SLC9A6 solute carrier family 9 member A6 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 10479)
Source: NCBI Gene (ID 10479)
Symbol: SLC9A6
Full name: solute carrier family 9 member A6
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: MRSA; MRXSCH; NHE6
Summary: 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]
Expression: Ubiquitous expression in brain (RPKM 26.2), adrenal (RPKM 4.9) and 23 other tissues
Orthologs: mouse
Gene size: 73433bp
Exon count: 21