DisGeNET - a database of gene-disease associations

Source: CLINGEN

Disease: Wolfram-Like Syndrome, Autosomal Dominant ×

Gene: WFS1 ×

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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:	7466
Gene Symbol:	WFS1

WFS1

wolframin ER transmembrane glycoprotein

0.528

0.846

1.6E-38

CUI:	C3280358
Disease:	Wolfram-Like Syndrome, Autosomal Dominant

Wolfram-Like Syndrome, Autosomal Dominant

disease

0.710

definitive

1.000

0

1998

2018