ABHD11, WBSCR21, PP1226, Abhydrolase domain-containing protein 11, Williams-Beuren syndrome chromosomal region 21 protein
This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Mar 2016],caution:It is uncertain whether Met-1 or Met-10 is the initiator.,sequence caution:Wrong choice of frame.,similarity:Belongs to the AB hydrolase superfamily.,tissue specificity:Ubiquitously expressed.,
