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KCNK9

This gene encodes a protein that contains multiple transmembrane regions and two pore-forming P domains and functions as a pH-dependent potassium channel. Amplification and overexpression of this gene have been observed in several types of human carcinomas. This gene is imprinted in the brain, with preferential expression from the maternal allele. A mutation in this gene was associated with Birk-Barel mental retardation dysmorphism syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]
Protein class

Disease related genes, FDA approved drug targets, Human disease related genes, Transporters, Voltage-gated ion channels

Predicted location

Membrane

Single cell type specificity

Group enriched (Excitatory neurons, Late spermatids, Inhibitory neurons)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Not detected

Interaction

Homodimer (Probable). Heterodimer with KCNK1.

Molecular function

Ion channel, Potassium channel

More Types Infomation

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For Research Use Only. Not For Clinical Use.

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