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Slc6a19

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Title: Slc6a19  
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Subject: Arterial tortuosity syndrome, Solute carrier family, SLC2A13, SLC2A14, SLC39A1
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Slc6a19

Solute carrier family 6 (neutral amino acid transporter), member 19
Identifiers
Symbols  ; B0AT1; HND
External IDs IUPHAR: GeneCards:
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)
RefSeq (protein)
Location (UCSC)
PubMed search

Solute carrier family 6 member 19 also known as the sodium-dependent neutral amino acid transporter B(0)AT1 or system B(0) neutral amino acid transporter AT1 is a protein that in humans is encoded by the SLC6A19 gene.[1]

Function

SLC6A19 is a system B(0) transporter that mediates epithelial resorption of neutral amino acids across the apical membrane in the kidney and intestine.[2][3]

Clinical significance

Mutations in the SLC6A19 gene cause Hartnup disease.[1][4]

References

  1. ^ a b
  2. ^
  3. ^
  4. ^

Further reading

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