Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
115019
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 26 member 9
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC26A9
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q32.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene is one member of a family of sulfate/anion transporter genes. Family members are well conserved in their genomic (number and size of exons) and protein (aa length among species) structures yet have markedly different tissue expression patterns.
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT646128 hsa-miR-618 HITS-CLIP 23824327
MIRT646127 hsa-miR-4640-3p HITS-CLIP 23824327
MIRT646126 hsa-miR-6871-3p HITS-CLIP 23824327
MIRT646125 hsa-miR-3065-3p HITS-CLIP 23824327
MIRT646124 hsa-miR-6887-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IDA 26801567
GO:0005254 Function Chloride channel activity IDA 17673510, 18769029, 19289574, 20658517, 22544634, 32818062
GO:0005254 Function Chloride channel activity TAS
GO:0005452 Function Solute:inorganic anion antiporter activity IDA 15800055, 22544634
GO:0005515 Function Protein binding IPI 28360110
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608481 14469 ENSG00000174502
Protein
UniProt ID Q7LBE3
Protein name Solute carrier family 26 member 9 (Anion transporter/exchanger protein 9)
Protein function Ion transporter that can act both as an ion channel and anion exchanger (PubMed:15800055, PubMed:17673510, PubMed:26801567, PubMed:32818062). Mainly acts as a chloride channel, which mediate uncoupled chloride anion transport in an alternate-acc
PDB 7CH1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00916 Sulfate_transp 71 469 Sulfate permease family Family
PF01740 STAS 520 733 STAS domain Domain
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in lung at the luminal side of the bronchiolar and alveolar epithelium of lung. To a lower extent, also expressed in pancreas and prostate. {ECO:0000269|PubMed:11834742}.
Sequence
Sequence length 791
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
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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
Cystic Fibrosis cystic fibrosis N/A N/A GenCC
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 33832101
Asthma Associate 34884866, 35328418
Autoimmune Diseases Associate 34944008
Bronchiectasis Associate 34884866
Cystic Fibrosis Associate 23670970, 24550193, 25771386, 28171547, 30716472, 30807572, 31581148, 31697830, 33674211, 34884866, 36206743
Diabetes Mellitus Associate 23670970, 31581148
Exocrine Pancreatic Insufficiency Associate 25771386
Huntington Disease Associate 22466613
Inflammation Associate 34884866
Lung Diseases Associate 28171547