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Protein-coding gene in the species Homo sapiens

DOT1L

DOT1L
All data from the card 19
Aliases
DOT1L, DOT1, KMT4, DOT1 like histone lysine methyltransferase
External IDs
OMIM: 607375; MGI: 2143886; GeneCards: DOT1L
PDB
Human UniProt search: PDBe RCSB
2.1.1.360
↗
Chr.
Chromosome 19 (human)
Band
19p13.3
End
2,232,578 bp
Chr.
Chromosome 10 (mouse)
Band
10|10 C1
End
80,631,295 bp
BioGPS
More reference expression data
Databases
NCBI: entry; OMA: entry
Species
Human
Entrez
84444
Ensembl
ENSG00000104885
UniProt
Q8TEK3
RefSeq (mRNA)
NM_032482
RefSeq (protein)
NP_115871
Location (UCSC)
Chr 19: 2.16 – 2.23 Mb

DOT1-like (Disruptor of telomeric silencing 1-like), histone H3K79 methyltransferase (S. cerevisiae), also known as DOT1L, is a protein found in humans, as well as other eukaryotes.

DOT1L has been reported to play an important role in the processes of mixed-lineage leukemia (MLL)-rearranged leukemias. DOT1L also plays a role in spermatogenesis, where it acts as a transcriptional activator for genes responsible for the histone-to-protamine transition.

Small molecule inhibitors of Dot1L catalytic activity have been developed.

All three forms of H3K79 methylation (H3K79me1; H3K79me2; H3K79me3) are catalyzed by DOT1 in yeast or DOT1L in mammals. H3K79 methylation participates in the DNA damage response and has multiple roles in nucleotide excision repair and sister chromatid recombinational repair.

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Text from Wikipedia, CC BY-SA 4.0 · Source article