Primary Identifier | IPR032964 | Type | Family |
Short Name | GPR179 |
description | GPR179 is a probable G-protein coupled receptor that plays a critical role in DBC (depolarising bipolar cell) signal transduction []. Mutations in the GPR179 gene cause autosomal recessive complete congenital stationary night blindness (CSNB), which is characterised by an ON-bipolar retinal cell dysfunction []. |