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BUD23, BUD23 rRNA methyltransferase and ribosome maturation factor

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BUD23, BUD23 rRNA methyltransferase and ribosome maturation factor

  • This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011]

  • Gene Synonyms (HASJ4442, HUSSY-3, MERM1, PP3381, WBMT, WBSCR22, probable 18S rRNA (guanine-N(7))-methyltransferase, Williams-Beuren candidate region putative methyltransferase, Williams-Beuren syndrome chromosomal region 22 protein, Williams-Beuren syndrome chromosome region 22, bud site selection protein 23 homolog, metastasis-related methyltransferase 1, rRNA methyltransferase and ribosome maturation factor, ribosome biogenesis methyltransferase WBSCR22,)
  • NCBI Gene ID: 114049
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>O43709
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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

BUD23 rRNA methyltransferase and ribosome maturation factor interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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