Genomics England
GMS Panels
Panels
Genes and Entities

SEPHS1

selenophosphate synthetase 1
OMIM: 600902
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
neurodevelopmental disorder, MONDO:0700092, SEPHS1-related neurodevelopmental disorder
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 10.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Ververi-Brady syndrome 2, OMIM:621325, Neurodevelopmental disorder, MONDO:0700092