+ |
KIRREL3 | up-regulates
|
Synaptic_plasticity |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269077 |
|
|
Homo sapiens |
|
pmid |
sentence |
32503885 |
We demonstrate that ectopic Kirrel3 expression in CA1 neurons specifically induces ectopic DG synapse formation, providing direct evidence that Kirrel3 plays an instructive role in synapse development. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Tissue: |
Brain |
+ |
KIRREL3 | up-regulates activity
binding
|
CASK |
0.47 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269078 |
|
|
Homo sapiens |
|
pmid |
sentence |
33853164 |
A Missense De Novo Variant in the CASK-interactor KIRREL3 Gene Leading to Neurodevelopmental Disorder with Mild Cerebellar Hypoplasia. KIRREL3 is a gene important for the central nervous system development-in particular for the process of neuronal migration, axonal fasciculation, and synaptogenesis-and colocalizes and cooperates in neurons with CASK gene. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Tissue: |
Cerebellum |
+ |
KIRREL3 | up-regulates activity
binding
|
DLG4 |
0.38 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269079 |
|
|
Mus musculus |
Dopaminergic Neuron |
pmid |
sentence |
28381988 |
We here report that, through its C-terminal PDZ domain-binding motif, Neph2 directly interacts with postsynaptic density (PSD)-95, an abundant excitatory postsynaptic scaffolding protein. Moreover, Neph2 protein is detected in the brain PSD fraction and interacts with PSD-95 in synaptosomal lysates. Functionally, loss of Neph2 in mice leads to age-specific defects in the synaptic connectivity of DG neurons. |
|
Publications: |
1 |
Organism: |
Mus Musculus |