Genomics England
GMS Panels
Panels
Genes and Entities

SRRM2

serine/arginine repetitive matrix 2
OMIM: 606032
PanelMode of inheritanceDetails
1 panel
Green
in Intellectual disability - microarray and sequencing
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
SRRM2-related developmental disorder (monoallelic)