CYLD:Ensemblv90

CYLD lysine 63 deubiquitinase
OMIM: 605018, ClinGen, DECIPHER

11 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 11 panels
Amber CYLD in Early-onset Dementia Level 2: Neurology and neurodevelopmental disorders Version 1.52 Component of the following Super Panels: Neurodegenerative disease - adult onset Progressive Neurological Conditions	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes Frontotemporal dementia and/or amytrophic lateral sclerosis 8, MIM# 619132
Amber CYLD in Motor Neurone Disease Level 2: Neurology and neurodevelopmental disorders Version 1.39 Component of the following Super Panels: Neurodegenerative disease - adult onset Neuromuscular Superpanel Progressive Neurological Conditions	4 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Victorian Clinical Genetics Services Phenotypes Frontotemporal dementia and/or amytrophic lateral sclerosis 8, MIM# 619132
Green CYLD in Mendeliome Version 1.3802	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Brooke-Spiegler syndrome, 605041 Cylindromatosis, familial, 132700 Trichoepithelioma, multiple familial, 1, 601606 Frontotemporal dementia and/or amytrophic lateral sclerosis 8, MIM# 619132
Red CYLD in CGC_86 Version 0.3	0 reviews	Other	Sources CGC_86 Phenotypes Spiegler-Brooke syndrome
Red CYLD in NCGC Version 0.3	0 reviews	Other	Sources NCGC Phenotypes Spiegler-Brooke syndrome
Red CYLD in TCGA_PANCAN_2018 Version 0.3	0 reviews	Other	Sources TCGA_PANCAN_2018 Phenotypes Spiegler-Brooke syndrome
Green CYLD in Facial papules Level 2: Dermatological disorders Version 1.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes familial cylindromatosis MONDO:0007565
Amber CYLD in Early-onset Dementia Level 2: Neurology and neurodevelopmental disorders Version 2.0	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Literature Expert Review Amber Phenotypes Frontotemporal dementia and/or amytrophic lateral sclerosis 8, MIM# 619132
Amber CYLD in Motor Neurone Disease Level 2: Neurology and neurodevelopmental disorders Version 2.0	4 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Literature Expert Review Amber Phenotypes Frontotemporal dementia and/or amytrophic lateral sclerosis 8, MIM# 619132
Red CYLD in TCGA_PANCAN_2018 Version 1.0	0 reviews	Other	Sources TCGA_PANCAN_2018 Phenotypes Spiegler-Brooke syndrome
Green CYLD in Facial papules Level 2: Dermatological disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Phenotypes familial cylindromatosis MONDO:0007565