Homo sapiens Protein: ABHD11
Summary
InnateDB Protein IDBP-377863.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ABHD11
Protein Name abhydrolase domain containing 11
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000392945
InnateDB Gene IDBG-20342 (ABHD11)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations Note=ABHD11 is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region.
Tissue Specificity Ubiquitously expressed. {ECO:0000269PubMed:12073013}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
Experimentally validated
Total 5 [view]
Protein-Protein 5 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
GO:0016787 hydrolase activity
Biological Process
GO:0008150 biological_process
GO:0008152 metabolic process
Cellular Component
GO:0005575 cellular_component
Protein Structure and Domains
PDB ID
InterPro IPR029058 Alpha/Beta hydrolase fold
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8NFV4
PhosphoSite PhosphoSite-Q8NFV4
TrEMBL
UniProt Splice Variant
Entrez Gene 83451
UniGene Hs.647045
RefSeq
HUGO HGNC:16407
OMIM
CCDS
HPRD 15658
IMGT
EMBL AC073846 AF217971 AF412030 AF412031 AF412032 AY053499 AY053500 BC008251 BC011712 BC067750
GenPept AAG17214 AAH08251 AAH11712 AAH67750 AAL14848 AAL14849 AAM62312 AAM62313 AAM62314 AAS07472