Kcnj10 Channel [kanál KCNJ10]
- Terms
-
Kir4.1 Protein
Potassium inwardly rectifying channel subfamily J member 10
Potassium Inwardly-Rectifying Channel, Subfamily J, Member 10
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.
- DUI
- D000098854 MeSH Browser
- CUI
- M000767442
- History note
- 2025 (2004)
- Public note
- 2025; KCNJ10 CHANNEL was indexed under POTASSIUM CHANNELS, INWARDLY RECTIFYING 2004-2024
Allowable subheadings
- AD
- administration & dosage
- AE
- adverse effects
- AG
- agonists
- AN
- analysis
- AI
- antagonists & inhibitors
- BI
- biosynthesis
- BL
- blood
- CF
- cerebrospinal fluid
- CS
- chemical synthesis
- CH
- chemistry
- CL
- classification
- DF
- deficiency
- DE
- drug effects
- EC
- economics
- GE
- genetics
- HI
- history
- IM
- immunology
- IP
- isolation & purification
- ME
- metabolism
- PK
- pharmacokinetics
- PD
- pharmacology
- PH
- physiology
- PO
- poisoning
- RE
- radiation effects
- ST
- standards
- SD
- supply & distribution
- TU
- therapeutic use
- TO
- toxicity
- UL
- ultrastructure
- UR
- urine
KCNJ10 protein, human Chemical MeSH Browser
Kcnj10 protein, mouse Chemical MeSH Browser
Kcnj10 protein, rat Chemical MeSH Browser