AMN

amnion associated transmembrane protein
OMIM: 605799, Gene2Phenotype

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green AMN in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
  • Victorian Clinical Genetics Services
Phenotypes
  • Imerslund-Grasbeck syndrome 2, MIM# 618882

Green AMN in Proteinuria


Level 2: Renal and urinary tract disorders
Version 0.225

Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • Renal Glomerular Disease_SuperPanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    • Expert list
    Phenotypes
    • Megaloblastic anemia-1, Norwegian type, MIM#261100

    Green AMN in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category A gene
    • Expert Review Green
    Phenotypes
    • Megaloblastic anemia-1, Norwegian type

    Green AMN in Red cell disorders


    Level 2: Haematological disorders
    Version 1.24

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Yorkshire and North East GLH
    • NHS GMS
    • Wessex and West Midlands GLH
    • North West GLH
    • London South GLH
    Phenotypes
    • Imerslund-Grasbeck syndrome 2, MIM# 618882

    No list AMN in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    Phenotypes
    • Imerslund-Grasbeck syndrome 2 (MIM#618882)

    Green AMN in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category A gene
    • BeginNGS
    Phenotypes
    • Megaloblastic anemia-1, Norwegian type, MIM#618882
    Tags
    • treatable
    • haematological

    Green AMN in Vitamin metabolism disorders


    Level 2: Metabolic disorders
    Version 1.6

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • NHS GMS
    Phenotypes
    • Imerslund-Grasbeck syndrome 2 MIM#618882
    • Disorders of cobalamin absorption, transport and metabolism