PRR9
Description
The PRR9 (proline rich 9) is a protein-coding gene located on chromosome 1.
Proline rich 9 is a protein that in humans is encoded by the PRR9 gene.
PRR9 is also known as -.
Associated Diseases
- Griscelli syndrome type 3
- uncombable hair syndrome
- oculocutaneous albinism type 3
- microcephaly-albinism-digital anomalies syndrome
- Tietz syndrome
- ermine phenotype
- hypotrichosis simplex
- Waardenburg syndrome, IIa 2F
- Clouston syndrome
- Waardenburg syndrome type 2A