MAX

MYC associated factor X
OMIM: 154950, Gene2Phenotype

9 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 9 panels
Green MAX in Neuroendocrine cancer pertinent cancer susceptibility Level 3: Pertinent cancer susceptibility gene panel Level 2: Cancer Programme Version 1.5	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes {Pheochromocytoma, susceptibility to}, OMIM:171300
Green MAX in Adult solid tumours for rare disease Level 3: Tumour syndromes Level 2: Tumour syndromes Version 1.42	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Expert list Phenotypes {Pheochromocytoma, susceptibility to}, OMIM:171300
Green MAX in Childhood solid tumours Level 2: Cancer susceptibility Version 5.9 Latest signed off version: v5.0 (30 Apr 2025)	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green NHS GMS Phenotypes {Pheochromocytoma, susceptibility to}, OMIM:171300
Green MAX in Multiple endocrine tumours Level 3: Breast and endocrine Level 2: Tumour syndromes Version 1.15	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Emory Genetics Laboratory Phenotypes {Pheochromocytoma, susceptibility to}, OMIM:171300
Green MAX in Inherited phaeochromocytoma and paraganglioma Level 3: Breast and endocrine Level 2: Tumour syndromes Version 1.12	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Eligibility statement prior genetic testing Radboud University Medical Center, Nijmegen Illumina TruGenome Clinical Sequencing Services UKGTN Emory Genetics Laboratory Phenotypes pheochromocytomas (PHEOs), paragangliomas (PGLs) Hereditary Paraganglioma-Pheochromocytoma Syndrome {Pheochromocytoma, susceptibility to}, 171300
Green MAX in Inherited phaeochromocytoma and paraganglioma excluding NF1 Level 2: Endocrinology Version 3.10 Latest signed off version: v3.0 (7 Aug 2024)	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green NHS GMS Phenotypes {Pheochromocytoma, susceptibility to}, OMIM:171300 Hereditary Paraganglioma-Pheochromocytoma Syndrome
Green MAX in Adult solid tumours cancer susceptibility Level 2: Cancer susceptibility Version 2.35 Latest signed off version: v2.2 (18 Feb 2020)	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources NHS GMS Expert Review Green Expert list Phenotypes {Pheochromocytoma, susceptibility to}, OMIM:171300 Familial Pheochromocytoma, adrenal
Green MAX in Fetal anomalies Level 2: Fetal (including NIPD) Version 6.140 Latest signed off version: v6.0 (30 Apr 2025)	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green NHS GMS Phenotypes Polydactyly-macrocephaly syndrome, OMIM:620712
Green MAX in Neurological segmental overgrowth Level 2: Neurology Version 3.3 Latest signed off version: v3.0 (30 Oct 2024) Component of the following Super Panels: Cerebral malformation	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green NHS GMS Literature Phenotypes Polydactyly-macrocephaly syndrome, OMIM:620712