DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Behcet Syndrome ×

Gene: TFCP2L1 ×

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

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	29842
Gene Symbol:	TFCP2L1

TFCP2L1

CUI:	C0004943
Disease:	Behcet Syndrome

Behcet Syndrome

0.100

GeneticVariation

GWASDB

Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study.

2012