QuickView for GEMIN5;jsessionid=8EBD2EFE5EF633894CDAF5DB2055BA8A (gene)

1. A Biallelic Truncating Variant in the TPR Domain of GEMIN5 Associated with Intellectual Disability a…
2. SMN regulates GEMIN5 expression and acts as a modifier of GEMIN5-mediated neurodegeneration.
3. Functional and structural deficiencies of Gemin5 variants associated with neurological disorders.
4. Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder.
5. The RBS1 domain of Gemin5 is intrinsically unstructured and interacts with RNA through conserved Arg…

There were no clinical trials for GEMIN5;jsessionid=8EBD2EFE5EF633894CDAF5DB2055BA8A