- decreased grip strength / IMPC
- decreased prepulse inhibition / IMPC
- increased mean corpuscular hemoglobin concentration / IMPC
- decreased body weight / IMPC
- increased circulating alkaline phosphatase level / IMPC
- thrombocytopenia / IMPC
- impaired glucose tolerance / IMPC
- male infertility / IMPC
- decreased airway resistance / IMPC
- increased fasting circulating glucose level / IMPC
- short tibia / IMPC
- hyperactivity / IMPC
- abnormal snout morphology / IMPC
- small testis / IMPC
- abnormal testis morphology / IMPC
- decreased eosinophil cell number / IMPC
- decreased exploration in new environment / IMPC
- increased freezing behavior / IMPC
- increased circulating aspartate transaminase level / IMPC
- decreased mean platelet volume / IMPC
- decreased lung elastance / IMPC
B6NCrl;B6N-Atm1Brd Marchf6tm1a(EUCOMM)Hmgu/Ph
Status | Available to order |
EMMA ID | EM:11675 |
Citation information | RRID:IMSR_EM:11675 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 | B6NCrl;B6N-Atm1Brd Marchf6tm1a(EUCOMM)Hmgu/Ph |
Alternative name | HEPD0773_3_A09 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Marchf6tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Marchf6 |
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 | Institute of Molecular Genetics |
Provider affiliation | Department of Transgenic Models of Diseases, Institute of Molecular Genetics |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0773_3_A09. 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 |
Animals used for archiving | heterozygous C57BL/6NCrl males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Benign adult familial myoclonic epilepsy / Orphanet_86814
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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