IMPC phenotypes (allele matching)
C57BL/6NTac-Cacna1aem1(IMPC)H/H
| Status | Available to order |
| EMMA ID | EM:12442 |
| International strain name | C57BL/6NTac-Cacna1aem1(IMPC)H/H |
| Alternative name | |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Cacna1aem1(IMPC)H |
| Gene/Transgene symbol | Cacna1a |
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
- Familial paroxysmal ataxia / Orphanet_97
- Undetermined early-onset epileptic encephalopathy / Orphanet_442835
- Spinocerebellar ataxia type 6 / Orphanet_98758
- Benign paroxysmal torticollis of infancy / Orphanet_71518
- Familial or sporadic hemiplegic migraine / Orphanet_569
- Lennox-Gastaut syndrome / Orphanet_2382