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. [provided by RefSeq, Jul 2008].
Colnaghi, Jones, Cotto-Rios, Schindler, Hanenberg, Huang: "Patient-derived C-terminal mutation of FANCI causes protein mislocalization and reveals putative EDGE motif function in DNA repair." in: Blood, Vol. 117, Issue 7, pp. 2247-56, (2011) (PubMed).
Yuan, El Hokayem, Zhou, Zhang: "FANCI protein binds to DNA and interacts with FANCD2 to recognize branched structures." in: The Journal of biological chemistry, Vol. 284, Issue 36, pp. 24443-52, (2009) (PubMed).
Chu, Wang, Lu, Chou, Yang, Chang: "Involvement of p29 in DNA damage responses and Fanconi anemia pathway." in: Carcinogenesis, Vol. 30, Issue 10, pp. 1710-6, (2009) (PubMed).
Aliases for FANCI 抗体
Fanconi anemia complementation group I (FANCI) 抗体 Fanconi anemia, complementation group I (Fanci) 抗体 KIAA1794 抗体