COPS7A (COP9 signalosome subunit 7A)
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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50813 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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COP9 signalosome subunit 7A |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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COPS7A |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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CSN7, CSN7A, SGN7a |
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Chromosome
Chromosome number
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12 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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12p13.31 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a component of the COP9 signalosome, an evolutionarily conserved multi-subunit protease that regulates the activity of the ubiquitin conjugation pathway. Alternatively spliced transcript variants that encode the same protein have been de |
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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 | Q9UBW8 | |||||||||||||||
| Protein name | COP9 signalosome complex subunit 7a (SGN7a) (Signalosome subunit 7a) (Dermal papilla-derived protein 10) (JAB1-containing signalosome subunit 7a) | |||||||||||||||
| Protein function | Component of the COP9 signalosome complex (CSN), a complex involved in various cellular and developmental processes. The CSN complex is an essential regulator of the ubiquitin (Ubl) conjugation pathway by mediating the deneddylation of the culli | |||||||||||||||
| PDB | 4D10 , 4D18 , 4WSN | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Widely expressed. Expressed at high level in brain, heart and skeletal muscle. {ECO:0000269|PubMed:12020345}. | |||||||||||||||
| Sequence |
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| Sequence length | 275 | |||||||||||||||
| 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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