SLC6A17 (solute carrier family 6 member 17)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 388662 |
| Gene name | Solute carrier family 6 member 17 |
| Gene symbol | SLC6A17 |
| Synonyms (NCBI Gene) |
MRT48NTT4
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| Chromosome | 1 |
| Chromosome location | 1p13.3 |
| Summary | The protein encoded by this gene is a member of the SLC6 family of transporters, which are responsible for the presynaptic uptake of most neurotransmitters. The encoded vesicular transporter is selective for proline, glycine, leucine and alanine. In mouse |
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SNPs
SNP information provided by dbSNP.
2
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miRNA
miRNA information provided by mirtarbase database.
199
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
42
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q9H1V8 | ||||||||||
| Protein name | Sodium-dependent neutral amino acid transporter SLC6A17 (Sodium-dependent neurotransmitter transporter NTT4) (Solute carrier family 6 member 17) | ||||||||||
| Protein function | Synaptic vesicle transporter with apparent selectivity for neutral amino acids. The transport is sodium-coupled but chloride-independent, likely driven by the proton electrochemical gradient generated by vacuolar H(+)-ATPase in an overall electr | ||||||||||
| Family and domains |
Pfam
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| Sequence | |||||||||||
| Sequence length | 727 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
45
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