1. Genes and Genomic Entities
  2. MYT1L

MYT1L

myelin transcription factor 1 like
OMIM: 613084, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Green MYT1L in Severe early-onset obesity


Level 2: Endocrinology
Version 6.1
Latest signed off version: v6.0 (6 May 2026)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
  • Literature
Phenotypes
  • obesity
  • Mental retardation, autosomal dominant 39, OMIM:616521
Red MYT1L in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 7.10
Latest signed off version: v7.0 (6 May 2026)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • PAGE DD-Gene2Phenotype
Phenotypes
  • MYT1L syndrome
Green MYT1L in DDG2P


Version 7.1
Latest signed off version: v7.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • DD-Gene2Phenotype
    Phenotypes
    • MYT1L syndrome
    Green MYT1L in Intellectual disability


    Level 2: Developmental disorders
    Version 10.17
    Latest signed off version: v10.0 (6 May 2026)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green
    Phenotypes
    • Mental retardation, autosomal dominant 39, 616521
    • MRD39
    • Intellectual disability
    • obesity