SLC9A9
Gene Information
- Official Symbol: SLC9A9
- Official Name: solute carrier family 9 member A9
- Aliases and Previous Symbols: N/A
- Entrez ID: 285195
- UniProt: Q8IVB4
- Interactions: BioGRID
- PubMed articles: Open PubMed
- OMIM: Open OMIM
Function Summary
- Entrez Summary: 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].
- UniProt Summary: May act in electroneutral exchange of protons for Na(+) across membranes. Involved in the effusion of Golgi luminal H(+) in exchange for cytosolic cations. Involved in organelle ion homeostasis by contributing to the maintenance of the unique acidic pH values of the Golgi and post-Golgi compartments in the cell. {ECO:0000269|PubMed:15522866}.
CRISPR Data
Essentiality in NALM6
- Essentiality Rank: 12536
- Expression level (log2 read counts): 2.34