CORO7 (coronin 7)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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79585 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Coronin 7 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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CORO7 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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0610011B16Rik, CRN7, POD1 |
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Chromosome
Chromosome number
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16 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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16p13.3 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of the coronin protein family. However, unlike other coronin proteins, it is not an actin-binding protein but rather functions as an F-actin regulator directing anterograde Golgi to endosome transport. The encoded protein has tw |
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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 | P57737 | |||||||||||||||||||||||||||||||||||||||||||||
| Protein name | Coronin-7 (Crn7) (70 kDa WD repeat tumor rejection antigen homolog) | |||||||||||||||||||||||||||||||||||||||||||||
| Protein function | F-actin regulator involved in anterograde Golgi to endosome transport: upon ubiquitination via 'Lys-33'-linked ubiquitin chains by the BCR(KLHL20) E3 ubiquitin ligase complex, interacts with EPS15 and localizes to the trans-Golgi network, where | |||||||||||||||||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Widely expressed. Expressed in the spleen, peripheral leukocytes, testes, brain, thymus and small intestine. {ECO:0000269|PubMed:21130766}. | |||||||||||||||||||||||||||||||||||||||||||||
| Sequence |
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| Sequence length | 925 | |||||||||||||||||||||||||||||||||||||||||||||
| Interactions | View interactions | |||||||||||||||||||||||||||||||||||||||||||||
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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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