KCNT1 Products

Description

FUNCTION: Outwardly rectifying potassium channel subunit that may co-assemble with other Slo-type channel subunits. Activated by high intracellular sodium or chloride levels. Activated upon stimulation of G-protein coupled receptors, such as CHRM1 and GRIA1. May be regulated by calcium in the absence of sodium ions (in vitro). ; Tissue specificity: Highest expression in liver, brain and spinal cord. Lowest expression in skeletal muscle.

Bioinformatics

Entrez	57582 Human
Uniprot	NM_020822 Human Q5JUK3 Human
Product By Gene ID	57582
Alternate Names	potassium channel subfamily T member 1 bA100C15.2 SLACK KCa4.1KIAA1422FLJ41282 potassium channel, subfamily T, member 1

Diseases related to KCNT1

Discover more about diseases related to KCNT1.

Epilepsy
Encephalopathies
Epilepsies, Partial
Partial Seizure
Developmental Delay (disorder)
Malignant Paraganglionic Neoplasm
Epilepsy, Frontal Lobe

Pathways for KCNT1

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Transport
Pathogenesis
Secretion

PTMs for KCNT1

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Phosphorylation

Bioinformatics Tool for KCNT1

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