Espn^spdz
Spontaneous Allele Detail

Summary

• Symbol: Espn^spdz
• Name: espin; spindizzy
• MGI ID: MGI:6470866
• Gene: Espn Location: Chr4:152204788-152236828 bp, - strand Genetic Position: Chr4, 82.9 cM, cytoband E1
• Alliance: Espn^spdz page

Mutation origin

• Strain of Origin: C57BL/6N

Mutation description

• Allele Type: Spontaneous (Null/knockout)
• Mutation: Intragenic deletion
• Mutation details: A spontaneous mutation produced a deletion that produces a disruption in intron 15-16 between g.4:152122586 and g.4:152123017 (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 Espn Mutation: 37 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)