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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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MIRAGE
solute carrier family 6 member 17
Summary
- Gene Symbol
-
- SLC6A17
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Amino-acid transport
- Cell projection
- Cytoplasmic vesicle
- Disease variant
- Glycoprotein
- Intellectual disability
- Neurotransmitter transport
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Sodium transport
- Symport
- Synapse
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9H1V8 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| neurotransmitter transport | ||
| brain development | ||
| neutral amino acid transport | ||
| glycine transport | ||
| glycine transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane | ||
| synaptic vesicle | ||
| synaptic vesicle | ||
| membrane | ||
| synaptic vesicle membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| symporter activity |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- sodium-dependent neutral amino acid
- Functional Category
-
- E: Amino acid transport and metabolism
- K: Transcription
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| leucine transport |
| sodium ion transmembrane transport |
| symporter activity |
| InterPro |
|---|
| Neutral amino acid SLC6 transporter |
| Sodium |
| Sodium |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0081212 | autosomal recessive intellectual developmental disorder 48 |
