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The Drug-Drug Interactions Ontology
Last uploaded:
February 11, 2016
| Id | http://purl.obolibrary.org/obo/dinto_4078
http://purl.obolibrary.org/obo/dinto_4078
|
|---|---|
| Preferred Name | sodium channel protein type 9 subunit alpha |
| Synonyms |
hne-na
voltage-gated sodium channel subunit alpha nav1.7
sodium channel protein type ix subunit alpha
neuroendocrine sodium channel
peripheral sodium channel 1
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| prefLabel | sodium channel protein type 9 subunit alpha
|
|---|---|
| label | sodium channel protein type 9 subunit alpha
|
| Definition | Mediates the voltage-dependent sodium ion permeability of excitable membranes. Assuming opened or closed conformations in response to the voltage difference across the membrane, the protein forms a sodium-selective channel through which Na(+) ions may pass in accordance with their electrochemical gradient. It is a tetrodotoxin-sensitive Na(+) channel isoform. Plays a role in pain mechanisms, especially in the development of inflammatory pain
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| type | |
| is modulated by | |
| is inhibited by | |
| Synonym |
hne-na
voltage-gated sodium channel subunit alpha nav1.7
sodium channel protein type ix subunit alpha
neuroendocrine sodium channel
peripheral sodium channel 1
|
| OrganismClass | human
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| xref |
UniProt ID:Q15858
DrugBank:1995
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| definition source | DrugBank Database
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| prefixIRI | obo2:dinto_4078
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| related with | |
| is pharmacological target of | |
| Gene | scn9a
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| subClassOf |
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| No notes to display |