DisGeNET - a database of gene-disease associations

Gene: MYL4 ×

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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:	4635
Gene Symbol:	MYL4

MYL4

CUI:	C1843687
Disease:	ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)

ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)

0.300

GermlineCausalMutation

ORPHANET

A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation.

2016