C57BL/6J-Scn9aem1H/H
| Status | Available to order |
| EMMA ID | EM:14647 |
| International strain name | C57BL/6J-Scn9aem1H/H |
| Alternative name | SCN9A-DEL713-EM1-B6 |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Scn9aem1H |
| Gene/Transgene symbol | Scn9a |
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
- Hereditary sensory and autonomic neuropathy type 2 / Orphanet_970
- Channelopathy-associated congenital insensitivity to pain / Orphanet_88642
- Paroxysmal extreme pain disorder / Orphanet_46348
- Sodium channelopathy-related small fiber neuropathy / Orphanet_306577
- Primary erythromelalgia / Orphanet_90026