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GeneQ6168793· pop 7· linked from 96 articles

Also known as Kell blood group precursor, X-linked Kx blood group, KX, MCLDS, NA, NAC, X1k, XKR1

protein-coding gene in the species Homo sapiens

Gene data

XK
Name
X-linked Kx blood group antigen, Kell and VPS13A binding protein
Type
protein-coding
Chromosome
X
Position
37,685,791–37,732,130 (+)
Aliases
KX, NA, NAC, X1k, XKR1
RefSeq RNA
NM_021083.4, XM_011543978.4, XM_054327716.1
RefSeq protein
NP_066569.1, XP_011542280.1, XP_054183691.1

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].

via MyGene.info

Wikidata facts

Show 5 more facts
HomoloGene ID
36393
genomic start
37685791
genomic end
37591383
cytogenetic location
Xp21.1
Sources (5)

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