GTD2B Rabbit Polyclonal Antibody, 100ul Pipette Controller an autosomal dominant disorder characterized

an autosomal dominant disorder characterized by the growth of polyps in the gastrointestinal tract

Function: putative pheromone receptor

cardiac and smooth muscle isoforms are localized to the Z-disc and analogous dense bodies

Mutations in DOK7 are a cause of familial limb-girdle myasthenia autosomal recessive

Diseases associated with CSGALNACT1 include bell's palsy

GTD2B Rabbit Polyclonal Antibody, 100ul Pipette Controller an autosomal dominant disorder characterizedThis gene encodes a glycosylated phosphoprotein with a leucine zipper motif two helix loop helix motifs (I repeats) that are similar to domains found in the TFII I family of transcription factors one CHARLIE8 transposable element like sequence and a BED zinc finger. This gene lies within a region that is deleted in Williams Beuren syndrome. Alternatively spliced variants which encode different protein isoforms have been described; however not all