RGR

retinal G protein coupled receptor

Ensembl:
ENSG00000148604
UniProt:
P47804
OMIM:
600342
Synonyms:
RP44

Cilia effects upon perturbation of RGR

Ciliogenesis screen results (5 screens)

  • Kim2016: Not Reported
  • Wheway et al. 2015 (siRNA) [siRNA]: Ciliogenesis Defect (z=-2.57) PMID:26167766
  • Breslow et al. 2018 (CRISPR) [CRISPR]: No Significant Effect PMID:29459680
  • Roosing et al. 2015 (siRNA) [siRNA]: No effect PMID:26595381
  • Pusapati et al. 2018 (CRISPR) [CRISPR]: Positive Regulator (Hh signaling, neg_rank=313, lfc=-2.39) PMID:30270045

Phenotypes

Human ciliopathy phenotype:
retinitis pigmentosa

Subcellular localization

cilia associated gene

Functional category

  • Ciliary assembly/disassembly
  • Signaling (Hedgehog, GPCRs, ion channels)

Function

Mutations in the RGR gene cause Retinitis Pigmentosa (PMID: 10581022, 21067480).