2071
|
|
|
ATP13A3 divergent transcript |
LINC00884 |
Curated: N/A
Unreviewed: N/A
|
2072
|
|
|
ATPase 13A4 |
- |
Curated: Bipolar disorder, Digestive system disease, Major depressive disorder
Unreviewed: Apraxia, Autism, Autism Spectrum Disorder, Breast neoplasm, Optic atrophy, Parkinson disease, Rolandic epilepsy, Schizophrenia
|
2073
|
|
|
ATP13A4 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
2074
|
|
|
ATPase 13A5 |
- |
Curated: Hodgkin lymphoma
Unreviewed: Allergic contact dermatitis, Benign familial pemphigus, Schizophrenia
|
2075
|
|
|
ATP13A5 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
2076
|
|
|
ATPase Na+/K+ transporting subunit alpha 1 |
CMT2DD, HOMGSMR2 |
Curated: Charcot-marie-tooth disease, Bipolar disorder, Cushing syndrome, Hyperaldosteronism, Hypertension, Hypothyroidism, Intellectual developmental disorder, Myocardial infarction, Myocardial ischemia, Neurodevelopmental disorder, Neuromuscular disease, Vestibular disease, Charcot-Marie-tooth disease, axonal, type 2DD
Unreviewed: N/A
|
2077
|
|
|
ATP1A1 antisense RNA 1 |
ATP1A1OS, C1orf203 |
Curated: N/A
Unreviewed: Charcot-Marie-Tooth Disease
|
2078
|
|
|
ATPase Na+/K+ transporting subunit alpha 2 |
DEE98, FARIMPD, FHM2, MHP2 |
Curated: Alternating hemiplegia of childhood, Benign neonatal epilepsy, Bipolar disorder, Developmental and epileptic encephalopathy, Dysphasia, Epilepsy, Hemiplegic migraine, Hypertension, Migraine, Polymicrogyria, Spastic ataxia, fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies, hemiplegic migraine-developmental and epileptic encephalopathy spectrum
Unreviewed: Adrenal Hypoplasia, X-Linked, Alternating Hemiplegia, Anxiety Disorder, Aphasia, Apraxia, Arthrogryposis multiplex congenita, Ataxia, Autism, Benign Epilepsy, Bipolar Disorder, Blast crisis, Brain disease, Brain edema, Cerebellar ataxia, Cerebral Microangiopathy, Cerebral palsy, Choreoathetosis, Cognition disorder, Common Migraine, Confusion, Congenital adrenal hyperplasia, Congenital adrenal hypoplasia, Craniocerebral trauma, Developmental disability, Duchenne muscular dystrophy, Dysarthria, Dystonia, Encephalopathy, Epilepsy And Migraine, Epileptic encephalopathy, Episodic Ataxia, Episodic quadriplegia, Febrile seizures, Gallbladder neoplasm, Glioma, Hearing Loss, Hemiplegia/hemiparesis, Hemiplegic Migraine, Hepatoblastoma, Hydrops Fetalis, Hypokalemic Periodic Paralysis, Intellectual developmental disorder, Lung carcinoma, Malformation of cortical development, Melas syndrome, Mental retardation, Microcephaly, Migraine with Aura, Migraine, sporadic hemiplegic, Motor neuron disease, Movement disorder, Movement Disorders, Nervous System Disorder, Neuroblastoma, Nystagmus, Paresis, Patent foramen ovale, Peripheral nervous system disease, Psychotic disorders, Retinitis Pigmentosa, Secundum atrial septal defect, Seizure, Seizures, Squamous cell carcinoma
|
2079
|
|
|
ATPase Na+/K+ transporting subunit alpha 3 |
AHC2, ATP1A1, CAPOS, DEE99, DYT12, RDP |
Curated: Alternating hemiplegia of childhood, Anhedonia, Autism, Bipolar disorder, Capos syndrome, Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss, Neurodevelopmental disorder, Congenital epicanthus, Congestive heart failure, Bipolar depression, Major depressive disorder, Developmental and epileptic encephalopathy, Dyskinesia, Dystonia, Epilepsy, Esophageal atresia, Global developmental delay, Heart failure, Non-specific syndromic intellectual disability, Osteoarthritis, Parkinson disease, Seizures, Ventricular dysfunction, ATP1A3-associated neurological disorder
Unreviewed: Adrenal Hypoplasia, X-Linked, Alternating Hemiplegia, Anxiety Disorder, Aphasia, Arthritis, Ataxia, Ataxia telangiectasia, Atrioventricular block, Auditory Neuropathy, Bilateral vestibulopathy, Bipolar Disorder, Bradycardia, Brain disease, CAPOS Syndrome, Cardiac arrhythmias, Cardiovascular disease, Cerebellar ataxia, Cerebellar Ataxia-Areflexia-Pes Cavus-Optic Atrophy-Sensorineural Hearing Loss Syndrome, Cerebellar atrophy, Cerebellar Diseases, Cerebral palsy, Chorea, Choreoathetosis, Cognition disorder, Cognitive disorder, Congenital adrenal hyperplasia, Congenital adrenal hypoplasia, Congenital Epicanthus, Congenital myasthenic syndrome, Congenital Pes Cavus, Congestive Heart Failure, Cortical development malformation, Deglutition disorder, Development Disorder, Developmental Delay, Developmental disability, Dysarthria, Dyskinetic Syndrome, Dysmorphic Features, Dysphagia, Dystonia-Parkinsonism, Epileptic encephalopathy, Episodic Ataxia, Episodic quadriplegia, Febrile seizures, Glioblastoma, Glioma, Headache, Hearing Loss, Heart Failure, Hemiplegia, Hemiplegic migraine, Hereditary spastic paraplegia, Hyperkinesia, Impaired Cognition, Intellectual developmental disorder, Long qt syndrome, Major Affective Disorder, Mental Depression, Mental retardation, Microcephaly, Migraine, Mitochondrial disease, Mood disorder, Mood swings, Motor delay, Motor Disorders, Movement disorder, Movement Disorders, Multiple Congenital Anomalies, Myocardial Infarction, Myoclonic Dystonia, Myotonic dystrophy, Neoplasms, Nervous System Disorder, Neurodevelopmental Disorders, Neuromuscular disease, Nystagmus, Optic Atrophy, Osteoarthrosis Deformans, Pancreatic adenocarcinoma, Paralysis, Paresis, Parkinsonian disease, Paroxysmal dystonia, Peripheral nervous system disease, Pigmentary Disorder, Reticulate, With Systemic Manifestations, Polymicrogyria, Proliferative Diabetic Retinopathy, Psychotic disorders, Ramsay Hunt Paralysis Syndrome, Retinoschisis, X-Linked, Sagittal craniosynostosis, Schizophrenia, Secondary parkinson disease, Septicemia, Spasms X-Linked, Status Epilepticus, Taurodontism, Ventricular fibrillation
|
2080
|
|
|
ATPase Na+/K+ transporting subunit alpha 4 |
ATP1A1, ATP1AL2 |
Curated: Autism, Gout
Unreviewed: Adenoma, Adrenocortical adenoma, Adrenocortical carcinoma, Aldosterone-Producing Adrenal Cortex Adenoma, Alzheimer disease, Anthracosis, Anxiety disorder, Bipolar Disorder, Cardiomyopathy, Cerebellar ataxia, Charcot-Marie-Tooth Disease, Conn Adenoma, Conn Syndrome, Cushing syndrome, Deafness, Demyelinating diseases, Developmental Delay, Diabetic Nephropathy, Esophagus Neoplasm, Essential tremor, Fuchs endothelial dystrophy, Gastroenteritis, Glioblastoma, Glioma, Gouty arthritis, Headache, Hearing loss, Heart disease, Hemiplegic Migraine, Henoch-Schonlein Nephritis, Hepatocellular carcinoma, Hereditary sensory and autonomic neuropathy, Hyperaldosteronism, Hypertension, Hypomagnesemia, Intellectual developmental disorder, Kidney Cancer, Kidney neoplasm, Liver carcinoma, Lung Cancer, Lung carcinoma, Major depressive disorder, Malignant Neoplasm, Mental retardation, Migraine, Myeloid leukemia, Myocardial Infarction, Myocardial Ischemia, Neoplasms, Nephrolithiasis, Nervous system disease, Pancreatic ductal carcinoma, Papillary Adenoma, Paraplegia, Peripheral nervous system disease, Prostatic neoplasm, Renal Carcinoma, Rheumatoid arthritis, Seizure, Seizures, Seminoma, Sensorimotor neuropathy, Small cell lung carcinoma, Spastic paraplegia, Status Epilepticus, Testicular neoplasm, Thyroid cancer, Vascular disease, Vesicular Stomatitis, Vestibular Diseases
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