Genomics England
GMS Panels
Panels
Genes and Entities

ICK

intestinal cell kinase
OMIM: 612325
PanelMode of inheritanceDetails
7 panels
Green
in Clefting
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.102
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 3.122
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980
Green
in Neurological ciliopathies
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 3.15
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980
Green
in Renal ciliopathies
Component of the following Super Panels:
  • - Cystic renal disease
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980
Green
in Skeletal ciliopathies
Component of the following Super Panels:
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 3.14
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980
Green
in Skeletal dysplasia
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 4.31
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980
Green
in Unexplained young onset end-stage renal disease
R-numbers: R257
Signed-off version 3.11
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980