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| Nomenclature |
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Symbol:
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Gpr132tm1Witt
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Name:
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G protein-coupled receptor 132;
targeted mutation 1, Owen N Witte
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MGI ID: |
MGI:2388138 |
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Synonyms: |
G2A- |
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Gene:
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Gpr132
Location:
Chr12:112850876-112860916 bp, - strand
Genetic Position: Chr12,
61.25 cM, cytoband F2
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:69473
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Parent Cell Line:
| Not Specified (ES Cell) |
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Strain of Origin:
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129X1/SvJ
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Mutation description |
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Allele
Type: | |
Targeted (Reporter) |
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Mutations: | |
Insertion, Intragenic deletion |
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Mutation details: The 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)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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| References |
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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
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All: |
8 reference(s)
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