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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

CACNA1F binds CAV1 and AP1S2. 1 / 1

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"Mutations in the CACNA1F gene, which encodes Cav1.4 LTCC α1 subunits, have been associated with several X-linked visual disorders including Åland Island Eye Disease (AIED) xref , cone-rod dystrophy (CORDX3) xref , X-linked retinal disorder (XRD) xref , night blindness-associated transient tonic down-gaze (NATTD) xref and incomplete congenital stationary night blindness (iCSNB, CSNB2) 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...