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The Drug-Drug Interactions Ontology
Last uploaded:
February 11, 2016
| Id | http://purl.obolibrary.org/obo/dinto_3317
http://purl.obolibrary.org/obo/dinto_3317
|
|---|---|
| Preferred Name | amiloride-sensitive cation channel 1, neuronal |
| Synonyms |
asic2
acid-sensing ion channel 2
amiloride-sensitive brain sodium channel
mammalian degenerin homolog
bnc1
brain sodium channel 1
amiloride-sensitive cation channel neuronal 1
bnac1
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| prefLabel | amiloride-sensitive cation channel 1, neuronal
|
|---|---|
| label | amiloride-sensitive cation channel 1, neuronal
|
| Definition | Cation channel with high affinity for sodium, which is gated by extracellular protons and inhibited by the diuretic amiloride. Also permeable for Li(+) and K(+). Generates a biphasic current with a fast inactivating and a slow sustained phase. Heteromeric channel assembly seems to modulate
|
| type | |
| is inhibited by | |
| Synonym |
asic2
acid-sensing ion channel 2
amiloride-sensitive brain sodium channel
mammalian degenerin homolog
bnc1
brain sodium channel 1
amiloride-sensitive cation channel neuronal 1
bnac1
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|
| OrganismClass | human
|
| xref |
UniProt ID:Q16515
DrugBank:749
|
| definition source | DrugBank Database
|
| prefixIRI | obo2:dinto_3317
|
| Gene | accn1
|
| subClassOf |
| Delete | Subject | Author | Type | Created |
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| No notes to display |