Genes | GeDiPNet - Gene Disease Pathway & Associations

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8331 to 8340 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
8331	58529	MYOZ1	Myozenin 1	CS-2, FATZ, MYOZ	Atrial fibrillation
8332	51778	MYOZ2	Myozenin 2	C4orf5, CMH16, CS-1, FATZ-2	Alzheimer disease, Attention deficit hyperactivity disorder, Cardiomyopathy, Hypertrophic cardiomyopathy, Diabetes mellitus type 2
8333	84665	MYPN	Myopalladin	CMD1DD, CMH22, CMYO24, CMYP24, MYOP, NEM11, RCM4	Alzheimer disease, Atrial fibrillation, Cap myopathy, Cardiomyopathy, Dilated cardiomyopathy, Nemaline myopathy, Kidney disease, Obstructive pulmonary disease, Congenital myopathy, Restrictive cardiomyopathy, Gastroesophageal reflux disease, Hypertrophic cardiomyopathy, Inflammatory bowel disease, Left ventricular disease, Left ventricular noncompaction cardiomyopathy, Psoriasis View all (1 more)
8334	339344	MYPOP	Myb related transcription factor, partner of profilin	P42pop	Neurotic disorder, Osteoarthritis, Diabetes mellitus type 2
8335	745	MYRF	Myelin regulatory factor	11orf9, C11orf9, CUGS, MMERV, MRF, NNO1, Ndt80, pqn-47	Ankylosing spondylitis, Aortic stenosis, Asthma, Eczema, Neoplasms, Bipolar disorder, Cardiac-urogenital syndrome, Ischemic stroke, Colorectal adenoma, Colorectal cancer, Congenital diaphragmatic hernia, Congenital heart defects, Coronary artery disease, Crohn disease, Developmental disability View all (20 more)
8336	196446	MYRFL	Myelin regulatory factor like	C12orf15, C12orf28, bcm1377	Attention deficit hyperactivity disorder, Conduct disorder, Osteoarthritis
8337	25924	MYRIP	Myosin VIIA and Rab interacting protein	SLAC2-C, SLAC2C	Alzheimer disease, Lymphoblastic leukemia, Connective tissue disease, Male reproductive system disease, Mixed connective tissue disease, Pulmonary edema
8338	114803	MYSM1	Myb like, SWIRM and MPN domains 1	2A-DUB, 2ADUB, BMFS4	Aortic stenosis, Aortic valve disease, Bone marrow failure syndromes, Congenital progressive bone marrow failure-b-cell immunodeficiency-skeletal dysplasia syndrome, Diabetic retinopathy, Willis-ekbom disease
8339	4661	MYT1	Myelin transcription factor 1	C20orf36, MTF1, MYTI, NZF2, PLPB1, ZC2H2C1, ZC2HC4A	Asthma, Autism, Bell's palsy, Breast cancer, Cervical cancer, Craniofacial microsomia, Diverticular disease, Goldenhar syndrome, Intellectual developmental disorder, Movement disorder, Periodic limb movement disorder, Willis-ekbom disease, Schizoaffective disorder, Hereditary spastic paraplegia, Diabetes mellitus type 2
8340	23040	MYT1L	Myelin transcription factor 1 like	MRD39, NZF1, ZC2H2C2, ZC2HC4B, myT1-L	Eczema, Attention deficit hyperactivity disorder, Autism, Color vision deficiency, Diabetic retinopathy, Iga nephropathy, Inflammatory skin disease, Insomnia, Intellectual developmental disorder, Major depressive disorder, Colorectal adenoma, Mood disorder, Neurodevelopmental disorder, Neurotic disorder, Psoriasis View all (6 more)

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