PanelApp (stage)
  1. Genes and Genomic Entities
  2. NEUROG3

NEUROG3

neurogenin 3
OMIM: 604882, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green NEUROG3 in Congenital Diarrhoea


Level 2: Gastroenterological disorders
Version 1.13

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Diarrhoea 4, malabsorptive, congenital, MIM# 610370

Green NEUROG3 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Diarrhoea 4, malabsorptive, congenital, MIM# 610370

Green NEUROG3 in Monogenic Diabetes


Level 2: Endocrine disorders
Version 0.134

Component of the following Super Panels:

  • Metabolic Disorders Superpanel

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • UKGTN
    Phenotypes
    • congenital malabsorptive diarrhea 4 MONDO:0012479

    Green NEUROG3 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category C gene
    Phenotypes
    • Diarrhoea 4, malabsorptive, congenital, MIM# 610370

    Green NEUROG3 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category C gene
    • BeginNGS
    Phenotypes
    • Diarrhoea 4, malabsorptive, congenital, MIM# 610370
    Tags
    • treatable
    • gastrointestinal