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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ephb4tm1And
targeted mutation 1, David J Anderson
MGI:2183162
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ephb4tm1And/Ephb4tm1And involves: 129S7/SvEvBrd * C57BL/6J MGI:3687749


Genotype
MGI:3687749
hm1
Allelic
Composition
Ephb4tm1And/Ephb4tm1And
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ephb4tm1And mutation (1 available); any Ephb4 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• growth retardation, arrested heart development and lack of blood flow by E9.5-E10
• degeneration and necrosis by E10.5

embryo
• apparent at E9.5-E10
• remodeling defects most severe at the primitive plexus stage around E9.5
• most severe "on the venous side"

cardiovascular system
• problems remodeling blood vessels apparently independent of heart defects
• fine branching of the head vasculature not seen at E9.5-10 but extensive fusion of the capillary network
• both arterial and venous intersomatic vessels fused and truncated
• failure to remodel multiple small vessels into a single larger vessel
• development of the anterior cardinal vein is disrupted
• failure of myocardial trabeculation by E10
• incomplete heart looping at E7.5-9 but heartbeat and blood flow still detectable
• endocardium fails to expand
• heart fails to enlarge between E9 and E9.5

growth/size/body
• apparent at E9.5-E10

muscle
• failure of myocardial trabeculation by E10





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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
12/10/2024
MGI 6.24
The Jackson Laboratory