History:GENE:DPT    GENE:FUT3    GENE:CIRH1A    GENE:MMP12    GENE:COMP    

Gene Expression: SLC12A3

Gene Data

  • Gene Symbol: SLC12A3
  • Gene ID: 6559
  • Synonyms: NCC, NCCT, TSC
  • Description: solute carrier family 12 (sodium/chloride transporter), member 3
  • Database Refs: HGNC:10912, MIM:600968, Ensembl:ENSG00000070915, HPRD:02984, Vega:OTTHUMG00000133284
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 28 exons in this gene. (More about DEXSeq here)

Cluster Associations

This gene is associated with the following clusters: No Clusters were found

Disease Associations

This gene is associated with the following diseases. Clicking on the disease will take you to the disease association entry for that disease.

This gene is associated with 39 diseases, scroll to view all:
  1. Adrenal cortex disease
  2. Adrenal gland disease
  3. Adrenal gland hyperfunction
  4. Articular cartilage disease
  5. Bartter disease
  6. Basilar artery occlusion
  7. Brain disease
  8. Calcinosis
  9. Calcium metabolism disease
  10. Cardiovascular system disease
  11. Cartilage disease
  12. Central nervous system disease
  13. Cerebrovascular accident
  14. Cerebrovascular disease
  15. Disease
  16. Disease of anatomical entity
  17. Disease of metabolism
  18. Endocrine system disease
  19. Essential hypertension
  20. Gitelman syndrome
  21. Hyperaldosteronism
  22. Hypertension
  23. Hypokalemia
  24. Inborn errors of metabolism
  25. Inborn errors renal tubular transport
  26. Kidney disease
  27. Mineral metabolism disease
  28. Nephrocalcinosis
  29. Nephrolithiasis
  30. Nervous system disease
  31. Papilledema
  32. Polyhydramnios
  33. Pseudogout
  34. Pseudohypoaldosteronism
  35. Pseudotumor cerebri
  36. Ureteral disease
  37. Ureterolithiasis
  38. Urinary system disease
  39. Vascular disease

Stage Associations

This gene is associated with the following stages: No Stages were found