SLC47A2 (solute carrier family 47 member 2)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 146802 |
| Gene name | Solute carrier family 47 member 2 |
| Gene symbol | SLC47A2 |
| Synonyms (NCBI Gene) |
MATE2MATE2-BMATE2-KMATE2K
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| Chromosome | 17 |
| Chromosome location | 17p11.2 |
| Summary | This gene encodes a protein belonging to a family of transporters involved in excretion of toxic electrolytes, both endogenous and exogenous, through urine and bile. This transporter family shares homology with the bacterial MATE (multidrug and toxin extr |
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miRNA
miRNA information provided by mirtarbase database.
14
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
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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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Q86VL8 | |||||||||||||||
| Protein name | Multidrug and toxin extrusion protein 2 (MATE-2) (hMATE-2) (Kidney-specific H(+)/organic cation antiporter) (Solute carrier family 47 member 2) | |||||||||||||||
| Protein function | Multidrug efflux pump that functions as a H(+)/organic cation antiporter. Mediates the efflux of cationic compounds, such as the model cations, tetraethylammonium (TEA) and 1-methyl-4-phenylpyridinium (MPP+), the platinum-based drug oxaliplatin | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: [Isoform 1]: High expression in kidney. Very small expression in adrenal gland and lung. {ECO:0000269|PubMed:16807400, ECO:0000269|PubMed:21419862}.; TISSUE SPECIFICITY: [Isoform 3]: High expression in kidney. Very small expression in | |||||||||||||||
| Sequence |
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| Sequence length | 602 | |||||||||||||||
| 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.).
4
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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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