CYTSA Rabbit Polyclonal Antibody, 100ul Bottles CDKL3 was identified as a

CDKL3 was identified as a gene absent in leukemic patients with chromosome 5q deletion

NFKB1/p105

A mutation in this gene results in nonsyndromic mental retardation-3

The dysregulation of the signaling pathways mediated by this protein may be the cause of the APLL

CYTSA Rabbit Polyclonal Antibody, 100ul Bottles CDKL3 was identified as aThis gene encodes a coiled coil domain containing protein. The encoded protein may play a critical role in actin cytoskeletal reorganization during facial morphogenesis. Mutations in this gene are a cause of oblique facial clefting 1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. A read through transcript composed of SPECC1L (sperm antigen with calponin homology and coiled coil domains 1 like)