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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Hdac3tm1Swh
targeted mutation 1, Scott W Heibert
MGI:3793477
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Hdac3tm1Swh/Hdac3tm1.1Swh involves: 129S6/SvEvTac * FVB/N MGI:3795941
cn2
Hdac3tm1Swh/Hdac3tm1.1Swh
Tg(Mx1-cre)1Cgn/0
involves: 129S6/SvEvTac * C57BL/6 * CBA MGI:3795938
cn3
Hdac3tm1Swh/Hdac3tm1.1Swh
Tg(CAG-cre/Esr1*)5Amc/0
involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N MGI:3795942
cn4
Hdac3tm1Swh/Hdac3tm1.1Swh
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
involves: 129S6/SvEvTac * C57BL/6 * DBA MGI:3795939


Genotype
MGI:3795941
cn1
Allelic
Composition
Hdac3tm1Swh/Hdac3tm1.1Swh
Genetic
Background
involves: 129S6/SvEvTac * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hdac3tm1.1Swh mutation (0 available); any Hdac3 mutation (33 available)
Hdac3tm1Swh mutation (0 available); any Hdac3 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• several markers of DNA damage are increased in MEFs at 72 h after adenoviral cre infection
• blocking progression through the cell cycle by serum starving cells reduces the amount of DNA damage detected
• sensitivity to DNA damage by ionizing radiation is also increased in adenoviral cre infected MEFs
• impaired cell cycle progression prior to metaphase in adenoviral cre infected MEFs
• viral cre infected cells display about a 2 h delay in moving from S phase through G2/M and re-entering G1
• by 120 h post adenoviral cre infection about 20 - 30% of MEFs are dying
• about a 2-fold reduction in BrdU positive MEFs after adenoviral cre infection




Genotype
MGI:3795938
cn2
Allelic
Composition
Hdac3tm1Swh/Hdac3tm1.1Swh
Tg(Mx1-cre)1Cgn/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hdac3tm1.1Swh mutation (0 available); any Hdac3 mutation (33 available)
Hdac3tm1Swh mutation (0 available); any Hdac3 mutation (33 available)
Tg(Mx1-cre)1Cgn mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
liver/biliary system
• 2 weeks after the final pIpC injection liver size is increased about 2-fold
• gradual increase in hypertrophic hepatocytes with grainy cytoplasm following pIpC injections
• 2 weeks after the final pIpC injection liver weight is increased about 2-fold
• dramatic depletion of glycogen in hepatocytes after pIpC injections
• gradual increase in hypertrophic hepatocytes with grainy cytoplasm following pIpC injections
• after pIpC injections

homeostasis/metabolism
• dramatic depletion of glycogen in hepatocytes after pIpC injections

growth/size/body
• 2 weeks after the final pIpC injection liver size is increased about 2-fold
• gradual increase in hypertrophic hepatocytes with grainy cytoplasm following pIpC injections
• 2 weeks after the final pIpC injection liver weight is increased about 2-fold




Genotype
MGI:3795942
cn3
Allelic
Composition
Hdac3tm1Swh/Hdac3tm1.1Swh
Tg(CAG-cre/Esr1*)5Amc/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hdac3tm1.1Swh mutation (0 available); any Hdac3 mutation (33 available)
Hdac3tm1Swh mutation (0 available); any Hdac3 mutation (33 available)
Tg(CAG-cre/Esr1*)5Amc mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• impaired cell cycle progression prior to metaphase in tamoxifen treated MEFs
• in MEFs following tamoxifen treatment
• several markers of DNA damage are increased in MEFs after tamoxifen treatment

homeostasis/metabolism
• several markers of DNA damage are increased in MEFs after tamoxifen treatment




Genotype
MGI:3795939
cn4
Allelic
Composition
Hdac3tm1Swh/Hdac3tm1.1Swh
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * DBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hdac3tm1.1Swh mutation (0 available); any Hdac3 mutation (33 available)
Hdac3tm1Swh mutation (0 available); any Hdac3 mutation (33 available)
Speer6-ps1Tg(Alb-cre)21Mgn mutation (6 available); any Speer6-ps1 mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• unlike homozygous null mice, mice with loss of expression in the liver after birth are viable

liver/biliary system
• at 6 - 8 weeks of age, but not at P17, the number of proliferating cells is increased
• by P28 livers are hypertrophic
• ratio of liver weight to body weight is increased to about 25 - 30% compared to about 5% in heterozygous mice
• dramatic depletion of glycogen in hepatocytes
• up to a 17-fold increase in triglyceride levels in the liver at P17
• cells with abnormal cytoplasm are apparent at P17
• accumulation of lipid droplets
• elevated triglyceride levels at P17
• treating mice with rapamycin reduces neutral lipid accumulation but does not alter the increase in liver size
• by P28

homeostasis/metabolism
• present by 6 weeks of age but not at P17
• at 10 weeks of age fasting glucose level is almost 2-fold lower than in control littermates
• however, glucose tolerance is not significantly different from controls
• slightly lower at P17
• dramatic decrease by P28 which persists as mice age
• dramatic depletion of glycogen in hepatocytes
• increases with age
• up to a 17-fold increase in triglyceride levels in the liver at P17

growth/size/body
• by 4 - 6 weeks of age
• by P28 livers are hypertrophic
• ratio of liver weight to body weight is increased to about 25 - 30% compared to about 5% in heterozygous mice

adipose tissue
• visibly leaner with a substantial reduction in visceral adipose tissue by 6 - 8 weeks of age

cellular
• at 6 - 8 weeks of age, but not at P17, the number of proliferating cells is increased





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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
12/10/2024
MGI 6.24
The Jackson Laboratory