Abhydrolase domain-containing protein 11 also known as Williams-Beuren syndrome chromosomal region 21 protein (WBSCR21) is an
enzyme that in humans is encoded by the ABHD11gene.[5][6]
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.
Alternatively spliced transcript variants have been described, but their biological validity has not been determined.[6]
Abhydrolase domain-containing protein 11 also known as Williams-Beuren syndrome chromosomal region 21 protein (WBSCR21) is an
enzyme that in humans is encoded by the ABHD11gene.[5][6]
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.
Alternatively spliced transcript variants have been described, but their biological validity has not been determined.[6]