1. Genes and Genomic Entities
  2. FBXO25

FBXO25

F-box protein 25
OMIM: 609098, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
No list FBXO25 in DDG2P


Version 4.3
Latest signed off version: v4.0 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Removed
    • DD-Gene2Phenotype
    Phenotypes
    • F-BOX ONLY PROTEIN 25 609098
    Tags
    • curated_removed
    Red FBXO25 in Intellectual disability

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 6.11
    Latest signed off version: v6.0 (1 May 2024)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Expert Review Red
    Phenotypes
    • Expression in brain