ATP7A
(redirected from FLJ17790)ATP7A
A gene on chromosome Xq21.1 that encodes a transmembrane protein that functions in copper transport across membranes, localising to the trans-Golgi network.Molecular pathology
ATP7A mutations cause Menkes disease, occipital horn syndrome and X-linked cutis laxa.
Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.