PWP2

PWP2

PWP2

Protein-coding gene in the species Homo sapiens


Periodic tryptophan protein 2 homolog is a protein that in humans is encoded by the PWP2 gene.[5][6]

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Function

This protein is involved in the assembly of small subunit of ribosome.[6]


References

  1. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  2. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. Yamakawa K, Gao DQ, Korenberg JR (Dec 1996). "A periodic tryptophan protein 2 gene homologue (PWP2H) in the candidate region of progressive myoclonus epilepsy on 21q22.3". Cytogenet Cell Genet. 74 (1–2): 140–5. doi:10.1159/000134402. PMID 8893822.

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