CSK (C-terminal Src kinase)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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1445 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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C-terminal Src kinase |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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CSK |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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Chromosome
Chromosome number
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15 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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15q24.1 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene is involved in multiple pathways, including the regulation of Src family kinases. It plays an important role in T-cell activation through its association with the protein encoded by the protein tyrosine phosphatase, non-re |
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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 | P41240 | ||||||||||||||||||||
| Protein name | Tyrosine-protein kinase CSK (EC 2.7.10.2) (C-Src kinase) (Protein-tyrosine kinase CYL) | ||||||||||||||||||||
| Protein function | Non-receptor tyrosine-protein kinase that plays an important role in the regulation of cell growth, differentiation, migration and immune response. Phosphorylates tyrosine residues located in the C-terminal tails of Src-family kinases (SFKs) inc | ||||||||||||||||||||
| PDB | 1BYG , 1CSK , 3D7T , 3D7U , 3EAC , 3EAZ | ||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed in lung and macrophages. {ECO:0000269|PubMed:1371489}. | ||||||||||||||||||||
| Sequence | |||||||||||||||||||||
| Sequence length | 450 | ||||||||||||||||||||
| 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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