CNTNAP5
Description
The CNTNAP5 (contactin associated protein family member 5) is a protein-coding gene located on chromosome 2.
CNTNAP5 is also known as caspr5.
Associated Diseases
- refractive error
- posterior cortical atrophy
- Alzheimer disease
- substance abuse
- benign adult familial myoclonic epilepsy
- hemolytic anemia due to diphosphoglycerate mutase deficiency
