Genomics England
GMS Panels
Panels
Genes and Entities

GMNN

geminin, DNA replication inhibitor
OMIM: 602842
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.15
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.195
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Meier-Gorlin syndrome 6, OMIM:616835, Meier-Gorlin syndrome 6, MONDO:0014794
Green
in Severe microcephaly
R-numbers: R88
Signed-off version 6.8
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Meier-Gorlin syndrome 6, OMIM:616835, Microcephalic primordial dwarfism