Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9356
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 22 member 6
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC22A6
Synonyms (NCBI Gene) Gene synonyms aliases
HOAT1, OAT1, PAHT, ROAT1
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q12.3
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is involved in the sodium-dependent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and may be localized to the basolateral membrane. Four
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT646399 hsa-miR-296-3p HITS-CLIP 23824327
MIRT646398 hsa-miR-1470 HITS-CLIP 23824327
MIRT646397 hsa-miR-4667-3p HITS-CLIP 23824327
MIRT646396 hsa-miR-6832-3p HITS-CLIP 23824327
MIRT646395 hsa-miR-6734-3p HITS-CLIP 23824327
Transcription factors
Transcription factor Regulation Reference
HNF4A Unknown 17344191
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005452 Function Inorganic anion exchanger activity IDA 15037815
GO:0005515 Function Protein binding IPI 16189514, 19060904
GO:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane IDA 14749323
GO:0005901 Component Caveola IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607582 10970 ENSG00000197901
Protein
UniProt ID Q4U2R8
Protein name Solute carrier family 22 member 6 (Organic anion transporter 1) (hOAT1) (PAH transporter) (hPAHT) (Renal organic anion transporter 1) (hROAT1)
Protein function Secondary active transporter that functions as a Na(+)-independent organic anion (OA)/dicarboxylate antiporter where the uptake of one molecule of OA into the cell is coupled with an efflux of one molecule of intracellular dicarboxylate such as
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00083 Sugar_tr 101 518 Sugar (and other) transporter Family
Tissue specificity TISSUE SPECIFICITY: Strongly expressed in kidney (PubMed:10049739, PubMed:10462545, PubMed:10964714, PubMed:9887087, PubMed:9950961). Expressed at lower level in liver, skeletal muscle, brain and placenta (PubMed:10049739, PubMed:10462545, PubMed:9887087,
Sequence
Sequence length 563
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Folate transport and metabolism   Organic anion transport
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Tumoral calcinosis Tumoral calcinosis rs104894343, rs104894344, rs745655924, rs137853086, rs375879489, rs761396172, rs137853087, rs137853091, rs137853088, rs137853089, rs137853090, rs766750282, rs760830864, rs786205250, rs267606841
View all (4 more)
12803500
Unknown
Disease term Disease name Evidence References Source
Insomnia Insomnia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Acute Kidney Injury Associate 26277839
Carcinoma Renal Cell Inhibit 32461965
Diabetic Nephropathies Inhibit 23949796
Gout Associate 35406626
Gyrate Atrophy Associate 2893548
Inflammation Associate 35245485
Juvenile gout Associate 12472777
Renal Insufficiency Chronic Associate 29795395
Stevens Johnson Syndrome Associate 25876064
Vascular Diseases Associate 35245485