NSUN5, NOP2/Sun RNA methyltransferase 5

NSUN5, NOP2/Sun RNA methyltransferase 5

• This gene encodes 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. [provided by RefSeq, Jul 2013]

• Gene Synonyms (NOL1, NOL1R, NSUN5A, WBSCR20, WBSCR20A, p120, p120(NOL1), 28S rRNA (cytosine-C(5))-methyltransferase, probable 28S rRNA (cytosine-C(5))-methyltransferase, NOL1-related protein, NOL1/NOP2/Sun domain family member 5, NOP2/Sun RNA methyltransferase family member 5, NOP2/Sun domain family, member 5, NOP2/Sun domain family, member 5A, Williams Beuren syndrome chromosome region 20A, Williams-Beuren syndrome chromosomal region 20A protein, Williams-Beuren syndrome critical region protein 20 copy A, putative methyltransferase NSUN5,)
• NCBI Gene ID: 55695
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q96P11
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

NOP2/Sun RNA methyltransferase 5 interacts with:

• heterogeneous nuclear ribonucleoprotein L like
  pleckstrin homology domain containing A4

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.