SLC14A2 (solute carrier family 14 member 2)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 8170 |
| Gene name | Solute carrier family 14 member 2 |
| Gene symbol | SLC14A2 |
| Synonyms (NCBI Gene) |
HUT2UT-A2UT2UTAUTRhUT-A6
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| Chromosome | 18 |
| Chromosome location | 18q12.3 |
| Summary | The protein encoded by this gene belongs to the urea transporter family. In mammalian cells, urea is the chief end product of nitrogen catabolism, and plays an important role in the urinary concentration mechanism. This protein is expressed in the inner m |
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miRNA
miRNA information provided by mirtarbase database.
191
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
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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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Q15849 | |||||||||||||||
| Protein name | Urea transporter 2 (Solute carrier family 14 member 2) (Urea transporter, kidney) | |||||||||||||||
| Protein function | [Isoform 1]: Mediates the transport of urea driven by a concentration gradient across the cell membrane of the renal inner medullary collecting duct which is critical to the urinary concentrating mechanism. {ECO:0000269|PubMed:11502588, ECO:0000 | |||||||||||||||
| PDB | 8BLO , 8XD7 , 8XD9 , 8XDA , 8XDB , 8XDC , 8XDD , 8XDE | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: [Isoform 1]: Epressed in the inner medulla of the kidney (at protein level). {ECO:0000269|PubMed:11502588}.; TISSUE SPECIFICITY: [Isoform 2]: Expressed in the kidney. {ECO:0000269|PubMed:8647271}. | |||||||||||||||
| Sequence |
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| Sequence length | 920 | |||||||||||||||
| 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 categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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