Chemicals and Drugs

Kcnj10 Channel

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.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

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.

MeSH Record

Classification

Broader headings

Related Concepts

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MeSH Record

Synonyms

3 entry terms
  • Kir4.1 Protein
  • Potassium Inwardly-Rectifying Channel, Subfamily J, Member 10
  • Potassium inwardly rectifying channel subfamily J member 10

MeSH Record

Aspects Covered

30 allowable subheadings

Indexed with the subheadings administration & dosage, adverse effects, agonists, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.

MeSH Record

History Note

2025 (2004)

MeSH Hierarchy

Tree Numbers

  1. D12.776w.157w.530w.400w.600w.450w.513
  2. D12.776w.543w.550w.450w.750w.450w.513
  3. D12.776w.543w.585w.400w.750w.450w.513

AMA Style

References

  1. National Library of Medicine. Kcnj10 Channel. Medical Subject Headings (MeSH). 2026. Unique ID D000098854. http://id.nlm.nih.gov/mesh/2026/D000098854
  2. Kcnj10 Channel. In: Wikidata. https://www.wikidata.org/wiki/Q21113510