DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Parkinson Disease ×

Gene: PLEKHM1 ×

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:	9842
Gene Symbol:	PLEKHM1

PLEKHM1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.100

GeneticVariation

GWASDB

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.

22438815

2012

Entrez Id:	9842
Gene Symbol:	PLEKHM1

PLEKHM1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.100

GeneticVariation

GWASDB

Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.

21738487

2011

Entrez Id:	9842
Gene Symbol:	PLEKHM1

PLEKHM1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.100

GeneticVariation

GWASDB

Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.

20070850

2010

Entrez Id:	9842
Gene Symbol:	PLEKHM1

PLEKHM1

CUI:	C0030567
Disease:	Parkinson Disease

Parkinson Disease

0.100

GeneticVariation

GWASDB

Genome-wide association study reveals genetic risk underlying Parkinson's disease.

19915575

2009