Previous symbols: TYRO1. Aliases: Hek8.
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 |
|---|---|---|
| Preaxial Digit Brachydactyly-Webbed Fingers | causative germline |
mechanism: Deletion of the EPHA4-PAX3 Regulatory Boundary
|
| Borjeson-Forssman-Lehmann syndrome | no genetic record |
mechanism: Ephrin receptor transcriptional dysregulation
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.