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Protein / target

Protein cereblon

Encoded byCRBNQ96SW2Homo sapiensSwiss-Prot
Clinically validated
Therapeutic maturity
3
Approved medicines
Open Targets target-level
View by indication →
30
Clinical trials
Small-molecule tractable
Druggability
Approved Drug

Protein at a glance

Biological role

Transmembrane transporter binding

Strongest disease association

congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome

Via encoding gene CRBN · Genetic evidence · score 0.94

Therapeutic position

Established drug target

Small molecules

Derived from structured UniProt, Open Targets and literature data on this page.

Protein profile

UniProt 2026_02

Canonical identity and biological annotation from UniProt.

Function overview

Substrate recognition component of a DCX (DDB1-CUL4-X-box) E3 protein ligase complex that mediates the ubiquitination and subsequent proteasomal degradation of target proteins, such as MEIS2, ILF2 or GLUL.

View complete UniProt function annotation

Substrate recognition component of a DCX (DDB1-CUL4-X-box) E3 protein ligase complex that mediates the ubiquitination and subsequent proteasomal degradation of target proteins, such as MEIS2, ILF2 or GLUL (PubMed:26990986, PubMed:33009960). Normal degradation of key regulatory proteins is required for normal limb outgrowth and expression of the fibroblast growth factor FGF8 (PubMed:20223979, PubMed:24328678, PubMed:25043012, PubMed:25108355). Maintains presynaptic glutamate release and consequently cognitive functions, such as memory and learning, by negatively regulating large-conductance calcium-activated potassium (BK) channels in excitatory neurons (PubMed:18414909, PubMed:29530986). Likely to function by regulating the assembly and neuronal surface expression of BK channels via its interaction with KCNT1 (PubMed:18414909). May also be involved in regulating anxiety-like behaviors via a BK channel-independent mechanism (By similarity). Plays a negative role in TLR4 signaling by interacting with TRAF6 and ECSIT, leading to inhibition of ECSIT ubiquitination, an important step of the signaling (PubMed:31620128)

Subcellular location

CytoplasmNucleusMembrane
Domains and Gene Ontology detail (18)

Domains & features

Lon N-terminalCULT

Gene Ontology

  • CCul4A-RING E3 ubiquitin ligase complex
  • Ccytoplasm
  • Ccytosol
  • Cmembrane
  • Cnucleus
  • Cperinuclear region of cytoplasm
  • Fmetal ion binding
  • Ftransmembrane transporter binding
  • Plimb development
  • Plocomotory exploration behavior
  • Pnegative regulation of monoatomic ion transmembrane transport
  • Pnegative regulation of protein-containing complex assembly

442 aa · 51 kDa · 2 isoforms

Biological roles

Reactome v97

What this protein does, drawn together from its UniProt function, Gene Ontology terms and Reactome pathways.

Synaptic signallingUniProtIon channel gatingGOGrowth-factor signallingUniProt
View supporting evidence

Synaptic signalling

  • ·Substrate recognition component of a DCX (DDB1-CUL4-X-box) E3 protein ligase complex tha…

Ion channel gating

  • ·negative regulation of monoatomic ion transmembrane transport

Growth-factor signalling

  • ·Substrate recognition component of a DCX (DDB1-CUL4-X-box) E3 protein ligase complex tha…
View underlying pathways (1)

Concepts derived from UniProt GO Reactome — each badge above shows which sources supported that role.

Interaction neighbourhood

STRING v12.0

Proteins with the strongest functional or physical association. Node size and line weight reflect STRING confidence; hover or select a partner to inspect one association.

CUL4BDDB1RBX1IKZF1CUL4AIKZF3CSNK1A1GSPT1ZFP91BRD4CRBN

10 strongest partners — larger node and heavier line mean higher confidence

Functional and physical associations from STRING v12.0. Only associations with this protein are drawn — partner-to-partner links are not part of this evidence.

Approved medicines with mapped indications

3 medicines · 5 areas

Approved therapies targeting this protein, grouped by what they are approved to treat — the disease-first view of the medicines below. Relationships come from the canonical approved-indication graph (ChEMBL phase-4), the same source as the drug cards.

Immune System Diseases3 medicines
Multiple Myeloma3 medicines
Anemia1 medicine
Lymphoma, Mantle-Cell1 medicine
Myelodysplastic Syndromes1 medicine

Approved indications from ChEMBL (phase-4), via the canonical drug→disease graph.

Drugs targeting this protein

3

How approved and investigational drugs engage this protein — mechanism and action type, direct vs complex targeting, and how broadly each acts across other targets. A drug-first view (the section above groups the approved ones disease-first); direct binders with few recorded targets are listed first.

Thalidomide
ApprovedInhibitor

CRL4(CRBN) E3 ubiquitin ligase inhibitor

Indicated for Immune System Diseases, Multiple Myeloma

Acts on a complex — shared with DDB1, CUL4A, RBX1 · 1 of 4 recorded protein targets

lenalidomide
ApprovedInhibitor

CRL4(CRBN) E3 ubiquitin ligase inhibitor

Indicated for Anemia, Immune System Diseases, Lymphoma, Mantle-Cell, Multiple Myeloma

Acts on a complex — shared with DDB1, CUL4A, RBX1 · 1 of 4 recorded protein targets

pomalidomide
ApprovedInhibitor

CRL4(CRBN) E3 ubiquitin ligase inhibitor

Indicated for Immune System Diseases, Multiple Myeloma

Acts on a complex — shared with DDB1, CUL4A, RBX1 · 1 of 4 recorded protein targets

ChEMBL mechanism, action type, target identity and approved indications. Open Targets clinical status.

Translational evidence

Open Targets 26

Why this target matters therapeutically, strongest evidence first. Disease associations are gene-level (via the gene that encodes this protein) and open into the full confidence synthesis; the development universe, tractability and safety annotations are target-level, from Open Targets.

Strongest disease associations · via encoding gene CRBN

Gene-level evidence surfaced through the gene CRBNthat encodes this protein — not a direct protein–disease relationship. Ranked by Forefront's causal-directness weighting, so genetically- and clinically-evidenced diseases lead over ones that merely share the literature.

congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
0.94Well supported

Genetic evidence dominant · Open Targets 0.57

Multiple Myeloma
0.86Well supported

Clinical evidence dominant · Open Targets 0.68

Retinitis pigmentosa and erythrocytic microcytosis
0.84Well supported

Genetic evidence dominant · Open Targets 0.51

Autosomal recessive non-syndromic intellectual disability
0.80Well supported

Genetic evidence dominant · Open Targets 0.60

Genetic Diseases, Inborn
0.77Well supported

Genetic evidence dominant · Open Targets 0.47

View evidence synthesis (5)
congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndromeWell supported
0.94
agreement 0.821.00
Genetic100%

Open Targets aggregate 0.57 · 1 independent evidence family

Multiple MyelomaWell supported
0.86
agreement 0.730.99
Clinical60%Pathway29%Literature10%

Open Targets aggregate 0.68 · 3 independent evidence families

Retinitis pigmentosa and erythrocytic microcytosisWell supported
0.84
agreement 0.720.97
Genetic88%Animal model13%

Open Targets aggregate 0.51 · 2 independent evidence families

Autosomal recessive non-syndromic intellectual disabilityWell supported
0.80
agreement 0.660.94
Genetic96%Literature4%

Open Targets aggregate 0.60 · 2 independent evidence families

Genetic Diseases, InbornWell supported
0.77
agreement 0.650.89
Genetic100%

Open Targets aggregate 0.47 · 1 independent evidence family

This ranking differs from Open Targets' own: re-weighting moves genetically-evidenced diseases above more heavily co-mentioned ones. The evidence agreement range shows how closely the independent evidence families agree — it is not a statistical confidence interval, and nothing here is fitted to outcome data. Derived from Open Targets evidence types under Forefront weighting; the per-type scores above show the calculation.

Show all associations
Multiple Myeloma0.68
Autosomal recessive non-syndromic intellectual disability0.60
Myelodysplastic syndrome0.57
congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome0.57
Lymphoma, Follicular0.57
Lymphoma, Mantle-Cell0.56
Retinitis pigmentosa and erythrocytic microcytosis0.51
Immune System Diseases0.50
Anemia0.49
Genetic Diseases, Inborn0.47

Drug development

4 compounds recorded · 3 approved · 1 in clinical development

Open Targets' development universe — every compound recorded against the target at any stage, not all approved medicines. Distinct from the 3 drugs that target this protein in Forefront's canonical graph (3 with a mapped approved indication, shown above): these count different sets and are not a subset relation.

View all recorded compounds (4)
LENALIDOMIDEApproval
THALIDOMIDEApproval
POMALIDOMIDEApproval
IBERDOMIDEPhase 3

Open Targets known-drugs universe. Drug name and highest clinical stage only — the disease relationship is NOT read from this slice (it carries trial-context noise); approved indications come from the canonical graph above.

Tractability

Small moleculesStrong

Approved Drug and Structure with Ligand support this modality.

AntibodiesEmerging

Feasibility evidence (uniprot loc med conf) — no clinical-stage drug of this modality recorded.

Protein degradersEmerging

Feasibility evidence (literature and uniprot ubiquitination) — no clinical-stage drug of this modality recorded.

View underlying tractability evidence (9)
SM · Approved DrugSM · Structure with LigandSM · High-Quality LigandAB · UniProt loc med confPR · LiteraturePR · UniProt UbiquitinationPR · Database UbiquitinationPR · Half-life DataPR · Small Molecule Binder

Raw Open Targets tractability assessment buckets, by modality.

Clinical trials

30

Trials of drugs that target this protein — reached indirectly through those drugs, so a trial listed here studies the drug, not the protein. Ranked by active status, then clinical phase and recency, and spread across the targeting drugs.

View all trials (26)

ClinicalTrials.gov via the drug-target graph.

What's happening now

12

Recent therapeutic activity around this target — regulatory actions, clinical trials and safety signals for 2 drugs that target this protein, plus publications where such a drug is a genuine subject. Every item is reached indirectly through the drug, not the protein itself; incidental mentions (a paper that merely measures a drug) and press items are excluded.

  1. Trial status changed2026-07-31

    A Phase 3b, Multicenter, Open-label, Daratumumab Long-term Extension Study

    Status changed to Active, not recruiting · ClinicalTrials.gov · via lenalidomide

  2. Trial status changed2026-07-30

    64407564MMY3009: A Phase 3 Randomized Study Comparing Talquetamab in Combination With Pomalidomide (Tal-P), Talquetamab in Combination With Teclistamab (Tal-Tec), and Investigator's Choice of Either Elotuzumab, Pomalidomide, and Dexamethasone (EPd) or Pom

    Status changed to Active, not recruiting · ClinicalTrials.gov · via pomalidomide

  3. Label change2026-07-22

    Label change: LENALIDOMIDE (NDA021880)

    fda · regulatory · fda · via lenalidomide

  4. Trial status changed2026-07-20

    A Phase II Trial of Tafasitamab and Lenalidomide Followed by Tafasitamab and ICE as Salvage Therapy for Transplant Eligible Patients With Relapsed/ Refractory Large B-Cell Lymphoma

    Status changed to Active, not recruiting · ClinicalTrials.gov · via lenalidomide

  5. Label change2026-06-15

    Label change: LENALIDOMIDE (ANDA201452)

    fda · regulatory · fda · via lenalidomide

  6. Supplemental approval2026-04-27

    Supplemental approval: LENALIDOMIDE (ANDA201452)

    fda · regulatory · fda · via lenalidomide

  7. Supplemental approval2026-04-27

    Supplemental approval: LENALIDOMIDE (NDA021880)

    fda · regulatory · fda · via lenalidomide

  8. New publication2022-03-01
    Safety, Activity, and Long-term Outcomes of Pomalidomide in the Treatment of Kaposi Sarcoma among Individuals with or without HIV Infection.

    Clinical cancer research : an official journal of the American Association for Cancer Research · 2022 · 38 citations · Europe PMC · via pomalidomide

  9. Safety communication2016-05-10

    Drug Safety Update: Pomalidomide (Imnovid▼): risk of hepatitis B reactivation

    mhra · safety · mhra · via pomalidomide

  10. Safety communication2014-12-11

    Drug Safety Update: Lenalidomide (Revlimid): risk of serious hepatic adverse drug reactions

    mhra · safety · mhra · via lenalidomide

  11. Safety communication2014-12-11

    Drug Safety Update: Lenalidomide (Revlimid▼): update on risk of second primary malignancy

    mhra · safety · mhra · via lenalidomide

  12. Safety communication2014-12-11

    Drug Safety Update: Lenalidomide: risk of thrombosis and thromboembolism

    mhra · safety · mhra · via lenalidomide

Objective event titles are shown unmodified; the event kind and significance line are derived from structured fields. Forefront AttentionEvent stream aggregating Europe PMC Regulatory filings ClinicalTrials.gov.