SLC30A2

solute carrier family 30 member 2
OMIM: 609617, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green SLC30A2 in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Zinc deficiency, transient neonatal , MIM#608118

Green SLC30A2 in Metal Metabolism Disorders


Level 2: Metabolic disorders
Version 0.47

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    Phenotypes
    • Zinc deficiency, transient neonatal , MIM#608118
    • Disorders of zinc metabolism