MEL-1A-R Polyclonal Antibody, 100ul Cell Culture Flasks Mutations in this gene are

Mutations in this gene are a cause of Charcot-Marie-Tooth disease type 4D

unlike NT1 receptor

Gene Ontology (GO) annotations related to this gene include calcium channel activity

Mutations in this gene are the cause of protein Z deficiency

MEL-1A-R Polyclonal Antibody, 100ul Cell Culture Flasks Mutations in this gene areMTNR1A encodes one of two high affinity forms of a receptor for melatonin, the primary hormone secreted by the pineal gland. This receptor is a G protein coupled, 7 transmembrane receptor that is responsible for melatonin effects on mammalian circadian rhythm and reproductive alterations affected by day length. The receptor is an integral membrane protein that is readily detectable and localized to two specific regions of the brain. The hypothalamic