Homo sapiens Gene: WDR65
Summary
InnateDB Gene IDBG-408221.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol WDR65
Gene Name WD repeat domain 65
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000243710
Encoded Proteins
WD repeat domain 65
WD repeat domain 65
WD repeat domain 65
WD repeat domain 65
WD repeat domain 65
WD repeat domain 65
cilia and flagella associated protein 57
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This protein encoded by this gene belongs to the WD repeat-containing family of proteins, which function in the formation of protein-protein complexes in a variety of biological pathways. This family member is thought to function in craniofacial development, possibly in the fusion of lip and palate. A missense mutation in this gene is associated with Van der Woude syndrome 2. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 1:43172149-43254358
Strand Forward strand
Band p34.2
Transcripts
ENST00000372492 ENSP00000361570
ENST00000428122 ENSP00000416933
ENST00000528956 ENSP00000435310
ENST00000529956 ENSP00000434133
ENST00000525227 ENSP00000434671
ENST00000533339 ENSP00000432547
ENST00000534615
ENST00000610710 ENSP00000479773
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
GO:0016192 vesicle-mediated transport
Cellular Component
GO:0016020 membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.735676 Hs.739028
RefSeq NM_001167965 NM_001195831 NM_152498 XM_005270520 XM_006710382 XM_006710383
HUGO
OMIM
CCDS CCDS479 CCDS72768
HPRD 08717
IMGT
EMBL
GenPept
RNA Seq Atlas