1. Genes and Genomic Entities
  2. JMJD1C

JMJD1C

jumonji domain containing 1C
OMIM: 604503, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red JMJD1C in DDG2P


Version 8.1
Latest signed off version: v8.0 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • DD-Gene2Phenotype
    Phenotypes
    • JMJD1C-related neurodevelopmental disorder
    Amber JMJD1C in Intellectual disability


    Level 2: Developmental disorders
    Version 11.28
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Expert Review
    Phenotypes
    • Intellectual disability
    • Autism
    Tags
    • watchlist