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 2025 (updated 12/03/2025)

Home
Disease group
Disease
Gene
Gene product
References
Search
Statistics

Gene symbol and protein	Gene Location	All allelic disease phenotypes - locus/disease symbols
TCAP Telethonin	17q12	* Dilated cardiomyopathy, 1N - (2.16, 10.27, 10.51) * Congenital musuclar dystrophy with telethonin defect - (2.16, 10.27, 10.51) * Muscular dystrophy, limb-girdle, type 2G - LGMD2G (2.16, 10.27, 10.51) * Hypertrophic cardiomyopathy related to TCAP - CMH25 (2.16, 10.27, 10.51)