DisGeNET - a database of gene-disease associations

Source: MGD

Disease: Hypertrophic neuropathy of infancy ×

Gene: MTMR2 ×

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:	8898
Gene Symbol:	MTMR2

MTMR2

CUI:	C1408174
Disease:	Hypertrophic neuropathy of infancy

Hypertrophic neuropathy of infancy

0.200

Biomarker

MGD

An animal model for Charcot-Marie-Tooth disease type 4B1.

16249189

2005

Entrez Id:	8898
Gene Symbol:	MTMR2

MTMR2

CUI:	C1408174
Disease:	Hypertrophic neuropathy of infancy

Hypertrophic neuropathy of infancy

0.200

Biomarker

MGD

Disruption of Mtmr2 produces CMT4B1-like neuropathy with myelin outfolding and impaired spermatogenesis.

15557122

2004