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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 |
|
|
| protein localization to paranode region of axon |
|
|
| mitochondrion organization |
|
|
| cytoskeleton organization |
|
|
| cytoskeleton organization |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane |
|
|
| membrane |
|
|
| paranodal junction |
|
|
| paranode region of axon |
|
|
| paranode region of axon |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding |
|
|
| SH3 domain binding |
|
|
| signaling receptor activity |
|
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060558 | lethal congenital contracture syndrome |
Ortholog
| Species | Gene ID | Alliance of Genome Resources |
|---|---|---|
| 53321 | MGI:1858201 | |
| 84008 | RGD:70902 | |
| 178167 | WB:WBGene00003772 | |
| 39387 | FB:FBgn0013997 |
