rs104894459
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel p.M96T variant of NRL and shRNA-based suppression and replacement of NRL mutants associated with autosomal dominant retinitis pigmentosa.
|
21981118 |
2012 |
rs104894459
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Next-generation genetic testing for retinitis pigmentosa.
|
22334370 |
2012 |
rs397514516
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Next-generation genetic testing for retinitis pigmentosa.
|
22334370 |
2012 |
rs397514516
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel p.M96T variant of NRL and shRNA-based suppression and replacement of NRL mutants associated with autosomal dominant retinitis pigmentosa.
|
21981118 |
2012 |
rs104894459
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activity.
|
17335001 |
2007 |
rs397514516
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activity.
|
17335001 |
2007 |
rs104894459
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families.
|
15994872 |
2005 |
rs397514516
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families.
|
15994872 |
2005 |
rs104894459
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function.
|
15591106 |
2004 |
rs397514516
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function.
|
15591106 |
2004 |
rs104894459
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosa.
|
11879142 |
2002 |
rs397514516
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosa.
|
11879142 |
2002 |
rs104894459
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosa.
|
11385710 |
2001 |
rs397514516
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosa.
|
11385710 |
2001 |
rs104894459
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
A mutation in NRL is associated with autosomal dominant retinitis pigmentosa.
|
10192380 |
1999 |
rs397514516
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.800 |
GeneticVariation |
UNIPROT |
A mutation in NRL is associated with autosomal dominant retinitis pigmentosa.
|
10192380 |
1999 |
rs104894459
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs397514516
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs743271
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
Body Height
|
|
0.700 |
GeneticVariation |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
rs2071586
|
Entrez Id: |
4901;5106 |
Gene Symbol: |
NRL;PCK2 |
NRL;PCK2
|
Intelligence
|
|
0.700 |
GeneticVariation |
GWASCAT |
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
|
29844566 |
2018 |
rs757038765
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.700 |
GeneticVariation |
UNIPROT |
Next-generation genetic testing for retinitis pigmentosa.
|
22334370 |
2012 |
rs757038765
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.700 |
GeneticVariation |
UNIPROT |
Novel p.M96T variant of NRL and shRNA-based suppression and replacement of NRL mutants associated with autosomal dominant retinitis pigmentosa.
|
21981118 |
2012 |
rs104894463
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.700 |
GeneticVariation |
UNIPROT |
Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activity.
|
17335001 |
2007 |
rs757038765
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.700 |
GeneticVariation |
UNIPROT |
Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activity.
|
17335001 |
2007 |
rs757038765
|
Entrez Id: |
4901 |
Gene Symbol: |
NRL |
NRL
|
RETINITIS PIGMENTOSA 27
|
|
0.700 |
GeneticVariation |
UNIPROT |
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families.
|
15994872 |
2005 |