Statements (29)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:protein
|
| gptkbp:alternativeName |
gptkb:Neural_cell_adhesion_molecule_L1
gptkb:L1 |
| gptkbp:associatedWith |
CRASH syndrome (in human homolog)
|
| gptkbp:cellularComponent |
gptkb:plasma_membrane
axon growth cone |
| gptkbp:domain |
Ig-like C2-type domain
Fibronectin type-III domain |
| gptkbp:Entrez_Gene_ID |
16796
|
| gptkbp:expressedIn |
gptkb:nervous_system
|
| gptkbp:fullName |
gptkb:L1_cell_adhesion_molecule
|
| gptkbp:function |
cell adhesion
axon guidance neuronal migration |
| gptkbp:gene |
L1cam
|
| https://www.w3.org/2000/01/rdf-schema#label |
mouse L1cam
|
| gptkbp:locatedOnChromosome |
X
|
| gptkbp:location |
X A1
|
| gptkbp:molecularWeight |
140 kDa
|
| gptkbp:mutationAssociatedWith |
neurological defects
|
| gptkbp:organism |
gptkb:Mus_musculus
|
| gptkbp:orthologIn |
human L1CAM
|
| gptkbp:postTranslationalModification |
phosphorylation
glycosylation |
| gptkbp:sequence |
1257 amino acids
|
| gptkbp:UniProtID |
P32020
|
| gptkbp:bfsParent |
gptkb:L1CAM
|
| gptkbp:bfsLayer |
7
|