SLC9A9, solute carrier family 9 member A9

SLC9A9, solute carrier family 9 member A9

• 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]

• Gene Synonyms (sodium/hydrogen exchanger 9, Na(+)/H(+) exchanger 9, putative protein product of Nbla00118, sodium/proton exchanger NHE9, solute carrier family 9 (sodium/hydrogen exchanger), solute carrier family 9, subfamily A (NHE9, cation proton antiporter 9), member 9, AUTS16, NHE9,)
• NCBI Gene ID: 285195
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q8IVB4
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

solute carrier family 9 member A9 interacts with:

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.