DisGeNET - a database of gene-disease associations

Source: GENOMICS_ENGLAND

Disease: Night blindness, congenital stationary ×

Gene: CACNA2D4 ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Gene Full Name

DSI _g

DPI _g

pLI

Disease

Type

Score _gda

EL_gda

EI _gda

N.PMIDs

N.SNPs _gda

First Ref.

LastRef.

Entrez Id:	93589
Gene Symbol:	CACNA2D4

CACNA2D4

calcium voltage-gated channel auxiliary subunit alpha2delta 4

0.716

0.269

1.5E-34

CUI:	C0339535
Disease:	Night blindness, congenital stationary

Night blindness, congenital stationary

disease

0.510

strong

0.667

0

2009

2016