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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Use1tm1.2Aha
targeted mutation 1.2, Akihiro Harada
MGI:3842571
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Use1tm1.2Aha/Use1tm1.2Aha involves: BALB/cJ * C57BL/6 * SJL MGI:3842579
cn2
Use1tm1.1Aha/Use1tm1.2Aha involves: BALB/cJ * C57BL/6 * SJL MGI:3842578
cn3
Use1tm1.1Aha/Use1tm1.2Aha
Tg(Pcp2-cre)2Mpin/0
involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL MGI:3842577


Genotype
MGI:3842579
hm1
Allelic
Composition
Use1tm1.2Aha/Use1tm1.2Aha
Genetic
Background
involves: BALB/cJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Use1tm1.2Aha mutation (1 available); any Use1 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:3842578
cn2
Allelic
Composition
Use1tm1.1Aha/Use1tm1.2Aha
Genetic
Background
involves: BALB/cJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Use1tm1.1Aha mutation (1 available); any Use1 mutation (18 available)
Use1tm1.2Aha mutation (1 available); any Use1 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• increase in the percentage of MEF cells with vacuolated ER structures and decrease in the percentage of cells with vesiculated ER structures with time following adenoviral cre treatment
• in MEFs after adenoviral cre treatment
• expression analysis indicates increased endoplasmic reticulum stress following adenoviral cre treatment
• protein transport from the endoplasmic reticulum to the Golgi complex is impaired




Genotype
MGI:3842577
cn3
Allelic
Composition
Use1tm1.1Aha/Use1tm1.2Aha
Tg(Pcp2-cre)2Mpin/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Pcp2-cre)2Mpin mutation (1 available)
Use1tm1.1Aha mutation (1 available); any Use1 mutation (18 available)
Use1tm1.2Aha mutation (1 available); any Use1 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• display cerebellar ataxia after 10 weeks of age
• after 10 weeks of age

nervous system





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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
04/16/2024
MGI 6.23
The Jackson Laboratory