Efnb3^lltw
Spontaneous Allele Detail

Summary

• Symbol: Efnb3^lltw
• Name: ephrin B3; lilting walker
• MGI ID: MGI:5578532
• Gene: Efnb3 Location: Chr11:69444918-69451031 bp, - strand Genetic Position: Chr11, 42.8 cM
• Alliance: Efnb3^lltw page

Ataxia of a Efnb3^lltw/Efnb3^lltw mouse

Show the 1 phenotype image(s) involving this allele.

Mutation origin

• Strain of Origin: C57BL/6J

Mutation description

• Allele Type: Spontaneous (Not Specified)
• Mutation: Single point mutation
• Mutation details: A spontaneous C-to-T mutation (G-to-A on negative gene strand) results in a glycine to glutamic acid change at codon 244 (p.G244E). (J:222308, J:223790)
• 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 Efnb3 Mutation: 11 strains or lines available

References

• Original: J:223790 Harris BS, et al., Lilting walker, a spontaneous mutation that causes ataxia. MGI Direct Data Submission. 2015
• All: 2 reference(s)