Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
116966
Gene name Gene Name - the full gene name approved by the HGNC.
WD repeat domain 17
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
WDR17
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q34.2
Summary Summary of gene provided in NCBI Entrez Gene.
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
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017936 hsa-miR-335-5p Microarray 18185580
MIRT707195 hsa-miR-4789-3p HITS-CLIP 21572407
MIRT707194 hsa-miR-4643 HITS-CLIP 21572407
MIRT707193 hsa-miR-5580-3p HITS-CLIP 21572407
MIRT707192 hsa-miR-466 HITS-CLIP 21572407
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
609005 16661 ENSG00000150627
Protein
UniProt ID Q8IZU2
Protein name WD repeat-containing protein 17
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00400 WD40 73 112 WD domain, G-beta repeat Repeat
PF12894 ANAPC4_WD40 400 491 Anaphase-promoting complex subunit 4 WD40 domain Repeat
PF00400 WD40 556 595 WD domain, G-beta repeat Repeat
PF00400 WD40 599 638 WD domain, G-beta repeat Repeat
PF00400 WD40 642 681 WD domain, G-beta repeat Repeat
Sequence
MAWMTYISNWFEQDDWYEGLQRANMSQVRQVGLLAAGCQPWNKDVCAASGDRFAYCATLA
IYIYQLDHRYNEFKLHAIMSEHKKTITAISWCPHNPDLFASGSTDNLVIIWNVAEQKVIA
KLDSTKGIPASLSWCWNAEDVVAFVSHRGPLFIWTISGPDSGVIVHKDAHSFLSDICMFR
WHTHQKGKVVFGHIDGSLSIFHPGNKNQKHVLRPESLEGTDEEDPVTALEWDPLSTDYLL
VVNLHYGIRLVDSESLSCITTFNLPSAAASVQCLAWVPSAPGMFITGDSQVGVLRIWNVS
RTTPIDNLKLKKTGFHCLHVLNSPPRKKFSVQSPTKNHYTSSTSEAVPPPTLTQNQAFSL
PPGHAVCCFLDGGVGLYDMGAKKWDFLRDLGHVETIFDCKFKPDDPNLLATASFDGTIKV
WDINTLTAVYTSPGNEGVIYSLSWAPGGLNCIAGGTSRNGAFIWNVQKGKIIQRFNEHGT
NGIFCIAWSHK
DSKRIATCSSDGFCIIRTIDGKVLHKYKHPAAVFGCDWSQNNKDMIATG
CEDTNVRVYYVATSSDQPLKVFSGHTAKVFHVKWSPLREGILCSGSDDGTVRIWDYTQDA
CINILNGHTAPVRGLMWNTEIPYLLISGSWDYTIKVWD
TREGTCVDTVYDHGADVYGLTC
HPSRPFTMASCSRDSTVRLWS
LTALVTPVQINILADRSWEEIIGNTDYAIEPGTPPLLCG
KVSRDIRQEIEKLTANSQVKKLRWFSECLSPPGGSDNLWNLVAVIKGQDDSLLPQNYCKG
IMHLKHLIKFRTSEAQELTTVKMSKFGGGIGVPAKEERLKEAAEIHLRLGQIQRYCELMV
ELGEWDKALSIAPGVSVKYWKKLMQRRADQLIQEDKDDVIPYCIAIGDVKKLVHFFMSRG
QLKEALLVAQAACEGNMQPLHVSVPKGASYSDDIYKEDFNELLHKVSKELAEWYFQDGRA
VLAACCHLAIDNIELAMAYLIRGNELELAVCVGTVLGESAAPATHYALELLARKCMMISV
CFPCVGYSVPFCYVNRNLAADLLLMIPDNELHLIKLCAFYPGCTEEINDLHDKCKLPTVE
ECMQLAETARADDNIFETVKYYLLSQEPEKALPIGISFVKEYISSSDWTLDTIYPVLDLL
SYIRTEKLLLHTCTEARNELLILCGYIGALLAIRRQYQSIVPALYEYTSQLLKRREVSVP
LKIEYLSEELDAWRACTQSTNRSLEDSPYTPPSDSQRMIYATLLKRLKEESLKGIIGPDY
VTGSNLPSHSDIHISCLTGLKIQGPVFFLEDGKSAISLNDALMWAKVNPFSPLGTGIRLN
PF
Sequence length 1322
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Insomnia Insomnia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Lymphoma T Cell Peripheral Associate 26536348