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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

NOP2/Sun domain family, member 5 pseudogene 2

This gene shares high sequence similarity with several genes in the Williams Beuren Syndrome critical region and its deletion is associated with this disorder. Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Feb 2010] (from NCBI)
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Top mentioned proteins: SET, fibrillin-1, RCC1, elastin
Papers on WBSCR20B
A map of human protein interactions derived from co-expression of human mRNAs and their orthologs.
Marcotte et al., Austin, United States. In Mol Syst Biol, 2007
We further validate uncharacterized proteins implicated by the associations in ribosome biogenesis, including WBSCR20C, associated with Williams-Beuren syndrome.
Identification of additional transcripts in the Williams-Beuren syndrome critical region.
Reymond et al., Genève, Switzerland. In Hum Genet, 2002
Here, we report the characterization of WBSCR16, WBSCR17, WBSCR18, WBSCR20A, WBSCR20B, WBSCR20C, WBSCR21, WBSCR22, and WBSCR23, nine novel genes contained in the WBS commonly deleted region or its flanking sequences.
Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome.
Grzeschik et al., Marburg an der Lahn, Germany. In Cytogenet Cell Genet, 2000
A highly similar putative gene, WBSCR20B, flanks the WBS deletion at the telomeric side.
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