Back to discover

SCGN

Gene

secretagogin, EF-hand calcium binding protein

HGNCHGNC:16941EnsemblENSG00000079689NCBI Gene10590
Locus: gene with protein productLocation: 6p22.2

Also known as

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

Also known asSECRET · DJ501N12.8 · SEGN · CALBL
View full nomenclature history (5)
Alias symbolsSECRET, DJ501N12.8, SEGN, CALBL
Alias namescalbindin-like

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
Coronary Artery Disease
Epstein-Barr Virus Infections
Diabetes Mellitus, Type 2
Iron Metabolism Disorders
Non-alcoholic Fatty Liver Disease
Arthritis, Rheumatoid

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.

EF-hand domain containing

Provenance

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