C57BL/6N-Mfn2tm1b(EUCOMM)Wtsi/Ieg
Status | Available to order |
EMMA ID | EM:10115 |
International strain name | C57BL/6N-Mfn2tm1b(EUCOMM)Wtsi/Ieg |
Alternative name | EPD0382_7_B07 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Mfn2tm1b(EUCOMM)Wtsi |
Gene/Transgene symbol | Mfn2 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
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 EPD0382_7_B07. For further details on the construction of this clone see the page at the IMPC portal. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele (Gt(ROSA)26Sor |
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/6NTac |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Multiple symmetric lipomatosis / Orphanet_2398
- Autosomal dominant Charcot-Marie-Tooth disease type 2A2 / Orphanet_99947
- Hereditary motor and sensory neuropathy type 6 / Orphanet_90120
- Hereditary motor and sensory neuropathy type 5 / Orphanet_64751
- Severe early-onset axonal neuropathy due to MFN2 deficiency / Orphanet_90118
IMPC phenotypes (allele matching)
MGI phenotypes (gene matching)
- decreased embryo size / MGI
- decreased trophoblast giant cell number / MGI
- abnormal axonal transport / MGI
- abnormal trophoblast layer morphology / MGI
- abnormal mitochondrion morphology / MGI
- abnormal mitochondrial physiology / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- embryonic lethality during organogenesis, incomplete penetrance / MGI
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).