Gene Gene information from NCBI Gene database.
Entrez ID 284129
Gene name Solute carrier family 26 member 11
Gene symbol SLC26A11
Synonyms (NCBI Gene)
-
Chromosome 17
Chromosome location 17q25.3
Summary This gene encodes a member of the solute linked carrier 26 family of anion exchangers. Members of this family of proteins are essential for numerous cellular functions including homeostasis and intracellular electrolyte balance. The encoded protein is a s
miRNA miRNA information provided by mirtarbase database.
89
miRTarBase ID miRNA Experiments Reference
MIRT1357467 hsa-miR-1228 CLIP-seq
MIRT1357468 hsa-miR-329 CLIP-seq
MIRT1357469 hsa-miR-362-3p CLIP-seq
MIRT1357470 hsa-miR-514 CLIP-seq
MIRT1357471 hsa-miR-514b-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
37
GO ID Ontology Definition Evidence Reference
GO:0005254 Function Chloride channel activity IEA
GO:0005254 Function Chloride channel activity ISS
GO:0005515 Function Protein binding IPI 32296183
GO:0005654 Component Nucleoplasm IDA
GO:0005764 Component Lysosome IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610117 14471 ENSG00000181045
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86WA9
Protein name Sodium-independent sulfate anion transporter (Solute carrier family 26 member 11)
Protein function Sodium-independent anion exchanger mediating bicarbonate, chloride, sulfate and oxalate transport (By similarity). Exhibits sodium-independent sulfate anion transporter activity that may cooperate with SLC26A2 to mediate DIDS-sensitive sulfate u
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00916 Sulfate_transp 48 441 Sulfate permease family Family
PF01740 STAS 470 576 STAS domain Domain
Tissue specificity TISSUE SPECIFICITY: Detected in all tissues tested with highest expression observed in brain, kidney, HEVEC and placenta and lowest in pancreas, skeletal muscle, liver, lung and heart. {ECO:0000269|PubMed:11087667, ECO:0000269|PubMed:12626430}.
Sequence
Sequence length 606
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Multifunctional anion exchangers
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Gastric cancer Uncertain significance rs374746901 RCV005932520
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 37511575
Neoplasms Associate 35568949
Sarcoma Associate 35568949