S23A1 Rabbit Polyclonal Antibody, 50ul Sampling Tubes A mutation in this gene

A mutation in this gene results in one form of Zellweger syndrome

form a gene cluster on chromosome 2q

and is a member of a small gene family

This receptor is known to be expressed in normal enterochromaffin cells and in gastrointestinal neuroendocrine carcinoma cells

Knockout studies in mice suggested the role of this

S23A1 Rabbit Polyclonal Antibody, 50ul Sampling Tubes A mutation in this geneThe absorption of vitamin C into the body and its distribution to organs requires two sodium dependent vitamin C transporters. This gene encodes one of the two transporters. The encoded protein is active in bulk vitamin C transport involving epithelial surfaces. Previously this gene had an official symbol of SLC23A2. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.