PanelApp (test)
  1. Genes and Genomic Entities
  2. MICAL1

MICAL1

microtubule associated monooxygenase, calponin and LIM domain containing 1
OMIM: 607129, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber MICAL1 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Autosomal dominant epilepsy with auditory features (ADEAF)

Amber MICAL1 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Autosomal dominant epilepsy with auditory features (ADEAF)

    Amber MICAL1 in Focal Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.14

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • GREP
    Phenotypes
    • Autosomal dominant epilepsy with auditory features (ADEAF)