XK (also known as Kell blood group precursor) is a protein found on human red blood cells and other tissues which is responsible for the Kx antigen which helps determine a person's blood type.
Clinical significance The Kx antigen plays a role in matching blood for blood transfusions. Mutation of XK protein may lead to McLeod syndrome, a multi-system disorder characterized by hemolytic anemia, myopathy, acanthocytosis, and chorea. XK is located on the X chromosome (cytogenetic band Xp21.1) and absence of the XK protein is an X-linked disease.
Clinical diagnostic Clinical testing in patient care for Kx antigen follows published minimum quality and operational requirements, similar to red cell genotyping for any of the other recognized blood group systems. Molecular analysis can identify gene variants (alleles) that may affect Kx antigen expression on the red cell membrane.
Function XK is a membrane transport protein of unknown action.
References
External links GeneReviews/NCBI/NIH/UW entry on McLeod Neuroacanthocytosis Syndrome XK at BGMUT Blood Group Antigen Gene Mutation Database at NCBI, NIH XK+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)





