KCNK9 Products

Description

The KCNK9 gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. This open channel is highly expressed in the cerebellum. It is inhibited by extracellular acidification and arachidonic acid, and

Bioinformatics

Entrez	51305 Human
Uniprot	NP_057685 Human
Product By Gene ID	51305
Alternate Names	KT3.2 potassium channel, subfamily K, member 9 TASK-3

Diseases related to KCNK9

Discover more about diseases related to KCNK9.

Hypoxia
Nervousness
Malignant Neoplasms
Neoplasms
Epilepsy
Hyperaldosteronism
Pain
Acidosis
Hypertensive Disease
Melanoma
Mammary Neoplasms
Malignant Paraganglionic Neoplasm
Conn Syndrome
Cell Transformation, Neoplastic
Sclerosis
Adenoma
Neoplasm Metastasis
Malignant Neoplasm Of Breast
Carcinoma
Chimera Disorder

Pathways for KCNK9

View related products by pathway and learn more about each of the pathways below.

Localization
Secretion
Transport
Membrane Depolarization
Cell Death
Aldosterone Secretion
Cell Proliferation
Genetic Transfer
Pathogenesis
Endoplasmic Reticulum Localization
Cell Migration
Programmed Cell Death
Brain Development
Fertilization
Hypersensitivity
Reflex
Blastocyst Formation
Reverse Transcription
Hormone Secretion
Oncogenesis

PTMs for KCNK9

Learn more about PTMs related to KCNK9.

Phosphorylation
Methylation

Bioinformatics Tool for KCNK9

Discover related pathways, diseases and genes to KCNK9. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.