| Name | oculocutaneous albinism 5 (autosomal recessive) |
| Synonyms | OCA7 |
| NCBI Gene ID | 101926885 |
| API | |
| Download Associations | |
| Predicted Functions |
![]() |
| Co-expressed Genes |
![]() |
| Expression in Tissues and Cell Lines |
![]() |
OCA5 has 1 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 1 datasets.
Click the + buttons to view associations for OCA5 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| OMIM Gene-Disease Associations | phenotypes associated with OCA5 gene from the curated OMIM Gene-Disease Associations dataset. | |