DisGeNET - a database of gene-disease associations

Familial schizencephaly, C2931870

Gene: EMX2 ×

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:	2018
Gene Symbol:	EMX2

EMX2

0.320

Biomarker

disease

BEFREE

EMX2-independent familial schizencephaly: clinical and genetic analyses.

2005

Entrez Id:	2018
Gene Symbol:	EMX2

EMX2

0.320

GeneticVariation

disease

BEFREE

Familial schizencephaly associated with EMX2 mutation.

1997

Entrez Id:	2018
Gene Symbol:	EMX2

EMX2

0.320

Biomarker

disease

CTD_human