Gene symbol and protein
Gene Location
All allelic disease phenotypes - locus/disease symbols
TTN
titin

2q31
* Congenital myopathy with fatal cardiomyopathy - (1.28, 3.31, 4.2, 5.13, 10.8, 10.33)
* Cardiomyopathy, familial hypertrophic, 9 - CMH9 (1.28, 3.31, 4.2, 5.13, 10.8, 10.33)
* Tibial muscular dystrophy, tardive - TMD (1.28, 3.31, 4.2, 5.13, 10.8, 10.33)
* Hereditry myopathy with early respiratory failure - HMERF (1.28, 3.31, 4.2, 5.13, 10.8, 10.33)
* Autosomal dominant myopathy with proximal muscle weakness and early respiratory - (1.28, 3.31, 4.2, 5.13, 10.8, 10.33)
* Cardiomyopathy, dilated, 1G - CMD1G (1.28, 3.31, 4.2, 5.13, 10.8, 10.33)
* Limb girdle muscular dystrophy 2J (autosomal recessive) - LGMD2J (1.28, 3.31, 4.2, 5.13, 10.8, 10.33)

Gene symbol and protein	Gene Location	All allelic disease phenotypes - locus/disease symbols
TTN titin	2q31	* Congenital myopathy with fatal cardiomyopathy - (1.28, 3.31, 4.2, 5.13, 10.8, 10.33) * Cardiomyopathy, familial hypertrophic, 9 - CMH9 (1.28, 3.31, 4.2, 5.13, 10.8, 10.33) * Tibial muscular dystrophy, tardive - TMD (1.28, 3.31, 4.2, 5.13, 10.8, 10.33) * Hereditry myopathy with early respiratory failure - HMERF (1.28, 3.31, 4.2, 5.13, 10.8, 10.33) * Autosomal dominant myopathy with proximal muscle weakness and early respiratory - (1.28, 3.31, 4.2, 5.13, 10.8, 10.33) * Cardiomyopathy, dilated, 1G - CMD1G (1.28, 3.31, 4.2, 5.13, 10.8, 10.33) * Limb girdle muscular dystrophy 2J (autosomal recessive) - LGMD2J (1.28, 3.31, 4.2, 5.13, 10.8, 10.33)