Previous symbols: C21orf60. Aliases: B17, C2TA, DKFZP434M035.
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 |
|---|---|---|
| DONSON-Related Microcephalic Primordial Dwarfism | causative germline |
mechanism: Reduced DONSON Protein Level
subtype: MGS-like; MISSLA; MMS; Seckel-like
|
| Meier-Gorlin syndrome | causative |
mechanism: Impaired CMG Helicase Assembly and Origin Firing
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.