Homo sapiens Protein: MMRN1 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-30172.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | MMRN1 | ||||||||||||||||||
Protein Name | multimerin 1 | ||||||||||||||||||
Synonyms | ECM; EMILIN4; GPIa*; MMRN; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000264790 | ||||||||||||||||||
InnateDB Gene | IDBG-30170 (MMRN1) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | Carrier protein for platelet (but not plasma) factor V/Va. Plays a role in the storage and stabilization of factor V in platelets. Upon release following platelet activation, may limit platelet and plasma factor Va-dependent thrombin generation. Ligand for integrin alpha-IIb/beta-3 and integrin alpha-V/beta-3 on activated platelets, and may function as an extracellular matrix or adhesive protein. {ECO:0000269PubMed:16363244, ECO:0000269PubMed:19132231, ECO:0000269PubMed:7629143}. | ||||||||||||||||||
Subcellular Localization | Secreted {ECO:0000305}. | ||||||||||||||||||
Disease Associations | Note=Deficiency in multimerin-1 due to proteolytic degradation within the platelet alpha granules is associated with an autosomal dominant bleeding disorder (factor V Quebec). {ECO:0000269PubMed:8652809}. | ||||||||||||||||||
Tissue Specificity | Synthesized by endothelial cells and megakaryocytes. Stored in platelet alpha granules and endothelial cell Weibel-Palade bodies, following activation of these cells, it is released and attached to megakaryocytes, platelets, endothelium and subendothelium of blood vessels. Not found in plasma. Found in vascular tissues such as placenta, lung, and liver. {ECO:0000269PubMed:7629143, ECO:0000269PubMed:8514871}. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 3 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 |
IPR000742
Epidermal growth factor-like domain IPR001073 Complement C1q protein IPR001881 EGF-like calcium-binding domain IPR008983 Tumour necrosis factor-like domain IPR011489 EMI domain |
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PFAM |
PF00008
PF00386 PF07645 PF07546 |
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PRINTS |
PR00007
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PIRSF | |||||||||||||||||||
SMART |
SM00181
SM00110 SM00179 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q13201 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q13201 | ||||||||||||||||||
TrEMBL | E7EPG1 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 22915 | ||||||||||||||||||
UniGene | Hs.708404 | ||||||||||||||||||
RefSeq | NP_031377 | ||||||||||||||||||
HUGO | HGNC:7178 | ||||||||||||||||||
OMIM | 601456 | ||||||||||||||||||
CCDS | CCDS3635 | ||||||||||||||||||
HPRD | 03267 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AC093759 AK125557 AK313566 BC063848 CH471057 U27109 | ||||||||||||||||||
GenPept | AAC52065 AAH63848 AAY40957 BAC86201 BAG36340 EAX06038 | ||||||||||||||||||