|Name||oculocutaneous albinism 5 (autosomal recessive)|
|NCBI Gene ID||101926885|
|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
|OMIM Gene-Disease Associations||phenotypes associated with OCA5 gene from the curated OMIM Gene-Disease Associations dataset.|