Home News About DMDM Database Statistics Research Publications Contact  

Mutations on the Protein: P02545 From Positions: 133 To 166

17
11
0
6


Swiss-Prot Disease: VAR_016913
p.ARG133LEU
N/A
N/A
Lipodystrophy, familial partial, 2 (FPLD2)


Swiss-Prot Disease: VAR_017657
p.ARG133PRO
N/A
N/A
Emery-Dreifuss muscular dystrophy 2, autosomal dominant (EDMD2)


Swiss-Prot Disease: VAR_070176
p.ARG166PRO
N/A
N/A
Cardiomyopathy, dilated 1A (CMD1A)


Swiss-Prot Disease: VAR_070175
p.GLU138LYS
N/A
N/A
Hutchinson-Gilford progeria syndrome (HGPS)


Swiss-Prot Disease: VAR_017659
p.GLU145LYS
N/A
N/A
Hutchinson-Gilford progeria syndrome (HGPS)


Swiss-Prot Disease: VAR_017660
p.GLU161LYS
N/A
N/A
Cardiomyopathy, dilated 1A (CMD1A)


Swiss-Prot Disease: VAR_017658
p.LEU140ARG
N/A
N/A
Hutchinson-Gilford progeria syndrome (HGPS)


Swiss-Prot Disease: VAR_039760
p.LEU140PRO
N/A
N/A
Emery-Dreifuss muscular dystrophy 2, autosomal dominant (EDMD2)


Swiss-Prot Disease: VAR_034707
p.SER143PHE
N/A
N/A
Hutchinson-Gilford progeria syndrome (HGPS)


Swiss-Prot Disease: VAR_039761
p.SER143PRO
N/A
N/A
Cardiomyopathy, dilated 1A (CMD1A)


Swiss-Prot Disease: VAR_039762
p.THR150PRO
N/A
N/A
Emery-Dreifuss muscular dystrophy 2, autosomal dominant (EDMD2)


OMIM Disease: 150330.0027
p.ARG133LEU
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2||HUTCHINSON-GILFORD PROGERIA SYNDROME, CHILDHOOD-ONSET, INCLUDED


OMIM Disease: 150330.0032
p.ARG133PRO
N/A
N/A
EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT


OMIM Disease: 150330.0024
p.GLU145LYS
N/A
N/A
HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL


OMIM Disease: 150330.0028
p.GLU161LYS
N/A
N/A
CARDIOMYOPATHY, DILATED, 1A


OMIM Disease: 150330.0031
p.LEU140ARG
N/A
N/A
HUTCHINSON-GILFORD PROGERIA SYNDROME, CHILDHOOD-ONSET


OMIM Disease: 150330.0034
p.SER143PHE
N/A
N/A
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED






   |   1000 Hilltop Circle, Baltimore, MD 21250   |   Department of Biological Sciences   |   Phone: 410-455-2258