DisGeNET - a database of gene-disease associations

GRN-related frontotemporal dementia, C3811918

Gene: UBQLN2 ×

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

Gene

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	29978
Gene Symbol:	UBQLN2

UBQLN2

0.040

GeneticVariation

disease

BEFREE

Pathogenic mutation of ubiquilin 2 (UBQLN2) causes neurodegeneration in amyotrophic lateral sclerosis and frontotemporal lobar degeneration.

27456931

2016

Entrez Id:	29978
Gene Symbol:	UBQLN2

UBQLN2

0.040

GeneticVariation

disease

BEFREE

Mutations in ubiquilin 2 (Ubqln2) is linked to amyotrophic lateral sclerosis and frontotemporal lobar degeneration.

25388785

2015

Entrez Id:	29978
Gene Symbol:	UBQLN2

UBQLN2

0.040

GeneticVariation

disease

BEFREE

UBQLN2 variant of unknown significance in frontotemporal lobar degeneration.

25179229

2015

Entrez Id:	29978
Gene Symbol:	UBQLN2

UBQLN2

0.040

Biomarker

disease

BEFREE

Screening UBQLN-2 in French frontotemporal lobar degeneration and frontotemporal lobar degeneration-amyotrophic lateral sclerosis patients.

23582661

2013