PanelApp
  1. Genes and Genomic Entities
  2. CD151

CD151

CD151 molecule (Raph blood group)
OMIM: 602243, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Red CD151 in Haematuria_Alport


Level 2: Renal and urinary tract disorders
Version 1.2

Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • Renal Glomerular Disease_SuperPanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057

    Green CD151 in Epidermolysis bullosa


    Level 2: Dermatological disorders
    Version 1.22

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057

    Green CD151 in Mendeliome


    Version 1.3512

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057

    Green CD151 in Proteinuria


    Level 2: Renal and urinary tract disorders
    Version 0.231

    Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • Renal Glomerular Disease_SuperPanel

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review Green
    • Expert list
    Phenotypes
    • Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057

    Amber CD151 in Deafness_IsolatedAndComplex


    Level 2: Hearing and ear disorders
    Version 1.238

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057

    Red CD151 in Fetal anomalies


    Version 1.465

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Genomics England PanelApp
    Phenotypes
    • Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057