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MIRAGE
Inactive sodium-dependent neutral amino acid transporter B(0)AT3
Summary
- UniProt ID
- Q96N87
- Gene Symbol
-
- B0AT3
- SLC6A18
- XTRP2
- Gene ID
- 348932
- Organism
- Homo sapiens (human)
External Links
- PubChem
- Q96N87
- The Human Metabolome Database
- HMDBP09076
- Re-Glyco
- Q96N87
Annotation
- Keyword
-
- Amino-acid transport
- Glycoprotein
- Neurotransmitter transport
- Reference proteome
- Symport
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| plasma membrane |
| apical plasma membrane |
| brush border membrane |
| GO Term |
|---|
| sodium ion transmembrane transport |
| neutral amino acid transport |
| neurotransmitter transport |
| amino acid transport |
| renal amino acid absorption |
| GO Term |
|---|
| amino acid transmembrane transporter activity |
| neutral L-amino acid:sodium:chloride symporter activity |
Sequence
MAHAPEPDPAACDLGDERPKWDNKAQYLLSCTGFAVGLGNIWRFPYLCQTYGGGAFLIPYVIALVFEGIPIFHVELAIGQRLRKGSVGVWTAISPYLSGVGLGCVTLSFLISLYYNTIVAWVLWYLLNSFQHPLPWSSCPPDLNRTGFVEECQGSSAVSYFWYRQTLNITADINDSGSIQWWLLICLAASWAVVYMCVIRGIETTGKVIYFTALFPYLVLTIFLIRGLTLPGATKGLIYLFTPNMHILQNPRVWLDAATQIFFSLSLAFGGHIAFASYNSPRNDCQKDAVVIALVNRMTSLYASIAVFSVLGFKATNDYEHCLDRNILSLINDFDFPEQSISRDDYPAVLMHLNATWPKRVAQLPLKACLLEDFLDKSASGPGLAFVVFTETDLHMPGAPVWAMLFFGMLFTLGLSTMFGTVEAVITPLLDVGVLPRWVPKEALTGLVCLVCFLSATCFTLQSGNYWLEIFDNFAASPNLLMLAFLEVVGVVYVYGMKRFCDDIAWMTGRRPSPYWRLTWRVVSPLLLTIFVAYIILLFWKPLRYKAWNPKYELFPSRQEKLYPGWARAACVLLSLLPVLWVPVAALAQLLTRRRRTWRDRDARPDTDMRPDTDTRPDTDMRPDTDMR
Glycosylation Sites
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Amino acid transport across the plasma membrane | Homo sapiens |
| Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria | Homo sapiens |
| Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria | Homo sapiens |
| Na+/Cl- dependent neurotransmitter transporters | Homo sapiens |
