PDE6B (Entrez ID: 5158)

Entrez Gene ID 5158
Official Gene Symbol PDE6B (GeneCards)
Full name phosphodiesterase 6B
Location 4p16.3
Other ids Vega : OTTHUMG00000159909
MIM : 180072
HGNC : HGNC:8786
Ensembl : ENSG00000133256
Other names rd1, PDEB, RP40, CSNB3, CSNBAD2, GMP-PDEbeta
Summary Photon absorption triggers a signaling cascade in rod photoreceptors that activates cGMP phosphodiesterase (PDE), resulting in the rapid hydrolysis of cGMP, closure of cGMP-gated cation channels, and hyperpolarization of the cell. PDE is a peripheral membrane heterotrimeric enzyme made up of alpha, beta, and gamma subunits. This gene encodes the beta subunit. Mutations in this gene result in retinitis pigmentosa and autosomal dominant congenital stationary night blindness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]

Variants

Found 2 variants in this database.