RBPJL

Gene

recombination signal binding protein for immunoglobulin kappa J region like

HGNCHGNC:13761 EnsemblENSG00000124232 NCBI Gene11317

Locus: gene with protein productLocation: 20q13.12

Also known as

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

Also known asRBPSUHL · RBP-L · SUH · SUHL

View full nomenclature history (6)

Previous symbolsRBPSUHL

Alias symbolsRBP-L, SUH, SUHL

Previous namesrecombining binding protein suppressor of hairless (Drosophila)-like, recombination signal binding protein for immunoglobulin kappa J region-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.

Diabetes Mellitus, Type 2

Neoplasms

Hereditary sensory and autonomic neuropathy

Esophageal Squamous Cell Carcinoma

Pancreatic Neoplasms

Diabetes Mellitus

Pancreatitis

Carcinoma, Pancreatic Ductal

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.

PTF1 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.