DisGeNET - a database of gene-disease associations

Night Blindness, Congenital Stationary, Type 1A, C3495587

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs62637027

NYX

0.800

GeneticVariation

UNIPROT

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

11062471

2000

dbSNP:

rs62637027

NYX

0.800

GeneticVariation

UNIPROT

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

11062472

2000

dbSNP:

rs62637027

NYX

0.800

CausalMutation

CLINVAR

dbSNP:

rs62637020

NYX

0.700

GeneticVariation

UNIPROT

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

11062471

2000

dbSNP:

rs62637020

NYX

0.700

GeneticVariation

UNIPROT

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

11062472

2000

dbSNP:

rs62637023

NYX

0.700

GeneticVariation

UNIPROT

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

11062471

2000

dbSNP:

rs62637023

NYX

0.700

GeneticVariation

UNIPROT

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

11062472

2000

dbSNP:

rs62637024

NYX

0.700

GeneticVariation

UNIPROT

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

11062471

2000

dbSNP:

rs62637024

NYX

0.700

GeneticVariation

UNIPROT

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

11062472

2000

dbSNP:

rs62637025

NYX

0.700

GeneticVariation

UNIPROT

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

11062471

2000

dbSNP:

rs62637025

NYX

0.700

GeneticVariation

UNIPROT

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

11062472

2000

dbSNP:

rs62637026

NYX

0.700

GeneticVariation

UNIPROT

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

11062472

2000

dbSNP:

rs62637026

NYX

0.700

GeneticVariation

UNIPROT

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

11062471

2000

dbSNP:

rs62637028

NYX

0.700

GeneticVariation

UNIPROT

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

11062471

2000

dbSNP:

rs62637028

NYX

0.700

GeneticVariation

UNIPROT

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

11062472

2000

dbSNP:

rs62637030

NYX

0.700

GeneticVariation

UNIPROT

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

11062471

2000

dbSNP:

rs62637030

NYX

0.700

GeneticVariation

UNIPROT

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

11062472

2000

dbSNP:

rs62637032

NYX

0.700

GeneticVariation

UNIPROT

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

11062471

2000

dbSNP:

rs62637032

NYX

0.700

GeneticVariation

UNIPROT

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

11062472

2000

dbSNP:

rs62637033

NYX

0.700

GeneticVariation

UNIPROT

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

11062471

2000

dbSNP:

rs62637033

NYX

0.700

GeneticVariation

UNIPROT

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

11062472

2000

dbSNP:

rs62637034

NYX

0.700

GeneticVariation

UNIPROT

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

11062471

2000

dbSNP:

rs62637034

NYX

0.700

GeneticVariation

UNIPROT

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

11062472

2000

dbSNP:

rs62637035

NYX

0.700

GeneticVariation

UNIPROT

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

11062472

2000

dbSNP:

rs62637035

NYX

0.700

GeneticVariation

UNIPROT

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

11062471

2000