YY1AP1

YY1 associated protein 1
OMIM: 607860, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green YY1AP1 in Mendeliome


Version 2.0

1 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 2.0

3 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Grange syndrome MIM#602531

Green YY1AP1 in Cerebral vascular malformations


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Genomics England PanelApp
  • Expert Review Green
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Grange syndrome, 602531

Amber YY1AP1 in Spontaneous coronary artery dissection


Level 2: Cardiovascular disorders
Version 1.0

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