erythropoietin

Summary
Gene Symbol
  • EPO
Organism
Homo sapiens (human)
NCBI Gene
2056
PubChem
2056
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Congenital erythrocytosis
  • Direct protein sequencing
  • Disease variant
  • Disulfide bond
  • Erythrocyte maturation
  • Glycoprotein
  • Hormone
  • Pharmaceutical
  • Reference proteome
  • Secreted
  • Signal
Proteins
Displaying all 2 entries
UniProt Protein Name
P01588
G9JKG7
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Erythropoietin
Functional Category
  • E: Amino acid transport and metabolism
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying entries 1 - 10 of 31 in total
DO ID Disease Name Source
DOID:0050852 limb ischemia
DOID:0080290 familial erythrocytosis 5
DOID:10652 Alzheimer's disease
DOID:11713 diabetic angiopathy
DOID:11832 visual epilepsy
DOID:1184 nephrotic syndrome
DOID:1289 neurodegenerative disease
DOID:13025 retinopathy of prematurity
DOID:13268 porphyria
DOID:14330 Parkinson's disease

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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: December 9, 2024