SLC7A14

solute carrier family 7 member 14
OMIM: 615720, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SLC7A14 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Retinitis pigmentosa 68, MIM# MIM#615725
Tags
  • disputed

Red SLC7A14 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 Red
    • Royal Melbourne Hospital
    Phenotypes
    • Retinitis pigmentosa 68, 615725 (3)
    Tags
    • disputed