Previous symbols: HOX1K.
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 |
|---|---|---|
| Bilateral Microtia-Deafness-Cleft Palate Syndrome | causative |
mechanism: HOXA2 Loss of Function; Impaired Transactivation of the Long-Range HMX1 Enhancer
subtype: AD-Microtia; AR-MHIC
|
| Fetal Valproate Syndrome | no genetic record |
mechanism: Disturbed Cranial Neural Crest Formation and Migration
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.