Genomics England
GMS Panels
Panels
Genes and Entities

ORC1

origin recognition complex subunit 1
OMIM: 601902
PanelMode of inheritanceDetails
4 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.6
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
MEIER-GORLIN SYNDROME 1 224690
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Meier-Gorlin syndrome 1, OMIM:224690
Green
in Severe microcephaly
R-numbers: R88
Signed-off version 6.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Meier-Gorlin syndrome 1, OMIM:224690, Microcephalic primordial dwarfism
Green
in Skeletal dysplasia
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 6.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Meier-Gorlin syndrome 1, OMIM:224690