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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fzd9+
wild type
MGI:2437134
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Fzd9tm1Uta/Fzd9+ involves: 129X1/SvJ MGI:4946081
ht2
Fzd9tm1Sjp/Fzd9+ involves: C57BL/6J MGI:3586705


Genotype
MGI:4946081
ht1
Allelic
Composition
Fzd9tm1Uta/Fzd9+
Genetic
Background
involves: 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fzd9tm1Uta mutation (1 available); any Fzd9 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• reduction in cortical thickness of femurs
• decrease in bone rate formation
• vertebral bodies and femora exhibit decreased biomechanical competence

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Williams-Beuren syndrome DOID:1928 OMIM:194050
J:169924




Genotype
MGI:3586705
ht2
Allelic
Composition
Fzd9tm1Sjp/Fzd9+
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fzd9tm1Sjp mutation (1 available); any Fzd9 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E14.5, there is a slight increase, less than that in homozygotes, in M-phase precursor cells in the medial cortical wall compared to wild-type mice
• at E14.5, the number of apoptotic cells in the dentate analage is less than in homozygotes but still increased compared to wild-type mice
• a decrease in the number of dentate granule cells and an increase in the hilar mossy cell number, intermediate to that detected in homozygous mutants, are seen





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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
07/08/2026
MGI 6.24
The Jackson Laboratory