FANCD2 Polyclonal Antibody, 50ul Shaker&Mixing Mutations in this gene are

Mutations in this gene are associated with the autosomal recessive disorder congenital disorder of glycosylation| type IIk

An important paralog of PSKH1 is CAMK2D

The protein encoded by this gene contains a type 1 thrombospondin domain| which is present in thrombospondin| a number of proteins involved in the complement pathway| as well as in extracellular matrix proteins

are described

The product of this gene is involved in the response of gonadal tissues to follicle-stimulating hormone

FANCD2 Polyclonal Antibody, 50ul Shaker&Mixing 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