_03775":null,"SJAG_03781":null,"SJAG_03782":null,"SJAG_03784":null,"SJAG_03786":null,"SJAG_03788":null,"SJAG_03789":null,"SJAG_03791":null,"SJAG_03793":null,"SJAG_03794":null,"SJAG_03797":null,"SJAG_03798":null,"SJAG_03799":null,"SJAG_03802":null,"SJAG_03805":null,"SJAG_03810":null,"SJAG_03811":null,"SJAG_03815":null,"SJAG_03818":null,"SJAG_03821":null,"SJAG_03825":null,"SJAG_03828":null,"SJAG_03835":null,"SJAG_03838":null,"SJAG_03839":null,"SJAG_03842":null,"SJAG_03845":null,"SJAG_03847":null,"SJAG_03849":null,"SJAG_03852":null,"SJAG_03854":null,"SJAG_03855":null,"SJAG_03856":null,"SJAG_03857":null,"SJAG_03859":null,"SJAG_03862":null,"SJAG_03863":null,"SJAG_03865":null,"SJAG_03868":null,"SJAG_03872":null,"SJAG_03876":null,"SJAG_03879":null,"SJAG_03881":null,"SJAG_03882":null,"SJAG_03883":null,"SJAG_03884":null,"SJAG_03886":null,"SJAG_03888":null,"SJAG_03889":null,"SJAG_03890":null,"SJAG_03891":null,"SJAG_03892":null,"SJAG_03893":null,"SJAG_03896":null,"SJAG_03901":null,"SJAG_03903":null,"SJAG_03907":null,"SJAG_03915":null,"SJAG_03919":null,"SJAG_03921":null,"SJAG_03922":null,"SJAG_03924":null,"SJAG_03932":null,"SJAG_03934":null,"SJAG_03936":null,"SJAG_03937":null,"SJAG_03949":null,"SJAG_03950":null,"SJAG_03955":null,"SJAG_03958":null,"SJAG_03959":null,"SJAG_03963":null,"SJAG_03964":null,"SJAG_03971":null,"SJAG_03977":null,"SJAG_03983":null,"SJAG_03986":null,"SJAG_03990":null,"SJAG_03996":null,"SJAG_03998":null,"SJAG_04002":null,"SJAG_04003":null,"SJAG_04007":null,"SJAG_04009":null,"SJAG_04011":null,"SJAG_04012":null,"SJAG_04013":null,"SJAG_04015":null,"SJAG_04016":null,"SJAG_04020":null,"SJAG_04021":null,"SJAG_04022":null,"SJAG_04023":null,"SJAG_04025":null,"SJAG_04027":null,"SJAG_04029":null,"SJAG_04030":null,"SJAG_04031":null,"SJAG_04032":null,"SJAG_04033":null,"SJAG_04036":null,"SJAG_04042":null,"SJAG_04043":null,"SJAG_04044":null,"SJAG_04051":null,"SJAG_04054":null,"SJAG_04055":null,"SJAG_04060":null,"SJAG_04061":null,"SJAG_04062":null,"SJAG_04066":null,"SJAG_04069":null,"SJAG_04070":null,"SJAG_04072":null,"SJAG_04074":null,"SJAG_04077":null,"SJAG_04079":null,"SJAG_04082":null,"SJAG_04083":null,"SJAG_04084":null,"SJAG_04085":null,"SJAG_04086":null,"SJAG_04088":null,"SJAG_04089":null,"SJAG_04091":null,"SJAG_04092":null,"SJAG_04093":null,"SJAG_04097":null,"SJAG_04100":null,"SJAG_04106":null,"SJAG_04107":null,"SJAG_04108":null,"SJAG_04109":null,"SJAG_04112":null,"SJAG_04114":null,"SJAG_04118":null,"SJAG_04121":null,"SJAG_04123":null,"SJAG_04125":null,"SJAG_04126":null,"SJAG_04128":null,"SJAG_04129":null,"SJAG_04130":null,"SJAG_04131":null,"SJAG_04144":null,"SJAG_04147":null,"SJAG_04148":null,"SJAG_04150":null,"SJAG_04153":null,"SJAG_04155":null,"SJAG_04156":null,"SJAG_04157":null,"SJAG_04159":null,"SJAG_04160":null,"SJAG_04161":null,"SJAG_04163":null,"SJAG_04166":null,"SJAG_04168":null,"SJAG_04169":null,"SJAG_04170":null,"SJAG_04172":null,"SJAG_04174":null,"SJAG_04175":null,"SJAG_04176":null,"SJAG_04177":null,"SJAG_04179":null,"SJAG_04181":null,"SJAG_04182":null,"SJAG_04183":null,"SJAG_04187":null,"SJAG_04188":null,"SJAG_04190":null,"SJAG_04191":null,"SJAG_04192":null,"SJAG_04197":null,"SJAG_04198":null,"SJAG_04201":null,"SJAG_04202":null,"SJAG_04204":null,"SJAG_04211":null,"SJAG_04212":null,"SJAG_04213":null,"SJAG_04214":null,"SJAG_04219":null,"SJAG_04220":null,"SJAG_04227":null,"SJAG_04229":null,"SJAG_04232":null,"SJAG_04233":null,"SJAG_04234":null,"SJAG_04235":null,"SJAG_04242":null,"SJAG_04248":null,"SJAG_04249":null,"SJAG_04253":null,"SJAG_04256":null,"SJAG_04261":null,"SJAG_04263":null,"SJAG_04264":null,"SJAG_04266":null,"SJAG_04268":null,"SJAG_04270":null,"SJAG_04271":null,"SJAG_04273":null,"SJAG_04274":null,"SJAG_04275":null,"SJAG_04276":null,"SJAG_04282":null,"SJAG_04283":null,"SJAG_04285":null,"SJAG_04286":null,"SJAG_04287":null,"SJAG_04289":null,"SJAG_04290":null,"SJAG_04291":null,"SJAG_04292":null,"SJAG_04297":null,"SJAG_04299":null,"SJAG_04300":null,"SJAG_04303":null,"SJAG_04304":null,"SJAG_04306":null,"SJAG_04307":null,"SJAG_04309":null,"SJAG_04311":null,"SJAG_04312":null,"SJAG_04320":null,"SJAG_04324":null,"SJAG_04326":null,"SJAG_04332":null,"SJAG_04334":null,"SJAG_04335":null,"SJAG_04337":null,"SJAG_04338":null,"SJAG_04342":null,"SJAG_04343":null,"SJAG_04344":null,"SJAG_04347":null,"SJAG_04350":null,"SJAG_04352":null,"SJAG_04354":null,"SJAG_04355":null,"SJAG_04357":null,"SJAG_04359":null,"SJAG_04360":null,"SJAG_04366":null,"SJAG_04368":null,"SJAG_04369":null,"SJAG_04371":null,"SJAG_04372":null,"SJAG_04375":null,"SJAG_04379":null,"SJAG_04380":null,"SJAG_04381":null,"SJAG_04383":null,"SJAG_04384":null,"SJAG_04385":null,"SJAG_04388":null,"SJAG_04390":null,"SJAG_04394":null,"SJAG_04397":null,"SJAG_04399":null,"SJAG_04400":null,"SJAG_04403":null,"SJAG_04404":null,"SJAG_04407":null,"SJAG_04408":null,"SJAG_04410":null,"SJAG_04414":null,"SJAG_04417":null,"SJAG_04427":null,"SJAG_04429":null,"SJAG_04431":null,"SJAG_04434":null,"SJAG_04436":null,"SJAG_04449":null,"SJAG_04452":null,"SJAG_04453":null,"SJAG_04454":null,"SJAG_04455":null,"SJAG_04456":null,"SJAG_04457":null,"SJAG_04458":null,"SJAG_04459":null,"SJAG_04460":null,"SJAG_04461":null,"SJAG_04463":null,"SJAG_04465":null,"SJAG_04466":null,"SJAG_04467":null,"SJAG_04470":null,"SJAG_04472":null,"SJAG_04473":null,"SJAG_04474":null,"SJAG_04475":null,"SJAG_04476":null,"SJAG_04477":null,"SJAG_04478":null,"SJAG_04480":null,"SJAG_04481":null,"SJAG_04482":null,"SJAG_04484":null,"SJAG_04486":null,"SJAG_04487":null,"SJAG_04491":null,"SJAG_04495":null,"SJAG_04496":null,"SJAG_04499":null,"SJAG_04501":null,"SJAG_04505":null,"SJAG_04511":null,"SJAG_04516":null,"SJAG_04518":null,"SJAG_04519":null,"SJAG_04520":null,"SJAG_04521":null,"SJAG_04531":null,"SJAG_04534":null,"SJAG_04535":null,"SJAG_04536":null,"SJAG_04539":null,"SJAG_04540":null,"SJAG_04541":null,"SJAG_04544":null,"SJAG_04548":null,"SJAG_04549":null,"SJAG_04551":null,"SJAG_04554":null,"SJAG_04559":null,"SJAG_04563":null,"SJAG_04565":null,"SJAG_04567":null,"SJAG_04573":null,"SJAG_04577":null,"SJAG_04579":null,"SJAG_04580":null,"SJAG_04581":null,"SJAG_04586":null,"SJAG_04587":null,"SJAG_04590":null,"SJAG_04595":null,"SJAG_04602":null,"SJAG_04607":null,"SJAG_04609":null,"SJAG_04611":null,"SJAG_04612":null,"SJAG_04617":null,"SJAG_04618":null,"SJAG_04626":null,"SJAG_04627":null,"SJAG_04628":null,"SJAG_04629":null,"SJAG_04631":null,"SJAG_04633":null,"SJAG_04634":null,"SJAG_04638":null,"SJAG_04649":null,"SJAG_04650":null,"SJAG_04651":null,"SJAG_04652":null,"SJAG_04653":null,"SJAG_04655":null,"SJAG_04656":null,"SJAG_04657":null,"SJAG_04658":null,"SJAG_04660":null,"SJAG_04663":null,"SJAG_04665":null,"SJAG_04666":null,"SJAG_04672":null,"SJAG_04674":null,"SJAG_04679":null,"SJAG_04681":null,"SJAG_04682":null,"SJAG_04688":null,"SJAG_04693":null,"SJAG_04695":null,"SJAG_04699":null,"SJAG_04700":null,"SJAG_04704":null,"SJAG_04709":null,"SJAG_04710":null,"SJAG_04711":null,"SJAG_04713":null,"SJAG_04724":null,"SJAG_04726":null,"SJAG_04728":null,"SJAG_04735":null,"SJAG_04741":null,"SJAG_04744":null,"SJAG_04746":null,"SJAG_04747":null,"SJAG_04751":null,"SJAG_04754":null,"SJAG_04756":null,"SJAG_04758":null,"SJAG_04760":null,"SJAG_04762":null,"SJAG_04763":null,"SJAG_04764":null,"SJAG_04765":null,"SJAG_04771":null,"SJAG_04772":null,"SJAG_04774":null,"SJAG_04776":null,"SJAG_04778":null,"SJAG_04781":null,"SJAG_04783":null,"SJAG_04784":null,"SJAG_04814":null,"SJAG_04815":null,"SJAG_04817":null,"SJAG_04818":null,"SJAG_04824":null,"SJAG_04825":null,"SJAG_04827":null,"SJAG_04837":null,"SJAG_04841":null,"SJAG_04842":null,"SJAG_04843":null,"SJAG_04844":null,"SJAG_04845":null,"SJAG_04846":null,"SJAG_04847":null,"SJAG_04848":null,"SJAG_04849":null,"SJAG_04858":null,"SJAG_04859":null,"SJAG_04861":null,"SJAG_04863":null,"SJAG_04865":null,"SJAG_04866":null,"SJAG_04870":null,"SJAG_04871":null,"SJAG_04874":null,"SJAG_04877":null,"SJAG_04878":null,"SJAG_04879":null,"SJAG_04880":null,"SJAG_04885":null,"SJAG_04888":null,"SJAG_04890":null,"SJAG_04891":null,"SJAG_04894":null,"SJAG_04896":null,"SJAG_04897":null,"SJAG_04901":null,"SJAG_04902":null,"SJAG_04907":null,"SJAG_04912":null,"SJAG_04917":null,"SJAG_04920":null,"SJAG_04921":null,"SJAG_04927":null,"SJAG_04928":null,"SJAG_04932":null,"SJAG_04935":null,"SJAG_04936":null,"SJAG_04938":null,"SJAG_04939":null,"SJAG_04943":null,"SJAG_04944":null,"SJAG_04946":null,"SJAG_04948":null,"SJAG_04950":null,"SJAG_04953":null,"SJAG_04960":null,"SJAG_04963":null,"SJAG_04964":null,"SJAG_04966":null,"SJAG_04968":null,"SJAG_04969":null,"SJAG_04970":null,"SJAG_04972":null,"SJAG_04973":null,"SJAG_04974":null,"SJAG_04977":null,"SJAG_04978":null,"SJAG_04980":null,"SJAG_04981":null,"SJAG_04987":null,"SJAG_04988":null,"SJAG_04990":null,"SJAG_04998":null,"SJAG_04999":null,"SJAG_05000":null,"SJAG_05003":null,"SJAG_05004":null,"SJAG_05007":null,"SJAG_05008":null,"SJAG_05009":null,"SJAG_05010":null,"SJAG_05011":null,"SJAG_05014":null,"SJAG_05015":null,"SJAG_05018":null,"SJAG_05019":null,"SJAG_05021":null,"SJAG_05023":null,"SJAG_05024":null,"SJAG_05027":null,"SJAG_05029":null,"SJAG_05030":null,"SJAG_05032":null,"SJAG_05033":null,"SJAG_05179":null,"SJAG_05184":null,"SJAG_05185":null,"SJAG_05192":null,"SJAG_05193":null,"SJAG_05195":null,"SJAG_05197":null,"SJAG_05198":null,"SJAG_05205":null,"SJAG_05206":null,"SJAG_05208":null,"SJAG_05210":null,"SJAG_05211":null,"SJAG_05214":null,"SJAG_05216":null,"SJAG_05222":null,"SJAG_05223":null,"SJAG_05225":null,"SJAG_05228":null,"SJAG_05230":null,"SJAG_05232":null,"SJAG_05240":null,"SJAG_05243":null,"SJAG_05245":null,"SJAG_05248":null,"SJAG_05252":null,"SJAG_05253":null,"SJAG_05256":null,"SJAG_05260":null,"SJAG_05261":null,"SJAG_05266":null,"SJAG_05276":null,"SJAG_05277":null,"SJAG_05283":null,"SJAG_05287":null,"SJAG_05290":null,"SJAG_05303":null,"SJAG_05304":null,"SJAG_05312":null,"SJAG_05314":null,"SJAG_05316":null,"SJAG_05329":null,"SJAG_05331":null,"SJAG_05332":null,"SJAG_05333":null,"SJAG_05334":null,"SJAG_05337":null,"SJAG_05343":null,"SJAG_05346":null,"SJAG_05351":null,"SJAG_05413":null,"SJAG_05694":null,"SJAG_05926":null,"SJAG_05978":null,"SJAG_06270":null,"SJAG_06309":null,"SJAG_06355":null,"SJAG_06440":null,"SJAG_06576":null,"SJAG_06588":null,"SJAG_06592":null,"SJAG_06599":null,"SJAG_06612":null,"SJAG_06621":null,"SJAG_06622":null,"SJAG_06636":null,"SJAG_07000":null,"SJAG_07011":null,"SJAG_07013":null,"SJAG_07014":null,"SJAG_07017":null,"SJAG_16457":null,"SJAG_16460":null},"genotype_count":0,"in_subsets":["cc_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"cytosol","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"PMID:31956022":null},"secondary_identifiers":["Wikipedia:Cytosol","NIF_Subcellular:sao101633890"],"termid":"GO:0005829","terms_by_termid":{"GO:0000015":null,"GO:0002144":null,"GO:0005829":null,"GO:0005832":null,"GO:0005945":null,"GO:0005971":null,"GO:0022625":null,"GO:0022626":null,"GO:0022627":null,"GO:0033596":null,"GO:0072380":null,"GO:0090730":null,"GO:0097361":null,"GO:0099128":null,"GO:0120510":null,"GO:1904564":null}}


id: GO:0008237
data:
  {"annotated_genes":["SJAG_00573","SJAG_02809","SJAG_04215","SJAG_04651","SJAG_01896","SJAG_01816","SJAG_01088","SJAG_02503","SJAG_02900","SJAG_00969","SJAG_02033","SJAG_01430","SJAG_04533","SJAG_00662","SJAG_00546","SJAG_04858","SJAG_03396","SJAG_00479","SJAG_00795","SJAG_00181","SJAG_01004","SJAG_04514","SJAG_00720","SJAG_02341","SJAG_02244","SJAG_04641","SJAG_03752","SJAG_00762","SJAG_03648","SJAG_00406","SJAG_01528","SJAG_03022","SJAG_01312","SJAG_02419","SJAG_01281","SJAG_06636","SJAG_03586","SJAG_04497","SJAG_00742","SJAG_03429","SJAG_03407","SJAG_01542","SJAG_01179","SJAG_03147","SJAG_04103","SJAG_00764","SJAG_03686","SJAG_03393","SJAG_00451","SJAG_03744","SJAG_02397","SJAG_01838","SJAG_00730","SJAG_01321","SJAG_03009"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[89153,97518,98313,99597,106440,110152,114093,114601],"is_not":false,"summary":null,"term":"GO:0008237"},{"annotations":[114685,111214,109792,93646,115399,88009,95902,105274,99367,114613,113066,94802,91150,114259,96046,105108,104095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140492"},{"annotations":[97343,102774,113897,92897,87762,88017,105227,109502],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070006"},{"annotations":[73798,93975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004181"},{"annotations":[101750,96244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070573"},{"annotations":[97818,101700,110448,112634,108656,116099,91818,118173,89079,89761,96833,100539,96843,100580,105054,107540],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004222"},{"annotations":[113652,115642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008235"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of peptide bonds by a mechanism in which water acts as a nucleophile, one or two metal ions hold the water molecule in place, and charged amino acid side chains are ligands for the metal ions.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidase activity","termid":"GO:0008233"}],"gene_count":55,"genes_by_uniquename":{"SJAG_00181":null,"SJAG_00406":null,"SJAG_00451":null,"SJAG_00479":null,"SJAG_00546":null,"SJAG_00573":null,"SJAG_00662":null,"SJAG_00720":null,"SJAG_00730":null,"SJAG_00742":null,"SJAG_00762":null,"SJAG_00764":null,"SJAG_00795":null,"SJAG_00969":null,"SJAG_01004":null,"SJAG_01088":null,"SJAG_01179":null,"SJAG_01281":null,"SJAG_01312":null,"SJAG_01321":null,"SJAG_01430":null,"SJAG_01528":null,"SJAG_01542":null,"SJAG_01816":null,"SJAG_01838":null,"SJAG_01896":null,"SJAG_02033":null,"SJAG_02244":null,"SJAG_02341":null,"SJAG_02397":null,"SJAG_02419":null,"SJAG_02503":null,"SJAG_02809":null,"SJAG_02900":null,"SJAG_03009":null,"SJAG_03022":null,"SJAG_03147":null,"SJAG_03393":null,"SJAG_03396":null,"SJAG_03407":null,"SJAG_03429":null,"SJAG_03586":null,"SJAG_03648":null,"SJAG_03686":null,"SJAG_03744":null,"SJAG_03752":null,"SJAG_04103":null,"SJAG_04215":null,"SJAG_04497":null,"SJAG_04514":null,"SJAG_04533":null,"SJAG_04641":null,"SJAG_04651":null,"SJAG_04858":null,"SJAG_06636":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140096","GO:0003824","GO:0016787","GO:0008233","GO:0003674"],"is_obsolete":false,"name":"metallopeptidase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-5211340","Reactome:R-HSA-2220976","Reactome:R-HSA-9604264","Reactome:R-HSA-5211391","Reactome:R-HSA-9662837","Reactome:R-HSA-5211387","Reactome:R-HSA-157632","Reactome:R-HSA-9759522","Reactome:R-HSA-5211405","Reactome:R-HSA-157629","Reactome:R-HSA-193679","Reactome:R-HSA-2730752","Reactome:R-HSA-5211400","Reactome:R-HSA-2220944","Reactome:R-HSA-8986181","Reactome:R-HSA-9013284","Reactome:R-HSA-2022368","Reactome:R-HSA-2022393","Reactome:R-HSA-2022396","Reactome:R-HSA-2022399","Reactome:R-HSA-3928660","Reactome:R-HSA-5211356","Reactome:R-HSA-2666278"],"synonyms":[{"name":"metalloprotease activity","type":"narrow"},{"name":"metalloproteinase activity","type":"narrow"}],"termid":"GO:0008237","terms_by_termid":{"GO:0004181":null,"GO:0004222":null,"GO:0008235":null,"GO:0008237":null,"GO:0070006":null,"GO:0070573":null,"GO:0140492":null}}


id: MONDO:0021723
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tightness of the vaginal wall during vaginal penetration including sexual intercourse. It is caused by involuntary spasm of the pelvic floor muscles, and results in painful intercourse or failure to have intercourse. It may due to psychological conditions, trauma in the vaginal area, or vaginal infection.","definition_xrefs":["NCIT:C78703"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vaginal disorder","termid":"MONDO:0001433"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vaginismus","secondary_identifiers":["MEDGEN:412150","MESH:D052065","ICD10CM:N94.2","UMLS:C2004487"],"synonyms":[{"name":"myalgia of pelvic floor","type":"exact"},{"name":"vaginismus","type":"exact"}],"termid":"MONDO:0021723","xrefs":{"Monarch":{"xref_id":"0021723"}}}


id: MONDO:0014077
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cobblestone lissencephaly without muscular or ocular involvement is a form of cobblestone lissencephaly characterized by a constellation of brain malformations which can either exist alone or in conjunction with minimal muscular and ocular abnormalities. The clinical features of the disease include severe developmental delay, increased head circumference, hydrocephalus and seizures.","definition_xrefs":["Orphanet:352682"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cobblestone lissencephaly","termid":"MONDO:0018869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"cobblestone lissencephaly without muscular or ocular involvement","secondary_identifiers":["MEDGEN:767571","OMIM:615191","UMLS:C3554657","GARD:17526","DOID:0112230"],"synonyms":[{"name":"LIS5","type":"related"},{"name":"cobblestone lissencephaly without muscular or eye involvement","type":"exact"},{"name":"cobblestone lissencephaly without muscular or ocular involvement","type":"exact"},{"name":"lissencephaly 5","type":"related"},{"name":"lissencephaly type 2 without muscular or eye involvement","type":"exact"},{"name":"lissencephaly type 2 without muscular or ocular involvement","type":"exact"},{"name":"lissencephaly type 5","type":"exact"}],"termid":"MONDO:0014077","xrefs":{"Monarch":{"xref_id":"0014077"}}}


id: PBO:0051466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable (I)-38 (pseudogene)","termid":"PBO:0051466"}


id: PBO:0034763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine tRNA C32 methyl transferase Trm141","termid":"PBO:0034763"}


id: GO:0052403
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism stops, prevents, or reduces the frequency, rate or extent of symbiont enzyme activity. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation by host of symbiont catalytic activity (obsolete GO:0052403)","synonyms":[{"name":"down regulation by host of symbiont enzyme activity","type":"exact"},{"name":"down regulation by host of symbiont protein function","type":"broad"},{"name":"down-regulation by host of symbiont enzyme activity","type":"exact"},{"name":"down-regulation by host of symbiont protein function","type":"broad"},{"name":"downregulation by host of symbiont enzyme activity","type":"exact"},{"name":"downregulation by host of symbiont protein function","type":"broad"},{"name":"inhibition by host of symbiont enzyme activity","type":"narrow"},{"name":"inhibition by host of symbiont protein function","type":"narrow"},{"name":"inhibition of symbiont enzyme activity","type":"exact"},{"name":"inhibition of symbiont protein function","type":"broad"},{"name":"negative regulation by host of symbiont enzyme activity","type":"exact"},{"name":"negative regulation by host of symbiont molecular function","type":"broad"}],"termid":"GO:0052403"}


id: PBO:0072097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S12 pseudogene 28","termid":"PBO:0072097"}


id: MONDO:0035734
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary angioedema","termid":"MONDO:0019623"}],"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":"hereditary angioedema with normal C1inh not related to F12 or PLG variant","secondary_identifiers":["UMLS:C5681601","Orphanet:599418","GARD:22406","MEDGEN:1843147"],"termid":"MONDO:0035734","xrefs":{"Monarch":{"xref_id":"0035734"}}}


id: MONDO:0031332
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A bleeding syndrome characterized by spontaneous mucocutaneous bleeding and an exaggerated response to trauma due to a constitutional thrombocytopenia","definition_xrefs":["Orphanet:849"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Glanzmann thrombasthenia","termid":"MONDO:0100326"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"Glanzmann thrombasthenia 1","secondary_identifiers":["NCIT:C61249","OMIM:273800","GARD:15240","DOID:2219","MESH:D013915","SCTID:32942005"],"synonyms":[{"name":"BDPLT2","type":"exact"},{"name":"Diacyclothrombopathia 2B 3A","type":"related"},{"name":"GP IIb-IIIa Complex, deficiency of","type":"related"},{"name":"GT","type":"related"},{"name":"Glanzmann thrombasthenia","type":"broad"},{"name":"Glanzmann thrombasthenia 1","type":"exact"},{"name":"Glanzmann thrombasthenia type A","type":"related"},{"name":"Glanzmann's thrombasthenia","type":"broad"},{"name":"Platelet fibrinogen receptor, deficiency of","type":"related"},{"name":"Platelet glycoprotein 2B 3A deficiency","type":"related"},{"name":"Platelet glycoprotein IIb-IIIa deficiency","type":"related"},{"name":"Thrombocytasthenia","type":"exact"},{"name":"bleeding disorder, Platelet-type, 2","type":"related"},{"name":"deficiency of GP 2B 3A complex","type":"related"},{"name":"deficiency of GP IIb-IIIa complex","type":"exact"},{"name":"deficiency of glycoprotein complex IIb-IIIa","type":"exact"},{"name":"deficiency of platelet fibrinogen receptor","type":"exact"},{"name":"glycoprotein Complex IIb-IIIa, deficiency of","type":"related"},{"name":"glycoprotein IIb/IIIa defect","type":"exact"},{"name":"platelet glycoprotein IIb-IIIa deficiency","type":"exact"},{"name":"platelet-type bleeding disorder 2","type":"exact"},{"name":"thrombasthenia","type":"exact"},{"name":"thrombasthenia of Glanzmann and Naegeli","type":"exact"}],"termid":"MONDO:0031332","xrefs":{"Monarch":{"xref_id":"0031332"}}}


id: SO:0002023
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A nucleic tag which is used in a ligation step of library preparation process to allow pooling of samples while maintaining ability to identify individual source material and creation of a multiplexed library.","definition_xrefs":["PMID:22574170","OBO:prs"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tag","termid":"SO:0000324"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiplexing_sequence_identifier","synonyms":[{"name":"multiplexing sequence identifier","type":"exact"}],"termid":"SO:0002023"}


id: MONDO:0017735
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"aortic valve stenosis","termid":"MONDO:0042981"}],"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":"congenital aortic valve stenosis","secondary_identifiers":["ICD9:746.3","GARD:18786","MedDRA:10010371","MEDGEN:509030","UMLS:C0152417","Orphanet:3093","SCTID:18546004","icd11.foundation:1824398514"],"termid":"MONDO:0017735","xrefs":{"Monarch":{"xref_id":"0017735"}}}


id: FYPO:0006104
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of retrotransposon integration is decreased.","definition_xrefs":["PMID:26358720","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transposition","termid":"FYPO:0000591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"decreased retrotransposon integration","synonyms":[{"name":"decreased retrotransposon integration during mitotic cell cycle","type":"related"},{"name":"decreased retrotransposon integration during vegetative growth","type":"exact"},{"name":"decreased transposon integration involved in RNA-mediated transposition","type":"exact"},{"name":"reduced retrotransposon integration","type":"exact"}],"termid":"FYPO:0006104"}


id: MONDO:0011311
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete glaucoma 1, open angle, F (obsolete MONDO:0011311)","secondary_identifiers":["MESH:C566383","OMIM:603383"],"synonyms":[{"name":"GLC1F","type":"related"},{"name":"glaucoma 1, open angle, F","type":"exact"},{"name":"glaucoma 1, open angle, type F","type":"exact"},{"name":"glaucoma, primary open angle, adult-onset","type":"related"}],"termid":"MONDO:0011311","xrefs":{"Monarch":{"xref_id":"0011311"}}}


id: GO:1902604
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of N-(4-aminobenzoyl)-L-glutamate across a membrane.","definition_xrefs":["GOC:TermGenie","GOC:pr","GO_REF:0000069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"p-aminobenzoyl-glutamate transport","termid":"GO:0015814"},{"relation_name":"is_a","term_name":"dipeptide transmembrane transport","termid":"GO:0035442"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transport","termid":"GO:1905039"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179","GO:0055085"],"is_obsolete":false,"name":"p-aminobenzoyl-glutamate transmembrane transport","synonyms":[{"name":"N-(4-aminobenzoyl)-L-glutamate transmembrane transport","type":"exact"}],"termid":"GO:1902604"}


id: PBO:0070207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 134 pseudogene","termid":"PBO:0070207"}


id: PBO:0075067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 116-30","termid":"PBO:0075067"}


id: PBO:0062509
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily I member 1 pseudogene","termid":"PBO:0062509"}


id: FYPO:0006507
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which duplication of DNA sequences in the subtelomeric region occur more frequently than in wild type cells during G0 phase.","definition_xrefs":["PomBase:mah","PMID:29167439"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased gross chromosomal rearrangement","termid":"FYPO:0001740"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000641","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased subtelomeric DNA amplification during G0","synonyms":[{"name":"increased occurrence of subtelomeric DNA amplification during G0","type":"exact"},{"name":"increased subtelomeric DNA amplification during cell quiescence","type":"exact"},{"name":"increased subtelomeric DNA amplification during quiescence","type":"exact"},{"name":"increased subtelomeric DNA sequence duplication during G0","type":"exact"},{"name":"increased subtelomeric amplification during G0","type":"exact"}],"termid":"FYPO:0006507"}


id: MONDO:0016946
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete partial trisomy of the short arm of chromosome 9 (obsolete MONDO:0016946)","termid":"MONDO:0016946","xrefs":{"Monarch":{"xref_id":"0016946"}}}


id: PBO:0081370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 208","termid":"PBO:0081370"}


id: PBO:0057690
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1279","termid":"PBO:0057690"}


id: FYPO:0001905
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the number, structure, and orientation of microtubules in the mitotic spindle are normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component during vegetative growth","termid":"FYPO:0001313"},{"relation_name":"part_of","term_name":"normal mitotic spindle","termid":"FYPO:0001399"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal mitotic spindle microtubules","synonyms":[{"name":"normal mitotic spindle microtubules during vegetative growth","type":"exact"},{"name":"normal spindle microtubules during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001905"}


id: GO:1905580
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ERBB3 signaling pathway.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:27353365","GOC:als"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of ERBB signaling pathway","termid":"GO:1901186"},{"relation_name":"is_a","term_name":"regulation of ERBB3 signaling pathway","termid":"GO:1905578"},{"relation_name":"positively_regulates","term_name":"ERBB3 signaling pathway","termid":"GO:0038129"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of ERBB3 signaling pathway","synonyms":[{"name":"activation of ERBB3 signaling pathway","type":"narrow"},{"name":"activation of ERBB3 signalling pathway","type":"narrow"},{"name":"activation of HER3 signaling pathway","type":"narrow"},{"name":"activation of receptor tyrosine-protein kinase erbB-3 signaling pathway","type":"narrow"},{"name":"positive regulation of ERBB3 signalling pathway","type":"exact"},{"name":"positive regulation of HER3 signaling pathway","type":"exact"},{"name":"positive regulation of receptor tyrosine-protein kinase erbB-3 signaling pathway","type":"exact"},{"name":"up regulation of ERBB3 signaling pathway","type":"exact"},{"name":"up regulation of ERBB3 signalling pathway","type":"exact"},{"name":"up regulation of HER3 signaling pathway","type":"exact"},{"name":"up regulation of receptor tyrosine-protein kinase erbB-3 signaling pathway","type":"exact"},{"name":"up-regulation of ERBB3 signaling pathway","type":"exact"},{"name":"up-regulation of ERBB3 signalling pathway","type":"exact"},{"name":"up-regulation of HER3 signaling pathway","type":"exact"},{"name":"up-regulation of receptor tyrosine-protein kinase erbB-3 signaling pathway","type":"exact"},{"name":"upregulation of ERBB3 signaling pathway","type":"exact"},{"name":"upregulation of ERBB3 signalling pathway","type":"exact"},{"name":"upregulation of HER3 signaling pathway","type":"exact"},{"name":"upregulation of receptor tyrosine-protein kinase erbB-3 signaling pathway","type":"exact"}],"termid":"GO:1905580"}


id: GO:1903142
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of establishment of endothelial barrier.","definition_xrefs":["GOC:als","GOC:TermGenie","GO_REF:0000058","PMID:24851274"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of endothelial cell development","termid":"GO:1901552"},{"relation_name":"is_a","term_name":"regulation of establishment of endothelial barrier","termid":"GO:1903140"},{"relation_name":"positively_regulates","term_name":"establishment of endothelial barrier","termid":"GO:0061028"}],"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 endothelial barrier","synonyms":[{"name":"activation of establishment of endothelial barrier","type":"narrow"},{"name":"up regulation of establishment of endothelial barrier","type":"exact"},{"name":"up-regulation of establishment of endothelial barrier","type":"exact"},{"name":"upregulation of establishment of endothelial barrier","type":"exact"}],"termid":"GO:1903142"}


id: PBO:0051455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 6-57","termid":"PBO:0051455"}


id: GO:0180032
data:
  {"annotated_genes":["SJAG_00581"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[108933],"is_not":false,"summary":null,"term":"GO:0180032"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: histone H4 N6-acetyl-L-lysine (position 5) + H2O = histone H4 L-lysine (position 5) + acetate. This reaction represents the removal of an acetyl group from lysine at position 5 of the histone H4 protein.","definition_xrefs":["PMID:37459529"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H4K deacetylase activity","termid":"GO:0141051"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00581":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019213"},{"rel_name":"is_a","termid":"GO:0033558"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0019213","GO:0003674","GO:0003824","GO:0033558","GO:0140096"],"is_obsolete":false,"name":"histone H4K5 deacetylase activity, hydrolytic mechanism","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"histone H4K5 deacetylase activity","type":"broad"}],"termid":"GO:0180032","terms_by_termid":{"GO:0180032":null}}


id: GO:0019535
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of ferric-vibriobactin ions from one side of a membrane to the other.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iron chelate transmembrane transporter activity","termid":"GO:0015603"}],"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":"ferric-vibriobactin transmembrane transporter activity","termid":"GO:0019535"}


id: PBO:0046407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enhancer of polycomb homolog 2","termid":"PBO:0046407"}


id: PBO:0089752
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription elongation factor TFIIS","termid":"PBO:0089752"}


id: PBO:0034472
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-premature_mitotic_spindle_elongation","termid":"PBO:0034472"}


id: PATO:0001825
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A wetness quality that is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"wet","termid":"PATO:0001823"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased wetness","termid":"PATO:0001825"}


id: GO:0021584
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to the pons. This process pertains to the initial formation of a structure from unspecified parts. The pons lies above the medulla and next to the cerebellum. The pons conveys information about movement from the cerebral hemisphere to the cerebellum.","definition_xrefs":["GOC:dgh","GO_REF:0000021","GOC:dph","ISBN:0838580343","GOC:jid","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"hindbrain formation","termid":"GO:0021576"},{"relation_name":"part_of","term_name":"pons morphogenesis","termid":"GO:0021583"}],"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":"pons formation","termid":"GO:0021584"}


id: PATO:0002224
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An angular shape quality inhering in a bearer by virtue of the bearer's having a single angle in its length giving the bearer the form of the letter V.","definition_xrefs":["PATOC:JE"],"direct_ancestors":[{"relation_name":"is_a","term_name":"angular","termid":"PATO:0001977"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-shaped","termid":"PATO:0002224"}


id: GO:0034673
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of inhibin, type III transforming growth factor beta receptor (also known as betaglycan), and the type II activin receptor ActRII. The complex is thought to negatively regulate the activity of activin B.","definition_xrefs":["GOC:BHF","PMID:10746731"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"inhibin-betaglycan-ActRII complex","termid":"GO:0034673"}


id: GO:0097312
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Any constituent part of the biofilm matrix, a structure lying external to bacterial cells. A biofilm is an aggregate of surface-associated bacteria, and the biofilm matrix is the envelope of polymeric substances that surrounds the bacteria.","definition_xrefs":["Wikipedia:Biofilm","GOC:imk","PMID:22571672"],"gene_count":0,"genotype_count":0,"name":"obsolete bacterial biofilm matrix component (obsolete GO:0097312)","synonyms":[{"name":"biofilm matrix part","type":"exact"}],"termid":"GO:0097312"}


id: PBO:0061623
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nudix hydrolase 7","termid":"PBO:0061623"}


id: PBO:0084113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Helicase encoded by the Y' element of subtelomeric regions; highly expressed in the mutants lacking the telomerase component TLC1; potentially phosphorylated by Cdc28p","termid":"PBO:0084113"}


id: PBO:0034648
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_SUMO_chain_length","termid":"PBO:0034648"}


id: PBO:0080953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger BED-type containing 6","termid":"PBO:0080953"}


id: MONDO:0006312
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, localized, nodular and well-circumscribed neoplasm usually seen as a congenital neoplasm or in the first year of life. It is characterized by a biphasic growth pattern and is composed of small, undifferentiated mesenchymal cells associated with branching thin-walled vessels and more mature neoplastic spindle cells with abundant eosinophilic cytoplasm in a collagenous stroma.","definition_xrefs":["NCIT:C7052"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"benign digestive system neoplasm","termid":"MONDO:0000385"},{"relation_name":"excluded_subClassOf","term_name":"benign connective and soft tissue neoplasm","termid":"MONDO:0000654"},{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"},{"relation_name":"is_a","term_name":"benign perivascular tumor","termid":"MONDO:0003342"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myofibroma","secondary_identifiers":["ONCOTREE:MF","EFO:1000389","UMLS:C1266121","ICDO:8824/0","MEDGEN:220420","MESH:D047708","DOID:4386"],"synonyms":[{"name":"infantile hemangiopericytoma","type":"related"},{"name":"lipoleiomyoma","type":"exact"},{"name":"myofibroma","type":"exact"},{"name":"myofibroma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0006312","xrefs":{"Monarch":{"xref_id":"0006312"}}}


id: SO:0000020
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of double stranded RNA where the bases do not conform to WC base pairing. The loop is closed on both sides by canonical base pairing. If the interruption to base pairing occurs on one strand only, it is known as a bulge.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA_motif","termid":"SO:0000715"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA_internal_loop","synonyms":[{"name":"RNA internal loop","type":"exact"}],"termid":"SO:0000020"}


id: GO:1990951
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The assembly and organization of the manchette, a tubular array of microtubules, possibly also containing actin filaments, that extends from the perinuclear ring surrounding the spermatid nucleus to the flagellar axoneme.","definition_xrefs":["PMID:24440897","GOC:krc","PMID:26792866","PMID:22319670"],"gene_count":0,"genotype_count":0,"name":"obsolete manchette assembly (obsolete GO:1990951)","termid":"GO:1990951"}


id: GO:0050310
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: sulfite + 2 ferricytochrome c + H2O = sulfate + 2 ferrocytochrome c.","definition_xrefs":["MetaCyc:SULFITE-DEHYDROGENASE-RXN","EC:1.8.2.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, cytochrome as acceptor","termid":"GO:0016669"}],"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":"sulfite dehydrogenase activity","secondary_identifiers":["RHEA:14281"],"synonyms":[{"name":"sulfite cytochrome c reductase activity","type":"related"},{"name":"sulfite-cytochrome c oxidoreductase activity","type":"related"},{"name":"sulfite:ferricytochrome-c oxidoreductase activity","type":"related"},{"name":"sulphite dehydrogenase activity","type":"exact"}],"termid":"GO:0050310"}


id: GO:0080056
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Vascular tissue pattern formation as it occurs in the petal of vascular plants.","definition_xrefs":["PMID:17369435"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xylem and phloem pattern formation","termid":"GO:0010051"}],"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":"petal vascular tissue pattern formation","termid":"GO:0080056"}


id: MOD:00157
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-tryptophan residue to an L-tryptophan quinone.","definition_xrefs":["Unimod:392#W","DeltaMass:0","PubMed:2028257","RESID:AA0148"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon oxygenated residue","termid":"MOD:00679"},{"relation_name":"is_a","term_name":"modified L-tryptophan residue","termid":"MOD:00918"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-tryptophyl quinone","synonyms":[{"name":"(2S)-2-amino-3-(6,7-dioxo-1H-indol-3-yl)propanoic acid","type":"exact"},{"name":"2-amino-3-(6,7-dioxo-6,7-dihydro-1H-indol-3-yl)-propionic acid","type":"exact"},{"name":"3-[(2S)-2-amino-2-carboxyethyl]-6,7-indolinedione","type":"exact"},{"name":"6,7 Dione (from Tryptophan)","type":"exact"},{"name":"L-tryptophyl quinone","type":"exact"},{"name":"MOD_RES Tryptophylquinone","type":"exact"},{"name":"N-(3-carboxy-1-oxopropyl)-L-tryptophan","type":"exact"},{"name":"Quinone","type":"related"},{"name":"TrpQ","type":"exact"},{"name":"quinone","type":"related"}],"termid":"MOD:00157"}


id: PBO:0060085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 32","termid":"PBO:0060085"}


id: MONDO:0000029
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete corticosterone methyloxidase deficiency (obsolete MONDO:0000029)","termid":"MONDO:0000029","xrefs":{"Monarch":{"xref_id":"0000029"}}}


id: FYPO:0000596
data:
  {"alleles_by_uniquename":{"SJAG_03689:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03689","name":"dcr1delta","uniquename":"SJAG_03689:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118589],"is_not":false,"summary":null,"term":"FYPO:0000596"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which transposition is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03689":null},"genotype_count":1,"genotypes_by_uniquename":{"dcr1delta":{"display_name":"dcr1delta","display_uniquename":"dcr1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03689:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal transposition","references_by_uniquename":{"PMID:35226668":null},"single_locus_annotated_genes":["SJAG_03689"],"single_locus_genotype_uniquenames":["dcr1delta"],"synonyms":[{"name":"normal transposable element transposition","type":"exact"},{"name":"normal transposition during mitotic cell cycle","type":"related"},{"name":"normal transposition during vegetative growth","type":"exact"},{"name":"transposable element transposition: normal","type":"related"}],"termid":"FYPO:0000596","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000162":null,"FYPO:0000596":null,"FYPO_EXT:0000001":null}}


id: PBO:0076290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synapsin III","termid":"PBO:0076290"}


id: PBO:0039843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGAP11A-SCG5 readthrough","termid":"PBO:0039843"}


id: GO:0015478
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of oligosaccharide, sized less than 1000 Da, from one side of a membrane to the other. The transmembrane portions of porins consist exclusively of beta-strands which form a beta-barrel. They are found in the outer membranes of Gram-negative bacteria, mitochondria, plastids and possibly acid-fast Gram-positive bacteria.","definition_xrefs":["GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharide transmembrane transporter activity","termid":"GO:0015157"},{"relation_name":"is_a","term_name":"porin activity","termid":"GO:0015288"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"oligosaccharide transporting porin activity","synonyms":[{"name":"raffinose porin","type":"narrow"}],"termid":"GO:0015478"}


id: MONDO:0020157
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete syndromic palpebral coloboma (obsolete MONDO:0020157)","secondary_identifiers":["Orphanet:98566"],"termid":"MONDO:0020157","xrefs":{"Monarch":{"xref_id":"0020157"}}}


id: GO:0106212
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which centromeres dissociate from the spindle pole body, contributing to the rearrangement of chromosomes into the orientation characteristic of meiotic prophase I.","definition_xrefs":["PMID:27611693","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome organization involved in meiotic cell cycle","termid":"GO:0070192"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"centromere detachment from spindle pole body involved in meiotic chromosome organization","synonyms":[{"name":"centromere detachment from SPB involved in meiotic chromosome organization","type":"exact"},{"name":"centromere detachment from spindle pole body involved in chromosome organization involved in meiotic cell cycle","type":"exact"}],"termid":"GO:0106212"}


id: PBO:0042279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCZ1 homolog B, vacuolar protein trafficking and biogenesis associated","termid":"PBO:0042279"}


id: GO:0018208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification of peptidyl-proline.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-amino acid modification","termid":"GO:0018193"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"peptidyl-proline modification","termid":"GO:0018208"}


id: FYPO:0000538
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of protein secretion is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein secretion during vegetative growth","termid":"FYPO:0000536"},{"relation_name":"is_a","term_name":"decreased protein transport during vegetative growth","termid":"FYPO:0000541"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000138","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"decreased protein secretion during vegetative growth","synonyms":[{"name":"decreased protein secretion during mitotic cell cycle","type":"related"},{"name":"protein secretion: decreased","type":"related"},{"name":"reduced protein secretion during vegetative growth","type":"exact"}],"termid":"FYPO:0000538"}


id: PATO:0001579
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality inhering in a bearer by virtue of the bearer's disposition to shrink or contract.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality","termid":"PATO:0001018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"contractility","termid":"PATO:0001579"}


id: GO:0090080
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of a fibroblast growth factor receptor binding to one of its physiological ligands resulting in an increase in the rate or frequency of a MAPKKK cascade.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibroblast growth factor receptor signaling pathway","termid":"GO:0008543"},{"relation_name":"is_a","term_name":"positive regulation of MAPK cascade","termid":"GO:0043410"}],"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"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of MAPKKK cascade by fibroblast growth factor receptor signaling pathway","synonyms":[{"name":"positive regulation of MAPKKK cascade by fibroblast growth factor receptor signalling pathway","type":"exact"}],"termid":"GO:0090080"}


id: GO:0106176
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The volume enclosed by the membrane of a clathrin-coated endocytic vesicle.","definition_xrefs":["GOC:pde","PMID:2516741"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocytic vesicle lumen","termid":"GO:0071682"},{"relation_name":"part_of","term_name":"clathrin-coated endocytic vesicle","termid":"GO:0045334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0031410"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0031410"],"is_obsolete":false,"name":"clathrin-coated endocytic vesicle lumen","termid":"GO:0106176"}


id: PBO:0091420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NAD binding dehydrogenase family protein, human DHDH ortholog, unknown biological role, implicated in carbohydrate metabolic process","termid":"PBO:0091420"}


id: GO:0038112
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by interleukin-8 binding to its receptor on the surface of a cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:nhn","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"},{"relation_name":"part_of","term_name":"cellular response to interleukin-8","termid":"GO:0098759"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"interleukin-8-mediated signaling pathway","synonyms":[{"name":"IL-8-mediated signaling pathway","type":"exact"},{"name":"interleukin-8-mediated signalling pathway","type":"exact"}],"termid":"GO:0038112"}


id: GO:0004262
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of proteins with broad specificity, and of BZ-Arg-OET > Ac-Tyr-OET. Does not hydrolyze peptide amides.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete cerevisin activity (obsolete GO:0004262)","synonyms":[{"name":"baker's yeast proteinase B","type":"related"},{"name":"brewer's yeast proteinase","type":"narrow"},{"name":"cerevisin activity","type":"exact"},{"name":"peptidase beta","type":"related"},{"name":"proteinase yscB activity","type":"narrow"},{"name":"yeast proteinase B activity","type":"narrow"}],"termid":"GO:0004262"}


id: PBO:0057243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 448","termid":"PBO:0057243"}


id: PBO:0041130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BTB domain containing 10","termid":"PBO:0041130"}


id: MONDO:0850078
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":"non-syndromic non-specific multisutural craniosynostosis","secondary_identifiers":["Orphanet:620158","MEDGEN:1842261","UMLS:C5680398","GARD:22475"],"termid":"MONDO:0850078","xrefs":{"Monarch":{"xref_id":"0850078"}}}


id: GO:0032242
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the directed movement of a nucleoside into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nucleobase-containing compound transport","termid":"GO:0032239"},{"relation_name":"regulates","term_name":"nucleoside transport","termid":"GO:0015858"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of nucleoside transport","termid":"GO:0032242"}


id: GO:0036465
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The trafficking of synaptic vesicles from the pre-synaptic membrane so the vesicle can dock and prime for another round of exocytosis and neurotransmitter release. Recycling occurs after synaptic vesicle exocytosis, and is necessary to replenish presynaptic vesicle pools, sustain transmitter release and preserve the structural integrity of the presynaptic membrane. Recycling can occur following transient fusion with the presynaptic membrane (kiss and run), or via endocytosis of presynaptic membrane.","definition_xrefs":["GOC:pad","PMID:23245563","GOC:PARL","GOC:bf","PMID:15217342","PMID:22026965"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport","termid":"GO:0006810"},{"relation_name":"is_a","term_name":"establishment of localization in cell","termid":"GO:0051649"},{"relation_name":"part_of","term_name":"synaptic vesicle cycle","termid":"GO:0099504"}],"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"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0016192","GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"synaptic vesicle recycling","synonyms":[{"name":"kiss-and-run synaptic vesicle recycling","type":"narrow"},{"name":"kiss-and-stay synaptic vesicle recycling","type":"narrow"}],"termid":"GO:0036465"}


id: MONDO:0002088
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinal vein occlusion","termid":"MONDO:0006951"}],"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":"partial retinal vein occlusion","secondary_identifiers":["MEDGEN:78753","SCTID:65593009","UMLS:C0271080","NCIT:C35341","DOID:1726"],"synonyms":[{"name":"partial occlusion of retinal vein","type":"exact"},{"name":"partial retinal vein occlusion","type":"exact"}],"termid":"MONDO:0002088","xrefs":{"Monarch":{"xref_id":"0002088"}}}


id: GO:1902047
data:
  {"annotated_genes":["SJAG_04469","SJAG_02125","SJAG_02060","SJAG_02344","SJAG_02059"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105859],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902267"},{"annotations":[110383,57728,116790,108905,108899,108911],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903711"},{"annotations":[108900,110384,116791,109806,108912,68396,108906],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903710"}]},"cv_name":"biological_process","definition":"The process in which a polyamine macromolecule is transported across a membrane.","definition_xrefs":["GOC:vw","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyamine transport","termid":"GO:0015846"},{"relation_name":"is_a","term_name":"transmembrane transport","termid":"GO:0055085"}],"gene_count":5,"genes_by_uniquename":{"SJAG_02059":null,"SJAG_02060":null,"SJAG_02125":null,"SJAG_02344":null,"SJAG_04469":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"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:0055085","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"polyamine transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["GO:1905122"],"synonyms":[{"name":"polyamine import","type":"related"},{"name":"polyamine uptake","type":"related"}],"termid":"GO:1902047","terms_by_termid":{"GO:1902267":null,"GO:1903710":null,"GO:1903711":null}}


id: MONDO:0032753
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spastic ataxia","termid":"MONDO:0017845"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spastic ataxia 9, autosomal recessive","secondary_identifiers":["UMLS:C5193100","MEDGEN:1680026","OMIM:618438"],"synonyms":[{"name":"SPASTIC ATAXIA 9, AUTOSOMAL RECESSIVE","type":"related"},{"name":"SPAX9","type":"related"}],"termid":"MONDO:0032753","xrefs":{"Monarch":{"xref_id":"0032753"}}}


id: PBO:0047740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibronectin type III domain containing 3C, pseudogene","termid":"PBO:0047740"}


id: PBO:0050826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydroxypyruvate isomerase (putative)","termid":"PBO:0050826"}


id: PR:Q09671
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC5H10.10 gene.","definition_xrefs":["UniProtKB:Q09671","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":"NADPH dehydrogenase C5H10.10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC5H10.10","synonyms":[{"name":"Old yellow enzyme homolog 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPAC5H10.10","type":"exact"}],"termid":"PR:Q09671"}


id: GO:0004445
data:
  {"annotated_genes":["SJAG_00063","SJAG_04545"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[107758],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052659"},{"annotations":[110619,107759],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052658"}]},"cv_name":"molecular_function","definition":"Catalysis of the reactions: D-myo-inositol 1,4,5-trisphosphate + H2O = myo-inositol 1,4-bisphosphate + phosphate, and 1D-myo-inositol 1,3,4,5-tetrakisphosphate + H2O = 1D-myo-inositol 1,3,4-trisphosphate + phosphate.","definition_xrefs":["EC:3.1.3.56"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol trisphosphate phosphatase activity","termid":"GO:0046030"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00063":null,"SJAG_04545":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0016788","GO:0003674"],"is_obsolete":false,"name":"inositol-polyphosphate 5-phosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"1D-myo-inositol-1,4,5-trisphosphate 5-phosphohydrolase activity","type":"narrow"},{"name":"5PTase activity","type":"related"},{"name":"D-myo-inositol 1,4,5-triphosphate 5-phosphatase activity","type":"narrow"},{"name":"D-myo-inositol 1,4,5-trisphosphate 5-phosphatase activity","type":"narrow"},{"name":"D-myo-inositol(1,4,5)/(1,3,4,5)-polyphosphate 5-phosphatase activity","type":"related"},{"name":"Ins(1,4,5)P(3) 5-phosphatase activity","type":"narrow"},{"name":"Ins(1,4,5)P3 5-phosphatase activity","type":"narrow"},{"name":"Ins(1,4,5)P3/Ins(1,3,4,5)P4 5-phosphatase activity","type":"related"},{"name":"InsP(3)/Ins(1,3,4,5)P(4) 5-phosphatase activity","type":"narrow"},{"name":"InsP3/Ins(1,3,4,5)P4 5-phosphatase activity","type":"narrow"},{"name":"L-myo-inositol 1,4,5-trisphosphate-monoesterase activity","type":"broad"},{"name":"inosine triphosphatase activity","type":"related"},{"name":"inositol 1,4,5-trisphosphate phosphatase activity","type":"broad"},{"name":"inositol phosphate 5-phosphomonoesterase activity","type":"broad"},{"name":"inositol polyphosphate-5-phosphatase activity","type":"related"},{"name":"inositol triphosphate 5-phosphomonoesterase activity","type":"related"},{"name":"inositol trisphosphate phosphomonoesterase activity","type":"related"},{"name":"inositol-1,4,5-trisphosphate 5-phosphatase activity","type":"narrow"},{"name":"inositol-1,4,5-trisphosphate/1,3,4,5-tetrakisphosphate 5-phosphatase activity","type":"related"},{"name":"myo-inositol-1,4,5-trisphosphate 5-phosphatase activity","type":"narrow"},{"name":"type I inositol-polyphosphate phosphatase activity","type":"related"},{"name":"type II inositol polyphosphate 5-phosphatase activity","type":"related"},{"name":"type II inositol-1,4,5-trisphosphate 5-phosphatase activity","type":"narrow"}],"termid":"GO:0004445","terms_by_termid":{"GO:0052658":null,"GO:0052659":null}}


id: PBO:0055984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat transmembrane neuronal 2","termid":"PBO:0055984"}


id: PBO:0017447
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-participates_in_a_biotic-biotic_interaction_with","termid":"PBO:0017447"}


id: MONDO:0010094
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spondylocarpotarsal synostosis (SCT) syndrome is a skeletal dysplasia clinically characterized by postnatal progressive vertebral fusions frequently manifesting as block vertebrae, contributing to an undersized trunk and a disproportionate short stature, scoliosis, lordosis, carpal and tarsal synostosis, with club feet and a mild facial dysmorphism.","definition_xrefs":["Orphanet:3275"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone development disease","termid":"MONDO:0005497"},{"relation_name":"is_a","term_name":"filamin-related bone disorder","termid":"MONDO:0019690"},{"relation_name":"is_a","term_name":"spondylodysplastic dysplasia","termid":"MONDO:0019694"}],"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":"spondylocarpotarsal synostosis syndrome","secondary_identifiers":["MESH:C535780","UMLS:C1848934","GARD:4974","DOID:0090116","OMIM:272460","SCTID:702351004","ICD9:758.89","MEDGEN:341339"],"synonyms":[{"name":"SCT","type":"exact"},{"name":"Synspondylism","type":"exact"},{"name":"Synspondylism congenital","type":"related"},{"name":"Synspondylism, congenital","type":"related"},{"name":"congenital scoliosis with unilateral unsegmented bar","type":"exact"},{"name":"congenital synspondylism","type":"exact"},{"name":"scoliosis, congenital with unilateral unsegmented bar","type":"related"},{"name":"scoliosis, congenital, with unilateral unsegmented Bar","type":"related"},{"name":"spondylocarpotarsal syndrome","type":"exact"},{"name":"spondylocarpotarsal synostosis","type":"exact"},{"name":"spondylocarpotarsal synostosis syndrome","type":"exact"},{"name":"vertebral fusion with carpal coalition","type":"exact"}],"termid":"MONDO:0010094","xrefs":{"Monarch":{"xref_id":"0010094"}}}


id: MONDO:1010065
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dermatomyositis characterized by the presence of anti-Mi2 autoantibodies.","definition_xrefs":["PMID:31279808"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatomyositis","termid":"MONDO:0016367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0005093"],"is_obsolete":false,"name":"anti-Mi2 dermatomyositis","termid":"MONDO:1010065","xrefs":{"Monarch":{"xref_id":"1010065"}}}


id: PBO:0061087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NK2 homeobox 5","termid":"PBO:0061087"}


id: PBO:0012561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine phosphatase Stp1","termid":"PBO:0012561"}


id: GO:0047376
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: all-trans-retinyl palmitate + H2O = all-trans-retinol + H+ + palmitate.","definition_xrefs":["RHEA:13933"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinyl-palmitate esterase activity","termid":"GO:0050253"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0016788","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"all-trans-retinyl-palmitate hydrolase, all-trans-retinol forming activity","secondary_identifiers":["Reactome:R-HSA-2429643","KEGG_REACTION:R02368","MetaCyc:3.1.1.64-RXN","Reactome:R-HSA-2404140"],"synonyms":[{"name":"all-trans-retinyl-palmitate acylhydrolase activity","type":"broad"},{"name":"all-trans-retinyl-palmitate hydrolase activity","type":"broad"},{"name":"retinyl-palmitate palmitohydrolase activity","type":"broad"}],"termid":"GO:0047376"}


id: PBO:0086952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Regulator of dynein, involved in intracellular transport; part of the dynein/dynactin pathway; targets dynein to microtubule tips, which is necessary for sliding of microtubules along bud cortex; serves at interface between dynein's ATPase site and its microtubule binding stalk, causing individual dynein motors to remain attached to microtubules for long periods; synthetic lethal with bni1; homolog of human LIS1, mutations in which cause the severe brain disorder lissencephaly","termid":"PBO:0086952"}


id: GO:0018629
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: quinolin-2-ol + NADH + H+ + O2 = 2,5,6-trihydroxy-5,6-dihydroquinoline + NAD+.","definition_xrefs":["EC:1.14.12.16"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of two atoms of oxygen into one donor","termid":"GO:0016708"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"2-hydroxyquinoline 5,6-dioxygenase activity","secondary_identifiers":["MetaCyc:1.14.12.16-RXN","RHEA:10976","UM-BBD_reactionID:r0052"],"synonyms":[{"name":"2-oxo-1,2-dihydroquinoline 5,6-dioxygenase activity","type":"exact"},{"name":"quinolin-2(1H)-one 5,6-dioxygenase activity","type":"related"},{"name":"quinolin-2-ol 5,6-dioxygenase activity","type":"related"},{"name":"quinolin-2-ol,NADH:oxygen oxidoreductase (5,6-hydroxylating)","type":"related"}],"termid":"GO:0018629"}


id: PBO:0075200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide G pseudogene 12","termid":"PBO:0075200"}


id: GO:0002452
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of replacing receptors on B cells, in which RAG gene expression allows continued light-chain gene rearrangement and expression of a new light change which combines with the previous heavy chain to form a new receptor.","definition_xrefs":["ISBN:0781735149","GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatic recombination of immunoglobulin gene segments","termid":"GO:0016447"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006310"}],"interesting_parent_ids":["GO:0006259","GO:0010467","GO:0008150","GO:0006310"],"is_obsolete":false,"name":"B cell receptor editing","synonyms":[{"name":"B lymphocyte receptor editing","type":"exact"},{"name":"B-cell receptor editing","type":"exact"},{"name":"B-lymphocyte receptor editing","type":"exact"}],"termid":"GO:0002452"}


id: PBO:0077781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TONSL antisense RNA 1","termid":"PBO:0077781"}


id: PBO:0050553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human papillomavirus (type 18) integration site 2","termid":"PBO:0050553"}


id: PBO:0058047
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4268","termid":"PBO:0058047"}


id: GO:0052202
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism stops, prevents, or reduces the frequency, rate or extent of the deposition of callose by the host in its cell walls, occurring as part of the defense response of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation by symbiont of defense-related host cell wall callose deposition (obsolete GO:0052202)","synonyms":[{"name":"down regulation by symbiont of defense-related host cell wall callose deposition","type":"exact"},{"name":"down-regulation by symbiont of defense-related host cell wall callose deposition","type":"exact"},{"name":"downregulation by symbiont of defense-related host cell wall callose deposition","type":"exact"},{"name":"inhibition by symbiont of defense-related host cell wall callose deposition","type":"narrow"},{"name":"negative regulation by organism of defense-related callose deposition in other organism involved in symbiotic interaction","type":"broad"},{"name":"negative regulation by organism of defense-related cell wall callose deposition in other organism involved in symbiotic interaction","type":"broad"},{"name":"negative regulation by symbiont of defense-related host callose deposition","type":"broad"}],"termid":"GO:0052202"}


id: GO:1904326
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of circadian sleep/wake cycle, wakefulness.","definition_xrefs":["PMID:10923657","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of circadian sleep/wake cycle, wakefulness","termid":"GO:0010840"},{"relation_name":"is_a","term_name":"negative regulation of circadian rhythm","termid":"GO:0042754"},{"relation_name":"is_a","term_name":"negative regulation of behavior","termid":"GO:0048521"},{"relation_name":"negatively_regulates","term_name":"circadian sleep/wake cycle, wakefulness","termid":"GO:0042746"}],"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 circadian sleep/wake cycle, wakefulness","synonyms":[{"name":"down regulation of circadian sleep/wake cycle, wakefulness","type":"exact"},{"name":"down-regulation of circadian sleep/wake cycle, wakefulness","type":"exact"},{"name":"downregulation of circadian sleep/wake cycle, wakefulness","type":"exact"},{"name":"inhibition of circadian sleep/wake cycle, wakefulness","type":"narrow"}],"termid":"GO:1904326"}


id: PR:O43017
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- swd3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O43017"],"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":"set1 complex component swd3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC354.03","synonyms":[{"name":"COMPASS component swd3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Set1C component swd3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-swd3","type":"exact"},{"name":"complex proteins associated with set1 protein swd3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O43017"}


