C57BL/6N-Atm1Brd Lmnatm1a(EUCOMM)Wtsi/IcsOrl
Status | Available to order |
EMMA ID | EM:09954 |
International strain name | C57BL/6N-Atm1Brd Lmnatm1a(EUCOMM)Wtsi/IcsOrl |
Alternative name | EPD0419_6_A02 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Lmnatm1a(EUCOMM)Wtsi, |
Gene/Transgene symbol | Lmna |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0419_6_A02. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Familial partial lipodystrophy, Dunnigan type / Orphanet_2348
- Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome / Orphanet_2229
- Charcot-Marie-Tooth disease type 2B1 / Orphanet_98856
- Hutchinson-Gilford progeria syndrome / Orphanet_740
- Heart-hand syndrome, Slovenian type / Orphanet_168796
- Restrictive dermopathy / Orphanet_1662
- Congenital muscular dystrophy due to LMNA mutation / Orphanet_157973
- LMNA-related cardiocutaneous progeria syndrome / Orphanet_363618
- Autosomal semi-dominant severe lipodystrophic laminopathy / Orphanet_280365
- Mandibuloacral dysplasia with type A lipodystrophy / Orphanet_90153
- Atypical Werner syndrome / Orphanet_79474
- Autosomal recessive Emery-Dreifuss muscular dystrophy / Orphanet_98855
- Autosomal dominant Emery-Dreifuss muscular dystrophy / Orphanet_98853
- Familial dilated cardiomyopathy with conduction defect due to LMNA mutation / Orphanet_300751
- Familial isolated arrhythmogenic ventricular dysplasia, right dominant form / Orphanet_293910
- Familial isolated arrhythmogenic ventricular dysplasia, biventricular form / Orphanet_293899
- Familial isolated arrhythmogenic ventricular dysplasia, left dominant form / Orphanet_293888
- Familial isolated dilated cardiomyopathy / Orphanet_154
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