The SLC9A6 gene homepage

General information
Gene symbol SLC9A6
Gene name solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
Chromosome X
Chromosomal band q26.3
Imprinted Unknown
Genomic reference NG_017160.1
Transcript reference NM_001042537.1, NM_006359.2
Exon/intron information NM_001042537.1 exon/intron table
Associated with diseases ID, MRXSCH
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 100
Unique public DNA variants reported 69
Individuals with public variants 67
Hidden variants 16
Download all this gene's data Download all data
Notes Alias KIAA0267, NHE6.
Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created September 13, 2012
Date last updated September 17, 2021
Version SLC9A6:210917

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_001042537.1.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL
HGNC 11079
Entrez Gene 10479
PubMed articles SLC9A6
OMIM - Gene 300231
OMIM - Diseases MRXSCH (mental retardation, X-linked, syndromic, Christianson type (MRXSCH))
GeneCards SLC9A6
GeneTests SLC9A6
Orphanet SLC9A6

Active transcripts




NCBI ID     

NCBI Protein ID     

00000342 X solute carrier family 9 (sodium/hydrogen exchanger), member 6, transcript variant 2 NM_006359.2 NP_006350.1 97
00023864 X solute carrier family 9 (sodium/hydrogen exchanger), member 6, transcript variant 1 NM_001042537.1 NP_001036002.1 85

Copyright & disclaimer
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