A1ATR Polyclonal Antibody, 50ul Reservoirs and Zellweger syndrome

and Zellweger syndrome

similarity:Belongs to the tubulin family

This gene encodes a microsomal protein expressed at high levels in androgen-sensitive tissues such as the prostate

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

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

A1ATR Polyclonal Antibody, 50ul Reservoirs and Zellweger syndromeThis 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.