C3HeB/FeJ-Ttnm2Mhda/Ieg
Status | Available to order |
EMMA ID | EM:09081 |
International strain name | C3HeB/FeJ-Ttnm2Mhda/Ieg |
Alternative name | TtnD27407GMhda |
Strain type | Induced Mutant Strains : Chemically-induced |
Allele/Transgene symbol | Ttnm2Mhda, |
Gene/Transgene symbol | Ttn |
Information from provider
Provider | Martin Hrabe de Angelis |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum München |
Genetic information | Missense mutation 82220A->G; internal lab code Ttn-01 |
Phenotypic information | Homozygous:no visible phenotype, viableHeterozygous:no visible phenotype |
References | None available |
Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | not known |
Immunocompromised | not known |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C3H |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Classic multiminicore myopathy / Orphanet_324604
- Childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome / Orphanet_466921
- Familial isolated arrhythmogenic ventricular dysplasia, biventricular form / Orphanet_293899
- Familial isolated arrhythmogenic ventricular dysplasia, left dominant form / Orphanet_293888
- Tibial muscular dystrophy / Orphanet_609
- Familial isolated dilated cardiomyopathy / Orphanet_154
- Autosomal recessive centronuclear myopathy / Orphanet_169186
- Titin-related limb-girdle muscular dystrophy R10 / Orphanet_140922
- Hereditary myopathy with early respiratory failure / Orphanet_178464
- Early-onset myopathy with fatal cardiomyopathy / Orphanet_289377
- Familial isolated arrhythmogenic ventricular dysplasia, right dominant form / Orphanet_293910
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