SLCO3A1 (solute carrier organic anion transporter family member 3A1)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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28232 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Solute carrier organic anion transporter family member 3A1 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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SLCO3A1 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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OATP-D, OATP-RP3, OATP3A1, OATPD, OATPRP3, SLC21A11 |
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Chromosome
Chromosome number
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15 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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15q26.1 |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | ||||||||||||||||
| UniProt ID | Q9UIG8 | |||||||||||||||
| Protein name | Solute carrier organic anion transporter family member 3A1 (OATP3A1) (Organic anion transporter polypeptide-related protein 3) (OATP-RP3) (OATPRP3) (Organic anion-transporting polypeptide D) (OATP-D) (PGE1 transporter) (Sodium-independent organic anion tr | |||||||||||||||
| Protein function | Putative organic anion antiporter with apparent broad substrate specificity. Recognizes various substrates including thyroid hormone L-thyroxine, prostanoids such as prostaglandin E1 and E2, bile acids such as taurocholate, glycolate and glycoch | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Generally the expression of isoform 1 is higher than that of isoform 2. {ECO:0000269|PubMed:16971491}.; TISSUE SPECIFICITY: [Isoform 1]: Expressed in placental trophoblasts (PubMed:10873595, PubMed:12409283). Expressed in pancreas, kid | |||||||||||||||
| Sequence | ||||||||||||||||
| Sequence length | 710 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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