# terms

id: GO:0031391
data:
  {"annotated_genes":["SJAG_02182","SJAG_01010","SJAG_00272","SJAG_04150","SJAG_00729"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[65976,74335,78794,79482,114662],"is_not":false,"summary":null,"term":"GO:0031391"}]},"cv_name":"cellular_component","definition":"A pentameric replication factor C (RLC) complex, which unloads the DNA polymerase processivity factor proliferating cell nuclear antigen (PCNA) from chromatin and has roles in telomere length regulation and other aspects of genome stability. In Saccharomyces the subunits are known as Elg1p, Rfc2p, Rfc3p, Rfc4p, and Rfc5p.","definition_xrefs":["PMID:23499004","PMID:14614842","PMID:27664980"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"},{"relation_name":"part_of","term_name":"chromosome","termid":"GO:0005694"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00272":null,"SJAG_00729":null,"SJAG_01010":null,"SJAG_02182":null,"SJAG_04150":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005694","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"Elg1 RFC-like complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"Elg1-RFC","type":"exact"},{"name":"Elg1-RLC","type":"exact"},{"name":"RFC (Elg1)","type":"exact"}],"termid":"GO:0031391","terms_by_termid":{"GO:0031391":null}}


id: MONDO:0018854
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A life-threatening, rapidly progressive thrombotic disorder affecting mainly neonates and children that is characterized by purpuric skin lesions and disseminated intravascular coagulation. PF may progress rapidly to multi-organ failure caused by thrombotic occlusion of small and medium-sized blood vessels. There are two forms of PF that are classified according to triggering mechanisms: acute infectious (the most common form), and idiopathic PF.","definition_xrefs":["Orphanet:49566"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purpura fulminans","termid":"MONDO:0000809"},{"relation_name":"is_a","term_name":"thrombotic disease","termid":"MONDO:0000831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"acquired purpura fulminans","secondary_identifiers":["MedDRA:10037556","SCTID:725157006","GARD:18838","UMLS:C4510896","MESH:D014884","MEDGEN:1377273","MESH:D055665"],"synonyms":[{"name":"acquired PF","type":"exact"},{"name":"acquired purpura fulminans","type":"exact"}],"termid":"MONDO:0018854","xrefs":{"Monarch":{"xref_id":"0018854"}}}


id: MONDO:0015169
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This syndrome is characterized by chronic diarrhea in infancy or childhood in association with intestinal glucoamylase deficiency.","definition_xrefs":["Orphanet:103907"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of carbohydrate transmembrane transport and absorption","termid":"MONDO:0017706"},{"relation_name":"is_a","term_name":"chronic diarrheal disease","termid":"MONDO:0044751"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066","MONDO:0004335"],"is_obsolete":false,"name":"chronic diarrhea due to glucoamylase deficiency","secondary_identifiers":["SCTID:716277000","icd11.foundation:2084206046","GARD:19838","MEDGEN:898614","UMLS:C4275068","NANDO:2200911"],"synonyms":[{"name":"chronic diarrhea due to glucoamylase deficiency","type":"exact"},{"name":"maltase glucoamylase deficiency","type":"related"},{"name":"maltase-glucoamylase deficiency","type":"exact"}],"termid":"MONDO:0015169","xrefs":{"Monarch":{"xref_id":"0015169"}}}


id: PBO:0043054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcineurin like EF-hand protein 2","termid":"PBO:0043054"}


id: FYPO:0001318
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular response phenotype in which the cellular response to a chemical stimulus is normal in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular response to chemical stimulus","termid":"FYPO:0000953"},{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"},{"relation_name":"is_a","term_name":"cellular response phenotype during vegetative growth","termid":"FYPO:0001342"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0000257","FYPO:0001320","FYPO:0000298"],"is_obsolete":false,"name":"normal cellular response to chemical stimulus during vegetative growth","synonyms":[{"name":"normal cellular response to chemical stimulus during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001318"}


id: PBO:0038290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase feature property types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sgd_identifier","termid":"PBO:0038290"}


id: PBO:0074804
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 13I","termid":"PBO:0074804"}


id: GO:0009658
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of the chloroplast.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plastid organization","termid":"GO:0009657"}],"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":"chloroplast organization","synonyms":[{"name":"chloroplast organisation","type":"exact"},{"name":"chloroplast organization and biogenesis","type":"related"}],"termid":"GO:0009658"}


id: PBO:0029536
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_microcolony,_small_cells_(obsolete_FYPO:0002186)","termid":"PBO:0029536"}


id: PBO:0109318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Prp19 complex subunit Cdc5/Cef1","termid":"PBO:0109318"}


id: MONDO:0009210
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital factor V deficiency is an inherited bleeding disorder due to reduced plasma levels of factor V (FV) and characterized by mild to severe bleeding symptoms.","definition_xrefs":["Orphanet:326"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemorrhagic disease","termid":"MONDO:0002243"},{"relation_name":"is_a","term_name":"factor V deficiency","termid":"MONDO:0020586"},{"relation_name":"is_a","term_name":"inherited blood coagulation disorder","termid":"MONDO:0021181"}],"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":"congenital factor V deficiency","secondary_identifiers":["DOID:2216","MedDRA:10048930","UMLS:C0015499","GARD:2237","MEDGEN:4633","OMIM:227400","NCIT:C98938","SCTID:88776002"],"synonyms":[{"name":"Owren Parahemophilia","type":"related"},{"name":"Owren disease","type":"exact"},{"name":"Parahemophilia","type":"exact"},{"name":"Proaccelerin deficiency","type":"exact"},{"name":"congenital factor V deficiency","type":"exact"},{"name":"deficiency, labile","type":"exact"},{"name":"factor 5 deficiency","type":"related"},{"name":"factor V deficiency","type":"related"},{"name":"hereditary Factor V deficiency","type":"exact"},{"name":"hereditary factor V deficiency","type":"exact"},{"name":"hereditary hypoproaccelerinaemia","type":"exact"},{"name":"labile Factor deficiency","type":"related"},{"name":"labile factor deficiency","type":"exact"}],"termid":"MONDO:0009210","xrefs":{"Monarch":{"xref_id":"0009210"}}}


id: MOD:00160
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-asparagine residue to an N4-glycosyl-L-asparagine.","definition_xrefs":["PubMed:1694179","RESID:AA0151#var","PubMed:5490222","PubMed:111247"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-glycosylated residue","termid":"MOD:00006"},{"relation_name":"is_a","term_name":"modified L-asparagine residue","termid":"MOD:00903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"N4-glycosyl-L-asparagine","synonyms":[{"name":"N4GlycoAsn","type":"exact"}],"termid":"MOD:00160"}


id: RO:0002489
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x starts ends with y if and only if the time point at which x starts is equivalent to the time point at which y starts. Formally: x existence starts with y iff α(x) = α(y).","direct_ancestors":[{"relation_name":"is_a","term_name":"existence_starts_during","termid":"RO:0002488"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"existence_starts_with","termid":"RO:0002489"}


id: FYPO:0003166
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 a cell has two nuclei and one septum, but both nuclei are in a single compartment on one side of the septum. Arises when a cell undergoes septation despite abnormal chromosome segregation, producing inviable daughter cells, and in which the septum forms in a position that partitions both nuclei into one compartment. Cell separation may or may not be completed.","definition_xrefs":["PomBase:vw","PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"monoseptate","termid":"FYPO:0001225"},{"relation_name":"has_part","term_name":"mislocalized nucleus during vegetative growth","termid":"FYPO:0002071"},{"relation_name":"is_a","term_name":"mislocalized nucleus during vegetative growth","termid":"FYPO:0002071"},{"relation_name":"is_a","term_name":"septated vegetative cell","termid":"FYPO:0002342"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"monoseptate vegetative cell with binucleate and anucleate compartments","secondary_identifiers":["FYPO:0004699"],"synonyms":[{"name":"abnormal nuclear segregation","type":"related"},{"name":"binucleate monoseptate cell with nuclei grouped","type":"related"},{"name":"monoseptate cell with binucleate and anucleate compartments during vegetative growth","type":"exact"},{"name":"monoseptate vegetative cell with binucleate and anucleate compartments during mitotic cell cycle","type":"related"},{"name":"monoseptate vegetative cell with binucleate and anucleate compartments following abnormal chromosome segregation","type":"exact"},{"name":"nuclear missegregation","type":"related"},{"name":"septation following abnormal chromosome segregation, with binucleate and anucleate compartment formation","type":"exact"},{"name":"septation following abnormal chromosome segregation, with binucleate cell formation","type":"exact"},{"name":"unequal nuclear partitioning","type":"related"}],"termid":"FYPO:0003166"}


id: GO:0072234
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of a metanephric nephron tubule over time, from its initial formation to the mature structure. A metanephric nephron tubule is an epithelial tube that is part of the metanephric nephron, the functional part of the metanephros.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephron tubule development","termid":"GO:0072080"},{"relation_name":"is_a","term_name":"metanephric tubule development","termid":"GO:0072170"},{"relation_name":"is_a","term_name":"metanephric nephron epithelium development","termid":"GO:0072243"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric nephron tubule development","termid":"GO:0072234"}


id: GO:0042945
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of D-serine from one side of a membrane to the other. D-serine is the D-enantiomer of 2-amino-3-hydroxypropanoic acid.","definition_xrefs":["GOC:mah","GOC:mtg_transport","GOC:jl","ISBN:0815340729","GOC:jsg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"D-amino acid transmembrane transporter activity","termid":"GO:0042943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"D-serine transmembrane transporter activity","synonyms":[{"name":"D-serine permease activity","type":"exact"},{"name":"D-serine transporter activity","type":"broad"}],"termid":"GO:0042945"}


id: SO:0000932
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript that, at least in part, encodes one or more proteins that has not been edited.","direct_ancestors":[{"relation_name":"is_a","term_name":"protein_coding_primary_transcript","termid":"SO:0000120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pre_edited_mRNA","synonyms":[{"name":"pre-edited mRNA","type":"exact"}],"termid":"SO:0000932"}


id: MONDO:0013053
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type is a rare syndrome with cardiac malformations, characterized by prenatal-onset growth retardation (low birth weight and short stature), hypotonia, developmental delay and intellectual disability associated with microcephaly and craniofacial (low anterior hairline, hypotelorism, thick lips with carp-shaped mouth, high-arched palate, low-set ears), cardiac (conotruncal heart malformations such as tetralogy of Fallot) and skeletal (hypoplastic thumbs and first metacarpals) abnormalities.","definition_xrefs":["Orphanet:217026"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart disorder","termid":"MONDO:0005267"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"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":"microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type","secondary_identifiers":["GARD:17116","MESH:C567850","OMIM:612946","SCTID:719395001","UMLS:C2751878","MEDGEN:414129"],"synonyms":[{"name":"Hadziselimovic syndrome","type":"exact"},{"name":"microcephaly-faciocardioskeletal syndrome","type":"exact"}],"termid":"MONDO:0013053","xrefs":{"Monarch":{"xref_id":"0013053"}}}


id: GO:0086092
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A cardiac conduction process that modulates the extent of heart contraction, changing the force with which blood is propelled.","definition_xrefs":["GOC:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of the force of heart contraction","termid":"GO:0002026"},{"relation_name":"is_a","term_name":"cardiac conduction","termid":"GO:0061337"}],"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 the force of heart contraction by cardiac conduction","termid":"GO:0086092"}


id: PBO:0111345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis protein","termid":"PBO:0111345"}


id: GO:0003192
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process pertaining to the initial formation of the mitral valve from unspecified parts. This process begins with the specific processes that contribute to the appearance of the discrete structure and ends when the structural rudiment is recognizable.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrioventricular valve formation","termid":"GO:0003190"},{"relation_name":"part_of","term_name":"mitral valve morphogenesis","termid":"GO:0003183"}],"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":"mitral valve formation","termid":"GO:0003192"}


id: GO:0098627
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: phospho-L-arginyl-[protein] +H2O = L-arginyl-[protein] + phosphate.","definition_xrefs":["PMID:23770242","RHEA:43380"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphoprotein phosphatase activity","termid":"GO:0004721"},{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid phosphorus-nitrogen bonds","termid":"GO:0016825"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0004721","GO:0140096","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"protein arginine phosphatase activity","secondary_identifiers":["EC:3.9.1.2"],"termid":"GO:0098627"}


id: PBO:0065105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRKAR2B antisense RNA 1","termid":"PBO:0065105"}


id: PBO:0067737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 36","termid":"PBO:0067737"}


id: MONDO:0020669
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm involving the paranasal sinuses.","definition_xrefs":["NCIT:C7487"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system cancer","termid":"MONDO:0000376"},{"relation_name":"is_a","term_name":"sensory system cancer","termid":"MONDO:0000649"},{"relation_name":"is_a","term_name":"skull cancer","termid":"MONDO:0002132"},{"relation_name":"is_a","term_name":"paranasal sinus neoplasm","termid":"MONDO:0005289"}],"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 cancer","secondary_identifiers":["UMLS:C0153474","MEDGEN:56305"],"synonyms":[{"name":"malignant accessory sinus neoplasm","type":"exact"},{"name":"malignant accessory sinus tumor","type":"exact"},{"name":"malignant accessory sinus tumour","type":"exact"},{"name":"malignant neoplasm of accessory sinus","type":"exact"},{"name":"malignant neoplasm of paranasal sinus","type":"exact"},{"name":"malignant neoplasm of the accessory sinus","type":"exact"},{"name":"malignant neoplasm of the paranasal sinus","type":"exact"},{"name":"malignant paranasal sinus neoplasm","type":"exact"},{"name":"malignant paranasal sinus tumor","type":"exact"},{"name":"malignant paranasal sinus tumour","type":"exact"},{"name":"malignant tumor of accessory sinus","type":"exact"},{"name":"malignant tumor of paranasal sinus","type":"exact"},{"name":"malignant tumor of the accessory sinus","type":"exact"},{"name":"malignant tumor of the paranasal sinus","type":"exact"},{"name":"malignant tumour of accessory sinus","type":"exact"},{"name":"malignant tumour of paranasal sinus","type":"exact"},{"name":"malignant tumour of the accessory sinus","type":"exact"},{"name":"malignant tumour of the paranasal sinus","type":"exact"}],"termid":"MONDO:0020669","xrefs":{"Monarch":{"xref_id":"0020669"}}}


id: PBO:0031049
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_modification","termid":"PBO:0031049"}


id: GO:0141130
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont inhibits or disrupts translation of mRNA into protein in its host by inactivating its ribosomes.","definition_xrefs":["PMID:1324134"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host translation","termid":"GO:0039604"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated inactivation of host ribosome","synonyms":[{"name":"symbiont-mediated host ribosome inactivation","type":"exact"}],"termid":"GO:0141130"}


id: GO:0051952
data:
  {"annotated_genes":["SJAG_00991","SJAG_03970","SJAG_03591","SJAG_05346","SJAG_02605"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89856],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905533"},{"annotations":[93518,100662,112367,95102],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905589"},{"annotations":[95103,93519,100663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905534"},{"annotations":[95104],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905626"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the directed movement of amines into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"amine transport","termid":"GO:0015837"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00991":null,"SJAG_02605":null,"SJAG_03591":null,"SJAG_03970":null,"SJAG_05346":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of amine transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0051952","terms_by_termid":{"GO:1905533":null,"GO:1905534":null,"GO:1905589":null,"GO:1905626":null}}


id: PBO:0062806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oxysterol binding protein like 6","termid":"PBO:0062806"}


id: PBO:0050807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hepatocellular carcinoma up-regulated long non-coding RNA","termid":"PBO:0050807"}


id: PBO:0060955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NFKB inhibitor alpha","termid":"PBO:0060955"}


id: MONDO:0016280
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sarcoma involving a uterine cervix.","definition_xrefs":["MONDO:patterns/sarcoma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervical cancer","termid":"MONDO:0002974"},{"relation_name":"is_a","term_name":"sarcoma","termid":"MONDO:0005089"}],"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":"sarcoma of cervix uteri","secondary_identifiers":["GARD:20493","ICD10CM:C53.0","UMLS:C5679807","MEDGEN:1842604","Orphanet:213797"],"synonyms":[{"name":"cervical malignant mesenchymal tumor","type":"exact"},{"name":"cervical malignant mesenchymal tumour","type":"exact"},{"name":"cervical sarcoma","type":"exact"},{"name":"malignant mesenchymal tumor of cervix uteri","type":"exact"},{"name":"malignant mesenchymal tumour of cervix uteri","type":"exact"},{"name":"sarcoma of uterine cervix","type":"exact"},{"name":"uterine cervix sarcoma","type":"exact"}],"termid":"MONDO:0016280","xrefs":{"Monarch":{"xref_id":"0016280"}}}


id: PBO:0081310
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 92","termid":"PBO:0081310"}


id: PBO:0039396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANAPC1 pseudogene 1","termid":"PBO:0039396"}


id: PBO:0011483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1-5,6,7,8-tetrahydrofolate (THF) synthase, trifunctional enzyme","termid":"PBO:0011483"}


id: PBO:0065840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB9A, member RAS oncogene family pseudogene 5","termid":"PBO:0065840"}


id: GO:0033550
data:
  {"annotated_genes":["SJAG_03263","SJAG_02000","SJAG_02013"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72761,93441,96817],"is_not":false,"summary":null,"term":"GO:0033550"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: MAP kinase tyrosine phosphate + H2O = MAP kinase tyrosine + phosphate.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein tyrosine phosphatase activity","termid":"GO:0004725"},{"relation_name":"is_a","term_name":"MAP kinase phosphatase activity","termid":"GO:0033549"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02000":null,"SJAG_02013":null,"SJAG_03263":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0004721"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0004721","GO:0140096","GO:0016787","GO:0016788"],"is_obsolete":false,"name":"MAP kinase tyrosine phosphatase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"tyrosine-specific MAP kinase phosphatase activity","type":"exact"}],"termid":"GO:0033550","terms_by_termid":{"GO:0033550":null}}


id: PBO:0031656
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_re-entry_into_mitotic_cell_cycle_after_pheromone_arrest","termid":"PBO:0031656"}


id: FYPO:0002939
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 an RNA catabolic process that degrades mRNA encoded in the nucleus is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","GO:0000956"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"},{"relation_name":"is_a","term_name":"cellular metabolism phenotype during vegetative growth","termid":"FYPO:0001348"},{"relation_name":"is_a","term_name":"normal RNA metabolic process","termid":"FYPO:0004850"}],"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":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001320","FYPO:0001312"],"is_obsolete":false,"name":"normal nuclear mRNA catabolic process","synonyms":[{"name":"normal nuclear mRNA breakdown","type":"exact"},{"name":"normal nuclear mRNA catabolic process during mitotic cell cycle","type":"related"},{"name":"normal nuclear mRNA catabolic process during vegetative growth","type":"exact"},{"name":"normal nuclear mRNA catabolism","type":"exact"},{"name":"normal nuclear mRNA degradation","type":"exact"},{"name":"normal nuclear-transcribed mRNA catabolic process","type":"exact"}],"termid":"FYPO:0002939"}


id: PBO:0016088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase like PAN complex subunit Ppk26","termid":"PBO:0016088"}


id: PBO:0081497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 395","termid":"PBO:0081497"}


id: MONDO:1010839
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Gangliosidosis that occurs in emu.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gangliosidosis, non-human animal","termid":"MONDO:1010167"},{"relation_name":"is_a","term_name":"lysosomal storage disease, emu","termid":"MONDO:1010858"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gangliosidosis, emu","secondary_identifiers":["OMIA:000401-8790"],"termid":"MONDO:1010839","xrefs":{"Monarch":{"xref_id":"1010839"}}}


id: PR:O74847
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A brain protein 44-like protein that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04225","PRO:DNx","PANTHER:PTHR14154:SF3"],"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":"mitochondrial pyruvate carrier 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1235.11","secondary_identifiers":["UniProtKB:O74847"],"synonyms":[{"name":"MPC1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-MPC1","type":"exact"}],"termid":"PR:O74847"}


id: MONDO:0006494
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete thyroid disease (obsolete MONDO:0006494)","termid":"MONDO:0006494","xrefs":{"Monarch":{"xref_id":"0006494"}}}


id: GO:0004099
data:
  {"annotated_genes":["SJAG_03013"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[93548],"is_not":false,"summary":null,"term":"GO:0004099"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: chitin + H2O = chitosan + acetate.","definition_xrefs":["EC:3.5.1.41"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"},{"relation_name":"is_a","term_name":"deacetylase activity","termid":"GO:0019213"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03013":null},"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:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0019213"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0019213","GO:0016787","GO:0016810"],"is_obsolete":false,"name":"chitin deacetylase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:10464","MetaCyc:CHITIN-DEACETYLASE-RXN"],"synonyms":[{"name":"chitin amidohydrolase activity","type":"related"}],"termid":"GO:0004099","terms_by_termid":{"GO:0004099":null}}


id: GO:0033633
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of cell-cell adhesion mediated by integrin.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell-cell adhesion","termid":"GO:0022408"},{"relation_name":"is_a","term_name":"negative regulation of cell adhesion mediated by integrin","termid":"GO:0033629"},{"relation_name":"is_a","term_name":"regulation of cell-cell adhesion mediated by integrin","termid":"GO:0033632"},{"relation_name":"negatively_regulates","term_name":"cell-cell adhesion mediated by integrin","termid":"GO:0033631"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of cell-cell adhesion mediated by integrin","synonyms":[{"name":"negative regulation of cell-cell adhesion mediated by integrin complex","type":"exact"}],"termid":"GO:0033633"}


id: PBO:0076340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptotagmin 8","termid":"PBO:0076340"}


id: PBO:0043908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytokine receptor like factor 1","termid":"PBO:0043908"}


id: PBO:0003596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centrin binding repeats","termid":"PBO:0003596"}


id: PBO:0084895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial translation elongation factor Tu (EF-Tu); involved in fundamental pathway of mtDNA homeostasis; comprises both GTPase and guanine nucleotide exchange factor activities, while these activities are found in separate proteins in S. pombe and humans; rare mutations in human mitochondrial elongation factor Tu (EFTu) associated with severe lactic acidosis, rapidly progressive fatal encephalopathy, severe infantile macrocystic leukodystrophy with micropolygyria","termid":"PBO:0084895"}


id: GO:0006701
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of progesterone, a steroid hormone produced in the ovary which prepares and maintains the uterus for pregnancy. Also found in plants.","definition_xrefs":["PMID:14613534","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C21-steroid hormone biosynthetic process","termid":"GO:0006700"},{"relation_name":"is_a","term_name":"ketone biosynthetic process","termid":"GO:0042181"},{"relation_name":"is_a","term_name":"progesterone metabolic process","termid":"GO:0042448"},{"relation_name":"is_a","term_name":"olefinic compound biosynthetic process","termid":"GO:0120255"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006629","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"progesterone biosynthetic process","synonyms":[{"name":"progesterone anabolism","type":"exact"},{"name":"progesterone biosynthesis","type":"exact"},{"name":"progesterone formation","type":"exact"},{"name":"progesterone synthesis","type":"exact"}],"termid":"GO:0006701"}


id: GO:0039592
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont interferes with the progression of the host mitotic cell cycle from G2 phase to M phase, leading to arrest in G2 phase. The arrest in G2/M allows some viruses to replicate their genome before cells enter mitosis. Alternatively, it can inhibit the antiviral immune response by preventing the clonal expansion of infected lymphocytes.","definition_xrefs":["PMID:10946289","VZ:876","PMID:12208959","PMID:9882364"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host cell cycle progression","termid":"GO:0044071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated arrest of host cell cycle during G2/M transition","synonyms":[{"name":"host G2/M cell cycle arrest by virus","type":"narrow"},{"name":"perturbation by virus of G2/M transition of host mitotic cell cycle","type":"narrow"},{"name":"suppression by virus of G2/M transition of host mitotic cell cycle","type":"narrow"}],"termid":"GO:0039592"}


id: PBO:0078901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gln (CTG) 10-1","termid":"PBO:0078901"}


id: PBO:0034343
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-starts_with","termid":"PBO:0034343"}


id: FYPO:0003596
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 formation of the mature 3' end of an snRNA molecule is abnormal.","definition_xrefs":["GO:0034472","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal RNA 3'-end processing","termid":"FYPO:0007918"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0005447","FYPO:0000294","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal snRNA 3'-end processing","synonyms":[{"name":"abnormal snRNA 3'-end processing during mitotic cell cycle","type":"related"},{"name":"abnormal snRNA 3'-end processing during vegetative growth","type":"exact"}],"termid":"FYPO:0003596"}


id: FYPO:0006041
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 metaphase chromosome recapture is decreased.","definition_xrefs":["PMID:27146110","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic metaphase chromosome recapture","termid":"FYPO:0005362"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"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:0000641"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000337","FYPO:0001320","FYPO:0000641","FYPO:0000138","FYPO:0000002","FYPO:0000631","FYPO:0001985"],"is_obsolete":false,"name":"decreased rate of mitotic metaphase chromosome recapture","synonyms":[{"name":"decreased rate of chromosome recapture during mitosis","type":"exact"},{"name":"decreased rate of chromosome recapture during mitotic metaphase","type":"exact"},{"name":"decreased rate of kinetochore retrieval in mitotic metaphase","type":"exact"},{"name":"decreased rate of metaphase chromosome recapture during mitotic cell cycle","type":"related"},{"name":"decreased rate of mitotic kinetochore retrieval","type":"exact"},{"name":"decreased rate of mitotic metaphase chromosome recapture during vegetative growth","type":"exact"},{"name":"decreased rate of mitotic metaphase chromosome retrieval to the spindle pole body","type":"exact"},{"name":"decreased rate of mitotic sister kinetochore recapture","type":"exact"},{"name":"increased time to mitotic metaphase chromosome recapture","type":"related"},{"name":"reduced rate of mitotic metaphase chromosome recapture","type":"exact"}],"termid":"FYPO:0006041"}


id: PBO:0039233
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AKTIP pseudogene 2","termid":"PBO:0039233"}


id: GO:0022406
data:
  {"annotated_genes":["SJAG_04023","SJAG_03005","SJAG_03536","SJAG_04413","SJAG_01324","SJAG_04978","SJAG_03347","SJAG_01598","SJAG_01697","SJAG_01168","SJAG_05184","SJAG_01633","SJAG_01437","SJAG_03170","SJAG_04966","SJAG_02699","SJAG_03416","SJAG_00053","SJAG_00280","SJAG_03499","SJAG_01564","SJAG_04221","SJAG_02626","SJAG_01305","SJAG_01929","SJAG_01116","SJAG_03848","SJAG_02320","SJAG_02587","SJAG_04370","SJAG_03710","SJAG_01772","SJAG_03552","SJAG_00171","SJAG_00029","SJAG_04417","SJAG_00380"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96402],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016240"},{"annotations":[120016,62843,60905,99237,92178,62217,113495,73544],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061817"},{"annotations":[72129],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048211"},{"annotations":[71620,81767,118458,76452,71664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990456"},{"annotations":[81970],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071562"},{"annotations":[117043,108838],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990854"},{"annotations":[96094],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140057"},{"annotations":[101300,102104,102915,114524,111634,77853,111478,73653,79534,119401],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048278"},{"annotations":[81761,60665,92347,94104,76803,71463,120072,81499],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006904"}]},"cv_name":"biological_process","definition":"The initial attachment of a membrane or protein to a target membrane. Docking requires only that the proteins come close enough to interact and adhere.","definition_xrefs":["PMID:27875684","GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process","termid":"GO:0009987"}],"gene_count":37,"genes_by_uniquename":{"SJAG_00029":null,"SJAG_00053":null,"SJAG_00171":null,"SJAG_00280":null,"SJAG_00380":null,"SJAG_01116":null,"SJAG_01168":null,"SJAG_01305":null,"SJAG_01324":null,"SJAG_01437":null,"SJAG_01564":null,"SJAG_01598":null,"SJAG_01633":null,"SJAG_01697":null,"SJAG_01772":null,"SJAG_01929":null,"SJAG_02320":null,"SJAG_02587":null,"SJAG_02626":null,"SJAG_02699":null,"SJAG_03005":null,"SJAG_03170":null,"SJAG_03347":null,"SJAG_03416":null,"SJAG_03499":null,"SJAG_03536":null,"SJAG_03552":null,"SJAG_03710":null,"SJAG_03848":null,"SJAG_04023":null,"SJAG_04221":null,"SJAG_04370":null,"SJAG_04413":null,"SJAG_04417":null,"SJAG_04966":null,"SJAG_04978":null,"SJAG_05184":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"membrane docking","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0022406","terms_by_termid":{"GO:0006904":null,"GO:0016240":null,"GO:0048211":null,"GO:0048278":null,"GO:0061817":null,"GO:0071562":null,"GO:0140057":null,"GO:1990456":null,"GO:1990854":null}}


id: PBO:0083538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified ORF YBR175W; null mutant is viable and sporulation defective","termid":"PBO:0083538"}


id: GO:0018838
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-mandelate = (R)-mandelate.","definition_xrefs":["EC:5.1.2.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"racemase and epimerase activity, acting on hydroxy acids and derivatives","termid":"GO:0016856"}],"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:0016853"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016853"],"is_obsolete":false,"name":"mandelate racemase activity","secondary_identifiers":["UM-BBD_reactionID:r0091","RHEA:13945","MetaCyc:MANDELATE-RACEMASE-RXN"],"termid":"GO:0018838"}


id: PBO:0026655
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_negative_regulation_of_transcription_by_glucose","termid":"PBO:0026655"}


id: PBO:0086483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative, non-essential component vacuolar ATPase; conserved in fungi; SWAT-GFP fusion protein localizes to vacuole membrane; partially overlaps the dubious genes YPR169W-A, YPR170W-A and YRP170C","termid":"PBO:0086483"}


id: PBO:0067000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 4, pseudogene","termid":"PBO:0067000"}


id: PBO:0017496
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MFS family transmembrane transporter Mfs2 (predicted)","termid":"PBO:0017496"}


id: RO:0002637
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of mesoparasite of","direct_ancestors":[{"relation_name":"is_a","term_name":"parasitized_by","termid":"RO:0002445"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_mesoparasite","termid":"RO:0002637"}


id: GO:1902813
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of BMP signaling pathway involved in determination of lateral mesoderm left/right asymmetry.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:10499580","GOC:mr"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of BMP signaling pathway involved in determination of lateral mesoderm left/right asymmetry (obsolete GO:1902813)","synonyms":[{"name":"down regulation of BMP signaling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"},{"name":"down regulation of BMP signaling pathway involved in lateral mesoderm left/right asymmetry determination","type":"exact"},{"name":"down regulation of BMP signalling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"},{"name":"down-regulation of BMP signaling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"},{"name":"down-regulation of BMP signaling pathway involved in lateral mesoderm left/right asymmetry determination","type":"exact"},{"name":"down-regulation of BMP signalling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"},{"name":"downregulation of BMP signaling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"},{"name":"downregulation of BMP signaling pathway involved in lateral mesoderm left/right asymmetry determination","type":"exact"},{"name":"downregulation of BMP signalling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"},{"name":"inhibition of BMP signaling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"narrow"},{"name":"inhibition of BMP signaling pathway involved in lateral mesoderm left/right asymmetry determination","type":"narrow"},{"name":"inhibition of BMP signalling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"narrow"},{"name":"negative regulation of BMP signaling pathway involved in lateral mesoderm left/right asymmetry determination","type":"exact"},{"name":"negative regulation of BMP signalling pathway involved in determination of lateral mesoderm left/right asymmetry","type":"exact"}],"termid":"GO:1902813"}


id: GO:0010116
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of abscisic acid.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of abscisic acid biosynthetic process","termid":"GO:0010115"},{"relation_name":"is_a","term_name":"positive regulation of isoprenoid metabolic process","termid":"GO:0045828"},{"relation_name":"is_a","term_name":"positive regulation of lipid biosynthetic process","termid":"GO:0046889"},{"relation_name":"is_a","term_name":"positive regulation of alcohol biosynthetic process","termid":"GO:1902932"},{"relation_name":"positively_regulates","term_name":"abscisic acid biosynthetic process","termid":"GO:0009688"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"positively_regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"positive regulation of abscisic acid biosynthetic process","synonyms":[{"name":"activation of abscisic acid biosynthetic process","type":"narrow"},{"name":"positive regulation of abscisic acid anabolism","type":"exact"},{"name":"positive regulation of abscisic acid biosynthesis","type":"exact"},{"name":"positive regulation of abscisic acid formation","type":"exact"},{"name":"positive regulation of abscisic acid synthesis","type":"exact"},{"name":"stimulation of abscisic acid biosynthetic process","type":"narrow"},{"name":"up regulation of abscisic acid biosynthetic process","type":"exact"},{"name":"up-regulation of abscisic acid biosynthetic process","type":"exact"},{"name":"upregulation of abscisic acid biosynthetic process","type":"exact"}],"termid":"GO:0010116"}


id: GO:0014711
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of branchiomeric skeletal muscle development. Branchiomeric skeletal muscle development is the process whose specific outcome is the progression of the branchiomeric skeletal muscle over time, from its formation to the mature structure.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of skeletal muscle tissue development","termid":"GO:0048641"},{"relation_name":"regulates","term_name":"branchiomeric skeletal muscle development","termid":"GO:0014707"}],"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 branchiomeric skeletal muscle development","termid":"GO:0014711"}


id: GO:1901709
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving (+)-larreatricin.","definition_xrefs":["PMID:12960376","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lignan metabolic process","termid":"GO:0009806"},{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"(+)-larreatricin metabolic process","synonyms":[{"name":"(+)-larreatricin metabolism","type":"exact"}],"termid":"GO:1901709"}


id: MONDO:1012326
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"premature senesence, non-human animal","termid":"MONDO:1011784"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"premature senesence, rabbit","secondary_identifiers":["OMIA:001213-9986"],"termid":"MONDO:1012326","xrefs":{"Monarch":{"xref_id":"1012326"}}}


id: FYPO:0002246
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of glucose binding by a gene product (usually a protein) in a mutant is increased. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal monosaccharide binding","termid":"FYPO:0002245"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"increased glucose binding","termid":"FYPO:0002246"}


id: MONDO:0007925
data:
  {"annotated_genes":["SJAG_03424","SJAG_01548"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87455,87456],"is_not":false,"summary":null,"term":"MONDO:0007925"}]},"cv_name":"mondo","definition":"A myelodysplastic syndrome characterized by a deletion between bands q31 and 33 on chromosome 5. The number of blasts in the bone marrow and blood is <5%. The bone marrow is usually hypercellular or normocellular with increased number of often hypolobated megakaryocytes. The peripheral blood shows macrocytic anemia. This syndrome occurs predominantly but not exclusively in middle age to older women. The prognosis is good and transformation to acute leukemia is rare. (WHO, 2001)","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macrocytic anemia","termid":"MONDO:0002281"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 5","termid":"MONDO:0016904"},{"relation_name":"is_a","term_name":"myelodysplastic syndrome","termid":"MONDO:0018881"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01548":null,"SJAG_03424":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"myelodysplastic syndrome associated with isolated del(5q)","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD10CM:D46.C","icd11.foundation:420472577","SCTID:277597005","UMLS:C0740302","OMIM:153550","NCIT:C6867","ICDO:9986/3","GARD:8723","DOID:0090016","MEDGEN:196625","Orphanet:86841","MESH:C535323"],"synonyms":[{"name":"5Q minus syndrome","type":"exact"},{"name":"5Q- syndrome","type":"exact"},{"name":"5q deletion syndrome","type":"related"},{"name":"5q syndrome","type":"related"},{"name":"5q- syndrome","type":"exact"},{"name":"5q- syndrome, refractory macrocytic anaemia due to 5q deletion","type":"exact"},{"name":"5q- syndrome, refractory macrocytic anemia due to 5q deletion","type":"exact"},{"name":"MAR","type":"related"},{"name":"chromosome 5q deletion syndrome","type":"exact"},{"name":"macrocytic Anemia, refractory, due to 5Q deletion","type":"related"},{"name":"macrocytic anemia, refractory, due to 5q deletion, somatic","type":"exact"},{"name":"megakaryocytes, unilobular nucleated","type":"related"},{"name":"myelodysplastic syndrome associated with isolated del (5q) chromosome Abnormality","type":"exact"},{"name":"myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality","type":"exact"},{"name":"myelodysplastic syndrome with 5q deletion","type":"exact"},{"name":"myelodysplastic syndrome with isolated del(5q)","type":"exact"},{"name":"refractory macrocytic anaemia due to 5q deletion","type":"related"},{"name":"refractory macrocytic anemia due to 5q deletion","type":"related"}],"termid":"MONDO:0007925","terms_by_termid":{"MONDO:0007925":null},"xrefs":{"Monarch":{"xref_id":"0007925"}}}


id: GO:0044168
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The irregular network of unit membranes, visible only by electron microscopy, that occurs in the host cell cytoplasm of many eukaryotic cells. The membranes form a complex meshwork of tubular channels, which are often expanded into slitlike cavities called cisternae. The host rough ER has ribosomes adhering to the outer surface.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell endoplasmic reticulum","termid":"GO:0044165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host cell rough endoplasmic reticulum","synonyms":[{"name":"host rough endoplasmic reticulum","type":"exact"}],"termid":"GO:0044168"}


id: PBO:0005370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing coactivator SRRM1 (predicted)","termid":"PBO:0005370"}


id: PBO:0071170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 10","termid":"PBO:0071170"}


id: FYPO:0000229
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An inviable phenotype observed in the vegetative growth phase of the life cycle in which a cell undergoes septation despite abnormal mitotic nuclear division, such that the septum physically divides the nucleus into two parts, giving rise to inviable daughter cells.","definition_xrefs":["PomBase:vw","PomBase:mah","PomBase:jh"],"direct_ancestors":[{"relation_name":"has_part","term_name":"abnormal mitotic sister chromatid segregation","termid":"FYPO:0000141"},{"relation_name":"has_part","term_name":"premature septum assembly","termid":"FYPO:0003250"},{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid segregation","termid":"FYPO:0000141"},{"relation_name":"is_a","term_name":"inviable vegetative cell","termid":"FYPO:0001489"},{"relation_name":"is_a","term_name":"premature septum assembly","termid":"FYPO:0003250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"has_part","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0000337"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"has_part","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000337","FYPO:0001985","FYPO:0000631","FYPO:0001320","FYPO:0000002","FYPO:0000004","FYPO:0000641","FYPO:0000032"],"is_obsolete":false,"name":"cut","secondary_identifiers":["FYPO:0000322","FYPO:0000323"],"synonyms":[{"name":"cut during mitotic cell cycle","type":"related"},{"name":"cut during vegetative growth","type":"exact"},{"name":"mitotic catastrophe","type":"related"},{"name":"septation following abnormal nuclear division","type":"exact"}],"termid":"FYPO:0000229"}


id: PBO:0081152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZFP91-CNTF readthrough (NMD candidate)","termid":"PBO:0081152"}


id: PBO:0071529
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L34 pseudogene 32","termid":"PBO:0071529"}


id: MONDO:0015907
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epimetaphyseal skeletal dysplasia","secondary_identifiers":["GARD:2176","Orphanet:1819"],"termid":"MONDO:0015907","xrefs":{"Monarch":{"xref_id":"0015907"}}}


id: GO:0012501
data:
  {"annotated_genes":["SJAG_03258","SJAG_01527","SJAG_00737"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98330],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0012502"},{"annotations":[75810,81290],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0043065"}]},"cv_name":"biological_process","definition":"A process which begins when a cell receives an internal or external signal and activates a series of biochemical events (signaling pathway). The process ends with the death of the cell.","definition_xrefs":["GOC:mtg_apoptosis","GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell death","termid":"GO:0008219"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00737":null,"SJAG_01527":null,"SJAG_03258":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"programmed cell death","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0016244","Wikipedia:Programmed_cell_death","Reactome:R-HSA-5357801"],"synonyms":[{"name":"PCD","type":"related"},{"name":"RCD","type":"related"},{"name":"caspase-independent apoptosis","type":"related"},{"name":"caspase-independent cell death","type":"narrow"},{"name":"non-apoptotic programmed cell death","type":"narrow"},{"name":"nonapoptotic programmed cell death","type":"narrow"},{"name":"regulated cell death","type":"broad"}],"termid":"GO:0012501","terms_by_termid":{"GO:0012502":null,"GO:0043065":null}}


id: GO:0016848
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the breakage of a bond between carbon and any halogen atom.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lyase activity","termid":"GO:0016829"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"carbon-halide lyase activity","secondary_identifiers":["EC:4.5.-.-"],"termid":"GO:0016848"}


id: GO:1990419
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an elemental metal stimulus.","definition_xrefs":["PMID:22688007"],"gene_count":0,"genotype_count":0,"name":"obsolete response to elemental metal (obsolete GO:1990419)","synonyms":[{"name":"response to elemental metal","type":"exact"}],"termid":"GO:1990419"}


id: PBO:0051568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 13 receptor subunit alpha 2","termid":"PBO:0051568"}


id: GO:0030377
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with the urokinase plasminogen activator to initiate a change in cell activity.","definition_xrefs":["GOC:mah","PMID:16456079"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor activity","termid":"GO:0038023"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"urokinase plasminogen activator receptor activity","secondary_identifiers":["Wikipedia:Urokinase_receptor"],"synonyms":[{"name":"U-plasminogen activator receptor activity","type":"exact"},{"name":"uPAR","type":"exact"},{"name":"urokinase plasminogen activator receptor","type":"exact"}],"termid":"GO:0030377"}


id: GO:0047113
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a quinone + an aldehyde + H2O = a carboxylate + a quinol + H+.","definition_xrefs":["RHEA:13881"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors","termid":"GO:0016903"}],"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":"aldehyde dehydrogenase (quinone) activity","secondary_identifiers":["EC:1.2.5.2","MetaCyc:1.2.99.3-RXN"],"synonyms":[{"name":"aldehyde dehydrogenase (acceptor) activity","type":"related"},{"name":"aldehyde dehydrogenase (pyrroloquinoline-quinone)","type":"related"},{"name":"aldehyde:(pyrroloquinoline-quinone) oxidoreductase activity","type":"related"}],"termid":"GO:0047113"}


id: GO:0009692
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving ethylene (C2-H4, ethene), a simple hydrocarbon gas that can function in plants as a growth regulator.","definition_xrefs":["ISBN:0387969845"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkene metabolic process","termid":"GO:0043449"}],"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":"ethylene metabolic process","synonyms":[{"name":"ethene metabolic process","type":"exact"},{"name":"ethene metabolism","type":"exact"},{"name":"ethylene metabolism","type":"exact"}],"termid":"GO:0009692"}


id: MONDO:0016732
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete dysembryoplastic neuroepithelial tumor (obsolete MONDO:0016732)","termid":"MONDO:0016732","xrefs":{"Monarch":{"xref_id":"0016732"}}}


id: PBO:0086485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative nucleotide sugar transporter; has similarity to Vrg4p","termid":"PBO:0086485"}


id: PBO:0074643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 35B","termid":"PBO:0074643"}


id: PBO:0087314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Small subunit of the clathrin-associated adaptor complex AP-2; AP-2 is involved in protein sorting at the plasma membrane; related to the sigma subunit of the mammalian plasma membrane clathrin-associated protein (AP-2) complex","termid":"PBO:0087314"}


id: PATO:0000503
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A phase which occurs during the light cycle.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phase","termid":"PATO:0000083"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"light phase","termid":"PATO:0000503"}


id: PBO:0087622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the core form of RNA polymerase transcription factor TFIIH; has both protein kinase and DNA-dependent ATPase/helicase activities; essential for transcription and nucleotide excision repair; interacts with Tfb4p","termid":"PBO:0087622"}


id: PBO:0113087
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic protein required for sporulation; targeted to vacuole via AP-3 pathway","termid":"PBO:0113087"}


id: GO:0019863
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an immunoglobulin of the IgE isotype.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin binding","termid":"GO:0019865"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"IgE binding","termid":"GO:0019863"}


id: GO:1905161
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a phagocytic vesicle.","definition_xrefs":["GOC:bf","GOC:PARL","GOC:TermGenie","GO_REF:0000087","PMID:23303671"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to organelle","termid":"GO:0033365"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"protein localization to phagocytic vesicle","synonyms":[{"name":"protein localisation in phagocytic vesicle","type":"exact"},{"name":"protein localisation to phagocytic vesicle","type":"exact"},{"name":"protein localisation to phagosome","type":"exact"},{"name":"protein localization in phagocytic vesicle","type":"exact"},{"name":"protein recruitment to phagosome","type":"exact"}],"termid":"GO:1905161"}


id: PBO:0055431
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 2861","termid":"PBO:0055431"}


id: MONDO:0003332
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An ovarian mature teratoma characterized by the presence of aberrant thyroid tissue with morphologic changes identical to thyroid carcinoma. Patients may present with abdominal mass and unusual symptoms due to thyrotoxicosis, or with Meigs syndrome (ascites and pleural effusion).","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"teratoma with malignant transformation","termid":"MONDO:0006444"},{"relation_name":"is_a","term_name":"struma ovarii","termid":"MONDO:0006980"},{"relation_name":"is_a","term_name":"immature ovarian teratoma","termid":"MONDO:0018369"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant struma ovarii","secondary_identifiers":["ICDO:9090/3","MEDGEN:137777","DOID:5208","NCIT:C4291","UMLS:C0334525"],"synonyms":[{"name":"struma ovarii, malignant","type":"exact"},{"name":"struma ovarii, malignant (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0003332","xrefs":{"Monarch":{"xref_id":"0003332"}}}


id: PBO:0047822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box O3","termid":"PBO:0047822"}


id: GO:0097621
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2.","definition_xrefs":["PMID:15279562","PMID:16129825","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH2 group of donors, oxygen as acceptor","termid":"GO:0016641"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"monoamine oxidase activity","secondary_identifiers":["EC:1.4.3.4"],"synonyms":[{"name":"amine:oxygen oxidoreductase (deaminating) activity","type":"exact"}],"termid":"GO:0097621"}


id: GO:0090032
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of steroid hormones,compounds with a 1, 2, cyclopentanoperhydrophenanthrene nucleus that act as hormones.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of steroid biosynthetic process","termid":"GO:0010894"},{"relation_name":"is_a","term_name":"negative regulation of hormone biosynthetic process","termid":"GO:0032353"},{"relation_name":"is_a","term_name":"regulation of steroid hormone biosynthetic process","termid":"GO:0090030"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"negative regulation of steroid hormone biosynthetic process","termid":"GO:0090032"}


id: PBO:0053317
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 51","termid":"PBO:0053317"}


id: PR:Q9UUH1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A leptin receptor overlapping transcript-like 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00143"],"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":"vacuolar protein sorting-associated protein 55 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC630.11","secondary_identifiers":["UniProtKB:Q9UUH1"],"synonyms":[{"name":"Spom972h-LEPROTL1","type":"exact"}],"termid":"PR:Q9UUH1"}


id: MONDO:0020175
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete malignant tumor of palpebral epidermis (obsolete MONDO:0020175)","termid":"MONDO:0020175","xrefs":{"Monarch":{"xref_id":"0020175"}}}


id: PBO:0066345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulator of chromosome condensation 2 pseudogene 7","termid":"PBO:0066345"}


id: MONDO:0006301
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, well-circumscribed renal cortical neoplasm affecting females more often than males. Polycythemia has been reported in twelve-percent of patients.","definition_xrefs":["NCIT:C27253"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal adenoma","termid":"MONDO:0002395"}],"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":"metanephric adenoma","secondary_identifiers":["DOID:6404","EFO:1000373","ICDO:8325/0","UMLS:C1266045","ICDO:8191/0","MEDGEN:266093"],"synonyms":[{"name":"metanephric adenoma","type":"exact"},{"name":"metanephric adenoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0006301","xrefs":{"Monarch":{"xref_id":"0006301"}}}


id: PBO:0057020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 107","termid":"PBO:0057020"}


id: PBO:0089008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit VI","termid":"PBO:0089008"}


id: PBO:0080554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WBP1 pseudogene 1","termid":"PBO:0080554"}


id: PBO:0081984
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and SCAN domain containing 10","termid":"PBO:0081984"}


id: PBO:0088228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydantoin racemase family","termid":"PBO:0088228"}


id: GO:1990848
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of removal of reactive oxygen species in a cell.","definition_xrefs":["PMID:24118096"],"gene_count":0,"genotype_count":0,"name":"obsolete Positive regulation of removal of reactive oxygen species (obsolete GO:1990848)","termid":"GO:1990848"}


id: MONDO:0019916
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 16 disorder","termid":"MONDO:0700023"},{"relation_name":"is_a","term_name":"uniparental disomy","termid":"MONDO:0700086"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maternal uniparental disomy of chromosome 16","secondary_identifiers":["UMLS:C4750769","GARD:19336","Orphanet:96185","icd11.foundation:635736420","MEDGEN:1650997"],"synonyms":[{"name":"UPD(16)mat","type":"exact"},{"name":"maternal uniparental disomy of chromosome type 16","type":"exact"}],"termid":"MONDO:0019916","xrefs":{"Monarch":{"xref_id":"0019916"}}}


id: GO:0101031
data:
  {"annotated_genes":["SJAG_02378","SJAG_03320","SJAG_02926","SJAG_00447","SJAG_03570","SJAG_04121","SJAG_00609","SJAG_01002"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[78480,79846,81491,75292,71490,77858,74347,79752],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005832"}]},"cv_name":"cellular_component","definition":"A protein complex required for the non-covalent folding or unfolding, maturation, stabilization or assembly or disassembly of macromolecular structures. Usually active during or immediately after completion of translation. Many chaperone complexes contain heat shock proteins.","definition_xrefs":["GOC:bhm","PMID:21855797"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00447":null,"SJAG_00609":null,"SJAG_01002":null,"SJAG_02378":null,"SJAG_02926":null,"SJAG_03320":null,"SJAG_03570":null,"SJAG_04121":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":"protein folding chaperone complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"chaperone complex","type":"broad"}],"termid":"GO:0101031","terms_by_termid":{"GO:0005832":null}}


id: PBO:0070386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rhophilin associated tail protein 1","termid":"PBO:0070386"}


id: PATO:0001368
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A surface feature shape quality inhering in a bearer by virtue of the bearer's having an irregularly toothed edge.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serration","termid":"PATO:0001976"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"erose","synonyms":[{"name":"jagged","type":"related"}],"termid":"PATO:0001368"}


id: MONDO:0004554
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An angiomyolipoma occurring in childhood.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood kidney neoplasm","termid":"MONDO:0002730"},{"relation_name":"is_a","term_name":"kidney angiomyolipoma","termid":"MONDO:0004555"}],"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":"childhood kidney angiomyolipoma","secondary_identifiers":["NCIT:C6565","MEDGEN:272468","DOID:8410","UMLS:C1333000"],"synonyms":[{"name":"childhood renal angiomyolipoma","type":"exact"},{"name":"kidney angiomyolipoma of childhood","type":"exact"},{"name":"paediatric kidney angiomyolipoma","type":"exact"},{"name":"paediatric renal angiomyolipoma","type":"exact"},{"name":"pediatric kidney angiomyolipoma","type":"exact"},{"name":"pediatric renal angiomyolipoma","type":"exact"}],"termid":"MONDO:0004554","xrefs":{"Monarch":{"xref_id":"0004554"}}}


id: MONDO:0012259
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Colloid cysts of the third ventricle are non-cancerous brain lesions. The third ventricle is a cavity in the brain that is filled with cerebral spinal fluid (CSF). Colloid cysts can cause blockages resulting in a build up of CSF in the brain (hydrocephalus) and increased pressure. Some colloid cysts are asymptomatic while others cause neurological symptoms, such as headaches, swelling of the optic nerve (papilledema), and drop attacks. When symptoms are present onset tends to be in the third to sixth decade of life. While uncommon, symptoms of colloid cyst can become life threatening.","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"colloid cysts of third ventricle","secondary_identifiers":["MESH:C535966","MEDGEN:82744","OMIM:609363","UMLS:C0266481"],"synonyms":[{"name":"colloid cysts of third ventricle","type":"exact"},{"name":"neuroepithelial cysts of third ventricle","type":"related"}],"termid":"MONDO:0012259","xrefs":{"Monarch":{"xref_id":"0012259"}}}


id: GO:1901410
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of tetrapyrrole biosynthetic process from glutamate.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of tetrapyrrole biosynthetic process","termid":"GO:1901463"},{"relation_name":"is_a","term_name":"regulation of glutamate metabolic process","termid":"GO:2000211"},{"relation_name":"regulates","term_name":"tetrapyrrole biosynthetic process from glutamate","termid":"GO:0033526"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0033013"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006520","GO:0033013","GO:0044281"],"is_obsolete":false,"name":"regulation of tetrapyrrole biosynthetic process from glutamate","synonyms":[{"name":"regulation of tetrapyrrole anabolism from glutamate","type":"exact"},{"name":"regulation of tetrapyrrole biosynthesis from glutamate","type":"exact"},{"name":"regulation of tetrapyrrole formation from glutamate","type":"exact"},{"name":"regulation of tetrapyrrole synthesis from glutamate","type":"exact"}],"termid":"GO:1901410"}


id: SO:1000060
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The amino acid change following from the codon change does not change the gross properties (size, charge, hydrophobicity) of the amino acid at that position.","definition_xrefs":["EBI:www.ebi.ac.uk/mutations/recommendations/mutevent.html"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000060 sequence_variant_causing_conservative_missense_codon_change_in_transcript (obsolete SO:1000060)","synonyms":[{"name":"mutation causing conservative missense codon change in transcript","type":"related"},{"name":"sequence variant causing conservative missense codon change in transcript","type":"exact"}],"termid":"SO:1000060"}


id: PBO:0034300
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-capable_of_inhibiting_or_preventing_pathological_process","termid":"PBO:0034300"}


id: PBO:0082487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Catabolic L-serine (L-threonine) deaminase; catalyzes the degradation of both L-serine and L-threonine; required to use serine or threonine as the sole nitrogen source, transcriptionally induced by serine and threonine","termid":"PBO:0082487"}


id: PBO:0059458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"minisatellite binding protein 2","termid":"PBO:0059458"}


id: GO:0071924
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of chemokine (C-C motif) ligand 22 (CCL22) due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah","PMID:18832724"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemokine production","termid":"GO:0032602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"chemokine (C-C motif) ligand 22 production","synonyms":[{"name":"C-C motif chemokine 22 production","type":"exact"},{"name":"CCL-22 production","type":"exact"},{"name":"CCL22 production","type":"exact"}],"termid":"GO:0071924"}


id: GO:0016634
data:
  {"annotated_genes":["SJAG_02876","SJAG_04944"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[81733],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004109"},{"annotations":[74233],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004729"}]},"cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which a CH-CH group acts as a hydrogen or electron donor and reduces oxygen.","definition_xrefs":["EC:1.3.3.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors","termid":"GO:0016627"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02876":null,"SJAG_04944":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0016634","terms_by_termid":{"GO:0004109":null,"GO:0004729":null}}


id: GO:0009923
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A tetrameric complex of four different subunits which catalyzes the elongation of a fatty acid chain 2 carbon units at a time in the synthesis of very long chain fatty acids.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"is_a","term_name":"endoplasmic reticulum protein-containing complex","termid":"GO:0140534"},{"relation_name":"is_a","term_name":"transferase complex","termid":"GO:1990234"},{"relation_name":"part_of","term_name":"endoplasmic reticulum membrane","termid":"GO:0005789"}],"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:0005783"},{"rel_name":"part_of","termid":"GO:0005789"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005783","GO:0005737","GO:0005789","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"fatty acid elongase complex","termid":"GO:0009923"}


id: GO:0071104
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an interleukin-9 stimulus.","definition_xrefs":["GOC:yaf","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cytokine","termid":"GO:0034097"}],"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 interleukin-9","synonyms":[{"name":"response to IL-9","type":"exact"}],"termid":"GO:0071104"}


id: PBO:0077150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TLC domain containing 1","termid":"PBO:0077150"}


id: GO:0031639
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which inactive plasminogen is processed to active plasmin. This process includes cleavage at an internal Arg-Val site to form an N-terminal A-chain and C-terminal B-chain held together by a disulfide bond, and can include further proteolytic cleavage events to remove the preactivation peptide.","definition_xrefs":["PMID:9548733"],"direct_ancestors":[{"relation_name":"is_a","term_name":"zymogen activation","termid":"GO:0031638"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0051604"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0051604","GO:0008150"],"is_obsolete":false,"name":"plasminogen activation","synonyms":[{"name":"cleavage of plasminogen to plasmin","type":"exact"}],"termid":"GO:0031639"}


id: GO:2001116
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a methanopterin.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pteridine-containing compound biosynthetic process","termid":"GO:0042559"},{"relation_name":"is_a","term_name":"organophosphate biosynthetic process","termid":"GO:0090407"},{"relation_name":"is_a","term_name":"methanopterin-containing compound metabolic process","termid":"GO:2001115"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0042559"}],"interesting_parent_ids":["GO:0008150","GO:0042559"],"is_obsolete":false,"name":"methanopterin-containing compound biosynthetic process","synonyms":[{"name":"methanopterin biosynthesis","type":"exact"}],"termid":"GO:2001116"}


id: PBO:0079948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP2 antisense RNA 1","termid":"PBO:0079948"}


id: PBO:0002663
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.1.137","termid":"PBO:0002663"}


id: GO:1905420
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any vascular smooth muscle cell differentiation that is involved in phenotypic switching.","definition_xrefs":["GOC:BHF","PMID:25089138","GOC:rph","GO_REF:0000060","GOC:BHF_miRNA","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vascular associated smooth muscle cell differentiation","termid":"GO:0035886"},{"relation_name":"is_a","term_name":"cell differentiation involved in phenotypic switching","termid":"GO:0090679"}],"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":"vascular associated smooth muscle cell differentiation involved in phenotypic switching","synonyms":[{"name":"VSMC differentiation involved in phenotypic dimorphism","type":"related"},{"name":"VSMC differentiation involved in phenotypic switching","type":"exact"},{"name":"vascular associated smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"vascular smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"vascular smooth muscle cell differentiation involved in phenotypic switching","type":"exact"}],"termid":"GO:1905420"}


id: PBO:0048468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glial cells missing transcription factor 1","termid":"PBO:0048468"}


id: GO:1904222
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of serine C-palmitoyltransferase activity.","definition_xrefs":["GOC:rl","GO_REF:0000059","GOC:BHF","GOC:TermGenie","PMID:16120614"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of transferase activity","termid":"GO:0051347"},{"relation_name":"is_a","term_name":"regulation of serine C-palmitoyltransferase activity","termid":"GO:1904220"}],"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 serine C-palmitoyltransferase activity","synonyms":[{"name":"activation of 3-oxosphinganine synthetase activity","type":"narrow"},{"name":"activation of SPT","type":"related"},{"name":"activation of acyl-CoA:serine C-2 acyltransferase decarboxylating","type":"related"},{"name":"activation of palmitoyl-CoA:L-serine C-palmitoyltransferase (decarboxylating) activity","type":"narrow"},{"name":"activation of serine C-palmitoyltransferase activity","type":"narrow"},{"name":"positive regulation of 3-oxosphinganine synthetase activity","type":"exact"},{"name":"positive regulation of SPT","type":"related"},{"name":"positive regulation of acyl-CoA:serine C-2 acyltransferase decarboxylating","type":"related"},{"name":"positive regulation of palmitoyl-CoA:L-serine C-palmitoyltransferase (decarboxylating) activity","type":"exact"},{"name":"up regulation of 3-oxosphinganine synthetase activity","type":"exact"},{"name":"up regulation of SPT","type":"related"},{"name":"up regulation of acyl-CoA:serine C-2 acyltransferase decarboxylating","type":"related"},{"name":"up regulation of palmitoyl-CoA:L-serine C-palmitoyltransferase (decarboxylating) activity","type":"exact"},{"name":"up regulation of serine C-palmitoyltransferase activity","type":"exact"},{"name":"up-regulation of 3-oxosphinganine synthetase activity","type":"exact"},{"name":"up-regulation of SPT","type":"related"},{"name":"up-regulation of acyl-CoA:serine C-2 acyltransferase decarboxylating","type":"related"},{"name":"up-regulation of palmitoyl-CoA:L-serine C-palmitoyltransferase (decarboxylating) activity","type":"exact"},{"name":"up-regulation of serine C-palmitoyltransferase activity","type":"exact"},{"name":"upregulation of 3-oxosphinganine synthetase activity","type":"exact"},{"name":"upregulation of SPT","type":"related"},{"name":"upregulation of acyl-CoA:serine C-2 acyltransferase decarboxylating","type":"related"},{"name":"upregulation of palmitoyl-CoA:L-serine C-palmitoyltransferase (decarboxylating) activity","type":"exact"},{"name":"upregulation of serine C-palmitoyltransferase activity","type":"exact"}],"termid":"GO:1904222"}


id: PBO:0017487
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-regulates","termid":"PBO:0017487"}


id: MONDO:0012421
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the ADCY1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 44","secondary_identifiers":["UMLS:C1857809","DOID:0110501","GARD:22620","MEDGEN:341854","OMIM:610154","MESH:C565716"],"synonyms":[{"name":"ADCY1 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"DFNB44","type":"narrow"},{"name":"autosomal recessive deafness 44","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 44","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in ADCY1","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 44","type":"narrow"},{"name":"deafness, autosomal recessive 44","type":"narrow"},{"name":"deafness, autosomal recessive type 44","type":"narrow"}],"termid":"MONDO:0012421","xrefs":{"Monarch":{"xref_id":"0012421"}}}


id: PBO:0060921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurofibromin 1 pseudogene 8","termid":"PBO:0060921"}


id: MONDO:0011299
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neurodegenerative disease with chorea in which the cause of the disease is a mutation in the PRNP gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"Huntington disease and related disorders","termid":"MONDO:0000167"},{"relation_name":"excluded_subClassOf","term_name":"movement disorder","termid":"MONDO:0005395"},{"relation_name":"is_a","term_name":"prion disease","termid":"MONDO:0005429"},{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"Huntington disease-like 1","secondary_identifiers":["UMLS:C1864112","OMIM:603218","Orphanet:157941","DOID:0090103","GARD:16985","MESH:C566398","MEDGEN:355137"],"synonyms":[{"name":"HDL1","type":"exact"},{"name":"HLN1","type":"exact"},{"name":"Huntington disease-like 1","type":"exact"},{"name":"Huntington disease-like type 1","type":"exact"},{"name":"Huntington's disease-like 1","type":"related"},{"name":"Huntington-like neurodegenerative disorder 1","type":"exact"},{"name":"Huntington-like neurodegenerative disorder, autosomal dominant","type":"related"},{"name":"PRNP neurodegenerative disease with chorea","type":"exact"},{"name":"autosomal dominant Huntington-like neurodegenerative disorder","type":"exact"},{"name":"early-onset prion disease with prominent psychiatric features","type":"exact"},{"name":"neurodegenerative disease with chorea caused by mutation in PRNP","type":"exact"},{"name":"prion disease, early-onset, with prominent psychiatric features","type":"related"}],"termid":"MONDO:0011299","xrefs":{"Monarch":{"xref_id":"0011299"}}}


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


id: PBO:0071130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 132","termid":"PBO:0071130"}


id: PBO:0040637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain abundant membrane attached signal protein 1","termid":"PBO:0040637"}


id: MONDO:0017294
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infantile glycerol kinase deficiency (GKD) is a severe form of GKD characterized clinically by poor feeding, failure to thrive, salt-wasting dehydration, vomiting, Addisonian pigmentation, hypotonia, and disorders of consciousness. Some patients have complex GKD associated with adrenal hypoplasia congenita and/or Duchenne muscular dystrophy (DMD) with manifestations including intellectual deficit, dysmorphic facial features, abnormal external genitalia, strabismus, seizures, and progressive lethargy.","definition_xrefs":["Orphanet:284408"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"isolated glycerol kinase deficiency","termid":"MONDO:0018459"},{"relation_name":"is_a","term_name":"inborn glycerol kinase deficiency","termid":"MONDO:0010613"},{"relation_name":"is_a","term_name":"disorder of gluconeogenesis","termid":"MONDO:0019225"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"glycerol kinase deficiency, infantile form","termid":"MONDO:0017294","xrefs":{"Monarch":{"xref_id":"0017294"}}}


id: GO:0003675
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete protein (obsolete GO:0003675)","synonyms":[{"name":"protein","type":"exact"}],"termid":"GO:0003675"}


id: PBO:0060803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit S6 pseudogene 1","termid":"PBO:0060803"}


id: GO:0030375
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. The function of a transcription cofactor that activates transcription in conjunction with a thyroid hormone-dependent nuclear receptor from a RNA polymerase II promoter; does not bind DNA itself.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete thyroid hormone receptor coactivator activity (obsolete GO:0030375)","synonyms":[{"name":"thyroid hormone receptor activator activity","type":"narrow"},{"name":"thyroid hormone receptor co-activator activity","type":"exact"}],"termid":"GO:0030375"}


id: GO:0052863
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 1-deoxy-D-xylulose 5-phosphate, the 5-phospho derivative of 1-deoxy-D-xylulose. 1-deoxy-D-xylulose 5-phosphate is an intermediate in the non-mevalonate pathway and a common precursor for isoprenoid, thiamin, and pyridoxol biosynthesis.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphate-containing compound metabolic process","termid":"GO:0006796"},{"relation_name":"is_a","term_name":"organophosphate metabolic process","termid":"GO:0019637"},{"relation_name":"is_a","term_name":"carbohydrate derivative metabolic process","termid":"GO:1901135"}],"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":"1-deoxy-D-xylulose 5-phosphate metabolic process","synonyms":[{"name":"(2R,3S)-2,3-dihydroxy-4-oxopentyl dihydrogen phosphate metabolic process","type":"exact"},{"name":"(2R,3S)-2,3-dihydroxy-4-oxopentyl dihydrogen phosphate metabolism","type":"exact"},{"name":"1-deoxy-D-xylulose 5-phosphate metabolism","type":"exact"}],"termid":"GO:0052863"}


id: PBO:0060510
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NSF attachment protein beta","termid":"PBO:0060510"}


id: PBO:0077221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane BAX inhibitor motif containing 4","termid":"PBO:0077221"}


id: PBO:0028844
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_Mei2_nuclear_dot","termid":"PBO:0028844"}


id: MONDO:0859393
data:
  {"annotated_genes":["SJAG_00213","SJAG_03436"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87347],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859575"},{"annotations":[87348],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859576"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00213":null,"SJAG_03436":null},"genotype_count":0,"is_obsolete":false,"name":"Atelis syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:620184"],"termid":"MONDO:0859393","terms_by_termid":{"MONDO:0859575":null,"MONDO:0859576":null},"xrefs":{"Monarch":{"xref_id":"0859393"}}}


id: GO:0046295
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of glycolate, the anion of hydroxyethanoic acid (glycolic acid).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycolate metabolic process","termid":"GO:0009441"},{"relation_name":"is_a","term_name":"primary alcohol biosynthetic process","termid":"GO:0034309"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"glycolate biosynthetic process","synonyms":[{"name":"glycolate anabolism","type":"exact"},{"name":"glycolate biosynthesis","type":"exact"},{"name":"glycolate formation","type":"exact"},{"name":"glycolate synthesis","type":"exact"}],"termid":"GO:0046295"}


id: FYPO:0004461
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of one or more regulation of sexual differentiation RNAs measured in a cell is lower than normal (i.e. lower than observed in wild-type cells) when the cell is subject to nitrogen starvation. Sexual differentiation RNAs are transcribed from genes whose products are involved in sexual differentiation, i.e. mating and sporulation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during nitrogen starvation","termid":"FYPO:0001152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0006551","FYPO:0001985"],"is_obsolete":false,"name":"decreased level of regulation of sexual differentiation gene mRNA during nitrogen starvation","synonyms":[{"name":"decreased level of regulation of sexual differentiation gene RNA during nitrogen starvation","type":"exact"},{"name":"decreased level of regulation of sexual differentiation gene mRNA during nitrogen depletion","type":"exact"},{"name":"decreased level of regulation of sexual differentiation gene mRNA during nitrogen deprivation","type":"exact"},{"name":"decreased level of regulation of sexual differentiation gene transcripts nitrogen starvation","type":"exact"},{"name":"decreased level of sexual differentiation regulation gene mRNA during nitrogen starvation","type":"exact"},{"name":"decreased regulation of sexual differentiation gene mRNA accumulation during nitrogen starvation","type":"related"},{"name":"reduced level of regulation of sexual differentiation gene mRNA during nitrogen starvation","type":"exact"}],"termid":"FYPO:0004461"}


id: GO:0000121
data:
  {"annotated_genes":["SJAG_04964"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[102056],"is_not":false,"summary":null,"term":"GO:0000121"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + sn-glycerol 1-phosphate = glycerol + phosphate.","definition_xrefs":["RHEA:46084"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04964":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0016788"],"is_obsolete":false,"name":"sn-glycerol 1-phosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:RXN-14964"],"synonyms":[{"name":"alpha-glycerol phosphatase activity","type":"related"},{"name":"alpha-glycerophosphatase activity","type":"related"},{"name":"glycerol 3-phosphatase activity","type":"related"},{"name":"glycerol 3-phosphate phosphohydrolase activity","type":"related"},{"name":"glycerol-1-phosphatase activity","type":"broad"},{"name":"glycerol-1-phosphate phosphohydrolase activity","type":"related"},{"name":"glycerol-3-phosphate phosphatase activity","type":"related"}],"termid":"GO:0000121","terms_by_termid":{"GO:0000121":null}}


id: MONDO:0015449
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Criss cross heart (CCH) is a cardiac malformation where the inflow streams of the two ventricles cross due to twisting of the heart about its major axis. The clinical features depend on the particular cardiac defects associated, like simple or corrected transposition of the great arteries and ventricular septal defects.","definition_xrefs":["Orphanet:1461"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital heart malformation","termid":"MONDO:0019512"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"criss-cross heart","secondary_identifiers":["MESH:D003420","MEDGEN:8181","UMLS:C0010334","ICD9:746.89","SCTID:253269002","GARD:18724"],"synonyms":[{"name":"criss-cross atrioventricular relationships","type":"exact"},{"name":"superoinferior ventricles","type":"exact"},{"name":"twisted atrioventricular connections","type":"exact"}],"termid":"MONDO:0015449","xrefs":{"Monarch":{"xref_id":"0015449"}}}


id: MONDO:0017346
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly is a rare form of diffuse large B-cell lymphoma occurring most commonly in patients over the age of 50 (usually between 70-75 years of age), without overt immunodeficiency, and presenting with nodal and extranodal involvement (in sites such as the stomach, lung, skin and pancreas) and B symptoms (fever, night sweats, weight loss). The tumor is characterized by an aggressive course and a short survival rate.","definition_xrefs":["Orphanet:289661"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Epstein-Barr virus-associated malignant lymphoproliferative disorder","termid":"MONDO:0017343"},{"relation_name":"is_a","term_name":"diffuse large B-cell lymphoma","termid":"MONDO:0018905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly","secondary_identifiers":["icd11.foundation:407807101","NCIT:C80281","UMLS:C2700007","MEDGEN:397690","ICDO:9680/3","SCTID:716788007","GARD:21150"],"synonyms":[{"name":"EBV Positive diffuse large B-cell lymphoma of the elderly","type":"exact"},{"name":"EBV-Positive diffuse large B-cell lymphoma, NOS","type":"exact"},{"name":"EBV-positive DLBCL of the elderly","type":"exact"},{"name":"Epstein-Barr Virus Positive diffuse large B-cell lymphoma of the elderly","type":"exact"},{"name":"Senile EBV-associated B-cell lymphoproliferative disorder","type":"exact"},{"name":"age-related EBV Positive B-cell lymphoproliferative disorder","type":"exact"}],"termid":"MONDO:0017346","xrefs":{"Monarch":{"xref_id":"0017346"}}}


id: PATO:0015004
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A increase in the ability of a process to produce its output.","definition_xrefs":["PATOC:PortlandMeetingFeb2015"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"increased process quality","termid":"PATO:0002304"},{"relation_name":"is_a","term_name":"process efficacy","termid":"PATO:0015002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased efficacy","termid":"PATO:0015004"}


id: GO:0045513
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to interleukin-27.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"interleukin-17 binding","termid":"GO:0019975"}],"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":"interleukin-27 binding","synonyms":[{"name":"IL-27 binding","type":"exact"}],"termid":"GO:0045513"}


id: GO:0010811
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of cell-substrate adhesion. Cell-substrate adhesion is the attachment of a cell to the underlying substrate via adhesion molecules.","definition_xrefs":["GOC:dph","GOC:tb","GOC:pf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell-substrate adhesion","termid":"GO:0010810"},{"relation_name":"is_a","term_name":"positive regulation of cell adhesion","termid":"GO:0045785"},{"relation_name":"positively_regulates","term_name":"cell-substrate adhesion","termid":"GO:0031589"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"positive regulation of cell-substrate adhesion","termid":"GO:0010811"}


id: GO:0010770
data:
  {"annotated_genes":["SJAG_03581","SJAG_00514","SJAG_02392"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96354,91638,97628],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051519"}]},"cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of cell morphogenesis contributing to cell differentiation. Cell morphogenesis involved in differentiation is the change in form (cell shape and size) that occurs when relatively unspecialized cells acquire specialized structural and/or functional features that characterize the cells, tissues, or organs of the mature organism or some other relatively stable phase of the organism's life history.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell development","termid":"GO:0010720"},{"relation_name":"is_a","term_name":"regulation of cell morphogenesis","termid":"GO:0022604"},{"relation_name":"positively_regulates","term_name":"cell morphogenesis","termid":"GO:0000902"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00514":null,"SJAG_02392":null,"SJAG_03581":null},"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 cell morphogenesis","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0010770","terms_by_termid":{"GO:0051519":null}}


id: FYPO:0004987
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to sunitinib. Cells stop growing (and may die) at a concentration of sunitinib that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0000003","FYPO:0005447","FYPO:0001985","FYPO:0002683"],"is_obsolete":false,"name":"sensitive to sunitinib","synonyms":[{"name":"hypersensitive to sunitinib","type":"exact"},{"name":"sensitive to sunitinib during mitotic cell cycle","type":"related"},{"name":"sensitive to sunitinib during vegetative growth","type":"exact"}],"termid":"FYPO:0004987"}


id: PBO:0035834
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-incomplete,_asymmetric_septum","termid":"PBO:0035834"}


id: PBO:0046057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 subunit H","termid":"PBO:0046057"}


id: FYPO:0004307
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A spindle phenotype in which the mitotic spindle is longer than normal during metaphase.","definition_xrefs":["PomBase:mah","PMID:10398680"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long mitotic spindle","termid":"FYPO:0000733"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0001985","FYPO:0001320","FYPO:0000120","FYPO:0000002","FYPO:0002399","FYPO:0005447"],"is_obsolete":false,"name":"long mitotic spindle during metaphase","synonyms":[{"name":"elongated mitotic spindle during metaphase","type":"exact"},{"name":"increased mitotic spindle length during metaphase","type":"exact"},{"name":"long bipolar mitotic spindle during metaphase","type":"exact"},{"name":"long mitotic spindle during metaphase during vegetative growth","type":"exact"},{"name":"long mitotic spindles during metaphase","type":"exact"},{"name":"long spindle during metaphase of mitosis","type":"exact"},{"name":"long spindle during mitotic metaphase","type":"exact"}],"termid":"FYPO:0004307"}


id: PBO:0004594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carbonic anhydrase (predicted)","termid":"PBO:0004594"}


id: GO:0002777
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of an antimicrobial peptide. Such peptides may have protective properties against bacteria, fungi, viruses, or protozoa.","definition_xrefs":["PMID:15638771","GOC:add","PMID:11807545","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide biosynthetic process","termid":"GO:0043043"},{"relation_name":"part_of","term_name":"antimicrobial peptide production","termid":"GO:0002775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"antimicrobial peptide biosynthetic process","termid":"GO:0002777"}


id: PBO:0068692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 73, pseudogene","termid":"PBO:0068692"}


id: PBO:0030615
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_cell_wall-degrading_enzymes","termid":"PBO:0030615"}


id: MONDO:0004484
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A melanoma that arises from the gallbladder.","definition_xrefs":["NCIT:C5735"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gallbladder cancer","termid":"MONDO:0005411"},{"relation_name":"is_a","term_name":"digestive system melanoma","termid":"MONDO:0045070"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"gallbladder melanoma","secondary_identifiers":["MEDGEN:232225","DOID:8167","UMLS:C1333749"],"synonyms":[{"name":"gall bladder melanoma","type":"exact"},{"name":"gall bladder melanoma (disease)","type":"exact"},{"name":"gallbladder malignant melanoma","type":"exact"},{"name":"gallbladder melanoma","type":"exact"},{"name":"malignant melanoma of gallbladder","type":"exact"},{"name":"malignant melanoma of the gallbladder","type":"exact"},{"name":"melanoma (disease) of gall bladder","type":"exact"},{"name":"melanoma of gallbladder","type":"exact"},{"name":"melanoma of the gallbladder","type":"exact"}],"termid":"MONDO:0004484","xrefs":{"Monarch":{"xref_id":"0004484"}}}


id: PBO:0084576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Merged open reading frame; does not encode a discreet protein; YKR004C-A was originally annotated as an independent ORF, but was later demonstrated to be an exon of an adjacent ORF, YKR004C","termid":"PBO:0084576"}


id: FYPO:0005278
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 glucose-repressed mRNAs measured in a cell is lower than normal (i.e. lower than observed in wild-type cells). Glucose-repressed mRNAs are transcribed from genes whose transcription is negatively regulated when glucose is present.","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:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0006551","FYPO:0005447"],"is_obsolete":false,"name":"decreased level of glucose-repressed gene mRNA during vegetative growth","synonyms":[{"name":"decreased glucose-repressed gene mRNA accumulation during vegetative growth","type":"related"},{"name":"decreased level of glucose-repressed gene RNA during vegetative growth","type":"exact"},{"name":"decreased level of glucose-repressed gene mRNA during mitotic cell cycle","type":"related"},{"name":"decreased level of glucose-repressed gene transcripts during vegetative growth","type":"exact"},{"name":"reduced level of glucose-repressed gene mRNA during vegetative growth","type":"exact"}],"termid":"FYPO:0005278"}


id: PBO:0026962
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_level_of_stress_responsive_gene_mRNA_during_cellular_response_to_phosphate_starvation","termid":"PBO:0026962"}


id: PBO:0044744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DExD-box helicase 21","termid":"PBO:0044744"}


id: PBO:0067471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 601, pseudogene","termid":"PBO:0067471"}


id: MONDO:1010209
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lymphosarcoma that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-hodgkin lymphoma, non-human animal","termid":"MONDO:1010214"},{"relation_name":"is_a","term_name":"lymphoid system disorder, non-human animal","termid":"MONDO:1011330"},{"relation_name":"is_a","term_name":"cancer, non-human animal","termid":"MONDO:1011828"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lymphosarcoma, non-human animal","secondary_identifiers":["OMIA:000615"],"termid":"MONDO:1010209","xrefs":{"Monarch":{"xref_id":"1010209"}}}


id: GO:0003177
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the pulmonary valve over time, from its formation to the mature structure.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"semi-lunar valve development","termid":"GO:1905314"}],"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":"pulmonary valve development","termid":"GO:0003177"}


id: GO:0000440
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The core TFIIH complex when it is part of the nucleotide-excision repair factor 3 (NEF3).","definition_xrefs":["PMID:7813015","GOC:krc","PMID:22572993","PMID:22308316","PMID:14500720","GOC:ew"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription factor TFIIH core complex","termid":"GO:0000439"},{"relation_name":"part_of","term_name":"nucleotide-excision repair factor 3 complex","termid":"GO:0000112"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0032991"},{"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:0005634","GO:0032991"],"is_obsolete":false,"name":"core TFIIH complex portion of NEF3 complex","secondary_identifiers":["GO:0000442"],"synonyms":[{"name":"SSL2-core TFIIH complex portion of NEF3 complex","type":"exact"}],"termid":"GO:0000440"}


id: PBO:0090499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ndc80 complex subunit Ndc80","termid":"PBO:0090499"}


id: PBO:0055624
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 3063","termid":"PBO:0055624"}


id: MONDO:1011451
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic pulmonary fibrosis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pneumonia, non-human animal","termid":"MONDO:0700110"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"idiopathic disease, non-human animal","termid":"MONDO:1011323"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"idiopathic pulmonary fibrosis, non-human animal","secondary_identifiers":["OMIA:001417"],"termid":"MONDO:1011451","xrefs":{"Monarch":{"xref_id":"1011451"}}}


id: GO:0075009
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Development of slender tubular outgrowth first produced by most symbiont spores immediately following germination on or near its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"spore germination","termid":"GO:0009847"}],"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":"germ tube formation","synonyms":[{"name":"germ tube formation on or near host","type":"exact"}],"termid":"GO:0075009"}


id: PR:O13747
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A BRCA1-associated protein that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01471","PANTHER:PTHR24007:SF8","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":"RING finger protein ETP1 homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC16E8.13","secondary_identifiers":["UniProtKB:O13747"],"synonyms":[{"name":"BRAP2 homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-BRAP","type":"exact"}],"termid":"PR:O13747"}


id: PBO:0059681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 47","termid":"PBO:0059681"}


id: MONDO:0026186
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic developmental defect of the eye (obsolete MONDO:0026186)","secondary_identifiers":["Orphanet:183557"],"termid":"MONDO:0026186","xrefs":{"Monarch":{"xref_id":"0026186"}}}


id: MONDO:0014941
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"distal arthrogryposis","termid":"MONDO:0019942"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arthrogryposis, distal, with impaired proprioception and touch","secondary_identifiers":["UMLS:C4310692","MEDGEN:934659","OMIM:617146"],"synonyms":[{"name":"DAIPT","type":"exact"},{"name":"arthrogryposis, distal, with impaired proprioception and touch","type":"exact"},{"name":"arthrogryposis, distal, with impaired proprioception and touch; DAIPT","type":"exact"}],"termid":"MONDO:0014941","xrefs":{"Monarch":{"xref_id":"0014941"}}}


id: PBO:0075738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal recognition particle 19","termid":"PBO:0075738"}


id: PBO:0077054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thyroid hormone responsive","termid":"PBO:0077054"}


id: GO:0019092
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a srRNA, small subunit ribosomal ribonucleic acid, is transported from the mitochondrial matrix into the cytosol.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial rRNA export from mitochondrion","termid":"GO:0019090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"mitochondrial srRNA export from mitochondrion","synonyms":[{"name":"export of mitochondrial srRNA","type":"broad"},{"name":"mitochondrial srRNA export","type":"exact"},{"name":"mitochondrial srRNA export from mitochondria","type":"exact"},{"name":"mitochondrial srRNA export out of mitochondrion","type":"exact"},{"name":"mitochondrial srRNA transport from mitochondrion","type":"exact"},{"name":"mitochondrial srRNA, mitochondrial export","type":"exact"}],"termid":"GO:0019092"}


id: PBO:0042472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CUB domain containing protein 1","termid":"PBO:0042472"}


id: PBO:0002290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U6 snRNP-associated protein Lsm6 (predicted)","termid":"PBO:0002290"}


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


id: PBO:0030905
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_level_during_vegetative_growth","termid":"PBO:0030905"}


id: PBO:0090308
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetylglucosamine-phosphate mutase","termid":"PBO:0090308"}


id: MONDO:0033169
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"curariform drugs toxicity","secondary_identifiers":["Orphanet:413693"],"termid":"MONDO:0033169","xrefs":{"Monarch":{"xref_id":"0033169"}}}


id: PBO:0068384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNF185 antisense RNA 1","termid":"PBO:0068384"}


id: GO:1902539
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A macropinocytosis which involves another organism.","definition_xrefs":["GOC:jl","GOC:TermGenie","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete multi-organism macropinocytosis (obsolete GO:1902539)","termid":"GO:1902539"}


id: PBO:0045351
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DONSON pseudogene 1","termid":"PBO:0045351"}


id: PATO:0001351
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A density quality which inheres in a bearer by virtue of some influence exerted by the bearer's mass on a given area.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Area_density"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mass density","termid":"PATO:0001019"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"area density","termid":"PATO:0001351"}


id: FYPO:0005093
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 duration of protein phosphorylation is shorter than normal during a cellular response to hydroxyurea. All phosphorylation may be affected, or only phosphorylation of specific proteins, or even specific sites within specific proteins.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein modification during vegetative growth","termid":"FYPO:0000329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002274","FYPO:0000002","FYPO:0001985","FYPO:0002494","FYPO:0001320"],"is_obsolete":false,"name":"decreased duration of protein phosphorylation during cellular response to hydroxyurea","synonyms":[{"name":"decreased duration of protein phosphorylation during cellular response to HU","type":"exact"},{"name":"decreased duration of protein phosphorylation during cellular response to hydroxyurea during mitotic cell cycle","type":"related"},{"name":"decreased duration of protein phosphorylation during cellular response to hydroxyurea during vegetative growth","type":"exact"},{"name":"reduced duration of protein phosphorylation during cellular response to hydroxyurea","type":"exact"}],"termid":"FYPO:0005093"}


id: PATO:0002349
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial quality inhering in a bearer by virtue of the bearer's being located toward the base of an organism relative to another entity.","definition_xrefs":["merriam-webster:http://www.merriam-webster.com/dictionary/basal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basal to","termid":"PATO:0002349"}


id: PBO:0072090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S12 pseudogene 21","termid":"PBO:0072090"}


id: GO:0043073
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The nucleus of a germ cell, a reproductive cell in multicellular organisms.","definition_xrefs":["CL:0000586","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus","termid":"GO:0005634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005634"],"is_obsolete":false,"name":"germ cell nucleus","synonyms":[{"name":"germ-cell nucleus","type":"exact"}],"termid":"GO:0043073"}


id: PBO:0054222
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 1603","termid":"PBO:0054222"}


id: FYPO:0004934
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 G1 phase of the mitotic cell cycle is higher than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased RNA level during vegetative growth","termid":"FYPO:0000825"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0006551","FYPO:0000002"],"is_obsolete":false,"name":"increased RNA level during mitotic G1 phase","synonyms":[{"name":"increased RNA accumulation during mitotic G1 phase","type":"related"},{"name":"increased RNA level during G1 phase of mitotic cell cycle","type":"exact"},{"name":"increased RNA level during mitotic G1 phase during vegetative growth","type":"exact"},{"name":"increased mRNA level during mitotic G1 phase","type":"narrow"},{"name":"increased transcript level during mitotic G1 phase","type":"exact"}],"termid":"FYPO:0004934"}


id: MONDO:0019608
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete 46,XX disorder of sex development induced by maternal-derived androgen (obsolete MONDO:0019608)","secondary_identifiers":["Orphanet:91144","icd11.foundation:293874628"],"synonyms":[{"name":"46,XX DSD induced by maternal-derived androgen","type":"exact"}],"termid":"MONDO:0019608","xrefs":{"Monarch":{"xref_id":"0019608"}}}


id: PATO:0020002
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A biological sex quality inhering in an individual or a population based upon genotypic composition that confers the capability for an organism to differentiate female gonads.","definition_xrefs":["PATOC:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genotypic sex","termid":"PATO:0020000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"female genotypic sex","termid":"PATO:0020002"}


id: GO:0000753
data:
  {"annotated_genes":["SJAG_01993","SJAG_02700","SJAG_02989","SJAG_01943","SJAG_02864","SJAG_01894"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90026,100070,100682,100763,116163,94286],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904600"}]},"cv_name":"biological_process","definition":"The change in form (cell shape and size) that occurs during sexual reproduction in order to facilitate direct contact between the compatible mating types in organisms that undergo conjugation cellular fusion.","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell morphogenesis","termid":"GO:0000902"},{"relation_name":"part_of","term_name":"conjugation with cellular fusion","termid":"GO:0000747"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01894":null,"SJAG_01943":null,"SJAG_01993":null,"SJAG_02700":null,"SJAG_02864":null,"SJAG_02989":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0000747"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0000747"],"is_obsolete":false,"name":"cell morphogenesis involved in conjugation with cellular fusion","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0007332"],"synonyms":[{"name":"shmoo orientation","type":"narrow"},{"name":"shmooing","type":"narrow"}],"termid":"GO:0000753","terms_by_termid":{"GO:1904600":null}}


id: PR:O14012
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC29A4.09 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14012"],"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":"ribosomal RNA-processing protein 17 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29A4.09","synonyms":[{"name":"Spom972h-SPAC29A4.09","type":"exact"}],"termid":"PR:O14012"}


id: PBO:0109609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A24","termid":"PBO:0109609"}


id: PBO:0027804
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_JM216","termid":"PBO:0027804"}


id: GO:0097479
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which a synaptic vesicle or vesicles are transported to, and/or maintained in, a specific location.","definition_xrefs":["GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle localization","termid":"GO:0051648"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"synaptic vesicle localization","synonyms":[{"name":"establishment and maintenance of synaptic vesicle localization","type":"exact"},{"name":"establishment and maintenance of synaptic vesicle position","type":"exact"},{"name":"synaptic vesicle localisation","type":"exact"}],"termid":"GO:0097479"}


id: PBO:0051940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integral membrane protein 2B","termid":"PBO:0051940"}


id: GO:0002489
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an antigen-presenting cell expresses a peptide antigen of endogenous origin on its cell surface in association with an MHC class Ib protein complex following intracellular transport via a TAP (transporter associated with antigen processing) pathway. The peptide is typically a fragment of a larger endogenous protein which has been degraded within the cell and is dependent on TAP transport from the cytosol to ER for association with the MHC class Ib molecule. Class Ib here refers to non-classical class I molecules, such as those of the HLA-E gene family.","definition_xrefs":["GOC:add","PMID:15928678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antigen processing and presentation of endogenous peptide antigen via MHC class Ib via ER pathway","termid":"GO:0002488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"antigen processing and presentation of endogenous peptide antigen via MHC class Ib via ER pathway, TAP-dependent","synonyms":[{"name":"TAP-dependent antigen processing and presentation of endogenous peptide antigen via MHC class Ib via ER pathway","type":"exact"},{"name":"TAP-dependent endogenous peptide antigen processing and presentation via MHC class Ib via ER pathway","type":"exact"},{"name":"endogenous peptide antigen processing and presentation via MHC class Ib via ER pathway, TAP-dependent","type":"exact"}],"termid":"GO:0002489"}


id: PBO:0071924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S4X pseudogene 1","termid":"PBO:0071924"}


id: GO:0030216
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a keratinocyte.","definition_xrefs":["GOC:mah","GOC:sdb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermal cell differentiation","termid":"GO:0009913"},{"relation_name":"part_of","term_name":"skin development","termid":"GO:0043588"}],"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":"keratinocyte differentiation","synonyms":[{"name":"keratinocyte cell differentiation","type":"exact"}],"termid":"GO:0030216"}


id: GO:0006536
data:
  {"annotated_genes":["SJAG_01903","SJAG_00937","SJAG_03457","SJAG_00359","SJAG_00695","SJAG_01592","SJAG_00495","SJAG_03434","SJAG_00529","SJAG_03306","SJAG_03266","SJAG_04145","SJAG_00714","SJAG_02235","SJAG_04054","SJAG_03224"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89610,92651,94712,104419,106553,113641,113737],"is_not":false,"summary":null,"term":"GO:0006536"},{"annotations":[73823,119583,96045],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019676"},{"annotations":[80097],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019544"},{"annotations":[60113,113066,119584],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097054"},{"annotations":[93483,81317],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006538"},{"annotations":[71936,79820],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010133"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving glutamate, the anion of 2-aminopentanedioic acid.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glutamine family amino acid metabolic process","termid":"GO:0009064"},{"relation_name":"is_a","term_name":"dicarboxylic acid metabolic process","termid":"GO:0043648"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00359":null,"SJAG_00495":null,"SJAG_00529":null,"SJAG_00695":null,"SJAG_00714":null,"SJAG_00937":null,"SJAG_01592":null,"SJAG_01903":null,"SJAG_02235":null,"SJAG_03224":null,"SJAG_03266":null,"SJAG_03306":null,"SJAG_03434":null,"SJAG_03457":null,"SJAG_04054":null,"SJAG_04145":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"glutamate metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Glutamic_acid"],"synonyms":[{"name":"glutamate metabolism","type":"exact"},{"name":"glutamic acid metabolic process","type":"exact"},{"name":"glutamic acid metabolism","type":"exact"}],"termid":"GO:0006536","terms_by_termid":{"GO:0006536":null,"GO:0006538":null,"GO:0010133":null,"GO:0019544":null,"GO:0019676":null,"GO:0097054":null}}


id: MONDO:0014398
data:
  {"annotated_genes":["SJAG_03585"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88016],"is_not":false,"summary":null,"term":"MONDO:0014398"}]},"cv_name":"mondo","definition":"Combined oxidative phosphorylation defect type 21 is a rare mitochondrial disease characterized by axial hypotonia with limb hypertonia, developmental delay, hyperlactatemia, central nervous system anomalies visible on magnetic resonance imaging (e.g. corpus callosum hypoplasia, lesions of the globus pallidus) and multiple deficiency of the mitochondrial respiratory chain complexes in muscle tissue, but not in fibroblasts or liver.","definition_xrefs":["Orphanet:420733"],"direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03585":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"combined oxidative phosphorylation defect type 21","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1638633","SCTID:763211004","OMIM:615918","GARD:17700","DOID:0111465","UMLS:C4706316"],"synonyms":[{"name":"COXPD21","type":"exact"},{"name":"TARS2 combined oxidative phosphorylation deficiency","type":"exact"},{"name":"combined oxidative phosphorylation deficiency 21","type":"related"},{"name":"combined oxidative phosphorylation deficiency caused by mutation in TARS2","type":"exact"},{"name":"combined oxidative phosphorylation deficiency type 21","type":"exact"}],"termid":"MONDO:0014398","terms_by_termid":{"MONDO:0014398":null},"xrefs":{"Monarch":{"xref_id":"0014398"}}}


id: PBO:0043415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclic nucleotide binding domain containing 1","termid":"PBO:0043415"}


id: GO:0047880
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-threitol + NADP+ = D-erythrulose + H+ + NADPH.","definition_xrefs":["EC:1.1.1.162","RHEA:18005"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"erythrulose reductase activity","secondary_identifiers":["KEGG_REACTION:R08573","MetaCyc:RXN-17773"],"synonyms":[{"name":"D-erythrulose reductase activity","type":"related"},{"name":"erythritol:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0047880"}


id: GO:0034349
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any apoptotic process in a glial cell, a non-neuronal cell of the nervous system.","definition_xrefs":["GOC:mtg_apoptosis","GOC:sart","CL:0000125"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apoptotic process","termid":"GO:0006915"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"glial cell apoptotic process","synonyms":[{"name":"apoptosis of glia","type":"exact"},{"name":"apoptosis of glial cells","type":"exact"},{"name":"glia apoptosis","type":"exact"},{"name":"glia programmed cell death by apoptosis","type":"exact"},{"name":"glial cell apoptosis","type":"narrow"},{"name":"glial cell programmed cell death by apoptosis","type":"exact"},{"name":"programmed cell death of glia by apoptosis","type":"exact"},{"name":"programmed cell death of glial cells by apoptosis","type":"exact"},{"name":"programmed cell death, glia","type":"exact"},{"name":"programmed cell death, glial cells","type":"exact"}],"termid":"GO:0034349"}


id: PBO:0002673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing associated factor Saf3","termid":"PBO:0002673"}


id: MONDO:0958326
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary macular dystrophy","termid":"MONDO:0020242"}],"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":"macular dystrophy with or without cone dysfunction","secondary_identifiers":["MEDGEN:1853300","OMIM:620762","UMLS:C5935594"],"termid":"MONDO:0958326","xrefs":{"Monarch":{"xref_id":"0958326"}}}


id: PBO:0087663
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the import motor (PAM complex); the PAM complex is a  component of the Translocase of the Inner Mitochondrial membrane (TIM23 complex); forms a 1:1 subcomplex with Pam18p and inhibits its cochaperone activity; contains a J-like domain","termid":"PBO:0087663"}


id: GO:0040018
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of growth of an organism to reach its usual body size.","definition_xrefs":["GOC:go_curators","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of multicellular organism growth","termid":"GO:0040014"},{"relation_name":"is_a","term_name":"positive regulation of developmental growth","termid":"GO:0048639"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"multicellular organism growth","termid":"GO:0035264"}],"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 multicellular organism growth","synonyms":[{"name":"positive regulation of body growth","type":"exact"},{"name":"positive regulation of body size","type":"exact"}],"termid":"GO:0040018"}


id: MONDO:0007590
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hemifacial hyperplasia is a rare morphological anomaly of the maxillofacial region characterized by unilateral overgrowth of all facial structures (bone, soft tissues, teeth), called true hemifacial hypertrophy, or overgrowth of one or more but not all facial structures, called partial hemifacial hypertrophy. It may be isolated or related to some syndromes (e.g. Beckwith-Wiedemann, Proteus, Klippel-Trenaunay-Weber, McCune-Albright syndrome, Neurofibromatosis type 1). It may be associated with airway obstruction, sensorineural hearing loss or swallowing difficulties.","definition_xrefs":["Orphanet:141145"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"macroglossia","termid":"MONDO:0015496"},{"relation_name":"is_a","term_name":"overgrowth syndrome","termid":"MONDO:0019716"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemifacial hypertrophy","secondary_identifiers":["icd11.foundation:2090544963","OMIM:133900","UMLS:C1399354","GARD:16971","MEDGEN:452987"],"synonyms":[{"name":"facial asymmetry","type":"related"},{"name":"facial hemihypertrophy","type":"related"},{"name":"hemifacial hyperplasia","type":"related"},{"name":"hemifacial hypertrophy","type":"exact"}],"termid":"MONDO:0007590","xrefs":{"Monarch":{"xref_id":"0007590"}}}


id: GO:0100063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that regulates dipeptide transmembrane transport.","definition_xrefs":["GOC:obol","GOC:cjm"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of dipeptide transmembrane transport by transcription from RNA polymerase II promoter (obsolete GO:0100063)","termid":"GO:0100063"}


id: PBO:0087238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Serine esterase; homolog of human neuropathy target esterase (NTE); Nte1p-mediated phosphatidylcholine turnover influences transcription factor Opi1p localization, affecting transcriptional regulation of phospholipid biosynthesis genes","termid":"PBO:0087238"}


id: MONDO:0018411
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An instance of rare female infertility due to hypothalamic-pituitary-gonadal axis disorder that is caused by a modification of the individual's genome.","definition_xrefs":["MONDO:patterns/genetic"],"gene_count":0,"genotype_count":0,"name":"obsolete rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin (obsolete MONDO:0018411)","secondary_identifiers":["Orphanet:400011"],"synonyms":[{"name":"genetic rare female infertility due to hypothalamic-pituitary-gonadal axis disorder","type":"exact"},{"name":"rare female infertility due to gonadotropic axis disorder of genetic origin","type":"exact"},{"name":"rare female infertility due to hypothalamic-pituitary-testicular axis disorder of genetic origin","type":"exact"}],"termid":"MONDO:0018411","xrefs":{"Monarch":{"xref_id":"0018411"}}}


id: GO:0036507
data:
  {"annotated_genes":["SJAG_01858"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[68113],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904380"}]},"cv_name":"biological_process","definition":"The removal of one or more mannose residues from a mannosylated protein.","definition_xrefs":["PMID:25092655","GOC:PARL","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein deglycosylation","termid":"GO:0006517"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01858":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein demannosylation","references_by_uniquename":{"GO_REF:0000002":null},"synonyms":[{"name":"protein de-mannosylation","type":"exact"}],"termid":"GO:0036507","terms_by_termid":{"GO:1904380":null}}


id: GO:1990214
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 protein levels in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:16840699","PMID:22233353"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation by symbiont of host protein levels (obsolete GO:1990214)","termid":"GO:1990214"}


id: PBO:0044222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTXN2 antisense RNA 1","termid":"PBO:0044222"}


id: PBO:0003520
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histidine-containing response regulator phosphotransferase Mpr1","termid":"PBO:0003520"}


id: PBO:0085807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; ECM18 has a paralog, ICT1, that arose from the whole genome duplication","termid":"PBO:0085807"}


id: MONDO:0003778
data:
  {"annotated_genes":["SJAG_02528","SJAG_02208","SJAG_04380","SJAG_01787","SJAG_02184","SJAG_02330","SJAG_03805","SJAG_02479","SJAG_03453","SJAG_02453","SJAG_00610","SJAG_02039","SJAG_01697","SJAG_04118","SJAG_02803","SJAG_02572","SJAG_03536","SJAG_00771","SJAG_01884","SJAG_04743","SJAG_00400","SJAG_00222"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87847],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030519"},{"annotations":[87080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012429"},{"annotations":[86909],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012471"},{"annotations":[86912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012472"},{"annotations":[87000],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014007"},{"annotations":[88397],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013767"},{"annotations":[87554,87555],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:8000024"},{"annotations":[88043],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012146"},{"annotations":[87410],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011336"},{"annotations":[88367],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013135"},{"annotations":[88119,88120,88121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010066"},{"annotations":[87806],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010600"},{"annotations":[87716],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011997"},{"annotations":[86793],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011971"},{"annotations":[87037],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010504"},{"annotations":[87839,87840],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958013"},{"annotations":[88171],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024541"},{"annotations":[88022],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013818"}]},"cv_name":"mondo","definition":"A disorder in which the immune system is unable to mount an adequate immune response.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"immune system disorder","termid":"MONDO:0005046"},{"relation_name":"is_a","term_name":"immune deficiency disease","termid":"MONDO:0009453"}],"gene_count":22,"genes_by_uniquename":{"SJAG_00222":null,"SJAG_00400":null,"SJAG_00610":null,"SJAG_00771":null,"SJAG_01697":null,"SJAG_01787":null,"SJAG_01884":null,"SJAG_02039":null,"SJAG_02184":null,"SJAG_02208":null,"SJAG_02330":null,"SJAG_02453":null,"SJAG_02479":null,"SJAG_02528":null,"SJAG_02572":null,"SJAG_02803":null,"SJAG_03453":null,"SJAG_03536":null,"SJAG_03805":null,"SJAG_04118":null,"SJAG_04380":null,"SJAG_04743":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"inborn error of immunity","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:2100204","MEDGEN:585013","ICD9:279.3","SCTID:58606001","NANDO:1200320","UMLS:C0398686","Orphanet:101997","NCIT:C3131","SCTID:234532001","DOID:612","MESH:D007153","GARD:19813"],"synonyms":[{"name":"IEI","type":"exact"},{"name":"antibody deficiency syndrome","type":"related"},{"name":"antibody deficiency syndromes","type":"related"},{"name":"deficiency syndrome, antibody","type":"related"},{"name":"deficiency syndrome, immunologic","type":"related"},{"name":"deficiency syndrome, immunological","type":"related"},{"name":"deficiency syndromes, antibody","type":"related"},{"name":"deficiency syndromes, immunologic","type":"related"},{"name":"deficiency syndromes, immunological","type":"related"},{"name":"hypoimmunity","type":"exact"},{"name":"immune deficiency disorder","type":"related"},{"name":"immunodeficiency syndrome","type":"related"},{"name":"immunologic deficiency syndrome","type":"related"},{"name":"immunological deficiency syndrome","type":"related"},{"name":"immunological deficiency syndromes","type":"related"},{"name":"inborn errors of immunity","type":"exact"},{"name":"primary immunodeficiency","type":"related"},{"name":"primary immunodeficiency disease","type":"exact"},{"name":"syndrome, antibody deficiency","type":"related"},{"name":"syndrome, immunologic deficiency","type":"related"},{"name":"syndrome, immunological deficiency","type":"related"},{"name":"syndromes, antibody deficiency","type":"related"},{"name":"syndromes, immunologic deficiency","type":"related"},{"name":"syndromes, immunological deficiency","type":"related"}],"termid":"MONDO:0003778","terms_by_termid":{"MONDO:0010066":null,"MONDO:0010504":null,"MONDO:0010600":null,"MONDO:0011336":null,"MONDO:0011971":null,"MONDO:0011997":null,"MONDO:0012146":null,"MONDO:0012429":null,"MONDO:0012471":null,"MONDO:0012472":null,"MONDO:0013135":null,"MONDO:0013767":null,"MONDO:0013818":null,"MONDO:0014007":null,"MONDO:0024541":null,"MONDO:0030519":null,"MONDO:0958013":null,"MONDO:8000024":null},"xrefs":{"Monarch":{"xref_id":"0003778"}}}


id: MOD:00969
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:346"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CAM-Cys vs PAM-Cys","termid":"MOD:00969"}


id: MONDO:0006483
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A morphologic finding indicating the presence of dysplastic changes in the transitional cell epithelium of the urinary tract.","definition_xrefs":["NCIT:C39856"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urothelial neoplasm","termid":"MONDO:0024337"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urothelial dysplasia","secondary_identifiers":["EFO:1000611","UMLS:C1275859","MEDGEN:266165"],"synonyms":[{"name":"transitional cell dysplasia of the urinary tract","type":"exact"},{"name":"urothelial dysplasia","type":"exact"}],"termid":"MONDO:0006483","xrefs":{"Monarch":{"xref_id":"0006483"}}}


id: PBO:0071295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L26 pseudogene 18","termid":"PBO:0071295"}


id: MONDO:0025370
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Tumors or cancer of the urogenital system in either the male or the female.","definition_xrefs":["MESH:D014565"],"gene_count":0,"genotype_count":0,"name":"obsolete urogenital neoplasm (obsolete MONDO:0025370)","synonyms":[{"name":"genito-urinary neoplasm","type":"related"},{"name":"genito-urinary neoplasms","type":"related"},{"name":"genitourinary neoplasm","type":"related"},{"name":"genitourinary neoplasms","type":"related"},{"name":"genitourinary system neoplasm","type":"exact"},{"name":"genitourinary system tumor","type":"exact"},{"name":"neoplasm of genitourinary system","type":"exact"},{"name":"neoplasm, genito-urinary","type":"related"},{"name":"neoplasm, genitourinary","type":"related"},{"name":"neoplasm, urogenital","type":"related"},{"name":"neoplasms, genito-urinary","type":"related"},{"name":"neoplasms, genitourinary","type":"related"},{"name":"neoplasms, urogenital","type":"related"},{"name":"tumor of genitourinary system","type":"exact"},{"name":"urogenital neoplasm","type":"exact"}],"termid":"MONDO:0025370","xrefs":{"Monarch":{"xref_id":"0025370"}}}


id: GO:0102757
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADPH + H2O = NADH + hydrogenphosphate.","definition_xrefs":["RHEA:60664","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"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:0016787"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"NADPH phosphatase activity","secondary_identifiers":["MetaCyc:RXN-7703"],"termid":"GO:0102757"}


id: PBO:0074844
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 36A","termid":"PBO:0074844"}


id: PBO:0091977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wtf meiotic drive antidote Wtf19","termid":"PBO:0091977"}


id: GO:0045163
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which voltage-gated potassium channels become localized together in high densities. In animals, voltage-gated potassium (Kv) channels are clustered beneath the myelin sheath in regions immediately adjacent to paranodes, called juxtaparanodes, and along the inner mesaxon within the internode.","definition_xrefs":["PMID:11456440"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuronal ion channel clustering","termid":"GO:0045161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0061024"],"is_obsolete":false,"name":"clustering of voltage-gated potassium channels","synonyms":[{"name":"Kv channel clustering","type":"exact"},{"name":"clustering of voltage gated potassium channels","type":"exact"},{"name":"clustering of voltage-dependent potassium channels","type":"exact"},{"name":"voltage-gated potassium channel clustering","type":"exact"}],"termid":"GO:0045163"}


id: PBO:0059308
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L50 pseudogene 4","termid":"PBO:0059308"}


id: FYPO:0002163
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the fungal-type cell wall is thinner than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell wall thickness during vegetative growth","termid":"FYPO:0006745"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002946"}],"interesting_parent_ids":["FYPO:0002946","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased cell wall thickness during vegetative growth","synonyms":[{"name":"decreased cell wall thickness during mitotic cell cycle","type":"related"},{"name":"reduced cell wall thickness during vegetative growth","type":"exact"},{"name":"thin cell wall during vegetative growth","type":"exact"}],"termid":"FYPO:0002163"}


id: GO:0034402
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which proteins required for 3'-end transcript processing become associated with the RNA polymerase II holoenzyme complex and the 3' end of a transcript.","definition_xrefs":["PMID:18195044"],"gene_count":0,"genotype_count":0,"name":"obsolete recruitment of 3'-end processing factors to RNA polymerase II holoenzyme complex (obsolete GO:0034402)","termid":"GO:0034402"}


id: GO:2000838
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of androstenedione secretion.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lipid transport","termid":"GO:0032369"},{"relation_name":"is_a","term_name":"negative regulation of hormone secretion","termid":"GO:0046888"},{"relation_name":"is_a","term_name":"regulation of androstenedione secretion","termid":"GO:2000837"},{"relation_name":"negatively_regulates","term_name":"androstenedione secretion","termid":"GO:0035941"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0023052"],"is_obsolete":false,"name":"negative regulation of androstenedione secretion","synonyms":[{"name":"negative regulation of androst-4-ene-3,17-dione secretion","type":"exact"}],"termid":"GO:2000838"}


id: PBO:0061635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nudix hydrolase 16","termid":"PBO:0061635"}


id: PBO:0003896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S21","termid":"PBO:0003896"}


id: GO:1902764
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of embryonic skeletal joint development.","definition_xrefs":["GO_REF:0000058","GOC:mr","GOC:TermGenie","PMID:16575901"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"regulation of embryonic skeletal joint development","termid":"GO:1902762"},{"relation_name":"positively_regulates","term_name":"embryonic skeletal joint development","termid":"GO:0072498"}],"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 embryonic skeletal joint development","synonyms":[{"name":"activation of embryonic skeletal joint development","type":"narrow"},{"name":"up regulation of embryonic skeletal joint development","type":"exact"},{"name":"up-regulation of embryonic skeletal joint development","type":"exact"},{"name":"upregulation of embryonic skeletal joint development","type":"exact"}],"termid":"GO:1902764"}


id: GO:1900785
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving naphtho-gamma-pyrone.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"naphtho-gamma-pyrone metabolic process","synonyms":[{"name":"naphtho-gamma-pyrone metabolism","type":"exact"},{"name":"naphtho-gamma-pyrones metabolic process","type":"related"},{"name":"naphtho-gamma-pyrones metabolism","type":"related"}],"termid":"GO:1900785"}


id: PR:O43085
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- dsc1 gene.","definition_xrefs":["UniProtKB:O43085","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":"DSC E3 ubiquitin ligase complex subunit 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC947.10","synonyms":[{"name":"Spom972h-dsc1","type":"exact"},{"name":"defective for SREBP cleavage protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O43085"}


id: MONDO:0014899
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An extremely rare multiple mitochondrial DNA deletion syndrome with markedly decreased deoxyguanosine kinase (DGUOK) activity in skeletal muscle characterized by a highly variable phenotype. Clinical manifestations include progressive external ophthalmoplegia, mitochondrial myopathy, recurrent rhabdomyolysis, lower motor neuron disease, mild cognitive impairment, sensory axonal neuropathy, optic atrophy, ataxia, hypogonadism and/or parkinsonism.","definition_xrefs":["Orphanet:329314"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"mitochondrial DNA depletion syndrome","termid":"MONDO:0018158"},{"relation_name":"is_a","term_name":"progressive external ophthalmoplegia with mitochondrial DNA deletions","termid":"MONDO:0000090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0004069","MONDO:0005066","MONDO:0005336"],"is_obsolete":false,"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4","secondary_identifiers":["GARD:17501","DOID:0111516","OMIM:617070","MEDGEN:934700","SCTID:733599009","UMLS:C4310733"],"synonyms":[{"name":"PEOB4","type":"exact"},{"name":"adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency","type":"exact"},{"name":"adult-onset multiple mtDNA deletion syndrome due to DGUOK deficiency","type":"exact"},{"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4","type":"exact"},{"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 4","type":"exact"},{"name":"progressive external ophthalmoplegia, autosomal recessive 4","type":"related"}],"termid":"MONDO:0014899","xrefs":{"Monarch":{"xref_id":"0014899"}}}


id: PBO:0065320
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine protease 43, pseudogene","termid":"PBO:0065320"}


id: PBO:0077114
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocase of inner mitochondrial membrane 23","termid":"PBO:0077114"}


id: PBO:0038643
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA thioesterase 11","termid":"PBO:0038643"}


id: MONDO:0025138
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A calicivirus infection of swine characterized by hydropic degeneration of the oral and cutaneous epithelia.","definition_xrefs":["MESH:D014720"],"direct_ancestors":[{"relation_name":"is_a","term_name":"swine disease","termid":"MONDO:0024990"},{"relation_name":"is_a","term_name":"Caliciviridae infectious disease, non-human animal","termid":"MONDO:0700208"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vesicular exanthema of swine","synonyms":[{"name":"swine vesicular Exanthemas","type":"related"},{"name":"swine vesicular exanthema","type":"related"}],"termid":"MONDO:0025138","xrefs":{"Monarch":{"xref_id":"0025138"}}}


id: PBO:0083988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glutaredoxin that employs a dithiol mechanism of catalysis; monomeric; activity is low and null mutation does not affect sensitivity to oxidative stress; GFP-fusion protein localizes to the cytoplasm; expression strongly induced by arsenic","termid":"PBO:0083988"}


id: PBO:0063740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHB1 pseudogene 5","termid":"PBO:0063740"}


id: MONDO:1011767
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"laminitis, non-human animal","secondary_identifiers":["OMIA:001225"],"termid":"MONDO:1011767","xrefs":{"Monarch":{"xref_id":"1011767"}}}


id: GO:0060094
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of glycinergic synaptic transmission. Glycinergic synaptic transmission is the process of communication from a neuron to another neuron across a synapse using the neurotransmitter glycine.","definition_xrefs":["GOC:dms","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of synaptic transmission","termid":"GO:0050806"},{"relation_name":"is_a","term_name":"regulation of synaptic transmission, glycinergic","termid":"GO:0060092"},{"relation_name":"positively_regulates","term_name":"synaptic transmission, glycinergic","termid":"GO:0060012"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of synaptic transmission, glycinergic","synonyms":[{"name":"positive regulation of glycinergic synaptic transmission","type":"exact"}],"termid":"GO:0060094"}


id: GO:0048724
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the epistomal sclerite over time, from its formation to the mature structure.","definition_xrefs":["GOC:rc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"clypeo-labral disc development","termid":"GO:0035213"}],"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":"epistomal sclerite development","termid":"GO:0048724"}


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


id: MONDO:0859243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities","secondary_identifiers":["UMLS:C5676975","MEDGEN:1812577","OMIM:619854"],"termid":"MONDO:0859243","xrefs":{"Monarch":{"xref_id":"0859243"}}}


id: GO:1903806
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of L-isoleucine from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["GO_REF:0000075","GOC:TermGenie","PMID:23895341"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"},{"relation_name":"is_a","term_name":"amino acid import across plasma membrane","termid":"GO:0089718"},{"relation_name":"is_a","term_name":"L-alpha-amino acid transmembrane transport","termid":"GO:1902475"},{"relation_name":"is_a","term_name":"isoleucine transmembrane transport","termid":"GO:1903714"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"L-isoleucine import across plasma membrane","secondary_identifiers":["GO:0090476","GO:0090477"],"synonyms":[{"name":"L-isoleucine import","type":"broad"},{"name":"L-isoleucine import into cell","type":"exact"},{"name":"isoleucine import","type":"broad"}],"termid":"GO:1903806"}


id: GO:0051709
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the killing by an organism of cells in another organism.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell killing","termid":"GO:0031341"},{"relation_name":"is_a","term_name":"modulation of process of another organism","termid":"GO:0035821"},{"relation_name":"regulates","term_name":"killing of cells of another organism","termid":"GO:0031640"}],"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 killing of cells of another organism","secondary_identifiers":["GO:0044531","GO:0052248","GO:0052433","GO:0052459"],"synonyms":[{"name":"modulation by organism of apoptotic process in other organism involved in symbiotic interaction","type":"narrow"},{"name":"modulation of programmed cell death in other organism","type":"narrow"},{"name":"modulation of programmed cell death in other organism involved in symbiotic interaction","type":"narrow"},{"name":"regulation of killing of cells of other organism","type":"exact"}],"termid":"GO:0051709"}


id: GO:0035514
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the removal of a methyl group from one or more nucleosides within a DNA molecule.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"demethylase activity","termid":"GO:0032451"},{"relation_name":"is_a","term_name":"catalytic activity, acting on DNA","termid":"GO:0140097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140097"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0140097","GO:0003824"],"is_obsolete":false,"name":"DNA demethylase activity","termid":"GO:0035514"}


id: MONDO:0013875
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any 3-methylglutaconic aciduria in which the cause of the disease is a mutation in the SERAC1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn mitochondrial metabolism disorder","termid":"MONDO:0004069"},{"relation_name":"is_a","term_name":"3-methylglutaconic aciduria","termid":"MONDO:0017359"},{"relation_name":"is_a","term_name":"disorder of phospholipids, sphingolipids and fatty acids biosynthesis","termid":"MONDO:0018117"},{"relation_name":"is_a","term_name":"SERAC1-related neurological disorder","termid":"MONDO:0100548"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0004069","MONDO:0002525","MONDO:0005066"],"is_obsolete":false,"name":"3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome","secondary_identifiers":["GARD:12963","SCTID:711409002","UMLS:C4040739","OMIM:614739","DOID:0110001","MEDGEN:873604","Orphanet:352328"],"synonyms":[{"name":"3-MGCA type IV (formerly)","type":"related"},{"name":"3-MGCA-4 (formerly)","type":"related"},{"name":"3-Methylglutaconic aciduria with dystonia-deafness, hepatopathy, encephalopathy, and Leigh-like syndrome","type":"related"},{"name":"3-Methylglutaconic aciduria, type 6","type":"related"},{"name":"3-methylglutaconic aciduria caused by mutation in SERAC1","type":"exact"},{"name":"3-methylglutaconic aciduria type 6","type":"exact"},{"name":"3-methylglutaconic aciduria type VI","type":"related"},{"name":"3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome","type":"exact"},{"name":"3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndrome","type":"exact"},{"name":"MEGDEL","type":"exact"},{"name":"MEGDEL syndrome","type":"exact"},{"name":"MGCA6","type":"exact"},{"name":"SERAC1 3-methylglutaconic aciduria","type":"exact"},{"name":"SERAC1 defect","type":"related"}],"termid":"MONDO:0013875","xrefs":{"Monarch":{"xref_id":"0013875"}}}


id: FYPO:0003479
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A signal transduction phenotype in which the MAPK cascade involved in cell wall organization or biogenesis is activated continuously.","definition_xrefs":["PMID:23934882","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation phenotype during vegetative growth","termid":"FYPO:0001334"},{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"},{"relation_name":"is_a","term_name":"signal transduction phenotype","termid":"FYPO:0003478"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0000298","FYPO:0005447"],"is_obsolete":false,"name":"constitutively activated MAPK cascade involved in cell wall organization or biogenesis","synonyms":[{"name":"constitutively activated MAPK cascade involved in cell wall organisation or biogenesis","type":"exact"},{"name":"constitutively activated Pmk1 MAPK cell integrity signaling","type":"narrow"},{"name":"continuous MAPK cascade involved in cell wall organization or biogenesis","type":"exact"}],"termid":"FYPO:0003479"}


id: PR:O36022
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mnn9 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O36022"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mannan polymerase complex subunit mnn9 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4F10.10c","synonyms":[{"name":"Spom972h-mnn9","type":"exact"}],"termid":"PR:O36022"}


id: GO:0046834
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of introducing one or more phosphate groups into a lipid, any member of a group of substances soluble in lipid solvents but only sparingly soluble in aqueous solvents.","definition_xrefs":["GOC:bf","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphorylation","termid":"GO:0016310"},{"relation_name":"is_a","term_name":"lipid modification","termid":"GO:0030258"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"lipid phosphorylation","termid":"GO:0046834"}


id: GO:0047159
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1-O-(1Z-alkenyl)-sn-glycero-3-phosphocholine + an acyl-CoA = 1-O-(1Z-alkenyl)-2-acyl-sn-glycero-3-phosphocholine + CoA.","definition_xrefs":["RHEA:10344"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acyltransferase activity","termid":"GO:0008374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016746","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"plasmalogen synthase activity","secondary_identifiers":["MetaCyc:PLASMALOGEN-SYNTHASE-RXN","EC:2.3.1.25"],"synonyms":[{"name":"1-alkenylglycerophosphocholine O-acyltransferase activity","type":"related"},{"name":"acyl-CoA:1-alkenylglycerophosphocholine O-acyltransferase activity","type":"related"}],"termid":"GO:0047159"}


id: MONDO:0021485
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the iris.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iris neoplasm","termid":"MONDO:0021224"},{"relation_name":"is_a","term_name":"benign neoplasm of eye","termid":"MONDO:0021454"}],"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":"benign neoplasm of iris","secondary_identifiers":["NCIT:C4555","icd11.foundation:549962833","MEDGEN:87560","ICD9:224.0","SCTID:189151003","UMLS:C0346374"],"synonyms":[{"name":"benign iris neoplasm","type":"exact"},{"name":"benign iris tumor","type":"exact"},{"name":"benign iris tumour","type":"exact"},{"name":"benign neoplasm of the iris","type":"exact"},{"name":"benign tumor of iris","type":"exact"},{"name":"benign tumor of the iris","type":"exact"},{"name":"benign tumour of iris","type":"exact"},{"name":"benign tumour of the iris","type":"exact"},{"name":"iris benign neoplasm","type":"exact"}],"termid":"MONDO:0021485","xrefs":{"Monarch":{"xref_id":"0021485"}}}


id: FYPO:0004568
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the presence, distribution, or morphology of the mitotic or meiotic spindle is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component","termid":"FYPO:0001233"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal spindle","termid":"FYPO:0004568"}


id: PBO:0054718
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 2127","termid":"PBO:0054718"}


id: GO:0075246
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of oospore formation, a process in which male and female gametangia develop and fuse to form a thick-walled resting spore of oomycetes.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of sexual sporulation resulting in formation of a cellular spore","termid":"GO:0043942"},{"relation_name":"is_a","term_name":"regulation of oospore formation","termid":"GO:0075244"},{"relation_name":"negatively_regulates","term_name":"oospore formation","termid":"GO:0075243"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"negative regulation of oospore formation","termid":"GO:0075246"}


id: FYPO:0004958
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 the mitochondrion differs from normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered RNA level during vegetative growth","termid":"FYPO:0001326"},{"relation_name":"is_a","term_name":"altered level of substance in mitochondrion","termid":"FYPO:0004957"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0006551","FYPO:0001320","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"altered RNA level in mitochondrion","synonyms":[{"name":"abnormal RNA level in mitochondrion","type":"exact"},{"name":"abnormal RNA level in mitochondrion during vegetative growth","type":"exact"},{"name":"abnormal mitochondrial RNA level","type":"exact"},{"name":"abnormal mitochondrial RNA level during vegetative growth","type":"exact"},{"name":"altered RNA level in mitochondrion during mitotic cell cycle","type":"related"},{"name":"altered mitochondrial RNA level","type":"exact"},{"name":"altered transcript level in mitochondrion","type":"exact"}],"termid":"FYPO:0004958"}


id: PBO:0002311
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.1.1.41","termid":"PBO:0002311"}


id: MONDO:0006909
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Proportionately decreased bodily growth due to failure of the pituitary gland to produce an adequate supply of growth hormone.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adrenal gland disorder","termid":"MONDO:0005495"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pituitary dwarfism","secondary_identifiers":["ICD9:253.3","MedDRA:10035083","MEDGEN:8506","MESH:D004393","EFO:1001109","SCTID:367460001","UMLS:C0013338"],"termid":"MONDO:0006909","xrefs":{"Monarch":{"xref_id":"0006909"}}}


id: MONDO:0023226
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":"gershinibaruch Leibo syndrome","termid":"MONDO:0023226","xrefs":{"Monarch":{"xref_id":"0023226"}}}


id: MONDO:0008708
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acrocallosal syndrome (ACS) is a polymalformative syndrome characterized by agenesis of corpus callosum (CC), distal anomalies of limbs, minor craniofacial anomalies and intellectual deficit.","definition_xrefs":["Orphanet:36"],"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"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"polydactyly-syndactyly-triphalangism","termid":"MONDO:0800066"},{"relation_name":"is_a","term_name":"KIF7-related ciliopathy","termid":"MONDO:0800463"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acrocallosal syndrome","secondary_identifiers":["SCTID:715951007","MESH:D055673","MEDGEN:162915","UMLS:C0796147","OMIM:200990","GARD:5721","NCIT:C84531","DOID:9250","icd11.foundation:1286493807"],"synonyms":[{"name":"ACLS","type":"exact"},{"name":"ACS","type":"exact"},{"name":"Joubert syndrome 12","type":"related"},{"name":"Joubert syndrome 12/15, digenic","type":"related"},{"name":"Schinzel acrocallosal syndrome","type":"exact"},{"name":"Schinzel syndrome 1","type":"exact"},{"name":"absence of corpus callosum with unusual facial appearance, mental deficiency, duplication of the halluces and polydactyly","type":"related"},{"name":"acrocallosal syndrome","type":"exact"},{"name":"acrocallosal syndrome, Schinzel type","type":"related"},{"name":"hallux Duplication, postaxial polydactyly, and absence of corpus callosum","type":"related"}],"termid":"MONDO:0008708","xrefs":{"Monarch":{"xref_id":"0008708"}}}


id: GO:0102960
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3beta-hydroxy-9beta-pimara-7,15-diene-19,6beta-olide + NAD(P) = momilactone A + H+ + NAD(P)H.","definition_xrefs":["EC:1.1.1.295"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"momilactone-A synthase [NAD(P)H] activity","secondary_identifiers":["MetaCyc:RXN-9290","RHEA:25363"],"termid":"GO:0102960"}


id: PBO:0011123
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanyl-nucleotide exchange factor Syt22","termid":"PBO:0011123"}


id: GO:0051500
data:
  {"annotated_genes":["SJAG_01248"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75266],"is_not":false,"summary":null,"term":"GO:0051500"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-tyrosyl-tRNATyr + H2O = D-tyrosine + tRNATyr. Removal of a D-tyrosine from a charged tRNA(Tyr).","definition_xrefs":["PMID:14527667","RHEA:25347"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-aminoacyl-tRNA deacylase activity","termid":"GO:0051499"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01248":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0140101"}],"interesting_parent_ids":["GO:0016788","GO:0003674","GO:0016787","GO:0140101","GO:0140098","GO:0003824"],"is_obsolete":false,"name":"D-tyrosyl-tRNA(Tyr) deacylase activity","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0051500","terms_by_termid":{"GO:0051500":null}}


id: MONDO:0958226
data:
  {"annotated_genes":["SJAG_02896"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88868],"is_not":false,"summary":null,"term":"MONDO:0958226"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02896":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"leukoencephalopathy, porphyria-related","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1862491","UMLS:C5935575","OMIM:620711"],"termid":"MONDO:0958226","terms_by_termid":{"MONDO:0958226":null},"xrefs":{"Monarch":{"xref_id":"0958226"}}}


id: MONDO:0019387
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Macrostomia-preauricular tags-external ophthalmoplegia syndrome combines macrostomia or abnormal mouth contour, preauricular tags, uni- or bilateral ptosis and external ophthalmoplegia. It was described in nine members of a Brazilian family. It is a new phenotype belonging to the so-called oculoauriculovertebral spectrum, resulting from a branchial arch anomaly. Transmission is autosomal dominant.","definition_xrefs":["Orphanet:83619"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"macrostomia-preauricular tags-external ophthalmoplegia syndrome","secondary_identifiers":["UMLS:C4509840","GARD:19044","MEDGEN:1391725"],"termid":"MONDO:0019387","xrefs":{"Monarch":{"xref_id":"0019387"}}}


id: GO:0048680
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the rate of axon regeneration.","definition_xrefs":["GOC:dph","GOC:lm","GOC:dgh","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of response to external stimulus","termid":"GO:0032103"},{"relation_name":"is_a","term_name":"regulation of axon regeneration","termid":"GO:0048679"},{"relation_name":"is_a","term_name":"positive regulation of neuron projection regeneration","termid":"GO:0070572"},{"relation_name":"is_a","term_name":"positive regulation of response to wounding","termid":"GO:1903036"},{"relation_name":"positively_regulates","term_name":"axon regeneration","termid":"GO:0031103"}],"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 axon regeneration","synonyms":[{"name":"activation of axon regeneration","type":"narrow"},{"name":"stimulation of axon regeneration","type":"narrow"},{"name":"up regulation of axon regeneration","type":"exact"},{"name":"up-regulation of axon regeneration","type":"exact"},{"name":"upregulation of axon regeneration","type":"exact"}],"termid":"GO:0048680"}


id: GO:1905179
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cardiac muscle tissue regeneration.","definition_xrefs":["PMID:23222520","GOC:rph","GOC:BHF_miRNA","GOC:BHF","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental growth","termid":"GO:0048640"},{"relation_name":"is_a","term_name":"regulation of cardiac muscle tissue regeneration","termid":"GO:1905178"},{"relation_name":"negatively_regulates","term_name":"cardiac muscle tissue regeneration","termid":"GO:0061026"}],"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 cardiac muscle tissue regeneration","synonyms":[{"name":"down regulation of cardiac muscle tissue regeneration","type":"exact"},{"name":"down-regulation of cardiac muscle tissue regeneration","type":"exact"},{"name":"downregulation of cardiac muscle tissue regeneration","type":"exact"},{"name":"inhibition of cardiac muscle tissue regeneration","type":"narrow"}],"termid":"GO:1905179"}


id: MONDO:0016699
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Myxopapillary ependymoma (MEPN) describes a slow growing ependymoma located almost exclusively in the conus medullaris-cauda equina-filum terminale region of the spinal cord, presenting in all age groups, and manifesting with variable symptoms such as neck pain, vomiting and unsteady gait and metastasis. It has a more aggressive disease course and is seen in the pediatric population.","definition_xrefs":["Orphanet:251643"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ependymal tumor","termid":"MONDO:0003266"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myxopapillary ependymoma","secondary_identifiers":["MESH:D004806","DOID:5075","UMLS:C0205769","ICDO:9394/1","MEDGEN:104717","ONCOTREE:MPE","NCIT:C3697","GARD:10633"],"synonyms":[{"name":"ependymoma, benign","type":"exact"},{"name":"myxopapillary ependymoma","type":"exact"},{"name":"myxopapillary ependymoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0016699","xrefs":{"Monarch":{"xref_id":"0016699"}}}


id: GO:0098696
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of neurotransmitter receptor localization to postsynaptic specialization membrane.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological quality","termid":"GO:0065008"},{"relation_name":"is_a","term_name":"regulation of protein localization to synapse","termid":"GO:1902473"},{"relation_name":"is_a","term_name":"regulation of receptor localization to synapse","termid":"GO:1902683"},{"relation_name":"is_a","term_name":"regulation of protein localization to cell periphery","termid":"GO:1904375"},{"relation_name":"is_a","term_name":"regulation of protein localization to membrane","termid":"GO:1905475"},{"relation_name":"regulates","term_name":"neurotransmitter receptor localization to postsynaptic specialization membrane","termid":"GO:0099645"}],"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 neurotransmitter receptor localization to postsynaptic specialization membrane","termid":"GO:0098696"}


id: PBO:0084409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lysophospholipase; hydrolyzes lysophosphatidylserine to release free fatty acid; involved in regulated cell death; localizes to both the nucleus and cytoplasm; contains a catalytic triad of Ser-His-Asp that is part of an alpha/beta hydrolase fold and a lipase motif (GXSXG); sequence similarity to Fsh2p and Fsh3p and the human candidate tumor suppressor and serine hydrolase, OVCA2","termid":"PBO:0084409"}


id: GO:0008905
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the transfer of a phosphate group from GTP or GDP to a mannose molecule.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete mannose-phosphate guanylyltransferase activity (obsolete GO:0008905)","termid":"GO:0008905"}


id: PBO:0052292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KH domain containing 1 like","termid":"PBO:0052292"}


id: GO:0071643
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of production of chemokine (C-C motif) ligand 4.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chemokine production","termid":"GO:0032642"},{"relation_name":"regulates","term_name":"chemokine (C-C motif) ligand 4 production","termid":"GO:0071606"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of chemokine (C-C motif) ligand 4 production","synonyms":[{"name":"regulation of CCL4 production","type":"exact"},{"name":"regulation of MIP-1b production","type":"exact"},{"name":"regulation of macrophage inflammatory protein production","type":"broad"}],"termid":"GO:0071643"}


id: GO:1990859
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an endothelin stimulus. Endothelin is any of three secretory vasoconstrictive peptides (endothelin-1, -2, -3).","definition_xrefs":["PMID:16365184"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to peptide hormone stimulus","termid":"GO:0071375"},{"relation_name":"is_a","term_name":"response to endothelin","termid":"GO:1990839"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to endothelin","termid":"GO:1990859"}


id: GO:0050739
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The cross-linking of a tyrosine residue to a tryptophan residue and a methionine residue to form S-[5'-(L-tryptoph-6'-yl)-L-tyrosin-3'-yl]-L-methionin-S-ium.","definition_xrefs":["RESID:AA0348"],"gene_count":0,"genotype_count":0,"name":"obsolete peptide cross-linking via S-[5'-(L-tryptoph-6'-yl)-L-tyrosin-3'-yl]-L-methionin-S-ium (obsolete GO:0050739)","termid":"GO:0050739"}


id: PBO:0038480
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily B member 5","termid":"PBO:0038480"}


id: GO:0110084
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of protein localization to cell division site involved in mitotic actomyosin contractile ring assembly.","definition_xrefs":["GOC:vw","PMID:29343550"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to cell division site involved in mitotic actomyosin contractile ring assembly","termid":"GO:0110082"},{"relation_name":"is_a","term_name":"negative regulation of mitotic actomyosin contractile ring assembly","termid":"GO:1903500"},{"relation_name":"is_a","term_name":"negative regulation of protein localization","termid":"GO:1903828"},{"relation_name":"negatively_regulates","term_name":"protein localization to cell division site involved in mitotic actomyosin contractile ring assembly","termid":"GO:1903476"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"negatively_regulates","termid":"GO:0030036"},{"rel_name":"regulates","termid":"GO:0000281"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"negatively_regulates","termid":"GO:0000281"},{"rel_name":"negatively_regulates","termid":"GO:0007049"},{"rel_name":"negatively_regulates","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0030036","GO:0044085","GO:0000281","GO:0007010","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"negative regulation of protein localization to cell division site involved in mitotic actomyosin contractile ring assembly","termid":"GO:0110084"}


id: PBO:0070361
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNY4 pseudogene 37","termid":"PBO:0070361"}


id: MONDO:0024351
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete familial pityriasis rubra pilaris (obsolete MONDO:0024351)","termid":"MONDO:0024351","xrefs":{"Monarch":{"xref_id":"0024351"}}}


id: GO:0071178
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of the intracellular domain of Notch4 (ICN4), the DNA-binding transcription factor RBP-Jkappa, and the transcriptional coactivator Mastermind-like-2 (MAML2); the complex is involved in transcriptional activation in response to Notch-mediated signaling.","definition_xrefs":["PMID:12370315"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"MAML2-RBP-Jkappa-ICN4 complex","synonyms":[{"name":"MAML2-RBP-Jkappa-Notch4 complex","type":"exact"}],"termid":"GO:0071178"}


id: GO:0009601
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a stimulus from an insect is received and converted into a molecular signal.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of other organism","termid":"GO:0098543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of insect","synonyms":[{"name":"perception of insect","type":"related"}],"termid":"GO:0009601"}


id: GO:0035449
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The component of a plastid thylakoid membrane consisting of gene products and protein complexes that are loosely bound to one of its surfaces, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:bf","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrinsic component of thylakoid membrane","termid":"GO:0035448"},{"relation_name":"is_a","term_name":"extrinsic component of plastid membrane","termid":"GO:0035452"},{"relation_name":"part_of","term_name":"plastid thylakoid membrane","termid":"GO:0055035"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"extrinsic component of plastid thylakoid membrane","synonyms":[{"name":"extrinsic to plastid thylakoid membrane","type":"narrow"},{"name":"peripheral to plastid thylakoid membrane","type":"exact"}],"termid":"GO:0035449"}


id: MONDO:0859209
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":"Zaki syndrome","secondary_identifiers":["OMIM:619648","UMLS:C5562037","MEDGEN:1794247","DOID:0070473"],"termid":"MONDO:0859209","xrefs":{"Monarch":{"xref_id":"0859209"}}}


id: MONDO:0010612
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"This syndrome is characterized by infantile hypotonia followed by onset of ataxia, cataract and intellectual deficit by preschool age. Cerebral atrophy was also reported.","definition_xrefs":["Orphanet:1397"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrocephaly-cerebellar agenesis syndrome","secondary_identifiers":["MEDGEN:375335","GARD:1200","OMIM:307010","UMLS:C1844005","MESH:C564407"],"synonyms":[{"name":"X-linked hydrocephalus-cerebellar agenesis-intellectual disability syndrome","type":"exact"},{"name":"cerebellum agenesis hydrocephaly","type":"related"},{"name":"hydrocephalus with cerebellar agenesis","type":"related"}],"termid":"MONDO:0010612","xrefs":{"Monarch":{"xref_id":"0010612"}}}


id: MONDO:0001939
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioma arising from the skin. It is characterized by the presence of epithelioid endothelial cells.","definition_xrefs":["NCIT:C7393"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin hemangioma","termid":"MONDO:0003110"},{"relation_name":"is_a","term_name":"epithelioid hemangioma","termid":"MONDO:0021169"}],"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":"skin epithelioid hemangioma","secondary_identifiers":["DOID:14308","MESH:D000796","SCTID:400131007","UMLS:C0002989","MEDGEN:297"],"synonyms":[{"name":"angiolymphoid cutaneous hyperplasia","type":"exact"},{"name":"angiolymphoid hyperplasia of skin","type":"exact"},{"name":"angiolymphoid hyperplasia of the skin","type":"exact"},{"name":"epithelioid hemangioma of skin","type":"exact"},{"name":"epithelioid hemangioma of the skin","type":"exact"},{"name":"histiocytoid hemangioma of skin","type":"exact"},{"name":"histiocytoid hemangioma of the skin","type":"exact"},{"name":"histiocytoid hemangioma of zone of skin","type":"exact"},{"name":"skin epithelioid hemangioma","type":"exact"},{"name":"zone of skin histiocytoid hemangioma","type":"exact"}],"termid":"MONDO:0001939","xrefs":{"Monarch":{"xref_id":"0001939"}}}


id: GO:0019650
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The anaerobic chemical reactions and pathways resulting in the breakdown of glucose into butanediol; effected by some members of the Enterobacteriaceae, e.g. Enterobacter, Erwinia, Klebsiella, and Serratia.","definition_xrefs":["ISBN:0198506732","GOC:nr","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucose metabolic process","termid":"GO:0006006"},{"relation_name":"is_a","term_name":"glycolytic fermentation","termid":"GO:0019660"},{"relation_name":"is_a","term_name":"butanediol metabolic process","termid":"GO:0034077"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006091","GO:0005975","GO:0044281"],"is_obsolete":false,"name":"glycolytic fermentation to butanediol","secondary_identifiers":["GO:0030646","Wikipedia:Butanediol_fermentation"],"synonyms":[{"name":"butanediol fermentation","type":"exact"},{"name":"glucose catabolic process to butanediol","type":"exact"},{"name":"glucose fermentation to butanediol","type":"exact"}],"termid":"GO:0019650"}


id: PBO:0061884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OPA1 antisense RNA 1","termid":"PBO:0061884"}


id: GO:0098810
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of neurotransmitter molecules from the extrasynaptic space into the presynaptic cytosol.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurotransmitter uptake","termid":"GO:0001504"},{"relation_name":"is_a","term_name":"establishment of localization in cell","termid":"GO:0051649"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"neurotransmitter reuptake","termid":"GO:0098810"}


id: PBO:0041697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium homeostasis modulator 3","termid":"PBO:0041697"}


id: GO:0043182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of transporting sodium ions into, and confining within, a vacuole.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vacuolar sequestering","termid":"GO:0043181"},{"relation_name":"part_of","term_name":"intracellular sodium ion homeostasis","termid":"GO:0006883"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0098771"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0098771","GO:0008150"],"is_obsolete":false,"name":"vacuolar sequestering of sodium ion","synonyms":[{"name":"sequestering of sodium ion (Na+) in vacuole","type":"exact"},{"name":"sequestration of sodium ion (Na+) in vacuole","type":"exact"},{"name":"sodium ion (Na+) retention in vacuole","type":"exact"},{"name":"sodium ion (Na+) storage in vacuole","type":"exact"},{"name":"vacuolar sequestering of sodium ion (Na+)","type":"exact"},{"name":"vacuolar sequestration of sodium ion (Na+)","type":"exact"},{"name":"vacuolar sodium ion (Na+) retention","type":"exact"},{"name":"vacuolar sodium ion (Na+) storage","type":"exact"}],"termid":"GO:0043182"}


id: PBO:0002332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chitin deacetylase Cda1","termid":"PBO:0002332"}


id: PR:O13950
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A signal recognition particle receptor subunit beta that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR19326:SF0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal recognition particle receptor subunit beta (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23H4.07c","secondary_identifiers":["UniProtKB:O13950"],"synonyms":[{"name":"SPAC23H4.07c","type":"related"},{"name":"SR-beta (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SRPRB","type":"exact"}],"termid":"PR:O13950"}


id: PBO:0071995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S6 pseudogene 24","termid":"PBO:0071995"}


id: PBO:0069294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 550, pseudogene","termid":"PBO:0069294"}


id: PBO:0116274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytosolic gamma-glutamyl kinase; catalyzes the first step in proline biosynthesis; required for nitrogen starvation-induced ribophagy but not for nonselective autophagy; PRO1 has a paralog, YHR033W, that arose from the whole genome duplication","termid":"PBO:0116274"}


id: PBO:0086742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; possible role in DNA metabolism and/or in genome stability; expression is heat-inducible","termid":"PBO:0086742"}


id: PBO:0040222
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arginyltransferase 1","termid":"PBO:0040222"}


id: PR:Q9P7H9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC105.03c gene.","definition_xrefs":["UniProtKB:Q9P7H9","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 transcriptional regulatory protein C105.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC105.03c","synonyms":[{"name":"Spom972h-SPAC105.03c","type":"exact"}],"termid":"PR:Q9P7H9"}


id: PATO:0001067
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001067 absolute strain (obsolete PATO:0001067)","termid":"PATO:0001067"}


id: MONDO:0000930
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive form of melanoma, frequently metastasizing to the lymph nodes. It presents as a papular or nodular raised skin lesion. It comprises approximately 10-15% of melanomas. Morphologically, it often displays an epithelioid appearance.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cutaneous melanoma","termid":"MONDO:0005012"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"nodular malignant melanoma","secondary_identifiers":["MEDGEN:83144","SCTID:254731001","UMLS:C0334424","NCIT:C4225","ICDO:8721/3","DOID:10047","EFO:0008515"],"synonyms":[{"name":"nodular cutaneous (skin) melanoma","type":"exact"},{"name":"nodular malignant melanoma of skin","type":"exact"},{"name":"nodular malignant melanoma of the skin","type":"exact"},{"name":"nodular malignant skin melanoma","type":"exact"},{"name":"nodular melanoma","type":"exact"},{"name":"nodular melanoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0000930","xrefs":{"Monarch":{"xref_id":"0000930"}}}


id: PBO:0000983
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cysteine synthase Cys12","termid":"PBO:0000983"}


id: MONDO:0011096
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Agammaglobulinemia, non-Bruton type (autosomal agammaglobulinemia) is a rare form of agammaglobulinemia, a primary immunodeficiency disease, and is characterized by variable immune dysfunction with frequent and recurrent bacterial infections and/or chronic diarrhea.","definition_xrefs":["Orphanet:33110"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated agammaglobulinemia","termid":"MONDO:0016462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"autosomal agammaglobulinemia","secondary_identifiers":["GARD:9640","MEDGEN:316941","MESH:C538056","UMLS:C1832241"],"synonyms":[{"name":"AGM","type":"exact"},{"name":"agammaglobulinemia, autosomal recessive, due to IGHM defect","type":"related"},{"name":"agammaglobulinemia, non-Bruton type","type":"exact"}],"termid":"MONDO:0011096","xrefs":{"Monarch":{"xref_id":"0011096"}}}


id: MONDO:0018281
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital muscular dystrophy with hyperlaxity is a rare, genetic neuromuscular disease characterized by congenital hypotonia, generalized, slowly progressive muscular weakness, and proximal joint contractures with distal joint hypermobility and hyperlaxity. Scoliosis or rigidity of the spine and delayed motor milestones are also frequently reported. Other manifestations include a long myopathic face and, in rare cases, respiratory failure, mild to moderate intellectual deficiency and short stature. Ambulation may be impaired with time.","definition_xrefs":["Orphanet:371007"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital muscular dystrophy","termid":"MONDO:0019950"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"congenital muscular dystrophy with hyperlaxity","secondary_identifiers":["GARD:21600","SCTID:763314009","MEDGEN:1633415","UMLS:C4706389"],"synonyms":[{"name":"CMDH","type":"exact"}],"termid":"MONDO:0018281","xrefs":{"Monarch":{"xref_id":"0018281"}}}


id: PBO:0059007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"monocyte to macrophage differentiation associated","termid":"PBO:0059007"}


id: PBO:0049905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hes family bHLH transcription factor 6","termid":"PBO:0049905"}


id: PBO:0070109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 23 pseudogene","termid":"PBO:0070109"}


id: PBO:0069868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1155, pseudogene","termid":"PBO:0069868"}


id: GO:0034924
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: cis-3,4-phenanthrenedihydrodiol-4-carboxylate = 3,4-dihydroxyphenanthrene + H+ + 2 e- + CO2.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete cis-3,4-phenanthrenedihydrodiol-4-carboxylate dehydrogenase activity (obsolete GO:0034924)","termid":"GO:0034924"}


id: GO:0033277
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A cell cycle in which mitosis is begun and progresses normally through the end of anaphase, but not completed, resulting in a cell with increased ploidy.","definition_xrefs":["GOC:mah","PMID:9573008"],"gene_count":0,"genotype_count":0,"name":"obsolete abortive mitotic cell cycle (obsolete GO:0033277)","synonyms":[{"name":"abortive mitosis","type":"related"}],"termid":"GO:0033277"}


id: MONDO:0000340
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A paralytic poliomyelitis in which the site of paralysis is the bulbospinal tract.","direct_ancestors":[{"relation_name":"is_a","term_name":"paralytic poliomyelitis","termid":"MONDO:0000341"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"bulbospinal polio","secondary_identifiers":["DOID:0050514"],"termid":"MONDO:0000340","xrefs":{"Monarch":{"xref_id":"0000340"}}}


id: GO:1904214
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of iodide transmembrane transport.","definition_xrefs":["GO_REF:0000058","PMID:20392814","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of inorganic anion transmembrane transport","termid":"GO:1903797"},{"relation_name":"is_a","term_name":"positive regulation of anion transmembrane transport","termid":"GO:1903961"},{"relation_name":"is_a","term_name":"positive regulation of iodide transport","termid":"GO:1904203"},{"relation_name":"is_a","term_name":"regulation of iodide transmembrane transport","termid":"GO:1904212"},{"relation_name":"positively_regulates","term_name":"iodide transmembrane transport","termid":"GO:1904200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of iodide transmembrane transport","synonyms":[{"name":"activation of iodide transmembrane transport","type":"narrow"},{"name":"up regulation of iodide transmembrane transport","type":"exact"},{"name":"up-regulation of iodide transmembrane transport","type":"exact"},{"name":"upregulation of iodide transmembrane transport","type":"exact"}],"termid":"GO:1904214"}


id: MONDO:1011835
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital cerebellar anomaly, non-human animal","secondary_identifiers":["OMIA:000176"],"termid":"MONDO:1011835","xrefs":{"Monarch":{"xref_id":"1011835"}}}


id: GO:0061147
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the endocardial endothelium over time, from its initial formation to the mature structure. The endocardium is an anatomical structure comprised of an endothelium and an extracellular matrix that forms the innermost layer of tissue of the heart, and lines the heart chambers.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endothelium development","termid":"GO:0003158"},{"relation_name":"part_of","term_name":"endocardium development","termid":"GO:0003157"}],"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":"endocardial endothelium development","termid":"GO:0061147"}


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


id: PBO:0044110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer/testis associated transcript 69","termid":"PBO:0044110"}


id: PBO:0000104
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"predominantly uniformly single copy (one to one)","termid":"PBO:0000104"}


id: PBO:0062242
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily BH member 1 pseudogene","termid":"PBO:0062242"}


id: PBO:0048135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FMR1 autosomal homolog 1","termid":"PBO:0048135"}


id: SO:0002196
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A (unitary) pseudogene that is stable in the population but importantly it has a functional alternative allele also in the population. i.e., one strain may have the gene, another strain may have the pseudogene. MHC haplotypes have allelic pseudogenes.","direct_ancestors":[{"relation_name":"is_a","term_name":"pseudogenic_rRNA","termid":"SO:0000777"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"allelic_pseudogenic_rRNA","synonyms":[{"name":"INSDC_feature:rRNA","type":"broad"},{"name":"INSDC_qualifier:allelic","type":"exact"},{"name":"allelic pseudogenic rRNA","type":"exact"}],"termid":"SO:0002196"}


id: PBO:0005386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA_pseudo anticodon AAC","termid":"PBO:0005386"}


id: GO:0052760
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2,4-dinitrophenol + H- = 2,4-dinitrophenol hydride Meisenheimer complex. Coenzyme F420 supplies the hydride (H-) in the reaction.","definition_xrefs":["PMID:11995829","UM-BBD_reactionID:r1071","GOC:mengo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete coenzyme F420-dependent 2,4-dinitrophenol reductase activity (obsolete GO:0052760)","synonyms":[{"name":"DNP reductase activity","type":"broad"},{"name":"coenzyme F420-dependent 2,4-dinitrophenol hydride transferase activity","type":"exact"}],"termid":"GO:0052760"}


id: PBO:0051670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inhibitor of growth family member 1","termid":"PBO:0051670"}


id: PBO:0085454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Posttranscriptional regulator of phosphate and glucose metabolism; facilitates PHO4 mRNA degradation by interacting with Pop2p; regulates PHO4 mRNA stability by binding to PHO4's 3'UTR in a phosphate-dependent manner; contains highly conserved YTH (YT521-B Homology) domain that exhibits RNA-binding activity; human homolog YTHDF2 can complement yeast null mutant","termid":"PBO:0085454"}


id: GO:1902427
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of water channel activity.","definition_xrefs":["PMID:22095752","GOC:TermGenie","GOC:nhn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transmembrane transporter activity","termid":"GO:0022898"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of water channel activity","synonyms":[{"name":"regulation of aquaporin","type":"narrow"},{"name":"regulation of aquaporin permeability","type":"narrow"}],"termid":"GO:1902427"}


id: PBO:0066694
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enriched in melanoma 3","termid":"PBO:0066694"}


id: PBO:0090184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial proline metabolism regulator","termid":"PBO:0090184"}


id: PBO:0044486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 27 subfamily B member 1","termid":"PBO:0044486"}


id: SO:0000415
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute to describe a feature that is invalidated due to polyA priming.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"invalidated","termid":"SO:0000790"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"invalidated_by_genomic_polyA_primed_cDNA","synonyms":[{"name":"invalidated by genomic polyA primed cDNA","type":"exact"}],"termid":"SO:0000415"}


id: PBO:0063255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PCDHB1 antisense RNA 1","termid":"PBO:0063255"}


id: GO:0046678
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 bacteriocin stimulus. A bacteriocin is a protein substance released by certain bacteria that kills but does not lyse closely related strains of bacteria. Specific bacteriocins attach to specific receptors on cell walls and induce specific metabolic block, e.g. cessation of nucleic acid or protein synthesis of oxidative phosphorylation.","definition_xrefs":["ISBN:0721662544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to antibiotic","termid":"GO:0046677"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"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 bacteriocin","synonyms":[{"name":"bacteriocin susceptibility/resistance","type":"related"}],"termid":"GO:0046678"}


id: MONDO:0016502
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hermansky-Pudlak syndrome without pulmonary fibrosis as a complication includes three relatively mild types (HPS-3, HPS-5 and HPS-6) of Hermansky-Pudlak syndrome (HPS), a multi-system disorder characterized by ocular or oculocutaneous albinism, bleeding diathesis and, in some cases, granulomatous colitis.","definition_xrefs":["Orphanet:231512"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Hermansky-Pudlak syndrome","termid":"MONDO:0019312"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005570","MONDO:0005066"],"is_obsolete":false,"name":"Hermansky-Pudlak syndrome without pulmonary fibrosis","secondary_identifiers":["ICD10CM:E70.3","icd11.foundation:1363499932","GARD:17169","MEDGEN:1842321","UMLS:C5679833"],"synonyms":[{"name":"HPS without pulmonary fibrosis","type":"exact"}],"termid":"MONDO:0016502","xrefs":{"Monarch":{"xref_id":"0016502"}}}


id: PR:Q9UTM4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A T-complex protein 1 subunit epsilon that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00509","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":"T-complex protein 1 subunit epsilon (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1420.02c","secondary_identifiers":["UniProtKB:Q9UTM4"],"synonyms":[{"name":"CCT-epsilon (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-CCT5","type":"exact"},{"name":"TCP-1-epsilon (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UTM4"}


id: GO:0055078
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the maintenance of an internal steady state of sodium ions within an organism or cell.","definition_xrefs":["GOC:jid","GOC:ai","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monoatomic cation homeostasis","termid":"GO:0055080"},{"relation_name":"is_a","term_name":"inorganic ion homeostasis","termid":"GO:0098771"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0098771"}],"interesting_parent_ids":["GO:0098771","GO:0008150"],"is_obsolete":false,"name":"sodium ion homeostasis","termid":"GO:0055078"}


id: GO:0036399
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a TCR signalosome.","definition_xrefs":["PMID:22426112","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"TCR signalosome assembly","synonyms":[{"name":"LAT signalosome assembly","type":"exact"},{"name":"linker for activation of T cells signalosome assembly","type":"exact"}],"termid":"GO:0036399"}


id: GO:0044270
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of organic and inorganic nitrogenous compounds.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete cellular nitrogen compound catabolic process (obsolete GO:0044270)","termid":"GO:0044270"}


id: PBO:0061350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleophosmin 1 pseudogene 8","termid":"PBO:0061350"}


id: PBO:0034222
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-contributes_to_morphology_of","termid":"PBO:0034222"}


id: MONDO:0032598
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"genetic developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 68","secondary_identifiers":["OMIM:618201","UMLS:C4748688","DOID:0112204","GARD:16310","MEDGEN:1648479"],"synonyms":[{"name":"DEE68","type":"exact"},{"name":"EIEE68","type":"exact"},{"name":"EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68","type":"exact"},{"name":"developmental and epileptic encephalopathy 68","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 68","type":"exact"}],"termid":"MONDO:0032598","xrefs":{"Monarch":{"xref_id":"0032598"}}}


id: PBO:0042511
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cadherin related family member 5","termid":"PBO:0042511"}


id: MOD:00870
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification produced by formation of an adduct with phenyl isocyanate.","definition_xrefs":["Unimod:411"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isocyanate reagent derivatized residue","termid":"MOD:00840"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phenyl isocyanate derivatized residue","synonyms":[{"name":"Phenylisocyanate","type":"related"},{"name":"phenyl isocyanate","type":"related"}],"termid":"MOD:00870"}


id: PBO:0084552
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of the seripauperin multigene family; encoded mainly in subtelomeric regions; induced during alcoholic fermentation; induced by low temperature and also by anaerobic conditions; negatively regulated by oxygen and repressed by heme","termid":"PBO:0084552"}


id: GO:0002527
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An increase in the internal diameter of blood vessels, especially arterioles or capillaries, usually resulting in a decrease in blood pressure contributing to an acute inflammatory response.","definition_xrefs":["GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vasodilation","termid":"GO:0042311"},{"relation_name":"part_of","term_name":"acute inflammatory response","termid":"GO:0002526"}],"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":"vasodilation involved in acute inflammatory response","synonyms":[{"name":"vasodilation during acute inflammatory response","type":"related"}],"termid":"GO:0002527"}


id: GO:0047264
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: heteroglycan + GDP-mannose = alpha-D-mannosylheteroglycan + GDP. 1,2- and 1,3-mannosyl bonds are formed.","definition_xrefs":["EC:2.4.1.48"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mannosyltransferase activity","termid":"GO:0000030"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016757","GO:0016740"],"is_obsolete":false,"name":"heteroglycan alpha-mannosyltransferase activity","synonyms":[{"name":"GDP mannose alpha-mannosyltransferase activity","type":"related"},{"name":"GDP-mannose:heteroglycan 2-(or 3-)-alpha-D-mannosyltransferase activity","type":"related"},{"name":"guanosine diphosphomannose-heteroglycan alpha-mannosyltransferase activity","type":"related"},{"name":"heteropolysaccharide alpha-mannosyltransferase activity","type":"exact"}],"termid":"GO:0047264"}


id: FYPO:0001628
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of L-valine measured in the vacuole is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in vacuole","termid":"FYPO:0001603"},{"relation_name":"is_a","term_name":"normal cellular valine level","termid":"FYPO:0002746"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001312","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal vacuolar valine level","synonyms":[{"name":"normal level of valine in vacuole","type":"exact"},{"name":"normal vacuolar L-valine level","type":"exact"},{"name":"normal vacuolar valine level during mitotic cell cycle","type":"related"},{"name":"normal vacuolar valine level during vegetative growth","type":"exact"}],"termid":"FYPO:0001628"}


id: PBO:0047135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 172 member A","termid":"PBO:0047135"}


id: FYPO:0001747
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 import of nickel ions into a cell is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal transport during vegetative growth","termid":"FYPO:0005973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"abnormal nickel import","synonyms":[{"name":"abnormal cellular nickel import","type":"exact"},{"name":"abnormal nickel cation import","type":"exact"},{"name":"abnormal nickel import across plasma membrane","type":"exact"},{"name":"abnormal nickel import during mitotic cell cycle","type":"related"},{"name":"abnormal nickel import during vegetative growth","type":"exact"},{"name":"abnormal nickel import into cell","type":"exact"},{"name":"abnormal nickel ion import","type":"exact"}],"termid":"FYPO:0001747"}


id: PBO:0079304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis-specific transcript, Y-linked 2","termid":"PBO:0079304"}


id: PBO:0109639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinoic acid early transcript 1F (pseudogene)","termid":"PBO:0109639"}


id: PBO:0049275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GSK3B interacting protein","termid":"PBO:0049275"}


id: MONDO:0006088
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A circumscribed neoplasm arising from the glandular epithelium of the appendix. Morphologically, it is characterized by a proliferation of neoplastic glandular cells and it is associated with dysplasia. According to the growth pattern, it may be classified as tubular, villous, or tubulovillous. The dysplasia is classified as mild, moderate, or severe.","definition_xrefs":["NCIT:C43550"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colon adenoma","termid":"MONDO:0000527"},{"relation_name":"is_a","term_name":"epithelial tumor of the appendix","termid":"MONDO:0018511"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"appendix adenoma","secondary_identifiers":["EFO:1000089","MEDGEN:312900","UMLS:C1706829"],"synonyms":[{"name":"appendix adenoma","type":"exact"},{"name":"vermiform appendix adenoma","type":"exact"}],"termid":"MONDO:0006088","xrefs":{"Monarch":{"xref_id":"0006088"}}}


id: PBO:0064057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 91","termid":"PBO:0064057"}


id: PBO:0035755
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_rate_of_medial_membrane_band_assembly","termid":"PBO:0035755"}


id: PBO:0042171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cellular communication network factor 2","termid":"PBO:0042171"}


id: GO:0102265
data:
  {"annotated_genes":["SJAG_03240"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[67142],"is_not":false,"summary":null,"term":"GO:0102265"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a 5,6-dihydrouracil47 in tRNA + NAD(P) = H+ + a uracil47 in tRNA + NAD(P)H.","definition_xrefs":["GOC:pz","EC:1.3.1.89"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA dihydrouridine synthase activity","termid":"GO:0017150"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03240":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0140098","GO:0016491","GO:0140101"],"is_obsolete":false,"name":"tRNA-dihydrouridine47 synthase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["MetaCyc:RXN-12457"],"termid":"GO:0102265","terms_by_termid":{"GO:0102265":null}}


id: PBO:0003300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coatomer alpha subunit (predicted)","termid":"PBO:0003300"}


id: PBO:0091546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces pombe specific protein, expressed during meiotic cell cycle","termid":"PBO:0091546"}


id: PBO:0003795
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beige protein homolog (predicted)","termid":"PBO:0003795"}


id: PBO:0073105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sidekick cell adhesion molecule 1","termid":"PBO:0073105"}


id: MONDO:0017894
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute myeloid leukemia with CEBPA somatic mutations is a subtype of acute myeloid leukemia with recurrent genetic abnormalities, characterized by clonal proliferation of myeloid blasts harboring somatic mutations of the CEBPA gene in the bone marrow, blood and, rarely, other tissues. It can present with anemia, thrombocytopenia, and other nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly).","definition_xrefs":["Orphanet:319480"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"acute myeloid leukemia with CEBPA somatic mutations","secondary_identifiers":["GARD:17451","SCTID:764855007","DOID:0081095","NCIT:C82433","UMLS:C4707178","MEDGEN:1640289"],"synonyms":[{"name":"AML with CEBPA somatic mutations","type":"exact"},{"name":"AML with mutated CEBPA","type":"exact"},{"name":"acute myeloid Leukaemia with mutated CEBPA","type":"exact"},{"name":"acute myeloid Leukaemia with non-germline mutated CEBPA","type":"exact"},{"name":"acute myeloid Leukemia with mutated CEBPA","type":"exact"},{"name":"acute myeloid Leukemia with non-germline mutated CEBPA","type":"exact"},{"name":"non-familial acute myeloid leukaemia with mutated CEBPA","type":"exact"},{"name":"non-familial acute myeloid leukemia with mutated CEBPA","type":"exact"}],"termid":"MONDO:0017894","xrefs":{"Monarch":{"xref_id":"0017894"}}}


id: FYPO:0004886
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the nuclear envelope is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to nucleus during vegetative growth","termid":"FYPO:0001424"},{"relation_name":"is_a","term_name":"abnormal protein localization to nuclear envelope during vegetative growth","termid":"FYPO:0004885"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"abolished protein localization to nuclear envelope during vegetative growth","synonyms":[{"name":"abolished protein localisation to nuclear envelope during vegetative growth","type":"exact"},{"name":"abolished protein localization to nuclear envelope during mitotic cell cycle","type":"related"},{"name":"protein localization to nuclear envelope abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0004886"}


id: MONDO:0000104
data:
  {"annotated_genes":["SJAG_01007"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86827],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008787"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypochromic microcytic anemia","termid":"MONDO:0000387"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01007":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"anemia, hypochromic microcytic with iron overload","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:388759","MESH:C567144","OMIMPS:206100","UMLS:C2673913"],"synonyms":[{"name":"anemia, hypochromic microcytic, with iron overload","type":"exact"}],"termid":"MONDO:0000104","terms_by_termid":{"MONDO:0008787":null},"xrefs":{"Monarch":{"xref_id":"0000104"}}}


id: MONDO:0010375
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked intellectual disability-epilepsy syndrome","termid":"MONDO:0016160"},{"relation_name":"is_a","term_name":"hereditary hyperekplexia","termid":"MONDO:0021022"},{"relation_name":"is_a","term_name":"genetic developmental and epileptic encephalopathy","termid":"MONDO:0100062"},{"relation_name":"is_a","term_name":"X-linked complex neurodevelopmental disorder","termid":"MONDO:0100148"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0005066","MONDO:0005027"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 8","secondary_identifiers":["MEDGEN:375581","UMLS:C1845102","GARD:17010","OMIM:300607","MESH:C564474","Orphanet:163985","DOID:0080215"],"synonyms":[{"name":"DEE8","type":"exact"},{"name":"EIEE8","type":"exact"},{"name":"developmental and epileptic encephalopathy 8","type":"exact"},{"name":"early infantile epileptic encephalopathy 8","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 8","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 8","type":"exact"},{"name":"hyperekplexia and epilepsy","type":"related"},{"name":"hyperekplexia-epilepsy syndrome","type":"exact"}],"termid":"MONDO:0010375","xrefs":{"Monarch":{"xref_id":"0010375"}}}


id: GO:0070439
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A transcriptional repressor complex that contains a heterodimer of the bHLH-ZIP proteins Mad and Max, plus mSin3A, a homolog of the yeast Sin3p.","definition_xrefs":["PMID:7889570"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II transcription repressor complex","termid":"GO:0090571"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0032991"],"is_obsolete":false,"name":"Mad-Max-mSin3A complex","termid":"GO:0070439"}


id: PR:O94319
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein SEC13 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03972","PANTHER:PTHR11024:SF2","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":"protein transport protein sec13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC215.15","secondary_identifiers":["UniProtKB:O94319"],"synonyms":[{"name":"Spom972h-SEC13","type":"exact"}],"termid":"PR:O94319"}


id: PBO:0073947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC20A1 divergent transcript","termid":"PBO:0073947"}


id: PBO:0071071
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 73","termid":"PBO:0071071"}


id: GO:0106150
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of zearalenone, a mycotoxin produced by several Fusarium species, is most commonly found as a contaminant in stored grain and has chronic estrogenic effects on mammals.","definition_xrefs":["PMID:16517624","PMID:20578001","GOC:ach"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macrolide biosynthetic process","termid":"GO:0033068"},{"relation_name":"is_a","term_name":"mycotoxin biosynthetic process","termid":"GO:0043386"},{"relation_name":"is_a","term_name":"phenol-containing compound biosynthetic process","termid":"GO:0046189"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"zearalenone biosynthetic process","termid":"GO:0106150"}


id: GO:0042944
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of D-alanine from one side of a membrane to the other. D-alanine is the D-enantiomer of 2-aminopropanoic acid.","definition_xrefs":["GOC:jl","ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alanine transmembrane transporter activity","termid":"GO:0022858"},{"relation_name":"is_a","term_name":"D-amino acid transmembrane transporter activity","termid":"GO:0042943"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"D-alanine transmembrane transporter activity","synonyms":[{"name":"D-alanine transporter activity","type":"broad"}],"termid":"GO:0042944"}


id: GO:0120141
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the activity of any ecdysone receptor signaling pathway.","definition_xrefs":["GOC:ha","PMID:23072462"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular steroid hormone receptor signaling pathway","termid":"GO:0033143"},{"relation_name":"is_a","term_name":"regulation of cellular response to alcohol","termid":"GO:1905957"},{"relation_name":"regulates","term_name":"ecdysone receptor signaling pathway","termid":"GO:0035076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of ecdysone receptor signaling pathway","synonyms":[{"name":"regulation of ecdysone receptor-mediated signaling pathway","type":"exact"}],"termid":"GO:0120141"}


id: PBO:0016887
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endocytic docking protein Mso1","termid":"PBO:0016887"}


id: PBO:0068170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 477","termid":"PBO:0068170"}


id: GO:0009266
data:
  {"annotated_genes":["SJAG_04567","SJAG_02381","SJAG_01584","SJAG_01186","SJAG_03527","SJAG_00436","SJAG_04388","SJAG_03815","SJAG_04187","SJAG_04055"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[80708,106116],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070370"},{"annotations":[117341,117342,106803,97470,111827,111828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034605"},{"annotations":[92580],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071502"},{"annotations":[74864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031990"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a temperature stimulus.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to abiotic stimulus","termid":"GO:0009628"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00436":null,"SJAG_01186":null,"SJAG_01584":null,"SJAG_02381":null,"SJAG_03527":null,"SJAG_03815":null,"SJAG_04055":null,"SJAG_04187":null,"SJAG_04388":null,"SJAG_04567":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to temperature stimulus","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"response to thermal stimulus","type":"exact"}],"termid":"GO:0009266","terms_by_termid":{"GO:0031990":null,"GO:0034605":null,"GO:0070370":null,"GO:0071502":null}}


id: GO:0004558
data:
  {"annotated_genes":["SJAG_03824","SJAG_02131"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[103395,103396],"is_not":false,"summary":null,"term":"GO:0004558"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of terminal, non-reducing alpha-(1->4)-linked alpha-D-glucose residues with release of alpha-D-glucose.","definition_xrefs":["EC:3.2.1.20"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-glucosidase activity","termid":"GO:0090599"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02131":null,"SJAG_03824":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016798","GO:0016787"],"is_obsolete":false,"name":"alpha-1,4-glucosidase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:MALTODEXGLUCOSID-RXN","Reactome:R-HSA-5659879","Reactome:R-HSA-189102","Reactome:R-HSA-191108","Reactome:R-HSA-5659861","Reactome:R-HSA-189053","Reactome:R-HSA-191101","Reactome:R-HSA-5659899","Reactome:R-HSA-191116","Reactome:R-HSA-5659922","GO:0016982","GO:0004562"],"synonyms":[{"name":"acid maltase activity","type":"related"},{"name":"alpha-D-glucosidase activity","type":"related"},{"name":"alpha-D-glucoside glucohydrolase activity","type":"related"},{"name":"alpha-glucopyranosidase activity","type":"related"},{"name":"alpha-glucoside hydrolase activity","type":"related"},{"name":"glucoinvertase activity","type":"related"},{"name":"glucosidoinvertase activity","type":"related"},{"name":"glucosidosucrase activity","type":"related"},{"name":"lysosomal alpha-glucosidase activity","type":"broad"},{"name":"maltase-glucoamylase activity","type":"related"}],"termid":"GO:0004558","terms_by_termid":{"GO:0004558":null}}


id: PBO:0075041
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 116-4","termid":"PBO:0075041"}


id: FYPO:0000728
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which actin cortical patch assembly is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actin cortical patch organization","termid":"FYPO:0000790"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0004803","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abnormal actin cortical patch assembly","synonyms":[{"name":"abnormal F-actin patch assembly","type":"exact"},{"name":"abnormal actin cortical patch assembly during mitotic cell cycle","type":"related"},{"name":"abnormal actin cortical patch assembly during vegetative growth","type":"exact"},{"name":"abnormal actin patch assembly","type":"exact"}],"termid":"FYPO:0000728"}


id: PBO:0072223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S19 pseudogene 6","termid":"PBO:0072223"}


id: PBO:0086173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for the degradation of mutant 25S rRNAs; functions in Mms1 pathway of nonfunctional 25S rRNA decay; expression induced by DNA damage and null mutations confer increased resistance to hydroxyurea; N-terminal region has a leucine repeat and a WD40 repeat","termid":"PBO:0086173"}


id: GO:0060751
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental growth process in which a branch of a mammary gland duct elongates.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"branch elongation of an epithelium","termid":"GO:0060602"},{"relation_name":"part_of","term_name":"branching involved in mammary gland duct morphogenesis","termid":"GO:0060444"}],"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":"branch elongation involved in mammary gland duct branching","synonyms":[{"name":"mammary gland duct branch elongation","type":"exact"}],"termid":"GO:0060751"}


id: MONDO:0015497
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hypoglossia/aglossia (obsolete MONDO:0015497)","secondary_identifiers":["icd11.foundation:2087939516","Orphanet:156212"],"termid":"MONDO:0015497","xrefs":{"Monarch":{"xref_id":"0015497"}}}


id: GO:0070602
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of sister chromatid cohesion in the centromeric region of a chromosome.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sister chromatid cohesion","termid":"GO:0007063"},{"relation_name":"regulates","term_name":"centromeric sister chromatid cohesion","termid":"GO:0070601"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of centromeric sister chromatid cohesion","synonyms":[{"name":"regulation of sister chromatid cohesion at centromere","type":"exact"}],"termid":"GO:0070602"}


id: GO:0016158
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: myo-inositol hexakisphosphate + H2O = D-myo-inositol 1,2,4,5,6-pentakisphosphate + phosphate.","definition_xrefs":["EC:3.1.3.8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol hexakisphosphate phosphatase activity","termid":"GO:0004446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0016788","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"inositol hexakisphosphate 3-phosphatase activity","secondary_identifiers":["RHEA:16989","MetaCyc:RXN0-1001"],"synonyms":[{"name":"1-phytase activity","type":"related"},{"name":"3-phytase activity","type":"exact"},{"name":"myo-inositol-hexakisphosphate 3-phosphohydrolase activity","type":"related"},{"name":"myo-inositol-hexaphosphate 3-phosphohydrolase activity","type":"exact"},{"name":"phytase activity","type":"broad"},{"name":"phytate 1-phosphatase activity","type":"related"},{"name":"phytate 3-phosphatase activity","type":"exact"}],"termid":"GO:0016158"}


id: FYPO:0003595
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a single cell grows in a shape that consists of two curves in opposite directions.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vegetative cell shape","termid":"FYPO:0002196"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0000005"],"is_obsolete":false,"name":"S-shaped cell","synonyms":[{"name":"S-shaped vegetative cell","type":"exact"},{"name":"Z-shaped cell","type":"exact"},{"name":"kinked cell","type":"exact"},{"name":"kinky cell","type":"exact"},{"name":"sigmoid cell","type":"exact"}],"termid":"FYPO:0003595"}


id: RO:0002453
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"symbiotically_interacts_with","termid":"RO:0002440"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"host_of","termid":"RO:0002453"}


id: MONDO:0014534
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any microlissencephaly in which the cause of the disease is a mutation in the KATNB1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microlissencephaly","termid":"MONDO:0015204"}],"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":"lissencephaly 6 with microcephaly","secondary_identifiers":["UMLS:C4015525","DOID:0112236","MEDGEN:863962","OMIM:616212"],"synonyms":[{"name":"KATNB1 Microlissencephaly","type":"exact"},{"name":"KATNB1 microlissencephaly","type":"exact"},{"name":"LIS6","type":"related"},{"name":"Microlissencephaly caused by mutation in KATNB1","type":"exact"},{"name":"lissencephaly 6 with microcephaly","type":"exact"},{"name":"lissencephaly 6, with microcephaly","type":"exact"},{"name":"microlissencephaly caused by mutation in KATNB1","type":"exact"}],"termid":"MONDO:0014534","xrefs":{"Monarch":{"xref_id":"0014534"}}}


id: PBO:0027507
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-spores_sensitive_to_acetone","termid":"PBO:0027507"}


id: PBO:0114478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA (adenine) methyltransferase activity Bmt2/human SAMTOR (S-adenosylmethionine sensor for the MTOR) ortholog","termid":"PBO:0114478"}


id: MONDO:0018594
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Secondary polyarteritis nodosa (PAN) is a rare serious form of PAN characterized by vasculitis in a background of viral infection, primarily with hepatitis B virus (HBV).","definition_xrefs":["Orphanet:439746"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyarteritis nodosa","termid":"MONDO:0019170"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secondary polyarteritis nodosa","secondary_identifiers":["GARD:21831","MEDGEN:1843373","UMLS:C5680050"],"synonyms":[{"name":"Secondary PAN","type":"exact"},{"name":"secondary PAN","type":"exact"},{"name":"secondary periarteritis nodosa","type":"exact"}],"termid":"MONDO:0018594","xrefs":{"Monarch":{"xref_id":"0018594"}}}


id: SO:0001847
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A promoter element with consensus sequence TTTRTTTACA, bound by transcription factors with a forkhead DNA-binding domain.","definition_xrefs":["PMID:15195092"],"direct_ancestors":[{"relation_name":"is_a","term_name":"promoter_element","termid":"SO:0001659"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead_motif","synonyms":[{"name":"forkhead motif","type":"exact"}],"termid":"SO:0001847"}


id: PBO:0076911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor AP-2 alpha","termid":"PBO:0076911"}


id: PBO:0080331
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 95 pseudogene","termid":"PBO:0080331"}


id: PBO:0077494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 213","termid":"PBO:0077494"}


id: PR:P0CT83
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl1201 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P0CT83"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L12-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC16C4.13c","synonyms":[{"name":"Spom972h-rpl1201","type":"exact"}],"termid":"PR:P0CT83"}


id: PBO:0039909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cdc42 guanine nucleotide exchange factor 9","termid":"PBO:0039909"}


id: GO:0047839
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dATP + depurinated DNA = ribose triphosphate + DNA.","definition_xrefs":["EC:2.6.99.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring nitrogenous groups","termid":"GO:0016769"},{"relation_name":"is_a","term_name":"catalytic activity, acting on DNA","termid":"GO:0140097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140097"}],"interesting_parent_ids":["GO:0003824","GO:0016769","GO:0016740","GO:0003674","GO:0140097"],"is_obsolete":false,"name":"dATP(dGTP)-DNA purinetransferase activity","secondary_identifiers":["MetaCyc:DATPDGTP--DNA-PURINE-TRANSFERASE-RXN"],"synonyms":[{"name":"dATP(dGTP)--DNA purine transferase activity","type":"exact"},{"name":"dATP(dGTP):depurinated-DNA purine transferase activity","type":"related"}],"termid":"GO:0047839"}


id: PBO:0083840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Evolutionarily conserved kinetochore protein; part of multiple protein complexes, including the SCF ubiquitin ligase complex, the CBF3 complex that binds centromeric DNA, and the RAVE complex that regulates assembly of the V-ATPase; protein abundance increases in response to DNA replication stress","termid":"PBO:0083840"}


id: MONDO:0012460
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the LHFPL5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"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 67","secondary_identifiers":["OMIM:610265","UMLS:C1853223","DOID:0110518","GARD:22624","MEDGEN:343997","MESH:C565207"],"synonyms":[{"name":"DFNB67","type":"narrow"},{"name":"LHFPL5 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 67","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 67","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in LHFPL5","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 67","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 67","type":"exact"},{"name":"deafness, autosomal recessive 67","type":"narrow"},{"name":"deafness, autosomal recessive type 67","type":"narrow"}],"termid":"MONDO:0012460","xrefs":{"Monarch":{"xref_id":"0012460"}}}


id: MONDO:0003037
data:
  {"annotated_genes":["SJAG_00155","SJAG_00624","SJAG_03469","SJAG_01202"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014027"},{"annotations":[88183,88182],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014384"},{"annotations":[88005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032649"}]},"cv_name":"mondo","definition":"A congenital condition, usually due to genetic aberrations, that is characterized by a lack of hair growth on the head and/or body.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of pilosebaceous unit","termid":"MONDO:0002917"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00155":null,"SJAG_00624":null,"SJAG_01202":null,"SJAG_03469":null},"genotype_count":0,"is_obsolete":false,"name":"hypotrichosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:605389","UMLS:C0020678","ICD9:704.09","DOID:4535","MESH:D007039","SCTID:53602002","MEDGEN:6993","NCIT:C34720"],"termid":"MONDO:0003037","terms_by_termid":{"MONDO:0014027":null,"MONDO:0014384":null,"MONDO:0032649":null},"xrefs":{"Monarch":{"xref_id":"0003037"}}}


id: PBO:0034050
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_structural_homology_relationship_with","termid":"PBO:0034050"}


id: PBO:0017003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"box H/ACA small nucleolar RNA snR95","termid":"PBO:0017003"}


id: PBO:0060735
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase complex assembly factor 4","termid":"PBO:0060735"}


id: MONDO:0036595
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant sex cord-stromal tumor arising from the ovary. It is characterized by the presence of neoplastic Leydig cells. Signs and symptoms include hirsutism, menorrhagia and metrorrhagia. It may be associated with trisomy 8.","definition_xrefs":["NCIT:C2880"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian sertoli-stromal cell tumor","termid":"MONDO:0020807"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian Sertoli-Leydig cell tumor","secondary_identifiers":["SCTID:254866007","UMLS:C0003810","MEDGEN:2038"],"synonyms":[{"name":"Sertoli-Leydig cell tumor of ovary","type":"exact"},{"name":"Sertoli-Leydig cell tumor of the ovary","type":"exact"},{"name":"Sertoli-Leydig cell tumour of ovary","type":"exact"},{"name":"Sertoli-Leydig cell tumour of the ovary","type":"exact"},{"name":"Sertoli-Leydig neoplasm of ovary","type":"exact"},{"name":"Sertoli-Leydig neoplasm of the ovary","type":"exact"},{"name":"androblastoma","type":"exact"},{"name":"arrhenoblastoma","type":"exact"},{"name":"ovarian Sertoli-Leydig cell neoplasm","type":"exact"},{"name":"ovarian Sertoli-Leydig cell tumor","type":"exact"}],"termid":"MONDO:0036595","xrefs":{"Monarch":{"xref_id":"0036595"}}}


id: GO:0051620
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of norepinephrine into a cell, typically presynaptic neurons or glial cells. Norepinephrine (3,4-dihydroxyphenyl-2-aminoethanol) is a hormone secreted by the adrenal medulla and a neurotransmitter in the sympathetic peripheral nervous system and in some tracts of the CNS. It is also the biosynthetic precursor of epinephrine.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"norepinephrine transport","termid":"GO:0015874"},{"relation_name":"is_a","term_name":"catecholamine uptake","termid":"GO:0090493"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"norepinephrine uptake","synonyms":[{"name":"levarterenol reuptake","type":"exact"},{"name":"levarterenol uptake","type":"exact"},{"name":"noradrenaline reuptake","type":"exact"},{"name":"noradrenaline uptake","type":"exact"},{"name":"norepinephrine import","type":"exact"},{"name":"norepinephrine reuptake","type":"exact"}],"termid":"GO:0051620"}


id: PBO:0046876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 8 member A1","termid":"PBO:0046876"}


id: MONDO:0000061
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete microcephaly, primary, autosomal recessive (obsolete MONDO:0000061)","termid":"MONDO:0000061","xrefs":{"Monarch":{"xref_id":"0000061"}}}


id: PBO:0114288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisome mebbrane ubiquitin conjugating enzyme E2 Ubc16 Pex4","termid":"PBO:0114288"}


id: GO:0018085
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of conversion of a L-amino acid into its enantiomer, the corresponding D-amino acid.","definition_xrefs":["GOC:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-amino acid modification","termid":"GO:0018193"},{"relation_name":"is_a","term_name":"chiral amino acid racemization","termid":"GO:0018366"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0006520","GO:0008150"],"is_obsolete":false,"name":"peptidyl-L-amino acid racemization","termid":"GO:0018085"}


id: PBO:0074986
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 114-28","termid":"PBO:0074986"}


id: SO:1000105
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000105 sequence_variant_affecting_polypeptide_amino_acid_sequence (obsolete SO:1000105)","synonyms":[{"name":"mutation affecting polypeptide amino acid sequence","type":"related"},{"name":"sequence variant affecting polypeptide amino acid sequence","type":"exact"}],"termid":"SO:1000105"}


id: PR:G2TRJ7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1834.13 gene.","definition_xrefs":["UniProtKB:G2TRJ7","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 c1834.13 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1834.13","synonyms":[{"name":"Spom972h-SPAC1834.13","type":"exact"}],"termid":"PR:G2TRJ7"}


id: PBO:0078655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Lys (anticodon CTT) 8-1","termid":"PBO:0078655"}


id: MONDO:0016297
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetically highly heterogeneous otorhinolaryngologic disease, resulting from inner and/or middle ear or hearing nerve anomalies, typically characterized by bilateral, severe to profound hearing loss (mean sensorineural hearing impairment of 60 dB or more for 500-, 1,000-, and 2,000-Hz frequency tones in the better ear) which occurs before the onset of speech development and is not associated with visible external ear abnormalities or any other medical problems. It is usually nonprogressive and impedes oral language acquisition.","definition_xrefs":["Orphanet:216445"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nonsyndromic genetic hearing loss","termid":"MONDO:0019497"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497"],"is_obsolete":false,"name":"prelingual non-syndromic genetic hearing loss","secondary_identifiers":["SCTID:764098007","MEDGEN:1647959","UMLS:C4706679"],"synonyms":[{"name":"isolated prelingual genetic deafness","type":"narrow"},{"name":"prelingual non-syndromic genetic deafness","type":"narrow"},{"name":"prelingual non-syndromic genetic hearing loss","type":"exact"}],"termid":"MONDO:0016297","xrefs":{"Monarch":{"xref_id":"0016297"}}}


id: PBO:0058801
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 7843","termid":"PBO:0058801"}


id: _global:regulated_by
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"inverse of regulates","direct_ancestors":[{"relation_name":"is_a","term_name":"causally_downstream_of_or_within","termid":"_global:causally_downstream_of_or_within"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulated_by","secondary_identifiers":["RO:0002334"],"termid":"_global:regulated_by"}


id: MONDO:1010515
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Triploidy that occurs in blue-and-yellow macaw.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"triploidy, non-human animal","termid":"MONDO:1010031"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"triploidy, blue-and-yellow macaw","secondary_identifiers":["OMIA:001180-9226"],"termid":"MONDO:1010515","xrefs":{"Monarch":{"xref_id":"1010515"}}}


id: PBO:0091096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific protein Dhm2","termid":"PBO:0091096"}


id: GO:0110144
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Any constituent part of a magnetosome, a membrane-bound organelle that envelops particles of magnetic iron minerals in magnetotactic bacteria.","definition_xrefs":["PMID:27620945","GOC:aa"],"gene_count":0,"genotype_count":0,"name":"obsolete magnetosome part (obsolete GO:0110144)","termid":"GO:0110144"}


id: PBO:0050913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon induced protein with tetratricopeptide repeats 5","termid":"PBO:0050913"}


id: PBO:0040811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BICD cargo adaptor 2","termid":"PBO:0040811"}


id: GO:0002633
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of granuloma formation.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of granuloma formation","termid":"GO:0002631"},{"relation_name":"is_a","term_name":"positive regulation of chronic inflammatory response","termid":"GO:0002678"},{"relation_name":"is_a","term_name":"positive regulation of immune effector process","termid":"GO:0002699"},{"relation_name":"positively_regulates","term_name":"granuloma formation","termid":"GO:0002432"}],"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 granuloma formation","synonyms":[{"name":"activation of granuloma formation","type":"narrow"},{"name":"stimulation of granuloma formation","type":"narrow"},{"name":"up regulation of granuloma formation","type":"exact"},{"name":"up-regulation of granuloma formation","type":"exact"},{"name":"upregulation of granuloma formation","type":"exact"}],"termid":"GO:0002633"}


id: GO:0009178
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of pyrimidine deoxynucleoside monophosphate, a compound consisting of a pyrimidine base linked to a deoxyribose sugar esterified with phosphate on the sugar.","definition_xrefs":["GOC:go_curators","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleoside monophosphate catabolic process","termid":"GO:0009131"},{"relation_name":"is_a","term_name":"deoxyribonucleoside monophosphate catabolic process","termid":"GO:0009159"},{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleoside monophosphate metabolic process","termid":"GO:0009176"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"pyrimidine deoxyribonucleoside monophosphate catabolic process","synonyms":[{"name":"pyrimidine deoxyribonucleoside monophosphate breakdown","type":"exact"},{"name":"pyrimidine deoxyribonucleoside monophosphate catabolism","type":"exact"},{"name":"pyrimidine deoxyribonucleoside monophosphate degradation","type":"exact"}],"termid":"GO:0009178"}


id: GO:1900594
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving (+)-kotanin.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary metabolic process","termid":"GO:0019748"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"(+)-kotanin metabolic process","synonyms":[{"name":"(+)-kotanin metabolism","type":"exact"}],"termid":"GO:1900594"}


id: PBO:0047418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box and WD repeat domain containing 9","termid":"PBO:0047418"}


id: GO:0047053
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-scoulerine + [reduced NADPH--hemoprotein reductase] + O2 = (S)-cheilanthifoline + [oxidized NADPH--hemoprotein reductase] + 2 H2O.","definition_xrefs":["RHEA:20485"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water","termid":"GO:0016717"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"(S)-cheilanthifoline synthase activity","secondary_identifiers":["KEGG_REACTION:R03834","EC:1.14.19.65","MetaCyc:1.14.21.2-RXN"],"synonyms":[{"name":"(S)-scoulerine oxidase (methylenedioxy-bridge-forming) activity","type":"exact"}],"termid":"GO:0047053"}


id: GO:0016121
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of carotenes, hydrocarbon carotenoids.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carotene metabolic process","termid":"GO:0016119"},{"relation_name":"is_a","term_name":"terpene catabolic process","termid":"GO:0046247"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"carotene catabolic process","synonyms":[{"name":"carotene breakdown","type":"exact"},{"name":"carotene catabolism","type":"exact"},{"name":"carotene degradation","type":"exact"}],"termid":"GO:0016121"}


id: PATO:0000116
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000116 relative temperature sensitivity (obsolete PATO:0000116)","termid":"PATO:0000116"}


id: PBO:0049577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3.3 histone A","termid":"PBO:0049577"}


id: PBO:0073347
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serpin family B member 8 pseudogene 1","termid":"PBO:0073347"}


id: MONDO:0000200
data:
  {"annotated_genes":["SJAG_00136"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014646"}]},"cv_name":"mondo","definition":"Zimmermann-Laband syndrome (ZLS) is a rare disorder characterized by gingival fibromatosis, coarse facial appearance, and absence or hypoplasia of nails or terminal phalanges of hands and feet.","definition_xrefs":["Orphanet:3473"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00136":null},"genotype_count":0,"is_obsolete":false,"name":"Zimmermann-Laband syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:699447001","GARD:385","MEDGEN:208656","ICD9:759.89","icd11.foundation:8285962","UMLS:C0796013","OMIMPS:135500","MESH:C536725"],"synonyms":[{"name":"Laband syndrome","type":"exact"},{"name":"Laband-Zimmermann syndrome","type":"related"},{"name":"ZLS","type":"related"},{"name":"ZLS1","type":"related"},{"name":"Zimmerman Laband syndrome","type":"related"},{"name":"Zimmermann-Laband syndrome 1","type":"related"},{"name":"Zimmermann-Laband syndrome type 1","type":"exact"},{"name":"fibromatosis gingival, hepatosplenomegaly other anomalies","type":"related"},{"name":"gingival fibromatosis, abnormal fingers, fingernails, nose and ears, and splenomegaly","type":"related"},{"name":"gingival fibromatosis-hepatosplenomegaly-other anomalies syndrome","type":"exact"}],"termid":"MONDO:0000200","terms_by_termid":{"MONDO:0014646":null},"xrefs":{"Monarch":{"xref_id":"0000200"}}}


id: GO:0016804
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the release of a N-terminal proline from a peptide.","definition_xrefs":["EC:3.4.11.5"],"gene_count":0,"genotype_count":0,"name":"obsolete prolyl aminopeptidase activity (obsolete GO:0016804)","synonyms":[{"name":"Pro-X aminopeptidase activity","type":"related"},{"name":"cytosol aminopeptidase V","type":"related"},{"name":"proline aminopeptidase","type":"broad"},{"name":"proline iminopeptidase activity","type":"exact"},{"name":"prolyl aminopeptidase activity","type":"exact"}],"termid":"GO:0016804"}


id: GO:0030248
data:
  {"annotated_genes":["SJAG_00981"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[61242],"is_not":false,"summary":null,"term":"GO:0030248"}]},"cv_name":"molecular_function","definition":"Binding to cellulose.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide binding","termid":"GO:0030247"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00981":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"cellulose binding","references_by_uniquename":{"GO_REF:0000002":null},"termid":"GO:0030248","terms_by_termid":{"GO:0030248":null}}


id: PR:O74905
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl902 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74905"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L9-B (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC613.06","synonyms":[{"name":"Spom972h-rpl902","type":"exact"}],"termid":"PR:O74905"}


id: GO:0060613
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of a fat pad from its initial formation to its mature structure. A fat pad is an accumulation of adipose tissue.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adipose tissue development","termid":"GO:0060612"}],"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":"fat pad development","termid":"GO:0060613"}


id: GO:0140613
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + Mn2+(in) = ADP + H+ + Mn2+(out) + phosphate.","definition_xrefs":["PMID:11134055","RHEA:66820","PMID:15590060","PMID:21187401","PMID:15831496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"manganese ion transmembrane transporter activity","termid":"GO:0005384"},{"relation_name":"is_a","term_name":"P-type ion transporter activity","termid":"GO:0015662"},{"relation_name":"is_a","term_name":"ATPase-coupled monoatomic cation transmembrane transporter activity","termid":"GO:0019829"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"P-type manganese transporter activity","secondary_identifiers":["MetaCyc:RXN-20940"],"termid":"GO:0140613"}


id: PBO:0060740
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase complex assembly factor 5","termid":"PBO:0060740"}


id: GO:0010454
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency or rate of cell fate commitment. Cell fate commitment is the commitment of cells to specific cell fates and their capacity to differentiate into particular kinds of cells. Positional information is established through protein signals that emanate from a localized source within a cell (the initial one-cell zygote) or within a developmental field.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell fate commitment","termid":"GO:0010453"},{"relation_name":"is_a","term_name":"negative regulation of cell differentiation","termid":"GO:0045596"},{"relation_name":"negatively_regulates","term_name":"cell fate commitment","termid":"GO:0045165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of cell fate commitment","termid":"GO:0010454"}


id: PBO:0088269
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP-2 adaptor complex beta subunit Apl1","termid":"PBO:0088269"}


id: MOD:01510
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an N'-hydrogen atom of a histidine residue with the Applied Biosystems iTRAQ4plex-117 reporter+balance group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"},{"relation_name":"is_a","term_name":"iTRAQ4plex-117, mTRAQ heavy, reporter+balance reagent acylated residue","termid":"MOD:01506"},{"relation_name":"is_a","term_name":"iTRAQ4plex reporter+balance reagent N-acylated residue","termid":"MOD:01709"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ4plex-117 reporter+balance reagent N'-acylated histidine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"iTRAQ4plex","type":"related"}],"termid":"MOD:01510"}


id: PBO:0112999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha arrestin, Ub-ligase adaptor for Rsp5p; controls nutrient limitation-mediated endosomal recycling of the Gap1p amino acid permease; PY motif-containing adaptor involved in substrate-induced, Rsp5p-mediated ubiquitination and endocytosis of select plasma membrane localized amino acid transporters, such as Dip5p and Put4p; regulates intracellular pH; phosphorylated by Npr1p and by the Pcl7p-Pho85p cyclin-CDK complex; interacts with AP-1 subunit Apl4p","termid":"PBO:0112999"}


id: GO:0016751
data:
  {"annotated_genes":["SJAG_03163"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77513],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004149"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of a succinyl group to a sulfur atom on the acceptor molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-acyltransferase activity","termid":"GO:0016417"},{"relation_name":"is_a","term_name":"succinyltransferase activity","termid":"GO:0016748"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03163":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0016746","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"S-succinyltransferase activity","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0016751","terms_by_termid":{"GO:0004149":null}}


id: PBO:0061470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear receptor binding factor 2 pseudogene 5","termid":"PBO:0061470"}


id: PBO:0054236
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 1618","termid":"PBO:0054236"}


id: MONDO:0002263
data:
  {"annotated_genes":["SJAG_02426","SJAG_01156","SJAG_03720","SJAG_01419","SJAG_00103","SJAG_02690","SJAG_03698","SJAG_02294","SJAG_04148","SJAG_03418","SJAG_04394","SJAG_04738","SJAG_04206","SJAG_02339","SJAG_04950","SJAG_03051","SJAG_04703","SJAG_04114","SJAG_02748","SJAG_02643","SJAG_02954","SJAG_00377"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87140],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008840"},{"annotations":[87698],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009258"},{"annotations":[89031,86763],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011962"},{"annotations":[88889],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032747"},{"annotations":[88240,88239,88241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008170"},{"annotations":[88709],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030736"},{"annotations":[87372],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013689"},{"annotations":[88138],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054850"},{"annotations":[88968],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013972"},{"annotations":[87743],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014126"},{"annotations":[86779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0976232"},{"annotations":[87358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014843"},{"annotations":[88155,88156],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054862"},{"annotations":[87443],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030870"},{"annotations":[87852],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958035"},{"annotations":[88771],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010350"},{"annotations":[88343,88344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014321"}]},"cv_name":"mondo","definition":"A disease involving the female reproductive system.","direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive system disorder","termid":"MONDO:0005039"}],"gene_count":22,"genes_by_uniquename":{"SJAG_00103":null,"SJAG_00377":null,"SJAG_01156":null,"SJAG_01419":null,"SJAG_02294":null,"SJAG_02339":null,"SJAG_02426":null,"SJAG_02643":null,"SJAG_02690":null,"SJAG_02748":null,"SJAG_02954":null,"SJAG_03051":null,"SJAG_03418":null,"SJAG_03698":null,"SJAG_03720":null,"SJAG_04114":null,"SJAG_04148":null,"SJAG_04206":null,"SJAG_04394":null,"SJAG_04703":null,"SJAG_04738":null,"SJAG_04950":null},"genotype_count":0,"is_obsolete":false,"name":"female reproductive system disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:229","MEDGEN:65928","ICD9:629.9","NCIT:C27020","EFO:0009549","UMLS:C0236100","SCTID:310789003","MESH:D005831"],"synonyms":[{"name":"disease of female genital system","type":"related"},{"name":"disease of female reproductive system","type":"exact"},{"name":"disease or disorder of female reproductive system","type":"exact"},{"name":"disorder of female genital system","type":"exact"},{"name":"disorder of female genital tract","type":"related"},{"name":"disorder of female reproductive system","type":"exact"},{"name":"female reproductive disease","type":"exact"},{"name":"female reproductive system disease","type":"exact"},{"name":"female reproductive system disease or disorder","type":"exact"},{"name":"female reproductive system disorder","type":"exact"},{"name":"gynaecological disease","type":"related"},{"name":"gynecological disease","type":"related"}],"termid":"MONDO:0002263","terms_by_termid":{"MONDO:0008170":null,"MONDO:0008840":null,"MONDO:0009258":null,"MONDO:0010350":null,"MONDO:0011962":null,"MONDO:0013689":null,"MONDO:0013972":null,"MONDO:0014126":null,"MONDO:0014321":null,"MONDO:0014843":null,"MONDO:0030736":null,"MONDO:0030870":null,"MONDO:0032747":null,"MONDO:0054850":null,"MONDO:0054862":null,"MONDO:0958035":null,"MONDO:0976232":null},"xrefs":{"Monarch":{"xref_id":"0002263"}}}


id: PBO:0062516
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 K member 2 pseudogene","termid":"PBO:0062516"}


id: PATO:0002174
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An alignment quality inhering in a bearer by virtue of the bearer's being in a improper spatial positioning away from an additional entity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"misaligned with","termid":"PATO:0001654"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"misaligned away from","termid":"PATO:0002174"}


id: MONDO:0017322
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with defective bone mineralization (obsolete MONDO:0019705)","termid":"MONDO:0019705"},{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"},{"relation_name":"is_a","term_name":"inborn vitamin metabolic disorder","termid":"MONDO:0005528"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"disorders of vitamin D metabolism","secondary_identifiers":["GARD:21132","MEDGEN:1842308","Orphanet:289098","UMLS:C5681017"],"termid":"MONDO:0017322","xrefs":{"Monarch":{"xref_id":"0017322"}}}


id: MONDO:0012819
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The metabolic condition resulted from uncontrolled diabetes mellitus, in which the shift of acid-base status of the body toward the acid side because of loss of base or retention of acids other than carbonic acid is accompanied by the accumulation of ketone bodies in body tissues and fluids.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"type 2 diabetes mellitus","termid":"MONDO:0005148"},{"relation_name":"is_a","term_name":"diabetes mellitus","termid":"MONDO:0005015"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005015"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005015","MONDO:0004335","MONDO:0005066"],"is_obsolete":false,"name":"diabetic ketoacidosis","secondary_identifiers":["MEDGEN:8351","UMLS:C0011880","ICD9:250.10","EFO:1000897","DOID:1837","SCTID:420422005","MedDRA:10012671","ICD9:250.1","MESH:D016883"],"synonyms":[{"name":"KPD","type":"related"},{"name":"ketosis-prone diabetes mellitus","type":"exact"}],"termid":"MONDO:0012819","xrefs":{"Monarch":{"xref_id":"0012819"}}}


id: MONDO:0012431
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital diaphragmatic hernia in which the cause of the disease is a mutation in the ZFPM2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital diaphragmatic hernia","termid":"MONDO:0005711"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diaphragmatic hernia 3","secondary_identifiers":["MESH:C565710","MEDGEN:347546","UMLS:C1857781","GARD:15474","OMIM:610187"],"synonyms":[{"name":"DIH3","type":"related"},{"name":"ZFPM2 congenital diaphragmatic hernia","type":"exact"},{"name":"congenital diaphragmatic hernia caused by mutation in ZFPM2","type":"exact"},{"name":"diaphragmatic hernia 3","type":"exact"},{"name":"diaphragmatic hernia type 3","type":"exact"}],"termid":"MONDO:0012431","xrefs":{"Monarch":{"xref_id":"0012431"}}}


id: PBO:0070543
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 9","termid":"PBO:0070543"}


id: PBO:0112874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UFM1 specific peptidase 1","termid":"PBO:0112874"}


id: GO:1901200
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any negative regulation of calcium ion transport into cytosol that is involved in cellular response to salt stress.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of calcium ion transport into cytosol","termid":"GO:0010523"},{"relation_name":"part_of","term_name":"cellular response to salt stress","termid":"GO:0071472"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"negative regulation of calcium ion transport into cytosol involved in cellular response to salt stress","synonyms":[{"name":"negative regulation of calcium ion transport into cytosol involved in cellular response to ionic osmotic stress","type":"exact"},{"name":"negative regulation of calcium ion transport into cytosol involved in cellular salinity response","type":"exact"}],"termid":"GO:1901200"}


id: GO:0021651
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of rhombomere 1 is generated and organized. Rhombomeres are transverse segments of the developing rhombencephalon. Rhombomeres are lineage restricted, express different genes from one another, and adopt different developmental fates. Rhombomeres are numbered in an anterior to posterior order.","definition_xrefs":["GO_REF:0000021","GOC:jid","GOC:curators","GOC:dgh","GOC:cls","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhombomere morphogenesis","termid":"GO:0021593"},{"relation_name":"part_of","term_name":"rhombomere 1 development","termid":"GO:0021567"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"rhombomere 1 morphogenesis","termid":"GO:0021651"}


id: GO:1904174
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of histone demethylase activity (H3-K4 specific).","definition_xrefs":["GOC:TermGenie","PMID:24843136","GO_REF:0000059","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of histone demethylase activity (H3-K4 specific) (obsolete GO:1904174)","synonyms":[{"name":"down regulation of histone demethylase activity (H3-K4 specific)","type":"exact"},{"name":"down-regulation of histone demethylase activity (H3-K4 specific)","type":"exact"},{"name":"downregulation of histone demethylase activity (H3-K4 specific)","type":"exact"},{"name":"inhibition of histone demethylase activity (H3-K4 specific)","type":"narrow"}],"termid":"GO:1904174"}


id: PBO:0074399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 8","termid":"PBO:0074399"}


id: PBO:0044714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD/H-box helicase 11 like 1 (pseudogene)","termid":"PBO:0044714"}


id: MONDO:0019577
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"isolated congenital anonychia","termid":"MONDO:0019211"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anonychia-onychodystrophy syndrome","secondary_identifiers":["GARD:710","MEDGEN:350767","Orphanet:90390","MESH:C536378","UMLS:C1862840"],"termid":"MONDO:0019577","xrefs":{"Monarch":{"xref_id":"0019577"}}}


id: PR:O13811
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pdi2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13811"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein disulfide-isomerase C17H9.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17H9.14c","synonyms":[{"name":"Spom972h-pdi2","type":"exact"}],"termid":"PR:O13811"}


id: PBO:0051927
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ITGB8 antisense RNA 1","termid":"PBO:0051927"}


id: GO:0039645
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont interferes with the normal execution of the host cell G1/S transition checkpoint. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:24501404","VZ:880"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host cell cycle progression","termid":"GO:0044071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated perturbation of host cell cycle G1/S transition checkpoint","synonyms":[{"name":"G1/S host cell cycle checkpoint dysregulation by virus","type":"exact"},{"name":"modulation by virus of host G1/S transition checkpoint","type":"related"},{"name":"perturbation by virus of host G1/S transition checkpoint","type":"narrow"}],"termid":"GO:0039645"}


id: PBO:0017679
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methyltransferase with rhodanese domain (predicted)","termid":"PBO:0017679"}


id: PBO:0055954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 66","termid":"PBO:0055954"}


id: GO:0033415
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a UGA codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003723"}],"interesting_parent_ids":["GO:0003723","GO:0005488","GO:0060090","GO:0003674"],"is_obsolete":false,"name":"UGA codon-amino acid adaptor activity","synonyms":[{"name":"TGA codon-amino acid adaptor activity","type":"exact"}],"termid":"GO:0033415"}


id: PBO:0087231
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Seipin involved in lipid droplet (LD) assembly; controls lipid particle morphology, number, and size; promotes initiation of LD formation on the ER; ensures that LDs bud from the ER towards the cytosolic side of the membrane; forms a complex with Ldb16p at ER-LD contact sites, stabilizing these sites; null mutants have localized accumulation of phosphatidic acid (PA) marker proteins; BSCL2, human homolog implicated in congenital lipodystrophy, complements yeast null mutant","termid":"PBO:0087231"}


id: PBO:0051601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 24","termid":"PBO:0051601"}


id: GO:0047784
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + cortisol = CoA + cortisol 21-acetate.","definition_xrefs":["EC:2.3.1.27","RHEA:17073"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acetyltransferase activity","termid":"GO:0016413"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016746","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"cortisol O-acetyltransferase activity","secondary_identifiers":["MetaCyc:CORTISOL-O-ACETYLTRANSFERASE-RXN","KEGG_REACTION:R02837"],"synonyms":[{"name":"acetyl-CoA:cortisol O-acetyltransferase activity","type":"related"},{"name":"corticosteroid acetyltransferase activity","type":"related"},{"name":"corticosteroid-21-O-acetyltransferase activity","type":"related"},{"name":"cortisol acetyltransferase activity","type":"related"}],"termid":"GO:0047784"}


id: GO:0016227
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: L-cysteine + 'activated' tRNA = L-serine + tRNA containing a thionucleotide.","definition_xrefs":["EC:2.8.1.4"],"gene_count":0,"genotype_count":0,"name":"obsolete tRNA sulfurtransferase activity (obsolete GO:0016227)","synonyms":[{"name":"L-cysteine:tRNA sulfurtransferase activity","type":"related"},{"name":"RNA sulfurtransferase activity","type":"related"},{"name":"ribonucleate sulfurtransferase activity","type":"related"},{"name":"tRNA sulfurtransferase activity","type":"exact"},{"name":"tRNA sulphurtransferase activity","type":"exact"},{"name":"transfer RNA sulfurtransferase activity","type":"related"},{"name":"transfer RNA thiolase activity","type":"related"},{"name":"transfer ribonucleate sulfurtransferase activity","type":"related"}],"termid":"GO:0016227"}


id: PBO:0054844
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 2258","termid":"PBO:0054844"}


id: GO:0017190
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The acetylation of the N-terminal aspartic acid of proteins; catalyzed by aspartate N-acetyltransferase.","definition_xrefs":["RESID:AA0042"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-terminal protein amino acid acetylation","termid":"GO:0006474"},{"relation_name":"is_a","term_name":"peptidyl-aspartic acid modification","termid":"GO:0018197"}],"gene_count":0,"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":"N-terminal peptidyl-aspartic acid acetylation","termid":"GO:0017190"}


id: PBO:0030436
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_tRNA-Asp_C38_methylation","termid":"PBO:0030436"}


id: GO:0033462
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A triplet codon-amino acid adaptor activity that recognizes a GGC codon.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triplet codon-amino acid adaptor activity","termid":"GO:0030533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0060090","GO:0003723","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"GGC codon-amino acid adaptor activity","synonyms":[{"name":"glycine tRNA","type":"related"}],"termid":"GO:0033462"}


id: GO:1903527
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of membrane tubulation.","definition_xrefs":["GOC:pm","GO_REF:0000058","GOC:TermGenie","PMID:18388313"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"is_a","term_name":"regulation of membrane tubulation","termid":"GO:1903525"},{"relation_name":"positively_regulates","term_name":"plasma membrane tubulation","termid":"GO:0097320"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0061024"},{"rel_name":"regulates","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0061024"],"is_obsolete":false,"name":"positive regulation of membrane tubulation","synonyms":[{"name":"activation of membrane tubulation","type":"narrow"},{"name":"activation of plasma membrane tubulation","type":"narrow"},{"name":"positive regulation of plasma membrane tubulation","type":"exact"},{"name":"up regulation of membrane tubulation","type":"exact"},{"name":"up regulation of plasma membrane tubulation","type":"exact"},{"name":"up-regulation of membrane tubulation","type":"exact"},{"name":"up-regulation of plasma membrane tubulation","type":"exact"},{"name":"upregulation of membrane tubulation","type":"exact"},{"name":"upregulation of plasma membrane tubulation","type":"exact"}],"termid":"GO:1903527"}


id: FYPO:0004438
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A spindle phenotype in which the mitotic spindle is longer than normal during anaphase.","definition_xrefs":["PomBase:mah","PMID:17352737"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long mitotic spindle","termid":"FYPO:0000733"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000120"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0002399","FYPO:0000120"],"is_obsolete":false,"name":"long mitotic spindle during anaphase","synonyms":[{"name":"elongated mitotic spindle during anaphase","type":"exact"},{"name":"increased mitotic spindle length during anaphase","type":"exact"},{"name":"long bipolar mitotic spindle during anaphase","type":"exact"},{"name":"long mitotic spindle during anaphase during vegetative growth","type":"exact"},{"name":"long mitotic spindles during anaphase","type":"exact"},{"name":"long spindle during anaphase of mitosis","type":"exact"},{"name":"long spindle during mitotic anaphase","type":"exact"}],"termid":"FYPO:0004438"}


id: GO:0061299
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the vasculature of the retina is generated and organized.","definition_xrefs":["GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"retina vasculature development in camera-type eye","termid":"GO:0061298"}],"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":"retina vasculature morphogenesis in camera-type eye","synonyms":[{"name":"retinal vasculature morphogenesis","type":"exact"}],"termid":"GO:0061299"}


id: MONDO:0012894
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"osteoarthritis","termid":"MONDO:0005178"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoarthritis susceptibility 6","secondary_identifiers":["OMIM:612401","ICD9:715.96","SCTID:239873007"],"synonyms":[{"name":"OS6","type":"exact"},{"name":"osteoarthritis of knee","type":"related"},{"name":"osteoarthritis susceptibility 6","type":"exact"}],"termid":"MONDO:0012894","xrefs":{"Monarch":{"xref_id":"0012894"}}}


id: MONDO:1012627
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any progressive degenerative myeloencephalopathy that occurs in cattle due to a mutation in the PNPLA8 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"degenerative myeloencephalopathy, non-human animal","termid":"MONDO:1011866"},{"relation_name":"is_a","term_name":"hereditary neurological disease, non-human animal","termid":"MONDO:1012972"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progressive degenerative myeloencephalopathy, PNPLA8-related, cattle","secondary_identifiers":["OMIA:000827-9913"],"synonyms":[{"name":"Weaver syndrome, cattle","type":"related"},{"name":"bovine degenerative progressive myeloencephalopathy","type":"related"},{"name":"haplotype BHW, cattle","type":"related"},{"name":"myeloencephalopathy, progressive degenerative, PNPLA8-related, cattle","type":"exact"}],"termid":"MONDO:1012627","xrefs":{"Monarch":{"xref_id":"1012627"}}}


id: MOD:01915
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-alanine residue to N-formyl-L-alanine.","definition_xrefs":["PubMed:9334739","RESID:AA0576"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-formylated residue","termid":"MOD:00409"},{"relation_name":"is_a","term_name":"modified L-alanine residue","termid":"MOD:00901"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-formyl-L-alanine","synonyms":[{"name":"(2S)-2-(formylamino)propanoic acid","type":"exact"},{"name":"2-formamidopropanoic acid","type":"exact"},{"name":"2-formamidopropionic acid","type":"exact"},{"name":"N-formyl-L-alanine","type":"exact"}],"termid":"MOD:01915"}


id: MONDO:0021115
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A biologic subset of breast carcinoma defined by low to moderate expression of genes characteristic of luminal epithelial cells including estrogen receptor (ER), and high expression of GGH, LAPTM4B, and CCNE1. This subtype of breast cancer is associated with a good prognosis, although not as favorable as the luminal A subtype.","definition_xrefs":["NCIT:C53555"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast tumor luminal A or B","termid":"MONDO:0004990"}],"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":"luminal B breast carcinoma","secondary_identifiers":["MEDGEN:770986","UMLS:C3642346","DOID:0080674"],"synonyms":[{"name":"Luminal B","type":"exact"},{"name":"Luminal B breast cancer","type":"exact"},{"name":"Luminal B breast carcinoma","type":"exact"},{"name":"Luminal B estrogen receptor positive subtype of breast carcinoma","type":"exact"},{"name":"Luminal B oestrogen receptor positive subtype of breast carcinoma","type":"exact"},{"name":"Luminal B subtype of breast carcinoma","type":"exact"}],"termid":"MONDO:0021115","xrefs":{"Monarch":{"xref_id":"0021115"}}}


id: PATO:0000168
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000168 relative time (obsolete PATO:0000168)","termid":"PATO:0000168"}


id: FYPO:0006988
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 dimethylation of lysine at position 9 of histone H3 occurs to a greater extent than normal at transposable elements.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H3-K9 dimethylation during vegetative growth","termid":"FYPO:0000873"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002274","FYPO:0000002","FYPO:0001320","FYPO:0002494","FYPO:0001985"],"is_obsolete":false,"name":"increased histone H3-K9 dimethylation at transposable element during vegetative growth","synonyms":[{"name":"increased histone H3 K9 dimethylation at transposable element during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 dimethylation at transposable element during mitotic cell cycle","type":"related"},{"name":"increased histone H3-K9 dimethylation at transposon during vegetative growth","type":"exact"},{"name":"increased histone H3K9 dimethylation at transposable element during vegetative growth","type":"exact"},{"name":"increased histone H3K9me2 at transposable element during vegetative growth","type":"exact"},{"name":"increased histone lysine H3 K9 dimethylation at transposable element during vegetative growth","type":"exact"}],"termid":"FYPO:0006988"}


id: GO:0120221
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in maintaining the planar beating pattern of ciliary movement pattern. Connection between the outer doublets and the central pair via the radial spokes constrains ciliary movement to the planar beating pattern. Cilia that lack this connection, such as those in the embryonic node or Kupfer's vesicle, display radial movement.","definition_xrefs":["GOC:krc","PMID:26506310"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cilium movement","termid":"GO:0003352"}],"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":"maintenance of ciliary planar beating movement pattern","termid":"GO:0120221"}


id: GO:2001028
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of endothelial cell chemotaxis.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of endothelial cell migration","termid":"GO:0010595"},{"relation_name":"is_a","term_name":"positive regulation of chemotaxis","termid":"GO:0050921"},{"relation_name":"is_a","term_name":"regulation of endothelial cell chemotaxis","termid":"GO:2001026"},{"relation_name":"positively_regulates","term_name":"endothelial cell chemotaxis","termid":"GO:0035767"}],"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 endothelial cell chemotaxis","termid":"GO:2001028"}


id: GO:0008703
data:
  {"annotated_genes":["SJAG_00491"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[67107],"is_not":false,"summary":null,"term":"GO:0008703"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-amino-6-(5-phosphoribitylamino)uracil + NADP+ = 5-amino-6-(5-phosphoribosylamino)uracil + H+ + NADPH.","definition_xrefs":["RHEA:17845","EC:1.1.1.193"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00491":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"5-amino-6-(5-phosphoribosylamino)uracil reductase activity","references_by_uniquename":{"GO_REF:0000002":null},"secondary_identifiers":["KEGG_REACTION:R03458","MetaCyc:RIBOFLAVINSYNREDUC-RXN"],"synonyms":[{"name":"5-amino-6-(5'-phosphoribosylamino)uracil reductase activity","type":"exact"},{"name":"5-amino-6-(5-phosphoribitylamino)uracil:NADP+ 1'-oxidoreductase activity","type":"related"},{"name":"aminodioxyphosphoribosylaminopyrimidine reductase activity","type":"related"}],"termid":"GO:0008703","terms_by_termid":{"GO:0008703":null}}


id: PATO:0000823
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000823 quinine taste (obsolete PATO:0000823)","termid":"PATO:0000823"}


id: MONDO:1010517
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Holoprosencephaly that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"holoprosencephaly, non-human animal","termid":"MONDO:1010033"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"holoprosencephaly, horse","secondary_identifiers":["OMIA:000478-9796"],"termid":"MONDO:1010517","xrefs":{"Monarch":{"xref_id":"1010517"}}}


id: GO:0032228
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of GABAergic synaptic transmission, the process of communication from a neuron to another neuron across a synapse using the neurotransmitter gamma-aminobutyric acid (GABA).","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation of chemical synaptic transmission","termid":"GO:0050804"},{"relation_name":"regulates","term_name":"synaptic transmission, GABAergic","termid":"GO:0051932"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of synaptic transmission, GABAergic","termid":"GO:0032228"}


id: PBO:0062077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily A member 8 (gene/pseudogene)","termid":"PBO:0062077"}


id: GO:0016471
data:
  {"annotated_genes":["SJAG_04015","SJAG_03962","SJAG_01397","SJAG_00136","SJAG_04955","SJAG_01913","SJAG_00516","SJAG_02023","SJAG_01447","SJAG_00212","SJAG_05294","SJAG_02782","SJAG_03406","SJAG_01471","SJAG_01817"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[105703,91930,93826,62649,97430,101732,97611],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000220"},{"annotations":[61008,98393,111694,104467,100698,72896,89801,120593],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000221"}]},"cv_name":"cellular_component","definition":"A proton-transporting two-sector ATPase complex found in the vacuolar membrane, where it acts as a proton pump to mediate acidification of the vacuolar lumen.","definition_xrefs":["GOC:mah","ISBN:0716743663","PMID:16449553"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proton-transporting V-type ATPase complex","termid":"GO:0033176"},{"relation_name":"part_of","term_name":"vacuolar membrane","termid":"GO:0005774"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00136":null,"SJAG_00212":null,"SJAG_00516":null,"SJAG_01397":null,"SJAG_01447":null,"SJAG_01471":null,"SJAG_01817":null,"SJAG_01913":null,"SJAG_02023":null,"SJAG_02782":null,"SJAG_03406":null,"SJAG_03962":null,"SJAG_04015":null,"SJAG_04955":null,"SJAG_05294":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005773"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005773","GO:0005737"],"is_obsolete":false,"name":"vacuolar proton-transporting V-type ATPase complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"vacuolar hydrogen-translocating V-type ATPase complex","type":"exact"}],"termid":"GO:0016471","terms_by_termid":{"GO:0000220":null,"GO:0000221":null}}


id: PBO:0027404
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_chromatin_at_replication_origin","termid":"PBO:0027404"}


id: MONDO:0002713
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic neoplasm that involves the space between the vertebral periosteum and dura mater that surrounds the spinal cord.","definition_xrefs":["NCIT:C3019"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vertebral column disorder","termid":"MONDO:0000812"},{"relation_name":"is_a","term_name":"neoplasm","termid":"MONDO:0005070"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epidural spinal canal neoplasm","secondary_identifiers":["UMLS:C0014536","MESH:D015174","DOID:3618","MEDGEN:4504"],"synonyms":[{"name":"epidural neoplasm","type":"exact"},{"name":"epidural space neoplasm","type":"exact"},{"name":"epidural space tumor","type":"exact"},{"name":"epidural space tumour","type":"exact"},{"name":"epidural spinal canal neoplasm","type":"exact"},{"name":"epidural spinal canal tumor","type":"exact"},{"name":"epidural spinal canal tumors","type":"exact"},{"name":"epidural spinal canal tumour","type":"exact"},{"name":"epidural spinal canal tumours","type":"exact"},{"name":"epidural spinal neoplasms","type":"exact"},{"name":"epidural spinal tumors","type":"exact"},{"name":"epidural spinal tumours","type":"exact"},{"name":"epidural tumor","type":"exact"},{"name":"epidural tumour","type":"exact"},{"name":"extradural neoplasm","type":"exact"},{"name":"extradural spinal canal neoplasm","type":"exact"},{"name":"extradural spinal canal neoplasms","type":"exact"},{"name":"extradural spinal canal tumor","type":"exact"},{"name":"extradural spinal canal tumour","type":"exact"},{"name":"extradural spinal neoplasms","type":"exact"},{"name":"extradural spinal tumors","type":"exact"},{"name":"extradural spinal tumours","type":"exact"},{"name":"extradural tumor","type":"exact"},{"name":"extradural tumour","type":"exact"},{"name":"neoplasm of epidural space","type":"exact"},{"name":"neoplasm of epidural spinal canal","type":"exact"},{"name":"neoplasm of extradural spinal canal","type":"exact"},{"name":"neoplasm of the epidural spinal canal","type":"exact"},{"name":"neoplasm of the extradural spinal canal","type":"exact"},{"name":"tumor of epidural space","type":"exact"},{"name":"tumor of epidural spinal canal","type":"exact"},{"name":"tumor of extradural spinal canal","type":"exact"},{"name":"tumor of the epidural spinal canal","type":"exact"},{"name":"tumor of the extradural spinal canal","type":"exact"},{"name":"tumour of epidural space","type":"exact"},{"name":"tumour of epidural spinal canal","type":"exact"},{"name":"tumour of extradural spinal canal","type":"exact"},{"name":"tumour of the epidural spinal canal","type":"exact"},{"name":"tumour of the extradural spinal canal","type":"exact"}],"termid":"MONDO:0002713","xrefs":{"Monarch":{"xref_id":"0002713"}}}


id: SO:0001218
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An insertion that derives from another organism, via the use of recombinant DNA technology.","definition_xrefs":["SO:bm"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"transgenic","termid":"SO:0000781"},{"relation_name":"is_a","term_name":"insertion","termid":"SO:0000667"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transgenic_insertion","synonyms":[{"name":"transgenic insertion","type":"exact"}],"termid":"SO:0001218"}


id: PBO:0090819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cortical variant C2 domain protein, human FAM102A and FAM102B ortholog, implicated in signalling or endocytosis","termid":"PBO:0090819"}


id: PBO:0051083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy constant gamma 1 (G1m marker)","termid":"PBO:0051083"}


id: PBO:0056459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAS1 proto-oncogene like, G protein-coupled receptor","termid":"PBO:0056459"}


id: MONDO:0018201
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A germ cell tumor arising in an anatomic site other than the testis or ovary (e.g., central nervous system, lung, mediastinum, and retroperitoneum).","definition_xrefs":["NCIT:C3918"],"direct_ancestors":[{"relation_name":"is_a","term_name":"germ cell tumor","termid":"MONDO:0005040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"extragonadal germ cell tumor","secondary_identifiers":["GARD:9325","Orphanet:363579","MEDGEN:75506","UMLS:C0262963"],"synonyms":[{"name":"extragonadal germ cell neoplasm","type":"exact"},{"name":"extragonadal germ cell neoplasms","type":"exact"},{"name":"extragonadal germ cell tumor","type":"exact"},{"name":"neoplasm of extragonadal germ cell","type":"exact"},{"name":"neoplasm of the extragonadal germ cell","type":"exact"},{"name":"primary extragonadal germ cell tumor","type":"exact"},{"name":"primary extragonadal germ cell tumour","type":"exact"},{"name":"tumor of extragonadal germ cell","type":"exact"},{"name":"tumor of the extragonadal germ cell","type":"exact"},{"name":"tumour of extragonadal germ cell","type":"exact"},{"name":"tumour of the extragonadal germ cell","type":"exact"}],"termid":"MONDO:0018201","xrefs":{"Monarch":{"xref_id":"0018201"}}}


id: PATO:0001131
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001131 absolute ratio value (obsolete PATO:0001131)","termid":"PATO:0001131"}


id: PBO:0049323
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTF2A1 antisense RNA 1","termid":"PBO:0049323"}


id: GO:0097314
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of the apoptosome, a multisubunit protein complex involved in the signaling phase of the apoptotic process.","definition_xrefs":["GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"},{"relation_name":"part_of","term_name":"apoptotic signaling pathway","termid":"GO:0097190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0023052","GO:0044085","GO:0065003"],"is_obsolete":false,"name":"apoptosome assembly","synonyms":[{"name":"apoptosome formation","type":"exact"}],"termid":"GO:0097314"}


id: PBO:0046092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 4A2 pseudogene 3","termid":"PBO:0046092"}


id: PBO:0008880
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3-containing 90S preribosome complex subunit Cms1 (predicted)","termid":"PBO:0008880"}


id: GO:0019765
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:add"],"gene_count":0,"genotype_count":0,"name":"obsolete low affinity Fc receptor activity (obsolete GO:0019765)","synonyms":[{"name":"low affinity Fc receptor activity","type":"exact"}],"termid":"GO:0019765"}


id: PBO:0001810
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.2.2.21","termid":"PBO:0001810"}


id: MONDO:0013517
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Abnormal clinical manifestations of beta thalassemia that are as a result of the underlying genotype.","definition_xrefs":["SCDO:0000251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta thalassemia","termid":"MONDO:0019402"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"beta-thalassemia HBB/LCRB","secondary_identifiers":["OMIM:613985"],"synonyms":[{"name":"beta-thalassemia","type":"related"},{"name":"thalassemia, beta","type":"exact"},{"name":"thalassemia, hispanic gamma-delta-beta","type":"exact"}],"termid":"MONDO:0013517","xrefs":{"Monarch":{"xref_id":"0013517"}}}


id: MONDO:0000574
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete CD45 deficiency (obsolete MONDO:0000574)","termid":"MONDO:0000574","xrefs":{"Monarch":{"xref_id":"0000574"}}}


id: MONDO:1012180
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myoclonus epilepsy of Lafora, non-human animal","termid":"MONDO:1011627"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myoclonus epilepsy of Lafora, Eurasian elk","secondary_identifiers":["OMIA:000690-9852"],"termid":"MONDO:1012180","xrefs":{"Monarch":{"xref_id":"1012180"}}}


id: MONDO:0007600
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition in which the kidneys do not absorb certain substances into the body. These substances, such as cysteine, fructose, galactose, or glycogen, are lost in the urine. Fanconi syndrome is thought to be caused by genetic and environmental factors, and it may be diagnosed at any age. Symptoms of Fanconi syndrome include increased urine production (which may cause dehydration), weakness, and abnormalities of the bones.","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited Fanconi renotubular syndrome","termid":"MONDO:0100238"}],"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":"primary Fanconi syndrome","secondary_identifiers":["UMLS:C1857395","GARD:9118","MEDGEN:341765","NCIT:C123229","Orphanet:3337"],"synonyms":[{"name":"FRTS1","type":"narrow"},{"name":"Fanconi renotubular syndrome 1","type":"narrow"},{"name":"primary Fanconi renotubular syndrome","type":"narrow"}],"termid":"MONDO:0007600","xrefs":{"Monarch":{"xref_id":"0007600"}}}


id: GO:0019845
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. The function of a toxin formed by a microorganism and secreted into the surrounding medium.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete exotoxin activity (obsolete GO:0019845)","synonyms":[{"name":"exotoxin activity","type":"exact"}],"termid":"GO:0019845"}


id: FYPO:0004771
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 glycine measured in the vacuole is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in vacuole","termid":"FYPO:0001730"},{"relation_name":"is_a","term_name":"increased cellular amino acid level","termid":"FYPO:0003986"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased vacuolar glycine level","synonyms":[{"name":"increased level of glycine in vacuole","type":"exact"},{"name":"increased vacuolar glycine level during mitotic cell cycle","type":"related"},{"name":"increased vacuolar glycine level during vegetative growth","type":"exact"}],"termid":"FYPO:0004771"}


id: MONDO:0017831
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mild Canavan disease (CD) is a neurodegenerative disorder characterized by mild speech delay or motor development.","definition_xrefs":["Orphanet:314918"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Canavan disease","termid":"MONDO:0010079"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005066"],"is_obsolete":false,"name":"mild Canavan disease","secondary_identifiers":["MEDGEN:865564","GARD:17438","UMLS:C4017127"],"synonyms":[{"name":"juvenile Canavan disease","type":"exact"}],"termid":"MONDO:0017831","xrefs":{"Monarch":{"xref_id":"0017831"}}}


id: GO:0010648
data:
  {"annotated_genes":["SJAG_02169","SJAG_06270","SJAG_03592","SJAG_01983","SJAG_01297","SJAG_00266","SJAG_03185","SJAG_00990","SJAG_01464","SJAG_00824","SJAG_04943","SJAG_01253","SJAG_05346","SJAG_03974","SJAG_01245","SJAG_02013","SJAG_02514","SJAG_03501","SJAG_04825","SJAG_05000","SJAG_00642","SJAG_03508","SJAG_02451","SJAG_00875","SJAG_02389","SJAG_00289","SJAG_02233","SJAG_01142","SJAG_02392","SJAG_02231","SJAG_03355","SJAG_02858","SJAG_02379","SJAG_04249","SJAG_04910","SJAG_04551","SJAG_00229","SJAG_03678","SJAG_00526","SJAG_03486","SJAG_04259","SJAG_04455","SJAG_00293","SJAG_00883","SJAG_02336","SJAG_03089","SJAG_00209","SJAG_00169","SJAG_01679","SJAG_03072","SJAG_02000","SJAG_03353","SJAG_03799","SJAG_02426","SJAG_01114","SJAG_01386","SJAG_00610","SJAG_01790","SJAG_00975","SJAG_03126","SJAG_02481","SJAG_04522","SJAG_03681","SJAG_00457","SJAG_02311","SJAG_03263","SJAG_01184","SJAG_02765","SJAG_00991","SJAG_04206","SJAG_03893","SJAG_00424","SJAG_04462"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115622,109043,101373,92492,110070,113792,105688,116110,117741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902426"},{"annotations":[118222,109785,94523,102227,93862],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110034"},{"annotations":[102786,117968],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106057"},{"annotations":[101222,97632,109423,120182,108856,105596],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903138"},{"annotations":[103937,91209,104641],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902660"},{"annotations":[95972],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140499"},{"annotations":[97754,118927,101224,96815,93440,120183],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903753"},{"annotations":[108949,89973],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180040"},{"annotations":[95095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090029"},{"annotations":[74008],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046580"},{"annotations":[73225],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035024"},{"annotations":[95230,92496,101375,103065,94616,111993,97419,108911,74589,93508,106847,117744,94701,109044,109354],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031030"},{"annotations":[113544,93011,107702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000639"},{"annotations":[74852],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032007"},{"annotations":[97881,81620,108961,117969,89788,104810,114996,116416,100660,115814,118326,75338,75231,119893,111090,95101,62840,103249,101357,118890,106937,120086,111497],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904262"},{"annotations":[118115],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903940"}]},"cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of cell communication. 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id: PBO:0039606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alanyl aminopeptidase, membrane","termid":"PBO:0039606"}


id: PATO:0002324
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"The temporal relation between the end of the process with respect to a reference process.","definition_xrefs":["PATOC:LC"],"direct_ancestors":[{"relation_name":"is_a","term_name":"temporal distribution quality","termid":"PATO:0002323"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"offset quality","termid":"PATO:0002324"}


id: GO:0019150
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + D-ribulose = ADP + D-ribulose 5-phosphate.","definition_xrefs":["EC:2.7.1.47"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"},{"relation_name":"is_a","term_name":"carbohydrate kinase activity","termid":"GO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016301","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"D-ribulokinase activity","secondary_identifiers":["RHEA:17601","MetaCyc:D-RIBULOKIN-RXN"],"synonyms":[{"name":"ATP:D-ribulose 5-phosphotransferase activity","type":"related"},{"name":"D-ribulokinase (phosphorylating)","type":"related"}],"termid":"GO:0019150"}


id: PBO:0084116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Helicase-like protein encoded within the telomeric Y' element; induced by treatment with 8-methoxypsoralen and UVA irradiation; SWAT-GFP and mCherry fusion proteins localize to the nucleus","termid":"PBO:0084116"}


id: MONDO:0015004
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any dystonic disorder in which the cause of the disease is a mutation in the KMT2B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited dystonia","termid":"MONDO:0044807"}],"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":"dystonia 28, childhood-onset","secondary_identifiers":["DOID:0060936","Orphanet:589618","GARD:22359","UMLS:C4310633","MEDGEN:934600","EFO:0009301","OMIM:617284"],"synonyms":[{"name":"DYT28","type":"exact"},{"name":"KMT2B dystonic disorder","type":"exact"},{"name":"dystonia 28, childhood-onset","type":"exact"},{"name":"dystonia 28, childhood-onset; DYT28","type":"exact"},{"name":"dystonic disorder caused by mutation in KMT2B","type":"exact"}],"termid":"MONDO:0015004","xrefs":{"Monarch":{"xref_id":"0015004"}}}


id: GO:0005019
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with platelet-derived growth factor isoform PDGF-BB or PDGF-AB to initiate a change in cell activity.","definition_xrefs":["PMID:1657917"],"direct_ancestors":[{"relation_name":"is_a","term_name":"platelet-derived growth factor receptor activity","termid":"GO:0005017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016301","GO:0003674","GO:0003824","GO:0140096","GO:0016740","GO:0004672","GO:0038023"],"is_obsolete":false,"name":"platelet-derived growth factor beta-receptor activity","synonyms":[{"name":"PDGF beta-receptor activity","type":"exact"},{"name":"betaPDGF receptor activity","type":"related"}],"termid":"GO:0005019"}


id: MONDO:0013978
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the PNPT1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"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:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 70","secondary_identifiers":["DOID:0110521","GARD:22646","UMLS:C1824925","MEDGEN:760477","OMIM:614934"],"synonyms":[{"name":"DFNB70","type":"narrow"},{"name":"PNPT1 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 70","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 70","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in PNPT1","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 70","type":"narrow"},{"name":"deafness, autosomal recessive 70","type":"narrow"},{"name":"deafness, autosomal recessive type 70","type":"narrow"}],"termid":"MONDO:0013978","xrefs":{"Monarch":{"xref_id":"0013978"}}}


id: MONDO:0850122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lung adenocarcinoma","termid":"MONDO:0005061"}],"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":"solid adenocarcinoma with mucin production","secondary_identifiers":["DOID:0080306"],"termid":"MONDO:0850122","xrefs":{"Monarch":{"xref_id":"0850122"}}}


id: MONDO:0010822
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Warburg micro syndrome in which the cause of the disease is a mutation in the RAB3GAP1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Warburg micro syndrome","termid":"MONDO:0016649"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0006025","MONDO:0005328"],"is_obsolete":false,"name":"Warburg micro syndrome 1","secondary_identifiers":["OMIM:600118","DOID:0110716","MEDGEN:333142","UMLS:C1838625"],"synonyms":[{"name":"RAB3GAP1 Warburg micro syndrome","type":"exact"},{"name":"WARBM1","type":"exact"},{"name":"WARBURG micro syndrome 1","type":"related"},{"name":"Warburg micro syndrome 1","type":"exact"},{"name":"Warburg micro syndrome caused by mutation in RAB3GAP1","type":"exact"},{"name":"Warburg micro syndrome type 1","type":"exact"},{"name":"micro syndrome","type":"related"},{"name":"micro syndrome 1","type":"exact"}],"termid":"MONDO:0010822","xrefs":{"Monarch":{"xref_id":"0010822"}}}


id: PBO:0039282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALG1 like 11, pseudogene","termid":"PBO:0039282"}


id: PATO:0000355
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000355 enzyme composition value (obsolete PATO:0000355)","termid":"PATO:0000355"}


id: GO:0035429
data:
  {"annotated_genes":["SJAG_04905","SJAG_04920"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94264],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140270"},{"annotations":[91700],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0035432"}]},"cv_name":"biological_process","definition":"The process in which gluconate is transported across a membrane. Gluconate is the aldonic acid derived from glucose.","definition_xrefs":["ISBN:0198506732","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldonate transmembrane transport","termid":"GO:0042873"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04905":null,"SJAG_04920":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"gluconate transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0015725"],"synonyms":[{"name":"gluconate membrane transport","type":"exact"},{"name":"gluconate transport","type":"related"}],"termid":"GO:0035429","terms_by_termid":{"GO:0035432":null,"GO:0140270":null}}


id: PBO:0075737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRP14 pseudogene 5","termid":"PBO:0075737"}


id: PBO:0039675
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adaptor related protein complex 5 subunit beta 1","termid":"PBO:0039675"}


id: PBO:0062408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 35 pseudogene","termid":"PBO:0062408"}


id: PBO:0050831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypoxia up-regulated 1","termid":"PBO:0050831"}


id: FYPO:0006162
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to chromatin is normal (i.e. indistinguishable from wild type) during the first meiotic nuclear division.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization during meiosis","termid":"FYPO:0003790"},{"relation_name":"is_a","term_name":"normal protein localization to chromatin","termid":"FYPO:0006163"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to chromatin during meiosis I","synonyms":[{"name":"normal protein localisation to chromatin during meiosis I","type":"exact"},{"name":"normal protein localization to chromatin during first meiotic nuclear division","type":"exact"}],"termid":"FYPO:0006162"}


id: PBO:0087280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Short open reading frame, shows evidence of translation; may be new protein-coding gene that originated de novo from noncoding sequence; same allele found in at least 33 other S. cerevisiae strains; at least 3 strains have a second allele with three nucleotide substitutions leading to two amino acid differences","termid":"PBO:0087280"}


id: MONDO:0850230
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An urticaria that is characterized by the presence of urticaria for a period exceeding 6 weeks, assuming symptoms for most days of the week.","definition_xrefs":["DOID:0080747"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urticaria","termid":"MONDO:0005492"}],"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":"chronic urticaria","secondary_identifiers":["UMLS:C0263338","icd11.foundation:901000137","MEDGEN:537829"],"termid":"MONDO:0850230","xrefs":{"Monarch":{"xref_id":"0850230"}}}


id: GO:0005749
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A protein complex located in the mitochondrial inner membrane that forms part of the mitochondrial respiratory chain. Contains the four polypeptide subunits of succinate dehydrogenase, flavin-adenine dinucleotide and iron-sulfur. Catalyzes the oxidation of succinate by ubiquinone. Connects the TCA cycle with the respiratory chain.","definition_xrefs":["ISBN:0198547684","GOC:mtg_sensu","GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrial respiratory chain complex II, succinate dehydrogenase complex (ubiquinone) (obsolete GO:0005749)","synonyms":[{"name":"mitochondrial fumarate reductase complex","type":"exact"}],"termid":"GO:0005749"}


id: GO:0090022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of neutrophil chemotaxis. Neutrophil chemotaxis is the directed movement of a neutrophil cell, the most numerous polymorphonuclear leukocyte found in the blood, in response to an external stimulus, usually an infection or wounding.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of granulocyte chemotaxis","termid":"GO:0071622"},{"relation_name":"is_a","term_name":"regulation of neutrophil migration","termid":"GO:1902622"},{"relation_name":"regulates","term_name":"neutrophil chemotaxis","termid":"GO:0030593"}],"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 neutrophil chemotaxis","termid":"GO:0090022"}


id: GO:0098595
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The space between the membrane of an oocyte and a surrounding membranous structure (zona pellucida or perivitelline membrane).","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular region","termid":"GO:0005576"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005576"}],"interesting_parent_ids":["GO:0005576","GO:0005575"],"is_obsolete":false,"name":"perivitelline space","termid":"GO:0098595"}


id: PBO:0052862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 5-5","termid":"PBO:0052862"}


id: MONDO:0009684
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":"muscular hypertonia, lethal","secondary_identifiers":["MESH:C564982","MEDGEN:342600","UMLS:C1850827","OMIM:254120"],"synonyms":[{"name":"muscular hypertonia, lethal","type":"exact"}],"termid":"MONDO:0009684","xrefs":{"Monarch":{"xref_id":"0009684"}}}


id: PBO:0090123
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial inner membrane protein Mdm31, unknown biological role, interacts with ERMES","termid":"PBO:0090123"}


