Genomics England
GMS Panels
Panels
Genes and Entities

LMNB2

lamin B2
OMIM: 150341
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 6.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
LMNB2-related Primary Microcephaly
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 6.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Microcephaly 27, primary, autosomal dominant, OMIM:619180, microcephaly 27, primary, autosomal dominant, MONDO:0030929
Green
in Severe microcephaly
R-numbers: R88
Signed-off version 8.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Microcephaly 27, primary, autosomal dominant, OMIM:619180, microcephaly 27, primary, autosomal dominant, MONDO:0030929