S6A19 Polyclonal Antibody, 20ul Cryopreservation Mutations in this gene have

Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly

a repair-deficient mutant that exhibits hypersensitivity to a number of different DNA-damaging agents

Different polymorphic forms

The induction of this gene by ionizing radiation occurs in certain cell lines regardless of p53 status

This protein is implicated in tRNA

S6A19 Polyclonal Antibody, 20ul Cryopreservation Mutations in this gene haveThis gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder.