3811
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Synapse differentiation inducing 1 |
C20orf39, DSPC2, IFITMD5, TMEM90B |
Curated: Bipolar disorder, Asthma, Tourette syndrome, Osteonecrosis of the femoral head, Major depressive disorder, Metabolic syndrome, Ovarian cancer, Ovarian serous carcinoma, Periodontal disease, Periodontitis, Schizophrenia, Depression, Diabetes mellitus type 2
Unreviewed: Alzheimer disease, Breast neoplasm
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3812
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Synapse differentiation inducing 1 like |
CAPUCIN, DSPC1, IFITMD4, SynDIG2, TMEM90A |
Curated: Crohn disease, Kidney cancer, Metabolic syndrome, Niemann-pick disease, Open angle glaucoma, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm
Unreviewed: Alzheimer disease
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3813
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Spectrin repeat containing nuclear envelope protein 1 |
8B, AMC3, AMCM, ARCA1, C6orf98, CPG2, EDMD4, KASH1, MYNE1, Nesp1, SCAR8, dJ45H2.2 |
Curated: Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Emery-dreifuss muscular dystrophy, Autosomal recessive ataxia, Cerebellar ataxia, Bipolar disorder, Breast neoplasms, Cardiomyopathy, Dilated cardiomyopathy, Colorectal neoplasms, Atrioventricular block, Coronary artery disease, Bipolar depression, Endometriosis, Female infertility, Frontotemporal dementia, Intellectual developmental disorder, Amyotrophic lateral sclerosis, Lung cancer, Major depressive disorder, Muscular dystrophy, Nasopharyngeal carcinoma, Schizophrenia, Spastic ataxia, Spinocerebellar ataxia, Uterine fibroid, arthrogryposis multiplex congenita 3, myogenic type
Unreviewed: Adenocarcinoma, Adenoma, Amyotrophy, Anorexia nervosa, Anxiety Disorder, Arthrogryposis, Asthma, Ataxia, Ataxia telangiectasia, Atherosclerosis, Attention Deficit Hyperactivity Disorder, Autism Spectrum Disorder, Basal ganglia disease, Bipolar Disorder, Borderline personality disorder, Breast Cancer, Breast Carcinoma, Breast neoplasm, Bronchopulmonary Dysplasia, Bundle branch block, Carcinoma, Cardiac arrhythmias, Cerebellar Ataxia, Cerebellar atrophy, Cerebellar Diseases, Cognition disorder, Cognitive disorder, Colitis, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Congenital Clubfoot, Congenital muscular dystrophy, Congenital Pectus Excavatum, Contracture, Cryptorchidism, Depressed bipolar disorder, Development Disorder, Developmental delay, Developmental regression, Diabetes Mellitus, Distal arthrogryposis, Duchenne Muscular Dystrophy, Dysarthria, Elbow flexion contracture, Emery dreifuss muscular dystrophy, Emery-Dreifuss Muscular Dystrophy, Emery-Dreifuss Muscular Dystrophy, X-Linked, Epithelial ovarian carcinoma, Esophagus Neoplasm, Fanconi anemia, Friedreich Ataxia, Gerstmann-Straussler-Scheinker syndrome, Glioblastoma, Heart disease, Heart Diseases, Hepatocellular carcinoma, Hereditary pyropoikilocytosis, Horizontal nystagmus, Hyperopia, Hypertension, Hypertrophic cardiomyopathy, Ichthyosis, Leukemia, Limb-Girdle Muscular Dystrophy, Lipodystrophy, Liver Cancer, Liver carcinoma, Lung Cancer, Lung carcinoma, Lung neoplasms, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoma, Major Affective Disorder, Malignant Neoplasm, Mammary Neoplasms, Marfan Syndrome, Melanocytic nevus, Melanoma, Mental Depression, Mental Disorders, Mental retardation, Migraine, Mitochondrial disease, Motor delay, Motor Neuron Disease, Multiple Sclerosis, Myocardial infarction, Myogenic Arthrogryposis Multiplex Congenita, Myopathy, Myotonia congenita, Myotonic dystrophy, Nasopharyngeal Carcinoma, Neoplasms, Neuromuscular disease, Neuromuscular Diseases, Nevus, Nystagmus, Obesity, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pena Shokeir syndrome, Peripheral axonal neuropathy, Plexiform leiomyoma, Prostate cancer, Psoriatic arthritis, Ptosis, Renal cell carcinoma, Scleroderma, Scoliosis, Spastic paraplegia, Spinal muscular atrophy, Spinocerebellar Ataxia, Sprengel Deformity, Squamous cell carcinoma, Stomach neoplasms, Strabismus, Urinary bladder neoplasms, Uterine Fibroids, Ventricular fibrillation, Ventricular Septal Hypertrophy, Vocal Cord Paralysis
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3814
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SYNE1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: Spinocerebellar Ataxia
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3815
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SYNE1 antisense RNA 2 |
- |
Curated: N/A
Unreviewed: N/A
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3816
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Spectrin repeat containing nuclear envelope protein 2 |
EDMD5, KASH2, NUA, NUANCE, Nesp2, Nesprin-2, SYNE-2, TROPH |
Curated: Anorexia nervosa, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Autism, Emery-dreifuss muscular dystrophy, Bipolar disorder, Renal cell carcinoma, Cardiac arrhythmia, Cardioembolic stroke, Dilated cardiomyopathy, Cerebral palsy, Melanoma, Left ventricular disease, Long qt syndrome, Major depressive disorder, Obsessive-compulsive disorder, Prostate cancer, Psoriasis, Restrictive cardiomyopathy, Schizophrenia, Spastic ataxia, Tourette syndrome
Unreviewed: Amyotrophy, Atrial Fibrillation, Atrioventricular block, Brain disease, Breast Cancer, Breast neoplasm, Cardiomyopathy, Chromophobe Carcinoma, Colorectal neoplasm, Congenital muscular dystrophy, Congenital Pectus Excavatum, Developmental disability, Elbow flexion contracture, Emery dreifuss muscular dystrophy, Emery-Dreifuss Muscular Dystrophy, Emery-Dreifuss Muscular Dystrophy, X-Linked, Hepatocellular carcinoma, Heterotaxy syndrome, Hypertrophic cardiomyopathy, Ichthyosis, Intellectual developmental disorder, Kidney Disease, Kidney Failure, Leukemia, Limb-Girdle Muscular Dystrophy, Lipodystrophy, Liver carcinoma, Liver cirrhosis, Lung neoplasms, Lymphoblastic Leukemia, Malignant melanoma of skin, Malignant Neoplasm, Mental Depression, Muscular dystrophy, Neoplasms, Obesity, Pancreatic neoplasm, Papillary Renal Carcinoma, Paroxysmal atrial fibrillation, Periodontitis, Ptosis, Renal Carcinoma, Scoliosis, Sprengel Deformity, Urinary bladder neoplasms, Vocal Cord Paralysis
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3817
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Spectrin repeat containing nuclear envelope family member 3 |
C14orf139, C14orf49, KASH3, LINC00341, NCRNA00341, NET53, Nesp3 |
Curated: Atrial fibrillation, Obesity, Open angle glaucoma, Squamous cell carcinoma, Waldenstrom macroglobulinemia
Unreviewed: Arthritis, Dystonia, Lung neoplasms, Malignant Neoplasm
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3818
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SYNE3 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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3819
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Spectrin repeat containing nuclear envelope family member 4 |
C19orf46, DFNB76, KASH4, Nesp4 |
Curated: Isolated sensorineural deafness, Nonsyndromic intellectual disability, Deafness, Hearing loss, Nonsyndromic hearing loss, nonsyndromic genetic hearing loss
Unreviewed: Hearing Loss, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness
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3820
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Synaptic Ras GTPase activating protein 1 |
MRD5, RASA1, RASA5, SYNGAP |
Curated: Autism, Nonsyndromic intellectual disability, Blepharoptosis, Cerebellar ataxia, Neurodevelopmental disorder, Developmental disability, Epilepsy, Epilepsy with myoclonic atonic seizures, Developmental and epileptic encephalopathy, Global developmental delay, Inflammatory bowel disease, Insomnia, Intellectual developmental disorder, Alzheimer disease, Multiple sclerosis, Non-specific syndromic intellectual disability, Psoriasis, Rheumatoid arthritis, Schizophrenia, Systemic lupus erythematosus, complex neurodevelopmental disorder
Unreviewed: Absence epilepsy, Adenocarcinoma, Adrenal Gland Pheochromocytoma, alpha Thalassemia, Amyotrophic lateral sclerosis, Anaplastic Carcinoma, Angelman Syndrome, Aortic Aneurysm, Arteriosclerosis, Arteriovenous malformations, Astrocytoma, Ataxia, Atherosclerosis, Atrioventricular block, Attention Deficit Hyperactivity Disorder, Autism Spectrum Disorder, Autoimmune Diseases, Autoimmune hemolytic anemia, Benign Essential Blepharospasm, Bladder carcinoma, Bladder Neoplasm, Blepharospasm, Brain disease, Brain Neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Bronchiectasis, Burkitt`s Lymphoma, Camptodactyly of fingers, Capillary malformation, Capillary Malformation Without Arteriovenous Malformation, Capillary Malformation-Arteriovenous Malformation, Carcinoma, Carcinoma, Somatic, Cardiofaciocutaneous syndrome, Cardiomyopathy, Cerebellar vermis agenesis, Cerebral Atrophy, Cerebral cavernous malformation, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Choriocarcinoma, Cognition disorder, Cognitive disorder, Colitis, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Congenital Arteriovenous Malformation, Congenital heart defect, Congenital Hypotrichia, Congestive Heart Failure, Constipation, Costello syndrome, Cutaneous mastocytosis, Dermatitis, Development Disorder, Developmental And Epileptic Encephalopathy, Developmental Delay, Developmental regression, Diabetic neuropathy, Dowling-Degos Disease, Drachtman Weinblatt Sitarz syndrome, Ductal carcinoma, Dwarfism, Dyskinetic Syndrome, Dysmorphic Features, Dystonia, Eczema, Endometriosis, Epileptic encephalopathy, Esophagus Neoplasm, Eyelid disease, Facial dysmorphism syndrome, Fleck Corneal Dystrophy, Focal cortical dysplasia, Frontotemporal dementia, Gastroesophageal Reflux Disease, Generalized epilepsy, Glaucoma, Glioblastoma, Glioma, Growth disorder, Headache, Heart failure, Hepatocellular carcinoma, Hereditary Hemorrhagic Telangiectasia, Herpetic keratitis, Hydrops Fetalis, Hyperparathyroidism, Hypertension, Hypodontia, Hypoplasia Of Thumb, Hypotonic seizures, Hypotrichosis, Hypoxia, Impaired Cognition, Intracranial arteriovenous malformation, Intracranial hemorrhage, Invasive Duct and Lobular Carcinoma, Klippel-Trenaunay-Weber Syndrome, Language development disorders, Language Disorders, Laryngeal cleft, LEOPARD Syndrome, Leukemia, Lip and Oral Cavity Carcinoma, Liver Cancer, Liver carcinoma, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung disease, Lung Diseases, Lung neoplasms, Lupus Erythematosus, Lymphatic metastasis, Lymphoblastic Leukemia, Lymphoma, Macrotia, Malignant Neoplasm, Malignant Peripheral Nerve Sheath Tumor, Mammary Neoplasms, Martsolf Syndrome, Megalencephaly Cutis Marmorata Telangiectatica Congenita, Melanocytic nevus, Melanoma, Mental retardation, Microcephaly, Mitochondrial disease, Motor delay, Motor skills disorder, Mouth disease, Movement Disorders, Mucinous Adenocarcinoma, Multiple Acyl-CoA Dehydrogenase Deficiency, Multiple Congenital Anomalies, Myelodysplastic syndrome, Myeloid Leukemia, Myeloproliferative disorder, Myoclonic dystonia, Myoclonic Epilepsy, Myopia, Myositis, Myotonia Levior, Nasopharyngeal Carcinoma, Nausea, Neoplasms, Nervous System Disorder, Neurocutaneous Syndromes, Neurodegenerative Disorders, Neurodevelopmental Disorders, Neurofibroma, Neurofibromatosis, Neurofibromatosis-Noonan Syndrome, Neurofibrosarcoma, Non-Specifi Epileptic Encephalopathy, Non-Syndromic Intellectual Disability, Nonorganic Psychosis, Noonan Syndrome, Noonan-Like Syndrome With Loose Anagen Hair, Nystagmus, Obesity, Oligodendroglioma, Optic Atrophy, Osteosarcoma, Pancreatic cancer, Pancreatic carcinoma, Pancreatic neoplasm, Papilloma, Parathyroid Neoplasms, Parkes Weber Syndrome, Phakomatosis pigmentovascularis, Pheochromocytoma, Polycystic Ovary Syndrome, Posteriorly Rotated Ear, Prader-Willi Syndrome, Prostate cancer, Prostatic Diseases, Prostatic neoplasm, Prostatic Neoplasms, Psychosis, Ptosis, Pulmonary Fibrosis, Renal Carcinoma, Retinitis Pigmentosa, Retinitis Pigmentosa, X-Linked, Sarcoma, Seizures, Skin carcinoma, Speech Disorders, Squamous cell carcinoma, Status Epilepticus, Stomach Neoplasms, Strabismus, Strawberry Nevus Of Skin, Stroke, Sturge-Weber Syndrome, Syndactyly Of The Toes, Syndromic microphthalmia, Tetralogy of Fallot, Thyroid cancer, Trichohepatoenteric Syndrome, Tricuspid Atresia, Triple negative breast cancer, Triple Negative Breast Neoplasms, Tuberous Sclerosis, Urinary bladder cancer, Uterine neoplasm, Vascular disease, Vascular Diseases, Vascular malformation, Vein of galen aneurysm, Vulval varices, Warburg Micro Syndrome
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