MRT9 Gene

Name mental retardation, non-syndromic, autosomal recessive, 9
Synonyms MRT26
NCBI Gene ID 100101424
API
Download Associations
Predicted Functions View MRT9's ARCHS4 Predicted Functions.
Co-expressed Genes View MRT9's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MRT9's ARCHS4 Predicted Functions.

Functional Associations

MRT9 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 MRT9 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with MRT9 gene/protein from the curated CTD Gene-Disease Associations dataset.
OMIM Gene-Disease Associations phenotypes associated with MRT9 gene from the curated OMIM Gene-Disease Associations dataset.