1. Genes and Genomic Entities
  2. WNT7B

WNT7B

Wnt family member 7B
OMIM: 601967, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green WNT7B 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
  • NHS GMS
  • Expert Review Green
  • Expert Review
Phenotypes
  • Pulmonary hypoplasia
  • Diaphragmatic anomalies
  • Anophthalmia/Microphthalmia
  • Cardiac defects
Tags
  • gene-checked
Green WNT7B in DDG2P


Version 6.424
Latest signed off version: v6.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • WNT7B-related PDAC syndrome
    Tags
    • gene-checked