DisGeNET - a database of gene-disease associations

Source: CLINGEN

Disease: Usher Syndrome, Type II ×

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:	25861
Gene Symbol:	WHRN

WHRN

whirlin

0.670

0.385

7.7E-05

CUI:	C1568249
Disease:	Usher Syndrome, Type II

Usher Syndrome, Type II

disease

0.940

definitive

1.000

0

2003

2017