SLC66A1

solute carrier family 66 member 1
OMIM: 614760, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green SLC66A1 in Mendeliome


Version 2.10

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Retinitis pigmentosa, MONDO:0019200, PQLC2-related
Tags
  • new gene name

Green SLC66A1 in Retinitis pigmentosa


Level 2: Ophthalmological disorders
Version 1.0

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Retinitis pigmentosa, MONDO:0019200, PQLC2-related
    Tags
    • new gene name