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Mrps34m1Anu
Chemically induced Allele Detail
Summary
Symbol: Mrps34m1Anu
Name: mitochondrial ribosomal protein S34; mutation 1, Australian National University
MGI ID: MGI:5763565
Synonyms: ENU19:B6:MRPS34, Mrps34m1Apb, Mrps34mut
Gene: Mrps34  Location: Chr17:25114094-25115263 bp, + strand  Genetic Position: Chr17, 12.53 cM
Alliance: Mrps34m1Anu page
Mutation
origin
Strain of Origin:  C57BL/6JAnu
Mutation
description
Allele Type:    Chemically induced (ENU) (Hypomorph)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a T to C point mutation that results in the amino acid substitution of proline for leucine at position 68 (L668P). Western blot analysis confirmed the absence of protein expression in the heart and liver. (J:222643)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 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 Mrps34 Mutation:  9 strains or lines available
References
Original:  J:222643 Richman TR, et al., Mutation in MRPS34 compromises protein synthesis and causes mitochondrial dysfunction. PLoS Genet. 2015 Mar;11(3):e1005089
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
11/12/2024
MGI 6.24
The Jackson Laboratory