XIRP1
Description
The XIRP1 (xin actin binding repeat containing 1) is a protein-coding gene located on chromosome 3.
Prevents the breakdown of actin filaments.
XIRP1 is also known as CMYA1, Xin.
Associated Diseases
- left ventricular noncompaction
- dilated cardiomyopathy 1AA
- left ventricular noncompaction 10
- mitochondrial complex IV deficiency, nuclear type 22
- dilated cardiomyopathy 1W
- dilated cardiomyopathy 1CC
- dilated cardiomyopathy 1M
- dilated cardiomyopathy 2A
- dilated cardiomyopathy 1GG
- dilated cardiomyopathy 1I
- sick sinus syndrome 2, autosomal dominant
- atrial standstill
- dilated cardiomyopathy 1JJ
- Becker muscular dystrophy