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MIRAGE
Alpha-2-HS-glycoprotein

Summary
UniProt ID
P02765
Gene Symbol
  • AHSG
  • FETUA
  • PRO2743
Gene ID
197
Organism
Homo sapiens (human)
GlycoProtDB
GPDB0011331
GlyConnect
GlyGen
P02765
PubChem
P02765
The Human Metabolome Database
HMDBP07684
The O-GlcNAc Database
P02765
RaftProt
P02765
Re-Glyco
P02765
Annotation
Keyword
  • Direct protein sequencing
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Hypotrichosis
  • Intellectual disability
  • Mineral balance
  • Phosphoprotein
  • Reference proteome
  • Repeat
  • Secreted
  • Signal
Gene Ontology (GO)
Displaying all 10 entries
GO Term
extracellular region
extracellular space
extracellular matrix
collagen-containing extracellular matrix
endoplasmic reticulum lumen
Golgi apparatus
extracellular exosome
blood microparticle
secretory granule lumen
platelet alpha granule lumen
Subcellular Location(GO Annotation)

Subcellular in which this glycoprotein is expressed are highlighted in blue.

Annotation information from UniProt.
Sequence
MKSLVLLLCLAQLWGCHSAPHGPGLIYRQPNCDDPETEEAALVAIDYINQNLPWGYKHTLNQIDEVKVWPQQPSGELFEIEIDTLETTCHVLDPTPVARCSVRQLKEHAVEGDCDFQLLKLDGKFSVVYAKCDSSPDSAEDVRKVCQDCPLLAPLNDTRVVHAAKAALAAFNAQNNGSNFQLEEISRAQLVPLPPSTYVEFTVSGTDCVAKEATEAAKCNLLAEKQYGFCKATLSEKLGGAEVAVTCMVFQTQPVSSQPQPEGANEAVPTPVVDPDAPPSPPLGAPGLPPAGSPPDSHVLLAAPPGHQLHRAHYDLRHTFMGVVSLGSPSGEVSHPRKTRTVVQPSVGAAAGPVVPPCPGRIRHFKV
  • N : N-glycosylation Site
  • ___ : Potential Sequon
Glycosylation Sites
Displaying entries 1 - 10 of 16 in total
Position Description PubMed ID GlyTouCan ID Source
156 N-linked (GlcNAc...) (complex) asparagine
176 N-linked (GlcNAc...) (complex) asparagine
186
196
197
202
256
270 O-linked (GalNAc...) threonine
280 O-linked (GalNAc...) serine
293 O-linked (GalNAc...) serine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 4 entries
Pathway Name Organism
Neutrophil degranulation Homo sapiens
Platelet degranulation Homo sapiens
Post-translational protein phosphorylation Homo sapiens
Regulation of IGF Activity by IGFBP Homo sapiens
Disease
Displaying all 3 entries
DO ID Disease Name Source
DOID:0080628 alopecia-mental retardation syndrome 1
DOID:3393 coronary artery disease
DOID:9352 type 2 diabetes mellitus
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International Collaboration

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: December 8, 2025