Catenin- Alpha E/N Polyclonal Antibody, 100ul Virus Packaging An inactivating nonsense mutation localized

An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9

Several pseudogenes of this gene are found on other chromosomes

Mutations in this gene or its regulatory region cause hypobetalipoproteinemia

such as detergents and solvents

ABCA13 is a member of ABC gene subfamily A (ABCA)

Catenin- Alpha E/N Polyclonal Antibody, 100ul Virus Packaging An inactivating nonsense mutation localizedCTNNA1 encodes a member of the catenin family of proteins that play an important role in cell adhesion process by connecting cadherins located on the plasma membrane to the actin filaments inside the cell. The encoded mechanosensing protein (catenin alpha 1) contains three vinculin homology domains and undergoes conformational changes in response to cytoskeletal tension, resulting in the reconfiguration of cadherin actin filament connections. Certain