rs104894493
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
The crystal structure of the orphan nuclear receptor NR2E3/PNR ligand binding domain reveals a dimeric auto-repressed conformation.
24069298
2013
rs104894493
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome.
15459973
2004
rs104894493
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition.
11071390
2000
rs104894493
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration.
12963616
2003
rs104894493
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family.
19006237
2009
rs104894493
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.
10655056
2000
rs1278137915
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition.
11071390
2000
rs1278137915
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome.
15459973
2004
rs1278137915
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.
10655056
2000
rs1278137915
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration.
12963616
2003
rs1278137915
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Analysis of the involvement of the NR2E3 gene in autosomal recessive retinal dystrophies.
18294254
2008
rs1278137915
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family.
19006237
2009
rs1278137915
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity.
16225923
2005
rs1278137915
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
The crystal structure of the orphan nuclear receptor NR2E3/PNR ligand binding domain reveals a dimeric auto-repressed conformation.
24069298
2013
rs1303613101
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
rs1489149705
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration.
12963616
2003
rs1489149705
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity.
16225923
2005
rs1489149705
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family.
19006237
2009
rs1489149705
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.
10655056
2000
rs1489149705
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition.
11071390
2000
rs1489149705
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
The crystal structure of the orphan nuclear receptor NR2E3/PNR ligand binding domain reveals a dimeric auto-repressed conformation.
24069298
2013
rs1489149705
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Analysis of the involvement of the NR2E3 gene in autosomal recessive retinal dystrophies.
18294254
2008
rs1489149705
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome.
15459973
2004
rs752883545
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family.
19006237
2009
rs752883545
×
Entrez Id:
10002
Gene Symbol:
NR2E3
NR2E3
Enhanced S-Cone Syndrome
0.700
GeneticVariation
UNIPROT
Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity.
16225923
2005