Genomics England
GMS Panels
Panels
Genes and Entities

TLK2

tousled like kinase 2
OMIM: 608439
PanelMode of inheritanceDetails
2 panels
Green
in Intellectual disability - microarray and sequencing
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Mental retardation, autosomal dominant 57, OMIM:618050, Mental retardation, autosomal dominant 57, MONDO:0054837
Green
in Rare syndromic craniosynostosis or isolated multisuture synostosis
R-numbers: R100
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Mental retardation, autosomal dominant 57, OMIM:618050, Mental retardation, autosomal dominant 57, MONDO:0054837