Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "M"

861 to 870 of 898 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
861	4542	MYO1F	Myosin IF	-	Liver cirrhosis, Metabolic syndrome, Nonsyndromic hearing loss, Diabetes mellitus, type 2
862	64005	MYO1G	Myosin IG	HA2, HLA-HA2, MHAG	Bipolar disorder, Major depressive disorder, Schizoaffective disorder, Squamous cell carcinoma
863	283446	MYO1H	Myosin IH	CCHS2	Bipolar disorder, Haddad syndrome, Central hypoventilation syndrome, Color vision deficiency, Congenital central hypoventilation syndrome, Insomnia, Major depressive disorder, Migraine, Mood disorder, Neurotic disorder, Schizophrenia
864	53904	MYO3A	Myosin IIIA	DFNA90, DFNB30	Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss, Obesity, Diabetes mellitus, type 2
865	140469	MYO3B	Myosin IIIB	-	Androgenetic alopecia, Bruxism, Coronary aneurysm, Migraine, Obesity
866	4644	MYO5A	Myosin VA	GS1, MYH12, MYO5, MYR12	Cerebellar cortical atrophy, Diabetes mellitus, Hereditary elliptocytosis, Global developmental delay, Griscelli syndrome, Liver cirrhosis, Non-neoplastic peripheral nervous system disease, Nystagmus, Peripheral nervous system disease, Peripheral neuropathy, Schizophrenia, Diabetes mellitus, type 2
867	4645	MYO5B	Myosin VB	DIAR2, MVID1, PFIC10	Amphetamine or sympathomimetic abuse, Cholelithiasis, Congenital microvillous atrophy, Crohn disease, Diarrhea, Dysentery, Glioma, Intestinal disease, Liver neoplasm, Microvillus inclusion disease, Multiple sclerosis, Osteoarthritis, Progressive intrahepatic cholestasis, Schizophrenia, Hypertension
868	55930	MYO5C	Myosin VC	-	Breast cancer, Diabetes mellitus, Prostate cancer, Systemic lupus erythematosus, Diabetes mellitus, type 2
869	4646	MYO6	Myosin VI	DFNA22, DFNB37	Atrial fibrillation, Isolated sensorineural deafness, Nonsyndromic hearing loss, Congenital ear anomaly, Deafness, Autosomal dominant sensorineural deafness, Junctional epidermolysis bullosa, Essential tremor, Hearing impairment, Hearing loss, Hereditary hearing loss, Male infertility, Meniere disease, Osteoarthritis, Hearing loss with hypertrophic cardiomyopathy View all (3 more)
870	4647	MYO7A	Myosin VIIA	DFNA11, DFNB2, MYOVIIA, MYU7A, NSRD2, USH1B	Auditory neuropathy, Isolated sensorineural deafness, Nonsyndromic hearing loss, Congenital ear anomaly, Congenital nystagmus, Deafness, Global developmental delay, Hearing impairment, Hearing loss, Hereditary hearing loss, Hypoglycemia, Leber congenital amaurosis, Lewy body disease, Melanoma, Meniere disease View all (5 more)

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