UPF2

UPF2, regulator of nonsense mediated mRNA decay
OMIM: 605529, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red UPF2 in Speech apraxia


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert Review
  • Expert list
Phenotypes
  • Neurodevelopmental disorder (MONDO:0700092), UPF2-related