Gene entry
XK
X-linked Kx blood group antigen, Kell and VPS13A binding protein
- Chromosome
- X
- Cytoband
- Xp21.1
- Variants (rsID)
- 21
XK is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp21.1). Its official name is “X-linked Kx blood group antigen, Kell and VPS13A binding protein”. The reference table lists 21 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs104894953Pathogenicsingle nucleotide variantMcLeod neuroacanthocytosis syndrome
- rs104894954Pathogenicsingle nucleotide variantMcLeod neuroacanthocytosis syndrome
- rs28933690Pathogenicsingle nucleotide variantMcLeod neuroacanthocytosis syndrome
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.