Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
115111
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 26 member 7
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC26A7
Synonyms (NCBI Gene) Gene synonyms aliases
SUT2
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8q21.3
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 gene structure and protein length yet have markedly different tissue expression patterns. This gene has abundant and specific expression in the ki
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs774517670 C>T Likely-pathogenic Stop gained, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018335 hsa-miR-335-5p Microarray 18185580
MIRT023903 hsa-miR-1-3p Microarray 18668037
MIRT653673 hsa-miR-409-3p HITS-CLIP 23824327
MIRT653672 hsa-miR-3156-5p HITS-CLIP 23824327
MIRT653671 hsa-miR-33a-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:0001696 Process Gastric acid secretion IEA
GO:0005254 Function Chloride channel activity IDA 1183472
GO:0005737 Component Cytoplasm IDA 16524946
GO:0005768 Component Endosome IDA 16524946
GO:0005886 Component Plasma membrane TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608479 14467 ENSG00000147606
Protein
UniProt ID Q8TE54
Protein name Anion exchange transporter (Solute carrier family 26 member 7)
Protein function Acts as an anion channel mediating the transport of chloride, sulfate and oxalate ions (PubMed:11834742). Mediates the transport of bromide, iodide, nitrate, gluconate, thiocyanate and bicarbonate ions (By similarity). Its permeability towards b
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00916 Sulfate_transp 47 444 Sulfate permease family Family
PF01740 STAS 493 637 STAS domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in the thyroid gland (at protein level). Expressed in tonsillar high endothelial venule endothelial cells (HEVEC), placenta and in testis, expressed in a subgroup of basal cells in the epididymal ducts. {ECO:0000269|PubMed:11
Sequence
Sequence length 656
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Gastric acid secretion   Multifunctional anion exchangers
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
21822266
Unknown
Disease term Disease name Evidence References Source
Congenital Hypothyroidism congenital hypothyroidism GenCC
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 34516545
Autoimmune Diseases Associate 34944008
Congenital Hypothyroidism Associate 34200080
Diarrhea Associate 34270794
Hand Foot Syndrome Associate 34270794
HIV Infections Associate 21897333
Nausea Associate 34270794
Neuroendocrine Tumors Associate 34944008
Thyroid Cancer Papillary Associate 36465624
Thyroid Carcinoma Anaplastic Associate 27796151