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Descriptor English: WNK Lysine-Deficient Protein Kinase 1
Descriptor Spanish: Proteína Quinasa Deficiente en Lisina WNK 1
Descriptor proteína quinasa deficiente en lisina WNK1
Entry term(s) proteína quinasa deficiente en lisina WNK 1
Scope note: Serina-treonina cinasa que tiene un papel importante en la regulación de la homeostasis de los electrolitos y en la señalización, supervivencia y proliferación celular. Actúa como activador e inhibidor de los cotransportadores de cloruro acoplados a sodio y como inhibidor de los cotransportadores de cloruro acoplados a potasio. Las mutaciones del gen WNK1 se asocian a PSEUDOHIPOALDOSTERONISMO tipo 2C y a NEUROPATÍAS HEREDITARIAS SENSORIALES Y AUTONÓMICAS tipo 2A.
Descriptor Portuguese: Proteína Quinase 1 Deficiente de Lisina WNK
Descriptor French: Protéine kinase déficiente en lysine WNK-1
Entry term(s): WNK Lysine Deficient Protein Kinase 1
Tree number(s): D08.811.913.696.620.682.700.982
D12.776.476.563.982
D23.050.301.500.600.962
D23.050.705.552.600.925
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D000076204
Scope note: A serine-threonine kinase which plays an important role in the regulation of electrolyte homeostasis, cell signaling, survival, and proliferation. It functions as an activator and inhibitor of sodium-coupled chloride co-transporters and as an inhibitor of potassium-coupled chloride co-transporters. Mutations in the WNK1 gene are associated with type 2C PSEUDOHYPOALDOSTERONISM and type 2A HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES.
Allowable Qualifiers: AD administration & dosage
AE adverse effects
AI antagonists & inhibitors
AN analysis
BI biosynthesis
BL blood
CF cerebrospinal fluid
CH chemistry
CL classification
CS chemical synthesis
DE drug effects
DF deficiency
EC economics
GE genetics
HI history
IM immunology
IP isolation & purification
ME metabolism
PD pharmacology
PH physiology
PK pharmacokinetics
PO poisoning
RE radiation effects
SD supply & distribution
ST standards
TO toxicity
TU therapeutic use
UL ultrastructure
UR urine
Registry Number: EC 2.7.11.1
Previous Indexing: Intracellular Signaling Peptides and Proteins (2005-2017)
Minor Histocompatibility Antigens (2005-2017)
Protein-Serine-Threonine Kinases (2005-2017)
Public MeSH Note: 2018
History Note: 2018
DeCS ID: 57033
Unique ID: D000076204
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2018/01/01
Date of Entry: 2017/07/11
Revision Date: 2017/06/29
WNK Lysine-Deficient Protein Kinase 1 - Preferred
Concept UI M000632439
Scope note A serine-threonine kinase which plays an important role in the regulation of electrolyte homeostasis, cell signaling, survival, and proliferation. It functions as an activator and inhibitor of sodium-coupled chloride co-transporters and as an inhibitor of potassium-coupled chloride co-transporters. Mutations in the WNK1 gene are associated with type 2C PSEUDOHYPOALDOSTERONISM and type 2A HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES.
Preferred term WNK Lysine-Deficient Protein Kinase 1
Entry term(s) WNK Lysine Deficient Protein Kinase 1



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