[PMID 19088850] Polymorphisms within the novel type 2 diabetes risk locus MTNR1B determine beta-cell function.

[PMID 21526376] Association of Polymorphism in the Promoter of the Melatonin Receptor 1A Gene with Schizophrenia and with Insomnia Symptoms in Schizophrenia Patients

[PMID 22698518] Melatonin pathway genes are associated with progressive subtypes and disability status in multiple sclerosis among Finnish patients

[PMID 17632395] Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis.

[PMID 20050988] Association of disease-predisposition polymorphisms of the melatonin receptors and sunshine duration in the global human populations.

[PMID 21353709] Single nucleotide polymorphisms and mRNA expression for melatonin MT(2) receptor in depression.

[PMID 21711391] Association and evolutionary studies of the melatonin receptor 1B gene (MTNR1B) in the self-contained population of Sorbs from Germany.

[PMID 22759724] Polymorphisms in the melatonin receptor 1B gene and the risk of delirium

[PMID 23611530] Genetics of melatonin receptor type 2 is associated with left ventricular function in hypertensive patients treated according to guidelines.

[PMID 24969335] [Association between single nucleotide polymorphism of rs4753426 of melatonin receptor 1B gene and gestational diabetes mellitus]

[PMID 25898821] The polymorphisms of melatonin receptor 1B gene (MTNR1B) (rs4753426 and rs10830963) and susceptibility to adolescent idiopathic scoliosis: a meta-analysis


Parent Gene: MTNR1B

Importance: 1
Less common allele: T = 44%
More common allele: C = 56%
My Genotype: Log In