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SLC9A6


Official Full Name
solute carrier family 9 member A6
Organism
Homo sapiens
Gene ID
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

Cat.No. Product Name Price
SHH412356 shRNA set against Human SLC9A6 (NM_006359.2) Inquiry
SHH412360 shRNA set against Mouse SLC9A6 (NM_172780.3) Inquiry
SHL012806 shRNA set against Human SLC9A6(NM_001042537.1) Inquiry
SHL012960 shRNA set against Human SLC9A6(NM_006359.2) Inquiry
Cat.No. Product Name Price
CDFH018052 Human SLC9A6 cDNA Clone(NM_001042537.1) Inquiry
CDFH018053 Human SLC9A6 cDNA Clone(NM_001177651.1) Inquiry
CDFL012654 Mouse Slc9a6 cDNA Clone(NM_172780.3) Inquiry
MiUTR1H-09611 SLC9A6 miRNA 3'UTR clone Inquiry
MiUTR1H-09612 SLC9A6 miRNA 3'UTR clone Inquiry
CDCB183814 Rabbit SLC9A6 ORF clone (XM_008273247.1) Inquiry
CDCH083048 human SLC9A6 ORF clone (NM_001042537.1) Inquiry
CDCH083050 human SLC9A6 ORF clone (NM_001177651.1) Inquiry
CDCR271630 Mouse Slc9a6 ORF Clone(NM_172780.3) Inquiry
CDCS407117 Human SLC9A6 ORF Clone (BC049169) Inquiry
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