Gitelman syndrome

Summary
Synonym
  • HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA
Definition
A renal tubular transport disease that is has_material_basis_in mutations in genes that produce proteins involved in the kidneys' reabsorption of salt (sodium chloride or NaCl) from urine back into the bloodstream, thus impairing the kidneys' ability to reabsorb salt, leading to the loss of excess salt in the urine (salt wasting).
Super Class
autosomal recessive disease renal tubular transport disease
Disease Ontology
DOID:0050450
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
1188 CLCNKB chloride voltage-gated channel Kb
6559 SLC12A3 solute carrier family 12 member 3
Displaying all 4 entries
Gene ID Gene Symbol Description Source
12733 Clcnka chloride channel, voltage-sensitive Ka
20497 Slc12a3 solute carrier family 12, member 3
56365 Clcnkb chloride channel, voltage-sensitive Kb
69847 Wnk4 WNK lysine deficient protein kinase 4
Displaying all 2 entries
Gene ID Gene Symbol Description Source
54300 Slc12a3 solute carrier family 12 member 3
79430 Clcnkb chloride voltage-gated channel Kb
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
378616 clcnkb.L chloride channel, voltage-sensitive Kb L homeolog Xenopus laevis (African clawed frog)

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024