MRXS7 Gene

HGNC Family X-linked mental retardation
Name mental retardation, X-linked, syndromic 7
NCBI Gene ID 4429
API
Download Associations
Predicted Functions View MRXS7's ARCHS4 Predicted Functions.
Co-expressed Genes View MRXS7's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MRXS7's ARCHS4 Predicted Functions.

Functional Associations

MRXS7 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 MRXS7 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with MRXS7 gene/protein from the curated CTD Gene-Disease Associations dataset.
OMIM Gene-Disease Associations phenotypes associated with MRXS7 gene from the curated OMIM Gene-Disease Associations dataset.