Genes | GeDiPNet - Gene Disease Pathway & Associations

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7781 to 7790 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
7781	79006	METRN	Meteorin, glial cell differentiation regulator	C16orf23, c380A1.2	Ankylosing spondylitis, Atrial fibrillation, Insomnia
7782	284207	METRNL	Meteorin like, glial cell differentiation regulator	-	Neoplasms, Breast cancer, Cataract, Colorectal adenoma, Colorectal cancer, Diabetes mellitus type 2, Migraine
7783	4234	METTL1	Methyltransferase 1, tRNA methylguanosine	C12orf1, TRM8, TRMT8, YDL201w	Cortical development malformation, Multiple sclerosis
7784	51603	METTL13	Methyltransferase 13, eEF1A N-terminus and K55	5630401D24Rik, CGI-01, DFNB26, DFNB26M, DFNM1, EEF1AKNMT, KIAA0859, feat	Astrocytoma, Attention deficit hyperactivity disorder, Autism, Deafness, Parkinson disease
7785	57721	METTL14	Methyltransferase 14, N6-adenosine-methyltransferase non-catalytic subunit	hMETTL14	Cardiomyopathy, Edema, Diabetes mellitus type 2, Multiple myeloma, Necrosis, Ventricular dysfunction
7786	196074	METTL15	Methyltransferase 15, mitochondrial 12S rRNA N4-cytidine	METT5D1	Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cannabis abuse, Lymphocytic leukemia, Major depressive disorder, Neurotic disorder, Obesity, Obsessive-compulsive disorder, Obstructive sleep apnea syndrome, Open angle glaucoma, Osteoarthritis, Post-traumatic stress disorder, Psychiatric disorders View all (5 more)
7787	79066	METTL16	Methyltransferase 16, RNA N6-adenosine	METT10D	Central nervous system cancer, Glioblastoma, Glioma, Insomnia, Diabetes mellitus type 2
7788	151194	METTL21A	Methyltransferase 21A, HSPA lysine	FAM119A, HCA557b, HSPA-KMT	Schizophrenia, Amyotrophic lateral sclerosis
7789	196541	METTL21C	Methyltransferase 21C, AARS1 lysine	C13orf39	Color vision deficiency
7790	79091	METTL22	Methyltransferase 22, Kin17 lysine	C16orf68	Systemic scleroderma

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