SIA8B Polyclonal Antibody, 50ul Sampling Tubes Mutations in the corresponding AQP2

Mutations in the corresponding AQP2 gene cause a rare form of diabetes known as nephrogenic diabetes insipidus

Mutations in this gene are associated with arrhythmogenic right ventricular dysplasia-11

The homeobox D10 functions as a sequence-specific transcription factor that is expressed in the developing limb buds and is involved in differentiation and limb development

transient receptor potential cation channel) encodes a member of the polycystin protein family

SIA8B Polyclonal Antibody, 50ul Sampling Tubes Mutations in the corresponding AQP2The protein encoded by this gene is a type II membrane protein that is thought to catalyze the transfer of sialic acid from CMP sialic acid to N linked oligosaccharides and glycoproteins. The encoded protein may be found in the Golgi apparatus and may be involved in the production of polysialic acid, a modulator of the adhesive properties of neural cell adhesion molecule (NCAM1). This protein is a member of glycosyltransferase family 29.