Genes | GeDiPNet - Gene Disease Pathway & Associations

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All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

8311 to 8320 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
8311	140469	MYO3B	Myosin IIIB	-	Androgenetic alopecia, Bruxism, Coronary aneurysm, Migraine, Obesity
8312	4644	MYO5A	Myosin VA	GS1, MYH12, MYO5, MYR12	Cerebellar cortical atrophy, Diabetes mellitus, Hereditary elliptocytosis, Global developmental delay, Griscelli syndrome, Non-neoplastic peripheral nervous system disease, Nystagmus, Peripheral nervous system disease, Peripheral neuropathy, Schizophrenia, Diabetes mellitus type 2
8313	4645	MYO5B	Myosin VB	DIAR2, MVID1, PFIC10	Amphetamine or sympathomimetic abuse, Cholelithiasis, Congenital microvillous atrophy, Crohn disease, Glioma, Intestinal disease, Liver neoplasms, Microvillus inclusion disease, Multiple sclerosis, Osteoarthritis, Progressive intrahepatic cholestasis, Schizophrenia, Hypertension
8314	55930	MYO5C	Myosin VC	-	Breast cancer, Diabetes mellitus, Prostate cancer, Systemic lupus erythematosus, Diabetes mellitus type 2
8315	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)
8316	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)
8317	4648	MYO7B	Myosin VIIB	-	Clear cell renal cell carcinoma, Cor pulmonale, Heart disease, Kidney cancer, Neuromuscular disease
8318	4649	MYO9A	Myosin IXA	CMS24	Arthrogryposis, Bronchiectasis, Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndrome, Focal glomerulosclerosis, Gout, Myasthenic syndrome, Presynaptic congenital myasthenic syndrome
8319	4650	MYO9B	Myosin IXB	CELIAC4, MYR5	Asthma, Autism, Biliary tract cancer, Breast cancer, Cancer, Cardiovascular disease, Cervical cancer, Color vision deficiency, Colorectal cancer, Coronary artery disease, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Gastric ulcer View all (11 more)
8320	4653	MYOC	Myocilin	GLC1A, GPOA, JOAG, JOAG1, TIGR	Cardioembolic stroke, Congenital glaucoma, Congestive heart failure, Glaucoma, Heart failure, Hydrophthalmos, Ocular hypertension, Open angle glaucoma

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