NSD1

nuclear receptor binding SET domain protein 1
Identifiers
Symbol NSD1
Alt. symbols STO
Entrez 64324
HUGO 14234
OMIM 606681
RefSeq NM_172349
UniProt Q96L73
Other data
Locus Chr. 5 q35

NSD1 is a transcription coregulator protein[1] associated with Sotos syndrome[2] and Weaver syndrome.[3]

References

  1. ↑ 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. PMC 1170677 Freely accessible. PMID 9628876. doi:10.1093/emboj/17.12.3398.
  2. ↑ 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. PMID 11896389. doi:10.1038/ng863.
  3. ↑ 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. PMC 378618 Freely accessible. PMID 12464997. doi:10.1086/345647.


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.