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SLC14A1 (Urea transporter 1) is a gene. In the public catalogues the evidence so far is association rather than a proven role. This dossier gathers the 0 products (0 approved), 0 trials, 0 pathways and 0 resistance routes in the corpus that involve it, with external identifiers so it can be joined to UniProt, ChEMBL, Open Targets and the rest of biology.
Mediates the transport of urea driven by a concentration gradient across the cell membrane of erythrocytes. Also mediates the transport of urea across the cell membrane of the renal inner medullary collecting duct which is critical to the urinary concentrating mechanism. Facilitates water transport in erythrocytes. Location: Cell membrane; Basolateral cell membrane (UniProt). Locus 18q12.3 (HGNC).
No product in the corpus is aimed at this target yet.
No trial in the corpus names this target or one of its products.
No recorded escape route names this target.
No pathway diagram carries this target as a node.
No companion diagnostic in the registry measures this target.
No model entry for this target yet; check the cancer entries on the models page.
No open questions recorded for this target yet. Suggest one.
Query for this target: (TITLE:"SLC14A1" OR ABSTRACT:"SLC14A1" OR TITLE:"solute carrier family 14 member 1 Kidd blood group" OR ABSTRACT:"solute carrier family 14 member 1 Kidd blood group" OR TITLE:"Urea transporter 1" OR ABSTRACT:"Urea transporter 1" OR TITLE:"HsT1341" OR ABSTRACT:"HsT1341" OR TITLE:"RACH1" OR ABSTRACT:"RACH1" OR TITLE:"RACH2" OR ABSTRACT:"RACH2") AND (cancer OR tumor OR tumour OR oncology OR carcinoma OR lymphoma OR leukemia OR leukaemia OR myeloma OR sarcoma OR melanoma OR glioma). Results are unfiltered search hits about SLC14A1, not a curated reading list.
The dossier as machine-readable JSON, at /api/v1/dossiers/slc14a1.json: identifiers from HGNC, Ensembl, UniProt and ChEMBL, products with status, trials, pathways, hotspots, open questions and assays. The full entity record is in the open API at /api/v1/entities/slc14a1.json. Licence CC BY-NC 4.0.