Human Disease and Mouse Model Detail
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Human Disease
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Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 2; SEMDJL2
OMIM ID: 603546
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Synonyms
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Spondyloepimetaphyseal Dysplasia with Joint Laxity, Hall Type;
Spondyloepimetaphyseal Dysplasia with Joint Laxity, Leptodactylic Type;
Spondyloepimetaphyseal Dysplasia with Multiple Dislocations, Hall Type
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Kif22
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KIF22*
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1:1 Homology
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Analysis Tools