Previous symbols: ZNF6, MRX65. Aliases: CMPX1, ZNF4, ZNF5, dJ75N13.1, Zfp711, MRX97.
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 |
|---|---|---|
| Choroideremia-Deafness-Obesity Syndrome | cooperating | |
| Non-Syndromic X-Linked Intellectual Disability | causative |
mechanism: Convergent Disruption of Neuronal Function
subtype: MRX97
scoped to subtype: MRX97
|
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 |
|---|---|---|---|
| X-linked complex neurodevelopmental disorder MONDO:0100148 | XL | Definitive 2022-09-22 |
no dismech entry |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.