Aliases: WNT-12, SHFM6.
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 |
|---|---|---|
| Tooth Agenesis |
untyped
Pathogenic Variants
|
mechanism: WNT/beta-catenin Signaling Deficiency
subtype: WNT10B-related
scoped to subtype: WNT10B-related
|
| Split Hand-Foot Malformation | no genetic record |
mechanism: Apical Ectodermal Ridge Maintenance Failure
subtype: SHFM6
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.