XB-FEAT-5777344: Difference between revisions
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=kcnj10= | =kcnj10= | ||
This is the community wiki page for the gene ''kcnj10'' 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 ''kcnj10'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase. | ||
=nomenclature changes= | |||
08.23.2019 | |||
Human name has changed for Entrez Gene: 3766. From potassium voltage-gated channel subfamily J member 10 to potassium inwardly rectifying channel subfamily J member 10 | |||
=summary from NCBI for human KNCJ10= | |||
This gene encodes a member of the inward rectifier-type potassium channel family, characterized by having a greater tendency to allow potassium to flow into, rather than out of, a cell. The encoded protein may form a heterodimer with another potassium channel protein and may be responsible for the potassium buffering action of glial cells in the brain. Mutations in this gene have been associated with seizure susceptibility of common idiopathic generalized epilepsy syndromes. [provided by RefSeq, Jul 2008] | |||
Latest revision as of 07:35, 27 August 2019
kcnj10
This is the community wiki page for the gene kcnj10 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
08.23.2019
Human name has changed for Entrez Gene: 3766. From potassium voltage-gated channel subfamily J member 10 to potassium inwardly rectifying channel subfamily J member 10
summary from NCBI for human KNCJ10
This gene encodes a member of the inward rectifier-type potassium channel family, characterized by having a greater tendency to allow potassium to flow into, rather than out of, a cell. The encoded protein may form a heterodimer with another potassium channel protein and may be responsible for the potassium buffering action of glial cells in the brain. Mutations in this gene have been associated with seizure susceptibility of common idiopathic generalized epilepsy syndromes. [provided by RefSeq, Jul 2008]