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

WDPCP

WD repeat containing planar cell polarity effector
OMIM: 613580, ClinGen, DECIPHER

11 panels

Panel Reviews Mode of inheritance Details
11 panels

Red WDPCP in Bardet Biedl syndrome


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.10

Component of the following Super Panels:

  • Retinal Disorders Superpanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Bardet-Biedl syndrome 15, MIM# 615992

    Green WDPCP in Ciliopathies


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.62

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • Bardet-Biedl syndrome 15, MIM# 615992
    • OFD
    • Congenital heart defects, hamartomas of tongue, and polysyndactyly, 217085

    Green WDPCP in Mendeliome


    Version 1.2302

    		2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    • Victorian Clinical Genetics Services
    Phenotypes
    • Bardet-Biedl syndrome 15, MIM# 615992
    • OFD
    • Congenital heart defects, hamartomas of tongue, and polysyndactyly, 217085

    Green WDPCP in Polydactyly


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 0.281

    Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Bardet-Biedl syndrome 15, MIM# 615992
    • OFD
    • Congenital heart defects, hamartomas of tongue, and polysyndactyly, 217085

    Green WDPCP in Renal Ciliopathies and Nephronophthisis


    Level 2: Renal and urinary tract disorders
    Version 1.26

    Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • Renal Cystic Disease_SuperPanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • KidGen_CilioNephronop v38.1.0
    Phenotypes
    • Bardet-Biedl syndrome 15, MIM# 615992
    • OFD
    • Congenital heart defects, hamartomas of tongue, and polysyndactyly, 217085

    Green WDPCP 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
    • Bardet-Biedl syndrome 15, MIM# 615992
    • OFD
    • Congenital heart defects, hamartomas of tongue, and polysyndactyly, 217085

    Green WDPCP in Skeletal dysplasia

    Level 3: Skeletal dysplasias
    Level 2: Skeletal disorders
    Version 0.302

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    • Emory Genetics Laboratory
    Phenotypes
    • ?Bardet-Biedl syndrome 15, 615992
    • ?Congenital heart defects, hamartomas of tongue, and polysyndactyly 217085

    Red WDPCP 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 Review Green
    • Expert Review Red
    • Expert list
    • Victorian Clinical Genetics Services
    Phenotypes
    • ?Bardet-Biedl syndrome 15, 615992
    • ?Congenital heart defects, hamartomas of tongue, and polysyndactyly, 217085

    Green WDPCP in Syndromic Retinopathy


    Level 2: Ophthalmological disorders
    Version 0.219

    Component of the following Super Panels:

  • Retinal Disorders Superpanel

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • RetNet
    • Expert Review Green
    • Expert list
    • Victorian Clinical Genetics Services

    Green WDPCP in Fetal anomalies


    Version 1.313

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • KidGen_CilioNephronop v38.1.0
    Phenotypes
    • Bardet-Biedl syndrome 15, MIM# 615992
    • OFD
    • Congenital heart defects, hamartomas of tongue, and polysyndactyly, 217085

    Red WDPCP in Severe early-onset obesity


    Level 2: Endocrine disorders
    Version 1.13

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Genomics England PanelApp
    • Victorian Clinical Genetics Services
    Phenotypes
    • Bardet-Biedl syndrome 15, MIM# 615992