Previous symbols: PIP5K3. Aliases: MGC40423, KIAA0981, PIP5K, p235, ZFYVE29, FAB1.
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 |
|---|---|---|
| Corneal Dystrophy | no genetic record |
mechanism: Corneal Stromal Endosomal Sorting Defect
subtype: FCD
|
| Yunis-Varon Syndrome | no genetic record |
mechanism: PI(3,5)P2 Deficiency
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.