FANCG

FANCG
Identifiers
Aliases	FANCG, FAG, XRCC9, Fanconi anemia complementation group G, FA complementation group G
External IDs	OMIM: 602956; MGI: 1926471; HomoloGene: 3402; GeneCards: FANCG; OMA:FANCG - orthologs
Gene location (Human)
Chr.	Chromosome 9 (human)
End	35,080,004 bp
Gene location (Mouse)
Chr.	Chromosome 4 (mouse)
End	43,010,506 bp
RNA expression pattern
	Top expressed in
	ventricular zone; ; ganglionic eminence; ; right hemisphere of cerebellum; ; mucosa of transverse colon; ; granulocyte; ; body of pancreas; ; left testis; ; right testis; ; rectum; ; right frontal lobe;
	Top expressed in
	spermatocyte; ; aortic valve; ; neural layer of retina; ; spermatid; ; ascending aorta; ; yolk sac; ; seminiferous tubule; ; cumulus cell; ; granulocyte; ; thymus;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	damaged DNA binding; protein binding; signal transducer activity;
Cellular component	plasma membrane; nucleolus; Fanconi anaemia nuclear complex; mitochondrion; nucleus; nucleoplasm; cytoplasm; cytosol; intracellular anatomical structure;
Biological process	ovarian follicle development; response to radiation; mitochondrion organization; interstrand cross-link repair; DNA repair; spermatid development; cellular response to DNA damage stimulus; phosphorelay signal transduction system;
	Sources:Amigo / QuickGO
Orthologs
	2189
	60534
	ENSG00000221829
	ENSMUSG00000028453
	O15287
	Q9EQR6
	NM_004629
	NM_001163233; NM_053081
	NP_004620
	NP_001156705; NP_444311
	Wikidata
View/Edit Human	View/Edit Mouse

Fanconi anemia group G protein is a protein that in humans is encoded by the FANCG gene.