Previous symbols: C9orf157. Aliases: NOHLH, TEB2, bA100C15.3, bHLHe80, SPATA27.
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 |
|---|---|---|
| 46,XX Gonadal Dysgenesis | causative germline |
mechanism: Oocyte Development and Cellular-Homeostasis Failure
subtype: ODG5
scoped to subtype: ODG5
|
| Spermatogenic Failure 32 | causative |
mechanism: SOHLH1 Transcription Factor Loss of Function
|
Identity from HGNC (snapshot 2026-10-24). Page layers are described in the gene pages documentation.