SLC9A6 Chromosome X

Solute carrier family 9 member A6
65 variants 65 Health Risk

Upload your DNA to see your personal genotypes for variants in SLC9A6.

What This Gene Does
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]
Gene Info
Gene Group
Solute carrier family 9
Locus Type
gene with protein product
Location
Xq26.3
Ensembl
ENSG00000198689
Associated Conditions (8)
Christianson syndrome
Inborn genetic diseases
Nonpapillary renal cell carcinoma
Intellectual disability
Thyroid cancer
nonmedullary
1
6 conditions
Key Variants
All Variants (65)
RSID Category Clinical Significance Conditions
RS1382310975 Health Risk Conflicting classifications of pathogenicity Christianson syndrome, Inborn genetic diseases, Christianson syndrome
RS140158476 Health Risk Conflicting classifications of pathogenicity Christianson syndrome, Christianson syndrome
RS2070960570 Health Risk Conflicting classifications of pathogenicity Christianson syndrome, Christianson syndrome
RS2071570215 Health Risk Conflicting classifications of pathogenicity Christianson syndrome, Christianson syndrome
RS372679456 Health Risk Conflicting classifications of pathogenicity Christianson syndrome, Christianson syndrome
RS558960349 Health Risk Conflicting classifications of pathogenicity Christianson syndrome, Christianson syndrome
RS781949645 Health Risk Conflicting classifications of pathogenicity Christianson syndrome, Christianson syndrome, Christianson syndrome
RS782039050 Health Risk Conflicting classifications of pathogenicity Christianson syndrome, Christianson syndrome
RS782469016 Health Risk Conflicting classifications of pathogenicity Christianson syndrome, Christianson syndrome
RS782731165 Health Risk Conflicting classifications of pathogenicity Christianson syndrome, Nonpapillary renal cell carcinoma, Christianson syndrome
RS782759179 Health Risk Conflicting classifications of pathogenicity Christianson syndrome, Intellectual disability, Inborn genetic diseases
RS796053284 Health Risk Conflicting classifications of pathogenicity Christianson syndrome, Christianson syndrome
RS1569525357 Health Risk Likely pathogenic Christianson syndrome, Christianson syndrome
RS1569525894 Health Risk Likely pathogenic
RS1603201557 Health Risk Likely pathogenic Christianson syndrome, Christianson syndrome
RS1603201598 Health Risk Likely pathogenic
RS2089324047 Health Risk Likely pathogenic
RS2148143998 Health Risk Likely pathogenic Christianson syndrome, Thyroid cancer, nonmedullary
RS2148149936 Health Risk Likely pathogenic
RS2148156504 Health Risk Likely pathogenic Christianson syndrome, Christianson syndrome
RS2148174022 Health Risk Likely pathogenic
RS2148179162 Health Risk Likely pathogenic
RS2148189993 Health Risk Likely pathogenic Christianson syndrome, Christianson syndrome
RS2521182259 Health Risk Likely pathogenic Christianson syndrome, Christianson syndrome
RS2521219756 Health Risk Likely pathogenic Christianson syndrome, Christianson syndrome
RS2521310197 Health Risk Likely pathogenic Christianson syndrome, Christianson syndrome
RS2521333666 Health Risk Likely pathogenic Christianson syndrome, Christianson syndrome
RS2521333744 Health Risk Likely pathogenic Christianson syndrome, Christianson syndrome
RS1057519394 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS1064795183 Health Risk Pathogenic
RS122461162 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS149044510 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS1556617455 Health Risk Pathogenic Christianson syndrome, Thyroid cancer, nonmedullary
RS1556620027 Health Risk Pathogenic
RS1603198063 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS1603198937 Health Risk Pathogenic Intellectual disability, Intellectual disability
RS1603215383 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS1603219805 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS2071147098 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS2089536867 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2148169894 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS2148173968 Health Risk Pathogenic Christianson syndrome, Thyroid cancer, nonmedullary
RS2148201789 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS2521178978 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS2521310108 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS2521409119 Health Risk Pathogenic
RS2521459845 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS398122849 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS398123003 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
RS398124224 Health Risk Pathogenic Christianson syndrome, Christianson syndrome
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