×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
CausalMutation
disease
CLINVAR
Analysis of disease-linked rhodopsin mutations based on structure, function, and protein stability calculations.
21094163
2011
×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
CausalMutation
disease
CLINVAR
Rod photoreceptor temporal properties in retinitis pigmentosa.
21219898
2011
×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
CausalMutation
disease
CLINVAR
Autosomal dominant retinitis pigmentosa in Norway: a 20-year clinical follow-up study with molecular genetic analysis. Two novel rhodopsin mutations: 1003delG and I179F.
17488458
2007
×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
CausalMutation
disease
CLINVAR
Retinitis pigmentosa rhodopsin mutations L125R and A164V perturb critical interhelical interactions: new insights through compensatory mutations and crystal structure analysis.
12871954
2003
×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
GeneticVariation
disease
UNIPROT
A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness.
9888392
1999
×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
CausalMutation
disease
CLINVAR
Structure and function in rhodopsin: packing of the helices in the transmembrane domain and folding to a tertiary structure in the intradiscal domain are coupled.
9380676
1997
×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
GeneticVariation
disease
UNIPROT
Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.
7846071
1995
×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
CausalMutation
disease
CLINVAR
Further screening of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.
8088850
1994
×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
GeneticVariation
disease
UNIPROT
Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness.
8107847
1994
×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
CausalMutation
disease
CLINVAR
Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with autosomal dominant retinitis pigmentosa.
7981701
1994
×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
GeneticVariation
disease
UNIPROT
Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness.
8358437
1993
×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
Biomarker
disease
MGD
×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
Biomarker
disease
GENOMICS_ENGLAND
×
Entrez Id:
6010
Gene Symbol:
RHO
RHO
0.900
Biomarker
disease
CTD_human