About   Help   FAQ
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 (27 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 (27 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





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory