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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 | ||
| viral entry into host cell | ||
| riboflavin transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| 4-hydroxybutyrate receptor activity | ||
| riboflavin transmembrane transporter activity | ||
| virus receptor 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:0050694 | Brown-Vialetto-Van Laere syndrome | |
| DOID:0080786 | Brown-Vialetto-Van Laere syndrome 2 |
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 102123601 | MACFA41797 | |||
| 102168746 | CAPHI05042 | |||
| 102350237 | LATCH02657 | |||
| 103030771 | ASTMX13586 | |||
| 103107253 | ERIEU02145 | |||
| 103183623 | CALMI28014 | |||
| 103237620 | CHLSB17488 | |||
| 103272497 | CARSF03973 | |||
| 103656649 | URSMA31490 | |||
| 103735251 | NANGA20789 |
