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 1.147

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


Level 2: Immunology
Version 9.105
Latest signed off version: v9.91 (12 Aug 2026)

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


Level 2: Fetal (including NIPD)
Version 8.5
Latest signed off version: v8.0 (12 Aug 2026)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Bachmann-Bupp syndrome, OMIM:619075
Green ODC1 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 Green
    Phenotypes
    • ODC1-related developmental disorder (monoallelic)
    Green ODC1 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, imprinted status unknown
    Sources
    • Expert Review Green
    • Expert Review
    • Literature
    Phenotypes
    • Bachmann-Bupp syndrome, OMIM:619075