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sodium-hydrogen exchanger 5

belongs to a family of integral membrane proteins that play central roles in sodium, acid-base, and cell volume homeostasis; mutations in the coding region of the NHE5 gene as a cause for familial Familial Paroxysmal Kinesigenic Dyskinesia (PKD), is an autosomal dominant condition characterized by attacks of dystonia or chorea triggered by sudden movements;; amino acid sequence in first source; GenBank AF111173 (human); RefSeq NM_004594 (human), NM_138858 (rat)
Also Known As:
NHE-5 protein, human; NHE5 protein, human; Nhe5 protein, rat; SLC9A5 protein, human; Slc9a5 protein, mouse; Slc9a5 protein, rat; sodium hydrogen exhanger 5; solute carrier family 9 (sodium-hydrogen exchanger), isoform 5 protein, human; solute carrier family 9 (sodium/hydrogen exchanger), isoform 5 protein, rat; solute carrier family 9 (sodium/hydrogen exchanger), member 5 protein, mouse
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