Genomics England
GMS Panels
Panels
Genes and Entities

BCAS3

BCAS3, microtubule associated cell migration factor
OMIM: 607470
PanelMode of inheritanceDetails
3 panels
Green
in Childhood onset hereditary spastic paraplegia
R-numbers: R61
Signed-off version 5.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Syndromic neurodevelopmental disorder
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
BCAS3-related neurodevelopmental disorder with thinning of corpus callosum and cerebellar atrophy
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 6.13
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Syndromic neurodevelopmental disorder