CLCNKA Products

Description

The CLCNKA gene is a member of the CLC family of voltage-gated chloride channels. The encoded protein is predicted to have 12transmembrane domains, and requires a beta subunit called barttin to form a functional channel. It is thought tofunction in salt reabsor

Bioinformatics

Entrez	1187 Human
Uniprot	NP_004061 Human
Product By Gene ID	1187
Alternate Names	kidney, A hClC-Ka chloride channel KaMGC61490

Diseases related to CLCNKA

Discover more about diseases related to CLCNKA.

Bartter Disease
Disease Of Adrenal Medulla
Complete Hearing Loss
Diabetes Mellitus
Nephrogenic Diabetes Insipidus
Hypertensive Disease
Kidney Diseases
Heart Failure
Dehydration
Sensorineural Hearing Loss (disorder)
Alkalosis
Dysequilibrium Syndrome
Deprivation Of Water
Dent's Disease
Metabolic Alkalosis
Congenital Nephrogenic Diabetes Insipidus
Cardiac Failure Chronic
Deafness Congenital

Pathways for CLCNKA

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

Transport
Localization
Chloride Transport
Transepithelial Chloride Transport
Pathogenesis
Cellular Localization
Water Homeostasis
Kidney Development
Secretion
Protein Phosphorylation
Ion Transport
Endocytosis
Diuresis
Regulation Of Transport
Transepithelial Transport
Cell Division
Antiport
Amino Acid Transport
Water Transport
Regulation Of Ion Transport

PTMs for CLCNKA

Learn more about PTMs related to CLCNKA.

Phosphorylation
Glycosylation

Bioinformatics Tool for CLCNKA

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