- decreased grip strength / IMPC
- preweaning lethality, complete penetrance / IMPC
- decreased heart left ventricle size / IMPC
- thrombocytosis / IMPC
- increased circulating calcium level / IMPC
- decreased exploration in new environment / IMPC
- increased heart left ventricle size / IMPC
- abnormal heart left ventricle morphology / IMPC
- increased cardiac muscle contractility / IMPC
- increased circulating HDL cholesterol level / IMPC
- increased circulating cholesterol level / IMPC
- increased circulating serum albumin level / IMPC
- increased circulating total protein level / IMPC
- increased startle reflex / IMPC
- thick ventricular wall / IMPC
- decreased startle reflex / IMPC
- decreased lymphocyte cell number / IMPC
- decreased leukocyte cell number / IMPC
C57BL/6N-Atm1Brd Eftud2tm1a(KOMP)Wtsi/Ics
Status | Available to order |
EMMA ID | EM:10218 |
Citation information | RRID:IMSR_EM:10218 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | C57BL/6N-Atm1Brd Eftud2tm1a(KOMP)Wtsi/Ics |
Alternative name | EPD0586_1_C02 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Eftud2tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Eftud2 |
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 | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This mouse line originates from KOMP ES clone EPD0586_1_C02. 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 | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Animals used for archiving | heterozygous C57BL/6NCrl males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Mandibulofacial dysostosis-microcephaly syndrome / Orphanet_79113
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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