- malocclusion / MGI
- decreased body size / MGI
- circling / MGI
- hunched posture / MGI
- postnatal lethality / MGI
- premature death / MGI
- long incisors / MGI
- absent mesoderm / MGI
- increased embryonic tissue cell apoptosis / MGI
- abnormal primitive streak formation / MGI
- abnormal rostral-caudal axis patterning / MGI
- absent primitive node / MGI
- abnormal primitive streak elongation / MGI
- abnormal foregut morphology / MGI
- absent floor plate / MGI
- absent notochord / MGI
- abnormal somite shape / MGI
- abnormal developmental patterning / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal neural tube morphology / MGI
- kinked neural tube / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- abnormal primitive endoderm morphology / MGI
- decreased somite size / MGI
- fused somites / MGI
- embryonic-extraembryonic boundary constriction / MGI
- rostral body truncation / MGI
129-Foxa2tm1Jrt/H
| Status | Available to order |
| EMMA ID | EM:02526 |
| Citation information | RRID:IMSR_EM:02526 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
| International strain name | 129-Foxa2tm1Jrt/H |
| Alternative name | HNF3beta (Foxa2) |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Foxa2tm1Jrt |
| Gene/Transgene symbol | Foxa2 |
Information from provider
| Provider | Elizabeth Robertson |
| Provider affiliation | Sir William Dunn School of Pathology, University of Oxford |
| Genetic information | Coding sequence of Foxa2 replaced by neo expression construct, causing a loss of function at the Foxa2 locus. Can be used to study Foxa2 function during gastrulation. |
| Phenotypic information | Homozygous lethal at day 8 of gestation. |
| Breeding history | Backcrossed to 129/SvEv. |
| References |
|
| Homozygous fertile | no |
| Homozygous viable | no |
| Homozygous matings required | no |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Combined pituitary hormone deficiencies, genetic forms / Orphanet_95494
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- malocclusion / MGI
- abnormal cell death / MGI
- abnormal foregut morphology / MGI
- absent floor plate / MGI
- absent notochord / MGI
- decreased body size / MGI
- abnormal eye development / MGI
- circling / MGI
- abnormal gait / MGI
- hunched posture / MGI
- impaired righting response / MGI
- increased circulating triglyceride level / MGI
- increased circulating free fatty acid level / MGI
- absent mesoderm / MGI
- abnormal endoderm development / MGI
- abnormal somite development / MGI
- abnormal somite shape / MGI
- decreased embryo size / MGI
- reduced female fertility / MGI
- abnormal glucose homeostasis / MGI
- postnatal lethality / MGI
- premature death / MGI
- abnormal developmental patterning / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal neural tube morphology / MGI
- no abnormal phenotype detected / MGI
- abnormal primitive streak formation / MGI
- kinked neural tube / MGI
- abnormal nervous system development / MGI
- abnormal craniofacial development / MGI
- abnormal miscarriage rate / MGI
- long incisors / MGI
- abnormal rostral-caudal axis patterning / MGI
- abnormal metabolism / MGI
- abnormal paraxial mesoderm morphology / MGI
- absent estrous cycle / MGI
- absent estrus / MGI
- absent primitive node / MGI
- increased liver triglyceride level / MGI
- abnormal neuron differentiation / MGI
- mortality/aging / MGI
- neonatal lethality, incomplete penetrance / MGI
- embryonic lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- abnormal primitive endoderm morphology / MGI
- decreased somite size / MGI
- fused somites / MGI
- delayed heart development / MGI
- embryonic-extraembryonic boundary constriction / MGI
- rostral body truncation / MGI
- abnormal chordamesoderm morphology / MGI
- abnormal primitive streak elongation / MGI
- increased embryonic tissue cell apoptosis / MGI
Literature references
- FoxH1 (Fast) functions to specify the anterior primitive streak in the mouse.;Hoodless P A, Pye M, Chazaud C, Labbé E, Attisano L, Rossant J, Wrana J L, ;2001;Genes & development;15;1257-71; 11358869
- HNF-3 beta is essential for node and notochord formation in mouse development.;Ang S L, Rossant J, ;1994;Cell;78;561-74; 8069909
- Nato3 plays an integral role in dorsoventral patterning of the spinal cord by segregating floor plate/p3 fates via Nkx2.2 suppression and Foxa2 maintenance.;Mansour Abed AlFatah, Khazanov-Zisman Sophie, Netser Yaara, Klar Avihu, Ben-Arie Nissim, ;2014;Development (Cambridge, England);141;574-84; 24401371
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