4321
|
|
|
Myosin IIIB |
- |
Curated: Androgenetic alopecia, Bruxism, Coronary aneurysm, Migraine, Obesity
Unreviewed: Bardet-Biedl Syndrome, Endometrial neoplasm, Intracranial Aneurysm, Leukemia
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4322
|
|
|
MYO3B antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
4323
|
|
|
Myosin VA |
GS1, MYH12, MYO5, MYR12 |
Curated: 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
Unreviewed: Acrocephalopolydactyly, Age-related macular degeneration, Albinism, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Central nervous system disease, Cerebellar Hypoplasia, Cerebral cortical hemiatrophy, Colorectal Cancer, Colorectal neoplasm, Developmental Delay, Diabetes Mellitus, Diabetes mellitus, type 2, Dilated cardiomyopathy, Elejalde Disease, Esophageal squamous cell carcinoma, Glioblastoma, Hyperlipidemia, Hypertrophic cardiomyopathy, Hypopigmentation Disorder, Hypopigmentation-Immunodeficiency Disease, Hypoxia, Laryngeal Carcinoma, Malignant Neoplasm, Malignant Neoplasm Of Testis, Malignant testicular germ cell tumor, Melanoma, Mental retardation, Movement Disorders, Myopia, Neoplasms, Nervous system disease, Nervous System Diseases, Neuroblastoma, Neuroectodermal Melanolysosomal Disease, Optic Atrophy, Peripheral Neuropathy, Pheochromocytoma, Piebaldism, Prostate cancer, Retinal Diseases, Specific Learning Disorder, Squamous cell carcinoma, Stomach neoplasms, Strabismus, Stroke, Subcortical cerebral atrophy, Trichothiodystrophy
|
4324
|
|
|
Myosin VB |
DIAR2, MVID1, PFIC10 |
Curated: 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
Unreviewed: Adrenal Gland Pheochromocytoma, Atrophy, Attention Deficit Hyperactivity Disorder, Bipolar Disorder, Bulbospinal Atrophy, X-Linked, Cholestasis, Colorectal Cancer, Colorectal neoplasm, Congenital secretory diarrhea, Cyst, Developmental Delay, Diabetes mellitus, type 2, Diarrhea, Dysentery, Dyslexia, Endometrial neoplasm, Epilepsy, Fabry disease, Fanconi syndrome, Hyperchloremia, Inborn Errors Of Metabolism, Intestinal Diseases, Intrahepatic Cholestasis, Intrahepatic cholestasis of pregnancy, Kawasaki disease, Liver Cancer, Liver disease, Malabsorption Syndrome, Malnutrition, Microvillus Inclusion Disease, Mood Disorder, Myopia, Nasopharyngeal Carcinoma, Neoplasms, Nephrocalcinosis, Neuroblastoma, Pancreatic neoplasm, Paraganglioma, Pheochromocytoma, Pruritus, Stomach Carcinoma, Stomach Neoplasms, Trichohepatoenteric Syndrome, Usher Syndrome, Vipoma
|
4325
|
|
|
Myosin VB pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
4326
|
|
|
Myosin VB pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
4327
|
|
|
Myosin VB pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
4328
|
|
|
Myosin VC |
- |
Curated: Breast cancer, Diabetes mellitus, Prostate cancer, Systemic lupus erythematosus, Diabetes mellitus type 2
Unreviewed: Alzheimer disease, Diabetic Retinopathy, Hearing loss, Lewy Body Disease, Obesity, Parkinson disease, Pendred syndrome, Retinal Diseases, Squamous cell carcinoma
|
4329
|
|
|
Myosin VI |
DFNA22, DFNB37 |
Curated: Atrial fibrillation, Isolated sensorineural deafness, Nonsyndromic hearing loss, Congenital ear anomaly, Deafness, Autosomal dominant sensorineural deafness, Junctional epidermolysis bullosa, Essential tremor, Hearing loss, Hereditary hearing loss, Male infertility, Meniere disease, Osteoarthritis, Hearing loss with hypertrophic cardiomyopathy, Prostate cancer, Diabetes mellitus type 2, Waardenburg syndrome, nonsyndromic genetic hearing loss
Unreviewed: Amyotrophic Lateral Sclerosis, Atrial septal defect, Breast Cancer, Breast Carcinoma, Cardiomyopathy, Ciliopathy, Classical Hodgkin lymphoma, Colorectal Cancer, Colorectal neoplasm, Congenital heart defect, Coronary Heart Disease, Deafness with hypertrophic cardioyopathy, Deafness, Sensorineural, With Hypertrophic Cardiomyopathy, Endometriosis, Hearing Loss, Heart Diseases, Hypertension, Hypertrophic cardiomyopathy, Hypoxia, Liver carcinoma, Lung Cancer, Lung carcinoma, Lung neoplasms, Malignant Neoplasm, Melanoma, Myopathy, Myosin storage myopathy, Neoplasms, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Orofaciodigital syndrome, Osteoarthritis Of Hip, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Polycystic kidney disease, Polycystic ovary syndrome, Progressive Sensorineural Hearing Loss-Hypertrophic Cardiomyopathy Syndrome, Prostatic neoplasm, Prostatic Neoplasms, Sensorineural hearing loss, Severe congenital neutropenia, Skin cancer, Stomach Carcinoma, Stomach Neoplasms, Stroke, Tongue carcinoma
|
4330
|
|
|
Myosin VIIA |
DFNA11, DFNB2, MYOVIIA, MYU7A, NSRD2, USH1B |
Curated: Auditory neuropathy, Isolated sensorineural deafness, Nonsyndromic hearing loss, Congenital ear anomaly, Congenital nystagmus, Deafness, Global developmental delay, Hearing loss, Hereditary hearing loss, Hypoglycemia, Leber congenital amaurosis, Lewy body disease, Melanoma, Meniere disease, Optic atrophy, Pendred syndrome, Retinitis pigmentosa, Retinitis pigmentosa-deafness syndrome, Usher syndrome, Usher syndrome type 1, nonsyndromic genetic hearing loss
Unreviewed: Age-related macular degeneration, Anxiety Disorder, Atrophy, Auditory Neuropathy, Bardet-Biedl Syndrome, Blindness, Cardiomyopathy, Cataract, Cerebral cortical atrophy, Ciliopathies, Congenital Sensorineural Hearing Loss, Cystoid macular edema, Developmental Delay, Dilated cardiomyopathy, Disorder Of Eye, Epiretinal Membrane, Hallucinations, Hearing Loss, Hemianopsia, Hereditary Retinal Dystrophy, Intellectual developmental disorder, Leber Congenital Amaurosis, Low-frequency hearing loss, Lung Cancer, Lung carcinoma, Lung neoplasms, Mental Depression, Mental retardation, Microdontia, Motor delay, Multiple Congenital Anomalies, Myopia, Nemaline myopathy, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Nyctalopia, Nystagmus, Oculocerebrorenal syndrome, Retinal degeneration, Retinal detachment, Retinal Diseases, Retinal Dystrophy, Retinitis Pigmentosa, Rod-cone dystrophy, Schizophrenia, Sensorineural hearing loss, Stargardt disease, Stomach neoplasms, Strabismus, Subcortical cerebral atrophy, Usher Syndrome, Vestibular disease, Visual disorder
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