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

Their protein structures resemble small leucine-rich proteoglycans found in the extracellular matrix

and a low-affinity receptor for IgE

DMD patients carry mutations which cause premature translation termination (nonsense or frame shift mutations)

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.