Gene Symbol | SLC6A19 |
Entrez Gene ID | 340024 |
Full Name | solute carrier family 6 member 19 |
Synonyms | B0AT1,HND |
General protein information |
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Gene Type | protein-coding |
Organism | Homo sapiens(human) |
Genome | |
Summary | 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]. |
Disorder MIM: | |
Disorder Html: | Hartnup disorder, 234500 (3); Iminoglycinuria, digenic, 242600 (3); Hyperglycinuria, 138500 (3) |