MFN2 K357N - GET-Evidence

Note: This variant has not been sufficiently evaluated by a GET-Evidence editor.

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MFN2 K357N

(MFN2 Lys357Asn)

Short summary


Variant evidence
Computational -
Functional -
Case/Control -
Familial -
Clinical importance
Severity -
Treatability -
Penetrance -


Insufficiently evaluated pathogenic

(The "insufficiently evaluated" qualifier is assigned automatically based on the above evidence and importance scores.)

Inheritance pattern


Summary of published research, and additional commentary


Allele frequency

  • None available.



Other external references

  • GeneTests records for the MFN2 gene
    Charcot-Marie-Tooth Neuropathy Type 2
    Charcot-Marie-Tooth Neuropathy Type 2A
    Charcot-Marie-Tooth Neuropathy Type 2A2
  • Score: 0.998 (probably damaging)
    Web search results (7 hits -- see all)
  • Hereditary Motor Sensory Neuropathies: Charcot-Marie-Tooth
    MFN2 deficient mice: Lower mitochondrial mobility. MFN2 mutant protein: ... l Mitofusin 2 (MFN2) ; Chromosome 1p36.2; Dominant or Sporadic new mutation ...
    (MFN2) interaction that takes place in trans across two mitochondria. ... domain model of MFN2, showing the conserved GTPase domain and the proposed neck, ...
  • BMC Medical Genetics
    Recently, mutations in MFN2 have also been linked to. two rare forms of hereditary ... of MFN2. Electropherograms showing novel mutations in the MFN2 gene ...
  • WUSTL - Hereditary Motor Sensory Neuropathies: Charcot-Marie ...
    V244M; Pro251Ala; V273G; Arg280His; F284Y; K357N; E424G; Trp740Ser ... MFN2 deficiente topo: Inferiori mitocondriale mobilità. MFN2 proteina mutante: Possono ...
  • Ruhr-Universität Bochum PD Dr. med. Moritz Meins Dienstort ...
    Das MFN2-Protein ist ein Transmembranprotein, welches in der ... Schematische Darstellung des MFN2-Proteins in der mitochondrialen Außenmembran ...
  • Inherited Peripheral Neuropathies
    Newest Entries Submit Mutation Table Legend. last updated 17-Dec-07. Mutations in MFN2. Name. c.281G>A. Alias ... K357N. Region. EX11. CDS. Date Added: 24-Mar-05. ID: 719. Name. c.1271A>G ...
  • Inherited Peripheral Neuropathies
    Mutations in MFN2. Name. c.134A>G. Alias. Gln45Arg. Description. Point ... K357N. Region. EX11. CDS. Date Added: 24-Mar-05. ID: 719. Name. c.1081C>T. Alias. His361Tyr ...

Other in silico analyses

  • NBLOSUM100 score = 1
  • GET-Evidence autoscore = 6

Edit history

Gene search

"GENE" or "GENE A123C":

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