Aliases: Hek11.
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 |
|---|---|---|
| 6q16 Deletion Syndrome | risk factor germline |
mechanism: Reduced EPHA7 Gene Dosage
|
| Choroid Plexus Carcinoma |
untyped
Somatic Mutation
|
|
| 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.