P09544 (WNT2_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 128.
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-2 Alternative name(s): Int-1-like protein 1 Int-1-related protein Short name=IRP | ||||
| Gene names |
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| 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 | 360 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein. May be a signaling molecule which affects the development of discrete regions of tissues. Is likely to signal over only few cell diameters. |
| Subcellular location | |
| Tissue specificity | Expressed in brain in the thalamus, in fetal and adult lung and in placenta. Ref.6 |
| Post-translational modification | Palmitoylation at Ser-212 is required for efficient binding to frizzled receptors. It is also required for subsequent palmitoylation at Cys-76. Palmitoylation is necessary for proper trafficking to cell surface By similarity. |
| 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 – 25 | 25 | Potential | ||||||
| Chain | 26 – 360 | 335 | Protein Wnt-2 | PRO_0000041410 | |||||
Amino acid modifications | |||||||||
| Lipidation | 76 | 1 | S-palmitoyl cysteine By similarity | ||||||
| Lipidation | 212 | 1 | O-palmitoyl serine; by PORCN By similarity | ||||||
| Glycosylation | 295 | 1 | N-linked (GlcNAc...) Potential | ||||||
Natural variations | |||||||||
| Natural variant | 5 | 1 | L → R. Ref.6 | VAR_013865 | |||||
| Natural variant | 294 | 1 | C → F. Corresponds to variant rs1051751 [ dbSNP | Ensembl ]. | VAR_052954 | |||||
| Natural variant | 299 | 1 | R → W. Ref.6 | VAR_013866 | |||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant wingless." Wainwright B.J., Scambler P.J., Stanier P., Watson E.K., Bell G., Wicking C., Estivill X., Courtney M., Boue A., Pedersen P.S., Williamson R., Farrall M. EMBO J. 7:1743-1748(1988) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA]. Tissue: Lung. |
| [2] | Farrall M. Submitted (APR-1988) to the EMBL/GenBank/DDBJ databases Cited for: SEQUENCE REVISION. |
| [3] | "Cloning of human full-length CDSs in BD Creator(TM) system donor vector." Kalnine N., Chen X., Rolfs A., Halleck A., Hines L., Eisenstein S., Koundinya M., Raphael J., Moreira D., Kelley T., LaBaer J., Lin Y., Phelan M., Farmer A. Submitted (OCT-2004) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. |
| [4] | "The DNA sequence of human chromosome 7." Hillier L.W., Fulton R.S., Fulton L.A., Graves T.A., Pepin K.H., Wagner-McPherson C., Layman D., Maas J., Jaeger S., Walker R., Wylie K., Sekhon M., Becker M.C., O'Laughlin M.D., Schaller M.E., Fewell G.A., Delehaunty K.D., Miner T.L. Wilson R.K.Nature 424:157-164(2003) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [5] | "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] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. Tissue: Brain, Lung and Testis. |
| [6] | "Evidence supporting WNT2 as an autism susceptibility gene." Wassink T.H., Piven J., Vieland V.J., Huang J., Swiderski R.E., Pietila J., Braun T., Beck G., Folstein S.E., Haines J.L., Sheffield V.C. Am. J. Med. Genet. 105:406-413(2001) [PubMed] [Europe PMC] [Abstract] Cited for: VARIANTS ARG-5 AND TRP-299, TISSUE SPECIFICITY. |
| [7] | "No association between the WNT2 gene and autistic disorder." McCoy P.A., Shao Y., Wolpert C.M., Donnelly S.L., Ashley-Koch A., Abel H.L., Ravan S.A., Abramson R.K., Wright H.H., DeLong G.R., Cuccaro M.L., Gilbert J.R., Pericak-Vance M.A. Am. J. Med. Genet. 114:106-109(2002) [PubMed] [Europe PMC] [Abstract] Cited for: SHOWS THAT WNT2 IS NOT LINKED TO AUTISM SUSCEPTIBILITY. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | X07876 mRNA. Translation: CAA30725.1. BT019608 mRNA. Translation: AAV38415.1. AC002465 Genomic DNA. Translation: AAB67043.1. AC006326 Genomic DNA. Translation: AAD28351.1. BC029854 mRNA. Translation: AAH29854.1. BC078170 mRNA. Translation: AAH78170.1. |
| IPI | IPI00015175. |
| PIR | S00834. |
| RefSeq | NP_003382.1. NM_003391.2. |
| UniGene | Hs.567356. |
3D structure databases | |
| ProteinModelPortal | P09544. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | P09544. 4 interactions. |
| STRING | 9606.ENSP00000265441. |
PTM databases | |
| PhosphoSite | P09544. |
Polymorphism databases | |
| DMDM | 139750. |
Proteomic databases | |
| PaxDb | P09544. |
| PRIDE | P09544. |
Protocols and materials databases | |
| DNASU | 7472. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000265441; ENSP00000265441; ENSG00000105989. |
| GeneID | 7472. |
| KEGG | hsa:7472. |
| UCSC | uc003viz.3. human. |
Organism-specific databases | |
| CTD | 7472. |
| GeneCards | GC07M116916. |
| HGNC | HGNC:12780. WNT2. |
| HPA | CAB017098. HPA020920. |
| MIM | 147870. gene. |
| neXtProt | NX_P09544. |
| PharmGKB | PA37381. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG284879. |
| HOGENOM | HOG000039529. |
| HOVERGEN | HBG001595. |
| InParanoid | P09544. |
| KO | K00182. |
| OMA | DVMRAIG. |
| OrthoDB | EOG4255SV. |
| PhylomeDB | P09544. |
Enzyme and pathway databases | |
| Reactome | REACT_111102. Signal Transduction. |
Gene expression databases | |
| ArrayExpress | P09544. |
| Bgee | P09544. |
| CleanEx | HS_WNT2. |
| Genevestigator | P09544. |
| GermOnline | ENSG00000105989. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR005817. Wnt. IPR009140. Wnt2. IPR018161. Wnt_CS. [Graphical view] |
| PANTHER | PTHR12027. PTHR12027. 1 hit. PTHR12027:SF21. PTHR12027:SF21. 1 hit. |
| Pfam | PF00110. wnt. 1 hit. [Graphical view] |
| PRINTS | PR01842. WNT2PROTEIN. PR01349. WNTPROTEIN. |
| SMART | SM00097. WNT1. 1 hit. [Graphical view] |
| PROSITE | PS00246. WNT1. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| BindingDB | P09544. |
| ChEMBL | CHEMBL1255132. |
| GenomeRNAi | 7472. |
| NextBio | 29268. |
| SOURCE | Search... |
Entry information
| Entry name | WNT2_HUMAN | ||||||||
| Accession | Primary (citable) accession number: P09544 Secondary accession number(s): Q75N05, Q9UDP9 | ||||||||
| 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 7 Human chromosome 7: 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
