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 |
|---|---|---|
| Chromosome 15q24 Deletion Syndrome | unknown germline | |
| SIN3A-Related Intellectual Disability Syndrome |
causative
germline
loss of function
CLINGEN: definitive
|
mechanism: SIN3A Haploinsufficiency; SIN3A PAH1 Domain Partner-Binding Defect
subtype: Point mutation; SIN3A-spanning deletion
|
Identity from HGNC (snapshot 2026-10-24). Page layers are described in the gene pages documentation.