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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

SCN5A activates LQT type 3. 2 / 2

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"Among congenital LQTS, LQT type 3 (LQT3) caused by a mutation in the SCN5A gene, the alpha subunit of cardiac sodium channel Nav1.5, is usually diagnosed in only 10% of cases of genetically identified LQTS."

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"LQT type 3 (LQT3) syndrome is caused by mutations in the SCN5A gene that encodes Nav1.5."

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Our Sources:

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