DisGeNET - a database of gene-disease associations

NYX, nyctalopin, 60506

N. diseases: 36; N. variants: 20

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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs62637027

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

0.800

CausalMutation

CLINVAR

dbSNP:

rs62637020

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

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

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C3495587
Disease:

Night Blindness, Congenital Stationary, Type 1A

0.700

GeneticVariation

UNIPROT

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

11062471

2000