PanelApp
  1. Genes and Genomic Entities
  2. AMFR

AMFR

autocrine motility factor receptor
OMIM: 603243, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green AMFR in Mendeliome


Version 1.3512

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Spastic paraplegia 89, autosomal recessive, MIM# 620379
  • Inborn error of immunity, MONDO:0003778, AMFR-related

Red AMFR in Disorders of immune dysregulation


Level 2: Immunological disorders
Version 1.33

Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Expert Review
    Phenotypes
    • Inborn error of immunity, MONDO:0003778, AMFR-related

    Green AMFR in Hereditary Spastic Paraplegia - paediatric


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.102

    Component of the following Super Panels:

  • Hereditary Spastic Paraplegia Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Spastic paraplegia 89, autosomal recessive, MIM# 620379