- increased grip strength / IMPC
C57BL/6N-Atm1Brd Dnmt3atm1a(KOMP)Wtsi/WtsiOrl
Status | Available to order |
EMMA ID | EM:07510 |
International strain name | C57BL/6N-Atm1Brd Dnmt3atm1a(KOMP)Wtsi/WtsiOrl |
Alternative name | EPD0332_1_C06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Dnmt3atm1a(KOMP)Wtsi |
Gene/Transgene symbol | Dnmt3a |
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 EPD0332_1_C06. 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 | Institut de Transgenose, INTRAGENE, Orléans, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Sporadic pheochromocytoma/secreting paraganglioma / Orphanet_276621
- Tatton-Brown-Rahman syndrome / Orphanet_404443
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal bone structure / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- decreased circulating cholesterol level / IMPC
- increased grip strength / IMPC
- decreased lean body mass / IMPC
- decreased circulating glucose level / IMPC
- decreased exploration in new environment / IMPC
- decreased circulating HDL cholesterol level / IMPC
- increased total body fat amount / IMPC
- convulsive seizures / IMPC
- abnormal embryo size / IMPC
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