1. Genes and Genomic Entities
  2. P2RY8

P2RY8

P2Y receptor family member 8
OMIM: 300525, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red P2RY8 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.12
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review Unknown
    Sources
    • Expert Review Red
    Tags
    • Pseudoautosomal region 1