PanelApp (test)
  1. Genes and Genomic Entities
  2. SLC7A5

SLC7A5

solute carrier family 7 member 5
OMIM: 600182, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SLC7A5 in Mendeliome


Version 1.1902

review Unknown
Sources
  • Expert Review Red
  • Other
Phenotypes
  • Large neutral amino acid transporter deficiency (MIM#600182)

Red SLC7A5 in Aminoacidopathy


Level 2: Metabolic disorders
Version 1.128

Component of the following Super Panels:

  • Metabolic Disorders Superpanel

    		•  review Unknown
    Sources
    • Expert Review Red
    • Other
    Phenotypes
    • Large neutral amino acid transporter deficiency (MIM#600182)