MRT19 Gene

Name mental retardation, non-syndromic, autosomal recessive, 19
NCBI Gene ID 100852395
API
Download Associations
Predicted Functions View MRT19's ARCHS4 Predicted Functions.
Co-expressed Genes View MRT19's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MRT19's ARCHS4 Predicted Functions.

Functional Associations

MRT19 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 MRT19 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
OMIM Gene-Disease Associations phenotypes associated with MRT19 gene from the curated OMIM Gene-Disease Associations dataset.