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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Hey2tm1Uts
targeted mutation 1, Manuel F Utset
MGI:2387940
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Hey2tm1Uts/Hey2tm1Uts either: (involves: 129X1/SvJ) or (involves: C57BL/6) MGI:2673834


Genotype
MGI:2673834
hm1
Allelic
Composition
Hey2tm1Uts/Hey2tm1Uts
Genetic
Background
either: (involves: 129X1/SvJ) or (involves: C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hey2tm1Uts mutation (0 available); any Hey2 mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most progeny died within 10 days of birth
• homozygous mice represented 3% of the surviving progeny at weaning

cardiovascular system
• at P9, the pulmonary artery shows narrowing in mutant mice
• defects, including secondary ventricular hypertrophy, ventricular septal defect, overriding aorta, and pulmonic stenosis, are similar to human Tetralogy of Fallot
• tricuspid atresia
• observed in all mice examined during the prenatal and early postnatal period
• the abnormal shunting of blood between the pulmonary and systemic circulations was confirmed using a dye
• some animals showed a defect of the muscular septum
• abnormal pear-shape
• exhibited by mice that survived to the second postnatal week
• exhibited by mice that survived to the second postnatal week
• at E15.5, the leaflets of the left atrium pulmonic valve are fused
• at E15.5, the lumen of the pulmonary valve is narrow

muscle
• exhibited by mice that survived to the second postnatal week
• exhibited by mice that survived to the second postnatal week

growth/size/body
• exhibited by mice that survived to the second postnatal week
• exhibited by mice that survived to the second postnatal week

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
tetralogy of Fallot DOID:6419 OMIM:187500
J:79025





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory