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Descriptor English: Kcnj10 Channel
Descriptor Spanish: Canal Kcnj10
Descriptor Portuguese: Canal Kcnj10
Descriptor French: Without translation
Entry term(s): Kir4.1 Protein
Potassium Inwardly-Rectifying Channel, Subfamily J, Member 10
Potassium inwardly rectifying channel subfamily J member 10
Tree number(s): D12.776.157.530.400.600.450.513
D12.776.543.550.450.750.450.513
D12.776.543.585.400.750.450.513
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D000098854
Scope note: An Inwardly rectifying potassium channel expressed by GLIAL CELLS of the brain and in cells of the DISTAL KIDNEY TUBULES. Mutations in the KCNJ10 gene can cause SESAME SYNDROME.
Allowable Qualifiers: AD administration & dosage
AE adverse effects
AG agonists
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
Public MeSH Note: 2025; KCNJ10 CHANNEL was indexed under POTASSIUM CHANNELS, INWARDLY RECTIFYING 2004-2024
History Note: 2025 (2004)
DeCS ID: 60905
Unique ID: D000098854
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2025/01/01
Date of Entry: 2024/08/09
Revision Date: 2024/08/06
Kcnj10 Channel - Preferred
Concept UI M000767442
Scope note An Inwardly rectifying potassium channel expressed by GLIAL CELLS of the brain and in cells of the DISTAL KIDNEY TUBULES. Mutations in the KCNJ10 gene can cause SESAME SYNDROME.
Preferred term Kcnj10 Channel
Entry term(s) Kir4.1 Protein
Potassium Inwardly-Rectifying Channel, Subfamily J, Member 10
Potassium inwardly rectifying channel subfamily J member 10



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