CYLD

CYLD lysine 63 deubiquitinase
OMIM: 605018, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Amber CYLD in Early-onset Dementia Level 2: Neurology and neurodevelopmental disorders Version 1.24 Component of the following Super Panels: Neurodegenerative disease - adult onset Progressive Neurological Conditions	review	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 1.24 Component of the following Super Panels: Neurodegenerative disease - adult onset Neuromuscular Superpanel Progressive Neurological Conditions	review	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 1.1902	review	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 0.2	review	Other	Sources CGC_86 Phenotypes Spiegler-Brooke syndrome
Red CYLD in NCGC Version 0.2	review	Other	Sources NCGC Phenotypes Spiegler-Brooke syndrome
Red CYLD in TCGA_PANCAN_2018 Version 0.2	review	Other	Sources TCGA_PANCAN_2018 Phenotypes Spiegler-Brooke syndrome
Green CYLD in Facial papules Level 2: Dermatological disorders Version 1.0	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes familial cylindromatosis MONDO:0007565