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Phenotypes Associated with This Genotype
Genotype
MGI:4844009
Allelic
Composition
Hand1tm2.1(Hand1)Abfi/Hand1tm2.1(Hand1)Abfi
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hand1tm2.1(Hand1)Abfi mutation (0 available); any Hand1 mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• majority of embryos are viable to E10.5, with 8% viable to E12.5

cardiovascular system
• mice exhibit similar phenotypes to Hand1tm1(Hand1)Abfi but at a less severe penetrance
• reduced outflow tract cushions at E12.5
• septal cardiomyocytes are disorganized in the forming interventricular septum at E12.5
• decrease in ventricular wall thickness at E12
• pericardial hemorrhaging at E12.5

craniofacial
• craniofacial defects at E12.5

embryo
• mice exhibit similar phenotypes to Hand1tm1(Hand1)Abfi but at a less severe penetrance
• embryo turning is impaired
• severe caudal defects at E12.5
• embryos surviving to E12.5 are slightly smaller than wild-type
• hypoplastic limb buds at E12.5

growth/size/body
• embryos surviving to E12.5 are slightly smaller than wild-type

homeostasis/metabolism
• pericardial hemorrhaging at E12.5

cellular
• decrease in the rate of global cell proliferation at E9.5

limbs/digits/tail
• hypoplastic limb buds at E12.5


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)
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last database update
03/18/2025
MGI 6.24
The Jackson Laboratory