MAX:Ensemblv90

MYC associated factor X
OMIM: 154950, ClinGen, DECIPHER

17 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 17 panels
Amber MAX in Macrocephaly_Megalencephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 0.153	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes Polydactyly-macrocephaly syndrome, MIM# 620712
Green MAX in Mendeliome Version 1.3802	2 reviews	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 0.132	1 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 0.297 Component of the following Super Panels: Limb and Digital Malformations SuperPanel	2 reviews	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 1.130	1 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 1.508	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Polydactyly-macrocephaly syndrome, MIM# 620712
Red MAX in CGC_86 Version 0.3	0 reviews	Other	Sources CGC_86 Phenotypes Hereditary Paraganglioma-Pheochromocytoma Syndromes
Red MAX in NCGC Version 0.3	0 reviews	Other	Sources NCGC Phenotypes Hereditary Paraganglioma-Pheochromocytoma Syndromes
Red MAX in TCGA_PANCAN_2018 Version 0.3	0 reviews	Other	Sources TCGA_PANCAN_2018 Phenotypes Hereditary Paraganglioma-Pheochromocytoma Syndromes
Green MAX in Fetal anomalies Version 1.482	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Polydactyly-macrocephaly syndrome, MIM# 620712
Green MAX in Transplant Co-Morbidity Level 2: Screening Version 0.20	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Phenotypes {Pheochromocytoma, susceptibility to} 171300
Amber MAX in Macrocephaly_Megalencephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.0	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Literature Expert Review Amber Phenotypes Polydactyly-macrocephaly syndrome, MIM# 620712
Green MAX in Cancer Predisposition_Paediatric Level 2: Cancer Version 1.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes {Pheochromocytoma, susceptibility to}, MIM# 171300
Green MAX in Polydactyly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.0	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Literature Expert Review Green Phenotypes Polydactyly-macrocephaly syndrome, MIM# 620712
Green MAX in Additional findings_Adult Level 2: Screening Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Phenotypes {Pheochromocytoma, susceptibility to} 171300
Green MAX in Fetal anomalies Version 2.0	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Literature Expert Review Green Phenotypes Polydactyly-macrocephaly syndrome, MIM# 620712
Green MAX in Transplant Co-Morbidity Level 2: Screening Version 1.0	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes {Pheochromocytoma, susceptibility to} 171300