Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "M"

471 to 480 of 898 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
471	22877	MLXIP	MLX interacting protein	MIR, MONDOA, bHLHe36	Eczema, Gout, Inflammatory skin disease, Osteoarthritis, Psoriasis, Schizophrenia
472	51085	MLXIPL	MLX interacting protein like	CHREBP, MIO, MLX, MONDOB, WBSCR14, WS-bHLH, bHLHd14	Alzheimer disease, Astrocytoma, Atrial fibrillation, Cancer, Hepatocellular carcinoma, Central nervous system cancer, Cholecystolithiasis, Ischemic heart disease, Liver cirrhosis, Coronary artery disease, Diabetes mellitus, Hyperlipidemia, Lipoprotein lipase deficiency, Gallstones, Glioblastoma View all (14 more)
473	23417	MLYCD	Malonyl-CoA decarboxylase	MCD	Cardiomyopathy, Malonyl-coa decarboxylase deficiency, Intellectual developmental disorder, Keratoconus, Malonic aciduria, Neuroblastoma, Scoliosis, Diabetes mellitus type 2
474	166785	MMAA	Metabolism of cobalamin associated A	cblA	Cataract, Deficiency anemia, Megaloblastic anemia, Methylmalonic acidemia, Vitamin b deficiency, Vitamin b12 deficiency, Vitamin b12-unresponsive methylmalonic acidemia
475	326625	MMAB	Metabolism of cobalamin associated B	ATR, CFAP23, cblB, cob	Autoinflammatory syndrome, Cataract, Coronary artery disease, Major depressive disorder, Hyper-immunoglobulin d syndrome, Insomnia, Methylmalonic acidemia, Neurotic disorder, Polymyositis, Prostate cancer, Psychiatric disorders, Schizophrenia, Vitamin b12-unresponsive methylmalonic acidemia
476	25974	MMACHC	Metabolism of cobalamin associated C	cblC	Hemolytic uremic syndrome, Cobalamin c disease, Disorders of intracellular cobalamin metabolism, Methylmalonic acidemia, Retinitis pigmentosa
477	27249	MMADHC	Metabolism of cobalamin associated D	C2orf25, CL25022, HMAD, MACD, MAHCD, cblD	Lymphoblastic leukemia, Cobalamin c disease, Disorder of cobalamin metabolism and transport, Disorders of intracellular cobalamin metabolism, Homocystinuria with megaloblastic anemia, Methylmalonic acidemia, Vitamin b12-unresponsive methylmalonic acidemia
478	23531	MMD	Monocyte to macrophage differentiation associated	MMA, MMD1, PAQR11	Obesity, Schizophrenia
479	221938	MMD2	Monocyte to macrophage differentiation associated 2	PAQR10	Alzheimer disease
480	4311	MME	Membrane metalloendopeptidase	CALLA, CD10, CMT2T, NEP, SCA43, SFE	Alzheimer disease, Spinocerebellar ataxia, Breast neoplasms, Cerebral amyloid angiopathy, Charcot-marie-tooth disease, Congenital membranous nephropathy, Cryopyrin-associated periodic syndrome, Dejerine-sottas disease, Diabetic neuropathy, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Kidney failure, Liver cirrhosis, Membranous glomerulonephritis, Peripheral neuropathy View all (4 more)

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