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C1QTNF9B

Gene

C1q and TNF related 9B

HGNCHGNC:34072EnsemblENSG00000205863NCBI Gene387911
Locus: gene with protein productLocation: 13q12.12

Also known as

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

Also known asCTRP9B
View full nomenclature history (2)
Alias symbolsCTRP9B
Previous namesC1q and tumor necrosis factor related protein 9B

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.

Respiratory Tract Diseases
Wet macular degeneration
Obesity due to melanocortin 4 receptor deficiency
autosomal dominant hyperinsulinism due to SUR1 deficiency
autosomal dominant hyperinsulinism due to Kir6.2 deficiency
MODY
Hypoinsulinemic hypoglycemia and body hemihypertrophy

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.