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mt-Tkm1
Spontaneous Allele Detail
Summary
Symbol: mt-Tkm1
Name: mitochondrially encoded tRNA lysine; mutation 1
MGI ID: MGI:5606283
Synonyms: tRNALys7731
Gene: mt-Tk  Location: ChrMT:7700-7764 bp, + strand  Genetic Position: ChrMT, Syntenic
Alliance: mt-Tkm1 page
Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsMitochondria with a ChrM:7731G>A mutation in the mitochondrially encoded lysine tRNA were identified in P29 cells. Cybrids created in B82 cells lacking mitochondrial DNA and then transferred to TT2-F ES cells were introduced into 8-cell stage embryos of ICR mice. Cybrids were estimated to have 70% mutant DNA. (J:206827)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any mt-Tk Mutation:  0 strains or lines available
References
Original:  J:206827 Shimizu A, et al., Transmitochondrial mice as models for primary prevention of diseases caused by mutation in the tRNALys gene. Proc Natl Acad Sci U S A. 2014 Feb 25;111(8):3104-9
All:  3 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory