2181
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Curated: Ataxia with polyneuropathy, Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cerebellar atrophy, Charcot-marie-tooth disease, Cleft palate and bilateral cleft lip, Diabetes mellitus, Gonadal dysgenesis, Hypertrophy, Systemic lupus erythematosus, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Mitochondrial myopathy with sideroblastic anemia, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Optic neuropathy, Parkinson disease, Periodic paralysis, Rod-cone dystrophy, Postaxial polydactyly
Unreviewed: Acute Myeloid Leukemia, Adenocarcinoma, Amyotrophic Lateral Sclerosis, Asthenozoospermia, Ataxia, Ataxia and polyneuropathy, Ataxia Telangiectasia, Autism, Autoimmune disease, Autoimmune Diseases, Basal ganglia cysts, Brain disease, Brain neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Cardiomyopathy, apical hypertrophic and neuropathy, Carnitine acetyltransferase deficiency, Cerebral cortical atrophy, Charcot-Marie-Tooth Disease, Childhood obesity, Choreoathetosis, Cleft Palate And Bilateral Cleft Lip, Coenzyme Q10 Deficiency, Colorectal neoplasm, Coronary artery disease, Dementia, Demyelinating neuropathy, Developmental Delay, Developmental regression, Diabetes Mellitus, Diabetes mellitus, type 2, Diarrhea, Distal hereditary motor neuropathy, Down Syndrome, Dwarfism, Dysarthria, Dyskinetic Syndrome, Dysphagia, Epilepsy, Episodic ataxia, Esophageal neoplasm, Gastroesophageal Reflux Disease, Glomerulonephritis, Hearing Loss, Hemiplegia, Hemolytic uremic syndrome, Hereditary breast and ovarian cancer syndrome, Hereditary Leber Optic Atrophy, Hereditary spastic paraplegia, High Altitude Pulmonary Edema, Histiocytoid Cardiomyopathy, Holocarboxylase Synthetase Deficiency, Horizontal pendular nystagmus, Huntington disease, Hyperlipidemia, Hypertension, Hypertrophic cardiomyopathy, Hypogonadism, Iga nephropathy, Intellectual developmental disorder, Irritable bowel syndrome, Isolated ATP Synthase Deficiency, Kearns Sayre Syndrome, Kidney Disease, Lactic acidosis, Language development disorders, Learning disorders, Leigh Syndrome, Leprosy, Liver failure, Lung disease, Lupus Erythematosus, Lymphoblastic Leukemia, Major depressive disorder, Male infertility, Maternally Inherited Leigh Syndrome, MELAS Syndrome, Mental retardation, MERRF Syndrome, Metabolic Syndrome, Microcephaly, Migraine, Mitochondrial Cardiomyopathy, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Mitochondrial Myopathy And Sideroblastic Anemia, Mitochondrial Spastic Paraplegia, Mouth neoplasm, Multiple Sclerosis, Myocardial infarction, Myoclonic epilepsy with ragged red fibers, Myoclonic Seizures, Myopathy, Myopathy, lactic acidosis, and sideroblastic anemia, Neoplasms, Nervous system disease, Nervous System Diseases, Nervous System Disorder, Neurodegenerative disorder, Neurodegenerative Disorders, Neuropathy Ataxia And Retinis Pigmentosa, Nystagmus, Obesity, Ophthalmoplegia, Optic Atrophy, Osteoporosis, Osteosarcoma, Ovarian Failure, Paresis, Periodic Paralysis With Distal Motor Neuropathy, Peripheral axonal neuropathy, Peripheral nervous system disease, Peripheral Neuropathy, Polycystic ovary syndrome, Polyneuropathy, Postaxial hand polydactyly, Prostate cancer, Prostatic neoplasm, Pulmonary edema, Respiration Disorders, Respiratory Tract Diseases, Retinal Diseases, Retinal telangiectasia, Retinitis Pigmentosa, RHYNS Syndrome, Sarcoidosis, Schizophrenia, Seizure, Seizures, Sensorimotor neuropathy, Sensory neuropathy, Spastic ataxia, Spastic paraplegia, Spastic tetraparesis, Spinocerebellar Ataxia, Strabismus, Striatonigral Degeneration, Trichohepatoenteric Syndrome, Ventricular preexcitation, West Syndrome, Wolff-Parkinson-White Syndrome
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2182
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- |
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Curated: Ataxia with polyneuropathy, Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cerebellar atrophy, Charcot-marie-tooth disease, Cleft palate and bilateral cleft lip, Diabetes mellitus, Gonadal dysgenesis, Hypertrophy, Systemic lupus erythematosus, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Mitochondrial myopathy with sideroblastic anemia, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Optic neuropathy, Parkinson disease, Periodic paralysis, Rod-cone dystrophy, Postaxial polydactyly
Unreviewed: Acute Myeloid Leukemia, Adenocarcinoma, Amyotrophic Lateral Sclerosis, Asthenozoospermia, Ataxia, Ataxia and polyneuropathy, Ataxia Telangiectasia, Autism, Autoimmune disease, Autoimmune Diseases, Basal ganglia cysts, Brain disease, Brain neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Cardiomyopathy, apical hypertrophic and neuropathy, Carnitine acetyltransferase deficiency, Cerebral cortical atrophy, Charcot-Marie-Tooth Disease, Childhood obesity, Choreoathetosis, Cleft Palate And Bilateral Cleft Lip, Coenzyme Q10 Deficiency, Colorectal neoplasm, Coronary artery disease, Dementia, Demyelinating neuropathy, Developmental Delay, Developmental regression, Diabetes Mellitus, Diabetes mellitus, type 2, Diarrhea, Distal hereditary motor neuropathy, Down Syndrome, Dwarfism, Dysarthria, Dyskinetic Syndrome, Dysphagia, Epilepsy, Episodic ataxia, Esophageal neoplasm, Gastroesophageal Reflux Disease, Glomerulonephritis, Hearing Loss, Hemiplegia, Hemolytic uremic syndrome, Hereditary breast and ovarian cancer syndrome, Hereditary Leber Optic Atrophy, Hereditary spastic paraplegia, High Altitude Pulmonary Edema, Histiocytoid Cardiomyopathy, Holocarboxylase Synthetase Deficiency, Horizontal pendular nystagmus, Huntington disease, Hyperlipidemia, Hypertension, Hypertrophic cardiomyopathy, Hypogonadism, Iga nephropathy, Intellectual developmental disorder, Irritable bowel syndrome, Isolated ATP Synthase Deficiency, Kearns Sayre Syndrome, Kidney Disease, Lactic acidosis, Language development disorders, Learning disorders, Leigh Syndrome, Leprosy, Liver failure, Lung disease, Lupus Erythematosus, Lymphoblastic Leukemia, Major depressive disorder, Male infertility, Maternally Inherited Leigh Syndrome, MELAS Syndrome, Mental retardation, MERRF Syndrome, Metabolic Syndrome, Microcephaly, Migraine, Mitochondrial Cardiomyopathy, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Mitochondrial Myopathy And Sideroblastic Anemia, Mitochondrial Spastic Paraplegia, Mouth neoplasm, Multiple Sclerosis, Myocardial infarction, Myoclonic epilepsy with ragged red fibers, Myoclonic Seizures, Myopathy, Myopathy, lactic acidosis, and sideroblastic anemia, Neoplasms, Nervous system disease, Nervous System Diseases, Nervous System Disorder, Neurodegenerative disorder, Neurodegenerative Disorders, Neuropathy Ataxia And Retinis Pigmentosa, Nystagmus, Obesity, Ophthalmoplegia, Optic Atrophy, Osteoporosis, Osteosarcoma, Ovarian Failure, Paresis, Periodic Paralysis With Distal Motor Neuropathy, Peripheral axonal neuropathy, Peripheral nervous system disease, Peripheral Neuropathy, Polycystic ovary syndrome, Polyneuropathy, Postaxial hand polydactyly, Prostate cancer, Prostatic neoplasm, Pulmonary edema, Respiration Disorders, Respiratory Tract Diseases, Retinal Diseases, Retinal telangiectasia, Retinitis Pigmentosa, RHYNS Syndrome, Sarcoidosis, Schizophrenia, Seizure, Seizures, Sensorimotor neuropathy, Sensory neuropathy, Spastic ataxia, Spastic paraplegia, Spastic tetraparesis, Spinocerebellar Ataxia, Strabismus, Striatonigral Degeneration, Trichohepatoenteric Syndrome, Ventricular preexcitation, West Syndrome, Wolff-Parkinson-White Syndrome
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2183
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ATPase H+ transporting accessory protein 1 |
16A, ATP6IP1, ATP6S1, Ac45, CF2, VATPS1, XAP-3, XAP3 |
Curated: Congenital disorder of glycosylation, Immunodeficiency, Lymphoma, Intellectual developmental disorder, x-linked, congenital disorder of glycosylation type II
Unreviewed: Agammaglobulinemia, Breast neoplasm, Carcinogenesis, Central nervous system disease, Cirrhosis, Cognition disorder, Cutis Laxa, Distal Renal Tubular Acidosis, Dystonia, Exocrine pancreatic insufficiency, Fatty Liver, Glioma, Glycogen storage disease, Hearing Loss, Hepatocellular carcinoma, Hydrocephalus, Hyperopia, Hypospadias, Leukopenia, Liver failure, Myeloid Leukemia, Neoplasms, Nervous system disease, Spinocerebellar ataxia
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2184
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ATP6AP1 divergent transcript |
CH17-340M24.3 |
Curated: N/A
Unreviewed: N/A
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2185
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ATPase H+ transporting accessory protein 1 like (pseudogene) |
- |
Curated: N/A
Unreviewed: Breast Cancer, Breast Carcinoma, Breast neoplasm, Mammary Neoplasms, Marfan Syndrome, Stress Disorder
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2186
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ATPase H+ transporting accessory protein 2 |
(P)RR, APT6M8-9, ATP6IP2, ATP6M8-9, CDG2R, ELDF10, HT028, M8-9, MRXE, MRXSH, MSTP009, PRR, RENR, XMRE, XPDS |
Curated: Congenital disorder of glycosylation, Craniofacial abnormalities, Intellectual developmental disorder, x-linked, Parkinsonism with spasticity, x-linked, X-linked intellectual disability, X-linked parkinsonism-spasticity syndrome, ATP6AP2-related disorder
Unreviewed: Adenocarcinoma, Age-related macular degeneration, Agraphesthesia, Anophthalmia, Aortic Valve Insufficiency, Aortic Valve Sclerosis, Apraxia, Arteriosclerosis, Arthrocutaneouveal granulomatosis, Atherosclerosis, Atrial Fibrillation, Autoimmune Diseases, Autonomic Central Nervous System Diseases, Breast Cancer, Breast Carcinoma, Breast neoplasm, Bronchiolitis, Carcinogenesis, Cardiomyopathy, Cardiovascular disease, Cardiovascular Diseases, Cerebellar atrophy, Cerebral Atrophy, Cerebrovascular Disorders, Cirrhosis, Colorectal adenoma, Colorectal Cancer, Congenital anomalies of kidney and urinary tract, Congestive Heart Failure, Conn Adenoma, Conn Syndrome, Coronary artery disease, Coronary Heart Disease, Diabetes, Diabetes Insipidus, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic cardiomyopathy, Diabetic Nephropathy, Diabetic neuropathy, Diabetic Retinopathy, Ductal carcinoma, Dysautonomia, Eclampsia, Endometrial Cancer, Endometrial carcinoma, Endometrial neoplasm, Epidermolysis Bullosa, Epilepsy, Erythroblastic Leukemia, Glioblastoma, Glioma, Glomerulonephritis, Glomerulosclerosis, Glycogen Storage Disease, Graves Disease, Heart Failure, Hemangioma, Hyperglycemia, Hypertension, Hyperthyroidism, Hypoplasia Of Corpus Callosum, Hypotonic seizures, Iga nephropathy, Impaired Cognition, Inflammatory abnormality of the eye, Intellectual developmental disorder, Invasive Duct and Lobular Carcinoma, Kawasaki disease, Kidney Disease, Kidney Failure, Left Ventricular Hypertrophy, Liver carcinoma, Lung Cancer, Lung carcinoma, Lung neoplasms, Male infertility, Malignant Neoplasm, Mental Depression, Mental retardation, Mental Retardation with Epilepsy,X-Linked, Mental Retardation, X-Linked, Metabolic Syndrome, Motor delay, Multiple Sclerosis, Myocardial Infarction, Neoplasms, Nephrogenic Diabetes Insipidus, Nervous system disease, Neurodegenerative Disorders, Obesity, Pancreatic adenocarcinoma, Pancreatic ductal carcinoma, Pancreatic neoplasm, Papillary Craniopharyngioma, Parkinson disease, Parkinsonism-Spasticity Syndrome, X-Linked, Peritoneal Fibrosis, Pigmentary Disorder, Reticulate, With Systemic Manifestations, Proliferative Diabetic Retinopathy, Promyelocytic Leukemia, Prostate cancer, Pulmonary Fibrosis, Renal cell carcinoma, Scoliosis, Secondary parkinson disease, Seizure, Sleep Apnea, Squamous cell carcinoma, Strawberry Nevus Of Skin, Vascular disease
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2187
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ATPase H+ transporting V0 subunit a1 |
ATP6N1, ATP6N1A, DEE104, NEDEBA, Stv1, VPP1, Vph1, a1 |
Curated: Asthma, Autism, Cerebellar ataxia, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Esophageal atresia, Global developmental delay, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Seizures
Unreviewed: Breast neoplasm, Carcinogenesis, Carotid artery stenosis, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Encephalitis, Hepatoblastoma, Hypertension, Lung neoplasms, Malignant Neoplasm
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2188
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|
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ATPase H+ transporting V0 subunit a2 |
A2, ARCL, ARCL2A, ATP6A2, ATP6N1D, J6B7, RTF, STV1, TJ6, TJ6M, TJ6S, VPH1, WSS, a2V |
Curated: Alzheimer disease, Cutis laxa, Accessory skin tag, Congenital disorder of glycosylation, Desbuquois syndrome, Aplasia of the vermis, Benign pemphigus, Darier disease, Meckel-gruber syndrome, Rothmund-thomson syndrome, Wrinkly skin syndrome, autosomal recessive cutis laxa type 2A
Unreviewed: Acquired Kyphoscoliosis, Alopecia, Arteriosclerosis, Atherosclerosis, Bicuspid aortic valve, Bone Disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Cerebellar Ataxia, Cerebellar Hypoplasia, Congenital Clubfoot, Congenital Epicanthus, Congenital Exomphalos, Congenital kyphoscoliosis, Congenital Pectus Excavatum, Cortical development malformation, Crohn Disease, Cryptorchidism, Cutis Laxa, Dandy-Walker Syndrome, Dementia, Developmental Delay, Developmental dysplasia of the hip, Diabetic Retinopathy, Dwarfism, Ehlers-Danlos Syndrome, Encephalitis, Epilepsy, Frontal bossing, Geroderma Osteodysplastica, Glioblastoma, Glioma, Hemochromatosis, Hemorrhagic disease, Hepatitis c, High palate, Hypertension, Intracranial Aneurysm, Lipodystrophy, Liver cirrhosis, Lung Diseases, Lung neoplasms, Male infertility, Malignant Osteopetrosis, Mental retardation, Microcephaly, Microdontia, Microstomia, Mixed connective tissue disease, Motor delay, Myopia, Neoplasms, Osteopenia, Osteosclerosis, Ovarian neoplasm, Pachygyria, Polymicrogyria, Pulmonary Emphysema, Rheumatoid arthritis, Scoliosis, Skin abnormalities, Status Epilepticus, Strabismus, Uterine neoplasm, von Willebrand disorder, Woodhouse Sakati Syndrome, Wrinkly Skin Syndrome
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2189
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ATPase H+ transporting V0 subunit a4 |
A4, ATP6N1B, ATP6N2, DRTA3, RDRTA2, RTA1C, RTADR, STV1, VPH1, VPP2 |
Curated: Distal renal tubular acidosis, Color vision deficiency, Hearing loss
Unreviewed: Astrocytoma, Breast neoplasm, Cutis Laxa, Deafness, Diabetes mellitus, Diabetic neuropathy, Distal Renal Tubular Acidosis, Encephalitis, Fanconi syndrome, Growth disorder, Hearing Loss, Kidney disease, Kidney stone, Nephrocalcinosis, Nephrolithiasis, Renal Carcinoma, Renal Tubular Acidosis, Renal Tubular Acidosis with Sensorineural Hearing Loss, Sensorineural hearing loss, Venous thromboembolism
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2190
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ATPase H+ transporting V0 subunit b |
ATP6F, HATPL, VMA16 |
Curated: Schizophrenia
Unreviewed: Breast Cancer, Bronchopulmonary dysplasia, Hepatocellular carcinoma
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