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Hlftm1Schb
Targeted Allele Detail
Summary
Symbol: Hlftm1Schb
Name: hepatic leukemia factor; targeted mutation 1, Ueli Schibler
MGI ID: MGI:3045480
Synonyms: Hlf-, PAR bZIP-
Gene: Hlf  Location: Chr11:90227362-90281721 bp, - strand  Genetic Position: Chr11, 55.03 cM
Alliance: Hlftm1Schb page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:90854
Parent Cell Line:  D3 (ES Cell)
Strain of Origin:  129S2/SvPas
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA lacZ and PGK-neo replaced exon 2, which encodes the transactivation domain. RT-PCR did not detect transcripts in mutant mice. (J:90854)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Hlf Mutation:  15 strains or lines available
References
Original:  J:90854 Gachon F, et al., The loss of circadian PAR bZip transcription factors results in epilepsy. Genes Dev. 2004 Jun 15;18(12):1397-412
All:  12 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
04/23/2024
MGI 6.23
The Jackson Laboratory