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Kirrel2tm2b(KOMP)Wtsi
Targeted Allele Detail
Summary
Symbol: Kirrel2tm2b(KOMP)Wtsi
Name: kirre like nephrin family adhesion molecule 2; targeted mutation 2b, Wellcome Trust Sanger Institute
MGI ID: MGI:6285518
Synonyms: Kirrel2-
Gene: Kirrel2  Location: Chr7:30146959-30157115 bp, - strand  Genetic Position: Chr7, 18.36 cM
Alliance: Kirrel2tm2b(KOMP)Wtsi page
IMPC: Kirrel2 gene page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:272414
Parent Cell Line:  JM8A3.N1 (ES Cell)
Strain of Origin:  C57BL/6N-Atm1Brd
Project Collection: KOMP-CSD
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutation:    Intragenic deletion
 
Mutation detailsThe L1L2_Bact_P cassette was inserted at position 30154397 of Chromosome 7 upstream of the critical exons 3 and 4 (Build GRCm39). The cassette is composed of an FRT site followed by lacZ sequence and a loxP site. This first loxP site is followed by a neomycin resistance gene under the control of the human beta-actin promoter, SV40 polyA, a second FRT site and a second loxP site. A third loxP site is inserted downstream of exon 4 at position 30155529. Exons 3 and 4 are thus flanked by loxP sites. A null/knockout allele was created by cre recombinase expression in mice carrying the tm2a allele to remove the neo selection cassette and loxP-flanked exons 3 and 4. Further information on targeting strategies used for this and other IKMC alleles can be found at http://www.informatics.jax.org/mgihome/nomen/IKMC_schematics.shtml. In situ hybridization and immunohistochemical analyses confirmed the absence of transcript and protein expression in the vomeronasal organ (VNO) and on vomeronasal sensory neuron (VSN) axons of homozygous mutant mice, respectively. (J:272414)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 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 Kirrel2 Mutation:  24 strains or lines available
References
Original:  J:272414 Brignall AC, et al., Loss of Kirrel family members alters glomerular structure and synapse numbers in the accessory olfactory bulb. Brain Struct Funct. 2018 Jan;223(1):307-319
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
04/09/2024
MGI 6.23
The Jackson Laboratory