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| Nomenclature |
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Symbol:
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Flcntm1.1Lss
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Name:
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folliculin;
targeted mutation 1.1, Laura S Schmidt
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MGI ID: |
MGI:3774416 |
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Synonyms: |
BHDd |
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Gene:
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Flcn
Location:
Chr11:59791408-59810016 bp, - strand
Genetic Position: Chr11,
37.79 cM
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:130978
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Parent Cell Line:
| Not Specified (ES Cell) |
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Strain of Origin:
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Not Specified
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Mutation description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutation: | |
Intragenic deletion |
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Mutation details: Exon 7 was removed by germ-line, cre-mediated recombination. Deletion of exon 7 results in a frame shift and premature termination. This allele is expected to be null. (J:130978)
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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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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Flcn Mutation:
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10 strains or lines available |
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| References |
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Original: |
J:130978
Baba M et al.,
"Kidney-targeted Birt-Hogg-Dube gene inactivation in a mouse model: Erk1/2 and Akt-mTOR activation, cell hyperproliferation, and polycystic kidneys."
J Natl Cancer Inst 2008 Jan 16;100(2):140-54
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All: |
3 reference(s)
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