Aliases: D11S813E, ASM, ASM1, NCRNA00008, LINC00008, MIR675HG, GMRSP.
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 |
|---|---|---|
| Coal Workers Pneumoconiosis | susceptibility germline | |
| Beckwith-Wiedemann Syndrome |
untyped
Maternally expressed lncRNA within the IC1 imprinted region
|
mechanism: 11p15.5 Imprinting Dysregulation; IGF2 Overexpression
scoped to subtype: IC1 GoM
|
| 3-M Syndrome | no genetic record |
mechanism: Increased H19 Expression
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.