DisGeNET - a database of gene-disease associations

CAMTA1, calmodulin binding transcription activator 1, 23261

N. diseases: 112; N. variants: 24

Disease: Amyotrophic Lateral Sclerosis, Sporadic ×

Source: ALL

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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

Disease

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

CUI:	C1862941
Disease:	Amyotrophic Lateral Sclerosis, Sporadic

Amyotrophic Lateral Sclerosis, Sporadic

0.110

GeneticVariation

disease

BEFREE

Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.

27244217

2016

CUI:	C1862941
Disease:	Amyotrophic Lateral Sclerosis, Sporadic