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Monocarboxylate transporter 9

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Monocarboxylate transporter 9
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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]

Quick Facts SLC16A9, Identifiers ...
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Clinical relevance

Mutations in the SLC16A9 gene have been associated with carnitine levels in blood.[6]

References

Further reading

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