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Intellectual_disability

Gene: KCTD7

Red List (low evidence)

KCTD7 (potassium channel tetramerization domain containing 7)
EnsemblGeneIds (GRCh38): ENSG00000243335
EnsemblGeneIds (GRCh37): ENSG00000243335
OMIM: 611725, Gene2Phenotype
KCTD7 is in 9 panels

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Details

Sources
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Epilepsy, progressive myoclonic 3, with or without intracellular inclusions, 611726
OMIM
611725
Clinvar variants
Variants in KCTD7
Penetrance
Complete
Panels with this gene

History Filter Activity

8 Oct 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

KCTD7 was added to Intellectual_disabilitypanel. Sources: Radboud University Medical Center, Nijmegen