1. Genes and Genomic Entities
  2. EXOSC5

EXOSC5

exosome component 5
OMIM: 606492, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber EXOSC5 in Ataxia and cerebellar anomalies - narrow panel


Level 2: Neurology
Version 8.63
Latest signed off version: v8.0 (30 Apr 2025)

Component of the following Super Panels:

  • Hereditary ataxia and cerebellar anomalies - childhood onset

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Short stature
    • Motor developmental delays
    • Cerebellar hypoplasia
    • Ataxia
    Tags
    • Q4_24_NHS_review
    • Q4_24_promote_green
    Amber EXOSC5 in Fetal anomalies


    Level 2: Fetal (including NIPD)
    Version 6.140
    Latest signed off version: v6.0 (30 Apr 2025)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Amber
    Phenotypes
    • Cerebellar ataxia, brain abnormalities, and cardiac conduction defects, OMIM:619576