SLC4A7

solute carrier family 4 member 7
OMIM: 603353, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber SLC4A7 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Retinitis pigmentosa, MONDO:0019200, SLC4A7-related

Amber SLC4A7 in Retinitis pigmentosa_Autosomal Recessive/X-linked


Level 2: Ophthalmological disorders
Version 0.147

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • Retinitis Pigmentosa Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Retinitis pigmentosa, MONDO:0019200, SLC4A7-related