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ELOB

Gene

elongin B

HGNCHGNC:11619EnsemblENSG00000103363NCBI Gene6923
Locus: gene with protein productLocation: 16p13.3

Also known as

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

Also known asTCEB2 · SIII
View full nomenclature history (4)
Previous symbolsTCEB2
Alias symbolsSIII
Previous namestranscription elongation factor B (SIII), polypeptide 2 (18kDa, elongin B), transcription elongation factor B subunit 2

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.

HIV Infections
Diabetes Mellitus, Type 2
Neoplasms
Ovarian carcinoma
Cytomegalovirus Infections
Ovarian Neoplasms
Sleep Initiation and Maintenance Disorders

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.

Elongin complex

Provenance

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