XB-FEAT-5889668: Difference between revisions
imported>Xenbase gene generator No edit summary |
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This is the community wiki page for the gene ''unc80'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | This is the community wiki page for the gene ''unc80'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase. | ||
=nomenclature changes= | |||
05/29/2017 | |||
Human name has changed for Entrez Gene: 285175. From unc-80 homolog, NALCN activator to unc-80 homolog, NALCN channel complex subunit | |||
=summary= | |||
The protein encoded by this gene is a component of a voltage-independent 'leak' ion-channel complex, in which it performs essential functions, such as serving as a bridge between two other components (sodium leak channel non-selective and UNC79) and as a scaffold for Src kinases. Leak channels play an importnat role in establishment and maintenance of resting membrane potentials in neurons. Mutations in this gene are associated with congenital infantile encephalopathy, intellectual disability and growth issues. [provided by RefSeq, Aug 2016] | |||
Latest revision as of 08:59, 31 May 2017
unc80
This is the community wiki page for the gene unc80 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
05/29/2017 Human name has changed for Entrez Gene: 285175. From unc-80 homolog, NALCN activator to unc-80 homolog, NALCN channel complex subunit
summary
The protein encoded by this gene is a component of a voltage-independent 'leak' ion-channel complex, in which it performs essential functions, such as serving as a bridge between two other components (sodium leak channel non-selective and UNC79) and as a scaffold for Src kinases. Leak channels play an importnat role in establishment and maintenance of resting membrane potentials in neurons. Mutations in this gene are associated with congenital infantile encephalopathy, intellectual disability and growth issues. [provided by RefSeq, Aug 2016]