SLC6A17
Description
The SLC6A17 (solute carrier family 6 member 17) is a protein-coding gene located on chromosome 1.
SLC6A17 is also known as MRT48, NTT4.
Associated Diseases
- Intellectual developmental disorder, autosomal recessive 48
- Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome
