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The Drug-Drug Interactions Ontology
Last uploaded:
February 11, 2016
| Id | http://purl.obolibrary.org/obo/dinto_0023
http://purl.obolibrary.org/obo/dinto_0023
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|---|---|
| Preferred Name | voltage-dependent t-type calcium channel subunit alpha-1g |
| Synonyms |
cav3.1c
nbr13
voltage- gated calcium channel subunit alpha cav3.1
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| prefLabel | voltage-dependent t-type calcium channel subunit alpha-1g
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|---|---|
| label | voltage-dependent t-type calcium channel subunit alpha-1g
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| Definition | Voltage-sensitive calcium channels (VSCC) mediate the entry of calcium ions into excitable cells and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, gene expression, cell motility, cell division and cell death. The isoform alpha-1G gives rise to T-type calcium currents. T-type calcium channels belong to the "low-voltage activated (LVA)" group and are strongly blocked by mibefradil. A particularity of this type of channels is an opening at quite negative potentials and a voltage-dependent inactivation. T-type channels serve pacemaking functions in both central neurons and cardiac nodal cells and support calcium signaling in secretory cells and vascular smooth muscle. They may also be involved in the modulation of firing patterns of neurons which is important for information processing as well as in cell growth processes
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| type | |
| is inhibited by |
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| Synonym |
cav3.1c
nbr13
voltage- gated calcium channel subunit alpha cav3.1
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| OrganismClass | human
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| xref |
DrugBank:535
UniProt ID:O43497
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| definition source | DrugBank Database
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| prefixIRI | obo2:dinto_0023
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| is pharmacological target of |
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| Gene | cacna1g
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| subClassOf |
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| No notes to display |