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MIRAGE
contactin associated protein 1
Summary
- Gene Symbol
-
- CNTNAP1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Cell adhesion
- Cell junction
- Disease variant
- Disulfide bond
- EGF-like domain
- Glycoprotein
- Neuropathy
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Repeat
- SH3-binding
- Signal
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| P78357 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein localization to paranode region of axon | ||
| mitochondrion organization | ||
| cytoskeleton organization | ||
| cell adhesion | ||
| signal transduction |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| septate junction |
|
|
| membrane | ||
| paranodal junction | ||
| paranode region of axon | ||
| presynaptic active zone |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| SH3 domain binding | ||
| signaling receptor activity |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- contactin associated protein like 5
- Functional Category
-
- E: Amino acid transport and metabolism
- G: Carbohydrate transport and metabolism
- T: Signal transduction mechanisms
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060558 | lethal congenital contracture syndrome |
