MRGPRG
Description
The MRGPRG (MAS related GPR family member G) is a protein-coding gene located on chromosome 11.
MRGPRG, also known as G-protein coupled receptor 169 (GPR169), is a protein encoded by the MRGPRG gene in humans. It is an orphan G-protein coupled receptor.
MRGPRG is an orphan receptor, suggesting it might play a role in regulating nociceptor function and development. This could include processes related to the sensation or modulation of pain.
MRGPRG is also known as GPR169, MRGG.
Associated Diseases
- Griscelli syndrome type 3
- migraine disorder
- 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
- type 2 diabetes mellitus
