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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Hnf4atm1Dnl
targeted mutation 1, James E Darnell
MGI:2158682
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Hnf4atm1Dnl/Hnf4atm1Dnl either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6) MGI:3610559
hm2
Hnf4atm1Dnl/Hnf4atm1Dnl involves: 129S4/SvJae * C57BL/6 MGI:3700818


Genotype
MGI:3610559
hm1
Allelic
Composition
Hnf4atm1Dnl/Hnf4atm1Dnl
Genetic
Background
either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hnf4atm1Dnl mutation (0 available); any Hnf4a mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygotes die before E10.5

embryo
• at E8.5, homozygotes display severe disruption of embryonic development
• mutant embryos exhibit an aberrant and retarded gastrulation process
• at E8.5, the mutant embryonic ectoderm varies from a thin sphere at the center to a thicker columnar epithelial tube
• at E6.5-E8.5, homozygotes exhibit increased cell death in the embryonic ectoderm, esp. in the posterior region of the embryo
• in contrast, little cell death is noted in mutant embryonic mesoderm or endoderm
• at E5.5, homozygotes appear morphologically normal; however, starting at E6.5, mutant embryos are often smaller, displaying a growth delay of ~24 hrs
• at E7.5, mutant embryonic cavities appear to be less expanded than wild-type
• at E8.5, the mutant embryonic portion is often distorted in shape, appearing as a small sphere or ovoid in the distal region
• by E10.5, mutant embryos are composed primarily of extraembryonic tissues, giant trophoblast cells, parietal endoderm, and a small yolk sac; the embryonic region has degenerated
• at E7.5, mutant embryos lack an identifiable mesoderm and remain as a two-layered cylinder of ectoderm and endoderm similar to wild-type embryos at E6.5
• by E8.5, a third layer is present but appears largely abnormal; mesoderm differentiation is delayed by ~24 hrs
• homozygotes exhibit a delay of ~24 hrs in primitive streak and node formation
• at E8.5, the mutant extraembryonic region appears as a large mass of tissues with relatively small cavities
• at E7.5 and E8.5, mutant embryos lack a clearly identifiable allantois
• at E7.5 and E8.5, mutant embryos lack a clearly identifiable amnion
• at E7.5 and E8.5, mutant embryos lack a clearly identifiable chorion
• by E10.5, mutant embryos exhibit a small yolk sac

growth/size/body
• at E5.5, homozygotes appear morphologically normal; however, starting at E6.5, mutant embryos are often smaller, displaying a growth delay of ~24 hrs

cellular
• at E6.5-E8.5, homozygotes exhibit increased cell death in the embryonic ectoderm, esp. in the posterior region of the embryo
• in contrast, little cell death is noted in mutant embryonic mesoderm or endoderm




Genotype
MGI:3700818
hm2
Allelic
Composition
Hnf4atm1Dnl/Hnf4atm1Dnl
Genetic
Background
involves: 129S4/SvJae * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hnf4atm1Dnl mutation (0 available); any Hnf4a mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• embryos exhibit an increase in overall level of cell death; cell death is 2.3-fold higher in the distal region than the proximal region of the E6.5 embryo

embryo
• embryos exhibit an increase in overall level of cell death; cell death is 2.3-fold higher in the distal region than the proximal region of the E6.5 embryo
• smaller than control littermates at E6.5

growth/size/body
• smaller than control littermates at E6.5





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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
11/19/2024
MGI 6.24
The Jackson Laboratory