DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: QT interval feature (observable entity) ×

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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:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Impact of ancestry and common genetic variants on QT interval in African Americans.

23166209

2012

Entrez Id:	8671
Gene Symbol:	SLC4A4

SLC4A4

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Impact of ancestry and common genetic variants on QT interval in African Americans.

23166209

2012

Entrez Id:	9516
Gene Symbol:	LITAF

LITAF

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Impact of ancestry and common genetic variants on QT interval in African Americans.

23166209

2012

Entrez Id:	23019
Gene Symbol:	CNOT1

CNOT1

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval.

22726844

2012

Entrez Id:	6546
Gene Symbol:	SLC8A1

SLC8A1

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval.

22726844

2012

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval.

22726844

2012

Entrez Id:	481
Gene Symbol:	ATP1B1

ATP1B1

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

19305409

2009

Entrez Id:	1805
Gene Symbol:	DPT

DPT

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

19305409

2009

Entrez Id:	54147
Gene Symbol:	BACH1-IT3

BACH1-IT3

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.

19587794

2009

Entrez Id:	6331
Gene Symbol:	SCN5A

SCN5A

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

19305409

2009

Entrez Id:	79658
Gene Symbol:	ARHGAP10

ARHGAP10

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.

20031603

2009

Entrez Id:	23019
Gene Symbol:	CNOT1

CNOT1

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common variants at ten loci influence QT interval duration in the QTGEN Study.

19305408

2009

Entrez Id:	9516
Gene Symbol:	LITAF

LITAF

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

19305409

2009

Entrez Id:	5139
Gene Symbol:	PDE3A

PDE3A

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.

20031603

2009

Entrez Id:	93109
Gene Symbol:	TMEM44

TMEM44

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.

20031603

2009

Entrez Id:	388591
Gene Symbol:	RNF207

RNF207

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common variants at ten loci influence QT interval duration in the QTGEN Study.

19305408

2009

Entrez Id:	23019
Gene Symbol:	CNOT1

CNOT1

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

19305409

2009

Entrez Id:	101929265
Gene Symbol:	LINC01428

LINC01428

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.

19587794

2009

Entrez Id:	388591
Gene Symbol:	RNF207

RNF207

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

19305409

2009

Entrez Id:	9722
Gene Symbol:	NOS1AP

NOS1AP

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

19305409

2009

Entrez Id:	3784
Gene Symbol:	KCNQ1

KCNQ1

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

19305409

2009

Entrez Id:	5793
Gene Symbol:	PTPRG

PTPRG

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.

20031603

2009

Entrez Id:	27004
Gene Symbol:	TCL6

TCL6

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.

20031603

2009

Entrez Id:	3784
Gene Symbol:	KCNQ1

KCNQ1

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common variants at ten loci influence QT interval duration in the QTGEN Study.

19305408

2009

Entrez Id:	105370158
Gene Symbol:	LINC02343

LINC02343

CUI:	C0429028
Disease:	QT interval feature (observable entity)

QT interval feature (observable entity)

0.100

GeneticVariation

GWASDB

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.

19587794

2009