DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Crohn Disease ×

Gene: BTNL2 ×

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:	56244
Gene Symbol:	BTNL2

BTNL2

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.120

GeneticVariation

LHGDN

Analysis of the BTNL2 truncating splice site mutation in tuberculosis, leprosy and Crohn's disease.

2007