PanelApp
  1. Genes and Genomic Entities
  2. DCAF17

DCAF17

DDB1 and CUL4 associated factor 17
OMIM: 612515, ClinGen, DECIPHER

17 panels

Panel Reviews Mode of inheritance Details
17 panels

Red DCAF17 in Early-onset Parkinson disease


Level 2: Neurology and neurodevelopmental disorders
Version 2.49

Component of the following Super Panels:

  • Movement Disorders Superpanel
  • Neurodegenerative disease - adult onset
  • Progressive Neurological Conditions

    		•  1 review Unknown
    Sources
    • Expert Review Red
    • Melbourne Genomics Health Alliance Complex Neurology Flagship
    • Victorian Clinical Genetics Services

    Green DCAF17 in Differences of Sex Development


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.36

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Woodhouse-Sakati syndrome, MIM# 241080

    Green DCAF17 in Mendeliome


    Version 1.4215

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Woodhouse-Sakati syndrome, MIM# 241080

    Green DCAF17 in Regression


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.602

    		0 reviews Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green DCAF17 in Deafness_IsolatedAndComplex


    Level 2: Hearing and ear disorders
    Version 1.317

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Woodhouse-Sakati syndrome, MIM# 241080

    Green DCAF17 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.638

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Woodhouse-Sakati syndrome, MIM# 241080

    Green DCAF17 in Dystonia and Chorea


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.337

    Component of the following Super Panels:

  • Movement Disorders Superpanel
  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Woodhouse-Sakati syndrome MONDO:0009419
    • Dystonia

    Green DCAF17 in Leukodystrophy


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.392

    Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Woodhouse-Sakati syndrome, MIM# 241080

    Green DCAF17 in Monogenic Diabetes


    Level 2: Endocrine disorders
    Version 0.161

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Woodhouse-Sakati syndrome MONDO:0009419

    Green DCAF17 in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.111

    		0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Woodhouse-Sakati syndrome, 241080 (3)

    Green DCAF17 in Primary Ovarian Insufficiency_Premature Ovarian Failure

    Level 3: Gonadal and sex development disorders
    Level 2: Endocrine disorders
    Version 0.394

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Woodhouse-Sakati syndrome MIM#241080

    Green DCAF17 in Pituitary hormone deficiency

    Level 3: Pituitary disorders
    Level 2: Endocrine disorders
    Version 0.173

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    • Expert Review
    • Expert Review
    Phenotypes
    • Woodhouse-Sakati syndrome, MIM# 241080

    Green DCAF17 in Neurodegeneration with brain iron accumulation


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.3

    Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • GeneReviews
    • Expert Review Green
    Phenotypes
    • Woodhouse-Sakati syndrome

    Green DCAF17 in Prepair 1000+


    Level 2: Screening
    Version 2.15

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Woodhouse-Sakati syndrome MIM#241080

    Green DCAF17 in Prepair 500+


    Level 2: Screening
    Version 2.0

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Woodhouse-Sakati syndrome MIM#241080

    Green DCAF17 in Infertility and Recurrent Pregnancy Loss


    Version 1.78

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Woodhouse-Sakati syndrome, MIM# 241080
    • Hypergonadotropic/ Hypogonadotropic Hypogonadism

    Green DCAF17 in Hypogonadotropic hypogonadism

    Level 3: Pituitary disorders
    Level 2: Endocrine disorders
    Version 0.80

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review
    • Expert Review Green
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Woodhouse-Sakati syndrome, MIM# 241080