1. Genes and Genomic Entities
  2. ASMT

ASMT

acetylserotonin O-methyltransferase
OMIM: 300015, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red ASMT in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Tags
  • Pseudoautosomal region 1
Red ASMT 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 Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Red
    Tags
    • Pseudoautosomal region 1