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FANCI
FA complementation group IFLJ10719, KIAA1794
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]
Top validated antibodies |
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| Proteintech Group |  20789-1-AP |
4 references | Polyclonal |
WB
EL
ICC
IP
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| Invitrogen Antibodies | 20789-1-AP |
Polyclonal |
WB
ICC
IP
OA
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| NovoPro Bioscience Inc. | 110520 |
Polyclonal |
WB
EL
ICC
IP
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| FineTest Biotech | FNab03009 |
Polyclonal |
WB
EL
ICC
IP
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| Novus Biologicals | NB100-60447 |
1 references | Polyclonal |
WB
IP
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