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 |
|---|---|---|
| Autosomal Dominant Cerebellar Ataxia Type I |
untyped
SCA37 noncoding (ATTTC)n insertion in DAB1
|
mechanism: Non-polyglutamine Repeat Toxicity
subtype: SCA37
scoped to subtype: SCA37
|
| Reelin Pathway Lissencephaly | no genetic record |
mechanism: VLDLR-ApoER2-DAB1 Signal Transduction Failure
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.