DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Hypertensive disease ×

Gene: MEX3C ×

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:	51320
Gene Symbol:	MEX3C

MEX3C

CUI:	C0020538
Disease:	Hypertensive disease

Hypertensive disease

0.010

GeneticVariation

LHGDN

Implication of chromosome 18 in hypertension by sibling pair and association analyses: putative involvement of the RKHD2 gene.

2006