Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10479
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 9 member A6
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC9A6
Synonyms (NCBI Gene) Gene synonyms aliases
MRSA, MRXSCH, NDPACX, NHE6
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xq26.3
Summary Summary of gene provided in NCBI Entrez Gene.
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 wit
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs122461162 C>T Pathogenic Coding sequence variant, stop gained
rs139299794 C>T Conflicting-interpretations-of-pathogenicity, benign Coding sequence variant, synonymous variant, 5 prime UTR variant
rs151178361 G>A Conflicting-interpretations-of-pathogenicity, likely-benign Synonymous variant, coding sequence variant
rs190788663 C>T Conflicting-interpretations-of-pathogenicity 3 prime UTR variant
rs398122849 GGTGCTGCT>- Pathogenic Inframe deletion, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT027197 hsa-miR-103a-3p Sequencing 20371350
MIRT030928 hsa-miR-21-5p Microarray 18591254
MIRT031859 hsa-miR-16-5p Sequencing 20371350
MIRT048876 hsa-miR-93-5p CLASH 23622248
MIRT046279 hsa-miR-23b-3p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 18057008, 32296183
GO:0005739 Component Mitochondrion IDA 11940519
GO:0005768 Component Endosome IEA
GO:0005789 Component Endoplasmic reticulum membrane IDA 11641397
GO:0005886 Component Plasma membrane IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
300231 11079 ENSG00000198689
Protein
UniProt ID Q92581
Protein name Sodium/hydrogen exchanger 6 (Na(+)/H(+) exchanger 6) (NHE-6) (Solute carrier family 9 member 6)
Protein function Endosomal Na(+), K(+)/H(+) antiporter (PubMed:15522866, PubMed:28635961, PubMed:31676550, PubMed:32277048). Mediates the electroneutral exchange of endosomal luminal H(+) for a cytosolic Na(+) or K(+). By facilitating proton efflux, SLC9A6 count
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00999 Na_H_Exchanger 76 503 Sodium/hydrogen exchanger family Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. High expression in brain, skeletal muscle, and heart, but is also detected at lower levels in most other tissues. {ECO:0000269|PubMed:9507001}.
Sequence
Sequence length 669
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Cardiac muscle contraction   Sodium/Proton exchangers
Defective SLC9A6 causes X-linked, syndromic mental retardation,, Christianson type (MRXSCH)
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Christianson Syndrome christianson syndrome rs398122849, rs1569525357, rs398123003, rs1603215383, rs398124224, rs587784398, rs1603198063, rs587784399, rs1603201557, rs797044508, rs1603219805, rs796053290, rs782108464, rs886037619, rs122461162
View all (5 more)
N/A
Mental retardation intellectual disability rs1603198937, rs796053290 N/A
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Inhibit 25561733
Alzheimer's disease without Neurofibrillary tangles Associate 20395263
Angelman Syndrome Associate 18342287, 20949524
Ataxia Associate 18342287, 34791706
ATR X syndrome Associate 29275387
Atrophy Associate 29275387
Autism Spectrum Disorder Associate 29275387, 32722525
Body Dysmorphic Disorders Associate 26993267
Brain Diseases Associate 25818041
Depression Postpartum Associate 34791706