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Monocarboxylate transporter 9
Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia
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Monocarboxylate transporter 9 (MCT9, solute carrier family 16, member 9, SLC16A9) is a protein that in humans is encoded by the SLC16A9 gene.[5]
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Clinical relevance
Mutations in the SLC16A9 gene have been associated with carnitine levels in blood.[6]
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Further reading
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