SPP2

secreted phosphoprotein 2
OMIM: 602637, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SPP2 in Mendeliome


Version 1.3802

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Royal Melbourne Hospital
  • Expert Review Red
  • Expert Review Red
  • Royal Melbourne Hospital
Phenotypes
  • Autosomal dominant retinitis pigmentosa

Red SPP2 in Retinitis pigmentosa


Level 2: Ophthalmological disorders
Version 0.225

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Royal Melbourne Hospital
    • Expert Review Red
    • Expert Review Red
    • Royal Melbourne Hospital
    Phenotypes
    • Autosomal dominant retinitis pigmentosa