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XK

Official Full Name
X-linked Kx blood group antigen, Kell and VPS13A binding protein
Organism
Homo sapiens
GeneID
7504
Background
This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. [provided by RefSeq, Jul 2008]
Synonyms
KX; NA; NAC; X1k; XKR1;

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