Homo sapiens Protein: AGGF1 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-29865.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | AGGF1 | ||||||||||||||||||
Protein Name | angiogenic factor with G patch and FHA domains 1 | ||||||||||||||||||
Synonyms | |||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000316109 | ||||||||||||||||||
InnateDB Gene | IDBG-29861 (AGGF1) | ||||||||||||||||||
Protein Structure | |||||||||||||||||||
UniProt Annotation | |||||||||||||||||||
Function | Promotes angiogenesis and the proliferation of endothelial cells. Able to bind to endothelial cells and promote cell proliferation, suggesting that it may act in an autocrine fashion. {ECO:0000269PubMed:14961121}. | ||||||||||||||||||
Subcellular Localization | Cytoplasm {ECO:0000269PubMed:14961121}. Secreted {ECO:0000269PubMed:14961121}. Note=Cytoplasmic in microvascular endothelial cells. Upon angiogenesis, when endothelial cell tube formation is initiated, it is secreted. | ||||||||||||||||||
Disease Associations | Klippel-Trenaunay syndrome (KTS) [MIM:149000]: Congenital disease characterized by malformations of capillary (98% of KTS patients), venous (72%) and lymphatic (11%) vessels, and bony and soft tissue hypertrophy that leads to large cutaneous hemangiomata with hypertrophy of the related bones and soft tissues. {ECO:0000269PubMed:14961121}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | Widely expressed. Expressed in endothelial cells, vascular smooth muscle cells and osteoblasts. Expressed in umbilical vein endothelial cells and microvascular endothelial cells. {ECO:0000269PubMed:14961121}. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 18 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR000253
Forkhead-associated (FHA) domain IPR000467 G-patch domain IPR008984 SMAD/FHA domain |
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PFAM |
PF00498
PF01585 |
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PRINTS | |||||||||||||||||||
PIRSF | |||||||||||||||||||
SMART |
SM00240
SM00443 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q8N302 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q8N302 | ||||||||||||||||||
TrEMBL | A8K029 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 55109 | ||||||||||||||||||
UniGene | Hs.653659 | ||||||||||||||||||
RefSeq | NP_060516 | ||||||||||||||||||
HUGO | HGNC:24684 | ||||||||||||||||||
OMIM | 608464 | ||||||||||||||||||
CCDS | CCDS4035 | ||||||||||||||||||
HPRD | 07621 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AK001145 AK289394 AY500994 AY500996 BC002828 BC029382 CH471084 U84971 | ||||||||||||||||||
GenPept | AAB60856 AAH02828 AAH29382 AAR97615 AAR97617 BAA91519 BAF82083 EAW95787 | ||||||||||||||||||