PanelApp (staging)
  1. Genes and Genomic Entities
  2. STEAP3

STEAP3

STEAP3 metalloreductase
OMIM: 609671, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red STEAP3 in Mendeliome


Version 1.2302

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Anaemia, hypochromic microcytic, with iron overload 2, MIM# 615234

Red STEAP3 in Red cell disorders


Level 2: Haematological disorders
Version 1.29

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Wessex and West Midlands GLH
  • NHS GMS
Phenotypes
  • Anaemia, hypochromic microcytic, with iron overload 2 MIM# 615234

Red STEAP3 in Metal Metabolism Disorders


Level 2: Metabolic disorders
Version 0.45

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • NHS Genomic Medicine Service
    • Genomics England PanelApp
    Phenotypes
    • Anaemia, hypochromic microcytic, with iron overload 2 MIM# 615234