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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nodaltm1Mku
targeted mutation 1, Michael R Kuehn
MGI:2158730
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nodaltm1Mku/Nodaltm1Mku involves: 129S1/Sv MGI:3850217
ht2
Nodaltm1Mku/Nodaltm1.1Mku either: (involves: 129S1/Sv * FVB/N) or (involves: 129S1/Sv * C57BL/6J * FVB/N) MGI:2173523
ht3
NodalTgR(MPSVNeo)413.dRob/Nodaltm1Mku involves: 129S1/Sv MGI:3850216
cn4
Nodaltm1Mku/Nodaltm1Mku
Mesp1tm2(cre)Ysa/Mesp1+
Tg(Pitx2-lacZ)1Mbf/0
involves: 129S1/Sv * C57BL/6 * CBA MGI:4880743


Genotype
MGI:3850217
hm1
Allelic
Composition
Nodaltm1Mku/Nodaltm1Mku
Genetic
Background
involves: 129S1/Sv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nodaltm1Mku mutation (0 available); any Nodal mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• homozygotes are viable and fertile




Genotype
MGI:2173523
ht2
Allelic
Composition
Nodaltm1Mku/Nodaltm1.1Mku
Genetic
Background
either: (involves: 129S1/Sv * FVB/N) or (involves: 129S1/Sv * C57BL/6J * FVB/N)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nodaltm1.1Mku mutation (0 available); any Nodal mutation (42 available)
Nodaltm1Mku mutation (0 available); any Nodal mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• of those alive at E14.5 none survive to birth

embryo
• abnormalities in the primitive streak, node, and anterior visceral endoderm suggest that axial rotation is abnormal
• 20% of embryos develop with the anterior region outside the yolk sac (type II) and 29% of embryos develop completely outside the yolk sac (type III), the remainder develop within the yolk sac (type I)
• expression analysis indicates abnormal cell positions along the anterior posterior axis at E7.5
• defects in axial patterning become more pronounced by E8.5
• severe defects in anterior patterning are seen in all 3 types of embryos
• some embryos arrest prior to gastrulation
• at E8.5 type III embryos lack any apparent lateral plate mesoderm
• at E8.5 type I embryos lack normal asymmetric gene expression in the left lateral plate mesoderm
• type I embryos lack the normal ventral midline separation of the neural folds at E8.5
• in type II embryos the head neuroectoderm is disorganized with repeated foldings
• type II embryos lack a distinct floor plate in the trunk region
• in some type II embryos
• in some type II embryos the notochord is present in the trunk but ends abruptly at the level of the head
• in type III embryos the notochord end short of the most anterior region
• type I embryos lack a prechordal plate in the forebrain region at E8.5
• in type II and type III embryos
• expression analysis at E7.5 indicates truncation of the primitive streak
• at E7.5, the node appears to be more proximal in location compared to controls
• at E8.5 in type II embryos Nodal expressing cells are found across the midline rather than confined to the periphery as in controls
• at E8.5 type III embryos lack a recognizable node
• all type II embryos show fusion of somites across the midline
• some type III embryos have fused somites
• a constriction is present at the boundary
• the lateral edges of the mesodermal wings encroach on the anterior midline at the site where the anterior visceral endoderm normally contacts the underlying anterior embryonic ectoderm
• in distal locations cells with cuboidal shapes are present where in controls the cell are squamous in shape

nervous system
• in type II embryos the head neuroectoderm is disorganized with repeated foldings
• type II embryos lack a distinct floor plate in the trunk region
• type II and type III embryos lack demarcations between fore-, mid- and hindbrain regions
• seen in type I embryos at E14.5

digestive/alimentary system
• in a few type I embryos at E14.5 the stomach is located on the right side or shows incomplete rotation
• expression analysis suggests that type III embryos lack gut endoderm and there is no morphologically recognizable gut tube in these embryos
• in type II embryos no recognizable foregut pocket is found
• in type I embryos the foregut does not extend as far anteriorly as in controls
• abnormally narrow and prematurely closed in type II embryos

cardiovascular system
• randomized direction of looping in type I embryos
• type II and type III embryos fail to develop a heart tube
• in all type I embryos at E14.5

respiratory system
• in most type I embryos at E14.5

liver/biliary system
• in some type I embryos at E14.5 the liver is reduced in size and/or pale
• in some type I embryos at E14.5 the liver is reduced in size and/or pale

growth/size/body
• type II and type III embryos have a ventral orientation of the head
• in most type I embryos at E14.5




Genotype
MGI:3850216
ht3
Allelic
Composition
NodalTgR(MPSVNeo)413.dRob/Nodaltm1Mku
Genetic
Background
involves: 129S1/Sv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
NodalTgR(MPSVNeo)413.dRob mutation (0 available); any Nodal mutation (42 available)
Nodaltm1Mku mutation (0 available); any Nodal mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• expanded giant cell layer
• cell layer is expanded in thickness
• reduced in thickness




Genotype
MGI:4880743
cn4
Allelic
Composition
Nodaltm1Mku/Nodaltm1Mku
Mesp1tm2(cre)Ysa/Mesp1+
Tg(Pitx2-lacZ)1Mbf/0
Genetic
Background
involves: 129S1/Sv * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mesp1tm2(cre)Ysa mutation (3 available); any Mesp1 mutation (18 available)
Nodaltm1Mku mutation (0 available); any Nodal mutation (42 available)
Tg(Pitx2-lacZ)1Mbf mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular 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
06/12/2024
MGI 6.13
The Jackson Laboratory