PanelApp (staging)
  1. Genes and Genomic Entities
  2. ARMC9

ARMC9

armadillo repeat containing 9
OMIM: 617612, ClinGen, DECIPHER

8 panels

Panel Reviews Mode of inheritance Details
8 panels

Red ARMC9 in Cerebral Palsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.389

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Joubert syndrome 30, MIM#617622

Green ARMC9 in Ciliopathies


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.62

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
  • Expert Review Green
  • Expert list
Phenotypes
  • Joubert syndrome 30 617622 AR

Green ARMC9 in Joubert syndrome and other neurological ciliopathies


Level 2: Neurology and neurodevelopmental disorders
Version 1.28

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Joubert syndrome 30, MIM# 617622

Green ARMC9 in Mendeliome


Version 1.2302

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
  • Victorian Clinical Genetics Services
Phenotypes
  • Joubert syndrome 30, MIM#617622

Green ARMC9 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.63

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genetic Health Queensland
Phenotypes
  • Joubert syndrome 30, MIM# 617622

Red ARMC9 in Ataxia - paediatric


Level 2: Neurology and neurodevelopmental disorders
Version 1.30

Component of the following Super Panels:

  • Ataxia_Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert list
    • Expert Review Red
    • Royal Melbourne Hospital
    Phenotypes
    • Joubert syndrome 30, MIM#617622

    Amber ARMC9 in Syndromic Retinopathy


    Level 2: Ophthalmological disorders
    Version 0.219

    Component of the following Super Panels:

  • Retinal Disorders Superpanel

    		•  3 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert list
    • Expert Review Green
    • Expert list
    • Victorian Clinical Genetics Services
    Phenotypes
    • Joubert syndrome 30 MIM#617622

    Green ARMC9 in Fetal anomalies


    Version 1.313

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Expert list
    Phenotypes
    • Joubert syndrome 30, MIM# 617622