Gene Symbol:
DNMT1
HGNC:2976
Locus Group:
protein-coding gene
Locus Type:
gene with protein product
Location:
19p13.2
Filters:

Definitive classifications

autosomal dominant cerebellar ataxia, deafness and narcolepsy
AD
02/10/2017
Evaluated
04/21/2024
Submitted

Strong classifications

autosomal dominant cerebellar ataxia, deafness and narcolepsy
Submitted as: OMIM:604121
AD
10/09/2020
Evaluated
11/09/2020
Submitted
hereditary sensory neuropathy-deafness-dementia syndrome
Submitted as: OMIM:614116
AD
10/09/2020
Evaluated
11/09/2020
Submitted
autosomal dominant cerebellar ataxia, deafness and narcolepsy
Submitted as: OMIM:604121
AD
01/28/2021
Evaluated
03/31/2021
Submitted
autosomal dominant cerebellar ataxia, deafness and narcolepsy
Submitted as: OMIM:604121
AD
08/12/2020
Evaluated
11/30/2023
Submitted
hereditary sensory neuropathy-deafness-dementia syndrome
Submitted as: OMIM:614116
AD
08/12/2020
Evaluated
11/30/2023
Submitted

Supportive classifications

autosomal dominant cerebellar ataxia, deafness and narcolepsy
Submitted as: Orphanet:314404
AD
09/14/2021
Evaluated
09/14/2021
Submitted
hereditary sensory neuropathy-deafness-dementia syndrome
Submitted as: Orphanet:456318
AD
09/14/2021
Evaluated
09/14/2021
Submitted

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