- preweaning lethality, complete penetrance / IMPC
B6Brd;B6N-Tyrc-Brd Mtfmttm1e(KOMP)Wtsi/Wtsi
Status | Available to order |
EMMA ID | EM:12053 |
International strain name | B6Brd;B6N-Tyrc-Brd Mtfmttm1e(KOMP)Wtsi/Wtsi |
Alternative name | EPD0042_1_A05 |
Strain type | Targeted Mutant Strains : Targeted Non-conditional |
Allele/Transgene symbol | Mtfmttm1e(KOMP)Wtsi, |
Gene/Transgene symbol | Mtfmt |
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 KOMP ES clone EPD0042_1_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 | Wellcome Trust Sanger Institute, Hinxton, United Kingdom |
Animals used for archiving | heterozygous C57BL/6Brd-Tyr |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Leigh syndrome with leukodystrophy / Orphanet_255241
- Combined oxidative phosphorylation defect type 15 / Orphanet_319524
IMPC phenotypes (allele matching)
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