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DNM3

Introduction

Dynamin-3 is a protein that in humans is encoded by the DNM3 gene.[1][2] The protein encoded by this gene is a member of the dynamin family which possess mechanochemical properties involved in actin-membrane processes, predominantly in membrane budding.[3] DNM3 is upregulated in Sézary’s syndrome.[4]

References

References

  1. ↑ Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (May 1999). “Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro”. DNA Res. 5 (6): 355–64. doi:10.1093/dnares/5.6.355. PMID 10048485.
  2. ↑ “Entrez Gene: DNM3 dynamin 3”.
  3. ↑ Orth JD, McNiven MA (February 2003). “Dynamin at the actin-membrane interface”. Curr. Opin. Cell Biol. 15 (1): 31–9. doi:10.1016/S0955-0674(02)00010-8. PMID 12517701.
  4. ↑ Booken N, Gratchev A, Utikal J, Weiss C, Yu X, Qadoumi M, Schmuth M, Sepp N, Nashan D, Rass K, Tüting T, Assaf C, Dippel E, Stadler R, Klemke CD, Goerdt S (February 2008). “Sézary syndrome is a unique cutaneous T-cell lymphoma as identified by an expanded gene signature including diagnostic marker molecules CDO1 and DNM3”. Leukemia. 22 (2): 393–9. doi:10.1038/sj.leu.2405044. PMID 18033314.
Further reading

Further reading