Previous symbols: CLG4B.
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 |
|---|---|---|
| Metaphyseal anadysplasia |
untyped
Causal biallelic variant
|
mechanism: Biallelic MMP9 Loss of Function
subtype: Type 2
animal model: Mmp9/Mmp13 single- and double-knockout mouse
|
| Bacterial meningitis | no genetic record |
mechanism: Blood-Brain Barrier Disruption
|
| Hepatocellular Carcinoma | no genetic record |
mechanism: MMP9 Upregulation
|
| Preterm Premature Rupture of the Membranes | no genetic record |
mechanism: Matrix Metalloproteinase-Mediated Collagen Degradation in the Amniochorion
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.