Previous symbols: PPOL, ADPRT. Aliases: PARP, ARTD1, Poly-PARP, PARS.
Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| Aflatoxin-Related Hepatocellular Carcinoma | no genetic record |
mechanism: PARP1 DNA Repair Suppression
|
| Alzheimer Disease | no genetic record |
mechanism: PARP1-Mediated Parthanatos
|
| Ewing Sarcoma | no genetic record |
mechanism: PARP1-Supported Fusion Transcription
|
| Leber Congenital Amaurosis 9 | no genetic record |
mechanism: PARP Hyperactivation and Nuclear NAD+ Consumption
|
| Ovarian High-Grade Serous Carcinoma | no genetic record |
mechanism: PARP and Platinum Synthetic Lethality
|
| Spinocerebellar Ataxia, Autosomal Recessive 26 | no genetic record |
mechanism: PARP1 Trapping and Hyperactivation
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.