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KMT2E

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KMT2E
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesKMT2E, HDCMC04P, MLL5, NKp44L, lysine methyltransferase 2E, ODLURO, lysine methyltransferase 2E (inactive), SETD5B
External IDsOMIM: 608444; MGI: 1924825; HomoloGene: 18822; GeneCards: KMT2E; OMA:KMT2E - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_018682
NM_032187
NM_182931

NM_026984

RefSeq (protein)

NP_061152
NP_891847

NP_081260

Location (UCSC)Chr 7: 104.94 – 105.12 MbChr 5: 23.64 – 23.71 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Lysine methyltransferase 2E is a protein that in humans is encoded by the KMT2E gene. [5]

Function

This gene is a member of the myeloid/lymphoid or mixed-lineage leukemia (MLL) family and encodes a protein with an N-terminal PHD zinc finger and a central SET domain. Overexpression of the protein inhibits cell cycle progression. Alternate transcriptional splice variants have been characterized.

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000005483Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000029004Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: Lysine methyltransferase 2E". Retrieved 2016-06-02.

Further reading

  • Emerling BM, Bonifas J, Kratz CP, Donovan S, Taylor BR, Green ED, Le Beau MM, Shannon KM (2002). "MLL5, a homolog of Drosophila trithorax located within a segment of chromosome band 7q22 implicated in myeloid leukemia". Oncogene. 21 (31): 4849–54. doi:10.1038/sj.onc.1205615. PMID 12101424.


This article incorporates text from the United States National Library of Medicine, which is in the public domain.