DisGeNET - a database of gene-disease associations

RETINITIS PIGMENTOSA 44, C3151068

Gene: RGR ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	5995
Gene Symbol:	RGR

RGR

0.600

GeneticVariation

disease

UNIPROT

Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa.

1999

Entrez Id:	5995
Gene Symbol:	RGR

RGR

0.600

Biomarker

disease

CTD_human

Entrez Id:	5995
Gene Symbol:	RGR

RGR

0.600

Biomarker

disease

GENOMICS_ENGLAND