Homo sapiens Protein: ANKRD11
Summary
InnateDB Protein IDBP-47308.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ANKRD11
Protein Name ankyrin repeat domain 11
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000301030
InnateDB Gene IDBG-47304 (ANKRD11)
Protein Structure
UniProt Annotation
Function May recruit HDACs to the p160 coactivators/nuclear receptor complex to inhibit ligand-dependent transactivation.
Subcellular Localization Nucleus {ECO:0000269PubMed:15184363, ECO:0000269Ref.1}.
Disease Associations KBG syndrome (KBGS) [MIM:148050]: A syndrome characterized by macrodontia of the upper central incisors, distinctive craniofacial findings, short stature, skeletal anomalies, and neurologic involvement that includes global developmental delay, seizures, and intellectual disability. {ECO:0000269PubMed:21782149}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 18 experimentally validated interaction(s) in this database.
Experimentally validated
Total 18 [view]
Protein-Protein 18 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0001701 in utero embryonic development
GO:0001894 tissue homeostasis
GO:0035264 multicellular organism growth
GO:0042475 odontogenesis of dentin-containing tooth
GO:0048705 skeletal system morphogenesis
GO:0060323 head morphogenesis
GO:0060325 face morphogenesis
GO:0060348 bone development
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005886 plasma membrane
Protein Structure and Domains
PDB ID
InterPro IPR002110 Ankyrin repeat
IPR020683 Ankyrin repeat-containing domain
PFAM PF00023
PF13606
PF11929
PF12796
PRINTS PR01415
PIRSF
SMART SM00248
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q6UB99
PhosphoSite PhosphoSite-Q6UB99
TrEMBL
UniProt Splice Variant
Entrez Gene 29123
UniGene Hs.740440
RefSeq NP_037407
HUGO HGNC:21316
OMIM 611192
CCDS CCDS32513
HPRD 12456
IMGT
EMBL AC137932 AY373756 AY533563 BC069013
GenPept AAH69013 AAR25661 AAS45544