DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Hypertriglyceridemia ×

Gene: GCKR ×

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:	2646
Gene Symbol:	GCKR

GCKR

CUI:	C0020557
Disease:	Hypertriglyceridemia

Hypertriglyceridemia

0.490

GeneticVariation

GWASDB

Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.

23505323

2013

Entrez Id:	2646
Gene Symbol:	GCKR

GCKR

CUI:	C0020557
Disease:	Hypertriglyceridemia

Hypertriglyceridemia

0.490

GeneticVariation

GWASDB

Through GWAS, we identified common variants in APOA5, GCKR, LPL and APOB associated with HTG.

20657596

2010