MBL associated serine protease 1

Summary
Gene Symbol
  • MASP1
Aliases
  • C4/C2 activating component of Ra-reactive factor
  • MAP-1
  • MASP
  • MASP-3
  • Map44
  • mannose-binding lectin-associated serine protease 1
Organism
Homo sapiens (human)
External Links
NCBI Gene
5648
HGNC
6901
KEGG Gene ID
hsa:5648
PubChem
5648
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Autocatalytic cleavage
  • Calcium
  • Complement activation lectin pathway
  • Direct protein sequencing
  • Disease variant
  • Disulfide bond
  • EGF-like domain
  • Glycoprotein
  • Hydroxylation
  • Metal-binding
  • Reference proteome
  • Repeat
  • Secreted
  • Serine protease
  • Signal
  • Sushi
Proteins
Displaying 1 entry
UniProt Protein Name
P48740
  • Complement factor MASP-3
  • Complement-activating component of Ra-reactive factor
  • Mannose-binding lectin-associated serine protease 1
  • Mannose-binding protein-associated serine protease
  • Ra-reactive factor serine protease p100
  • Serine protease 5
Gene Ontology (GO)
Displaying all 2 entries
GO Term Evidence Code PMID
complement activation, lectin pathway
zymogen activation
GO Hierarchy
Disease
Disease Ontology
Displaying entries 81 - 90 of 118 in total
DO ID Disease Name Source
DOID:2007 degeneration of macula and posterior pole
DOID:2340 craniosynostosis
DOID:2377 multiple sclerosis
DOID:2893 cervix carcinoma
DOID:2921 glomerulonephritis
DOID:2957 pulmonary tuberculosis
DOID:3156 hypomelanosis of Ito
DOID:3526 cerebral infarction
DOID:3702 cervical adenocarcinoma
DOID:3748 esophagus squamous cell carcinoma
The Human Phenotype Ontology
Displaying entries 11 - 20 of 58 in total
HPO ID HPO Term
HP:0000377 Abnormal pinna morphology
HP:0000405 Conductive hearing impairment
HP:0000494 Downslanted palpebral fissures
HP:0000496 Abnormality of eye movement
HP:0000501 Glaucoma
HP:0000506 Telecanthus
HP:0000508 Ptosis
HP:0000524 Conjunctival telangiectasia
HP:0000537 Epicanthus inversus
HP:0000581 Blepharophimosis
Displaying all 2 entries
Disease ID Disease Name
ORPHA:293843
  • 3MC syndrome
OMIM:257920
  • 3MC syndrome 1
PubChem Disease
GHR Health Conditions
MedGen Diseases
OMIM Phenotypes
KEGG Diseases

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024