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 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.38
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review Not set
    Sources
    • Expert
    Amber NEUROG1 in Intellectual disability - microarray and sequencing

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 5.536
    Latest signed off version: v5.0 (22 Mar 2023)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay, OMIM:620469
    Tags
    • Q3_23_promote_green
    • Q3_23_NHS_review