Symbol
| CNTNAP1
| contributors: mct/pgu - updated : 23-11-2016
|
HGNC name
| contactin associated protein 1
|
HGNC id
| 8011
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
| germinal mutation
|  
|  
|  
|
appear to induce characteristic ultrastructural lesions of the paranodal region | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| nodal/paranodal axoplasm of shm mice lack paranodal junctions and contain large mitochondria and abnormal accumulations of cytoplasmic organelles that indicate altered axonal transport |