S38A8 Rabbit Polyclonal Antibody, 20ul Long RNA Synthesis Mutations in this gene were

Mutations in this gene were found in individuals with osteogenesis imperfecta

this protein is predominantly expressed in the sebaceous gland of the skin

This kinase is predominantly expressed in brain

An important paralog of this gene is ZNF718

hypertrophic DCM

S38A8 Rabbit Polyclonal Antibody, 20ul Long RNA Synthesis Mutations in this gene wereThis gene encodes a putative sodium dependent amino acid proton antiporter. The protein has eleven transmembrane domains an extracellular N terminus and an intracellular C terminal tail. The protein is a member of the SLC38 sodium coupled neutral amino acid transporter family of proteins. Mutations in this gene result in foveal hypoplasia with or without optic nerve misrouting and or anterior segment dysgenesis.