Gene table: search width pubmed_id = 8406488


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Charcot-Marie-Tooth neuropathy Type 2A2 - (AD)
14.48
15064763
8406488
MFN2 (1p36.22)
Mitofusin 2(M)
* Hereditary motor and sensory neuropathy 2A - CMT2A2A
* Charcot-Marie-Tooth disease, axonal, type 2A2B - CMT2A2B
* Hereditary motor and sensory neuropathy, type VIA with optic atrophy - HMSN6A