PanelApp
  1. Genes and Genomic Entities
  2. AGXT

AGXT

alanine-glyoxylate aminotransferase
OMIM: 604285, Gene2Phenotype

10 panels

Panel Reviews Mode of inheritance Details
10 panels

Green AGXT in Mendeliome


Version 1.3512

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hyperoxaluria, primary, type 1, MIM# 259900
  • MONDO:0009823
Tags
  • treatable
  • clinical trial

Green AGXT in Peroxisomal Disorders


Level 2: Metabolic disorders
Version 0.56

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  0 reviews Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green AGXT in Hereditary Neuropathy - complex


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.40

    Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Hyperoxaluria, primary, type 1, MIM#259900
    Tags
    • treatable
    • clinical trial

    Green AGXT in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.110

    		0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Hyperoxaluria, primary, type 1, 259900 (3)

    Green AGXT in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    		0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category A gene
    • Expert Review Green
    Phenotypes
    • Hyperoxaluria, primary, type 1

    Red AGXT in Fetal anomalies


    Version 1.465

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Genomics England PanelApp
    Phenotypes
    • Hyperoxaluria, primary, type 1, MIM# 259900 MONDO:0009823

    Green AGXT in Prepair 1000+


    Level 2: Screening
    Version 2.14

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Hyperoxaluria, primary, type 1, 259900 (3)

    Green AGXT in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category A gene
    Phenotypes
    • Hyperoxaluria, primary, type 1, MIM# 259900, MONDO:0009823
    Tags
    • treatable
    • clinical trial
    • metabolic

    Green AGXT in Renal Tubulopathies and related disorders


    Level 2: Renal and urinary tract disorders
    Version 1.22

    Component of the following Super Panels:

  • Kidneyome_SuperPanel

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Expert list
    • Victorian Clinical Genetics Services
    Phenotypes
    • MONDO:0009823
    • Hyperoxaluria, primary, type 1, MIM# 259900

    Green AGXT in Prepair 500+


    Level 2: Screening
    Version 2.0

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Hyperoxaluria, primary, type 1 MIM #259900