SYNCRIP

synaptotagmin binding cytoplasmic RNA interacting protein
OMIM: 616686, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red SYNCRIP in Periventricular Grey Matter Heterotopia


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
  • Expert Review Red
Phenotypes
  • SYNCRIP-related neurodevelopmental disorder