Aliases for FXYD3 Gene
- FXYD Domain Containing Ion Transport Regulator 3 2 3 5
- Sodium/Potassium-Transporting ATPase Subunit FXYD3 3 4
- FXYD Domain-Containing Ion Transport Regulator 3 2 3
- Chloride Conductance Inducer Protein Mat-8 3 4
- Mammary Tumor 8 KDa Protein 3 4
- PLML 3 4
- MAT8 3 4
- Phospholemman-Like Protein 3
- Phospholemman-Like 4
External Ids for FXYD3 Gene
Previous HGNC Symbols for FXYD3 Gene
Previous GeneCards Identifiers for FXYD3 Gene
This gene belongs to a small family of FXYD-domain containing regulators of Na+/K+ ATPases which share a 35-amino acid signature sequence domain, beginning with the sequence PFXYD, and containing 7 invariant and 6 highly conserved amino acids. This gene encodes a cell membrane protein that may regulate the function of ion-pumps and ion-channels. This gene may also play a role in tumor progression. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2008]
GeneCards Summary for FXYD3 Gene
FXYD3 (FXYD Domain Containing Ion Transport Regulator 3) is a Protein Coding gene. Among its related pathways are Cardiac conduction and Ion channel transport. Gene Ontology (GO) annotations related to this gene include ion channel activity and ATPase binding. An important paralog of this gene is FXYD4.
UniProtKB/Swiss-Prot for FXYD3 Gene
Associates with and regulates the activity of the sodium/potassium-transporting ATPase (NKA) which transports Na(+) out of the cell and K(+) into the cell (PubMed:17077088). Reduces glutathionylation of the NKA beta-1 subunit ATP1B1, thus reversing glutathionylation-mediated inhibition of ATP1B1 (PubMed:21454534). Induces a hyperpolarization-activated chloride current when expressed in Xenopus oocytes (PubMed:7836447).
Isoform 1: Decreases the apparent K+ and Na+ affinity of the sodium/potassium-transporting ATPase over a large range of membrane potentials.
Isoform 2: Decreases the apparent K+ affinity of the sodium/potassium-transporting ATPase only at slightly negative and positive membrane potentials and increases the apparent Na+ affinity over a large range of membrane potentials.