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XKR7 (XK-related protein 7) is a 579 amino acid multi-pass membrane protein that likely is a component of the XK/Kell complex of the Kell blood group system. The gene encoding XKR7 maps to human chromosome 20, which comprises approximately 2% of the human genome. Chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome.
C20orf159; dJ310O13.4; X Kell blood group precursor-related family, member 7; XK related 7; XK, Kell blood group complex subunit-related family, member 7; XKR7; XK-related protein 7; X-linked Kx blood group related 7; XRG7
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