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Glycan Structure Repository
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Glycomics MS raw data Repository
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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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Guidelines
MIRAGE
solute carrier family 17 member 8
Summary
- Gene Symbol
-
- SLC17A8
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Cell membrane
- Chloride channel
- Cytoplasmic vesicle
- Disease variant
- Glycoprotein
- Hearing
- Neurotransmitter transport
- Non-syndromic deafness
- Phosphate transport
- Proteomics identification
- Reference proteome
- Sodium transport
- Symport
- Synaptosome
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q8NDX2 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| neural retina development | ||
| monoatomic ion transport | ||
| ion transport | ||
| sensory perception of sound | ||
| L-glutamate transmembrane transport |
GO Hierarchy
biological process
localization [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of localization [inference]
regulation of transport [inference]
positive regulation of biological process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| multivesicular body | ||
| plasma membrane | ||
| synaptic vesicle membrane | ||
| synaptic vesicle membrane | ||
| chloride channel complex |
| GO Term | Evidence Code | PMID |
|---|---|---|
| chloride channel activity | ||
| L-glutamate transmembrane transporter activity | ||
| L-glutamate transmembrane transporter activity | ||
| neurotransmitter transmembrane transporter activity | ||
| sodium:phosphate symporter activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- transporter
- Functional Category
-
- C: Energy production and conversion
- E: Amino acid transport and metabolism
- T: Signal transduction mechanisms
| InterPro |
|---|
| MFS transporter superfamily |
| Major facilitator superfamily domain |
| Major facilitator superfamily |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110555 | autosomal dominant nonsyndromic deafness 25 |
