IndraLab

Statements

KCNH2 activates LQT syndrome type 2. 1 / 1

| 1

reach

"LQT syndrome type 2 (LQT2) is caused by a mutation in KCNH2 (also known as human ether-a-go-go, HERG), which encodes the alpha subunits of channels that generate I Kr, a rapid component of the delayed rectifier potassium current."

26274955

INDRA sources:

Colored badges next to statement headings correspond to evidence counts from knowledge sources, as shown below. Badges to the left of the | separator correspond to curated knowledge base sources, and badges to the right of it correspond to machine reading systems.

IndraLab

Statements

KCNH2 activates LQT syndrome type 2. 1 / 1

INDRA sources:

Databases

Reading