CCL24 (C-C motif chemokine ligand 24)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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6369 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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C-C motif chemokine ligand 24 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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CCL24 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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Ckb-6, MPIF-2, MPIF2, SCYA24 |
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Chromosome
Chromosome number
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7 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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7q11.23 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene belongs to the subfamily of small cytokine CC genes. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded |
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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 | O00175 | ||||||||||
| Protein name | C-C motif chemokine 24 (CK-beta-6) (Eosinophil chemotactic protein 2) (Eotaxin-2) (Myeloid progenitor inhibitory factor 2) (MPIF-2) (Small-inducible cytokine A24) | ||||||||||
| Protein function | Chemotactic for resting T-lymphocytes, and eosinophils (PubMed:9104803, PubMed:9365122). Has lower chemotactic activity for neutrophils but none for monocytes and activated lymphocytes (PubMed:9104803, PubMed:9365122). Is a strong suppressor of | ||||||||||
| PDB | 1EIG , 1EIH | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Activated monocytes and activated T lymphocytes. {ECO:0000269|PubMed:9104803}. | ||||||||||
| Sequence |
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| Sequence length | 119 | ||||||||||
| 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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