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Kcnn2fri
Spontaneous Allele Detail
Nomenclature
Symbol: Kcnn2fri
Name: potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2; frissonant
MGI ID: MGI:1856876
Gene: Kcnn2  Location: Chr18:45268860-45685883 bp, + strand  Genetic Position: Chr18, 24.34 cM, cytoband C
Mutation
origin
Strain of Origin:  C3H/HePas-KitW-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
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 3 anatomical structures
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:  24 strains or lines available
References
Original:  J:13711 Guenet JL, fri. Mouse News Lett. 1977;56:57
All:  3 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/12/2018
MGI 6.12
The Jackson Laboratory