|Name||optic atrophy 5 (autosomal dominant)|
|NCBI Gene ID||692222|
|Expression in Tissues and Cell Lines||
OPA5 has 15 functional associations with biological entities spanning 2 categories (disease, phenotype or trait, functional term, phrase or reference) extracted from 3 datasets.
Click the + buttons to view associations for OPA5 from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with OPA5 gene/protein from the curated CTD Gene-Disease Associations dataset.|
|GeneRIF Biological Term Annotations||biological terms co-occuring with OPA5 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.|
|OMIM Gene-Disease Associations||phenotypes associated with OPA5 gene from the curated OMIM Gene-Disease Associations dataset.|