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Q9BV38 (WDR18_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 92. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
WD repeat-containing protein 18
Gene names
Name:WDR18
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length432 AA.
Sequence statusComplete.
Protein existenceEvidence at protein level

General annotation (Comments)

Function

May play a role during development By similarity.

Sequence similarities

Belongs to the WD repeat WDR18 family.

Contains 6 WD repeats.

Sequence caution

The sequence AAC12679.1 differs from that shown. Reason: Erroneous initiation. Translation N-terminally shortened.

Ontologies

Keywords
   Coding sequence diversityPolymorphism
   DomainRepeat
WD repeat
   Molecular functionDevelopmental protein
   PTMPhosphoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological processmulticellular organismal development

Inferred from electronic annotation. Source: UniProtKB-KW

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 432432WD repeat-containing protein 18
PRO_0000051365

Regions

Repeat36 – 7540WD 1
Repeat78 – 11639WD 2
Repeat119 – 15840WD 3
Repeat170 – 21142WD 4
Repeat213 – 25745WD 5
Repeat267 – 30640WD 6

Amino acid modifications

Modified residue611Phosphotyrosine Ref.3

Natural variations

Natural variant1721A → T. Ref.2
Corresponds to variant rs2158367 [ dbSNP | Ensembl ].
VAR_031577
Natural variant2131L → F.
Corresponds to variant rs35068100 [ dbSNP | Ensembl ].
VAR_031578
Natural variant2641V → I.
Corresponds to variant rs11538683 [ dbSNP | Ensembl ].
VAR_031579

Experimental info

Sequence conflict198 – 1992Missing in AAC12679. Ref.1

Sequences

Sequence LengthMass (Da)Tools
Q9BV38 [UniParc].

Last modified April 3, 2007. Version 2.
Checksum: 0E00FA0DF124F82C

FASTA43247,405
        10         20         30         40         50         60 
MAAPMEVAVC TDSAAPMWSC IVWELHSGAN LLTYRGGQAG PRGLALLNGE YLLAAQLGKN 

        70         80         90        100        110        120 
YISAWELQRK DQLQQKIMCP GPVTCLTASP NGLYVLAGVA ESIHLWEVST GNLLVILSRH 

       130        140        150        160        170        180 
YQDVSCLQFT GDSSHFISGG KDCLVLVWSL CSVLQADPSR IPAPRHVWSH HALPITDLHC 

       190        200        210        220        230        240 
GFGGPLARVA TSSLDQTVKL WEVSSGELLL SVLFDVSIMA VTMDLAEHHM FCGGSEGSIF 

       250        260        270        280        290        300 
QVDLFTWPGQ RERSFHPEQD AGKVFKGHRN QVTCLSVSTD GSVLLSGSHD ETVRLWDVQS 

       310        320        330        340        350        360 
KQCIRTVALK GPVTNAAILL APVSMLSSDF RPSLPLPHFN KHLLGAEHGD EPRHGGLTLR 

       370        380        390        400        410        420 
LGLHQQGSEP SYLDRTEQLQ AVLCSTMEKS VLGGQDQLRV RVTELEDEVR NLRKINRDLF 

       430 
DFSTRFITRP AK 

« Hide

References

[1]"The DNA sequence and biology of human chromosome 19."
Grimwood J., Gordon L.A., Olsen A.S., Terry A., Schmutz J., Lamerdin J.E., Hellsten U., Goodstein D., Couronne O., Tran-Gyamfi M., Aerts A., Altherr M., Ashworth L., Bajorek E., Black S., Branscomb E., Caenepeel S., Carrano A.V. expand/collapse author list , Caoile C., Chan Y.M., Christensen M., Cleland C.A., Copeland A., Dalin E., Dehal P., Denys M., Detter J.C., Escobar J., Flowers D., Fotopulos D., Garcia C., Georgescu A.M., Glavina T., Gomez M., Gonzales E., Groza M., Hammon N., Hawkins T., Haydu L., Ho I., Huang W., Israni S., Jett J., Kadner K., Kimball H., Kobayashi A., Larionov V., Leem S.-H., Lopez F., Lou Y., Lowry S., Malfatti S., Martinez D., McCready P.M., Medina C., Morgan J., Nelson K., Nolan M., Ovcharenko I., Pitluck S., Pollard M., Popkie A.P., Predki P., Quan G., Ramirez L., Rash S., Retterer J., Rodriguez A., Rogers S., Salamov A., Salazar A., She X., Smith D., Slezak T., Solovyev V., Thayer N., Tice H., Tsai M., Ustaszewska A., Vo N., Wagner M., Wheeler J., Wu K., Xie G., Yang J., Dubchak I., Furey T.S., DeJong P., Dickson M., Gordon D., Eichler E.E., Pennacchio L.A., Richardson P., Stubbs L., Rokhsar D.S., Myers R.M., Rubin E.M., Lucas S.M.
Nature 428:529-535(2004) [PubMed: 15057824] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[2]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT THR-172.
Tissue: Brain and Lung.
[3]"Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer."
Rikova K., Guo A., Zeng Q., Possemato A., Yu J., Haack H., Nardone J., Lee K., Reeves C., Li Y., Hu Y., Tan Z., Stokes M., Sullivan L., Mitchell J., Wetzel R., Macneill J., Ren J.M. expand/collapse author list , Yuan J., Bakalarski C.E., Villen J., Kornhauser J.M., Smith B., Li D., Zhou X., Gygi S.P., Gu T.-L., Polakiewicz R.D., Rush J., Comb M.J.
Cell 131:1190-1203(2007) [PubMed: 18083107] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT TYR-61, MASS SPECTROMETRY.
Tissue: Lung carcinoma.
[4]"Initial characterization of the human central proteome."
Burkard T.R., Planyavsky M., Kaupe I., Breitwieser F.P., Buerckstuemmer T., Bennett K.L., Superti-Furga G., Colinge J.
BMC Syst. Biol. 5:17-17(2011) [PubMed: 21269460] [Abstract]
Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AC004528 Genomic DNA. Translation: AAC12679.1. Different initiation.
BC000040 mRNA. Translation: AAH00040.2.
BC001648 mRNA. Translation: AAH01648.1.
IPIIPI00032533.
RefSeqNP_077005.2. NM_024100.3.
UniGeneHs.325321.

3D structure databases

ProteinModelPortalQ9BV38.
SMRQ9BV38. Positions 13-407.
ModBaseSearch...

Protein-protein interaction databases

IntActQ9BV38. 5 interactions.
MINTMINT-1388285.
STRINGQ9BV38.

PTM databases

PhosphoSiteQ9BV38.

Polymorphism databases

DMDM143811475.

Proteomic databases

PeptideAtlasQ9BV38.
PRIDEQ9BV38.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000251289; ENSP00000251289; ENSG00000065268.
GeneID57418.
KEGGhsa:57418.
NMPDRfig|9606.3.peg.15250.
UCSCuc002lqm.1. human.

Organism-specific databases

CTD57418.
GeneCardsGC19P000935.
H-InvDBHIX0014566.
HGNCHGNC:17956. WDR18.
neXtProtNX_Q9BV38.
PharmGKBPA38269.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG16435.
GeneTreeENSGT00390000000289.
HOGENOMHBG717431.
HOVERGENHBG059735.
InParanoidQ9BV38.
OMAFCGGSDG.
OrthoDBEOG4PZJ6K.
PhylomeDBQ9BV38.

Gene expression databases

ArrayExpressQ9BV38.
BgeeQ9BV38.
CleanExHS_WDR18.
GenevestigatorQ9BV38.
GermOnlineENSG00000065268. Homo sapiens.

Family and domain databases

InterProIPR020472. G-protein_beta_WD-40_rep.
IPR015943. WD40/YVTN_repeat-like_dom.
IPR001680. WD40_repeat.
IPR011046. WD40_repeat-like_dom.
IPR019775. WD40_repeat_CS.
IPR017986. WD40_repeat_dom.
[Graphical view]
Gene3DG3DSA:2.130.10.10. WD40/YVTN_repeat-like. 1 hit.
PfamPF00400. WD40. 3 hits.
[Graphical view]
PRINTSPR00320. GPROTEINBRPT.
SMARTSM00320. WD40. 4 hits.
[Graphical view]
SUPFAMSSF50978. WD40_like. 1 hit.
PROSITEPS00678. WD_REPEATS_1. 2 hits.
PS50082. WD_REPEATS_2. 3 hits.
PS50294. WD_REPEATS_REGION. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio63562.

Entry information

Entry nameWDR18_HUMAN
AccessionPrimary (citable) accession number: Q9BV38
Secondary accession number(s): O60390, Q9BWR2
Entry history
Integrated into UniProtKB/Swiss-Prot: May 27, 2002
Last sequence update: April 3, 2007
Last modified: January 25, 2012
This is version 92 of the entry and version 2 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

Relevant documents

Human chromosome 19

Human chromosome 19: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

SIMILARITY comments

Index of protein domains and families