About   Help   FAQ
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





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