Q93098 (WNT8B_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 1, 2013.
Version 113.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Protein Wnt-8b | ||
| Gene names |
| ||
| Organism | Homo sapiens (Human) [Reference proteome] | ||
| Taxonomic identifier | 9606 [NCBI] | ||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 351 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| 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 | |
| Tissue specificity | Expression is restricted to the brain, and more specifically to the forebrain. Ref.1 |
| Sequence similarities | Belongs to the Wnt family. |
Ontologies
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 22 | 22 | Potential | ||||||
| Chain | 23 – 351 | 329 | Protein Wnt-8b | PRO_0000041450 | |||||
Amino acid modifications | |||||||||
| Glycosylation | 103 | 1 | N-linked (GlcNAc...) Potential | ||||||
| Glycosylation | 259 | 1 | N-linked (GlcNAc...) Potential | ||||||
Natural variations | |||||||||
| Natural variant | 11 | 1 | C → S. Corresponds to variant rs3793771 [ dbSNP | Ensembl ]. | VAR_020310 | |||||
| Natural variant | 53 | 1 | E → Q in a colorectal cancer sample; somatic mutation. Ref.5 | VAR_036288 | |||||
Experimental info | |||||||||
| Sequence conflict | 230 | 1 | G → A Ref.1 | ||||||
| Sequence conflict | 230 | 1 | G → A Ref.4 | ||||||
| Sequence conflict | 284 | 1 | R → L Ref.1 | ||||||
| Sequence conflict | 284 | 1 | R → L Ref.4 | ||||||
Sequences
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References
| « 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] [Europe PMC] [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] [Europe PMC] [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. Rogers J.Nature 429:375-381(2004) [PubMed] [Europe PMC] [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] [Europe PMC] [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. Velculescu V.E.Science 314:268-274(2006) [PubMed] [Europe PMC] [Abstract] Cited for: VARIANT [LARGE SCALE ANALYSIS] GLN-53. |
| + | Additional computationally mapped references. |
Cross-references
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. |
| IPI | IPI00004125. |
| RefSeq | NP_003384.2. NM_003393.3. |
| UniGene | Hs.421281. |
3D structure databases | |
| ProteinModelPortal | Q93098. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | 9606.ENSP00000340677. |
PTM databases | |
| PhosphoSite | Q93098. |
Polymorphism databases | |
| DMDM | 66774217. |
Proteomic databases | |
| PaxDb | Q93098. |
| PRIDE | Q93098. |
Protocols and materials databases | |
| DNASU | 7479. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000343737; ENSP00000340677; ENSG00000075290. |
| GeneID | 7479. |
| KEGG | hsa:7479. |
| UCSC | uc001krb.3. human. |
Organism-specific databases | |
| CTD | 7479. |
| GeneCards | GC10P102212. |
| HGNC | HGNC:12789. WNT8B. |
| HPA | HPA036570. |
| MIM | 601396. gene. |
| neXtProt | NX_Q93098. |
| PharmGKB | PA37390. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG277037. |
| HOGENOM | HOG000039529. |
| HOVERGEN | HBG001595. |
| InParanoid | Q93098. |
| KO | K00714. |
| OMA | KYFCVRK. |
| OrthoDB | EOG4CNQRC. |
| PhylomeDB | Q93098. |
Enzyme and pathway databases | |
| Reactome | REACT_111102. Signal Transduction. |
Gene expression databases | |
| Bgee | Q93098. |
| CleanEx | HS_WNT8B. |
| Genevestigator | Q93098. |
| GermOnline | ENSG00000075290. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR005817. Wnt. IPR013301. Wnt8. IPR018161. Wnt_CS. [Graphical view] |
| PANTHER | PTHR12027. PTHR12027. 1 hit. PTHR12027:SF6. PTHR12027:SF6. 1 hit. |
| Pfam | PF00110. wnt. 1 hit. [Graphical view] |
| PRINTS | PR01892. WNT8PROTEIN. PR01349. WNTPROTEIN. |
| SMART | SM00097. WNT1. 1 hit. [Graphical view] |
| PROSITE | PS00246. WNT1. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 7479. |
| NextBio | 29296. |
| SOURCE | Search... |
Entry information
| Entry name | WNT8B_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q93098 Secondary accession number(s): O00771, Q5VX55, Q8WYK9 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any 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 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 |

Clusters with
