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 |
|---|---|---|
| KATNB1-related Cortical Malformation |
untyped
Causative
|
mechanism: Biallelic KATNB1 Loss and Katanin Microtubule-Severing Defect
discussion: (unnamed)
|
| Lissencephaly Spectrum Disorders |
untyped
Loss of function
|
mechanism: Katanin p80 Deficiency in Dividing Neural Progenitors
subtype: LIS6/KATNB1
scoped to subtype: LIS6/KATNB1
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.