IRPL1 Polyclonal Antibody, 100ul Cell Senescence The product of KCNK12 has

The product of KCNK12 has not been shown to be a functional channel

Alternatively spliced transcript variants encoding different isoforms have been noted for PPP1R14A

Mutations in the genes that code for the collagen VI subunits result in the autosomal dominant disorder

lacking an intracellular serine/threonine kinase domain required for signaling

a state which is disrupted by inhibition of this novel serine protease

IRPL1 Polyclonal Antibody, 100ul Cell Senescence The product of KCNK12 hasThe protein encoded by this gene is a member of the interleukin 1 receptor family and is similar to the interleukin 1 accessory proteins. It is most closely related to interleukin 1 receptor accessory protein like 2 (IL1RAPL2). This gene and IL1RAPL2 are located at a region on chromosome X that is associated with X linked non syndromic mental retardation. Deletions and mutations in this gene were found in patients with mental retardation. This gene is