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PLXDC2

Gene

plexin domain containing 2

HGNCHGNC:21013EnsemblENSG00000120594NCBI Gene84898
Locus: gene with protein productLocation: 10p12.31

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asTEM7R · FLJ14623 · PLXDC2-OT
View full nomenclature history (4)
Alias symbolsTEM7R, FLJ14623, PLXDC2-OT
Alias namestumor endothelial marker 7-related precursor

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Spinal Cord Injuries
Hypopituitarism
Retinal Diseases
Respiratory Tract Infections
Diabetic Ketoacidosis
Liver Diseases

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-02-02.
Open TargetsGene–disease associations from the Open Targets Platform.