IMPC phenotypes (allele matching)
- preweaning lethality, incomplete penetrance / IMPC
C57BL/6NTac-Scn1bem1(IMPC)H/H
| Status | Available to order |
| EMMA ID | EM:12354 |
| International strain name | C57BL/6NTac-Scn1bem1(IMPC)H/H |
| Alternative name | |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Scn1bem1(IMPC)H |
| Gene/Transgene symbol | Scn1b |
Information from provider
| Provider | MRC, Medical Research Council |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
| Phenotypic information | Potential phenotyping data in the IMPC portal |
| References | None available |
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
- Dravet syndrome / Orphanet_33069
- Familial progressive cardiac conduction defect / Orphanet_871
- Early infantile epileptic encephalopathy / Orphanet_1934
- Generalized epilepsy with febrile seizures-plus / Orphanet_36387
IMPC phenotypes (gene matching)
- preweaning lethality, incomplete penetrance / IMPC