CYTSA Rabbit Polyclonal Antibody, 100ul Bottles CMTM5 encodes a member of

CMTM5 encodes a member of the chemokine-like factor superfamily

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

Mutations in SLC52A2 have been associated with Brown-Vialetto-Van Laere syndrome 2--an autosomal recessive progressive neurologic disorder characterized by deafness

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

It specifically recognizes phosphorylated cyclin-dependent kinase inhibitor 1B (CDKN1B| also referred to as p27 or KIP1) predominantly in S phase and int

CYTSA Rabbit Polyclonal Antibody, 100ul Bottles CMTM5 encodes a member ofThis 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)