P10767 (FGF6_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 1, 2013.
Version 128.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Web links·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Web links·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Fibroblast growth factor 6 Short name=FGF-6 Alternative name(s): Heparin secretory-transforming protein 2 Short name=HST-2 Short name=HSTF-2 Heparin-binding growth factor 6 Short name=HBGF-6 | ||||
| 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 | 208 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 | Plays an important role in the regulation of cell proliferation, cell differentiation, angiogenesis and myogenesis, and is required for normal muscle regeneration. Ref.6 |
| Subunit structure | Interacts with FGFR1, FGFR2 and FGFR4. Affinity between fibroblast growth factors (FGFs) and their receptors is increased by heparan sulfate glycosaminoglycans that function as coreceptors. Ref.6 |
| Subcellular location | |
| Tissue specificity | Leukemia cell lines with platelet/ megakaryocytic differentiation potential. |
| Sequence similarities | Belongs to the heparin-binding growth factors family. |
| Sequence caution | The sequence CAA40359.1 differs from that shown. Reason: Erroneous initiation. The sequence CAA40360.1 differs from that shown. Reason: Erroneous initiation. |
Ontologies
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||||
Molecule processing | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 37 | 37 | Potential | ||||||||
| Chain | 38 – 208 | 171 | Fibroblast growth factor 6 | PRO_0000008961 | |||||||
Amino acid modifications | |||||||||||
| Glycosylation | 45 | 1 | N-linked (GlcNAc...) Potential | ||||||||
| Disulfide bond | 90 ↔ 157 | Potential | |||||||||
Natural variations | |||||||||||
| Natural variant | 36 | 1 | V → A. Ref.2 Corresponds to variant rs11613495 [ dbSNP | Ensembl ]. | VAR_018882 | |||||||
| Natural variant | 63 | 1 | A → V. Ref.2 Corresponds to variant rs17183529 [ dbSNP | Ensembl ]. | VAR_018883 | |||||||
| Natural variant | 174 | 1 | D → V. Ref.2 Corresponds to variant rs7961645 [ dbSNP | Ensembl ]. | VAR_018884 | |||||||
| Natural variant | 191 | 1 | R → W. Ref.2 Corresponds to variant rs17183778 [ dbSNP | Ensembl ]. | VAR_018885 | |||||||
Experimental info | |||||||||||
| Sequence conflict | 100 | 1 | V → G in CAB37648. Ref.5 | ||||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Putative structure of the FGF6 gene product and role of the signal peptide." Coulier F., Batoz M., Marics I., de Lapeyriere O., Birnbaum D. Oncogene 6:1437-1444(1991) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]. |
| [2] | NIEHS SNPs program Submitted (MAR-2004) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA], VARIANTS ALA-36; VAL-63; VAL-174 AND TRP-191. |
| [3] | "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]. |
| [4] | "Human hst-2 (FGF-6) oncogene: cDNA cloning and characterization." Iida S., Yoshida T., Naito K., Sakamoto H., Katoh O., Hirohashi S., Sato T., Onda M., Sugimura T., Terada M. Oncogene 7:303-309(1992) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 11-208. |
| [5] | "Characterization of the HST-related FGF.6 gene, a new member of the fibroblast growth factor gene family." Marics I., Adelaide J., Raybaud F., Mattei M.-G., Coulier F., Planche J., de Lapeyriere O., Birnbaum D. Oncogene 4:335-340(1989) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 81-208. |
| [6] | "Receptor specificity of the fibroblast growth factor family." Ornitz D.M., Xu J., Colvin J.S., McEwen D.G., MacArthur C.A., Coulier F., Gao G., Goldfarb M. J. Biol. Chem. 271:15292-15297(1996) [PubMed] [Europe PMC] [Abstract] Cited for: INTERACTION WITH FGFR1; FGFR2 AND FGFR4, FUNCTION IN CELL PROLIFERATION. |
| [7] | "Fibroblast growth factor signalling: from development to cancer." Turner N., Grose R. Nat. Rev. Cancer 10:116-129(2010) [PubMed] [Europe PMC] [Abstract] Cited for: REVIEW. |
| + | Additional computationally mapped references. |
Web resources
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | X57075 Genomic DNA. Translation: CAA40358.1. X57075 Genomic DNA. Translation: CAA40359.1. Different initiation. X57075 Genomic DNA. Translation: CAA40360.1. Different initiation. AY581424 Genomic DNA. Translation: AAS79318.1. BC121097 mRNA. Translation: AAI21098.1. BC121098 mRNA. Translation: AAI21099.1. X63454 mRNA. Translation: CAA45054.1. X14071, X14072, X14073 Genomic DNA. Translation: CAB37648.2. |
| IPI | IPI00022396. |
| PIR | S20102. |
| RefSeq | NP_066276.2. NM_020996.1. |
| UniGene | Hs.166015. |
3D structure databases | |
| ProteinModelPortal | P10767. |
| ModBase | Search... |
Protein-protein interaction databases | |
| DIP | DIP-6035N. |
| STRING | 9606.ENSP00000228837. |
PTM databases | |
| PhosphoSite | P10767. |
Polymorphism databases | |
| DMDM | 1169676. |
Proteomic databases | |
| PaxDb | P10767. |
| PRIDE | P10767. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000228837; ENSP00000228837; ENSG00000111241. |
| GeneID | 2251. |
| KEGG | hsa:2251. |
| UCSC | uc001qmr.1. human. |
Organism-specific databases | |
| CTD | 2251. |
| GeneCards | GC12M004543. |
| HGNC | HGNC:3684. FGF6. |
| MIM | 134921. gene. |
| neXtProt | NX_P10767. |
| PharmGKB | PA28123. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG320285. |
| HOGENOM | HOG000236341. |
| HOVERGEN | HBG007580. |
| InParanoid | P10767. |
| KO | K04358. |
| OMA | EIAGVNW. |
| OrthoDB | EOG4N8R5V. |
| PhylomeDB | P10767. |
Enzyme and pathway databases | |
| Pathway_Interaction_DB | fgf_pathway. FGF signaling pathway. syndecan_4_pathway. Syndecan-4-mediated signaling events. |
| Reactome | REACT_111102. Signal Transduction. REACT_116125. Disease. REACT_6900. Immune System. |
Gene expression databases | |
| ArrayExpress | P10767. |
| Bgee | P10767. |
| CleanEx | HS_FGF6. |
| Genevestigator | P10767. |
| GermOnline | ENSG00000111241. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR008996. Cytokine_IL1-like. IPR002209. GF_heparin-bd. IPR002348. IL1_HBGF. [Graphical view] |
| PANTHER | PTHR11486. PTHR11486. 1 hit. |
| Pfam | PF00167. FGF. 1 hit. [Graphical view] |
| PRINTS | PR00263. HBGFFGF. PR00262. IL1HBGF. |
| SMART | SM00442. FGF. 1 hit. [Graphical view] |
| SUPFAM | SSF50353. Cytok_IL1_like. 1 hit. |
| PROSITE | PS00247. HBGF_FGF. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 2251. |
| NextBio | 9113. |
| SOURCE | Search... |
Entry information
| Entry name | FGF6_HUMAN | ||||||||
| Accession | Primary (citable) accession number: P10767 Secondary accession number(s): Q0VAE1 | ||||||||
| 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 12 Human chromosome 12: 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
