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SLC9A6

Official Full Name
solute carrier family 9 member A6
Organism
Homo sapiens
GeneID
10479
Background
This gene encodes a sodium-hydrogen exchanger that is amember of the solute carrier family 9. The encoded protein localizes to early and recycling endosomes and may be involved in regulating endosomal pH and volume. Defects in this gene are associated with X-linked syndromic cognitive disability, Christianson type. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010]
Synonyms
MRSA; NHE6; MRXSCH;

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