TSPOAP1

TSPO associated protein 1
OMIM: 610764, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red TSPOAP1 in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Green TSPOAP1 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.12
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    • Literature
    Phenotypes
    • Dystonia, intellectual disability and cerebellar atrophy
    Green TSPOAP1 in Childhood onset dystonia, chorea or related movement disorder


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

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    • Literature
    Phenotypes
    • Dystonia, intellectual disability and cerebellar atrophy