SDHAF2

succinate dehydrogenase complex assembly factor 2
OMIM: 613019, Gene2Phenotype

11 panels

Panel Reviews Mode of inheritance Details
11 panels

Green SDHAF2 in Incidentalome


Version 0.360

2 reviews MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Sources
  • Expert Review Green
  • Melbourne Genomics Health Alliance
  • Victorian Clinical Genetics Services
Phenotypes
  • Paragangliomas 2, MIM# 601650

Green SDHAF2 in Cancer Predisposition_Paediatric


Level 2: Cancer
Version 0.132

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Paragangliomas 2, MIM# 601650

Red SDHAF2 in Mitochondrial disease


Level 2: Metabolic disorders
Version 0.1085

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • 1 review Unknown
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Mitochondrial Flagship
    Phenotypes
    • Paragangliomas 2, MIM# 601650

    Green SDHAF2 in Additional findings_Adult


    Level 2: Screening
    Version 1.130

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance
    Phenotypes
    • Paragangliomas 2, MIM# 601650

    Amber SDHAF2 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • BabySeq Category B gene
    Phenotypes
    • Hereditary Paraganglioma-Pheochromocytoma Syndromes

    Amber SDHAF2 in Incidentalome_PREGEN_DRAFT


    Version 0.43

    1 review Unknown
    Sources
    • Expert Review Amber
    • NSW Health Pathology

    Amber SDHAF2 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

    0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • BabySeq Category B gene
    • Expert Review Amber
    Phenotypes
    • Hereditary Paraganglioma-Pheochromocytoma Syndromes

    Green SDHAF2 in Transplant Co-Morbidity


    Level 2: Screening
    Version 0.20

    0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance
    Phenotypes
    • Paragangliomas 2, MIM# 601650

    Green SDHAF2 in Paraganglioma_phaeochromocytoma


    Level 2: Cancer Predisposition
    Version 1.1

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    • Expert list
    Phenotypes
    • Paragangliomas 2, MONDO:0011121
    • Pheochromocytoma, MONDO:0008233
    • Hereditary pheochromocytoma-paraganglioma, MONDO:0017366
    • Pheochromocytoma/paraganglioma syndrome 2, MIM#601650

    Red SDHAF2 in Kidney Cancer


    Level 2: Cancer Predisposition
    Version 1.11

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Expert Review
    • Expert list
    Phenotypes
    • Renal carcinoma, MONDO:0005206
    • Hereditary pheochromocytoma-paraganglioma, MONDO:0017366
    • Pheochromocytoma/paraganglioma syndrome 2, MIM#601650

    Green SDHAF2 in Gastrointestinal Stromal Tumour


    Level 2: Cancer Predisposition
    Version 1.0

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    • Expert list
    Phenotypes
    • Gastrointestinal stromal tumor, MONDO:0011719
    • Hereditary pheochromocytoma-paraganglioma, MONDO:0017366
    • Pheochromocytoma/paraganglioma syndrome 2, MIM#601650