Sodium-dependent neutral amino acid transporter B(0)AT1
| solute carrier family 6 (neutral amino acid transporter), member 19 | |
|---|---|
| Identifiers | |
| Symbol | SLC6A19 |
| NCBI gene | 340024 |
| HGNC | 27960 |
| OMIM | 608893 |
| RefSeq | XM_291120 |
| Other data | |
| Locus | Chr. 5 p15 |
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.[1] SLC6A19 is a gene associated with Hartnup disease.[2]
References
- ^ Kleta R, Romeo E, Ristic Z; et al. (2004). "Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder". Nat. Genet. 36 (9): 999–1002. doi:10.1038/ng1405. PMID 15286787.
{{cite journal}}: Explicit use of et al. in:|author=(help); Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link) - ^ Seow HF, Bröer S, Bröer A; et al. (2004). "Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19". Nat. Genet. 36 (9): 1003–7. doi:10.1038/ng1406. PMID 15286788.
{{cite journal}}: Explicit use of et al. in:|author=(help); Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link)
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