C57BL/6N-Camk2btm1a(EUCOMM)Hmgu/Cnrm
Status | Available to order |
EMMA ID | EM:05782 |
International strain name | C57BL/6N-Camk2btm1a(EUCOMM)Hmgu/Cnrm |
Alternative name | HEPD0667_4_A12 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Camk2btm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Camk2b |
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 | CNR, Consiglio Nazionale delle Ricerche |
Provider affiliation | EMMA-Monterotondo Campus International Development, CNR, Consiglio Nazionale delle Ricerche |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0667_4_A12. 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 | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal dominant non-syndromic intellectual disability / Orphanet_178469
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- decreased body size / MGI
- decreased anxiety-related response / MGI
- ataxia / MGI
- impaired coordination / MGI
- abnormal nest building behavior / MGI
- abnormal object recognition memory / MGI
- reduced long term potentiation / MGI
- impaired balance / MGI
- abnormal long term depression / MGI
- abnormal long term potentiation / MGI
- abnormal voluntary movement / MGI
- nervous system phenotype / MGI
- abnormal synaptic plasticity / MGI
- homeostasis/metabolism phenotype / MGI
- behavior/neurological phenotype / MGI
- increased percent body fat/body weight / MGI
- slow postnatal weight gain / MGI
- impaired contextual conditioning behavior / MGI
- decreased grip strength / MGI
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