|Name||mental retardation, non-syndromic, autosomal recessive, 19|
|NCBI Gene ID||100852395|
|Expression in Tissues and Cell Lines||
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
|OMIM Gene-Disease Associations||phenotypes associated with MRT19 gene from the curated OMIM Gene-Disease Associations dataset.|