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Mmutem1Cpv
Endonuclease-mediated Allele Detail
Summary
Symbol: Mmutem1Cpv
Name: methylmalonyl-Coenzyme A mutase; endonuclease-mediated mutation 1, Charles P Venditti
MGI ID: MGI:7431125
Synonyms: Mmutp.R106C
Gene: Mmut  Location: Chr17:41245576-41272879 bp, + strand  Genetic Position: Chr17, 19.55 cM, cytoband C-D
Alliance: Mmutem1Cpv page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Endonuclease-mediated (Humanized sequence)
Mutation:    Nucleotide substitutions
 
Mutation detailsCRISPR/Cas9 technology generated an arginine to cysteine substitution at amino acid 106 (p.R106C). This corresponds to the human p.R108C pathogenic mutation classified as muto which results in the more common and severe form of methylmalonic acidemia. (J:332892)
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 Mmut Mutation:  34 strains or lines available
References
Original:  J:332892 Schneller JL, et al., In vivo genome editing at the albumin locus to treat methylmalonic acidemia. Mol Ther Methods Clin Dev. 2021 Dec 10;23:619-632
All:  1 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
12/10/2024
MGI 6.24
The Jackson Laboratory