NSD3

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Histone-lysine N-methyltransferase NSD3 is an enzyme that in humans is encoded by the NSD3 gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesNSD3, pp14328, WHSC1L1, WHISTLE, Wolf-Hirschhorn syndrome candidate 1-like 1, nuclear receptor binding SET domain protein 3, KMT3G, KMT3F
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NSD3
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesNSD3, pp14328, WHSC1L1, WHISTLE, Wolf-Hirschhorn syndrome candidate 1-like 1, nuclear receptor binding SET domain protein 3, KMT3G, KMT3F
External IDsOMIM: 607083; MGI: 2142581; HomoloGene: 56960; GeneCards: NSD3; OMA:NSD3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_017778
NM_023034

NM_001001735
NM_001081269
NM_001308481
NM_001308482

RefSeq (protein)

NP_060248
NP_075447

NP_001001735
NP_001074738
NP_001295410
NP_001295411

Location (UCSC)Chr 8: 38.27 – 38.38 MbChr 8: 26.09 – 26.21 Mb
PubMed search[3][4]
Wikidata
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This gene is related to the Wolf–Hirschhorn syndrome candidate-1 gene (NSD2) and encodes a protein with PWWP (proline-tryptophan-tryptophan-proline) domains. This protein methylates histone H3 at lysine residues 4 and 27, which represses gene transcription. Two alternatively spliced variants have been described.[6]

The NSD3 gene is amplified in several cancers, including lung cancer and head and neck cancer, and may play a role in carcinogenesis.[7][8]

References

Further reading

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