SMS

3C6K, 3C6M

SMS
SMS
Strwythurau
PDBHuman UniProt search: PDBe RCSB
Dynodwyr
CyfenwauSMS, MRSR, SPMSY, SRS, SpS, spermine synthase, MRXSSR
Dynodwyr allanolOMIM: 300105 HomoloGene: 88709 GeneCards: SMS
EC number2.5.1.22
Patrwm RNA pattern
Rhagor o gyfeiriadau
Orthologau
SpeciesBod dynolLlygoden
Entrez

6611

n/a

Ensembl

ENSG00000102172

n/a

UniProt

P52788

n/a

RefSeq (mRNA)

NM_001258423
NM_004595

n/a

RefSeq (protein)

NP_001245352
NP_004586

n/a

Lleoliad (UCSC)n/an/a
PubMed search[1]n/a
Wicidata
Gweld/Golygu Bod dynol

Protein sy'n cael ei godio yn y corff dynol gan y genyn SMS yw SMS a elwir hefyd yn Spermine synthase (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn blaen o gromosom X dynol, band Xp22.11.[2]

Cyfystyron

Yn aml mae gan enynnau lawer o gyfystyron. Mae hyn oherwydd eu bod yn aml yn cael eu darganfod gan nifer o bobl mewn cyd-destunau gwahanol heb wybod mai'r un genynnau oeddyn nhw. Hefyd mae gan wahanol gymunedau gwyddonol safonau gwahanol ar gyfer enwi genynnau. Dyma restr o gyfystyron ar gyfer y genyn SMS.

  • SRS
  • SpS
  • MRSR
  • SPMSY

Llyfryddiaeth

  • "Enhancing human spermine synthase activity by engineered mutations. ". PLoS Comput Biol. 2013. PMID 23468611.
  • "A rational free energy-based approach to understanding and targeting disease-causing missense mutations. ". J Am Med Inform Assoc. 2013. PMID 23408511.
  • "Revealing the Effects of Missense Mutations Causing Snyder-Robinson Syndrome on the Stability and Dimerization of Spermine Synthase. ". Int J Mol Sci. 2016. PMID 26761001.
  • Snyder-Robinson Syndrome. 1993. PMID 23805436.
  • "A Y328C missense mutation in spermine synthase causes a mild form of Snyder-Robinson syndrome.". Hum Mol Genet. 2013. PMID 23696453.

Cyfeiriadau

  1. ↑ "Human PubMed Reference:".
  2. ↑ SMS - Cronfa NCBI

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