Gene entry
KIF22
kinesin family member 22
- Chromosome
- 16
- Cytoband
- 16p11.2
- Variants (rsID)
- 4
KIF22 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p11.2). Its official name is “kinesin family member 22”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs193922921Pathogenicsingle nucleotide variantSpondyloepimetaphyseal dysplasia with multiple dislocations|Inborn genetic diseases
- rs193922922Pathogenicsingle nucleotide variantSpondyloepimetaphyseal dysplasia with multiple dislocations|Inborn genetic diseases
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.