solute carrier family 9, subfamily A (NHE9, cation proton antiporter 9), member 9

Symbol

SLC9A9 (may also be known as: None)

Organism

Human

Description

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. [provided by RefSeq, Mar 2012]

Orthologs

SymbolSpecies
nhx-5 Caenorhabditis elegans
Nhe3 Drosophila melanogaster
Slc9a9 Mus musculus
Slc9a9 Rattus norvegicus
NHX1 Saccharomyces cerevisiae
SPAC15A10.06 Schizosaccharomyces pombe

Links to external resources

Changes associated with this gene

GO Terms

GO IDGO TermGO Category
GO:0006811 ion transport biological_process
GO:0006812 cation transport biological_process
GO:0006814 sodium ion transport biological_process
GO:0006885 regulation of pH biological_process
GO:0055085 transmembrane transport biological_process
GO:0016020 membrane cellular_component
GO:0016021 integral to membrane cellular_component
GO:0031902 late endosome membrane cellular_component
GO:0055037 recycling endosome cellular_component
GO:0015297 antiporter activity molecular_function
GO:0015299 solute:hydrogen antiporter activity molecular_function
GO:0015385 sodium:hydrogen antiporter activity molecular_function