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MIRAGE
solute carrier family 13 member 5
Summary
- Gene Symbol
-
- SLC13A5
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Amelogenesis imperfecta
- Cell membrane
- Disease variant
- Epilepsy
- Glycoprotein
- Metal-binding
- Proteomics identification
- Reference proteome
- Sodium transport
- Symport
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q86YT5 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| oxaloacetate transport | ||
| oxaloacetate transport | ||
| fumarate transport | ||
| fumarate transport | ||
| alpha-ketoglutarate transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleoplasm | ||
| cytosol | ||
| plasma membrane | ||
| plasma membrane | ||
| plasma membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| organic acid:sodium symporter activity | ||
| protein binding | ||
| citrate transmembrane transporter activity | ||
| citrate transmembrane transporter activity | ||
| citrate transmembrane transporter activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Solute carrier family 13 member
- Functional Category
-
- E: Amino acid transport and metabolism
- G: Carbohydrate transport and metabolism
- P: Inorganic ion transport and metabolism
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| citrate transmembrane transporter activity |
| sodium ion transmembrane transport |
| solute |
| succinate transmembrane transporter activity |
| InterPro |
|---|
| Solute carrier family 13 |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080453 | developmental and epileptic encephalopathy 25 |
