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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ascl2+
wild type
MGI:2431340
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Ascl2tm1Alj/Ascl2+ involves: 129 * CD-1 MGI:3773268
ht2
Ascl2tm1.1Nagy/Ascl2+ involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:3847333
cx3
Ascl2tm1Alj/Ascl2+
Kcnq1ot1tm1.1Mjh/Kcnq1ot1+
involves: 129 * C57BL/6 * ICR MGI:3772941


Genotype
MGI:3773268
ht1
Allelic
Composition
Ascl2tm1Alj/Ascl2+
Genetic
Background
involves: 129 * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ascl2tm1Alj mutation (0 available); any Ascl2 mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• maternal inheritance of the mutant allele leads to embryonic death due to placental failure
• mice whom paternally inherit the mutant allele are viable

embryo
• chorion membrane is underdeveloped in embryos whom maternally inherit the mutant allele
• spongiotrophoblast fails to develop in embryos whom maternally inherit the mutant allele

cellular
• the paternal allele is functionally inactivated
• mice whom maternally inherit the mutant allele are functionally null homozygotes and die during embryogenesis
• mice whom paternally inherit the mutant allele are viable




Genotype
MGI:3847333
ht2
Allelic
Composition
Ascl2tm1.1Nagy/Ascl2+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ascl2tm1.1Nagy mutation (0 available); any Ascl2 mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• when this allele is inherited maternally, mice show reduced spongiotrophoblast cells compared with wild-type mice
• however, mice inheriting this allele paternally exhibit no defects




Genotype
MGI:3772941
cx3
Allelic
Composition
Ascl2tm1Alj/Ascl2+
Kcnq1ot1tm1.1Mjh/Kcnq1ot1+
Genetic
Background
involves: 129 * C57BL/6 * ICR
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ascl2tm1Alj mutation (0 available); any Ascl2 mutation (13 available)
Kcnq1ot1tm1.1Mjh mutation (0 available); any Kcnq1ot1 mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
N
• no embryonic lethality is observed in mice maternally inheriting the Ascl2tm1Alj allele

cellular
• embryonic lethality associated with maternal transmission of Ascl2tm1Alj allele is prevented by the addition of the Kcnq1tm1.1Mjh allele due to a lack of paternal imprinting of genes in the distal portion of chromosome 7





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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
01/13/2026
MGI 6.24
The Jackson Laboratory