Preferred Label : sodium-hydrogen exchanger 5;
MeSH note : 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);
CISMeF synonym : SLC9A5 protein, human; Slc9a5 protein, mouse; Slc9a5 protein, rat; solute carrier family 9 (sodium/hydrogen exchanger), member 5 protein, mouse; solute carrier family 9 (sodium/hydrogen exchanger), isoform 5 protein, rat;
MeSH synonym : sodium hydrogen exhanger 5;
MeSH hyponym : solute carrier family 9 (sodium-hydrogen exchanger), member 5 protein, mouse; NHE5 protein, human; NHE-5 protein, human; solute carrier family 9 (sodium-hydrogen exchanger), isoform 5 protein, human; Nhe5 protein, rat; solute carrier family 9 (sodium-hydrogen exchanger), isoform 5 protein, rat;
Is substance : O;
Origin ID : C117561;
UMLS CUI : C0764009;
MeSH term(s) associated for indexing
- Record concept(s)
- Semantic type(s)
