| Name | ATP synthase F1 subunit epsilon pseudogene 2 |
| Description | Predicted to enable hydrolase activity. Predicted to contribute to proton-transporting ATP synthase activity, rotational mechanism. Predicted to be involved in proton motive force-driven mitochondrial ATP synthesis. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
| NCBI Gene ID | 432369 |
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| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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ATP5F1EP2 has 5 functional associations with biological entities spanning 2 categories (disease, phenotype or trait, cell line, cell type or tissue) extracted from 2 datasets.
Click the + buttons to view associations for ATP5F1EP2 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CellMarker Gene-Cell Type Associations | cell types associated with ATP5F1EP2 gene from the CellMarker Gene-Cell Type Associations dataset. | |
| IMPC Knockout Mouse Phenotypes | phenotypes of mice caused by ATP5F1EP2 gene knockout from the IMPC Knockout Mouse Phenotypes dataset. | |
