Erythropoietin

Summary
UniProt ID
P01588
Gene Symbol
EPO
Gene ID
2056
Organism
Homo sapiens (human)
GlyConnect
GlyGen
P01588
PubChem
P01588
Re-Glyco
P01588
Annotation
Keyword
3D-structure Congenital erythrocytosis Direct protein sequencing Disease variant Disulfide bond Erythrocyte maturation Glycoprotein Hormone Pharmaceutical Proteomics identification Reference proteome Secreted Signal
Gene Ontology (GO)
GO Hierarchy
Sequence
MGVHECPAWLWLLLSLLSLPLGLPVLGAPPRLICDSRVLERYLLEAKEAENITTGCAEHCSLNENITVPDTKVNFYAWKRMEVGQQAVEVWQGLALLSEAVLRGQALLVNSSQPWEPLQLHVDKAVSGLRSLTTLLRALGAQKEAISPPDAASAAPLRTITADTFRKLFRVYSNFLRGKLKLYTGEACRTGDR
Glycosylation Sites
Displaying all 5 entries
Position Description PubMed ID GlyTouCan ID Source
51
  • N-linked (GlcNAc...) asparagine
65
  • N-linked (GlcNAc...) asparagine
110
  • N-linked (GlcNAc...) asparagine
153
  • O-linked (GalNAc...) serine
unknown
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Disease
Displaying entries 1 - 10 of 19 in total
DO ID Disease Name Source
DOID:11713 diabetic angiopathy
DOID:6432 pulmonary hypertension
DOID:10652 Alzheimer's disease
DOID:6000 congestive heart failure
DOID:3021 acute kidney failure
DOID:8947 diabetic retinopathy
DOID:13268 porphyria
DOID:1289 neurodegenerative disease
DOID:3891 placental insufficiency
DOID:1184 nephrotic syndrome

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: April 6, 2026