PanelApp
  1. Genes and Genomic Entities
  2. SSR3

SSR3

signal sequence receptor subunit 3
OMIM: 606213, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber SSR3 in Congenital Disorders of Glycosylation


Level 2: Metabolic disorders
Version 1.78

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Congenital disorder of glycosylation

    Amber SSR3 in Mendeliome


    Version 1.3512

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Congenital disorder of glycosylation