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The Drug-Drug Interactions Ontology
Last uploaded:
February 11, 2016
| Id | http://purl.obolibrary.org/obo/dinto_1994
http://purl.obolibrary.org/obo/dinto_1994
|
|---|---|
| Preferred Name | sodium channel subunit beta-3 |
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| prefLabel | sodium channel subunit beta-3
|
|---|---|
| label | sodium channel subunit beta-3
|
| Definition | Modulates channel gating kinetics. Causes unique persistent sodium currents. Inactivates the sodium channel opening more slowly than the subunit beta-1. Its association with neurofascin may target the sodium channels to the nodes of Ranvier of developing axons and retain these channels at the nodes in mature myelinated axons (By similarity)
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| type | |
| is inhibited by | |
| OrganismClass | human
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| xref |
UniProt ID:Q9NY72
DrugBank:6134
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| definition source | DrugBank Database
|
| prefixIRI | obo2:dinto_1994
|
| is pharmacological target of | |
| Gene | scn3b
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| subClassOf |
| Delete | Subject | Author | Type | Created |
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| No notes to display |