Del(18Ctxn3-Ccdc192)1Kcl
Spontaneous Allele Detail

Summary

• Symbol: Del(18Ctxn3-Ccdc192)1Kcl
• Name: deletion, Chr 18, King's College London 1
• MGI ID: MGI:6470868
• Synonyms: Rhythm, rthm
• Gene: Del(18Ctxn3-Ccdc192)1Kcl Location: unknown Genetic Position: Chr18, Syntenic

Mutation origin

• Strain of Origin: C57BL/6N

Mutation description

• Allele Type: Spontaneous (Null/knockout)
• Mutations: Intergenic deletion, Intragenic deletion
• Del(18Ctxn3-Ccdc192)1Kcl involves 201 genes/genome features (A330093E20Rik, Gm26262, Gm38337 ...) View all
• A spontaneous mutation produced the deletion (g.18:57437258_57740507; 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: 2 strains available Cell Lines: 0 lines available
• Carrying any Del(18Ctxn3-Ccdc192)1Kcl 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)