VWA5A
Description
The VWA5A (von Willebrand factor A domain containing 5A) is a protein-coding gene located on chromosome 11.
VWA5A, or Von Willebrand factor A domain containing 5A, is a protein encoded by the VWA5A gene in humans.
VWA5A is also known as BCSC-1, BCSC1, LOH11CR2A.
Associated Diseases
- breast cancer
- X-linked endothelial corneal dystrophy
- granular corneal dystrophy type I
- macular corneal dystrophy
- Thiel-Behnke corneal dystrophy
- corneal endothelial dystrophy
- Schnyder corneal dystrophy
- granular corneal dystrophy type II
- lattice corneal dystrophy type I
- autosomal dominant keratitis
- corneal dystrophy, Fuchs endothelial, 3
- X-linked corneal dermoid
- epithelial basement membrane dystrophy
- Peters anomaly
- cornea plana 2
- ring dermoid of cornea
- congenital glaucoma
