CD6 Polyclonal Antibody, 50ul[BT-AP01864] Cellular Function Assays Alternatively spliced transcript variants encoding

Alternatively spliced transcript variants encoding different proteins have been identified

This gene is a member of the Antp homeobox family and encodes a protein with a homeobox DNA-binding domain

NEPH1 is a member of the nephrin-like protein family

the most common form of syndromic deafness

Has also been implicated in tumor invasion and metastasis

CD6 Polyclonal Antibody, 50ul[BT-AP01864] Cellular Function Assays Alternatively spliced transcript variants encodingThe product of CLCN7 belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. CLCN7 encodes chloride channel 7. Defects in CLCN7 are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers