Male reproductive organ cancer

disease
On this page

Also known as cancer of male reproductive organmale genital neoplasmmale reproductive system neoplasmmalignant male reproductive organ neoplasmmalignant Male reproductive system neoplasmmalignant Male reproductive system tumormalignant Male reproductive system tumourmalignant neoplasm of male genital organ, site unspecifiedmalignant neoplasm of male reproductive organmalignant neoplasm of Male reproductive systemmalignant neoplasm of the Male reproductive systemmalignant tumor of male genital organmalignant tumor of Male reproductive systemmalignant tumor of the Male reproductive systemmalignant tumour of male genital organmalignant tumour of Male reproductive systemmalignant tumour of the Male reproductive systemneoplasm of male genital organtumor of male reproductive system

Summary

Male reproductive organ cancer (MONDO:0005836) is a cancer (an umbrella term covering 7 Mondo subtypes) with 22 GWAS associations across 12 studies and 3 clinical trials. Top therapeutic interventions include valproic acid. A subtype of reproductive system cancer — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Umbrella term: 7 Mondo subtypes
  • GWAS associations: 22
  • Clinical trials: 3

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namemale reproductive organ cancer
Mondo IDMONDO:0005836
EFOEFO:0007355
MeSHD005834
DOIDDOID:3856
NCITC8561
SNOMED CT363515000
UMLSC0153606
MedGen102279
Anatomy (UBERON)UBERON:0003135
Is cancer (heuristic)yes

Also known as: cancer of male reproductive organ · male genital neoplasm · male reproductive organ cancer · male reproductive system neoplasm · malignant male reproductive organ neoplasm · malignant Male reproductive system neoplasm · malignant Male reproductive system tumor · malignant Male reproductive system tumour · malignant neoplasm of male genital organ, site unspecified · malignant neoplasm of male reproductive organ · malignant neoplasm of Male reproductive system · malignant neoplasm of the Male reproductive system · malignant tumor of male genital organ · malignant tumor of Male reproductive system · malignant tumor of male reproductive system · malignant tumor of the Male reproductive system · malignant tumour of male genital organ · malignant tumour of Male reproductive system · malignant tumour of male reproductive system · malignant tumour of the Male reproductive system (+3 more)

Data availability: 22 GWAS associations (12 studies).

Disease family

This is a subtype of reproductive system cancer. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumorneoplastic disease or syndromeneoplasmcancerreproductive system cancermale reproductive organ cancer

Related subtypes (7): malignant Leydig cell tumor, malignant Sertoli cell tumor, female reproductive organ cancer, prepuce cancer, pituitary cancer, gonadoblastoma, Buschke Lowenstein tumor

Subtypes (7): epididymis cancer, penile cancer, spermatic cord cancer, carcinoma of Cowper glands, testicular cancer, prostate cancer, scrotum cancer

Genetics & variants

GWAS landscape

22 GWAS associations across 12 studies. Top hits map to 17 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
rs1918510631e-15KLF12G4.07
rs1480202842e-13LRATD1 - NBASA4.73
rs5411476033e-13LINC01804 - RNU5E-7PG3.24
rs754674949e-13SAMD3G3.76
rs5433581392e-12LINC01182 - LINC00504A4.46
rs9058398312e-12NWD2T3.61
rs5649066173e-12SOX7-AS1, PINX1, PINX1G3.56
rs5473003585e-12DTWD2G3.61
rs5693911745e-12PCDH15A2.35
rs3736251978e-12XDHG2.66
rs773610998e-12LINC01723C3.62
rs14521795131e-11PCAT1, CASC8C2.87
rs1482961951e-11TAFA5G3.03
rs5374567541e-11RAD52P1 - ZNF385BC4.01
rs1385209381e-11FARS2G2.35
rs1851967381e-11PTPRK - EEF1DP5T3.32
rs7663421042e-11CDC14AG2.33
rs5433698842e-11GABRG3G2.78
rs5482123842e-11RN7SKP181 - LINC02253T5.22
rs1438016622e-11SCN4A - PRR29-AS1G2.33
rs1877503014e-11CRISPLD2C2.28
rs21750581e-09RNU6-1073P - H3P29?

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90399477Zagkos L20248,988149,131Exploring the contribution of lifestyle to the impact of education on the risk of cancer through Mendelian randomization analysis.
GCST90477206Verma A20242,251412,592Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90477207Verma A2024594415,675Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90481512Verma A2024455416,284Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90479805Verma A2024453103,757Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90481511Verma A2024453103,757Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90481510Verma A202431453,258Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90651317Liu TY2025219105,312Diversity and longitudinal records: Genetic architecture of disease associations and polygenic risk in the Taiwanese Han population.
GCST90479804Verma A2024205104,425Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90481514Verma A2024205104,425Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding0
Tier 2: splice/UTR0
Tier 3: regulatory0
Tier 4: intronic/intergenic22

MAF distribution

BucketVariants
common (>=0.05)1
low_freq (0.01-0.05)0
rare (<0.01)21
unknown0

Functional consequences

ConsequenceCount
intron_variant18
intergenic_variant4

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
rs1918510631373799100G>A0intron_variantKLF121e-15Tier 4: intronic/intergenic
rs148020284214713353A>C0.001intron_variantLRATD1 - NBAS2e-13Tier 4: intronic/intergenic
rs541147603215849047G>A0.001intergenic_variantLINC01804 - RNU5E-7P3e-13Tier 4: intronic/intergenic
rs754674946130309090G>C0.001intergenic_variantSAMD39e-13Tier 4: intronic/intergenic
rs543358139414342045A>C,T0intergenic_variantLINC01182 - LINC005042e-12Tier 4: intronic/intergenic
rs905839831437257929T>C0intron_variantNWD22e-12Tier 4: intronic/intergenic
rs564906617810765973G>A,T0intron_variantSOX7-AS1, PINX1, PINX13e-12Tier 4: intronic/intergenic
rs5473003585118882153G>A0intron_variantDTWD25e-12Tier 4: intronic/intergenic
rs5693911741055206300A>G0.001intergenic_variantPCDH155e-12Tier 4: intronic/intergenic
rs373625197231352687G>A0intron_variantXDH8e-12Tier 4: intronic/intergenic
rs773610992012970412C>T0intron_variantLINC017238e-12Tier 4: intronic/intergenic
rs14521795138127291513C>G0.001intron_variantPCAT1, CASC81e-11Tier 4: intronic/intergenic
rs1482961952248657957G>A,T0intron_variantTAFA51e-11Tier 4: intronic/intergenic
rs5374567542179415808C>A0intron_variantRAD52P1 - ZNF385B1e-11Tier 4: intronic/intergenic
rs13852093865666366G>A0.003intron_variantFARS21e-11Tier 4: intronic/intergenic
rs1851967386128580049T>A,C,G0intron_variantPTPRK - EEF1DP51e-11Tier 4: intronic/intergenic
rs7663421041100379948G>A0.001intron_variantCDC14A2e-11Tier 4: intronic/intergenic
rs5433698841527497513G>A0.001intron_variantGABRG32e-11Tier 4: intronic/intergenic
rs5482123841596906564T>A,G0intron_variantRN7SKP181 - LINC022532e-11Tier 4: intronic/intergenic
rs1438016621763987260G>A,T0.002intron_variantSCN4A - PRR29-AS12e-11Tier 4: intronic/intergenic
rs1877503011684834381C>T0.001intron_variantCRISPLD24e-11Tier 4: intronic/intergenic
rs217505891005072C>A,G,T0.05intron_variantRNU6-1073P - H3P291e-09Tier 4: intronic/intergenic

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

Drugs indicated for this disease

0 approved, 7 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.

DrugDevelopment status
ClonidinePhase 3 (in late-stage trials)
DexamethasonePhase 3 (in late-stage trials)
EpinephrinePhase 3 (in late-stage trials)
FospropofolPhase 3 (in late-stage trials)
PropofolPhase 3 (in late-stage trials)
RopivacainePhase 3 (in late-stage trials)
St. John’S WortPhase 3 (in late-stage trials)

Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Daratumumab.

Clinical trials & evidence

Clinical trials

Clinical trials: 3.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE12
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01552434PHASE1TERMINATEDBevacizumab and Temsirolimus Alone or in Combination With Valproic Acid or Cetuximab in Treating Patients With Advanced or Metastatic Malignancy or Other Benign Disease
NCT03420963PHASE1TERMINATEDDonor Natural Killer Cells, Cyclophosphamide, and Etoposide in Treating Children and Young Adults With Relapsed or Refractory Solid Tumors
NCT02192333Not specifiedCOMPLETEDSurvivorship Care in Reducing Symptoms in Young Adult Cancer Survivors

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
VALPROIC ACID41