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

SCN1B binds SCN5A, TRPM4, GJA5, and LMNA. 2 / 2

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sparser

"Nineteen genes known or suspected to be involved in conduction defects were sequenced in these patients using the HaloPlex™ System, resulting in a mean coverage depth of 578 × per sample: SCN5A , SC[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

26820365

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sparser

"In this study we focused solely on the relevant 19 PCCD genes including SCN5A , SCN1B , TRPM4 , GJA5 and LMNA that have already been associated with isolated cardiac conduction defects together[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

26820365

Our Sources:

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