A1ATR Polyclonal Antibody, 50ul Reservoirs Mutations in this gene are

Mutations in this gene are associated with susceptibility to obesity in humans

which is necessary for homodimerization and for interaction with other leucine zipper proteins

DVL2 and/or DVL3)

similarity:Belongs to the tubulin family

Galactokinase is a major enzyme for the metabolism of galactose and its deficiency causes congenital cataracts during infancy and presenile cataracts in the adult population

A1ATR Polyclonal Antibody, 50ul Reservoirs Mutations in this gene areThis gene encodes a member of the serpin family of proteins a group of proteins that inhibit serine proteases. The encoded intracellular glycoprotein is localized at the endoplasmic reticulum. This gene is a polymorphic pseudogene with the non functional allele being predominant in some populations. Some individuals as represented by the reference genome allele contain a 2kb coding region deletion and a start code mutation.