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C1QL2

Gene

complement C1q like 2

HGNCHGNC:24181EnsemblENSG00000144119NCBI Gene165257
Locus: gene with protein productLocation: 2q14.2

Also known as

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

Also known asCTRP10 · C1QTNF10
View full nomenclature history (4)
Alias symbolsCTRP10, C1QTNF10
Previous namescomplement component 1, q subcomponent-like 2
Alias namesC1q and tumor necrosis factor related protein 10

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.

Endocrine System Diseases
Multiple Sclerosis
Hypertension, Portal
Skin Diseases
Placental abruption
Obesity disorder

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.

Gene family

HGNC gene-group membership.

C1q and TNF related

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.