CDON (cell adhesion associated, oncogene regulated)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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50937 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Cell adhesion associated, oncogene regulated |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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CDON |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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CDO, CDON1, HPE11, Ihog, ORCAM |
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Chromosome
Chromosome number
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11 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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11q24.2 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a cell surface receptor that is a member of the immunoglobulin superfamily. The encoded protein contains three fibronectin type III domains and five immunoglobulin-like C2-type domains. This protein is a member of a cell-surface receptor |
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SNPs
SNP information provided by dbSNP.
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||||||||||||||||||||||||||||||||
| UniProt ID | Q4KMG0 | ||||||||||||||||||||||||||||||||||||||||
| Protein name | Cell adhesion molecule-related/down-regulated by oncogenes | ||||||||||||||||||||||||||||||||||||||||
| Protein function | Component of a cell-surface receptor complex that mediates cell-cell interactions between muscle precursor cells. Promotes differentiation of myogenic cells (By similarity). | ||||||||||||||||||||||||||||||||||||||||
| PDB | 3D1M , 3N1F , 3N1Q | ||||||||||||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 1287 | ||||||||||||||||||||||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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