Previous symbols: LINC00889. Aliases: FHF2, FGF2, FLJ30672.
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 |
|---|---|---|
| Genetic Developmental and Epileptic Encephalopathy | causative |
mechanism: Genetic Lesion in an Ion Channel or Synaptic Gene
subtype: DEE90
scoped to subtype: DEE90
|
| Non-Syndromic X-Linked Intellectual Disability | causative |
mechanism: Convergent Disruption of Neuronal Function
subtype: IDX110
scoped to subtype: IDX110
|
| Major Depressive Disorder | no genetic record |
animal model: Astrocyte-specific Fgf13 knockout and overexpression mouse under chronic stress
discussion: (unnamed)
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.