PanelApp (stage)
  1. Genes and Genomic Entities
  2. CHRM5

CHRM5

cholinergic receptor muscarinic 5
OMIM: 118496, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red CHRM5 in Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic


Level 2: Renal and urinary tract disorders
Version 0.138

Component of the following Super Panels:

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

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Congenital anomaly of kidney and urinary tract, (MONDO:0019719), CHRM5-related

    Red CHRM5 in Mendeliome


    Version 1.1891

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Congenital anomaly of kidney and urinary tract, (MONDO:0019719), CHRM5-related