Medical Knowledge Cockpit hyperglycinuria

• Amino acid transport across the plasma membrane
  species not specified 3 genes

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SLC36A2

• Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters

SLC6A19

• Amino acid transport across mammalian intestinal and renal epithelia

SLC6A20

• Cloning, gene structure and genomic localization of an orphan transporter from mouse kidney with six alternatively-spliced isoforms