FANCI Products

Description

FANCI is the gene underlying Fanconi anemia complementation group I, a syndrome characterized by a predisposition to cancer, congenital malformations, and pancytopenia. At the cellular level, FANCI is involved in the S and G2 phase DNA damage checkpoint and in the repair of DNA double-strand breaks and cross-links.

Bioinformatics

Entrez	55215 Human
Uniprot	AAH04277 Human NM_018193 Human Q9NVI1 Human
Product By Gene ID	55215
Alternate Names	Fanconi anemia group I protein Fanconi anemia, complementation group I KIAA1794FLJ10719 Protein FACI

Research Areas for FANCI

Find related products by research area and learn more about each of the different research areas below.

Neuroscience
Stem Cell Markers

Related FANCI Blog Posts

Check out the latest blog posts on FANCI.

FANCD2 and DNA damage repair Fanconi anemia (FA) is a genetically inherited disorder that yields cytogenetic instability, hypersensitivity to DNA crosslinking compounds and defective DNA repair. A variety of genes have been identified within the FA pathway that are referred t...    Read more.

Fanconi Antibodies and Cancer Research We at Novus Biologicals have an extensive antibody databasedevoted to the 13 Fanconi anaemia complementation (FANC) genes, which are involved in the recognition and repair of damaged DNA.The core complex of 8 proteins (FANCA, B, C, E, F, G, L and M)...    Read more.

Read more FANCI related blogs.