PanelApp (stage)
  1. Genes and Genomic Entities
  2. ATL3

ATL3

atlastin GTPase 3
OMIM: 609369, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green ATL3 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Neuropathy, hereditary sensory, type IF, MIM# 615632

Green ATL3 in Hereditary Neuropathy_CMT - isolated


Level 2: Neurology and neurodevelopmental disorders
Version 1.48

Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Hereditary sensory neuropathy type IF
    • HSAN/SFN

    Green ATL3 in Pain syndromes


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.34

    Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Neuropathy, hereditary sensory, type IF, 615632
    • HSN1F

    Red ATL3 in Autonomic neuropathy


    Level 2: Autonomic Neuropathy
    Version 0.50

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • # 615632 NEUROPATHY, HEREDITARY SENSORY, TYPE IF
    • HSN1F