ATP7A wt Allele

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. (NCI Thesaurus)

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ATP7A Gene

This gene is involved in copper transport.

ATP6AP1 wt Allele

Human ATP6AP1 wild-type allele is located in the vicinity of Xq28 and is approximately 8 kb in length. This allele, which encodes…

ATP6AP1 Gene

This gene plays a role in organelle acidification.

ATP5E wt Allele

Human ATP5E wild-type allele is located in the vicinity of 20q13.32 and is approximately 7 kb in length. This allele, which encodes…

ATP5E Gene

This gene is involved in ATP synthesis.

ATP2C2 wt Allele

Human ATP2C2 wild-type allele is located in the vicinity of 16q24.1 and is approximately 96 kb in length. This allele, which encodes…