PanelApp
  1. Genes and Genomic Entities
  2. CDX2

CDX2

caudal type homeobox 2
OMIM: 600297, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

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


Level 2: Renal and urinary tract disorders
Version 0.127

Component of the following Super Panels:

  • Congenital abnormalities of the kidneys and urinary tract (CAKUT)_SuperPanel
  • Kidneyome_SuperPanel

    		•  2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • 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 1.3512

    		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 1.465

    		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