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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tektm1Dmt
targeted mutation 1, Daniel J Dumont
MGI:2159357
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Tektm1Dmt/Tektm1Dmt involves: 129S1/Sv * 129X1/SvJ MGI:3760539
hm2
Tektm1Dmt/Tektm1Dmt involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:3582528
cx3
Rasa1tm1Paw/Rasa1tm1Paw
Tektm1Dmt/Tektm1Dmt
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1) MGI:3040175
cx4
Tektm1Dmt/Tektm1Dmt
Tie1tm1Jpa/Tie1tm1Jpa
involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:3851553
cx5
Tektm1Dmt/Tek+
Tie1tm1Jpa/Tie1tm1Jpa
involves: 129S1/Sv * 129X1/SvJ * CD-1 MGI:3851554


Genotype
MGI:3760539
hm1
Allelic
Composition
Tektm1Dmt/Tektm1Dmt
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tektm1Dmt mutation (1 available); any Tek mutation (92 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
N
• allantois explants form normal vascular networks




Genotype
MGI:3582528
hm2
Allelic
Composition
Tektm1Dmt/Tektm1Dmt
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tektm1Dmt mutation (1 available); any Tek mutation (92 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygous embryos are present at E9.5 but absent at E10.5

cardiovascular system
• gaps are seen in the blood vessel walls in the head and electron microscopy revealed gaps in the vascular endothelial cells of the perinuclear plexus in the head
• no pericytes are found around the vascular endothelial cells
• vascular branching and sprouting are impaired and the complexity of the vascular network is decreased
• absent myocardial trabeculations at E9.5
• at E9.5 the endothelium lining the myocardium is less intricately folded and the endocardial lining appears collapsed and retracted from the myocardial wall
• most homozygous embryos have hemorrhages in the head

embryo
• at E9.5 the vitteline vasculature fails to reorganize into a mature branched network; however, the immature plexus forms normally

hematopoietic system
• multilineage hematopoietic stem cell clusters in the omphalomesenteric and vitelline arteries are absent and the number of hematopoietic cells produced in vitro is severely reduced

nervous system
• most homozygous embryos have hemorrhages in the head

muscle
• absent myocardial trabeculations at E9.5




Genotype
MGI:3040175
cx3
Allelic
Composition
Rasa1tm1Paw/Rasa1tm1Paw
Tektm1Dmt/Tektm1Dmt
Genetic
Background
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rasa1tm1Paw mutation (0 available); any Rasa1 mutation (34 available)
Tektm1Dmt mutation (1 available); any Tek mutation (92 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• at 16 somite stage, thinning of the dorsal aorta and aberrant ventral arteries seen
• heart is surrounded by a distended pericardium by E9.5
• by E9.5, local ruptures in the vasculature and leakage of blood into the body cavity occurred

embryo
• endothelial cells failed to reorganize into a vascular network




Genotype
MGI:3851553
cx4
Allelic
Composition
Tektm1Dmt/Tektm1Dmt
Tie1tm1Jpa/Tie1tm1Jpa
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tektm1Dmt mutation (1 available); any Tek mutation (92 available)
Tie1tm1Jpa mutation (2 available); any Tie1 mutation (67 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

cardiovascular system
• blood vessels in the dorsal, posterior portion of the mouse are enlarged and highly distorted compared to in wild-type mice
• blood vessel development fails to proceed to the dorsal portion of the body unlike in wild-type mice
• vessel integrity is compromised compared to in wild-type mice
• mice exhibit poor branching structures of the blood vessels in the head unlike wild-type mice
• blood vessels fail to organize into large and small vessels unlike in wild-type mice
• yolk sac vasculature is underdeveloped and lacks major blood vessels unlike in wild-type mice
• myocardial trabeculation in the ventricle is absent
• at E9.5, heart development is poor
• mice exhibit reduced endocardial tissue in the common atrial and ventricular chambers compared to in wild-type mice
• mice exhibit thin myocardial layer, poor maintenance of endocardial contact, and absence of trabeculations unlike in wild-type mice

embryo
• yolk sac vasculature is underdeveloped and lacks major blood vessels unlike in wild-type mice
• at E9.5, necrotic tissue is occasionally observed
• at E10.5, necrosis is widespread
• somites are disorganized and necrotic unlike in wild-type mice
• remodeling of primary yolk sac capillary plexus fails

homeostasis/metabolism
• at E9.5

growth/size/body

muscle
• myocardial trabeculation in the ventricle is absent

nervous system
• underdeveloped at E9.5

cellular
• at E9.5, necrotic tissue is occasionally observed
• at E10.5, necrosis is widespread




Genotype
MGI:3851554
cx5
Allelic
Composition
Tektm1Dmt/Tek+
Tie1tm1Jpa/Tie1tm1Jpa
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tektm1Dmt mutation (1 available); any Tek mutation (92 available)
Tie1tm1Jpa mutation (2 available); any Tie1 mutation (67 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

cardiovascular system
• maintenance of blood vessels in the head and extremities is poor
• atrial and ventricular endocardium is poorly maintained

homeostasis/metabolism





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory