RBL2

RB transcriptional corepressor like 2
OMIM: 180203, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber RBL2 in Intellectual disability - microarray and sequencing

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 5.536
Latest signed off version: v5.0 (22 Mar 2023)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Brunet-Wagner neurodevelopmental syndrome, OMIM:619690
    Tags
    • Q4_23_promote_green
    • Q4_23_NHS_review