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 1.141

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


Version 4.201
Latest signed off version: v4.0 (22 Mar 2023)

review Unknown
Sources
  • Literature
Phenotypes
  • primary immunodeficiency
Green ODC1 in DDG2P


Version 3.87
Latest signed off version: v3.1 (22 Mar 2023)

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 - microarray and sequencing

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 5.532
    Latest signed off version: v5.0 (22 Mar 2023)

    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
    • Global developmental delay
    • Intellectual disability
    • Macrocephaly
    • Alopecia
    • Ectodermal dysplasia
    Green ODC1 in Severe Paediatric Disorders


    Version 1.184

    review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Next Generation Children Project
    • Expert Review Green
    • Expert list
    Phenotypes
    • Global developmental delay
    • Ectodermal dysplasia
    • Alopecia
    • Intellectual disability
    • Macrocephaly