C57BL/6J-Kcna1em1H/H
| Status | Available to order |
| EMMA ID | EM:14626 |
| International strain name | C57BL/6J-Kcna1em1H/H |
| Alternative name | KCNA1-R417X-EM1-B6 |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Kcna1em1H |
| Gene/Transgene symbol | Kcna1 |
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:not knownHeterozygous:None reported |
| 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
- Episodic ataxia type 1 / Orphanet_37612
- Isolated autosomal dominant hypomagnesemia, Glaudemans type / Orphanet_199326
- Early infantile epileptic encephalopathy / Orphanet_1934
- Hereditary continuous muscle fiber activity / Orphanet_972
- Paroxysmal kinesigenic dyskinesia / Orphanet_98809