Proton-coupled amino acid transporter 2 deficiency

Type

Disease
Gene
- SLC36A2 / Solute Carrier Family 36 Member 2
  5q33.1
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Proton-assisted amino acid transporter
Disease group(s)
- 1.11 Disorders of amino acid transport
Child entries
- Hyperglycinuria