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Thrbtm1Mkni
Targeted Allele Detail
Summary
Symbol: Thrbtm1Mkni
Name: thyroid hormone receptor beta; targeted mutation 1, Marlies Knipper
MGI ID: MGI:3836780
Synonyms: Thrbtm1.1Sasr, TRbetaflox, TRbeta L2, TRbetalox
Gene: Thrb  Location: Chr14:4431611-4809435 bp, - strand  Genetic Position: Chr14, 7.08 cM, cytoband A3
Alliance: Thrbtm1Mkni page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:145941
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsLoxP sites were introduced 5' and 3' of exon 8 and an FRT site flanked neomycin resistance gene cassette was introduced downstream of the 3' loxP site in intron 8. The neo cassette was then removed by Flp-mediated recombination leaving behind a single FRT site. (J:145941)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 44 assay results
1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 2 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 Thrb Mutation:  41 strains or lines available
References
Original:  J:145941 Winter H, et al., Deafness in TRbeta mutants is caused by malformation of the tectorial membrane. J Neurosci. 2009 Feb 25;29(8):2581-7
All:  13 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