Previous symbols: AOP1. Aliases: MER5, AOP-1, SP-22.
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 |
|---|---|---|
| Spinocerebellar Ataxia, Autosomal Recessive 32 | causative germline loss of function |
mechanism: PRDX3 Loss of Function
|
| Corneal Dystrophy | no genetic record |
mechanism: Layer-Restricted Corneal Deposition or Cellular Failure
subtype: PPPCD
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.