CHD7 Rabbit Polyclonal Antibody, 50ul Liquid Storage Consumables This gene's protein is found

This gene's protein is found in the cytoplasm| yet it lacks the nuclear localization signals found in other subfamily members

Mutations in SLC22A5 (solute carrier family 22 member 5)are the cause of systemic primary carnitine deficiency (CDSP)

The kinase regulates the activities of several types of ion channels

cardiodilatin

CHD7 Rabbit Polyclonal Antibody, 50ul Liquid Storage Consumables This gene's protein is foundThis gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. Two transcript variants encoding different isoforms have been found for this gene.