1. Genes and Genomic Entities
  2. NEUROG1

NEUROG1

neurogenin 1
OMIM: 601726, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red NEUROG1 in Monogenic hearing loss


Level 2: Audiology
Version 6.35
Latest signed off version: v6.34 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review Not set
    Sources
    • Expert
    Green NEUROG1 in Intellectual disability


    Level 2: Developmental disorders
    Version 11.1
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    • Literature
    Phenotypes
    • Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay, OMIM:620469