×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
MFN2-associated lipomatosis: Clinical spectrum and impact on adipose tissue.
30158064
2019
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
Catalogue of inherited disorders found among the Irish Traveller population.
29358271
2018
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression.
28414270
2017
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
Genetic heterogeneity of motor neuropathies.
28251916
2017
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
CausalMutation
disease
CLINVAR
The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy.
26378787
2016
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
Biomarker
disease
GENOMICS_ENGLAND
Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes.
27604308
2016
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy.
26257172
2015
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
MFN2 deletion of exons 7 and 8: founder mutation in the UK population.
26114802
2015
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
Homozygous mutations in MFN2 cause multiple symmetric lipomatosis associated with neuropathy.
26085578
2015
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
CausalMutation
disease
CLINVAR
Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy.
26257172
2015
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
Genetic diagnosis of Charcot-Marie-Tooth disease in a population by next-generation sequencing.
25025039
2014
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
Diagnostic laboratory testing for Charcot Marie Tooth disease (CMT): the spectrum of gene defects in Norwegian patients with CMT and its implications for future genetic test strategies.
24053775
2013
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
Spectrum and frequencies of mutations in the MFN2 gene and its phenotypical expression in Czech hereditary motor and sensory neuropathy type II patients.
24126688
2013
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
BEFREE
Charcot-Marie-Tooth disease Type 2A2 (CMT2A2), caused by mitofusin 2 (MFN2 ) genes, has been clinically classified into two types: severe early-onset and mild benign.
22762946
2013
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
MFN2 mutations cause compensatory mitochondrial DNA proliferation.
22492563
2012
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
Biomarker
disease
GENOMICS_ENGLAND
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations.
21715711
2011
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
UNIPROT
The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan.
22206013
2011
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
CausalMutation
disease
CLINVAR
Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan.
21326314
2011
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
UNIPROT
MFN2 point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families.
20350294
2010
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
MFN2 point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families.
20350294
2010
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
Genotype-phenotype correlations in Charcot-Marie-Tooth disease type 2 caused by mitofusin 2 mutations.
20008656
2009
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
CLINVAR
Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations.
18458227
2008
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
UNIPROT
Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2).
16762064
2006
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
CausalMutation
disease
CLINVAR
Mitochondrial GTPase mitofusin 2 mutation in Charcot-Marie-Tooth neuropathy type 2A.
15549395
2005
×
Entrez Id:
9927
Gene Symbol:
MFN2
MFN2
0.810
GeneticVariation
disease
UNIPROT
Mitochondrial GTPase mitofusin 2 mutation in Charcot-Marie-Tooth neuropathy type 2A.
15549395
2005