Homo sapiens Protein: SRPX2 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-79194.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | SRPX2 | ||||||||||||||||||
Protein Name | sushi-repeat containing protein, X-linked 2 | ||||||||||||||||||
Synonyms | |||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000362095 | ||||||||||||||||||
InnateDB Gene | IDBG-79192 (SRPX2) | ||||||||||||||||||
Protein Structure | |||||||||||||||||||
UniProt Annotation | |||||||||||||||||||
Function | Acts as a ligand for the urokinase plasminogen activator surface receptor. Plays a role in angiogenesis by inducing endothelial cell migration and the formation of vascular network (cords). Involved in cellular migration and adhesion. Increases the phosphorylation levels of FAK. Interacts with and increases the mitogenic activity of HGF. Promotes synapse formation. May have a role in the perisylvian region, critical for language and cognitive development. {ECO:0000269PubMed:16497722, ECO:0000269PubMed:18718938, ECO:0000269PubMed:19065654, ECO:0000269PubMed:24179158}. | ||||||||||||||||||
Subcellular Localization | Secreted. Cytoplasm. Cell surface. Cell junction, synapse {ECO:0000250}. | ||||||||||||||||||
Disease Associations | Rolandic epilepsy with speech dyspraxia and mental retardation X-linked (RESDX) [MIM:300643]: A condition characterized by the association of rolandic seizures with oral and speech dyspraxia, and mental retardation. Rolandic seizures occur during a period of significant brain maturation. During this time, dysfunction of neural network activities such as focal discharges may be associated with specific developmental disabilities resulting in specific cognitive impairments of language, visuo-spatial abilities or attention. {ECO:0000269PubMed:16497722}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | Expressed in neurons of the rolandic area of the brain (at protein level). Highly expressed in the brain, placenta, lung, trachea, uterus, adrenal gland, heart, ovary and placenta. Weakly expressed in the peripheral blood, brain and bone marrow. Expressed in numerous cancer cell lines and in gastrointestinal cancer cells. Higher levels found in colorectal cancers than in normal colonic mucosa. {ECO:0000269PubMed:16497722, ECO:0000269PubMed:18718938, ECO:0000269PubMed:19065654, ECO:0000269PubMed:22242148, ECO:0000269PubMed:9864177}. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 1 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 |
IPR000436
Sushi/SCR/CCP IPR003410 Hyalin IPR012336 Thioredoxin-like fold |
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PFAM |
PF00084
PF02494 PF13098 PF13192 PF13462 PF13905 |
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PRINTS | |||||||||||||||||||
PIRSF | |||||||||||||||||||
SMART |
SM00032
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | O60687 | ||||||||||||||||||
PhosphoSite | PhosphoSite-O60687 | ||||||||||||||||||
TrEMBL | |||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 27286 | ||||||||||||||||||
UniGene | Hs.306339 | ||||||||||||||||||
RefSeq | NP_055282 | ||||||||||||||||||
HUGO | HGNC:30668 | ||||||||||||||||||
OMIM | 300642 | ||||||||||||||||||
CCDS | CCDS14471 | ||||||||||||||||||
HPRD | 06726 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AF060567 AF393649 AK075462 AL035608 AL390040 BC020733 | ||||||||||||||||||
GenPept | AAC15765 AAH20733 AAM73693 BAG52145 | ||||||||||||||||||