GTD2B Rabbit Polyclonal Antibody, 100ul Pipette Controller Three transcript variants encoding different

Three transcript variants encoding different isoforms have been found for CYB5A

Diseases associated with CSGALNACT1 include bell's palsy

this protein is likely involved in hair formation and spermatogenesis in human as well

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

GTD2B Rabbit Polyclonal Antibody, 100ul Pipette Controller Three transcript variants encoding differentThis 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