MAX

MYC associated factor X
OMIM: 154950, Gene2Phenotype

11 panels

Panel Reviews Mode of inheritance Details
11 panels

Amber MAX in Macrocephaly_Megalencephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.140

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Polydactyly-macrocephaly syndrome, MIM# 620712

Green MAX in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • {Pheochromocytoma, susceptibility to}, MIM# 171300
  • Polydactyly-macrocephaly syndrome, MIM# 620712

Green MAX in Cancer Predisposition_Paediatric


Level 2: Cancer
Version 0.131

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • {Pheochromocytoma, susceptibility to}, MIM# 171300

Green MAX in Polydactyly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.276

Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Polydactyly-macrocephaly syndrome, MIM# 620712

    Green MAX in Additional findings_Adult


    Level 2: Screening
    Version 0.166

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • {Pheochromocytoma, susceptibility to} 171300

    Green MAX in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Polydactyly-macrocephaly syndrome, MIM# 620712

    Red MAX in CGC_86


    Version 0.2

    review Other
    Sources
    • CGC_86
    Phenotypes
    • Hereditary Paraganglioma-Pheochromocytoma Syndromes

    Red MAX in NCGC


    Version 0.2

    review Other
    Sources
    • NCGC
    Phenotypes
    • Hereditary Paraganglioma-Pheochromocytoma Syndromes

    Red MAX in TCGA_PANCAN_2018


    Version 0.2

    review Other
    Sources
    • TCGA_PANCAN_2018
    Phenotypes
    • Hereditary Paraganglioma-Pheochromocytoma Syndromes

    Green MAX in Fetal anomalies


    Version 1.255

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Polydactyly-macrocephaly syndrome, MIM# 620712

    Green MAX in Transplant Co-Morbidity Superpanel


    Level 2: Screening
    Version 0.18

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert list
    • Expert Review Green
    Phenotypes
    • {Pheochromocytoma, susceptibility to} 171300