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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Bcas3tm1.1Msin
targeted mutation 1.1, Maneesha S Inamdar
MGI:6195663
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Bcas3tm1.1Msin/Bcas3tm1.1Msin involves: BALB/cJ * C57BL/6NCrlj * CBA/JNCrlj MGI:6195770


Genotype
MGI:6195770
hm1
Allelic
Composition
Bcas3tm1.1Msin/Bcas3tm1.1Msin
Genetic
Background
involves: BALB/cJ * C57BL/6NCrlj * CBA/JNCrlj
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bcas3tm1.1Msin mutation (0 available); any Bcas3 mutation (76 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

cardiovascular system
• impaired or random migration and are unable to form organized vessels
• fewer capillaries
• discontinuous intersomitic vessels
• unpatterned at E8.5
• discontinuous with reduced lumen
• impaired branching in head and heart vasculature
• reduced sprouting in head and heart vasculature
• reduced development
• fused atrioventricular canal
• collapsed, small heart chambers

embryo
• reduced number of somites at E9.5
• fetal vessels fail to invade into the developing placenta
• composed of mostly trophoblast giant cells
• lacking stratified layers
• few major blood vessels with irregular and fused vessels
• congested capillaries are lined by thinner endothelium

growth/size/body
• disorganized with reduced capillaries and impaired branching of intersomitic vessels at E9.5

cellular
• cell derived from the yolk sac exhibit reduced migration rates and loss of directionality





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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
04/30/2024
MGI 6.23
The Jackson Laboratory