FANCA Polyclonal Antibody, 50ul sgRNA customized design Mutations in this gene are

Mutations in this gene are associated with ectodermal dysplasia| and cleft lip/palate syndrome 3 (EEC3)

This enzyme highly contributes to the antioxidant defense system

this proteolipid is localized in compact myelin of cells in the nervous system and has been implicated in myelin biogenesis and/or function

2000 [PubMed 10799485])

The encoded protein may play a critical role in actin-cytoskeletal reorganization during facial morphogenesis

FANCA Polyclonal Antibody, 50ul sgRNA customized design Mutations in this gene areThe 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