Tissue expression
Cell line expression
Protein structure
FANCD2
FA complementation group D2FA-D2, FACD, FAD, FANCD
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 D2. This protein is monoubiquinated in response to DNA damage, resulting in its localization to nuclear foci with other proteins (BRCA1 AND BRCA2) involved in homology-directed DNA repair. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Top validated antibodies |
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Novus Biologicals | NB100-182 | 167 references | Polyclonal |
WB
ICC
IP
IHC
FC
BN
ChIP
|
|
GeneTex | GTX30142 | 10 references | Polyclonal |
WB
ICC
IP
IHC
FC
|
|
Invitrogen Antibodies | PA1-16548 | 1 references | Polyclonal |
WB
ICC
IP
IHC
FC
ChIP
OA
|
|
antibodies-online | ABIN151329 | 131 references | Polyclonal |
WB
ICC
IP
IHC
FC
|
|
Proteintech Group | 24006-1-AP | 1 references | Polyclonal |
WB
EL
IP
IHC |
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