SLC7A8

solute carrier family 7 member 8
OMIM: 604235, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SLC7A8 in Cataract


Level 2: Ophthalmological disorders
Version 0.626

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Cataract, MONDO:0005129, SLC7A8-related

Red SLC7A8 in Mendeliome


Version 1.4294

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
  • Literature
Phenotypes
  • Cataract, MONDO:0005129, SLC7A8-related