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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
sodium channel epithelial 1 subunit beta
Summary
- Gene Symbol
-
- SCNN1B
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Cytoplasmic vesicle
- Disease variant
- Glycoprotein
- Phosphoprotein
- Reference proteome
- Sodium channel
- Taste
- Transmembrane helix
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| mucus secretion | ||
| epithelial fluid transport | ||
| neutrophil-mediated killing of bacterium | ||
| sensory perception of salty taste | ||
| artery smooth muscle contraction |
GO Hierarchy
biological process
immune system process [inference]
metabolic process [inference]
cellular process [inference]
multicellular organismal process [inference]
homeostatic process [inference]
response to stimulus [inference]
localization [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| external side of plasma membrane | ||
| sodium channel complex | ||
| cytoplasmic vesicle membrane | ||
| apical plasma membrane | ||
| plasma membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| WW domain binding | ||
| ligand-gated sodium channel activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- sodium channel
- Functional Category
-
- E: Amino acid transport and metabolism
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| ligand-gated sodium channel activity |
| monoatomic ion transport |
| sodium channel activity |
| sodium ion transmembrane transport |
| InterPro |
|---|
| Epithelial sodium channel |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050477 | Liddle syndrome | |
| DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | |
| DOID:0080526 | bronchiectasis 1 | |
| DOID:1184 | nephrotic syndrome | |
| DOID:1289 | neurodegenerative disease | |
| DOID:14452 | hypokalemic periodic paralysis | |
| DOID:1485 | cystic fibrosis | |
| DOID:326 | ischemia | |
| DOID:4479 | pseudohypoaldosteronism |
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 20277 | MGI:104696 | MOUSE56436 | ||
| 24767 | RGD:3640 | RATNO18542 | ||
| 34299 | FB:FBgn0065109 | |||
| 174306 | WB:WBGene00006832 | |||
| 177494 | WB:WBGene00006748 | |||
| 181035 | WB:WBGene00000950 | |||
| 181101 | WB:WBGene00003174 | |||
| 181728 | WB:WBGene00003168 | |||
| 189058 | WB:WBGene00012137 | |||
| 191422 | WB:WBGene00022815 |
