GNB1

G protein subunit beta 1
OMIM: 139380
PanelMode of inheritanceDetails
5 panels
R-numbers: R57
Signed-off version 2.3
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Mental retardation, autosomal dominant 42 OMIM:616973, intellectual disability, autosomal dominant 42 MONDO:0014855
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Mental retardation, autosomal dominant 42 OMIM:616973, intellectual disability, autosomal dominant 42 MONDO:0014855
R-numbers: R21, R412
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Mental retardation, autosomal dominant 42 OMIM:616973, intellectual disability, autosomal dominant 42 MONDO:0014855
R-numbers: R59
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Mental retardation, autosomal dominant 42 OMIM:616973, intellectual disability, autosomal dominant 42 MONDO:0014855
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, NOT imprinted
Phenotypes
Mental retardation, autosomal dominant 42 OMIM:616973, intellectual disability, autosomal dominant 42 MONDO:0014855