PanelApp
  1. Genes and Genomic Entities
  2. INF2

INF2

inverted formin, FH2 and WH2 domain containing
OMIM: 610982, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green INF2 in Mendeliome


Version 1.3512

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Charcot-Marie-Tooth disease, dominant intermediate E, MIM# 614455
  • Glomerulosclerosis, focal segmental, 5, MIM# 613237

Green INF2 in Proteinuria


Level 2: Renal and urinary tract disorders
Version 0.231

Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • Renal Glomerular Disease_SuperPanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Charcot-Marie-Tooth disease, dominant intermediate E, MIM# 614455
    • Glomerulosclerosis, focal segmental, 5, MIM# 613237

    Green INF2 in Hereditary Neuropathy_CMT - isolated


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.68

    Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Charcot Marie Tooth disease, dominant intermediate E, 614455
    • HMSN