ⓘ WBSCR22

                                     

ⓘ WBSCR22

Uncharacterized methyltransferase WBSCR22 is an enzyme that in humans is encoded by the WBSCR22 gene.

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, Multisystem developmental pathology caused by deletion of contiguous genes at 7q11.23.

                                     
  • Grzeschik KH Apr 2002 Characterization of two novel genes, WBSCR 20 and WBSCR22 deleted in Williams - Beuren syndrome Cytogenet Cell Genet. 95 1 2
  • protein 3 is an enzyme that in humans is encoded by the WBSCR 17 gene. This gene encodes an N - acetylgalactosaminyltransferase, which has
  • Hum. Genet. 8 3 215 22 doi: 10.1038 sj.ejhg.5200435. PMID 10780788. Cairo S, Merla G, Urbinati F, et al. 2001 WBSCR 14, a gene mapping to the
  • NSUN5 POR RFC2 STX1A TBL2 TRIM50 TRIM73 TRIM74 WBSCR 14 WBSCR 18 WBSCR 21 WBSCR22 WBSCR 23 WBSCR 24 WBSCR 27 WBSCR 28 Williams syndrome is a microdeletion syndrome
  • X Cairo S, Merla G, Urbinati F, Ballabio A, Reymond A March 2001 WBSCR 14, a gene mapping to the Williams - - Beuren syndrome deleted region, is a
  • PMID 9184233. Cairo S, Merla G, Urbinati F, Ballabio A, Reymond A Mar 2001 WBSCR 14, a gene mapping to the Williams - - Beuren syndrome deleted region, is a
  • Peoples RJ, Cisco MJ, Kaplan P, Francke U Feb 1999 Identification of the WBSCR 9 gene, encoding a novel transcriptional regulator, in the Williams - Beuren
  • PMID 12418961. Cairo S, Merla G, Urbinati F, Ballabio A, Reymond A March 2001 WBSCR 14, a gene mapping to the Williams - - Beuren syndrome deleted region, is a
  • Green ED 2001 Divergent human and mouse orthologs of a novel gene WBSCR 15 Wbscr 15 reside within the genomic interval commonly deleted in Williams syndrome