SIRT6

sirtuin 6
OMIM: 606211, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber SIRT6 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.140
Latest signed off version: v6.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Fetal anomaly, HP:0034057
  • Neurodevelopmental disorder, MONDO:0700092