- increased circulating calcium level / IMPC
- increased circulating insulin level / IMPC
- increased heart weight / IMPC
- increased circulating alkaline phosphatase level / IMPC
- decreased circulating chloride level / IMPC
- fusion of vertebral arches / IMPC
- improved glucose tolerance / IMPC
- increased blood urea nitrogen level / IMPC
C57BL/6N-Atm1Brd Slc25a4tm1a(EUCOMM)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:06192 |
Citation information | RRID:IMSR_EM:06192 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 Slc25a4tm1a(EUCOMM)Wtsi/WtsiH |
Alternative name | EPD0369_5_A05 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Slc25a4tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Slc25a4 |
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 EUCOMM ES clone EPD0369_5_A05. 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 | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Animals used for archiving | homozygous C57BL/6NTac males |
Breeding at archiving centre | Frozen samples received. No breeding at archiving centre. Due to the possible presence of C57BL/6N-Atm1Brd/a, may produce agouti pups. |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome / Orphanet_1369
- Autosomal dominant progressive external ophthalmoplegia / Orphanet_254892
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased blood urea nitrogen level / IMPC
- decreased circulating chloride level / IMPC
- fusion of vertebral arches / IMPC
- increased circulating calcium level / IMPC
- increased heart weight / IMPC
- increased circulating insulin level / IMPC
- improved glucose tolerance / IMPC
- increased circulating alkaline phosphatase level / IMPC