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Kalrntm2.1Npl
Targeted Allele Detail
Summary
Symbol: Kalrntm2.1Npl
Name: kalirin, RhoGEF kinase; targeted mutation 2.1, Neuropeptide Laboratory
MGI ID: MGI:5551305
Synonyms: KalSRKO
Gene: Kalrn  Location: Chr16:33789443-34393647 bp, - strand  Genetic Position: Chr16, 24.27 cM
Alliance: Kalrntm2.1Npl page
Neuromuscular junctions are abnormal in Kalrntm2.1Npl/Kalrntm2.1Npl mice

Show the 2 phenotype image(s) involving this allele.

Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:206512
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExon 13, an exon in the spectrin repeat region (KalSR), was floxed. Flp-mediated recombination removed the neomycin resistance cassette. Cre-mediated recombination removed exon 13. Western blot analysis confirmed the loss of isoforms Kalirin7, 9 and 12 and deltaKalirin7 in the adult cortex. (J:206512)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Kalrn Mutation:  170 strains or lines available
References
Original:  J:206512 Mandela P, et al., Kalrn plays key roles within and outside of the nervous system. BMC Neurosci. 2012;13:136
All:  6 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
04/16/2024
MGI 6.23
The Jackson Laboratory