KCNK9

potassium two pore domain channel subfamily K member 9
OMIM: 605874
PanelMode of inheritanceDetails
2 panels
R-numbers: R21, R412
Signed-off version 5.80
MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Phenotypes
Birk-Barel syndrome, OMIM:612292
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 8.134
MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Phenotypes
Birk-Barel mental retardation dysmorphism syndrome 612292