AKT1 | Advancing Rare Disorders: Vascular mAlformation Research Network with CaNVAS

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This is a human gene. Genetic variants in AKT1 are found in proteus syndrome.

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The Advancing Rare Disorders: Vascular mAlformation Research Network with CaNVAS (ARDVARC) is part of the Rare Diseases Clinical Research Network (RDCRN), which is funded by the National Institutes of Health (NIH) and led by the National Center for Advancing Translational Sciences (NCATS) through its Division of Rare Diseases Research Innovation (DRDRI). ARDVARC is funded under grant number U54HL185006 as a collaboration between NCATS, and the National Heart, Lung, and Blood Institute (NHLBI). This website is hosted by the network’s Data Management and Coordinating Center at Cincinnati Children’s Hospital Medical Center, which is funded by NCATS and the National Institute of Neurological Disorders and Stroke (NINDS) under grant number TR002818. The content of this website is solely the responsibility of the ARDVARC administrative coordinating center at Children's Hospital of Philadelphia and does not necessarily represent the official views of the NIH.

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