Symbol Name ID

Lmna lamin A MGI:96794

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8 matching Alleles (1 Gene/Marker represented)

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                      Allele Symbol
Name                         Chr                Synonyms                      Category                                                                                                              Phenotypic Classes                                                                                                                                                                                       Human Diseases                                                                                

LmnaDhe
lamin A; disheveled hair and ears
                        3                                          Spontaneous           adipose, cellular, craniofacial, digestive/alimentary, endocrine/exocrine, growth/size, hearing/vestibular/ear, homeostasis, integument, limbs/digits/tail, mortality/aging, pigmentation, reproductive, skeleton, vision/eye  Hutchinson-Gilford Progeria Syndrome; HGPS 176670                                                                                                                             

Lmnatm1.1Otin
lamin A; targeted mutation 1.1, Carlos Lopez-Otin  3    LmnaG609G                             Targeted (knock-in)   adipose, behavior, cardiovascular, cellular, craniofacial, growth/size, hematopoietic, homeostasis, immune, integument, mortality/aging, muscle, reproductive, skeleton                                                        Hutchinson-Gilford Progeria Syndrome; HGPS 176670                                                                                                                             

Lmnatm1Gbon
lamin A; targeted mutation 1, Gisele Bonne           3    LmnaH222P                             Targeted (knock-in)   behavior, cardiovascular, growth/size, homeostasis, mortality/aging, muscle, respiratory                                                                                                                                       Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant; EDMD2 181350                                                                                                         

Lmnatm1Lgf
lamin A; targeted mutation 1, Loren G Fong
            3    LmnaHG                                Targeted (knock-out)  adipose, cellular, craniofacial, growth/size, integument, mortality/aging, skeleton                                                                                                                                            Hutchinson-Gilford Progeria Syndrome; HGPS 176670                                                                                                                             

Lmnatm1Stw
lamin A; targeted mutation 1, Colin L Stewart         3    Lmna-                                 Targeted (knock-out)  adipose, behavior, cellular, endocrine/exocrine, growth/size, hematopoietic, homeostasis, immune, mortality/aging, muscle, nervous system, reproductive, skeleton                                                              Cardiomyopathy, Dilated, 1A; CMD1A 115200; Charcot-Marie-Tooth Disease, Axonal, Type 2B1; CMT2B1 605588; Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant; EDMD2 181350

Lmnatm2.1Gbon
lamin A; targeted mutation 2.1, Gisele Bonne       3    LmnadeltaK32                          Targeted (other)      adipose, behavior, cardiovascular, cellular, growth/size, homeostasis, mortality/aging, muscle, renal/urinary                                                                                                                  Muscular Dystrophy, Congenital, Lmna-Related 613205                                                                                                                           

Lmnatm2Stw
lamin A; targeted mutation 2, Colin L Stewart         3    Lmnadelta9, LmnaL530P, ProgericL530P  Targeted (knock-in)   adipose, behavior, cardiovascular, cellular, craniofacial, digestive/alimentary, endocrine/exocrine, growth/size, hearing/vestibular/ear, integument, mortality/aging, muscle, reproductive, skeleton                          Hutchinson-Gilford Progeria Syndrome; HGPS 176670                                                                                                                             

Lmnatm3Stw
lamin A; targeted mutation 3, Colin L Stewart         3    LMNA-N195K                            Targeted (knock-in)   behavior, cardiovascular, growth/size, integument, mortality/aging, muscle                                                                                                                                                     Cardiomyopathy, Dilated, 1A; CMD1A 115200