Previous symbols: BRWD2. Aliases: KIAA1351, FLJ10506, WDR15, HH14, DR11, SRI1.
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 |
|---|---|---|
| Autosomal Recessive Non-Syndromic Intellectual Disability | causative germline |
mechanism: Loss of a Gene-Specific Molecular Function Required by Developing Neurons
subtype: MRT78
scoped to subtype: MRT78
|
| Kallmann Syndrome | causative |
mechanism: Defective GnRH neuron and olfactory axon migration
subtype: WDR11
scoped to subtype: WDR11
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.