CD58 Polyclonal Antibody, 100ul[BT-AP02005] Rotator Mutations in this gene are

Mutations in this gene are a cause of Treacher Collins syndrome (TCS)

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This gene is one of a cluster of highly related genes located at chromosomal region 19q13

Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia

it does form heterodimers with other EGF receptor family members which do have kinase activity

CD58 Polyclonal Antibody, 100ul[BT-AP02005] Rotator Mutations in this gene areCMTM4 belongs to the chemokine like factor gene superfamily, a novel family that is similar to the chemokine and the transmembrane 4 superfamilies of signaling molecules. CMTM4 is one of several chemokine like factor genes located in a cluster on chromosome 16. Alternatively spliced transcript variants encoding different isoforms have been identified.