Gene symbol and protein
Gene Location
All allelic disease phenotypes - locus/disease symbols
LMNA
lamin A/C

1q21.2-q21.3
* Cardiomyopathy, dilated, 1A - CMD1A (1.4, 1.5, 1.12, 10.26, 14.51)
* Lipodystrophy, familial partial, type 2 - FPLD2 (1.4, 1.5, 1.12, 10.26, 14.51)
* Muscular dystrophy, limb-girdle, type 1B - LGMD1B (1.4, 1.5, 1.12, 10.26, 14.51)
* Hutchinson-Gilford progeria syndrome - HGPS (1.4, 1.5, 1.12, 10.26, 14.51)
* Emery-Dreifuss muscular dystrophy, autosomal dominant - EDMD2 (1.4, 1.5, 1.12, 10.26, 14.51)
* Mandibuloacral dysplasia with type a lipodystrophy - MADA (1.4, 1.5, 1.12, 10.26, 14.51)
* restrictive dermopathy - (1.4, 1.5, 1.12, 10.26, 14.51)
* Emery-Dreifuss Autosomal recessive - EDMD3 (1.4, 1.5, 1.12, 10.26, 14.51)
* Charcot-Marie-Tooth disease, axonal, type 2B1 - CMT2B1 (1.4, 1.5, 1.12, 10.26, 14.51)

Gene symbol and protein	Gene Location	All allelic disease phenotypes - locus/disease symbols
LMNA lamin A/C	1q21.2-q21.3	* Cardiomyopathy, dilated, 1A - CMD1A (1.4, 1.5, 1.12, 10.26, 14.51) * Lipodystrophy, familial partial, type 2 - FPLD2 (1.4, 1.5, 1.12, 10.26, 14.51) * Muscular dystrophy, limb-girdle, type 1B - LGMD1B (1.4, 1.5, 1.12, 10.26, 14.51) * Hutchinson-Gilford progeria syndrome - HGPS (1.4, 1.5, 1.12, 10.26, 14.51) * Emery-Dreifuss muscular dystrophy, autosomal dominant - EDMD2 (1.4, 1.5, 1.12, 10.26, 14.51) * Mandibuloacral dysplasia with type a lipodystrophy - MADA (1.4, 1.5, 1.12, 10.26, 14.51) * restrictive dermopathy - (1.4, 1.5, 1.12, 10.26, 14.51) * Emery-Dreifuss Autosomal recessive - EDMD3 (1.4, 1.5, 1.12, 10.26, 14.51) * Charcot-Marie-Tooth disease, axonal, type 2B1 - CMT2B1 (1.4, 1.5, 1.12, 10.26, 14.51)