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solute carrier family 52 member 2
Summary
- Gene Symbol
-
- SLC52A2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Cell membrane
- Deafness
- Disease variant
- Host cell receptor for virus entry
- Proteomics identification
- Reference proteome
- Signal
- Transmembrane helix
- Transport
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| riboflavin metabolic process | ||
| riboflavin transport | ||
| riboflavin transport | ||
| viral entry into host cell |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane | ||
| plasma membrane | ||
| plasma membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| virus receptor activity | ||
| protein binding | ||
| riboflavin transmembrane transporter activity | ||
| riboflavin transmembrane transporter activity | ||
| riboflavin transmembrane transporter activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Solute carrier family 52 riboflavin transporter
- Functional Category
-
- E: Amino acid transport and metabolism
- M: Cell wall/membrane/envelope biogenesis
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| riboflavin transmembrane transporter activity |
| riboflavin transport |
| InterPro |
|---|
| Solute carrier family 52, riboflavin transporter |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080786 | Brown-Vialetto-Van Laere syndrome 2 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 52710 | Xenbase:XB-GENE-5786440 | MOUSE16438 | |
| 55065 | Xenbase:XB-GENE-5786440 | ||
| 69698 | FB:FBgn0039882 | ||
| 79581 | Xenbase:XB-GENE-5786440 | ||
| 113278 | FB:FBgn0039882 | ||
| 178842 | Xenbase:XB-GENE-5786440 | ||
| 311536 | FB:FBgn0039882 | ||
| 323832 | DANRE15287 | ||
| 362942 | Xenbase:XB-GENE-5786440 | RATNO39683 | |
| 431729 | FB:FBgn0039882 |
