DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Crohn Disease ×

Gene: PROSER1 ×

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:	80209
Gene Symbol:	PROSER1

PROSER1

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.010

GeneticVariation

LHGDN

An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29.

2008