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 1 - 10 of 118 in total
DO ID Disease Name Source
DOID:0040085 bacterial sepsis
DOID:0050865 tongue squamous cell carcinoma
DOID:0050881 inclusion body myopathy with Paget disease of bone and frontotemporal dementia
DOID:0060193 amyotrophic lateral sclerosis type 1
DOID:0060198 amyotrophic lateral sclerosis type 6
DOID:0060225 3MC syndrome
DOID:0060249 scoliosis
DOID:0060260 ptosis
DOID:0060261 congenital ptosis
DOID:0060262 gallbladder disease
The Human Phenotype Ontology
Displaying entries 51 - 58 of 58 in total
HPO ID HPO Term
HP:0004443 Lambdoidal craniosynostosis
HP:0005105 Abnormal nasal morphology
HP:0006216 Single interphalangeal crease of fifth finger
HP:0006394 Limited pronation/supination of forearm
HP:0008689 Bilateral cryptorchidism
HP:0008897 Postnatal growth retardation
HP:0009237 Short 5th finger
HP:0009891 Underdeveloped supraorbital ridges
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