274
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Microtubule associated protein RP/EB family member 2 |
CSCSC2, EB1, EB2, RP1 |
Curated: Brugada syndrome, Central nervous system cancer, Color vision deficiency, Developmental disability, Glioma, Hypertrophic cardiomyopathy, Scoliosis
Unreviewed: Albinism, Atrophy, Autoimmune disease, Carcinoma, Cataract, Choroideremia, Ciliopathy, Colorectal Cancer, Congenital Epicanthus, Congenital Exomphalos, Congenital Hypoplasia Of Penis, Congestive Heart Failure, Crohn disease, Cryptorchidism, Developmental Delay, Diabetes Mellitus, Disorder Of Eye, Down syndrome, Dwarfism, Dysmorphism, Emphysema, Glaucoma, Hearing Loss, Hyperinsulinism, Hypogonadism, Hypoplasia Of Corpus Callosum, Hypospadias, Intracranial Aneurysm, Keratoconus, Kidney Disease, Leber congenital amaurosis, Leukemia, Liver carcinoma, Lung carcinoma, Lymphoblastic Leukemia, Macular degeneration, Mental retardation, Methylmalonic acidemia, Michelin Tire Baby Syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Microstomia, Microtia, Motor delay, Multiple Benign Circumferential Skin Creases On Limbs, Multiple polyposis syndrome, Myopia, Neoplasms, Neuroblastoma, Nyctalopia, Nystagmus, Obesity, Optic Atrophy, Pancreatitis, Posteriorly Rotated Ear, Renal cell carcinoma, Retinal detachment, Retinal Diseases, Retinal Dystrophy, Retinitis Pigmentosa, Rheumatoid arthritis, Rod-cone dystrophy, Skin Creases, Congenital Symmetric Circumferential, Stomach neoplasms, Ulcerative colitis, Urogenital abnormalities, Usher syndrome, Vitamin d deficiency
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277
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Microtubule associated protein tau |
DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1, MTBT2, PPND, PPP1R103, TAU, Tau-PHF6, tau-40 |
Curated: Alzheimer disease, Androgenetic alopecia, Anxiety disorder, Ataxia, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Autism, Parkinson disease, Breast cancer, Hepatocellular carcinoma, Cardiac arrhythmia, Cardiomyopathy, Progressive supranuclear palsy, Cognition disorder, Degenerative disorder, Delirium, dementia, and cognitive disorders, Dementia, Dilated cardiomyopathy, Dyslexia, Temporal lobe epilepsy, Estrogen-receptor negative breast cancer, Frontotemporal dementia, Gastroesophageal reflux disease, Generalized anxiety disorder, Heart failure, Idiopathic pulmonary fibrosis, Interstitial lung disease, Hereditary parkinson disease, Learning disorders, Major depressive disorder, Memory disorders, Metabolic syndrome, Migraine, Mood disorder, Neurodegenerative disorder, Neurotic disorder, Open angle glaucoma, Osteoarthritis, Ovarian cancer, Parkinson-dementia syndrome, Post-traumatic stress disorder, Biliary cholangitis, Psychiatric disorders, Retinal detachment, Schizophrenia, Splenomegaly, Substance abuse, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2
Unreviewed: 22q13 monosomy syndrome, Abulia, Acquired Kyphoscoliosis, Age-Related Memory Disorders, Akinesia, Alexia, Alopecia, Alopecia, Male Pattern, Amnesia, Amyloid angiopathy, Amyloidosis, Amyotrophic Lateral Sclerosis, Androgenetic Alopecia, Anomia, Anxiety Disorder, Aphasia, Apnea, Apraxia, Arthritis, Astrocytoma, Ataxia telangiectasia, Atrial Fibrillation, Atrophy, Auditory perceptual disorder, Aural Atresia, Congenital, Autism spectrum disorder, Autoimmune disease, Autonomic Central Nervous System Diseases, Autonomic nervous system disease, B-Cell Lymphoma, Basal ganglia disease, Behavior Disorders, Behavioral Variant Of Frontotemporal Dementia, Biliary Cirrhosis, Blepharospasm, Brain atrophy, Brain disease, Brain injuries, Brain Neoplasms, Brain stem neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Broca Aphasia, Bulbospinal Atrophy, X-Linked, Calcinosis, Calcium metabolism disorders, Carcinoma, Cardiovascular disease, Cardiovascular Diseases, Cerebellar atrophy, Cerebellar diseases, Cerebral Amyloid Angiopathy, Cerebral Atrophy, Cerebral cortical atrophy, Cerebral Infarction, Cerebral Ischemia, Cerebral microangiopathy, Cerebral palsy, Cerebrovascular Disorders, Choriocarcinoma, Chromosome 17q21.31 deletion syndrome, CNS Disorder, Cognitive disorder, Colon Carcinoma, Colonic Neoplasms, Compulsive Hoarding, Congenital kyphoscoliosis, Congenital macrodactylia, Connective tissue disease, Cortical development malformation, Corticobasal Degeneration, Craniocerebral trauma, Creutzfeldt-Jakob disease, Crohn disease, CSF pleocytosis, Degenerative Brain Disorder, Degenerative Diseases, Central Nervous System, Delusions, Dementia Of Frontal Lobe, Deuteranomaly, Development Disorder, Developmental Delay, Developmental disability, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Diaphyseal dysplasia, Disruptive, impulse control, and conduct disorders, Distal myopathy, Down Syndrome, Duchenne muscular dystrophy, Dysarthria, Dysautonomia, Dyscalculia, Dysgraphia, Dysphagia, Dysphasia, Dyssomnia, Encephalitis, Encephalopathy With Neuroserpin Inclusion Bodies, Epilepsy, Epithelial ovarian carcinoma, Essential tremor, Facial dysmorphism, Focal dystonia, Frontal lobe epilepsy, Frontotemporal cerebral atrophy, Gerstmann-Straussler-Scheinker syndrome, Glaucoma, Glioblastoma, Glioma, Grammar-specific speech disorder, Graves ophthalmopathy, Hallucinations, Hearing loss, Heart disease, Hemimegalencephaly, Hereditary Diffuse Leukoencephalopathy With Spheroids, Hereditary folate malabsorption, Hereditary Leber Optic Atrophy, Hereditary spastic paraplegia, Huntington Disease, Hydrocephalus, Hyperglycemia, Hyperhomocysteinemia, Hyperinsulinism, Hyperkinesia, Hypoxia, Hypoxic-Ischemic Encephalopathy, Impaired Cognition, Inclusion body myopathy, Inclusion Body Myositis, Insomnia, Insulinoma, Intellectual developmental disorder, Ischemic Stroke, Kidney failure, Lafora Disease, Language development disorders, Language Disorders, Lateral Sclerosis, Learning Disorders, Leprosy, Lewy Body Disease, Limb apraxia, Liver carcinoma, Long qt syndrome, Lung carcinoma, Lung Diseases, Lymphoblastic Leukemia, Lymphocytic Leukemia, Malignant Neoplasm, Mammary Neoplasms, Melanoma, Memory Disorders, Meningioma, Mental Depression, Mental retardation, Mitochondrial complex deficiency, Mitochondrial disease, Mood Disorder, Motor neuron atrophy, Motor Neuron Disease, Movement disorder, Movement Disorders, Multiple polyposis syndrome, Multiple Sclerosis, Multiple system atrophy, Myocardial Diseases, Myocardial Infarction, Myositis, Myotonic Disorders, Myotonic dystrophy, Nail-Patella Syndrome, Narcolepsy, Nasopharyngeal Carcinoma, Neoplasms, Nervous system disease, Nervous System Diseases, Nervous System Disorder, Neuroblastoma, Neurodegenerative Disorders, Neurodevelopmental Disorders, Neurogenic bladder, Neuromuscular dysphagia, Neuropathy, Niemann-Pick Disease, Night blindness, congenital stationary, Nonfluent Aphasia, Nonorganic Psychosis, Normal pressure hydrocephalus, Obesity, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Oestrogen Receptor Positive Breast Cancer, Orthostatic hypotension, Osteoarthritis Of Hip, Osteoporosis, Ovarian Epithelial carcinoma, Ovarian neoplasm, Panic disorder, Parkinsonian disease, Paroxysmal atrial fibrillation, Peripheral Neuropathy, Pica, Pineal Gland Neoplasm, Pneumothorax, Prion disease, Progressive Non-Fluent Aphasia, Progressive supranuclear ophthalmoplegia, Progressive Supranuclear Palsy, Prostate cancer, Prostatic neoplasm, Psychosis, Psychotic disorders, Ramsay Hunt Paralysis Syndrome, Renal cell carcinoma, Respiratory Failure, Retrocollis, Rheumatoid arthritis, Sarcoma, Schilder disease, Secondary parkinson disease, Seizure, Semantic Dementia, Senile Dementia, Senile Paranoid Dementia, Senile Plaques, Sjogren syndrome, Sleep apnea, Sleep Disorders, Speech Disorders, Sphingomyelinase deficiency, Spinal muscular atrophy, Stereotyped Behavior, Stomach Carcinoma, Stomach Neoplasms, Stroke, Strudwick Syndrome, Supranuclear gaze palsy, Supranuclear Palsy, Supranuclear Palsy-Corticobasal Syndrome, Supranuclear Palsy-Parkinsonism Syndrome, Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome, Supranuclear Palsy-Pure Akinesia With Gait Freezing Syndrome, Syndactyly, Systemic sclerosis, Tauopathies, Temporal cortical atrophy, Torsades de pointes, Tremor, Ulcerative colitis, Vascular dementia, Vascular Diseases, Ventricular fibrillation, Visual disorder, Wernicke Encephalopathy, Willis-ekbom disease
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280
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Membrane associated ring-CH-type finger 1 |
MARCH-I, MARCH1, RNF171 |
Curated: Asthma, Central nervous system cancer, Kidney disease, Color vision deficiency, Coronary artery disease, Digestive system disease, Glioblastoma, Glioma, Hypertension, Insomnia, Mouth disease, Multiple sclerosis, Myocardial infarction, Ovarian cancer, Peripheral neuropathy, Pernicious anemia, Scoliosis, Small cell lung carcinoma, Stroke, Diabetes mellitus type 2
Unreviewed: Ankylosing Spondylitis, Autoimmune Diseases, Bladder carcinoma, Bladder Neoplasm, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Colorectal Cancer, Congestive Heart Failure, Crohn Disease, Cryptorchidism, Cystic Fibrosis, Dementia, Dextrocardia, Diabetes Insipidus, Diabetes Mellitus, Epilepsy, Esophageal Carcinoma, Exfoliation Syndrome, Febrile seizures, Gastroenteritis, Glaucoma, Heart Diseases, Heart Failure, Hyperlipidemia, Hypoglycemia, Inflammatory Bowel Disease, Ischemic Stroke, Kidney Disease, Liver Cancer, Liver carcinoma, Lung carcinoma, Lymphocytic Leukemia, Malignant Neoplasm, Melanoma, Mesothelioma, Metabolic Syndrome, Multiple Sclerosis, Myelodysplastic Syndrome, Neoplasms, Neurodegenerative disorder, Obesity, Ocular Hypertension, Osteosarcoma, Ovarian Epithelial carcinoma, Ovarian neoplasm, Prostate cancer, Pulmonary Fibrosis, Retinopathy, Rheumatoid arthritis, Schizophrenia, Schwartz-Jampel Syndrome, Senile Dementia, ST Segment Elevation Myocardial Infarction, Stevens-Johnson Syndrome, Stomach Carcinoma, Stomach Neoplasms, Thrombophilia, Thrombosis, Tongue carcinoma, Ulcerative colitis, Urinary bladder cancer, Urticaria, Ventricular arrhythmia, Xeroderma Pigmentosum
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