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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

STXBP1 binds THRA, UBE3A, COL11A1, MYH14, KATNAL2, GJB6, KCNQ4, and ARSD. 2 / 2

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"Mutations in different genes, such as STXBP1, KCNQ4, MYH14, GJB6, COL11A1, UBE3A, KATNAL2, and THRA, have also been associated with ASD [ xref ]."

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"One such study, by Yuen et al., found genetic aberrations in STXBP1 , UBE3A , KATNAL2 , THRA , KCNQ4 , MYH14 , GJB6 and COL11A1 , some of which have been previously associated with ASD and some with overlapping conditions such as hearing loss [ xref ]."

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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...