Slc16a2 (solute carrier family 16 (monocarboxylic acid transporters), member 2)

基因基本信息

Slc16a2 基因表型（MGI）

Homo- and hemizygous inactivation of this gene leads to abnormal thyroid hormone metabolism with no apparent neurological phenotype. Males hemizygous for a knock-out allele also show altered deiodinase enzymatic activities, reduced serum cholesterol and increased serum alkaline phosphatase levels.

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