Article snapshot taken from[REDACTED] with creative commons attribution-sharealike license.
Give it a read and then ask your questions in the chat.
We can research this topic together.
Protein-coding gene in the species Homo sapiens
For the cruise missile, see KSR-2.
Variations within the gene and its expression are hypothesized to play a key role in the phenotype of individuals with metabolic disease, alongside leptin-deficiency induced hyperphagia. While the exact mechanism is unclear, it is believed that KSR2 variations result in a disruption of the MAPK/ERK pathway, which can in turn lower the body's BMR. Since this normally accounts for about 70% of the total energy expenditure, a decrease results in excess energy storage, compared to an individual with a normal BMR on an isocaloric diet.
Besides human metabolism, KSR2 is also crucial for ovarian development in the cabbage beetle Colaphellus bowringi.