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Kcnn2bc-3J
Spontaneous Allele Detail
Nomenclature
Symbol: Kcnn2bc-3J
Name: potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2; bouncy 3 Jackson
MGI ID: MGI:1855967
Gene: Kcnn2  Location: Chr18:45268750-45685887 bp, + strand  Genetic Position: Chr18, 24.34 cM, cytoband C
Mutation
origin
Strain of Origin:  C3H/HeSn
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsA G-to-A point mutation at coding nucleotide 599/1394/1424 of the transcript (NM_080465/ENSMUST00000066890/NM_001312905) is predicted to result in premature truncation at tryptophan 200/465/475 of the encoded protein (NP_536713:p.W200*, ENSMUSP00000067884:p.W465*, NP_001299834:p.W475*). (J:222308)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structures
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 Kcnn2 Mutation:  6 strains or lines available
References
Original:  J:6710 Lane PW, et al., Chromosome 18 of the house mouse. J Hered. 1981 Nov-Dec;72(6):409-12
All:  3 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
04/13/2021
MGI 6.16
The Jackson Laboratory