About   Help   FAQ
Phenotypic Alleles
Query Results -- Summary
 Symbol
Name
ID
Lmna
lamin A
MGI:96794

8 matching Alleles (1 Gene/Marker represented)
                      Allele Symbol
Name Chr Synonyms Category Phenotypic Classes Human Diseases LmnaDhe
lamin A; disheveled hair and ears
images 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
images 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

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
04/08/2014
MGI 5.17
The Jackson Laboratory