1. Genes and Genomic Entities
  2. NR1I3

NR1I3

nuclear receptor subfamily 1 group I member 3
OMIM: 603881, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red NR1I3 in DDG2P


Version 8.2
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
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • EHMT1-LIKE INTELLECTUAL DISABILITY
    Red NR1I3 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 Red
    Phenotypes
    • EHMT1-like Intellectual disability