PanelApp (stage)
  1. Genes and Genomic Entities
  2. COG2

COG2

component of oligomeric golgi complex 2
OMIM: 606974, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red COG2 in Congenital Disorders of Glycosylation


Level 2: Metabolic disorders
Version 1.44

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Congenital disorder of glycosylation, type IIq (MIM# 617395)

    Red COG2 in Mendeliome


    Version 1.1891

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Congenital disorder of glycosylation, type IIq (MIM# 617395)