ZEB1

zinc finger E-box binding homeobox 1
OMIM: 189909, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green ZEB1 in Corneal Dystrophy


Level 2: Ophthalmological disorders
Version 1.10

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Corneal dystrophy, Fuchs endothelial, 6, MIM# 613270
  • Corneal dystrophy, posterior polymorphous, 3, MIM# 609141

Green ZEB1 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Corneal dystrophy, Fuchs endothelial, 6, MIM# 613270
  • Corneal dystrophy, posterior polymorphous, 3, MIM# 609141

Amber ZEB1 in Callosome


Level 2: Neurology and neurodevelopmental disorders
Version 0.522

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Corpus callosum abnormalities MONDO:0009022
Tags
  • SV/CNV