SLC39A7

solute carrier family 39 member 7
OMIM: 601416, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red SLC39A7 in Epidermolysis bullosa


Level 2: Dermatological disorders
Version 1.15

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Agammaglobulinaemia 9, autosomal recessive, MIM# 619693
  • Absent B cells
  • Agammaglobulinemia
  • Early onset infections

Green SLC39A7 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Agammaglobulinaemia 9, autosomal recessive, MIM# 619693
  • Antibody deficiency
  • early onset infections
  • blistering dermatosis
  • failure to thrive
  • thrombocytopaenia

Green SLC39A7 in Predominantly Antibody Deficiency


Level 2: Immunological disorders
Version 0.135

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Agammaglobulinaemia 9, autosomal recessive, MIM# 619693
    • Antibody deficiency
    • early onset infections
    • blistering dermatosis
    • failure to thrive
    • thrombocytopaenia

    Green SLC39A7 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.114

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Agammaglobulinaemia 9, autosomal recessive, MIM# 619693
    Tags
    • treatable
    • immunological