Previous symbols: ZFYVE20.
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 |
|---|---|---|
| Congenital Myelofibrosis with Anemia, Neutropenia, Developmental Delay, and Ocular Abnormalities | causative germline loss of function |
mechanism: RBSN Loss of Function
|
| Kariminejad Neurodevelopmental Syndrome | causative germline loss of function |
mechanism: RBSN FYVE-Domain Missense Variant
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.