PARP1

poly(ADP-ribose) polymerase 1
OMIM: 173870, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels
Red PARP1 in Familial Meniere Disease

Level 3: Other hearing and ear disorders
Level 2: Hearing and ear disorders
Version 1.4

review Not set
Sources
  • Literature
Red PARP1 in COVID-19 research


Level 2: Viral research
Version 1.147

review Unknown
Sources
  • Literature
Red PARP1 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
Red PARP1 in DDG2P


Version 8.2
Latest signed off version: v8.0 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • AUTOSOMAL RECESSIVE MENTAL RETARDATION
    Red PARP1 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 BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    Phenotypes
    • AUTOSOMAL RECESSIVE MENTAL RETARDATION