PanelApp (staging)
  1. Genes and Genomic Entities
  2. SLC11A2

SLC11A2

solute carrier family 11 member 2
OMIM: 600523, ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green SLC11A2 in Mendeliome


Version 1.2302

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Anaemia, hypochromic microcytic, with iron overload 1 MIM#206100

Red SLC11A2 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Anemia, hypochromic microcytic

Green SLC11A2 in Red cell disorders


Level 2: Haematological disorders
Version 1.29

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Yorkshire and North East GLH
  • NHS GMS
  • Wessex and West Midlands GLH
  • North West GLH
Phenotypes
  • Anaemia, hypochromic microcytic, with iron overload 1 MIM#206100

Green SLC11A2 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 BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS Genomic Medicine Service
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • AHMIO1
    • 206100 Anemia, hypochromic microcytic, with iron overload 1
    • AHMIO1 DMT1-related anemia
    • 206100 ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1
    • DMT1-related anemia

    Red SLC11A2 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.116

    		0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category C gene
    • Expert Review Red
    Phenotypes
    • Anemia, hypochromic microcytic