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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
L1 cell adhesion molecule
Summary
- Gene Symbol
-
- L1CAM
- Aliases
-
- CAML1
- CD171
- NCAM-L1
- neural cell adhesion molecule L1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell adhesion
- Cell membrane
- Cell projection
- Developmental protein
- Differentiation
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Glycoprotein
- Hereditary spastic paraplegia
- Hirschsprung disease
- Immunoglobulin domain
- Intellectual disability
- Neurogenesis
- Phosphoprotein
- Reference proteome
- Repeat
- Signal
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| P32004 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| axon development | ||
| cell migration | ||
| nervous system development |
|
|
| synapse organization | ||
| chemotaxis |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| focal adhesion | ||
| collagen-containing extracellular matrix | ||
| axonal growth cone |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| axon guidance receptor activity | ||
| protein binding | ||
| protein domain specific binding |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110791 | hereditary spastic paraplegia 3A | |
| DOID:0110792 | hereditary spastic paraplegia 4 | |
| DOID:0110793 | hereditary spastic paraplegia 41 | |
| DOID:0110794 | hereditary spastic paraplegia 42 | |
| DOID:0110795 | hereditary spastic paraplegia 43 | |
| DOID:0110796 | hereditary spastic paraplegia 44 | |
| DOID:0110797 | hereditary spastic paraplegia 45 | |
| DOID:0110798 | hereditary spastic paraplegia 46 | |
| DOID:0110800 | hereditary spastic paraplegia 48 | |
| DOID:0110801 | hereditary spastic paraplegia 49 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000218 | High palate |
| HP:0000238 | Hydrocephalus |
| HP:0000252 | Microcephaly |
| HP:0000256 | Macrocephaly |
| HP:0000280 | Coarse facial features |
| HP:0000486 | Strabismus |
| HP:0000639 | Nystagmus |
| HP:0000750 | Delayed speech and language development |
| HP:0001181 | Adducted thumb |
| HP:0001188 | Hand clenching |
| Disease ID | Disease Name |
|---|---|
| ORPHA:306617 |
|
| ORPHA:2182 |
|
| OMIM:304100 |
|
| ORPHA:1497 |
|
| OMIM:303350 |
|
| OMIM:307000 |
|
| ORPHA:2466 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 101609645 | JACJA24152 | ||
| 102422358 | MYOLU04240 | ||
| 117026748 | RHIFE17927 | ||
| 103232804 | CHLSB18895 | ||
| 108535072 | RHIBE35121 | ||
| 104661172 | RHIRO38358 | ||
| 114587370 | PODMU24316 | ||
| 107570628 | SINGR15504 | ||
| 107586533 | SINGR40598 | ||
| 106825621 | EQUAS31541 |
