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

Symbol:	Slc25a13em9Mvw
Name:	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13; endonuclease-mediated mutation 9, Michael Wiles
MGI ID:	MGI:6115007
Synonyms:	delta hs2313, eDlx23 null
Gene:	Slc25a13  Location: Chr6:6041218-6217173 bp, - strand  Genetic Position: Chr6, 2.3 cM, cytoband A1
Alliance:	Slc25a13em9Mvw page

Strain of Origin:

C57BL/6J

Allele Type:    Endonuclease-mediated (Not Specified) Mutation:    Intragenic deletion   Mutation details: This endonuclease-mediated 455 bp deletion from Chromosome 6: 6,058,558 bp - 6,059,012 bp (GRCM38.p4) within the Slc25a13 gene deletes the murine equivalent sequence to human enhancer hs2313, also referred to as eDlx23. (J:254776) Inheritance:    Not Specified

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:	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)