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Hnf4atm1Sad
Targeted Allele Detail
Summary
Symbol: Hnf4atm1Sad
Name: hepatic nuclear factor 4, alpha; targeted mutation 1, Stephen A Duncan
MGI ID: MGI:2385463
Synonyms: hnf4alphaloxP
Gene: Hnf4a  Location: Chr2:163348731-163414827 bp, + strand  Genetic Position: Chr2, 84.32 cM
Alliance: Hnf4atm1Sad page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:75121
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
    Single loxP sites in introns 1 and 2 flanked exon 2. (J:75121)
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: 226 assay results
5 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 3 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 Hnf4a Mutation:  27 strains or lines available
References
Original:  J:75121 Parviz F, et al., Generation of a conditionally null allele of hnf4alpha. Genesis. 2002 Feb;32(2):130-3
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
04/16/2024
MGI 6.23
The Jackson Laboratory