ZFPM2

zinc finger protein, FOG family member 2
OMIM: 603693, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green ZFPM2 in Congenital diaphragmatic hernia


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Diaphragmatic hernia 3, MIM# 610187

Amber ZFPM2 in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 1.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Amber
Phenotypes
  • Tetralogy of Fallot, MIM# 187500

Red ZFPM2 in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Red
Phenotypes
  • 46XY sex reversal 9 (MIM#616067)
Tags
  • refuted