Homo sapiens Protein: WDR65
Summary
InnateDB Protein IDBP-97364.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol WDR65
Protein Name WD repeat domain 65
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000361570
InnateDB Gene IDBG-408221 (WDR65)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations Van der Woude syndrome 2 (VWS2) [MIM:606713]: An autosomal dominant developmental disorder characterized by lower lip pits, cleft lip and/or cleft palate. {ECO:0000269PubMed:21574244}. Note=The disease may be 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 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
Cellular Component
Protein Structure and Domains
PDB ID
InterPro IPR001680 WD40 repeat
IPR009053 Prefoldin
IPR011047 Quinonprotein alcohol dehydrogenase-like superfamily
IPR017986 WD40-repeat-containing domain
PFAM PF00400
PRINTS
PIRSF
SMART SM00320
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q96MR6
PhosphoSite PhosphoSite-Q96MR6
TrEMBL E9PRV3
UniProt Splice Variant
Entrez Gene 149465
UniGene Hs.739028
RefSeq XP_005270577
HUGO HGNC:26485
OMIM 614259
CCDS
HPRD 08717
IMGT
EMBL AC093420 AK056562 AL139138 BC117280 BC117306
GenPept AAI17281 AAI17307 BAB71217 CAI18963