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Repository for lectin-assisted multimodality data
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MIRAGE
solute carrier family 5 member 5
Summary
- Gene Symbol
-
- SLC5A5
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Cell membrane
- Congenital hypothyroidism
- Cytoplasm
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Glycoprotein
- Phosphoprotein
- Reference proteome
- Sodium transport
- Symport
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q92911 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| thyroid hormone generation | ||
| monoatomic ion transport | ||
| ion transport | ||
| sodium ion transport | ||
| iodide transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleus | ||
| cytoplasm | ||
| plasma membrane | ||
| plasma membrane | ||
| plasma membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| sodium:iodide symporter activity | ||
| sodium:iodide symporter activity | ||
| sodium:iodide symporter activity | ||
| sodium:iodide symporter activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- solute carrier family 5 member 5
- Functional Category
-
- E: Amino acid transport and metabolism
- K: Transcription
- T: Signal transduction mechanisms
| InterPro |
|---|
| Sodium/glucose symporter superfamily |
| Sodium/solute symporter |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050328 | congenital hypothyroidism | |
| DOID:0112185 | thyroid dyshormonogenesis 1 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 6528 | Xenbase:XB-GENE-486472 | ||
| 8884 | FB:FBgn0052669 | ||
| 20537 | SGD:S000001008 | ||
| 43136 | Xenbase:XB-GENE-486472 | ||
| 64452 | SGD:S000001008 | ||
| 64522 | SGD:S000001008 | ||
| 109342 | SGD:S000001008 | ||
| 114479 | MOUSE60367 | ||
| 114613 | Xenbase:XB-GENE-486472 | RATNO11305 | |
| 159963 | FB:FBgn0250757 |
