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Fasntm1.1Sem
Targeted Allele Detail
Summary
Symbol: Fasntm1.1Sem
Name: fatty acid synthase; targeted mutation 1.1, Clay F Semenkovich
MGI ID: MGI:3765071
Synonyms: FAS-deficient
Gene: Fasn  Location: Chr11:120696672-120715373 bp, - strand  Genetic Position: Chr11, 84.56 cM
Alliance: Fasntm1.1Sem page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:127793
Parent Cell Line:  RW-4 (ES Cell)
Strain of Origin:  129X1/SvJ
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsMice carrying the Fasntm1Sem allele were crossed with Cre transgenic mice to remove exons 4-8 of the gene. Germline deletion of the exons was verified by PCR, and gene inactivation was demonstrated by a 50% reduction in enzyme activity in liver lysates from heterozygote. (J:127793)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Fasn Mutation:  89 strains or lines available
References
Original:  J:127793 Chakravarthy MV, et al., 'New' hepatic fat activates PPARalpha to maintain glucose, lipid, and cholesterol homeostasis. Cell Metab. 2005 May;1(5):309-22
All:  3 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
11/12/2024
MGI 6.24
The Jackson Laboratory