DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Ventricular Septal Defects ×

Gene: NTRK3 ×

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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:	4916
Gene Symbol:	NTRK3

NTRK3

CUI:	C0018818
Disease:	Ventricular Septal Defects

Ventricular Septal Defects

0.020

Biomarker

BEFREE

These findings suggest a novel pathophysiological mechanism involving NTRK3 in the development of VSDs.

25196463

2014

Entrez Id:	4916
Gene Symbol:	NTRK3

NTRK3

CUI:	C0018818
Disease:	Ventricular Septal Defects

Ventricular Septal Defects

0.020

AlteredExpression

BEFREE

The expression of NTRK3 in the VSD group and in the control group showed no significant differences at both mRNA and protein levels.

19187638

2009