Summary | Mutation origin | Mutation description | Find Mice (IMSR) | References

Symbol:	Slc25a13em7Mvw
Name:	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13; endonuclease-mediated mutation 7, Michael Wiles
MGI ID:	MGI:6115029
Synonyms:	Line 54
Gene:	Slc25a13  Location: Chr6:6041218-6217173 bp, - strand  Genetic Position: Chr6, 2.3 cM, cytoband A1
Alliance:	Slc25a13em7Mvw page

Strain of Origin:

C57BL/6J

Allele Type:    Endonuclease-mediated (Not Specified) Mutation:    Intragenic deletion   Mutation details: This CRISPR/Cas9 mediated mutation has a 25,420 bp deletion from Chr 6: 6,141,226 bp - 6,166,645 bp (GRCm38.p4) and a 2 bp TA insertion there. This deletion includes the putative hs1642 enhancer element and phylogenetically conserved region in exon 4. (J:254776) Inheritance:    Not Specified

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 Slc25a13 Mutation:	178 strains or lines available

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)