FANCI

FANCI
Identifiers
Aliases	FANCI, KIAA1794, Fanconi anemia complementation group I, FA complementation group I
External IDs	OMIM: 611360; MGI: 2384790; HomoloGene: 49530; GeneCards: FANCI; OMA:FANCI - orthologs
Gene location (Human)
Chr.	Chromosome 15 (human)
End	89,317,261 bp
Gene location (Mouse)
Chr.	Chromosome 7 (mouse)
End	79,100,012 bp
RNA expression pattern
	Top expressed in
	ventricular zone; ; secondary oocyte; ; testicle; ; ganglionic eminence; ; right testis; ; left testis; ; gonad; ; bone marrow cells; ; rectum; ; trabecular bone;
	Top expressed in
	otic vesicle; ; otic placode; ; spermatocyte; ; saccule; ; spermatid; ; fetal liver hematopoietic progenitor cell; ; primary oocyte; ; secondary oocyte; ; epiblast; ; zygote;
	More reference expression data
	; ;
	More reference expression data
Gene ontology
Molecular function	DNA binding; protein binding; DNA polymerase binding;
Cellular component	membrane; nucleus; nucleoplasm; cytosol;
Biological process	cell cycle; mitotic G2 DNA damage checkpoint signaling; positive regulation of protein ubiquitination; interstrand cross-link repair; cellular response to DNA damage stimulus; DNA repair;
	Sources:Amigo / QuickGO
Orthologs
	55215
	208836
	ENSG00000140525
	ENSMUSG00000039187
	Q9NVI1
	Q8K368
	NM_001113378; NM_018193; NM_001376910; NM_001376911
	NM_145946
	NP_001106849; NP_060663; NP_001363839; NP_001363840
	NP_666058
	Wikidata
View/Edit Human	View/Edit Mouse

Fanconi anemia, complementation group I (FANCI) also known as KIAA1794, is a protein which in humans is encoded by the FANCI gene. Mutations in the FANCI gene are known to cause Fanconi anemia.