- increased circulating calcium level / IMPC
- increased heart weight / IMPC
- increased bone mineral density / IMPC
- preweaning lethality, complete penetrance / IMPC
- increased circulating phosphate level / IMPC
- decreased circulating HDL cholesterol level / IMPC
- decreased circulating cholesterol level / IMPC
- hypertrophy / IMPC
- increased lean body mass / IMPC
- increased circulating sodium level / IMPC
- decreased erythrocyte cell number / IMPC
- decreased circulating serum albumin level / IMPC
- increased circulating glucose level / IMPC
C57BL/6-Ndufs3tm1c(EUCOMM)Wtsi/Ics
Status | Available to order |
EMMA ID | EM:05923 |
International strain name | C57BL/6-Ndufs3tm1c(EUCOMM)Wtsi/Ics |
Alternative name | Ndufs3 tm1c |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Ndufs3tm1c(EUCOMM)Wtsi |
Gene/Transgene symbol | Ndufs3 |
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 line originates from the C57BL/6NTac-Ndufs3tm1a(EUCOMM)Wtsi/Ics (EMMA ID EM:04157) strain, after breeding with a flp recombinase deleter line, to convert the original targeted tm1a allele (knock-out first allele) into a conditional tm1c allele. For further details on the construction of the tm1a allele see the relevant page at the IMPC portal. Removal of the targeting cassette using flp recombinase is required to convert the targeted tm1a into a conditional tm1c allele - more information on conversion to the b,c and d allele forms. Click here for more information on EUCOMM final vectors. |
Phenotypic information | Currently not available. Heterozygous Ndufs3 tm1c are viable. |
Breeding history | For production of the Ndufs3 tm1c line, Ndufs3 tm1a mice were crossed with N10 C57BL/6NTac flp recombinase (i.e. backcrossed 10x with C57BL/6NTac mice; original background C57BL/6J). |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | no |
Immunocompromised | not known |
Information from EMMA
Archiving centre | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Animals used for archiving | heterozygous C57BL/6N Tac, wild-type C57BL/6NTac |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Leigh syndrome with leukodystrophy / Orphanet_255241
- Isolated complex I deficiency / Orphanet_2609
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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