- muscle weakness / MGI
- paralysis / MGI
- decreased body weight / MGI
- decreased body size / MGI
- decreased anxiety-related response / MGI
- hypoactivity / MGI
- impaired coordination / MGI
- abnormal gait / MGI
- gliosis / MGI
- spongiform encephalopathy / MGI
- abnormal muscle tone / MGI
- muscle hypertonia / MGI
- jerky movement / MGI
C57BL/6NTac-Aspatm1a(EUCOMM)Wtsi/Ieg
Status | Available to order |
EMMA ID | EM:09271 |
International strain name | C57BL/6NTac-Aspatm1a(EUCOMM)Wtsi/Ieg |
Alternative name | EPD0038_4_F09 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Aspatm1a(EUCOMM)Wtsi, |
Gene/Transgene symbol | Aspa |
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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0038_4_F09. 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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6NTacUSA, wild-type C57BL/6NTacUSA |
Stage of embryos | 2-cell |
Disease and phenotype information
MGI allele-associated human disease models
Orphanet associated rare diseases, based on orthologous gene matching
- Severe Canavan disease / Orphanet_314911
- Mild Canavan disease / Orphanet_314918
MGI phenotypes (allele matching)
Information on how we integrate external resources can be found here
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