NSD1

NSD1
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	3OOI
Identifiers
Aliases	NSD1, ARA267, KMT3B, SOTOS, SOTOS1, STO, nuclear receptor binding SET domain protein 1
External IDs	OMIM: 606681 MGI: 1276545 HomoloGene: 32543 GeneCards: NSD1
Gene location (Human)
Chr.	Chromosome 5 (human)
End	177,300,213 bp
Gene location (Mouse)
Chr.	Chromosome 13 (mouse)
End	55,466,138 bp
RNA expression pattern
	Top expressed in
	sural nerve; ; Achilles tendon; ; ganglionic eminence; ; monocyte; ; sperm; ; thymus; ; corpus callosum; ; stromal cell of endometrium; ; cerebellar vermis; ; islet of Langerhans;
	Top expressed in
	ascending aorta; ; aortic valve; ; pineal gland; ; supraoptic nucleus; ; vas deferens; ; yolk sac; ; secondary oocyte; ; ganglionic eminence; ; cumulus cell; ; lacrimal gland;
	More reference expression data
	n/a
Gene ontology
Molecular function	methyltransferase activity; transferase activity; histone methyltransferase activity (H4-K20 specific); transcription corepressor activity; chromatin binding; transcription coregulator activity; metal ion binding; retinoid X receptor binding; thyroid hormone receptor binding; androgen receptor binding; retinoic acid receptor binding; estrogen receptor binding; histone-lysine N-methyltransferase activity; histone methyltransferase activity (H3-K36 specific); zinc ion binding; protein binding; RNA polymerase II cis-regulatory region sequence-specific DNA binding;
Cellular component	nucleoplasm; chromosome; nucleus; chromatin;
Biological process	regulation of transcription, DNA-templated; negative regulation of transcription by RNA polymerase II; transcription, DNA-templated; positive regulation of transcription, DNA-templated; methylation; regulation of peptidyl-serine phosphorylation; regulation of histone H3-K36 methylation; histone lysine methylation; histone methylation; regulation of RNA polymerase II regulatory region sequence-specific DNA binding; histone H3-K36 methylation; histone H4-K20 methylation; chromatin organization;
	Sources:Amigo / QuickGO
Orthologs
	64324
	18193
	ENSG00000165671
	ENSMUSG00000021488
	Q96L73
	O88491
	NM_022455; NM_172349; NM_001365684
	NM_008739
	NP_071900; NP_758859; NP_001352613
	n/a
	Wikidata
View/Edit Human	View/Edit Mouse

NSD1 (Nuclear receptor binding SET Domain Protein 1)^[5] is a transcription coregulator protein^[6] that encodes Histone Methyltransferase and is associated with Sotos syndrome^[7] and Weaver syndrome.^[8]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000165671 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000021488 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "NSD1 Gene". GeneCards human gene database. Weizmann Institute of Science. Retrieved 31 December 2017.
^ Huang N, vom Baur E, Garnier JM, Lerouge T, Vonesch JL, Lutz Y, Chambon P, Losson R (June 1998). "Two distinct nuclear receptor interaction domains in NSD1, a novel SET protein that exhibits characteristics of both corepressors and coactivators". EMBO J. 17 (12): 3398–412. doi:10.1093/emboj/17.12.3398. PMC 1170677. PMID 9628876.
^ Kurotaki N, Imaizumi K, Harada N, Masuno M, Kondoh T, Nagai T, Ohashi H, Naritomi K, Tsukahara M, Makita Y, Sugimoto T, Sonoda T, Hasegawa T, Chinen Y, Tomita Ha HA, Kinoshita A, Mizuguchi T, Yoshiura Ki K, Ohta T, Kishino T, Fukushima Y, Niikawa N, Matsumoto N (April 2002). "Haploinsufficiency of NSD1 causes Sotos syndrome". Nat. Genet. 30 (4): 365–6. doi:10.1038/ng863. PMID 11896389. S2CID 205357840.
^ Douglas J, Hanks S, Temple IK, Davies S, Murray A, Upadhyaya M, Tomkins S, Hughes HE, Cole TR, Rahman N (January 2003). "NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypes". Am. J. Hum. Genet. 72 (1): 132–43. doi:10.1086/345647. PMC 378618. PMID 12464997.

External links

GeneReviews/NCBI/NIH/UW entry on Sotos Syndrome
NSD1 protein, human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
NURSA C103

This article on a gene on human chromosome 5 is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000165671 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000021488 – Ensembl, 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] "NSD1 Gene". GeneCards human gene database. Weizmann Institute of Science. Retrieved 31 December 2017.

[pmid9628876-6] Huang N, vom Baur E, Garnier JM, Lerouge T, Vonesch JL, Lutz Y, Chambon P, Losson R (June 1998). "Two distinct nuclear receptor interaction domains in NSD1, a novel SET protein that exhibits characteristics of both corepressors and coactivators". EMBO J. 17 (12): 3398–412. doi:10.1093/emboj/17.12.3398. PMC 1170677. PMID 9628876.

[pmid11896389-7] Kurotaki N, Imaizumi K, Harada N, Masuno M, Kondoh T, Nagai T, Ohashi H, Naritomi K, Tsukahara M, Makita Y, Sugimoto T, Sonoda T, Hasegawa T, Chinen Y, Tomita Ha HA, Kinoshita A, Mizuguchi T, Yoshiura Ki K, Ohta T, Kishino T, Fukushima Y, Niikawa N, Matsumoto N (April 2002). "Haploinsufficiency of NSD1 causes Sotos syndrome". Nat. Genet. 30 (4): 365–6. doi:10.1038/ng863. PMID 11896389. S2CID 205357840.

[pmid12464997-8] Douglas J, Hanks S, Temple IK, Davies S, Murray A, Upadhyaya M, Tomkins S, Hughes HE, Cole TR, Rahman N (January 2003). "NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypes". Am. J. Hum. Genet. 72 (1): 132–43. doi:10.1086/345647. PMC 378618. PMID 12464997.

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NSD1

References

External links

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