DisGeNET - a database of gene-disease associations

Myoclonic Epilepsies, Progressive, C0751778

Gene: LMNB2 ×

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:	84823
Gene Symbol:	LMNB2

LMNB2

0.310

GeneticVariation

disease

BEFREE

Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia.

2015

Entrez Id:	84823
Gene Symbol:	LMNB2

LMNB2

0.310

Biomarker

disease

CTD_human