|Name||myopia 2 (high grade, autosomal dominant)|
|NCBI Gene ID||4658|
|Expression in Tissues and Cell Lines||
MYP2 has 19 functional associations with biological entities spanning 2 categories (disease, phenotype or trait, functional term, phrase or reference) extracted from 4 datasets.
Click the + buttons to view associations for MYP2 from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with MYP2 gene/protein from the curated CTD Gene-Disease Associations dataset.|
|GeneRIF Biological Term Annotations||biological terms co-occuring with MYP2 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.|
|HuGE Navigator Gene-Phenotype Associations||phenotypes associated with MYP2 gene by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.|
|OMIM Gene-Disease Associations||phenotypes associated with MYP2 gene from the curated OMIM Gene-Disease Associations dataset.|