KID Monoclonal Antibody, 100ul[BT-MCA0808] Peptide Modification Defects in this gene are

Defects in this gene are a cause of familial amyloidosis Finnish type (FAF)

Protein Wnt-16 have been implicated in oncogenesis and in several developmental processes

a characteristic unique to this subfamily

Pseudogenes corresponding to MRPL35 are found on chromosomes 6p

and appear to regulate cytoskeletal organization

KID Monoclonal Antibody, 100ul[BT-MCA0808] Peptide Modification Defects in this gene areThe protein encoded by this gene is a member of the kinesin like protein family. The family members are microtubule dependent molecular motors that transport organelles within cells and move chromosomes during cell division. The C terminal half of this protein has been shown to bind DNA. Studies with the Xenopus homolog suggests its essential role in metaphase chromosome alignment and maintenance. Alternatively spliced transcript variants encoding