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Repository for lectin-assisted multimodality data
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Guidelines
MIRAGE
contactin associated protein 2
Summary
- Gene Symbol
-
- CNTNAP2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Autism
- Cell adhesion
- Cell junction
- Cell projection
- Chromosomal rearrangement
- Disulfide bond
- EGF-like domain
- Epilepsy
- Glycoprotein
- Intellectual disability
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Repeat
- Signal
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| A0A090N7T7 |
|
| B2RCH4 |
|
| Q9UHC6 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| cell adhesion | ||
| brain development | ||
| learning | ||
| neuron recognition | ||
| cell population proliferation |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| early endosome | ||
| Golgi apparatus | ||
| voltage-gated potassium channel complex | ||
| voltage-gated potassium channel complex | ||
| cell surface |
| GO Term | Evidence Code | PMID |
|---|---|---|
| protease binding | ||
| protein binding | ||
| enzyme binding | ||
| transmembrane transporter binding |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- contactin-associated protein-like 2
- Functional Category
-
- G: Carbohydrate transport and metabolism
- M: Cell wall/membrane/envelope biogenesis
- T: Signal transduction mechanisms
| InterPro |
|---|
| Concanavalin A-like lectin/glucanase domain superfamily |
| EGF-like domain |
| Laminin G domain |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060041 | autism spectrum disorder | |
| DOID:0060244 | specific language impairment | |
| DOID:0090130 | cortical dysplasia-focal epilepsy syndrome | |
| DOID:11257 | social phobia | |
| DOID:12849 | autistic disorder | |
| DOID:13365 | reading disorder | |
| DOID:1470 | major depressive disorder | |
| DOID:4186 | articulation disorder | |
| DOID:4189 | mutism | |
| DOID:5419 | schizophrenia |
