DisGeNET - a database of gene-disease associations

Source: CTD_human

Disease: Congenital diaphragmatic hernia ×

Gene: CCL2 ×

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:	6347
Gene Symbol:	CCL2

CCL2

CUI:	C0235833
Disease:	Congenital diaphragmatic hernia

Congenital diaphragmatic hernia

0.310

Biomarker

CTD_human

We performed this study to evaluate the role of MCP-1 for the pathogenesis of PH in experimental CDH.

2018