Protein-coding gene in the species Homo sapiens
Solute carrier family 30 member 10 is aprotein that in humans is encoded by the SLC30A10gene .[ 5]
This gene is highly expressed in the liver and is inducible by manganese. Its protein product appears to be critical in maintaining manganese levels, and has higher specificity for manganese than zinc. Loss of function mutations appear to result in a pleomorphic phenotype, including dystonia and adult-onset parkinsonism. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Mar 2012].
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