Mus musculus Gene: Masp1
Summary
InnateDB Gene IDBG-149706.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Masp1
Gene Name mannan-binding lectin serine peptidase 1
Synonyms AW048060; CCPII; Crarf; Masp1/3
Species Mus musculus
Ensembl Gene ENSMUSG00000022887
Encoded Proteins
mannan-binding lectin serine peptidase 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
InnateDB Annotation from Orthologs
Summary
[Homo sapiens] MASP1 is an essential protease of both the lectin and alternative complement pathways, essential components of innate immunity, participating in the pathogenesis of inflammatory diseases and in host defence.
[Homo sapiens] MASP1 is crucial for classical complement activation, but is not required for the alternative pathway function.
[Homo sapiens] MASP1 forms a complex with MASP2 to activate the complement system.
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000127241:
This gene encodes a serine protease that functions as a component of the lectin pathway of complement activation. The complement pathway plays an essential role in the innate and adaptive immune response. The encoded protein is synthesized as a zymogen and is activated when it complexes with the pathogen recognition molecules of lectin pathway, the mannose-binding lectin and the ficolins. This protein is not directly involved in complement activation but may play a role as an amplifier of complement activation by cleaving complement C2 or by activating another complement serine protease, MASP-2. The encoded protein is also able to cleave fibrinogen and factor XIII and may may be involved in coagulation. A splice variant of this gene which lacks the serine protease domain functions as an inhibitor of the complement pathway. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 16:23451785-23520590
Strand Reverse strand
Band B1
Transcripts
ENSMUST00000089883 ENSMUSP00000087327
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 19 interaction(s) predicted by orthology.
Predicted by orthology
Total 19 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003824 catalytic activity
GO:0004252 serine-type endopeptidase activity
GO:0005509 calcium ion binding
GO:0005515 protein binding
GO:0008233 peptidase activity
GO:0042803 protein homodimerization activity
GO:0048306 calcium-dependent protein binding
Biological Process
GO:0001867 complement activation, lectin pathway
GO:0006508 proteolysis
GO:0045916 negative regulation of complement activation
Cellular Component
GO:0005615 extracellular space
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Innate Immune System pathway
Creation of C4 and C2 activators pathway
Ficolins bind to repetitive carbohydrate structures on the target cell surface pathway
Complement cascade pathway
Immune System pathway
Binding and Uptake of Ligands by Scavenger Receptors pathway
Scavenging by Class A Receptors pathway
Lectin pathway of complement activation pathway
Initial triggering of complement pathway
KEGG
Complement and coagulation cascades pathway
Staphylococcus aureus infection pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Lectin pathway of complement activation pathway
Initial triggering of complement pathway
Innate Immune System pathway
Binding and Uptake of Ligands by Scavenger Receptors pathway
Scavenging by Class A Receptors pathway
Creation of C4 and C2 activators pathway
Immune System pathway
Ficolins bind to repetitive carbohydrate structures on the target cell surface pathway
Complement cascade pathway
KEGG
Complement and coagulation cascades pathway
Staphylococcus aureus infection pathway
INOH
PID NCI
Cross-References
SwissProt P98064
TrEMBL
UniProt Splice Variant
Entrez Gene 17174
UniGene Mm.1213
RefSeq NM_008555
OMIM
CCDS CCDS37303
HPRD
IMGT
MGI ID MGI:88492
MGI Symbol Masp1
EMBL AB049755 AK031598 AY135525 AY135527 BC131637 BC131638 CH466521 D16492
GenPept AAI31638 AAI31639 AAN39850 BAA03944 BAB69688 BAC27469 EDK97670 EDK97671
RNA Seq Atlas 17174