DisGeNET - a database of gene-disease associations

Source: GENOMICS_ENGLAND

Gene: MYL1 ×

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

Gene Full Name

DSI _g

DPI _g

pLI

Disease

Type

Score _gda

EL_gda

EI _gda

N.PMIDs

N.SNPs _gda

First Ref.

LastRef.

Entrez Id:	4632
Gene Symbol:	MYL1

MYL1

myosin light chain 1

0.839

0.346

1.3E-04

CUI:	C0270960
Disease:	Congenital myopathy (disorder)

Congenital myopathy (disorder)

group

0.310

strong

1.000

0

2018

2018