Bartter disease type 4b

Summary
Synonym
  • BARTS4B
  • Bartter syndrome, type 4b, digenic
  • neonatal Bartter syndrome type 4B with sensorineural deafness
Definition
A Bartter disease that has_material_basis_in simultaneous mutation in both the CLCNKA and CLCNKB genes.
Super Class
Bartter disease
External Links
Disease Ontology
DOID:0110146
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1188 CLCNKB chloride voltage-gated channel Kb
Displaying all 2 entries
Gene ID Gene Symbol Description Source
12733 Clcnka chloride channel, voltage-sensitive Ka
56365 Clcnkb chloride channel, voltage-sensitive Kb
Displaying 1 entry
Gene ID Gene Symbol Description Source
79430 Clcnkb chloride voltage-gated channel Kb
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
378616 clcnkb.L chloride channel, voltage-sensitive Kb L homeolog Xenopus laevis (African clawed frog)

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024