Slc25a46em1Rstot
Endonuclease-mediated Allele Detail
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Symbol: |
Slc25a46em1Rstot |
Name: |
solute carrier family 25, member 46; endonuclease-mediated mutation 1, Rolf Stottmann |
MGI ID: |
MGI:6358090 |
Gene: |
Slc25a46 Location: Chr18:31713217-31743585 bp, - strand Genetic Position: Chr18, 17.79 cM
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Alliance: |
Slc25a46em1Rstot page
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Allele Type: |
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Endonuclease-mediated (Null/knockout) |
Mutation: |
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Intragenic deletion
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Mutation details: CRISPR/Cas9 genome editing technology was used to induce a 46-bp deletion in exon 8. The deletion causes a frameshift and a subsequent stop codon 15 amino acids downstream of the deleted sequences in the encoded protein.
(J:251671)
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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
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Carrying any Slc25a46 Mutation: |
24 strains or lines available
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Original: |
J:251671 Li Z, et al., Loss of SLC25A46 causes neurodegeneration by affecting mitochondrial dynamics and energy production in mice. Hum Mol Genet. 2017 Oct 01;26(19):3776-3791 |
All: |
2 reference(s) |
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