Homo sapiens Gene: WDR17
Summary
InnateDB Gene IDBG-45238.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol WDR17
Gene Name WD repeat domain 17
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000150627
Encoded Proteins
WD repeat domain 17
WD repeat domain 17
WD repeat domain 17
WD repeat domain 17
WD repeat domain 17
WD repeat domain 17
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a WD repeat-containing protein. It is abundantly expressed in retina and testis, and is thought to be a candidate gene for retinal disease. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 4:176065834-176182818
Strand Forward strand
Band q34.2
Transcripts
ENST00000280190 ENSP00000280190
ENST00000443118 ENSP00000426985
ENST00000508596 ENSP00000422763
ENST00000509792
ENST00000507824 ENSP00000422200
ENST00000513261 ENSP00000427502
ENST00000505894 ENSP00000426847
ENST00000508773
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
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.532056 Hs.617434
RefSeq NM_170710 NM_181265 XM_005262722 XM_005262723 XM_005262725 XM_006714078
HUGO
OMIM
CCDS CCDS3825 CCDS43284
HPRD 16417
IMGT
EMBL
GenPept
RNA Seq Atlas