"Gene or Genome"^^ . . _:b643389 . . "Human ATP7A wild-type allele is located within Xq13.2-q13.3 and is approximately 139 kb in length. This allele, which encodes copper-transporting ATPase 1 protein, plays a role in the localization of copper ions. Mutations in the gene are associated with both Menkes disease and occipital horn syndrome.NCIUniProt" . "ATP7A_wt_Allele"^^ . "MNKSYNCI" . "FLJ17790SYNCI" . _:b643389 . "C74974"^^ . "C2699122"^^ . "HGNC:869"^^ . "ATP7A wt Allele"^^ . "300011"^^ . "MKSYNCI" . "ATP7A wt Allele"^^ . _:b643389 . "ATPase, Cu++ Transporting, Alpha Polypeptide (Menkes Syndrome) wt AlleleSYNCI" . "ATP7A wt AllelePTNCI" . "538"^^ . "L06133"^^ . _:b643389 .