NSD1

Nuclear receptor binding SET domain protein 1
المعرفات
الأسماء المستعارة	nuclear receptor-binding SET domain-containing protein 1, androgen receptor-associated coregulator 267, H4-K20-HMTase, NR-binding SET domain-containing protein, lysine N-methyltransferase 3B, H3-K36-HMTase, androgen receptor coactivator 267 kDa protein, truncated nuclear receptor binding SET domain protein 1, androgen receptor-associated protein of 267 kDa, histone-lysine N-methyltransferase, H3 lysine-36 specific, nuclear receptor SET domain-containing protein 1, histone-lysine N-methyltransferase, H3 lysine-36 and H4 lysine-20 specific, NSD1
معرفات خارجية
أورثولوج
	n/a
	n/a
	n/a
	n/a
	n/a
	n/a
	ويكي بيانات
اعرض/عدّل إنسان

NSD1 هوَ بروتين يُشَفر بواسطة جين NSD1 في الإنسان.[1][2][3][4]

الوظيفة

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 (أبريل 2002)، "Haploinsufficiency of NSD1 causes Sotos syndrome"، Nat. Genet.، 30 (4): 365–6، doi:10.1038/ng863، PMID 11896389.
Douglas J, Hanks S, Temple IK, Davies S, Murray A, Upadhyaya M, Tomkins S, Hughes HE, Cole TR, Rahman N (يناير 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.
"NSD1 Gene"، GeneCards human gene database، Weizmann Institute of Science، مؤرشف من الأصل في 31 ديسمبر 2017، اطلع عليه بتاريخ 31 ديسمبر 2017.
Huang N, vom Baur E, Garnier JM, Lerouge T, Vonesch JL, Lutz Y, Chambon P, Losson R (يونيو 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.

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