DNA methyltransferase 1

Summary
Gene Symbol
  • DNMT1
Organism
Homo sapiens (human)
NCBI Gene
1786
PubChem
1786
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Acetylation
  • Activator
  • Alternative splicing
  • Chromatin regulator
  • DNA-binding
  • Deafness
  • Disease variant
  • Isopeptide bond
  • Methylation
  • Methyltransferase
  • Neuropathy
  • Nucleus
  • Phosphoprotein
  • Reference proteome
  • Repeat
  • Repressor
  • S-adenosyl-L-methionine
  • Transcription regulation
  • Ubl conjugation
  • Zinc-finger
Proteins
Displaying all 3 entries
UniProt Protein Name
I6L9H2
Q59FP7
P26358
  • CXXC-type zinc finger protein 9
  • DNA methyltransferase HsaI
  • MCMT
Gene Ontology (GO)
GO Hierarchy
Disease
Disease Ontology
Displaying entries 1 - 10 of 28 in total
DO ID Disease Name Source
DOID:0050548 hereditary sensory neuropathy
DOID:0050696 fetal alcohol spectrum disorder
DOID:0050968 autosomal dominant cerebellar ataxia, deafness and narcolepsy
DOID:0070158 hereditary sensory neuropathy type 1E
DOID:10283 prostate cancer
DOID:11054 urinary bladder cancer
DOID:11984 hypertrophic cardiomyopathy
DOID:12361 Graves' disease
DOID:1324 lung cancer
DOID:1682 congenital heart disease

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024