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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Shbtm1.1Miwe
targeted mutation 1.1, Michael Welsh
MGI:3721903
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Shbtm1.1Miwe/Shbtm1.1Miwe B6.129X1-Shbtm1.1Miwe MGI:3723305
hm2
Shbtm1.1Miwe/Shbtm1.1Miwe involves: 129X1/SvJ * C57BL/6 * FVB/N MGI:3723303
ht3
Shbtm1.1Miwe/Shb+ involves: 129X1/SvJ * C57BL/6 * FVB/N MGI:3723304


Genotype
MGI:3723305
hm1
Allelic
Composition
Shbtm1.1Miwe/Shbtm1.1Miwe
Genetic
Background
B6.129X1-Shbtm1.1Miwe
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shbtm1.1Miwe mutation (0 available); any Shb mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:3723303
hm2
Allelic
Composition
Shbtm1.1Miwe/Shbtm1.1Miwe
Genetic
Background
involves: 129X1/SvJ * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shbtm1.1Miwe mutation (0 available); any Shb mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• fewer than expected embryos are born
• however, mice that are born are viable, fertile and show no obvious defects

embryo
• mice produced from null parents exhibit severe malformations including resorptions or loss of embryo structures and mild malformations including tail rotation defects, neural tube closure defects or superficial hemorrhaging
• some mice have an open neural tube

cardiovascular system
• some mice exhibit external hemorrhaging

limbs/digits/tail
• some mice have tail defects such as a twisted tail

nervous system
• some mice have an open neural tube




Genotype
MGI:3723304
ht3
Allelic
Composition
Shbtm1.1Miwe/Shb+
Genetic
Background
involves: 129X1/SvJ * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shbtm1.1Miwe mutation (0 available); any Shb mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• authors state that the defects similar to those seen in homozygous mice are present in heterozygotes when one parent is homozygous and the other heterozygous for the null allele

reproductive system
• maternal inheritance of the null allele is increased
• at E10.5, mice carrying a maternal copy of the null allele were more common than those carrying a maternal wild-type copy
• transmission rations of wild-type to null allele are 31% to 54% at E10.5 and 19% to 81% during ovulation





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory