PanelApp (test)
  1. Genes and Genomic Entities
  2. WBP11:Ensemblv115

WBP11:Ensemblv115

WW domain binding protein 11
OMIM: 618083, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green WBP11 in Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic


Level 2: Renal and urinary tract disorders
Version 1.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
  • Literature
  • Expert Review Green
Phenotypes
  • Vertebral, cardiac, tracheoesophageal, renal, and limb defects, MIM# 619227
  • malformation syndrome affecting the cardiac, skeletal, gastrointestinal and renal systems

Green WBP11 in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
  • Expert Review Green
Phenotypes
  • Vertebral, cardiac, tracheoesophageal, renal, and limb defects, MIM# 619227