Del(10Map3k5-Map7)2Kcl
Spontaneous Allele Detail

Summary

• Symbol: Del(10Map3k5-Map7)2Kcl
• Name: deletion, Chr 10, King's College London 2
• MGI ID: MGI:6470869
• Synonyms: Del(10Map3k5-Map7)2Wtsi, Rhyme, rthm
• Gene: Del(10Map3k5-Map7)2Kcl Location: unknown Genetic Position: Chr10, Syntenic

Mutation origin

• Strain of Origin: C57BL/6N

Mutation description

• Allele Type: Spontaneous (Null/knockout)
• Mutations: Intergenic deletion, Intragenic deletion
• Del(10Map3k5-Map7)2Kcl involves 6 genes/genome features (Map3k5, Map7, Gm51795 ...) View all
• A spontaneous mutation produced a deletion (g.10:20116294_20153024del; GRCm38) (J:327181)
• Inheritance: Recessive

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 Del(10Map3k5-Map7)2Kcl Mutation: 1 strain or line 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)