SLCO3A1 (solute carrier organic anion transporter family member 3A1)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 28232 |
| Gene name | Solute carrier organic anion transporter family member 3A1 |
| Gene symbol | SLCO3A1 |
| Synonyms (NCBI Gene) |
OATP-DOATP-RP3OATP3A1OATPDOATPRP3SLC21A11
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| Chromosome | 15 |
| Chromosome location | 15q26.1 |
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miRNA
miRNA information provided by mirtarbase database.
309
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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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 from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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