IMPC phenotypes (gene matching)
- preweaning lethality, incomplete penetrance / IMPC
C57BL/6J-Syne1em1H/H
| Status | Available to order |
| EMMA ID | EM:13031 |
| International strain name | C57BL/6J-Syne1em1H/H |
| Alternative name | Syne1-R8253Q-EM1-B6 |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Syne1em1H |
| Gene/Transgene symbol | Syne1 |
Information from provider
| Provider | MRC-Harwell |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | For detailed information on the genetic description of this strain, please have a look at this report. |
| Phenotypic information | Homozygous:UnknownHeterozygous:None |
| Breeding history | Co-isogenic on original background |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | not known |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive ataxia, Beauce type / Orphanet_88644
- Autosomal dominant Emery-Dreifuss muscular dystrophy / Orphanet_98853
- Autosomal recessive myogenic arthrogryposis multiplex congenita / Orphanet_319332