lysine methyltransferase 5B

Summary
Gene Symbol
  • KMT5B
Organism
Homo sapiens (human)
NCBI Gene
51111
PubChem
51111
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Chromatin regulator
  • Chromosome
  • Disease variant
  • Intellectual disability
  • Isopeptide bond
  • Metal-binding
  • Methyltransferase
  • Myogenesis
  • Nucleus
  • Proteomics identification
  • Reference proteome
  • Repressor
  • S-adenosyl-L-methionine
  • Transcription regulation
  • Ubl conjugation
  • Zinc
Proteins
Displaying all 5 entries
UniProt Protein Name
A0A8V8TQB9
  • [histone H4]-lysine20 N-methyltransferase KMT5B
B7WNX0
  • [histone H4]-lysine20 N-methyltransferase KMT5B
B7Z5N2
  • [histone H4]-lysine20 N-methyltransferase KMT5B
Q4FZB7
  • Lysine N-methyltransferase 5B
  • Lysine-specific methyltransferase 5B
  • Suppressor of variegation 4-20 homolog 1
  • [histone H4]-N-methyl-L-lysine20 N-methyltransferase KMT5B
  • [histone H4]-lysine20 N-methyltransferase KMT5B
C9J6S5
  • [histone H4]-lysine20 N-methyltransferase KMT5B
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
histone-lysine n-methyltransferase
Functional Category
  • J: Translation, ribosomal structure and biogenesis
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0080232 autosomal dominant intellectual developmental disorder 51

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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: April 7, 2025