Kcnn2^fri
Spontaneous Allele Detail

Summary

• Symbol: Kcnn2^fri
• Name: potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2; frissonant
• MGI ID: MGI:1856876
• Gene: Kcnn2 Location: Chr18:45401927-45818950 bp, + strand Genetic Position: Chr18, 24.34 cM, cytoband C
• Alliance: Kcnn2^fri page

Mutation origin

• Strain of Origin: C3H/HePas-Kit^W-f

Mutation description

• Allele Type: Spontaneous
• Mutation: Intragenic deletion
• A 3441 bp deletion begins in the first coding exon and ends in the second intron. (J:177761)
• Inheritance: Recessive

Disease models

Expression

In Structures Affected by this Mutation:

3 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 0 strains available Cell Lines: 0 lines available
• Carrying any Kcnn2 Mutation: 43 strains or lines available

References

• Original: J:13711 Guenet JL, fri. Mouse News Lett. 1977;56:57
• All: 3 reference(s)