OncoSignal
Live from Open Targets Platform, fetched 2026-11-11 15:37 UTC. Every row links to its source record.

PRDM10 PR/SET domain 10

ENSG00000170325 · protein coding · Open Targets profile

Transcriptional activator, essential for early embryonic development and survival of embryonic stem cells (ESCs) (By similarity). Supports cell growth and survival during early development by transcriptionally activating the expression of the translation initiation factor EIF3B, to sustain global translation (By similarity). Activates the transcription of FLNC (PubMed:36440963). .

In 7 of 15 cancers, the evidence for PRDM10 comes mainly from inherited variants

Each row is a cancer, strongest overall evidence first. The two dots show how strong the inherited (germline) and tumour-mutation (somatic) evidence is; the line between them is the gap.

Inherited (germline) variantsMutations in tumours (somatic)
00.250.50.751Birt-Hogg-Dubé syndromeBirt-Hogg-Dubé syndromeBirt-Hogg-Dubé syndrome: germline 0.61benign lipomatous neoplasmbenign lipomatous neoplasmbenign lipomatous neoplasm: germline 0.48lipomalipomalipoma: germline 0.46male reproductive organ cancermale reproductive organ cancermale reproductive organ cancer: germline 0.19bone neoplasmbone neoplasmbone neoplasm: germline 0.17benign chondrogenic neoplasmbenign chondrogenic neoplasmbenign chondrogenic neoplasm: germline 0.08breast carcinomabreast carcinomabreast carcinoma: germline 0.03non-small cell lung carcinomanon-small cell lung carcinomasoft tissue neoplasmsoft tissue neoplasmhepatocellular carcinomahepatocellular carcinomaesophageal squamous cell carcinomaesophageal squamous cell carcinomarenal cell carcinomarenal cell carcinomalung carcinomalung carcinomalung cancerlung cancerlobular neoplasialobular neoplasia

Scores run from 0 (no evidence) to 1 (strongest). A missing dot at 0 means Open Targets holds no evidence of that kind. Source: Open Targets Platform, fetched live.

Tractability

PROTAC
UniProt Ubiquitination, Database Ubiquitination, Half-life Data

gnomAD loss of function constraint: o/e 0.48824000358581543 (upper bound 0.6002100110054016). Low values mean loss of function is poorly tolerated, a safety flag for inhibition.

Who runs trials of these drugs

No named investigators on registry trials of PRDM10's approved or late-stage drugs in the last three years.

No terminated, withdrawn or suspended trials of PRDM10's drugs are registered

All 0 drugs and clinical candidates as a table

Each drug, stage and indication links to its Open Targets record, where the trials and approvals behind it are listed. Salt forms (for example a mesylate) are listed as Open Targets records them, as separate entries.

DrugTypeHighest stageIndicationsSource records
No drugs or clinical candidates recorded.