WBSCR17: Proteins and Enzymes
WBSCR17 encodes an N-acetylgalactosaminyltransferase, which has 97% sequence identity to the mouse protein. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq]
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2 results for "WBSCR17 Proteins and Enzymes" in Products
2 results for "WBSCR17 Proteins and Enzymes" in Products
WBSCR17: Proteins and Enzymes
WBSCR17 encodes an N-acetylgalactosaminyltransferase, which has 97% sequence identity to the mouse protein. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq]
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| Applications: | WB, ELISA, MA, AP |
| Applications: | AC |