Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
284129
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 26 member 11
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC26A11
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q25.3
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610117 14471 ENSG00000181045
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Ischemic Stroke Ischemic stroke N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 37511575
Neoplasms Associate 35568949
Sarcoma Associate 35568949