DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Coronary Artery Disease ×

Gene: LPA ×

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:	4018
Gene Symbol:	LPA

LPA

CUI:	C1956346
Disease:	Coronary Artery Disease

Coronary Artery Disease

0.500

GeneticVariation

LHGDN

Association between lipoprotein(a) levels, apo(a) isoforms and family history of premature CAD in young Asian Indians.

18280807

2008

Entrez Id:	4018
Gene Symbol:	LPA

LPA

CUI:	C1956346
Disease:	Coronary Artery Disease

Coronary Artery Disease

0.500

GeneticVariation

LHGDN

We found 1 SNP that was associated with severe CAD: LPA I4399M (rs3798220).

17569884

2007

Entrez Id:	4018
Gene Symbol:	LPA

LPA

CUI:	C1956346
Disease:	Coronary Artery Disease

Coronary Artery Disease

0.500

AlteredExpression

LHGDN

Circulating transforming growth factor-beta1, lipoprotein(a) and cellular adhesion molecules in angiographically assessed coronary artery disease.

12940514

2003

Entrez Id:	4018
Gene Symbol:	LPA

LPA

CUI:	C1956346
Disease:	Coronary Artery Disease

Coronary Artery Disease

0.500

AlteredExpression

LHGDN

Plasma lipoprotein (a) levels are significantly elevated in patients with coronary artery disease as compared to controls.

11999088

2002