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mt-Trm2
Spontaneous Allele Detail
Nomenclature
Symbol: mt-Trm2
Name: mitochondrially encoded tRNA arginine; mutation 2
MGI ID: MGI:3832223
Synonyms: 9A
Gene: mt-Tr  Location: ChrMT:9808-9875 bp, + strand  Genetic Position: ChrMT, Syntenic
Mutation
origin
Strain of Origin:  various
Mutation
description
Allele Type:    Spontaneous
Mutation:    Nucleotide repeat expansion
    The adenine repeat in the D stem is polymorphic with 9 adenines in this allele. (J:67312, J:97969)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 4 strains available      Cell Lines: 0 lines available
Carrying any mt-Tr Mutation:  10 strains or lines available
Notes
This polymorphism is present in ALR/Lt, NOD/ShiLtDvs, and SKH2/J. A variant with 10 adenines is found in A/J, ALS/Lt, NOD/ShiLtJ and NZB/B1NJ.
References
Original:  J:67312 Johnson KR, et al., A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice. Nat Genet. 2001 Feb;27(2):191-4
All:  2 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
12/03/2019
MGI 6.14
The Jackson Laboratory