- abnormal tail movements / MGI
- abnormal posture / MGI
- impaired righting response / MGI
- apnea / MGI
- abnormal pain threshold / MGI
- abnormal nervous system electrophysiology / MGI
- impaired ability to fire action potentials / MGI
- abnormal thermal nociception / MGI
- abnormal mechanical nociception / MGI
- catalepsy / MGI
- hypoalgesia / MGI
- abnormal single cell response / MGI
- decreased thermal nociceptive threshold / MGI
- abnormal brain wave pattern / MGI
- behavior/neurological phenotype / MGI
- abnormal action potential / MGI
- hyperalgesia / MGI
- abnormal RR interval / MGI
- sinus bradycardia / MGI
B6;129-Scn10atm3(cre/ERT2)Jwo/H
Status | Available to order |
EMMA ID | EM:02603 |
Citation information | RRID:IMSR_EM:02603 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | B6;129-Scn10atm3(cre/ERT2)Jwo/H |
Alternative name | Nav1.8-CreERT2 |
Strain type | Targeted Mutant Strains : Knock-in |
Allele/Transgene symbol | Scn10atm3(cre/ERT2)Jwo |
Gene/Transgene symbol | Scn10a |
Information from provider
Provider | John Wood |
Provider affiliation | University College Lonodon |
Genetic information | The creERT2 gene was inserted at the endogenous ATG start site of the mouse Scn10a (Nav1.8) gene. This strain expresses the tamoxifen-inducible creERT2 recombinase in Scn10a (Nav1.8)-positive neurons in dorsal root ganglia. |
Phenotypic information | None observed. Heterozygous Scn10a (Nav1.8)-creERT2 can express enough cre recombinase to delete the floxed fragment, but it does not affect the expression of Scn10a in Scn10a-positive neurons in dorsal root ganglion. |
Breeding history | Mostly C57BL/6; between 3-4 crossings to C57BL/6. |
References |
|
Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Animals used for archiving | heterozygous C57BL/6 males |
Breeding at archiving centre | Males were archived upon arrival at the archiving centre. No breeding was performed. |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Romano-Ward syndrome / Orphanet_101016
- Sodium channelopathy-related small fiber neuropathy / Orphanet_306577
MGI phenotypes (gene matching)
Literature references
- Tamoxifen-inducible NaV1.8-CreERT2 recombinase activity in nociceptive neurons of dorsal root ganglia.;Zhao Jing, Nassar Mohammed A, Gavazzi Isabella, Wood John N, ;2006;Genesis (New York, N.Y. : 2000);44;364-71; 16850455
Information on how we integrate external resources can be found here
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