Previous symbols: RBM8. Aliases: ZNRP, BOV-1A, BOV-1B, BOV-1C, Y14.
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 |
|---|---|---|
| Mayer-Rokitansky-Kuster-Hauser_Syndrome | unknown | |
| Thrombocytopenia-Absent Radius Syndrome | causative |
mechanism: Reduced RBM8A Gene Dosage
variant: RBM8A rs139428292; RBM8A rs201779890
dataset: geo:GSE5781
|
An entry matches when ClinGen's MONDO disease is the entry's own disease term, a subtype term, or an exact-match mapping. An amber status marks an entry ClinGen supports the gene for (Definitive, Strong or Moderate) whose own record does not type it. A Limited, Disputed or Refuted tier on such an entry is not a gap.
| ClinGen disease | MOI | Classification | dismech entry |
|---|---|---|---|
| thrombocytopenia-absent radius syndrome MONDO:0010121 | AR | Definitive 2020-05-15 |
Thrombocytopenia-Absent Radius Syndrome
causative
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.