CD55 Polyclonal Antibody, 100ul[BT-AP02140] Human Genome Knockout Libraries Mutations in COL18A1 are associated

Mutations in COL18A1 are associated with Knobloch syndrome

the exchanger may play a key role in digitalis action

and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53)

Two related pseudogenes have been identified on chromosome X

This gene encodes a seven-transmembrane domain protein that functions to transport cystine out of lysosomes

CD55 Polyclonal Antibody, 100ul[BT-AP02140] Human Genome Knockout Libraries Mutations in COL18A1 are associatedCortactin, encoded by CTTN gene (formerly EMS1), was originally identified as a substrate of the Src kinase. It is a cytoskeletal protein that interacts with F actin and Arp2 3 complex and plays an important role in regulation of actin assembly and cytoskeleton dynamics. Overexpression of cortactin increases cell migration, and is thought to contribute to the invasive phennotype of breast cancer and several other tumors. Three isoforms of cortactin