Other Services

This Service

A database built with INDRA combining content from numerous readers and databases. This page allows you to curate the loaded statements. For more information please see the manual.

This Project

INDRA is developed by indralabs, a part of the Harvard Medical School Laboratory of Systems Pharmacology.

This project, indra_db, is also developed by the indralab team. For more information on how we procure our sources, you can go here. This work was funded by ARO grant W911NF‐15‐1‐0544 under the DARPA Communicating with Computers program.

IndraLab

Statements

SCN9A binds ATXN3. 1 / 1

| 1

➶

sparser

"Further supporting the notion of C1719 being pathogenic, this conserved cysteine was found mutated (C1756G) in SCN1A in a patient with severe myoclonic epilepsy in infancy ( xref ), an autosomal dominant condition (OMIM 607208) that has also been associated with mutations in SCN9A ( xref )."

20692858

Our Sources:

INDRA allows us to combine the results from a multitude of sources. In particular, the INDRA Database draws on the following...