Gene: DNMT1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1786
Gene Symbol: DNMT1
DNMT1 		0.310 GeneticVariation disease BEFREE Missense mutations in the DNMT1 gene have been previously associated with two neurological syndromes: hereditary sensory and autonomic neuropathy type 1 with dementia and deafness (HSAN1E) and autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN). 27277422 2016
Entrez Id: 1786
Gene Symbol: DNMT1
DNMT1 		0.310 Biomarker disease CTD_human Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss. 21532572 2011