IRPL1 Polyclonal Antibody, 100ul Cell Senescence Mutations in ITCH are a

Mutations in ITCH are a cause of syndromic multisystem autoimmune disease

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

The adiponectin receptors

lacking an intracellular serine/threonine kinase domain required for signaling

There is a pseudogene for TCEAL4 on chromosome 13

IRPL1 Polyclonal Antibody, 100ul Cell Senescence Mutations in ITCH are aThe 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