DisGeNET - a database of gene-disease associations

Gene: ACTG1 ×

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:	71
Gene Symbol:	ACTG1

ACTG1

CUI:	C1858172
Disease:	Deafness, Autosomal Dominant 20

Deafness, Autosomal Dominant 20

0.700

Biomarker

GENOMICS_ENGLAND

FISH localization of human cytoplasmic actin genes ACTB to 7p22 and ACTG1 to 17q25 and characterization of related pseudogenes.

1996