Gene Gene information from NCBI Gene database.
Entrez ID 65010
Gene name Solute carrier family 26 member 6
Gene symbol SLC26A6
Synonyms (NCBI Gene)
-
Chromosome 3
Chromosome location 3p21.31
Summary This gene belongs to the solute carrier 26 family, whose members encode anion transporter proteins. This particular family member encodes a protein involved in transporting chloride, oxalate, sulfate and bicarbonate. Alternatively spliced transcript varia
miRNA miRNA information provided by mirtarbase database.
104
miRTarBase ID miRNA Experiments Reference
MIRT733880 hsa-miR-411-3p Immunohistochemistry (IHC)Luciferase reporter assayWestern blotting 33772775
MIRT733880 hsa-miR-411-3p Immunohistochemistry (IHC)Luciferase reporter assayWestern blotting 33772775
MIRT733880 hsa-miR-411-3p Luciferase reporter assayWestern blottingqRT-PCR 33772775
MIRT1357905 hsa-miR-1202 CLIP-seq
MIRT1357906 hsa-miR-1291 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
106
GO ID Ontology Definition Evidence Reference
GO:0005254 Function Chloride channel activity IEA
GO:0005452 Function Solute:inorganic anion antiporter activity IDA 15548529, 27681177
GO:0005452 Function Solute:inorganic anion antiporter activity IEA
GO:0005452 Function Solute:inorganic anion antiporter activity IMP 20501439
GO:0005452 Function Solute:inorganic anion antiporter activity ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610068 14472 ENSG00000225697
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BXS9
Protein name Solute carrier family 26 member 6 (Anion exchange transporter) (Pendrin-like protein 1) (Pendrin-L1)
Protein function Apical membrane anion-exchanger with wide epithelial distribution that plays a role as a component of the pH buffering system for maintaining acid-base homeostasis. Acts as a versatile DIDS-sensitive inorganic and organic anion transporter that
PDB 8OPQ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00916 Sulfate_transp 90 480 Sulfate permease family Family
PF01740 STAS 531 738 STAS domain Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. Highest levels in kidney and pancreas. Lower expression in heart, skeletal muscle, liver and placenta. Also found in lung and brain. {ECO:0000269|PubMed:11087667, ECO:0000269|PubMed:11247665}.; TISSUE SPECIFICITY: [Isoform
Sequence
Sequence length 759
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Mineral absorption
Chemical carcinogenesis - reactive oxygen species
  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
Hyperoxaluria Uncertain significance rs2531501088 RCV003228829
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenoma Associate 19940027
Biliary Atresia Associate 21390152
Colorectal Neoplasms Associate 25193853
Congenital chloride diarrhea Associate 24350656
Diabetes Gestational Associate 31539142
Diabetic Ketoacidosis Associate 31539142
Enteritis Associate 35115415
Hyperoxaluria Associate 18951670, 21956166, 35115415
Kidney Calculi Associate 31042422, 35500753
Lung Neoplasms Associate 35500753