ⓘ WBSCR17

                                     

ⓘ WBSCR17

Putative polypeptide N-acetylgalactosaminyltransferase-like protein 3 is an enzyme that in humans is encoded by the WBSCR17 gene.

This gene encodes N-acetylgalactosaminyltransferase, which has 97% sequence identity with the mouse protein. This gene is deleted in Williams syndrome, Multisystem developmental pathology caused by deletion of contiguous genes at 7q11.23.

                                     
  • protein - like 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
  • 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
  • leucine rich repeats URG4: up - regulated gene 4 WBSCR17 polypeptide N - acetylgalactosaminyltransferase 17 WDR91 encoding protein WD repeat domain 91 ZC3HAV1:
  • 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
  • NSUN5 POR RFC2 STX1A TBL2 TRIM50 TRIM73 TRIM74 WBSCR 14 WBSCR 18 WBSCR 21 WBSCR 22 WBSCR 23 WBSCR 24 WBSCR 27 WBSCR 28 Williams syndrome is a microdeletion syndrome
  • 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