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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Engtm1Hma
targeted mutation 1, Helen M Arthur
MGI:2177822
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Engtm1Hma/Engtm1Hma involves: 129P2/OlaHsd MGI:3623406
hm2
Engtm1Hma/Engtm1Hma involves: 129P2/OlaHsd * C57BL/6J MGI:2177906
ht3
Engtm1Hma/Eng+ 129P2/OlaHsd-Engtm1Hma MGI:3623404
ht4
Engtm1Hma/Engtm2.1Hma involves: 129P2/OlaHsd * C57BL/6 MGI:3712891


Genotype
MGI:3623406
hm1
Allelic
Composition
Engtm1Hma/Engtm1Hma
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Engtm1Hma mutation (1 available); any Eng mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• smooth muscle cell differentiation is impaired

muscle
• smooth muscle cell differentiation is impaired




Genotype
MGI:2177906
hm2
Allelic
Composition
Engtm1Hma/Engtm1Hma
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Engtm1Hma mutation (1 available); any Eng mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos are present at E9.5 but die by E10.5

embryo
• exhibit defects in angiogenesis of the yolk sac, with fewer and less well-developed vascular channels and reduced numbers of red blood cells in many embryos
• exhibit developmental delay of about 0.5 day, as indicated by a delay in fusion of the dorsal aorta
• exhibit defects in hematopoiesis of the yolk sac, with reduced numbers of blood cells in the yolk sac

cardiovascular system
• fusion is delayed
• occasional embryos have a reduced cephalic capillary bed, however the appearance of the vasculature in the embryo (except for in the yolk sac) for the most part is normal
• exhibit defects in angiogenesis of the yolk sac, with fewer and less well-developed vascular channels and reduced numbers of red blood cells in many embryos
• almost all embryos have dilated outflow tracts
• the endothelial surface of the truncal cushions fails to organize in about half of homozygous embryos
• many embryos have abnormal cardiac looping
• almost all embryos have enlarged ventricles
• seen in many embryos

growth/size/body
• exhibit developmental delay of about 0.5 day, as indicated by a delay in fusion of the dorsal aorta

hematopoietic system
• exhibit defects in hematopoiesis of the yolk sac, with reduced numbers of blood cells in the yolk sac

homeostasis/metabolism
• seen in many embryos

muscle




Genotype
MGI:3623404
ht3
Allelic
Composition
Engtm1Hma/Eng+
Genetic
Background
129P2/OlaHsd-Engtm1Hma
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Engtm1Hma mutation (1 available); any Eng mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• occasional mice exhibit extensive dilated and weak-walled vessels
• elastin support fibers surrounding fragile vessels are disorganized and sparsely distributed
• smooth muscle cells surrounding the fragile vessels are disorganized and sparsely distributed

muscle
• smooth muscle cells surrounding the fragile vessels are disorganized and sparsely distributed




Genotype
MGI:3712891
ht4
Allelic
Composition
Engtm1Hma/Engtm2.1Hma
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Engtm1Hma mutation (1 available); any Eng mutation (41 available)
Engtm2.1Hma mutation (2 available); any Eng mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• mice are viable





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