Aliases: IL1RA, ICIL-1RA, IL1F3, IRAP, IL-1RN, MGC10430.
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 |
|---|---|---|
| Deficiency of the Interleukin-1 Receptor Antagonist | causative germline |
mechanism: Biallelic IL1RN Loss of Function
|
| Febrile Infection-Related Epilepsy Syndrome | susceptibility germline |
mechanism: Functional IL-1RA Deficiency (Permissive Host Factor)
|
| Vulvodynia | susceptibility | |
| Multisystem Inflammatory Syndrome in Children (MIS-C) |
untyped
Autoantigen target
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.