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Antibody detects endogenous levels of total hFANCI.
The 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 I. Alternative splicing results in two transcript variants encoding different isoforms.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Fanconi anemia group I protein; Fanconi anemia group I protein homolog; Fanconi anemia, complementation group I; Protein FACI
Gene Aliases: FANCI; KIAA1794
UniProt ID: (Human) Q9NVI1, (Mouse) Q8K368
Entrez Gene ID: (Human) 55215, (Rat) 100360594, (Mouse) 208836
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