PEG10

paternally expressed 10
OMIM: 609810, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber PEG10 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 8.31
Latest signed off version: v8.0 (12 Aug 2026)

review MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Sources
  • NHS GMS
  • Expert Review Amber
Phenotypes
  • Silver-Russell syndrome, MONDO:0008394