GINS2

GINS complex subunit 2
OMIM: 610609, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red GINS2 in Craniosynostosis


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.74

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Meier-Gorlin syndrome with craniosynostosis

Red GINS2 in Mendeliome


Version 1.4216

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Meier-Gorlin syndrome with craniosynostosis MONDO:0016817

Red GINS2 in Growth failure


Version 1.95

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Meier-Gorlin syndrome with craniosynostosis