EPN2 (epsin 2)
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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22905 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Epsin 2 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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EPN2 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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EHB21 |
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Chromosome
Chromosome number
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17 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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17p11.2 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a protein which interacts with clathrin and adaptor-related protein complex 2, alpha 1 subunit. The protein is found in a brain-derived clathrin-coated vesicle fraction and localizes to the peri-Golgi region and the cell periphery. The p |
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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 | O95208 | ||||||||||
| Protein name | Epsin-2 (EPS-15-interacting protein 2) | ||||||||||
| Protein function | Plays a role in the formation of clathrin-coated invaginations and endocytosis. | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Highest expression is found in brain. Detected at lower levels in lung and liver. {ECO:0000269|PubMed:10567358}. | ||||||||||
| Sequence |
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| Sequence length | 641 | ||||||||||
| 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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