Back to discover

C3orf38

Gene

chromosome 3 open reading frame 38

HGNCHGNC:28384EnsemblENSG00000179021NCBI Gene285237
Locus: gene with protein productLocation: 3p11.1

Also known as

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

Also known asMGC26717
View full nomenclature history (2)
Alias symbolsMGC26717
Alias namesdense incisors

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.

Smoking initiation
Fractures, Bone
Osteoporosis, Postmenopausal
Obesity disorder
Migraine Disorders
Attention Deficit Disorder with Hyperactivity
Overnutrition

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 2025-06-09.
Open TargetsGene–disease associations from the Open Targets Platform.