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SLC9A9
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For Research Use Only. Not For Clinical Use.
Background
This gene encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family. The encoded protein localizes the to the late recycling endosomes and may play an important role in maintaining cation homeostasis. Mutations in this gene are associated with autism susceptibility 16 and attention-deficit/hyperactivity disorder.
Protein class
Disease related genes, Human disease related genes, Metabolic proteins, Potential drug targets, Transporters
Predicted location
Membrane
Single cell type specificity
Group enriched (Oligodendrocytes, Microglial cells, Oligodendrocyte precursor cells, Inhibitory neurons, Astrocytes)
Immune cell specificity
Low immune cell specificity
Cell line specificity
Cell line enhanced (ASC diff, ASC TERT1, HSkMC, Karpas-707, RPMI-8226, U-266/70)
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