SMS (gene)

{{Short description|Protein-coding gene in the species Homo sapiens}}

{{Infobox_gene}}

Spermine synthase is an enzyme that in humans is encoded by the SMS gene.{{cite journal | author = Korhonen VP, Halmekyto M, Kauppinen L, Myohanen S, Wahlfors J, Keinanen T, Hyvonen T, Alhonen L, Eloranta T, Janne J | title = Molecular cloning of a cDNA encoding human spermine synthase | journal = DNA Cell Biol | volume = 14 | issue = 10 | pages = 841–7 |date=Nov 1995 | pmid = 7546290 | doi =10.1089/dna.1995.14.841 | last4 = Myöhänen }}{{cite journal |author1=Grieff M |author2=Whyte MP |author3=Thakker RV |author4=Mazzarella R | title = Sequence analysis of 139 kb in Xp22.1 containing spermine synthase and the 5' region of PEX | journal = Genomics | volume = 44 | issue = 2 | pages = 227–31 |date=Dec 1997 | pmid = 9299240 | doi = 10.1006/geno.1997.4876 }}{{cite web | title = Entrez Gene: SMS spermine synthase| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6611}}

The protein encoded by this gene belongs to the spermidine/spermine synthases family. This gene encodes a ubiquitous enzyme of polyamine metabolism.

References

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Further reading

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  • {{cite journal |author1=Snyder RD |author2=Robinson A |title=Recessive sex-linked mental retardation in the absence of other recognizable abnormalities. Report of a family |journal=Clinical Pediatrics |volume=8 |issue= 11 |pages= 669–74 |year= 1969 |pmid= 5823961 |doi=10.1177/000992286900801114 |s2cid=32198336 }}
  • {{cite journal |vauthors=Arena JF, Schwartz C, Ouzts L, etal |title=X-linked mental retardation with thin habitus, osteoporosis, and kyphoscoliosis: linkage to Xp21.3-p22.12 |journal=Am. J. Med. Genet. |volume=64 |issue= 1 |pages= 50–8 |year= 1996 |pmid= 8826448 |doi= 10.1002/(SICI)1096-8628(19960712)64:1<50::AID-AJMG7>3.0.CO;2-V }}
  • {{cite journal |title=Toward a complete human genome sequence |journal=Genome Res. |volume=8 |issue= 11 |pages= 1097–108 |year= 1999 |pmid= 9847074 |doi= 10.1101/gr.8.11.1097|last1=Sanger Centre |first1=The |last2=Washington University Genome Sequencing Cente |first2=The |doi-access=free }}
  • {{cite journal |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 |bibcode=2002PNAS...9916899M |doi-access=free }}
  • {{cite journal |vauthors=Gevaert K, Goethals M, Martens L, etal |title=Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides |journal=Nat. Biotechnol. |volume=21 |issue= 5 |pages= 566–9 |year= 2004 |pmid= 12665801 |doi= 10.1038/nbt810 |s2cid=23783563 }}
  • {{cite journal |vauthors=Cason AL, Ikeguchi Y, Skinner C, etal |title=X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome |journal=Eur. J. Hum. Genet. |volume=11 |issue= 12 |pages= 937–44 |year= 2004 |pmid= 14508504 |doi= 10.1038/sj.ejhg.5201072 |doi-access= free }}
  • {{cite journal |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |title=The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC) |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 }}
  • {{cite journal |vauthors=Rush J, Moritz A, Lee KA, etal |title=Immunoaffinity profiling of tyrosine phosphorylation in cancer cells |journal=Nat. Biotechnol. |volume=23 |issue= 1 |pages= 94–101 |year= 2005 |pmid= 15592455 |doi= 10.1038/nbt1046 |s2cid=7200157 }}
  • {{cite journal |vauthors=Ross MT, Grafham DV, Coffey AJ, etal |title=The DNA sequence of the human X chromosome |journal=Nature |volume=434 |issue= 7031 |pages= 325–37 |year= 2005 |pmid= 15772651 |doi= 10.1038/nature03440 | pmc=2665286 |bibcode=2005Natur.434..325R }}

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Category:Genes mutated in mice