MN1

MN1 proto-oncogene, transcriptional regulator
OMIM: 156100
PanelMode of inheritanceDetails
4 panels
R-numbers: R21, R412
Signed-off version 2.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CEBALID syndrome, OMIM:618774, CEBALID syndrome, MONDO:0032908
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 4.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CEBALID syndrome, OMIM:618774, CEBALID syndrome, MONDO:0032908
Component of the following Super Panels:
  • - Cerebral malformations
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CEBALID syndrome, OMIM:618774, CEBALID syndrome, MONDO:0032908
R-numbers: R67
Signed-off version 3.3
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CEBALID syndrome, OMIM:618774, CEBALID syndrome, MONDO:0032908