DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Cholelithiasis ×

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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:	64241
Gene Symbol:	ABCG8

ABCG8

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.200

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	54578
Gene Symbol:	UGT1A6

UGT1A6

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.180

GeneticVariation

GWASDB

A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.

22558097

2012

Entrez Id:	54657
Gene Symbol:	UGT1A4

UGT1A4

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.180

GeneticVariation

GWASDB

A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.

22558097

2012

Entrez Id:	54575
Gene Symbol:	UGT1A10

UGT1A10

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.180

GeneticVariation

GWASDB

A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.

22558097

2012

Entrez Id:	54577
Gene Symbol:	UGT1A7

UGT1A7

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.180

GeneticVariation

GWASDB

A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.

22558097

2012

Entrez Id:	54576
Gene Symbol:	UGT1A8

UGT1A8

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.180

GeneticVariation

GWASDB

A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.

22558097

2012

Entrez Id:	54600
Gene Symbol:	UGT1A9

UGT1A9

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.140

GeneticVariation

GWASDB

A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.

22558097

2012

Entrez Id:	54579
Gene Symbol:	UGT1A5

UGT1A5

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.140

GeneticVariation

GWASDB

A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.

22558097

2012

Entrez Id:	54659
Gene Symbol:	UGT1A3

UGT1A3

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.140

GeneticVariation

GWASDB

A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.

22558097

2012

Entrez Id:	23673
Gene Symbol:	STX12

STX12

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	3371
Gene Symbol:	TNC

TNC

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	9630
Gene Symbol:	GNA14

GNA14

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	29994
Gene Symbol:	BAZ2B

BAZ2B

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	7576
Gene Symbol:	ZNF28

ZNF28

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	1602
Gene Symbol:	DACH1

DACH1

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	55691
Gene Symbol:	FRMD4A

FRMD4A

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	50514
Gene Symbol:	DELEC1

DELEC1

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	85461
Gene Symbol:	TANC1

TANC1

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	348645
Gene Symbol:	C22orf34

C22orf34

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	283953
Gene Symbol:	TMEM114

TMEM114

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	4651
Gene Symbol:	MYO10

MYO10

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	137868
Gene Symbol:	SGCZ

SGCZ

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	91316
Gene Symbol:	GUSBP11

GUSBP11

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	83872
Gene Symbol:	HMCN1

HMCN1

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007

Entrez Id:	84665
Gene Symbol:	MYPN

MYPN

CUI:	C0008350
Disease:	Cholelithiasis

Cholelithiasis

0.100

GeneticVariation

GWASDB

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

17632509

2007