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Flcntm1.1Lss
Targeted Allele Detail
Summary
Symbol: Flcntm1.1Lss
Name: folliculin; targeted mutation 1.1, Laura S Schmidt
MGI ID: MGI:3774416
Synonyms: BHDd
Gene: Flcn  Location: Chr11:59682234-59700842 bp, - strand  Genetic Position: Chr11, 37.79 cM
Alliance: Flcntm1.1Lss page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:130978
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsExon 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)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 119 assay results
In Structures Affected by this Mutation: 5 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 Flcn Mutation:  40 strains or lines available
References
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
All:  4 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
04/16/2024
MGI 6.23
The Jackson Laboratory