Genomics England
GMS Panels
Panels
Genes and Entities

AKT2

AKT serine/threonine kinase 2
OMIM: 164731
PanelMode of inheritanceDetails
4 panels
Green
in Congenital hyperinsulinism
R-numbers: R144
Signed-off version 3.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Hypoinsulinemic hypoglycemia with hemihypertrophy, OMIM:240900, Hypoinsulinemic hypoglycemia and body hemihypertrophy, MONDO:0009416
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.15
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
AKT2-related hypoinsulinemic hypoglycemia and hemihypertrophy, OMIM:240900
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.195
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Hypoinsulinemic hypoglycemia with hemihypertrophy, OMIM:240900, Hypoinsulinemic hypoglycemia and body hemihypertrophy, MONDO:0009416
Green
in Monogenic diabetes
R-numbers: R141
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Diabetes mellitus, type II, 125853, Severe insulin resistance, partial lipodystrophy and diabetes