GINS3

GINS complex subunit 3
OMIM: 610610, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green GINS3 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Meier-Gorlin syndrome, MONDO:0016817, GINS3-related

Green GINS3 in Microcephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.269

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Meier-Gorlin syndrome, MONDO:0016817, GINS3-related

Green GINS3 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 0.285

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Meier-Gorlin syndrome, MONDO:0016817, GINS3-related

Green GINS3 in Growth failure


Version 1.76

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Meier-Gorlin syndrome, MONDO:0016817, GINS3-related

Red GINS3 in Fetal anomalies


Version 1.255

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
Phenotypes
  • Meier-Gorlin syndrome, MONDO:0016817, GINS3-related