NEK8

NIMA related kinase 8
OMIM: 609799
PanelMode of inheritanceDetails
4 panels
Component of the following Super Panels:
  • - Cystic renal disease
  • - Unexplained young onset end-stage renal disease
Signed-off version 5.4
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
polycystic kidney disease, MONDO:0020642, ?Nephronophthisis 9, OMIM:613824
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
RENAL-HEPATIC-PANCREATIC DYSPLASIA 2 615415, NEPHRONOPHTHISIS 9 613824
R-numbers: R21, R412
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
?Nephronophthisis 9, OMIM:613824, Nephronophthisis 9, MONDO:0013444, Renal-hepatic-pancreatic dysplasia 2, OMIM:615415, Renal-hepatic-pancreatic dysplasia 2, MONDO:0014174
Component of the following Super Panels:
  • - Cystic renal disease
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
  • - Unexplained young onset end-stage renal disease
Signed-off version 3.7
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Renal-hepatic-pancreatic dysplasia, ?Renal-hepatic-pancreatic dysplasia 2, 615415, Nephronophthisis, ?Nephronophthisis 9, 613824