|HGNC Family||X-linked mental retardation|
|Name||mental retardation, X-linked 49|
|NCBI Gene ID||4412|
|Expression in Tissues and Cell Lines||
MRX49 has 11 functional associations with biological entities spanning 2 categories (disease, phenotype or trait, functional term, phrase or reference) extracted from 3 datasets.
Click the + buttons to view associations for MRX49 from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with MRX49 gene/protein from the curated CTD Gene-Disease Associations dataset.|
|GeneRIF Biological Term Annotations||biological terms co-occuring with MRX49 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.|
|OMIM Gene-Disease Associations||phenotypes associated with MRX49 gene from the curated OMIM Gene-Disease Associations dataset.|