C57BL/6NTac-Atp1a3em3H/H
Status | Available to order |
EMMA ID | EM:13034 |
International strain name | C57BL/6NTac-Atp1a3em3H/H |
Alternative name | ATP1A3-N879T-EM3-B6N |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Atp1a3em3H, |
Gene/Transgene symbol | Atp1a3 |
Information from provider
Provider | MRC-Harwell |
Provider affiliation | Mammalian Genetics Unit, 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:UnknownHeterozygous:A couple have malformed teeth but not sure if this is a phenotype as could just be a background issue on the B6N that is prone to this. |
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
- Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome / Orphanet_1171
- Rapid-onset dystonia-parkinsonism / Orphanet_71517
- Alternating hemiplegia of childhood / Orphanet_2131
- Non-specific early-onset epileptic encephalopathy / Orphanet_442835
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