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SLC6A19

Index SLC6A19

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]

5 relations: Amino acid transporter, Cell membrane, Gene, Hartnup disease, Protein.

Amino acid transporter

An amino acid transporter is a membrane transport protein that transports amino acids.

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Cell membrane

The cell membrane (also known as the plasma membrane or cytoplasmic membrane, and historically referred to as the plasmalemma) is a biological membrane that separates the interior of all cells from the outside environment (the extracellular space).

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Gene

In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.

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Hartnup disease

Hartnup disease (also known as "pellagra-like dermatosis" and "Hartnup disorder") is an autosomal recessive metabolic disorder affecting the absorption of nonpolar amino acids (particularly tryptophan that can be, in turn, converted into serotonin, melatonin, and niacin).

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Protein

Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.

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Redirects here:

B0AT1, Neutral amino acid transporter member 19, SLC6A19 (gene), Sodium-dependent neutral amino acid transporter B(0)AT1, Solute carrier family 6 member 19, System B(0) neutral amino acid transporter AT1.

References

[1] https://en.wikipedia.org/wiki/SLC6A19

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