DisGeNET - a database of gene-disease associations

Source: ORPHANET

Disease: DYSTONIA 21 ×

Gene: DYT21 ×

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:	100885773
Gene Symbol:	DYT21

DYT21

CUI:	C3281236
Disease:	DYSTONIA 21

DYSTONIA 21

0.300

GermlineCausalMutation

ORPHANET

A high-penetrance form of late-onset torsion dystonia maps to a novel locus (DYT21) on chromosome 2q14.3-q21.3.

2011