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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Foxa2tm1Dnl
targeted mutation 1, James E Darnell
MGI:2158924
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Foxa2tm1Dnl/Foxa2tm1Dnl involves: 129P2/OlaHsd * C57BL/6J MGI:3849567
ht2
Foxa2tm1Dnl/Foxa2+ involves: 129P2/OlaHsd * C57BL/6J MGI:3849568


Genotype
MGI:3849567
hm1
Allelic
Composition
Foxa2tm1Dnl/Foxa2tm1Dnl
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxa2tm1Dnl mutation (0 available); any Foxa2 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

embryo
• at E9.5, endodermal cells are present but have not invaginated to form the gut tube
• at E7.5 the embryo has a tubular appearance and maintains little contact with the extraembryonic tissues
• at E9.5 embryos are either minute with few externally distinguishable landmarks or small, showing increased elongation compared to minute embryos but decreased compared to control littermates
• expression analysis indicates that notochord development is not initiated
• at E9.5 in many cases the paraxial mesoderm forms a continuous mass of tissue that traverses the midline under the neural tube
• the neural tube is closed at E9.5 but the dorsal and ventral regions appear abnormal with a high density of pyknotic nuclei primarily in the dorsal regions and an increase in thickness in the ventral regions
• at E9.5, expression analysis indicates failure of differentiation of floor plate cells at all axial levels
• at E8.5 and E9.5
• expression analysis indicates that notochord development is not initiated
• lack a distinct node at E7.5 and E8.5
• at E9.5 fewer than 10 somites are seen at the trunk level compared to more than 20 in control littermates
• at E9.5 somites are disarranged and in many cases the bilateral separation of segmented mesoderm is lost

cellular
• at E9.5 embryos contain increased numbers of dying cells
• at E9.5, expression analysis indicates absence of motor neuron differentiation in the ventral region of the neural tube

nervous system
• at E8.5 neural tissues are disordered and have prominent ridges
• at E9.5, expression analysis indicates absence of motor neuron differentiation in the ventral region of the neural tube
• the neural tube is closed at E9.5 but the dorsal and ventral regions appear abnormal with a high density of pyknotic nuclei primarily in the dorsal regions and an increase in thickness in the ventral regions
• at E9.5, expression analysis indicates failure of differentiation of floor plate cells at all axial levels

vision/eye
• fail to show signs of eye differentiation at E9.5

growth/size/body




Genotype
MGI:3849568
ht2
Allelic
Composition
Foxa2tm1Dnl/Foxa2+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxa2tm1Dnl mutation (0 available); any Foxa2 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• about 10% of mice die within 24 h of birth

growth/size/body
• seen in over 50% of mice

reproductive system
• almost 50% of females fail to pass through estrus
• fewer than 50% of females carry embryos to term

behavior/neurological
• many are unable to right themselves when placed on their backs
• circular gait

homeostasis/metabolism
• hepatic glucose output is elevated and hepatic insulin sensitivity is reduced in mice fed a high fat diet
• increased hepatic levels
• ketogenesis is significantly decreased in mice fed a standard chow diet and this reduction is more severe in mice fed a high fat diet
• beta-oxidation is reduced in mice fed a high fat diet

skeleton
• seen in over 50% of mice

craniofacial
• seen in over 50% of mice

liver/biliary system
• increased hepatic levels





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
04/30/2024
MGI 6.23
The Jackson Laboratory