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MITOMAP: Reported mtDNA Pathogenic Inversion(s)

(Last edited 07/01/05)

 

Inversion
Start (nt)
Inversion
Stop (nt)
Inversion
Size (bp)
Gene(s)
Affected
Amino Acids
Affected
Flanking
Structures
Patient
Phenotype

3902

3908

7 bp

ND1

In-frame substitution:
D199G, L200K, A201V

2-8bp inverted repeats

Mitochondrial Myopathy

Reference: Musumeci, O., Andreu, A.L., Shanske, S., Bresolin, N., Comi, G.P., Rothstein, R., Schon, E.A. and DiMauro, S. (2000). "Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathy." American Journal of Human Genetics 66(6):1900-1904.

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