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Fars2em1Chenk
Endonuclease-mediated Allele Detail
Summary
Symbol: Fars2em1Chenk
Name: phenylalanine-tRNA synthetase 2, mitochondrial; endonuclease-mediated mutation 1, Kun Chen
MGI ID: MGI:7621486
Gene: Fars2  Location: Chr13:36301373-36721569 bp, + strand  Genetic Position: Chr13, 14.44 cM, cytoband A5
Alliance: Fars2em1Chenk page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsCRISPR/cas9 mediated recombination using guide RNAs introduced a G to T mutation at position 424 (p.D142Y). This mutation disrupts the aminoacylation activity of the enzyme. (J:339244)
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: 0 strains available      Cell Lines: 0 lines available
Carrying any Fars2 Mutation:  44 strains or lines available
References
Original:  J:339244 Chen X, et al., Neuropathy-associated Fars2 deficiency affects neuronal development and potentiates neuronal apoptosis by impairing mitochondrial function. Cell Biosci. 2022 Jul 6;12(1):103
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
05/21/2024
MGI 6.23
The Jackson Laboratory