C57BL/6NTac-Atxn3tm1a(KOMP)Wtsi/WtsiPh
Status | Available to order |
EMMA ID | EM:08898 |
International strain name | C57BL/6NTac-Atxn3tm1a(KOMP)Wtsi/WtsiPh |
Alternative name | EPD0162_1_C04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Atxn3tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Atxn3 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0162_1_C04. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Machado-Joseph disease type 3 / Orphanet_276244
- Machado-Joseph disease type 2 / Orphanet_276241
- Machado-Joseph disease type 1 / Orphanet_276238
IMPC phenotypes (allele matching)
MGI phenotypes (gene matching)
- Purkinje cell degeneration / MGI
- abnormal Purkinje cell morphology / MGI
- impaired coordination / MGI
- decreased exploration in new environment / MGI
- neurodegeneration / MGI
- decreased vertical activity / MGI
- astrocytosis / MGI
- nervous system phenotype / MGI
- neuronal intranuclear inclusions / MGI
- behavior/neurological phenotype / MGI
- neuronal cytoplasmic inclusions / MGI
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