Slc25a13^em8Mvw
Endonuclease-mediated Allele Detail

Summary

• Symbol: Slc25a13^em8Mvw
• Name: solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13; endonuclease-mediated mutation 8, Michael Wiles
• MGI ID: MGI:6114753
• Synonyms: delta hs1642
• Gene: Slc25a13 Location: Chr6:6041218-6217173 bp, - strand Genetic Position: Chr6, 2.3 cM, cytoband A1
• Alliance: Slc25a13^em8Mvw page

Mutation origin

• Strain of Origin: C57BL/6J

Mutation description

• Allele Type: Endonuclease-mediated (Not Specified)
• Mutation: Intragenic deletion
• Mutation details: This endonuclease-mediated 440 bp deletion from Chromosome 6: 6,163,224 bp - 6,163,663 bp (GRCM38.p4) within the Slc25a13 gene deletes the murine equivalent sequence to human enhancer hs1642. (J:254776)
• Inheritance: Not Specified

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 1 strain available Cell Lines: 0 lines available
• Carrying any Slc25a13 Mutation: 179 strains or lines available

References

• Original: J:254776 Johnson KR, et al., Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice. Genetics. 2018 Mar;208(3):1165-1179
• All: 1 reference(s)