CRY1

cryptochrome circadian regulator 1
OMIM: 601933, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red CRY1 in Kleine-Levin syndrome

Level 3: Sleep disorders
Level 2: Neurology and neurodevelopmental disorders
Version 1.7

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Attention deficit/hyperactivity disorder (ADHD)
  • Delayed sleep phase disorder (DSPD)