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Intellectual_disability

Gene: CLCNKB

Red List (low evidence)

CLCNKB (chloride voltage-gated channel Kb)
EnsemblGeneIds (GRCh38): ENSG00000184908
EnsemblGeneIds (GRCh37): ENSG00000184908
OMIM: 602023, Gene2Phenotype
CLCNKB is in 6 panels

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Details

Sources
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Bartter syndrome, type 3, 607364Bartter syndrome, type 4b, digenic, 613090
OMIM
602023
Clinvar variants
Variants in CLCNKB
Penetrance
Complete
Panels with this gene

History Filter Activity

8 Oct 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

CLCNKB was added to Intellectual_disabilitypanel. Sources: Radboud University Medical Center, Nijmegen