This gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder. [provided by RefSeq, Jul 2008]
人 SLC6A19 (NM_001003841) cDNA克隆
| Accession: | NM_001003841 |
|---|---|
| 基因名称: | SLC6A19 |
| 基因别名: | HND; B0AT1 |
| 基因描述: | Homo sapiens solute carrier family 6 (neutral amino acid transporter), member 19 (SLC6A19), mRNA. |
| 种属: | Human |
| CDS区长度: | 1905 (查看编码区序列) |
| 翻译后氨基酸长度: | 634 (查看氨基酸序列) |
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