DisGeNET - a database of gene-disease associations

Gene: NTRK1 ×

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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:	4914
Gene Symbol:	NTRK1

NTRK1

CUI:	C0598589
Disease:	Inherited neuropathies

Inherited neuropathies

0.310

Biomarker

GENOMICS_ENGLAND

Novel 9 amino acid in-frame deletion in the NTRK1 tyrosine kinase domain in a patient with congenital insensitivity to pain with anhydrosis.

2017