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NSUN5

NOP2/Sun domain family, member 5

NSUN5 is a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms.

Gene Name: NOP2/Sun domain family, member 5
Synonyms: NSUN5, p120, NOL1-related protein, NOL1R, WBSCR20, Ynl022cL, NOL1, NSUN5A, WBSCR20A
Target Sequences: NM_018044 NP_060514.1 Q96P11

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PLEASE NOTE

For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).