Sertoli-Leydig cell tumor

disease
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Summary

Sertoli-Leydig cell tumor (MONDO:0002479) is a cancer with 1 cohort gene (1 CIViC-evidence somatic driver) and 2 clinical trials. Top therapeutic interventions include nivolumab.

At a glance

  • Classification: Cancer
  • Cohort genes: 1
  • Clinical trials: 2

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameSertoli-Leydig cell tumor
Mondo IDMONDO:0002479
MeSHD018310
DOIDDOID:2997
UMLSC0206723
MedGen61669
GARD0009967
Is cancer (heuristic)yes

Disease family

An umbrella term covering 1 Mondo subtype.

Classification path: disease › human disease › disease by body system or component › reproductive system disorder › reproductive system neoplasm › sex cord-stromal tumor › testicular sex cord-stromal neoplasm › Sertoli-Leydig cell tumor

Related subtypes (9): testicular lymphoma, testicular gonadoblastoma, testicular Leydig cell tumor, testicular granulosa cell tumor, testicular fibroma, testicular thecoma, testicular sertoli cell tumor, testicular fibrothecoma, testicular sex cord-stromal benign neoplasm

Subtypes (1): malignant Sertoli-Leydig cell tumor

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

Mendelian disease overlap and somatic drivers

GenCC: 0 · Orphanet: 7 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0

Somatic driver evidence (intOGen + CIViC, cohort fanout)

GeneintOGen roleCancer typesCIViC
DICER1LoFCOADREAD,CSCC,MEL,UCECCIViC #9533

Orphanet rare-disease linkage (cohort genes)

GeneOrphanet IDRare disease
DICER1Orphanet:276399Familial multinodular goiter
DICER1Orphanet:284343DICER1 tumor-predisposition syndrome
DICER1Orphanet:404476Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome
DICER1Orphanet:99757Embryonal rhabdomyosarcoma
DICER1Orphanet:99914Gynandroblastoma
DICER1Orphanet:99915Malignant granulosa cell tumor of the ovary
DICER1Orphanet:99916Malignant Sertoli-Leydig cell tumor of the ovary

Cohort genes → proteins

1 cohort genes, 1 distinct canonical proteins.

Evidence partition

SubsetGenes
civic_only1

Cohort genes (full)

SymbolHGNCEnsemblUniProtNameEvidence
DICER1HGNC:17098ENSG00000100697Q9UPY3Endoribonuclease Dicercivic_evidence

Cohort function summary

Lead sentence per gene, UniProt-curated.

SymbolProtein nameFunction (lead sentence)
DICER1Endoribonuclease DicerDouble-stranded RNA (dsRNA) endoribonuclease playing a central role in short dsRNA-mediated post-transcriptional gene silencing.

Protein-family classification

Druggable: 1 · Difficult: 0 · Unknown: 0 · Druggable fraction: 1.0

Family distribution

Cohort families vs a genome-wide background (hypergeometric, BH-FDR; fold = observed/expected). Counts kept; sorted by enrichment, so the catch-all Other/Unknown bucket no longer leads.

FamilyGenesFoldFDR
Enzyme (other)112.0×0.083

Per-gene assignment

SymbolFamilyDruggable?ECInterPro (top 3)
DICER1Enzyme (other)yes3.1.26.3RNase_III_dom, Helicase_C-like, PAZ_dom

Expression context

Cohort genes with no expression data: 0.

1 cohort gene are a single-cell marker in ≥1 SCXA experiment.

Breadth distribution (Bgee present_calls)

BucketGenes
narrow (1-5 tissues)0
moderate (6-20)0
broad (>20)1
unknown0

Top tissues across cohort

TissueCohort genes
caput epididymis1
cauda epididymis1
tongue squamous epithelium1

Per-gene tissue summary (top 30)

SymbolBgee breadthFANTOM5 breadthSCXATop tissues
DICER1295ubiquitousmarkercauda epididymis, caput epididymis, tongue squamous epithelium

Protein interactions among cohort

Intra-cohort edges: 0.

Hub genes (top 10 by interactor count)

SymbolInteractor count
DICER18,268

Structural data

PDB: 1 · AlphaFold-only: 0 · No structure: 0

Cohort genes with PDB structures (top 30)

SymbolUniProtPDB entries
DICER1Q9UPY321

Function

Pathway analysis

Distinct Reactome pathways touched by cohort: 5. Enrichment computed across 1 evidence-associated genes (1 with Reactome annotation).

Pathways by enrichment

Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

PathwayCohort genesFoldFDRSample cohort genes
tRNA-derived small RNA (tsRNA or tRNA-related fragment, tRF) biogenesis13806.7×0.001DICER1
Small interfering RNA (siRNA) biogenesis11142.0×0.002DICER1
Regulation of MITF-M-dependent genes involved in apoptosis1634.4×0.003DICER1
MicroRNA (miRNA) biogenesis1456.8×0.003DICER1
M-decay: degradation of maternal mRNAs by maternally stored factors1326.3×0.003DICER1

GO biological processes by enrichment

Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

GO termCohort genesFoldFDRSample cohort genes
positive regulation of Schwann cell differentiation18426.0×0.001DICER1
peripheral nervous system myelin formation15617.3×0.001DICER1
global gene silencing by mRNA cleavage15617.3×0.001DICER1
tRNA decay13370.4×0.001DICER1
negative regulation of Schwann cell proliferation12407.4×0.001DICER1
siRNA processing11872.4×0.002DICER1
RISC complex assembly11532.0×0.002DICER1
miRNA metabolic process11404.3×0.002DICER1
apoptotic DNA fragmentation11203.7×0.002DICER1
pre-miRNA processing11123.5×0.002DICER1
miRNA processing11053.2×0.002DICER1
nerve development1936.2×0.002DICER1
positive regulation of myelination1766.0×0.002DICER1
negative regulation of tumor necrosis factor-mediated signaling pathway1455.5×0.003DICER1
neuron projection morphogenesis1276.3×0.004DICER1
negative regulation of tumor necrosis factor production1251.5×0.004DICER1
negative regulation of gene expression169.1×0.015DICER1
negative regulation of transcription by RNA polymerase II117.7×0.056DICER1

Therapeutics

Drug target analysis

Approved (phase 4): 0 · Phase ≥3: 0 · Phased (≥1): 0 · Undrugged: 1

Druggability breadth: 1 of 1 evidence-associated genes (100%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).

Top cohort targets by molecule count

SymbolMoleculesMax phase
DICER100

Bioactivity and enzyme data

Enzyme cohort genes (≥1 EC): 1.

Cohort genes with ChEMBL bioactivity (full, sorted by assay count)

SymbolAssaysType breakdown
DICER18Binding:8

Cohort enzymes (BRENDA EC)

SymbolEC numbersNames
DICER13.1.26.3ribonuclease III

Pharmacogenomics

Cohort genes with a PharmGKB record: 1; with CPIC/DPWG dosing guidelines: 0.

No cohort gene has a CPIC/DPWG genotype-guided dosing guideline (PharmGKB).

Drug repurposing candidates

0 approved/phased drugs hit cohort targets but don’t yet appear in disease-level clinical trials. Target-inhibition rationale is strongest for cancer driver genes; a bioactivity hit is a screening signal, not a treatment claim.

Druggability pyramid

Cohort genes binned by druggability tier (high → low):

TierDefinitionGenesSymbols
AApproved (phase 4 drug)0
BPhased (≥1) drug, not yet approved0
CDruggable family + PDB, no drug1DICER1
DDruggable family + AlphaFold only, no drug0
EDifficult family or no structure, no drug0

Undrugged target profiles

1 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).

SymbolChEMBL assaysDrugged partners (top 3)
DICER18

Clinical trials & evidence

Clinical trials

Clinical trials: 2.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE21
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06638931PHASE2RECRUITINGAgnostic Therapy in Rare Solid Tumors
NCT03382158Not specifiedRECRUITINGInternational PPB/DICER1 Registry

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
NIVOLUMAB41