DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Amyotrophic Lateral Sclerosis ×

Gene: UNC13A ×

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:	23025
Gene Symbol:	UNC13A

UNC13A

CUI:	C0002736
Disease:	Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis

0.700

GeneticVariation

GWASDB

No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.

24234648

2014

Entrez Id:	23025
Gene Symbol:	UNC13A

UNC13A

CUI:	C0002736
Disease:	Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis

0.700

GeneticVariation

GWASDB

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.

22959728

2013

Entrez Id:	23025
Gene Symbol:	UNC13A

UNC13A

CUI:	C0002736
Disease:	Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis

0.700

GeneticVariation

GWASDB

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.

20801717

2010

Entrez Id:	23025
Gene Symbol:	UNC13A

UNC13A

CUI:	C0002736
Disease:	Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis

0.700

GeneticVariation

GWASDB

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.

19734901

2009