PanelApp
  1. Genes and Genomic Entities
  2. FANCG

FANCG

FA complementation group G
OMIM: 602956, ClinGen, DECIPHER

18 panels

Panel Reviews Mode of inheritance Details
18 panels

Green FANCG in Haematological malignancies


Level 2: Cancer susceptibility
Version 0.148

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Curated sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Fanconi anaemia G
  • AML, Leukaemia
  • Bone marrow failure
  • MDS
  • leukaemia
  • AML
  • Head and neck and anogenital squamous cell cancers, liver cancer, esophageal cancer, Squamous cell carcinoma: oral, GI, vulvar
  • Class: BM failure FA, (typ AR)

Green FANCG in Bone Marrow Failure


Level 2: Haematological disorders
Version 2.9

Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • Fanconi anaemia, complementation group G, MIM# 614082
    • MONDO:0013565

    Green FANCG in Chromosome Breakage Disorders


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 2.3

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Fanconi anaemia, complementation group G, MIM# 614082
    • MONDO:0013565

    Green FANCG in Mendeliome


    Version 2.612

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Fanconi anaemia, complementation group G, MIM# 614082
    • MONDO:0013565

    Green FANCG in Microcephaly


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 2.32

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Fanconi anemia, complementation group G MIM#614082

    Green FANCG in Cancer Predisposition_Paediatric


    Level 2: Cancer
    Version 1.2

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

    Green FANCG in Radial Ray Abnormalities


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 2.1

    Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • Fanconi anaemia, complementation group G, MIM# 614082
    • MONDO:0013565

    Green FANCG in Additional findings_Adult


    Level 2: Screening
    Version 3.1

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Fanconi anaemia, complementation group G, MIM# 614082

    Green FANCG in Homologous_recombination_deficiency_WTS_UMCCR


    Level 2: Cancer
    Version 1.0

    		0 reviews Unknown
    Sources
    • Literature
    • Expert Review Green
    Tags
    • umccr

    Amber FANCG in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.148

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Genetic Health Queensland
    Phenotypes
    • Fanconi anemia, complementation group G, MIM# 614082

    Green FANCG in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 1.0

    		0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Fanconi anemia, complementation group G, 614082 (3)

    Green FANCG in Additional findings_Paediatric


    Level 2: Screening
    Version 1.1

    		0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category A gene
    • Expert Review Green
    Phenotypes
    • Fanconi anaemia

    Green FANCG in Growth failure


    Version 2.28

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Victorian Clinical Genetics Services
    Phenotypes
    • Fanconi anaemia, complementation group G, MIM# 614082
    • MONDO:0013565

    Green FANCG in Fetal anomalies


    Version 2.83

    		2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Literature
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • Fanconi anaemia, complementation group G, MIM# 614082
    • MONDO:0013565

    Green FANCG in IBMDx study


    Version 1.2

    		1 review Unknown
    Sources
    • Expert Review Green
    • IBMDx Study
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • MONDO:0013565
    • Fanconi anaemia, complementation group G, MIM# 614082

    Green FANCG in Prepair 1000+


    Level 2: Screening
    Version 3.0

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Fanconi anemia, complementation group G, 614082 (3)

    Green FANCG in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 2.7

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category A gene
    Phenotypes
    • Fanconi anaemia, MIM#614082
    Tags
    • treatable
    • haematological

    Green FANCG in Prepair 500+


    Level 2: Screening
    Version 3.0

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Fanconi anaemia, complementation group G, MIM#614082