Entry |
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Symbol |
KCNJ10, KIR4.1
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Name |
potassium inwardly-rectifying channel subfamily J member 10
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Pathway |
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Disease |
H00605 | Deafness, autosomal recessive |
H00803 | Seizures-sensorineural deafness-ataxia-mental retardation-electrolyte imbalance (SESAME) |
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Brite |
KEGG Orthology (KO) [BR:ko00001]
09150 Organismal Systems
09154 Digestive system
04971 Gastric acid secretion
K05003 KCNJ10, KIR4.1; potassium inwardly-rectifying channel subfamily J member 10
09160 Human Diseases
09164 Neurodegenerative disease
05016 Huntington disease
K05003 KCNJ10, KIR4.1; potassium inwardly-rectifying channel subfamily J member 10
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04040 Ion channels
K05003 KCNJ10, KIR4.1; potassium inwardly-rectifying channel subfamily J member 10
Ion channels [BR:ko04040]
Voltage-gated cation channels
Potassium channel, inwardly-rectifying (Kir)
K05003 KCNJ10, KIR4.1; potassium inwardly-rectifying channel subfamily J member 10
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Other DBs |
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Genes |
» show all
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Reference |
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Authors |
Shuck ME, Piser TM, Bock JH, Slightom JL, Lee KS, Bienkowski MJ |
Title |
Cloning and characterization of two K+ inward rectifier (Kir) 1.1 potassium channel homologs from human kidney (Kir1.2 and Kir1.3). |
Journal |
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Sequence |
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Reference |
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Authors |
Chever O, Djukic B, McCarthy KD, Amzica F |
Title |
Implication of Kir4.1 channel in excess potassium clearance: an in vivo study on anesthetized glial-conditional Kir4.1 knock-out mice. |
Journal |
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Sequence |
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