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Gene information for FANCG (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID2189
Official gene symbolFANCG
Full nameFanconi anemia, complementation group G
Aliases,FAG,XRCC9,
Gene summaryThe Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group G. [provided by RefSeq]
LocationChromosome: 9   Locus: 9p13
Gene position35080013 - 35073835  Map Viewer
Gene orientationminus
Gene size6179 bp
Gene sequence
OMIM ID602956