Previous symbols: A1S9T, GXP1, UBE1. Aliases: UBE1X, POC20, CFAP124.
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 |
|---|---|---|
| Sweet Syndrome | somatic driver somatic |
mechanism: Clonal Myeloid Somatic Mutation
|
| VEXAS Syndrome | causative somatic |
mechanism: Somatic Pathogenic UBA1 Mutation in Hematopoietic Stem Cells
|
| Relapsing Polychondritis |
untyped
VEXAS syndrome overlap with relapsing polychondritis phenotype
somatic
|
|
| X-Linked Infantile Spinal Muscular Atrophy |
untyped
Causative
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.