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KIF22

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

KIF22
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Kinesin-like protein KIF22 is a protein that in humans is encoded by the KIF22 gene.[5][6][7]

Quick facts Available structures, PDB ...

The protein encoded by this gene is a member of kinesin-like protein family. This family of proteins are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. The C-terminal half of this protein has been shown to bind DNA. Studies with the Xenopus homolog suggests an essential role in metaphase chromosome alignment and maintenance.[7]

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Interactions

KIF22 has been shown to interact with SIAH1.[8]

Clinical relevance

Mutations in this gene have been shown to cause developmental disorders such as Spondyloepimetaphyseal dysplasia with joint laxity.[9]

References

Further reading

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