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C11orf58

Gene

chromosome 11 open reading frame 58

HGNCHGNC:16990EnsemblENSG00000110696NCBI Gene10944
Locus: gene with protein productLocation: 11p15.2

Also known as

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

Also known asSMAP · Hero20
View full nomenclature history (3)
Alias symbolsSMAP, Hero20
Alias namessmall acidic protein

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.

Neurodegenerative Diseases
Ovarian dysfunction
Self-injurious ideation
Hypertension
Diabetes Mellitus
Hair color

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 2024-12-06.
Open TargetsGene–disease associations from the Open Targets Platform.