Aliases: RNMX, hnRNP-G, HNRNPG.
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 |
|---|---|---|
| Severe X-linked Intellectual Disability Gustavson Type | causative germline |
mechanism: RBMX p.(Pro162del) In-Frame Deletion
|
| Shashi X-Linked Intellectual Disability Syndrome | causative germline |
mechanism: RBMX Loss of Function
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.