PanelApp
  1. Genes and Genomic Entities
  2. YY1AP1

YY1AP1

YY1 associated protein 1
OMIM: 607860, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green YY1AP1 in Mendeliome


Version 1.2374

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Grange syndrome, MIM# 602531
  • stenosis/occlusion of multiple arteries

Green YY1AP1 in Stroke


Level 2: Neurology and neurodevelopmental disorders
Version 1.16

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Grange syndrome MIM#602531

Green YY1AP1 in Cerebral vascular malformations


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Genomics England PanelApp
    • Expert Review Green
    Phenotypes
    • Grange syndrome, 602531

    Amber YY1AP1 in Spontaneous coronary artery dissection


    Level 2: Cardiovascular disorders
    Version 0.56

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Grange syndrome, MIM# 602531