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Gpr132tm1Witt
Targeted Allele Detail
Summary
Symbol: Gpr132tm1Witt
Name: G protein-coupled receptor 132; targeted mutation 1, Owen N Witte
MGI ID: MGI:2388138
Synonyms: G2A-
Gene: Gpr132  Location: Chr12:112814493-112831848 bp, - strand  Genetic Position: Chr12, 61.25 cM, cytoband F2
Alliance: Gpr132tm1Witt page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:69473
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129X1/SvJ
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsThe gene was disrupted by replacement of exon 2 (98% of the total coding sequence) with an IRES-lacZ-PGK-neo cassette. Absence of gene expression was confirmed by RT-PCR analysis of pre-B and -T cells from homozygous mutant animals. (J:69473)
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: 8 anatomical structure(s)
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 Gpr132 Mutation:  25 strains or lines available
References
Original:  J:69473 Le LQ, et al., Mice lacking the orphan G protein-coupled receptor G2A develop a late-onset autoimmune syndrome. Immunity. 2001 May;14(5):561-71
All:  17 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
11/19/2024
MGI 6.24
The Jackson Laboratory