DisGeNET - a database of gene-disease associations

WAGR Syndrome, C0206115

Gene: WT1 ×

Source: CURATED ×

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

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	7490
Gene Symbol:	WT1

WT1

0.800

ChromosomalRearrangement

disease

ORPHANET

The modifier effect of the BDNF gene in the phenotype of the WAGRO syndrome.

2013

Entrez Id:	7490
Gene Symbol:	WT1

WT1

0.800

Biomarker

disease

GENOMICS_ENGLAND

Entrez Id:	7490
Gene Symbol:	WT1

WT1

0.800

Biomarker

disease

CTD_human