GP179 Polyclonal Antibody, 100ul Pipette Controller MSH2 is frequently mutated in

MSH2 is frequently mutated in hereditary nonpolyposis colon cancer (HNPCC)

Diseases associated with TRAK2 include amyotrophic lateral sclerosis 2

Exon one encodes the leader peptide

This protein is expressed in the inner medulla of the kidney| and mediates rapid transepithelial urea transport across the inner medullary collecting duct

GP179 Polyclonal Antibody, 100ul Pipette Controller MSH2 is frequently mutated inThis gene encodes a member of the glutamate receptor subfamily of G protein coupled receptors. The encoded protein has an EGF like calcium binding domain and a seven transmembrane domain in the N terminal region of the protein. Mutations in this gene are associated with congenital stationary night blindness type 1E.