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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Dkk1tm1Sia
targeted mutation 1, Shinichi Aizawa
MGI:3777004
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Dkk1tm1Sia/Dkk1tm1Sia involves: C57BL/6 * CBA MGI:3795587
cx2
Dkk1tm1Sia/Dkk1tm1Sia
Sfrp1tm1Aksh/Sfrp1tm1Aksh
involves: 129 * C57BL/6 * CBA MGI:3795550
cx3
Dkk1tm1Sia/Dkk1tm1Sia
Sfrp1tm1Aksh/Sfrp1tm1Aksh
Sfrp2tm1Aksh/Sfrp2+
involves: 129 * C57BL/6 * CBA MGI:3795551
cx4
Dkk1tm1Sia/Dkk1tm1Sia
Sfrp1tm1Aksh/Sfrp1tm1Aksh
Sfrp2tm1Aksh/Sfrp2tm1Aksh
involves: 129 * C57BL/6 * CBA MGI:3795552


Genotype
MGI:3795587
hm1
Allelic
Composition
Dkk1tm1Sia/Dkk1tm1Sia
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dkk1tm1Sia mutation (0 available); any Dkk1 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E7.5, anterior neuroectoderm development is abnormal

embryo
• at E7.5, anterior neuroectoderm development is abnormal




Genotype
MGI:3795550
cx2
Allelic
Composition
Dkk1tm1Sia/Dkk1tm1Sia
Sfrp1tm1Aksh/Sfrp1tm1Aksh
Genetic
Background
involves: 129 * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dkk1tm1Sia mutation (0 available); any Dkk1 mutation (18 available)
Sfrp1tm1Aksh mutation (1 available); any Sfrp1 mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• 50% of mice exhibit irregular somatic segmentation and indistinct intersomitic boundaries




Genotype
MGI:3795551
cx3
Allelic
Composition
Dkk1tm1Sia/Dkk1tm1Sia
Sfrp1tm1Aksh/Sfrp1tm1Aksh
Sfrp2tm1Aksh/Sfrp2+
Genetic
Background
involves: 129 * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dkk1tm1Sia mutation (0 available); any Dkk1 mutation (18 available)
Sfrp1tm1Aksh mutation (1 available); any Sfrp1 mutation (19 available)
Sfrp2tm1Aksh mutation (1 available); any Sfrp2 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• intersomitic boundaries are absent in the posterior portion




Genotype
MGI:3795552
cx4
Allelic
Composition
Dkk1tm1Sia/Dkk1tm1Sia
Sfrp1tm1Aksh/Sfrp1tm1Aksh
Sfrp2tm1Aksh/Sfrp2tm1Aksh
Genetic
Background
involves: 129 * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dkk1tm1Sia mutation (0 available); any Dkk1 mutation (18 available)
Sfrp1tm1Aksh mutation (1 available); any Sfrp1 mutation (19 available)
Sfrp2tm1Aksh mutation (1 available); any Sfrp2 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• pre-somitic mesoderm is reduced
• however, the notochord and tail bud mesoderm are present





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory