GeneTable of Neuromuscular Disorders

This table has been prepared by Dr Gisèle Bonne ^* - PhD and by Pr. François Rivier ^** - MD, PhD

This website is developed and maintained by Dalil Hamroun^** - PhD

* Sorbonne Université-Inserm, Centre of Research in Myology , Paris, France.
** Chu de Montpellier, Montpellier. France.

GT_NMD 2024 (updated 17/01/2024)

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Gene symbol and protein	Gene Location	All allelic disease phenotypes - locus/disease symbols
DNM2 Dynamin 2	19p13.2	* Myopathy centronuclear, 1 - CNM1 (2.15, 3.19, 4.20, 12.91, 14.16) * Charcot-Marie-Tooth disease, dominant intermediate B - CMTDIB (2.15, 3.19, 4.20, 12.91, 14.16) * Lethal Congenital Contracture Syndrome 5 - LCCS5 (2.15, 3.19, 4.20, 12.91, 14.16)