About   Help   FAQ
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 (28 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 (28 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory