ABHD11 Products

Description

ABHD11 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. [provided by RefSeq]

Bioinformatics

Entrez	83451 Human
Uniprot	NM_148912 Human NP_683710 Human NP_683710.1 Human Q8NFV4 Human
Product By Gene ID	83451
Alternate Names	abhydrolase domain containing 11 abhydrolase domain-containing protein 11 EC 3.- PP1226 WBSCR21 Williams Beuren syndrome chromosome region 21 Williams-Beuren syndrome chromosomal region 21 protein

Research Areas for ABHD11

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Lipid and Metabolism