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MIRAGE
Defective SLCO2A1 causes primary, autosomal recessive hypertrophic osteoarthropathy 2 (PHOAR2)

Summary
Species
Homo sapiens
Reactome
PubChem
Click on a node on the pathway to see its details. Glycoproteins are marked with a glycoprotein icon in their name.
SPV: a JavaScript Signaling Pathway Visualizer, Bioinformatics, 2018
Displaying 1 entry
UniProt ID Protein Name Gene Symbol Pathway Viewer
Q92959 Solute carrier organic anion transporter family member 2A1
  • OATP2A1
  • SLC21A2
  • SLCO2A1
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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 8, 2025