1121
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Solute carrier family 17 member 7 |
BNPI, VGLUT1 |
Curated: Anhedonia, Bipolar disorder, Learning disorders, Memory disorders, Schizophrenia, Seizures
Unreviewed: Age-Related Memory Disorders, Alzheimer disease, Amyloidosis, Anxiety Disorder, Bipolar Disorder, Cerebellar Diseases, Clonic Seizures, Colorectal neoplasm, Dementia, Epilepsy, Febrile seizures, Friedreich Ataxia, Gallbladder neoplasm, Glioblastoma, Glioma, Hypertrophic cardiomyopathy, Hypotonic seizures, Intracranial aneurysm, Jacksonian Seizure, Learning Disorders, Lewy Body Disease, Memory Disorders, Mental Depression, Neoplasms, Nervous System Disorder, Oligodendroglioma, Parkinson disease, Seizure, Senile Dementia, Tourette Syndrome, Vulval varices
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1122
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Solute carrier family 17 member 8 |
DFNA25, VGLUT3 |
Curated: Auditory neuropathy, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hereditary hearing loss, Non-small cell lung carcinoma, Squamous cell carcinoma, nonsyndromic genetic hearing loss
Unreviewed: Anxiety Disorder, Atrophy, Biliary Cirrhosis, Carcinoma, Catalepsy, Hearing Loss, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Tourette syndrome, Vulval varices
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1123
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Solute carrier family 17 member 9 |
C20orf59, POROK8, VNUT |
Curated: Disseminated superficial actinic porokeratosis, Porokeratosis
Unreviewed: Carcinoma, Colorectal Cancer, Diabetes Mellitus, Disseminated Superficial Actinic Porokeratosis, Gestational diabetes, Hepatitis b, Kidney neoplasm, Malignant Neoplasm, Neoplasms, Renal cell carcinoma, Stomach Carcinoma, Stomach neoplasms
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1124
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Solute carrier family 18 member A1 |
CGAT, VAT1, VMAT1 |
Curated: Amyotrophic lateral sclerosis, Bipolar disorder, Bipolar depression, Major depressive disorder, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2
Unreviewed: Adenocarcinoma, Anorexia, Anxiety disorder, Asthenozoospermia, Autism, Autism Spectrum Disorder, Benign Prostatic Hyperplasia, Bipolar Disorder, Borderline personality disorder, Breast Cancer, Breast Carcinoma, Bronchopulmonary Dysplasia, Carcinoid tumor, Colorectal Cancer, Complement component deficiency, Disruptive, impulse control, and conduct disorders, Glioblastoma, Glioma, Impaired Cognition, Lung Cancer, Lung carcinoma, Lung neoplasms, Malignant Neoplasm, Mental Depression, Mental Disorders, Multiple Endocrine Neoplasia, Neoplasms, Neuroblastoma, Neurodegenerative Disorders, Obsessive-Compulsive Disorder, Ovarian neoplasm, Paraganglioma, Pheochromocytoma, Von Hippel-Lindau Syndrome
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1125
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|
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Solute carrier family 18 member A2 |
PKDYS2, SVAT, SVMT, VAT2, VMAT2 |
Curated: Bipolar disorder, Brain edema, Major depressive disorder, Nervous system disease, Parkinson disease, Secondary parkinson disease, Parkinsonism-dystonia, Schizophrenia, Depression
Unreviewed: Adrenal Gland Pheochromocytoma, Anxiety Disorder, Attention Deficit Hyperactivity Disorder, Bipolar Disorder, Borderline personality disorder, Brain Dopamine-Serotonin Vesicular Transport Disease, Brain injuries, Bronchopulmonary Dysplasia, Chromosomal instability, Cognition disorder, Developmental Delay, Developmental disability, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 1, Dysarthria, Dysautonomia, Dyssomnia, Dystonia, Ear Diseases, Epilepsy, Frontotemporal dementia, Gestational diabetes, Glioblastoma, Huntington Disease, Hypoparathyroidism-deafness-renal disease syndrome, Impaired Cognition, Lateral Sclerosis, Liver carcinoma, Long QT Syndrome, Lung Cancer, Lung carcinoma, Machado-Joseph Disease, Malignant Neoplasm, Mental Depression, Mental Depression With Psychotic Features, Mental Disorders, Mood Disorder, Movement disorder, Movement Disorders, Multiple Endocrine Neoplasia, Narcolepsy, Neoplasms, Nervous System Disorder, Neuroblastoma, Neurodegenerative Disorders, Neuroendocrine Tumors, Orofacial dyskinesia, Osteosarcoma, Paraganglioma, Parkinsonian disease, Parkinsonism-Dystonia, Pheochromocytoma, Polycystic Ovary Syndrome, Prostate adenocarcinoma, Prostate cancer, Prostatic neoplasm, Psychosis, Psychotic disorders, Ptosis, Ramsay Hunt Paralysis Syndrome, Sleep Disorders, Spastic tetraparesis, Spinocerebellar Ataxia, Stomach neoplasms, Stress Disorder, Vitiligo, Vitiligo-associated SYSTEMIC LUPUS ERYTHEMATOSUS, Von Hippel-Lindau Syndrome, Vulval varices
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1126
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|
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SLC18A2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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1127
|
|
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Solute carrier family 18 member A3 |
CMS21, VACHT |
Curated: Presynaptic congenital myasthenic syndrome, Congenital myasthenic syndrome, Fetal akinesia deformation sequence, Hodgkin lymphoma, Myasthenic syndrome, Pena-shokeir syndrome
Unreviewed: Acquired Kyphoscoliosis, Alzheimer disease, Arthrogryposis multiplex congenita, Ataxia, Bulbar palsy, Cardiomyopathy, Chronic obstructive pulmonary disease, Congenital kyphoscoliosis, Congenital Pectus Carinatum, Congestive Heart Failure, Constipation, Deglutition disorder, Dementia, Developmental dysplasia of the hip, Distal amyotrophy, Dysphagia, Epilepsy, Esotropia, Facial paralysis, Fetal Akinesia Deformation Sequence, Gastroesophageal Reflux Disease, Hearing Loss, Heart Failure, High palate, Impaired Cognition, Lambert-Eaton Myasthenic Syndrome, Learning disorders, Mental retardation, Motor delay, Myasthenia Gravis, Myasthenic Syndrome, Narcolepsy-Cataplexy Syndrome, Neurodegenerative Disorders, Nystagmus, Ocular albinism, Ophthalmoplegia, Parkinson disease, Pena Shokeir syndrome, Polyneuropathy, Ptosis, Respiratory Failure, Rett Syndrome, Senile Dementia, Sleep Apnea, Squamous cell carcinoma, Status Epilepticus, Sudden episodic apnea, Tourette syndrome, Ventricular dysfunction, Vulval varices
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1128
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|
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Solute carrier family 18 member B1 |
C6orf192, VPAT, dJ55C23.6 |
Curated: Parkinson disease
Unreviewed: Sepsis, Septicemia
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1129
|
|
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Solute carrier family 19 member 1 |
CHMD, FOLT, IFC-1, IFC1, IMD114, MEGAF, REFC, RFC, RFC1, RFT-1, hRFC, hSLC19A1 |
Curated: Autism, Cataract, Cleft lip, Cleft palate, Colonic neoplasms, Colorectal neoplasms, Combined immunodeficiency disease, Complete unilateral cleft lip, Discordant ventriculoarterial connection, Down syndrome, Glaucoma, Immunodeficiency, Knobloch syndrome, Macular dystrophy, Megaloblastic anemia, Nervous system disease, Nystagmus, Retinitis pigmentosa, Myopia, Transposition of the great arteries, Urinary bladder neoplasms, immunodeficiency 114, folate-responsive
Unreviewed: Adenocarcinoma, Adenoma, Adrenoleukodystrophy, Alopecia, Alzheimer disease, Amyotrophic lateral sclerosis, Aortic aneurysm, Aortic dissection, Arthritis, Ataxia, Atherosclerosis, Atrioventricular septal defect, Atrophy, Attention Deficit Hyperactivity Disorder, Autism spectrum disorder, Bilateral Vestibulopathy, Bladder carcinoma, Bladder Neoplasm, Bone marrow diseases, Brain Infarction, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Carcinoma Of The Head And Neck, Cardiovascular disease, Cardiovascular Diseases, Central Nervous System Lymphoma, Cerebellar Ataxia, Cerebellar Ataxia With Neuropathy And Bilateral Vestibular Areflexia Syndrome, Cerebellar ataxia, neuropathy and vestibular areflexia syndrome, Cerebellar atrophy, Cerebellar diseases, Cerebral Infarction, Charcot-Marie-Tooth Disease, Chorea, Cleft Lip With Or Without Cleft Palate, Cognition disorder, Colonic Neoplasms, Colorectal adenoma, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Congenital central hypoventilation syndrome, Congenital heart defect, Congenital heart defects, Congenital idiopathic intestinal pseudoobstruction, Congenital omphalocele, Congestive Heart Failure, Conotruncal cardiac defect, Conotruncal defect, Coronary artery disease, Coronary Heart Disease, Cough, Deglutition disorder, Dementia, Demyelinating diseases, Demyelinating neuropathy, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Nephropathy, Diffuse Lymphoma, Down Syndrome, Dysarthria, Dysautonomia, Dystonia, Episodic ataxia, Esophagitis, Esophagus Neoplasm, Folic Acid Deficiency, Gastrointestinal stromal tumor, Glycoprotein storage disease, Graft-versus-host disease, Head And Neck Carcinoma, Head and neck neoplasm, Hearing Loss, Heart Failure, Hematologic disease, Hematologic Neoplasms, Hepatocellular carcinoma, Hereditary folate malabsorption, Hereditary motor and sensory neuropathy, Hereditary sensory and autonomic neuropathy, Hyperglycemia, Hyperhomocysteinemia, Hypertension, Hypoxia, Impaired Cognition, Infertility, Intracranial Aneurysm, Ischemic Stroke, Kidney Disease, Laryngeal neoplasm, Leukemia, Leukopenia, Liver Cancer, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung Neoplasms, Lupus Erythematosus, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphocytosis, Lymphoma, Lynch syndrome, Malignant Neoplasm, Melanoma, Meningioma, Meningomyelocele, Mesothelioma, Miscarriage, Motor and Sensory Neuropathy, Multiple myeloma, Multiple Sclerosis, Multiple system atrophy, Myelodysplastic Syndrome, Myocardial Infarction, Myotonic dystrophy, Nance-Horan Syndrome, Neoplasms, Nephroblastoma, Nervous System Disorder, Neural Tube Defect, Neuroblastoma, Neutropenia, Non-Hodgkin lymphoma, Obesity, Oestrogen Receptor Positive Breast Cancer, Optic Atrophy, Osteoporosis, Osteosarcoma, Ovarian neoplasm, Pancreatic cancer, Papillary Adenoma, Parkinson disease, Pelvic Organ Prolapse, Polycystic ovary syndrome, Polyneuropathy, Prostate cancer, Prostatic neoplasm, Retinal Dystrophy, Retinitis Pigmentosa, Retinoblastoma, Rheumatoid arthritis, Sarcoma, Secondary parkinson disease, Sensorimotor neuropathy, Septicemia, Sjogren syndrome, Small cell lung carcinoma, Spastic ataxia, Spina Bifida, Spina bifida occulta, Spinal muscular atrophy, Stomach Carcinoma, Stomach Neoplasms, Stomatitis, Stroke, Systemic lupus erythematosus, Trisomy 21, Turner Syndrome, Urinary bladder cancer, Uterine disease, Uterine neoplasm, Vascular dementia, Vestibular disease, Wilms tumor
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1130
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|
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Solute carrier family 19 member 2 |
TC1, THMD1, THT1, THTR1, TRMA |
Curated: Megaloblastic anemia, Angioedema, Atrial fibrillation, Blood coagulation disorder, Cardiovascular disease, Venous hypertension, Venous insufficiency, Congenital ear anomaly, Cor pulmonale, Diabetes mellitus, Edema, Endometriosis, Heart disease, Lipoma, Thiamine-responsive megaloblastic anemia, Peripheral vascular disease, Retinitis pigmentosa, Hearing loss, Thrombophilia, Vascular disease, Venous thromboembolism
Unreviewed: Activated Protein C Resistance, Alstrom syndrome, Anemia, Anorexia, Atrial Septal Defect, Breast Cancer, Breast Carcinoma, Cobalamin deficiency, Colorectal Cancer, Colorectal Neoplasms, Cone-rod dystrophy, Congestive Heart Failure, Deafness, Deglutition disorder, Diabetes, Diabetes Mellitus, Diabetes mellitus transient neonatal, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Distal myopathy, Dwarfism, Hearing Loss, Ischemic stroke, Kidney Disease, Korsakoff psychosis, Leber Congenital Amaurosis, Malignant Neoplasm, Mason type diabetes, Mitochondrial disease, Monogenic Diabetes, Myeloid Leukemia, Neural Tube Defect, Nystagmus, Optic Atrophy, Osteoarthritis, Osteoporosis, Retinal degeneration, Retinal Diseases, Retinal Dystrophy, Retinitis Pigmentosa, Sepsis, Sideroblastic Anemia, Stroke, Thiamine Deficiency, Thiamine Responsive Megaloblastic Anemia Syndrome, Thrombocytopenia, Thyroid Diseases, Ventricular ectopy, Ventricular septal defect, Visual disorder, Wolfram syndrome
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