Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "M"

741 to 750 of 893 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
741	4543	MTNR1A	Melatonin receptor 1A	MEL-1A-R, MT1	Autism, Breast cancer, Prostate cancer, Schizophrenia
742	4544	MTNR1B	Melatonin receptor 1B	FGQTL2, MEL-1B-R, MT2	Autism, Dental caries, Diabetes mellitus, Diabetes mellitus type 2, Diabetic neuropathy, Gestational diabetes, Metabolic syndrome, Neurotic disorder, Obesity, Polycystic ovary syndrome, Schizophrenia
743	25821	MTO1	Mitochondrial tRNA translation optimization 1	CGI-02, COXPD10	Combined oxidative phosphorylation deficiency, Global developmental delay, Mitochondrial disease
744	2475	MTOR	Mechanistic target of rapamycin kinase	FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS	Breast neoplasms, Hepatocellular carcinoma, Non-small-cell lung carcinoma, Renal cell carcinoma, Small cell carcinoma, Cebalid syndrome, Colonic neoplasms, Diabetes mellitus type 2, Dupuytren contracture, Endocrine system disease, Focal cortical dysplasia, Glioblastoma, Hemimegalencephaly, Hepatomegaly, Hypertension View all (18 more)
745	55149	MTPAP	Mitochondrial poly(A) polymerase	PAPD1, SPAX4, TENT6	Spastic ataxia optic atrophy dysarthria syndrome, Melanoma, Mitochondrial disease, Spastic ataxia
746	136319	MTPN	Myotrophin	GCDP, V-1	Bone disease, Cartilage disease, Dementia, Dry eye syndrome, Obesity, Periodontitis, Venous thromboembolism
747	4548	MTR	5-methyltetrahydrofolate-homocysteine methyltransferase	HMAG, MS, cblG	Autism, Bipolar disorder, Breast neoplasms, Ischemic stroke, Cleft lip, Cleft palate, Complete unilateral cleft lip, Major depressive disorder, Digestive system disease, Intracellular cobalamin metabolism disorder, Epilepsy, Gastrointestinal disease, Heart disease, Hematologic disease, Homocystinuria with megaloblastic anemia View all (11 more)
748	51250	MTRES1	Mitochondrial transcription rescue factor 1	C6orf203, HSPC230, PRED31	Prostate cancer, Hypertension
749	9617	MTRF1	Mitochondrial translation release factor 1	MRF1, MTTRF1, RF1	Cardiovascular disease
750	91574	MTRFR	Mitochondrial translation release factor in rescue	C12orf65, COXPD7, SPG55, mtRF-R	Alzheimer disease, Asthma, Spastic paraplegia, Combined oxidative phosphorylation deficiency, Endometriosis, Developmental and epileptic encephalopathy, Hereditary motor and sensory neuropathies, Leigh syndrome, Metabolic syndrome, Mitochondrial disease, Mitochondrial encephalomyopathy, Neurodevelopmental disorder, Optic atrophy, Osteoarthritis, Retinitis pigmentosa View all (4 more)

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