IndraLab

Statements

KCN activates KCNQ2. 2 / 2

| 2

reach

"Potassium channel, voltage-gated, kqt-like subfamily, member 2 (KCNQ2) pathogenic variants cause benign neonatal epilepsy and KCNQ2-related encephalopathy."

| PMC

➶

reach

"A significant proportion of cases have a genetic origin, and the most frequently mutated gene is KCNQ2, encoding Kv7.2, a voltage dependent potassium channel subunit, leading to so called KCNQ2 related epileptic encephalopathy (KCNQ2-REE)."

32239694

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

KCN activates KCNQ2. 2 / 2

INDRA sources:

Databases

Reading