1. Genes and Genomic Entities
  2. SLC7A14

SLC7A14

solute carrier family 7 member 14
OMIM: 615720, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red SLC7A14 in Retinal disorders

Level 3: Posterior segment abnormalities
Level 2: Ophthalmological disorders
Version 5.4
Latest signed off version: v5.0 (1 May 2024)

review Not set
Sources
  • NHS GMS
  • Expert Review Red
Phenotypes
  • Retinitis pigmentosa 68, 615725 (3)