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| Nomenclature |
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Symbol:
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Fnip1LPAB.1
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Name:
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folliculin interacting protein 1;
LPAB.1
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MGI ID: |
MGI:5437714 |
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Gene:
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Fnip1
Location:
Chr11:54438199-54518235 bp, + strand
Genetic Position: Chr11,
32.13 cM
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Mutation
origin |
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Strain of Origin:
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C57BL/6J
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Mutation
description |
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Allele
Type: | |
Chemically induced (ENU) |
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Mutation: | |
Intragenic deletion |
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Mutation details: ENU mutagenesis induced a 32 bp deletion that results in a premature stop codon at residue 293. Real-time PCR confirmed the absence of transcript expression. (J:187318)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Fnip1 Mutation:
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1 strain or line available |
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| References |
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Original: |
J:187318
Park H et al.,
"Disruption of Fnip1 reveals a metabolic checkpoint controlling B lymphocyte development."
Immunity 2012 May 25;36(5):769-81
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All: |
1 reference(s)
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Analysis Tools
