GLMN

glomulin, FKBP associated protein
OMIM: 601749, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green GLMN in Mendeliome


Version 1.2302

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Glomuvenous malformations MIM#138000

Green GLMN in Vascular Malformations_Germline


Level 2: Cardiovascular disorders
Version 1.12

Component of the following Super Panels:

  • Vascular Malformations SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Glomuvenous malformations, MIM# 138000

    Green GLMN in Vascular Malformations_Somatic


    Level 2: Cardiovascular disorders
    Version 1.14

    Component of the following Super Panels:

  • Vascular Malformations SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Glomuvenous malformations (138000)

    Red GLMN in Fetal anomalies


    Version 1.313

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Genomics England PanelApp
    Phenotypes
    • Glomuvenous malformations MIM#138000