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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
- Glycoprotein
- Metal-binding
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Sodium transport
- Symport
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q92911 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| thyroid hormone generation |
|
|
| thyroid hormone generation |
|
|
| sodium ion transport |
|
|
| iodide transport |
|
|
| iodide transport |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleus |
|
|
| cytoplasm |
|
|
| cytoplasm |
|
|
| plasma membrane |
|
|
| plasma membrane |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| organic acid:sodium symporter activity |
|
|
| protein binding |
|
|
| sodium:iodide symporter activity |
|
|
| sodium:iodide symporter activity |
|
|
| sodium:iodide symporter activity |
|
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 |
|---|---|---|
| 114613 | RGD:69267 | |
| 43136 | FB:FBgn0250757 | |
| 326229 | FB:FBgn0052669 |
