PanelApp
  1. Genes and Genomic Entities
  2. CDX2

CDX2

caudal type homeobox 2
OMIM: 600297, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green CDX2 in Congenital anomalies of the kidney and urinary tract (CAKUT)


Level 2: Renal and urinary tract disorders
Version 0.201

Component of the following Super Panels:

  • Kidneyome_SuperPanel

    		•  2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    • Expert Review Green
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • Genetic multiple congenital anomalies/dysmorphic syndrome, MONDO:0043005
    • Congenital abnormalities of anus, renal and urogenital system, vertebrae and/or the limbs

    Green CDX2 in Mendeliome


    Version 1.4559

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Genetic multiple congenital anomalies/dysmorphic syndrome, MONDO:0043005
    • Congenital abnormalities of anus, renal and urogenital system, vertebrae and/or the limbs

    Green CDX2 in Fetal anomalies


    Version 1.543

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Genetic multiple congenital anomalies/dysmorphic syndrome, MONDO:0043005
    • Congenital abnormalities of anus, renal and urogenital system, vertebrae and/or the limbs