SDCCAG8

serologically defined colon cancer antigen 8
OMIM: 613524, Gene2Phenotype

13 panels

Panel Reviews Mode of inheritance Details
13 panels

Green SDCCAG8 in Bardet Biedl syndrome


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.10

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Bardet-Biedl syndrome 16, MIM# 615993
    • MONDO:0014444

    Green SDCCAG8 in Ciliopathies


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.54

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • Bardet-Biedl syndrome 16, MIM# 615993
    • MONDO:0014444
    • Senior-Loken syndrome 7, MIM# 613615
    • MONDO:0013326
    • Nephronophthisis

    Green SDCCAG8 in Mendeliome


    Version 1.1891

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Bardet-Biedl syndrome 16, MIM# 615993
    • MONDO:0014444
    • Senior-Loken syndrome 7, MIM# 613615
    • MONDO:0013326
    • Nephronophthisis

    Red SDCCAG8 in Polydactyly


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 0.276

    Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • Bardet-Biedl syndrome 16, MIM# 615993

    Green SDCCAG8 in Renal Ciliopathies and Nephronophthisis


    Level 2: Renal and urinary tract disorders
    Version 1.22

    Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • Renal Cystic Disease_SuperPanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • KidGen_CilioNephronop v38.1.0
    Phenotypes
    • Bardet-Biedl syndrome 16, MIM# 615993
    • MONDO:0014444
    • Senior-Loken syndrome 7, MIM# 613615
    • MONDO:0013326
    • Nephronophthisis

    Green SDCCAG8 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Bardet-Biedl syndrome 16, MIM# 615993
    • MONDO:0014444
    • Senior-Loken syndrome 7, MIM# 613615
    • MONDO:0013326
    • Nephronophthisis

    Red SDCCAG8 in Skeletal dysplasia

    Level 3: Skeletal dysplasias
    Level 2: Skeletal disorders
    Version 0.285

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review Red
    • Emory Genetics Laboratory
    • Victorian Clinical Genetics Services
    Phenotypes
    • Bardet-Biedl syndrome 16, 615993

    Green SDCCAG8 in Syndromic Retinopathy


    Level 2: Ophthalmological disorders
    Version 0.209

    Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • RetNet
    Phenotypes
    • Bardet-Biedl syndrome 16, MIM# 615993
    • MONDO:0014444
    • Senior-Loken syndrome 7, MIM# 613615
    • MONDO:0013326

    Green SDCCAG8 in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.109

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Bardet-Biedl syndrome 16, 615993 (3)

    Green SDCCAG8 in Fetal anomalies


    Version 1.255

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • KidGen_CilioNephronop v38.1.0
    Phenotypes
    • Bardet-Biedl syndrome 16, MIM# 615993
    • MONDO:0014444
    • Senior-Loken syndrome 7, MIM# 613615
    • MONDO:0013326
    • Nephronophthisis

    Green SDCCAG8 in Severe early-onset obesity


    Level 2: Endocrine disorders
    Version 1.10

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Victorian Clinical Genetics Services
    Phenotypes
    • Bardet-Biedl syndrome 16, MIM# 615993
    • MONDO:0014444

    Green SDCCAG8 in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Bardet-Biedl syndrome 16, 615993 (3)

    Green SDCCAG8 in Prepair 500+


    Level 2: Screening
    Version 1.1

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Bardet-Biedl syndrome 16, 615993 (3)