DCUN1D5 (defective in cullin neddylation 1 domain containing 5)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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84259 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Defective in cullin neddylation 1 domain containing 5 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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DCUN1D5 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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DCNL5, SCCRO5 |
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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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11q22.3 |
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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 | Q9BTE7 | ||||||||||
| Protein name | DCN1-like protein 5 (DCNL5) (DCUN1 domain-containing protein 5) (Defective in cullin neddylation protein 1-like protein 5) (Squamous cell carcinoma-related oncogene 5) | ||||||||||
| Protein function | Contributes to the neddylation of all cullins by transferring NEDD8 from N-terminally acetylated NEDD8-conjugating E2s enzyme to different cullin C-terminal domain-RBX complexes which is necessary for the activation of cullin-RING E3 ubiquitin l | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Weakly expressed in testis, skin and immune tissues (thymus, spleen and lymph nodes). {ECO:0000269|PubMed:26906416}. | ||||||||||
| Sequence |
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| Sequence length | 237 | ||||||||||
| Interactions | View interactions | ||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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