Previous symbols: C17orf27, KIAA1618, MYMY2. Aliases: KIAA1554, NET57, ALO17.
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 |
|---|---|---|
| Coronary Vasospasm | susceptibility | |
| Moyamoya Disease | susceptibility |
mechanism: RNF213 loss-of-function Hippo-YAP/TAZ-VEGFR2 activation; RNF213-TRAF2-mediated NF-κB-IL-6 amplification; RNF213-associated angiogenic and remodeling dysregulation
subtype: Moyamoya disease 2
scoped to subtype: Moyamoya disease 2
|
| Congenital Renal Artery Stenosis |
untyped
Rare monogenic vasculopathy gene in midaortic syndrome
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.