NEK6 Polyclonal Antibody, 50ul Diagnostic Probes & Oligos Defects in ITGA7 are associated

Defects in ITGA7 are associated with congenital myopathy

the specific function of GPRC5D has not yet been determined

|subunit:Interacts with ATF7IP| ATF7IP2| POGZ| HCFC1| AATF and PHC2

a progressive neurologic developmental disorder and one of the most common causes of mental retardation in females

It functions through either direct interaction with components of the antigen receptor complexes

NEK6 Polyclonal Antibody, 50ul Diagnostic Probes & Oligos Defects in ITGA7 are associatedThe protein encoded by this gene is a kinase required for progression through the metaphase portion of mitosis. Inhibition of the encoded protein can lead to apoptosis. This protein also can enhance tumorigenesis by suppressing tumor cell senescence. Several transcript variants encoding a few different isoforms have been found for this gene.