Genomics England
GMS Panels
Panels
Genes and Entities

TCF12

transcription factor 12
OMIM: 600480
PanelMode of inheritanceDetails
5 panels
Green
in Common craniosynostosis syndromes
R-numbers: R99
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Craniosynostosis 3 615314
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.3
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CORONAL CRANIOSYNOSTOSIS
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CORONAL CRANIOSYNOSTOSIS
Green
in Hydrocephalus
R-numbers: R86
Signed-off version 4.6
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Craniosynostosis 3, OMIM:615314
Green
in Rare syndromic craniosynostosis or isolated multisuture synostosis
R-numbers: R100
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Craniosynostosis 3, 615314, Craniosynostosis 3