Gene: MTMR2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8898
Gene Symbol: MTMR2
MTMR2 		0.230 Biomarker group MGD An animal model for Charcot-Marie-Tooth disease type 4B1. 16249189 2005
Entrez Id: 8898
Gene Symbol: MTMR2
MTMR2 		0.230 Biomarker group MGD Disruption of Mtmr2 produces CMT4B1-like neuropathy with myelin outfolding and impaired spermatogenesis. 15557122 2004
Entrez Id: 8898
Gene Symbol: MTMR2
MTMR2 		0.230 GeneticVariation group BEFREE Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B). 10586229 1999
Entrez Id: 8898
Gene Symbol: MTMR2
MTMR2 		0.230 GeneticVariation group BEFREE Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B). 9521281 1998
Entrez Id: 8898
Gene Symbol: MTMR2
MTMR2 		0.230 Biomarker group BEFREE Hereditary motor and sensory neuropathy (HMSN) with focally folded myelin sheaths, or Charcot-Marie-Tooth type 4B (CMT4B), is a distinct clinical entity belonging to the heterogeneous group of autosomal recessive demyelinating neuropathies. 8817346 1996