DNMT1:Ensemblv90

DNA methyltransferase 1
OMIM: 126375, ClinGen, DECIPHER

13 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 13 panels
Green DNMT1 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	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources ClinGen Expert Review Green Phenotypes Hereditary sensory neuropathy-deafness-dementia syndrome, MONDO:0013584
Green DNMT1 in Mendeliome Version 1.3802	3 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Literature ClinGen Expert Review Green Phenotypes Hereditary sensory neuropathy-deafness-dementia syndrome, MONDO:0013584
Green DNMT1 in Regression Level 2: Neurology and neurodevelopmental disorders Version 0.601	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green DNMT1 in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.304	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Literature ClinGen Expert Review Green Phenotypes Hereditary sensory neuropathy-deafness-dementia syndrome, MONDO:0013584
Green DNMT1 in Ataxia - adult onset Level 2: Neurology and neurodevelopmental disorders Version 1.62 Component of the following Super Panels: Neurodegenerative disease - adult onset Neuromuscular Superpanel Progressive Neurological Conditions	3 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Literature ClinGen Expert Review Green Phenotypes Hereditary sensory neuropathy-deafness-dementia syndrome, MONDO:0013584
Green DNMT1 in Ataxia Level 2: Neurology and neurodevelopmental disorders Version 1.162 Component of the following Super Panels: Ataxia_Superpanel Neuromuscular Superpanel Progressive Neurological Conditions	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green ClinGen Literature Phenotypes Hereditary sensory neuropathy-deafness-dementia syndrome, MONDO:0013584
Green DNMT1 in Hereditary Neuropathy_CMT - isolated Level 2: Neurology and neurodevelopmental disorders Version 1.68 Component of the following Super Panels: Hereditary Neuropathy_CMT_IsolatedAndComplex Neuromuscular Superpanel Progressive Neurological Conditions	3 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Literature ClinGen Expert Review Green Phenotypes Hereditary sensory neuropathy-deafness-dementia syndrome, MONDO:0013584
Green DNMT1 in Early-onset Dementia Level 2: Neurology and neurodevelopmental disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green ClinGen Phenotypes Hereditary sensory neuropathy-deafness-dementia syndrome, MONDO:0013584
Green DNMT1 in Regression Level 2: Neurology and neurodevelopmental disorders Version 1.0	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services
Green DNMT1 in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green ClinGen Literature Phenotypes Hereditary sensory neuropathy-deafness-dementia syndrome, MONDO:0013584
Green DNMT1 in Ataxia - adult onset Level 2: Neurology and neurodevelopmental disorders Version 2.0	3 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green ClinGen Literature Phenotypes Hereditary sensory neuropathy-deafness-dementia syndrome, MONDO:0013584
Green DNMT1 in Ataxia Level 2: Neurology and neurodevelopmental disorders Version 2.0	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Literature ClinGen Expert Review Green Phenotypes Hereditary sensory neuropathy-deafness-dementia syndrome, MONDO:0013584
Green DNMT1 in Hereditary Neuropathy_CMT - isolated Level 2: Neurology and neurodevelopmental disorders Version 2.0	3 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green ClinGen Literature Phenotypes Hereditary sensory neuropathy-deafness-dementia syndrome, MONDO:0013584