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Phenotypes Associated with This Genotype
Genotype
MGI:2674072
Allelic
Composition
H1f2tm2Ais/H1f2tm2Ais
H1f3tm2Ais/H1f3tm2Ais
H1f4tm2Ais/H1f4tm2Ais
Genetic
Background
involves: 129/Sv * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
H1f2tm2Ais mutation (0 available); any H1f2 mutation (17 available)
H1f3tm2Ais mutation (0 available); any H1f3 mutation (8 available)
H1f4tm2Ais mutation (0 available); any H1f4 mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no triple homozygotes are born
• no triple homozygous embryos after E11.5
• only about 25% as many embryos at E10.5 as expected

cardiovascular system
• no visible blood or blood vessels at E10.5

embryo
• arrested posterior development while anterior development remained normal at E9.5
• partial or complete axis duplication in early somite stage embryos (n=2)
• embryos between E7.5 and E11.5 are reduced in size
• retarded development based on somite number
• E10.5 embryos with 16-18 somites as opposed to an expected 26-30 somites
• varied from mild to more severe (splayed anterior neural tube)
• no visible blood or blood vessels at E10.5
• failed chorioallantoic fusion at E9.5

growth/size/body
• embryos between E7.5 and E11.5 are reduced in size
• retarded development based on somite number
• E10.5 embryos with 16-18 somites as opposed to an expected 26-30 somites

limbs/digits/tail
• at E9.5

nervous system
• varied from mild to more severe (splayed anterior neural tube)


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
01/28/2026
MGI 6.24
The Jackson Laboratory