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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 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:0110815 | hereditary spastic paraplegia 64 | |
| DOID:0110816 | hereditary spastic paraplegia 7 | |
| DOID:0110817 | hereditary spastic paraplegia 72A | |
| DOID:0110818 | hereditary spastic paraplegia 73 | |
| DOID:0110820 | hereditary spastic paraplegia 75 | |
| DOID:0110822 | hereditary spastic paraplegia 77 | |
| DOID:0110823 | hereditary spastic paraplegia 8 | |
| DOID:0110824 | hereditary spastic paraplegia 9A | |
| DOID:0110825 | hereditary spastic paraplegia 9B | |
| DOID:0110881 | holoprosencephaly 1 |
- 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 |
|---|---|---|---|
| 101590171 | OCTDE23673 | ||
| 100028028 | MONDO35982 | ||
| 114030882 | VOMUR30213 | ||
| 105867318 | MICMU07290 | ||
| 100949201 | OTOGA01197 | ||
| 101065574 | TAKRU38243 | ||
| 102020500 | CHILA24756 | ||
| 105707107 | AOTNA39726 | ||
| 101034097 | SAIBB38855 | ||
| 101969264 | ICTTR08590 |
