SLC6A19

SLC6A19

protein
name=solute carrier family 6 (neutral amino acid transporter), member 19
caption=


width=
HGNCid=27960
Symbol=SLC6A19
AltSymbols=
EntrezGene=340024
OMIM=608893
RefSeq=XM_291120
UniProt=
PDB=
ECnumber=
Chromosome=5
Arm=p
Band=15
LocusSupplementaryData=

SLC6A19 is a gene associated with Hartnup disease.cite journal |author=Seow HF, Bröer S, Bröer A, "et al" |title=Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19 |journal=Nat. Genet. |volume=36 |issue=9 |pages=1003–7 |year=2004 |month=September |pmid=15286788 |doi=10.1038/ng1406 |url=http://dx.doi.org/10.1038/ng1406]

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