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DCLRE1B

Gene

DNA cross-link repair 1B

HGNCHGNC:17641EnsemblENSG00000118655NCBI Gene64858
Locus: gene with protein productLocation: 1p13.2

Also known as

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

Also known asSNM1B · FLJ12810 · FLJ13998 · APOLLO
View full nomenclature history (6)
Alias symbolsSNM1B, FLJ12810, FLJ13998, APOLLO
Previous namesDNA cross-link repair 1B (PSO2 homolog, S. cerevisiae)
Alias namesPSO2 homolog (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.

Thyroid gland carcinoma
Coronary Artery Disease
Breast Neoplasms
Basal cell carcinoma
Myocardial Infarction
Heart Diseases

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.

DNA cross-link repair family

Provenance

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