- 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 |
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 |
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
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