Kmt2d^m1Wtsi
Spontaneous Allele Detail

Summary

• Symbol: Kmt2d^m1Wtsi
• Name: lysine (K)-specific methyltransferase 2D; mutation 1, Wellcome Trust Sanger Institute
• MGI ID: MGI:7565307
• Gene: Kmt2d Location: Chr15:98729550-98769085 bp, - strand
• Alliance: Kmt2d^m1Wtsi page

Mutation origin

• Strain of Origin: C57BL/6N-A^tm1Brd

Mutation description

• Allele Type: Spontaneous (Not Specified)
• Mutation: Intragenic deletion
• A spontaneous mutation resulted in the loss of 9 amino acids (ENSMUST00000023741, p.586594del). (J:327181)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 2 strains available Cell Lines: 0 lines available
• Carrying any Kmt2d Mutation: 169 strains or lines available

References

• Original: J:327181 Lewis MA, et al., Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme. BMC Biol. 2022 Mar 17;20(1):67
• All: 1 reference(s)