DELXQ21 Gene

Name Choroideremia, deafness, and mental retardation
Synonyms CXDELQ21
NCBI Gene ID 100887743
API
Download Associations
Predicted Functions View DELXQ21's ARCHS4 Predicted Functions.
Co-expressed Genes View DELXQ21's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View DELXQ21's ARCHS4 Predicted Functions.

Functional Associations

DELXQ21 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 DELXQ21 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
OMIM Gene-Disease Associations phenotypes associated with DELXQ21 gene from the curated OMIM Gene-Disease Associations dataset.