DisGeNET - a database of gene-disease associations

Source: MGD

Disease: Usher Syndrome, Type I ×

Gene: MYO7A ×

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:	4647
Gene Symbol:	MYO7A

MYO7A

myosin VIIA

0.585

0.423

1.6E-38

CUI:	C1568247
Disease:	Usher Syndrome, Type I

Usher Syndrome, Type I

disease

1.000

definitive

0.990

0

1956

2020