ODC1

ornithine decarboxylase 1
OMIM: 165640, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels
Red ODC1 in COVID-19 research


Level 2: Viral research
Version 1.146

review Unknown
Sources
  • Literature
Red ODC1 in Primary immunodeficiency or monogenic inflammatory bowel disease


Level 2: Immunology
Version 8.78
Latest signed off version: v8.0 (30 Apr 2025)

review Unknown
Sources
  • Literature
Phenotypes
  • primary immunodeficiency
Green ODC1 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.140
Latest signed off version: v6.0 (30 Apr 2025)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Bachmann-Bupp syndrome, OMIM:619075
Green ODC1 in DDG2P


Version 6.424
Latest signed off version: v6.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • ODC1-related developmental disorder (monoallelic)
    Green ODC1 in Intellectual disability


    Level 2: Developmental disorders
    Version 9.285
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Expert Review
    • Literature
    Phenotypes
    • Bachmann-Bupp syndrome, OMIM:619075