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)

Haploinsufficiency of this protein can cause maternal riboflavin deficiency

RIN1 binds c-Abl and

This enzyme highly contributes to the antioxidant defense system

2000 [PubMed 10799485])

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