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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Shb+
wild type
MGI:2432093
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Shbtm1.1Miwe/Shb+ involves: 129X1/SvJ * C57BL/6 * FVB/N MGI:3723304


Genotype
MGI:3723304
ht1
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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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
05/21/2024
MGI 6.23
The Jackson Laboratory