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Reviewed, UniProtKB/Swiss-Prot Q93098 (WNT8B_HUMAN)

Last modified July 13, 2010. Version 85. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (5) | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents
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Names and originHide

Protein namesRecommended name:
Protein Wnt-8b
Gene names
Name:WNT8B
OrganismHomo sapiens (Human) [Complete proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo
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Protein attributesHide

Sequence length351 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceEvidence at transcript level.
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General annotation (Comments)Hide

Function

Ligand for members of the frizzled family of seven transmembrane receptors. May play an important role in the development and differentiation of certain forebrain structures, notably the hippocampus. Ref.1

Subcellular location

Secretedextracellular spaceextracellular matrix.

Tissue specificity

Expression is restricted to the brain, and more specifically to the forebrain. Ref.1

Sequence similarities

Belongs to the Wnt family.

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OntologiesHide

Keywords
   Biological processWnt signaling pathway
   Cellular componentExtracellular matrix
Secreted
   Coding sequence diversityPolymorphism
   DomainSignal
   Molecular functionDevelopmental protein
   PTMGlycoprotein
   Technical termComplete proteome
Gene Ontology (GO)
   Biological processWnt receptor signaling pathway, calcium modulating pathway

Inferred from electronic annotation. Source: InterPro

cell-cell signaling

Traceable author statement. Source: ProtInc

nervous system development

Traceable author statement. Source: ProtInc

signal transduction

Traceable author statement. Source: ProtInc

   Cellular componentproteinaceous extracellular matrix

Inferred from electronic annotation. Source: UniProtKB-SubCell

   Molecular functionsignal transducer activity

Traceable author statement. Source: ProtInc

Complete GO annotation...
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Sequence annotation (Features)Hide

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Signal peptide1 – 2222 Potential
Chain23 – 351329Protein Wnt-8b
PRO_0000041450

Amino acid modifications

Glycosylation1031N-linked (GlcNAc...) Potential
Glycosylation2591N-linked (GlcNAc...) Potential

Natural variations

Natural variant111C → S. [dbSNP:rs3793771]
VAR_020310
Natural variant531E → Q in a colorectal cancer sample; somatic mutation. Ref.5
VAR_036288

Experimental info

Sequence conflict2301G → A Ref.1
Sequence conflict2301G → A Ref.4
Sequence conflict2841R → L Ref.1
Sequence conflict2841R → L Ref.4
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SequencesHide

Sequence LengthMass (Da)Tools
Q93098-1 [UniParc].

Last modified May 24, 2005. Version 3.
Checksum: DD242070948813F8

FASTA35138,721
        10         20         30         40         50         60 
MFLSKPSVYI CLFTCVLQLS HSWSVNNFLM TGPKAYLIYS SSVAAGAQSG IEECKYQFAW 

        70         80         90        100        110        120 
DRWNCPERAL QLSSHGGLRS ANRETAFVHA ISSAGVMYTL TRNCSLGDFD NCGCDDSRNG 

       130        140        150        160        170        180 
QLGGQGWLWG GCSDNVGFGE AISKQFVDAL ETGQDARAAM NLHNNEAGRK AVKGTMKRTC 

       190        200        210        220        230        240 
KCHGVSGSCT TQTCWLQLPE FREVGAHLKE KYHAALKVDL LQGAGNSAAG RGAIADTFRS 

       250        260        270        280        290        300 
ISTRELVHLE DSPDYCLENK TLGLLGTEGR ECLRRGRALG RWERRSCRRL CGDCGLAVEE 

       310        320        330        340        350 
RRAETVSSCN CKFHWCCAVR CEQCRRRVTK YFCSRAERPR GGAAHKPGRK P 

« Hide

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ReferencesHide

« Hide 'large scale' references
[1]"A novel mammalian Wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrain."
Lako M., Lindsay S., Bullen P., Wilson D.I., Robson S.C., Strachan T.
Hum. Mol. Genet. 7:813-822(1998) [PubMed: 9536085] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA], FUNCTION, TISSUE SPECIFICITY.
[2]"Up-regulation of WNT8B mRNA in human gastric cancer."
Saitoh T., Mine T., Katoh M.
Int. J. Oncol. 20:343-348(2002) [PubMed: 11788899] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA].
Tissue: Fetal brain.
[3]"The DNA sequence and comparative analysis of human chromosome 10."
Deloukas P., Earthrowl M.E., Grafham D.V., Rubenfield M., French L., Steward C.A., Sims S.K., Jones M.C., Searle S., Scott C., Howe K., Hunt S.E., Andrews T.D., Gilbert J.G.R., Swarbreck D., Ashurst J.L., Taylor A., Battles J. expand/collapse author list , Bird C.P., Ainscough R., Almeida J.P., Ashwell R.I.S., Ambrose K.D., Babbage A.K., Bagguley C.L., Bailey J., Banerjee R., Bates K., Beasley H., Bray-Allen S., Brown A.J., Brown J.Y., Burford D.C., Burrill W., Burton J., Cahill P., Camire D., Carter N.P., Chapman J.C., Clark S.Y., Clarke G., Clee C.M., Clegg S., Corby N., Coulson A., Dhami P., Dutta I., Dunn M., Faulkner L., Frankish A., Frankland J.A., Garner P., Garnett J., Gribble S., Griffiths C., Grocock R., Gustafson E., Hammond S., Harley J.L., Hart E., Heath P.D., Ho T.P., Hopkins B., Horne J., Howden P.J., Huckle E., Hynds C., Johnson C., Johnson D., Kana A., Kay M., Kimberley A.M., Kershaw J.K., Kokkinaki M., Laird G.K., Lawlor S., Lee H.M., Leongamornlert D.A., Laird G., Lloyd C., Lloyd D.M., Loveland J., Lovell J., McLaren S., McLay K.E., McMurray A., Mashreghi-Mohammadi M., Matthews L., Milne S., Nickerson T., Nguyen M., Overton-Larty E., Palmer S.A., Pearce A.V., Peck A.I., Pelan S., Phillimore B., Porter K., Rice C.M., Rogosin A., Ross M.T., Sarafidou T., Sehra H.K., Shownkeen R., Skuce C.D., Smith M., Standring L., Sycamore N., Tester J., Thorpe A., Torcasso W., Tracey A., Tromans A., Tsolas J., Wall M., Walsh J., Wang H., Weinstock K., West A.P., Willey D.L., Whitehead S.L., Wilming L., Wray P.W., Young L., Chen Y., Lovering R.C., Moschonas N.K., Siebert R., Fechtel K., Bentley D., Durbin R.M., Hubbard T., Doucette-Stamm L., Beck S., Smith D.R., Rogers J.
Nature 429:375-381(2004) [PubMed: 15164054] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[4]"Isolation and characterization of WNT8B, a novel human Wnt gene that maps to 10q24."
Lako M., Strachan T., Curtis A.R.J., Lindsay S.
Genomics 35:386-388(1996) [PubMed: 8661156] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 23-317.
[5]"The consensus coding sequences of human breast and colorectal cancers."
Sjoeblom T., Jones S., Wood L.D., Parsons D.W., Lin J., Barber T.D., Mandelker D., Leary R.J., Ptak J., Silliman N., Szabo S., Buckhaults P., Farrell C., Meeh P., Markowitz S.D., Willis J., Dawson D., Willson J.K.V. expand/collapse author list , Gazdar A.F., Hartigan J., Wu L., Liu C., Parmigiani G., Park B.H., Bachman K.E., Papadopoulos N., Vogelstein B., Kinzler K.W., Velculescu V.E.
Science 314:268-274(2006) [PubMed: 16959974] [Abstract]
Cited for: VARIANT [LARGE SCALE ANALYSIS] GLN-53.
+Additional computationally mapped references.
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Cross-referencesHide

Sequence databases

EMBL
GenBank
DDBJ
Y11094 mRNA. Translation: CAA71968.1.
Y11108 Genomic DNA. Translation: CAA71994.1.
AB073637 mRNA. Translation: BAB83924.1.
AL359759, AL133352 Genomic DNA. Translation: CAH71991.1.
AL133352, AL359759 Genomic DNA. Translation: CAH73565.1.
X91940 mRNA. Translation: CAA63017.1.
IPIIPI00004125.
RefSeqNP_003384.2.
UniGeneHs.421281

3D structure databases

ModBaseSearch...

Protein-protein interaction databases

STRINGQ93098.

Proteomic databases

PRIDEQ93098.

Genome annotation databases

EnsemblENST00000343737; ENSP00000340677; ENSG00000075290; Homo sapiens. [Genome view]
GeneID7479.
KEGGhsa:7479.
UCSCuc001krb.1. human.

Organism-specific databases

CTD7479.
GeneCardsGC10P102212.
H-InvDBHIX0035306.
HGNCHGNC:12789. WNT8B.
MIM601396. gene.
PharmGKBPA37390.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG14592.
HOGENOMHBG446188.
HOVERGENHBG001595.
InParanoidQ93098.
OMAKWEKRSC.
OrthoDBEOG9XH2JW.
PhylomeDBQ93098.

Enzyme and pathway databases

ReactomeREACT_14797. Signaling by GPCR.

Gene expression databases

ArrayExpressQ93098.
BgeeQ93098.
CleanExHS_WNT8B.
GenevestigatorQ93098.
GermOnlineENSG00000075290. Homo sapiens.

Family and domain databases

InterProIPR013301. Wnt8.
IPR005816. Wnt_grthfactor.
IPR018161. Wnt_grthfactor_CS.
IPR005817. Wnt_SF.
[Graphical view]
PANTHERPTHR12027. Wnt. 1 hit.
PfamPF00110. wnt. 1 hit.
[Graphical view]
PRINTSPR01892. WNT8PROTEIN.
PR01349. WNTPROTEIN.
SMARTSM00097. WNT1. 1 hit.
[Graphical view]
PROSITEPS00246. WNT1. 1 hit.
[Graphical view]
ProtoNetSearch...

Other Resources

NextBio29296.
SOURCESearch...
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Entry informationHide

Entry nameWNT8B_HUMAN
AccessionPrimary (citable) accession number: Q93098
Secondary accession number(s): O00771, Q5VX55, Q8WYK9
Entry history
Integrated into UniProtKB/Swiss-Prot: November 1, 1997
Last sequence update: May 24, 2005
Last modified: July 13, 2010
This is version 85 of the entry and version 3 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectHPI (Human Proteome Initiative)
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.
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Relevant documentsHide

Human chromosome 10

Human chromosome 10: 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

MIM cross-references

Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot

SIMILARITY comments

Index of protein domains and families

Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents