GATM Rabbit Polyclonal Antibody, 100ul Hepatocytes Diseases associated with HSPA14 include

Diseases associated with HSPA14 include tetralogy of fallot

The protein encoded by MAP3K10 is a member of the serine/threonine kinase family

Defects in this gene are a cause of xeroderma pigmentosum complementation group F (XP-F)

High levels of type XVI collagen have been found in fibroblasts and keratinocytes

coli mismatch repair gene mutS

GATM Rabbit Polyclonal Antibody, 100ul Hepatocytes Diseases associated with HSPA14 includeThis gene encodes a mitochondrial enzyme that belongs to the amidinotransferase family. This enzyme is involved in creatine biosynthesis whereby it catalyzes the transfer of a guanido group from L arginine to glycine resulting in guanidinoacetic acid the immediate precursor of creatine. Mutations in this gene cause arginine: glycine amidinotransferase deficiency an inborn error of creatine synthesis characterized by mental retardation language