DisGeNET - a database of gene-disease associations

TREM2, triggering receptor expressed on myeloid cells 2, 54209

N. diseases: 239; N. variants: 28

Disease: Dystonia ×

Source: ALL

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

Disease

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

CUI:	C0013421
Disease:	Dystonia

Dystonia

0.300

Biomarker

phenotype

GENOMICS_ENGLAND

Parkinsonism, movement disorders and genetics in frontotemporal dementia.

26891767

2016

CUI:	C0013421
Disease:	Dystonia

Dystonia

0.300

Biomarker

phenotype

GENOMICS_ENGLAND

The genetic causes of basal ganglia calcification, dementia, and bone cysts: DAP12 and TREM2.

15883308

2005

CUI:	C0013421
Disease:	Dystonia

Dystonia

0.300

Biomarker

phenotype

GENOMICS_ENGLAND