SAMD11
Description
The SAMD11 (sterile alpha motif domain containing 11) is a protein-coding gene located on chromosome 1.
SAMD11 might contribute to the development of photoreceptor cells in the eye.
SAMD11 is also known as MRS.
Associated Diseases
- retinitis pigmentosa
- uncombable hair syndrome
- schizophrenia 15
- Griscelli syndrome type 3
- Phelan-McDermid syndrome
- hypotrichosis simplex
- Clouston syndrome
- Waardenburg syndrome, IIa 2F
- Potocki-Lupski syndrome
- respiratory distress syndrome in premature infants
