Name Cogan-type congential oculomotor apraxia
NCBI Gene ID 266710
Download Associations
Predicted Functions View COMA's ARCHS4 Predicted Functions.
Co-expressed Genes View COMA's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View COMA's ARCHS4 Predicted Functions.

Functional Associations

COMA has 2 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 2 datasets.

Click the + buttons to view associations for COMA from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with COMA gene/protein from the curated CTD Gene-Disease Associations dataset.
OMIM Gene-Disease Associations phenotypes associated with COMA gene from the curated OMIM Gene-Disease Associations dataset.