Aliases: JJAZ1, KIAA0160, CHET9.
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 |
|---|---|---|
| Malignant Peripheral Nerve Sheath Tumor |
untyped
Somatic PRC2-core loss of function
|
mechanism: PRC2 Core Complex Inactivation
|
| NF1 Microdeletion Syndrome |
untyped
Co-deleted PRC2 subunit increasing MPNST risk
|
mechanism: SUZ12 Haploinsufficiency and Elevated MPNST Risk
|
| Neurofibroma | no genetic record |
mechanism: Malignant Transformation to MPNST
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.