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Repository for lectin-assisted multimodality data
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Guidelines
MIRAGE
Disks large homolog 4
Summary
- UniProt ID
- Q62108
- Gene Symbol
-
- Dlg4
- Dlgh4
- Psd95
- Gene ID
- 13385
- Organism
- Mus musculus (house mouse)
Annotation
- Keyword
-
- Alternative splicing
- Cell membrane
- Cell projection
- Cytoplasm
- Palmitate
- Phosphoprotein
- Reference proteome
- Repeat
- SH3 domain
- Synapse
- Ubl conjugation
- Gene Ontology (GO)
| GO Term |
|---|
| cortical cytoskeleton |
| cytoplasm |
| plasma membrane |
| membrane |
| cell junction |
| dendrite |
| neuromuscular junction |
| dendrite cytoplasm |
| synapse |
| postsynaptic membrane |
Sequence
MDCLCIVTTKKYRYQDEDTPPLEHSPAHLPNQANSPPVIVNTDTLEAPGYELQVNGTEGEMEYEEITLERGNSGLGFSIAGGTDNPHIGDDPSIFITKIIPGGAAAQDGRLRVNDSILFVNEVDVREVTHSAAVEALKEAGSIVRLYVMRRKPPAEKIIEIKLIKGPKGLGFSIAGGVGNQHIPGDNSIYVTKIIEGGAAHKDGRLQIGDKILAVNSVGLEDVMHEDAVAALKNTYDVVYLKVAKPSNAYLSDSYAPPDITTSYSQHLDNEISHSSYLGTDYPTAMTPTSPRRYSPVAKDLLGEEDIPREPRRIVIHRGSTGLGFNIVGGEDGEGIFISFILAGGPADLSGELRKGDQILSVNGVDLRNASHEQAAIALKNAGQTVTIIAQYKPEEYSRFEAKIHDLREQLMNSSLGSGTASLRSNPKRGFYIRALFDYDKTKDCGFLSQALSFHFGDVLHVIDASDEEWWQARRVHSDSETDDIGFIPSKRRVERREWSRLKAKDWGSSSGSQGREDSVLSYETVTQMEVHYARPIIILGPTKDRANDDLLSEFPDKFGSCVPHTTRPKREYEIDGRDYHFVSSREKMEKDIQAHKFIEAGQYNSHLYGTSVQSVREVAEQGKHCILDVSANAVRRLQAAHLHPIAIFIRPRSLENVLEINKRITEEQARKAFDRATKLEQEFTECFSAIVEGDSFEEIYHKVKRVIEDLSGPYIWVPARERL
Glycosylation Sites
G46503DX
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Activation of Ca-permeable Kainate Receptor | Mus musculus |
| LGI-ADAM interactions | Mus musculus |
| Neurexins and neuroligins | Mus musculus |
| RAF/MAP kinase cascade | Mus musculus |
| RHO GTPases activate CIT | Mus musculus |
| Synaptic adhesion-like molecules | Mus musculus |
| Trafficking of AMPA receptors | Mus musculus |
| Unblocking of NMDA receptors, glutamate binding and activation | Mus musculus |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060041 | autism spectrum disorder | |
| DOID:1928 | Williams-Beuren syndrome |
