OTUD7A (OTU deubiquitinase 7A)
| Gene | |
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
161725 |
|
Gene name
Gene Name - the full gene name approved by the HGNC.
|
OTU deubiquitinase 7A |
|
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
|
OTUD7A |
|
Synonyms (NCBI Gene)
Gene synonyms aliases
|
C15orf16, C16ORF15, CEZANNE2, NEDHS, OTUD7 |
|
Chromosome
Chromosome number
|
15 |
|
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
15q13.3 |
|
Summary
Summary of gene provided in NCBI Entrez Gene.
|
The protein encoded by this gene is a deubiquitinizing enzyme and possible tumor suppressor. The encoded protein acts on TNF receptor associated factor 6 (TRAF6) to control nuclear factor kappa B expression. However, this gene is downregulated by SNAIL1 i |
|
miRNA
miRNA information provided by mirtarbase database.
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
|
|||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||
|
Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
|
|||||||
|
|||||||
| Protein | |||||||||||||||||||||
| UniProt ID | Q8TE49 | ||||||||||||||||||||
| Protein name | OTU domain-containing protein 7A (EC 3.4.19.12) (Zinc finger protein Cezanne 2) | ||||||||||||||||||||
| Protein function | Deubiquitinase, which cleaves 'Lys-11'-linked polyubiquitin chains. Might be required for PA28-20S proteasome assembly (Probable). | ||||||||||||||||||||
| PDB | 2L2D | ||||||||||||||||||||
| Family and domains |
Pfam
|
||||||||||||||||||||
| Sequence |
|
||||||||||||||||||||
| Sequence length | 926 | ||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||
|
Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
|
|||||||
|
|||||||
|
Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
|
|||||||||||||||||||||
|
|||||||||||||||||||||
|
|||||||||||||||||||||