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SEC23B

Gene

SEC23 homolog B, COPII component

HGNCHGNC:10702EnsemblENSG00000101310NCBI Gene10483
Locus: gene with protein productLocation: 20p11.23

Also known as

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

Also known asCDAN2 · CDA-II · CDAII · HEMPAS
View full nomenclature history (8)
Previous symbolsCDAN2
Alias symbolsCDA-II, CDAII, HEMPAS
Previous namesSEC23 homolog B, COPII coat complex component, Sec23 (S. cerevisiae) homolog B, congenital dyserythropoietic anemia, type II, Sec23 homolog B (S. cerevisiae)

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.

Genetic Diseases, Inborn
Neoplasms
immunoglobulin G4-related sclerosing disease

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.

Coat protein complex II

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-07-04.
Open TargetsGene–disease associations from the Open Targets Platform.