{"code":"C24385","name":"FANCG Gene","terminology":"ncit","version":"26.09d","conceptStatus":"DEFAULT","leaf":false,"active":true,"synonyms":[{"name":"FANCG Gene","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"caDSR"},{"name":"FANCG","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"CCPS"},{"name":"FANCG Gene","termType":"DN","type":"FULL_SYN","typeCode":"P90","source":"CTRP"},{"name":"FANCG","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"GDC"},{"name":"FANCG","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"HGNC","code":"HGNC:3588"},{"name":"FA Complementation Group G Gene","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"FANCG","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"FANCG Gene","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"FANCG Gene","type":"Display_Name","typeCode":"P107"},{"name":"FANCG Gene","type":"Preferred_Name","typeCode":"P108"}],"definitions":[{"definition":"This gene is involved in the maintenance of genomic integrity and nuclear signal transduction. Allelic variants of the gene are involved in Fanconi syndrome.","code":"P97","type":"DEFINITION","source":"NCI"}],"properties":[{"code":"P322","type":"Contributing_Source","value":"CCPS"},{"code":"P322","type":"Contributing_Source","value":"CTRP"},{"code":"P322","type":"Contributing_Source","value":"GDC"},{"code":"P369","type":"HGNC_ID","value":"HGNC:3588"},{"code":"P366","type":"Legacy Concept Name","value":"FANCG_Gene"},{"code":"P375","type":"Maps_To","value":"FANCG"},{"code":"P100","type":"OMIM_Number","value":"602956"},{"code":"P106","type":"Semantic_Type","value":"Gene or Genome"},{"code":"P207","type":"UMLS_CUI","value":"C1333532"}]}