1281
|
|
|
Solute carrier family 25 member 6 pseudogene 6 |
- |
Curated: N/A
Unreviewed: N/A
|
1282
|
|
|
Solute carrier family 26 member 1 |
CAON, CAON1, EDM4, HYSULF, SAT-1, SAT1 |
Curated: Alzheimer disease, Developmental and epileptic encephalopathy, Hyperoxaluria, Mucopolysaccharidosis, Nephrolithiasis, Pfaundler-hurler syndrome, Polymyositis, Urolithiasis
Unreviewed: Adenocarcinoma, Adenoma, Anxiety Disorder, Asthma, Autism Spectrum Disorder, Carcinoma, Diabetic retinopathy, Diastrophic Dysplasia, Gastrointestinal Diseases, Hurler-Scheie Syndrome, Intestinal Neoplasms, Kidney stone, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Mammary Neoplasms, Melanoma, Multiple myeloma, Neoplasms, Nephrocalcinosis, Nephronophthisis, Parkinson disease, Pfaundler-Hurler Syndrome, Schizophrenia
|
1283
|
|
|
Solute carrier family 26 member 10, pseudogene |
SLC26A10 |
Curated: N/A
Unreviewed: N/A
|
1284
|
|
|
Solute carrier family 26 member 11 |
- |
Curated: Mucopolysaccharidosis, Stroke
Unreviewed: Breast neoplasm, Ischemic Stroke, Myeloid Leukemia, Sarcoma
|
1285
|
|
|
Solute carrier family 26 member 2 |
D5S1708, DTD, DTDST, EDM4, MST153, MSTP157 |
Curated: Achondrogenesis, Atelosteogenesis, Bone disease, Brachydactyly, Carnevale syndrome, Congenital cartilage disorder, Connective tissue disease, Craniofacial abnormalities, De la chapelle dysplasia, Desbuquois syndrome, Diastrophic dysplasia, Diastrophic dysplasia, broad bone-platyspondylic variant, Ear disease, Epiphyseal dysplasia, Juvenile idiopathic arthritis, Marshall syndrome, Osteochondrodysplasias, Oligoarticular juvenile idiopathic arthritis, Skeletal dysplasia, SLC26A2-related skeletal dysplasia
Unreviewed: Acquired Clubfoot, Acquired Kyphoscoliosis, Adenoma, Arthritis, Asthma, Bone Disease, Breast Cancer, Breast neoplasm, Camptodactyly of fingers, Clubfoot, Colon Carcinoma, Colonic Neoplasms, Congenital Camptodactyly, Congenital Clubfoot, Congenital Epicanthus, Congenital Exomphalos, Congenital kyphoscoliosis, Conn Syndrome, Cryptorchidism, Cystic hygroma, Cystic lesions of the pinnae, De La Chapelle Dysplasia, Diastrophic Dwarfism, Diastrophic Dysplasia, Dwarfism, Ear Diseases, Elbow flexion contracture, Facial midline hemangioma, Fibrosarcoma, Frontal bossing, Glabellar hemangioma, Hernia, Femoral, Hip Contracture, Hydrops Fetalis, Irritable Bowel Syndrome, Juvenile arthritis, Knee osteoarthritis, Laryngostenosis, Lung carcinoma, Lung Neoplasms, Macrocephaly, Malignant Neoplasm, Mesothelioma, Metabolic Diseases, Micrognathism, Micromelia, Movement Disorders, Mucopolysaccharidosis, Multiple Epiphyseal Dysplasia, Neoplasms, Osteoarthritis, Osteochondrodysplasia, Osteoporosis, Osteosclerosis, Otosclerosis, Pancreatic Diseases, Pierre-Robin Syndrome, Plagiocephaly, Pulmonary hypoplasia, Scoliosis, Short femur, Spinal cord compression, Spondylolysis, Squamous cell carcinoma, Stargardt disease, Stomach Carcinoma, Stomach Neoplasms, Thoracic hypoplasia, Tracheobronchomalacia, Ulcerative colitis, Visceral angiomatosis
|
1286
|
|
|
Solute carrier family 26 member 3 |
CLD, DRA |
Curated: Cholecystolithiasis, Ulcerative colitis, Congenital chloride diarrhea, Congenital secretory diarrhea, Hydrops fetalis, Intestinal obstruction
Unreviewed: Achondrogenesis, Adenocarcinoma, Adenoma, Adenomatous Polyposis, Asthma, Autoimmune Diseases, Barrett esophagus, Bartter syndrome, Breast Cancer, Breast Carcinoma, Brooke-Spiegler Syndrome, Cardiovascular Abnormalities, Cirrhosis, Cleidocranial Dysplasia, Colitis, Colonic neoplasm, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Congenital disorder of glycosylation, Congenital Heart Disease, Cystic Fibrosis, Cystitis, Deafness, Dermatitis, Diabetes Insipidus, Diabetes Mellitus, Diabetes mellitus, type 1, Diarrhea, Diastrophic Dysplasia, Dysentery, Eczema, End Stage Liver Disease, Eosinophilic Leukemia, Fatty Liver, Gastrointestinal Diseases, Gitelman syndrome, Glioblastoma, Glioma, Graves Disease, Hematopoietic Neoplasms, Hyperaldosteronism, Hypereosinophilic syndrome, Hyperoxaluria, Hypochloremia, Hypokalemia, Infertility, Inflammatory Bowel Disease, Intestinal Cancer, Lactose Intolerance, Leprosy, Liver carcinoma, Liver Cirrhosis, Liver Fibrosis, Lung Diseases, Lymphoblastic Leukemia, Lymphoma, Male infertility, Malignant Neoplasm, Malnutrition, Melasma, Metabolic alkalosis, Microvillus Inclusion Disease, Mineralocorticoid Excess Syndrome, Multiple Epiphyseal Dysplasia, Multiple myeloma, Myopathy, Neoplasms, Nephrocalcinosis, Neurodegenerative Disorders, Non-Alcoholic Fatty Liver Disease, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pendred syndrome, Prostatic neoplasm, Pulmonary Emphysema, Rheumatoid arthritis, Rickets, Sclerosing Cholangitis, SEBASTIAN SYNDROME, Septicemia, Spermatocele, Subfertility, Systemic lupus erythematosus, Vipoma, Vitamin D Deficiency
|
1287
|
|
|
Solute carrier family 26 member 4 |
DFNB4, EVA, PDS, TDH2B |
Curated: Congenital hypothyroidism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Thyroid agenesis, Congenital ear anomaly, Congenital hypothyroidism due to absence of thyroid gland, Deafness, Hearing loss, Hereditary hearing loss, Pendred syndrome, Prostatic neoplasms, Wolff-parkinson-white syndrome
Unreviewed: Achondrogenesis, Acoustic Neuroma, Adenoma, Adrenal Gland Pheochromocytoma, Allergic rhinitis, Aplastic anemia, Apraxia, Arteriosclerosis, Asthma, Atherosclerosis, Auditory Neuropathy, Autism, Bartter syndrome, Brain Infarction, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Cardiomegaly, Carotid artery stenosis, Cholestanol storage disease, Chromophobe Carcinoma, Chronic Obstructive Pulmonary Disease, Classical Hodgkin lymphoma, Cochlear diseases, Compensated hypothyroidism, Congenital chloride diarrhea, Congenital Hypothyroidism, Congenital Ichthyosis, Congenital Nonbullous Ichthyosiform Erythroderma, Congenital Sensorineural Hearing Loss, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Craniosynostosis, Cystic Fibrosis, Dementia, Developmental Delay, Diastrophic Dysplasia, Distal Renal Tubular Acidosis, Dwarfism, Epidermolysa bullosa simplex and limb girdle muscular dystrophy, Euthyroid Goiter, Graves Disease, Hashimoto Disease, Headache, Hearing Loss, Hepatitis b, Hodgkin Disease, Hyperaldosteronism, Hyperparathyroidism, Hypersomnia, Hypertension, Hyperthyroidism, Hypothyroidism, Ichthyosis, Impaired Cognition, Kidney Disease, Left Ventricular Hypertrophy, Leukemia, Low-frequency hearing loss, Lung Diseases, Lymphoma, Macroglossia, Malignant Neoplasm, Megalencephaly, Polymicrogyria, Polydactyly, Hydrocephalus Syndrome, Mental Disorders, Mental retardation, Metabolic alkalosis, Metabolic syndrome, Migraine, Mineralocorticoid Excess Syndrome, Mondini Defect, Multiple Epiphyseal Dysplasia, Myeloid leukemia, Myocardial Infarction, Nasal polyp, Nasal polyposis, Neoplasms, Neurodegenerative disorder, Neutrophilia, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Oncocytoma of kidney, Pancytopenia, Papillary thyroid cancer, Papillary thyroid carcinoma, Paraganglioma, Pendred Syndrome, Pheochromocytoma, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Pseudohypoaldosteronism, Pulmonary arterial hypertension, Pulmonary hypertension, Retinoblastoma, Rhinitis, Rhinosinusitis With Nasal Polyps, Seizures, Senile Dementia, Sensorineural hearing loss, Sinusitis, Sjogren syndrome, Sleep Apnea, Speech Disorders, Stress Disorder, Thoracic disease, Thyroid Agenesis, Thyroid cancer, Thyroid Carcinoma, Thyroid disease, Thyroid Diseases, Thyroid Dysgenesis, Thyroid dyshormonogenesis, Thyroid Hormone Resistance, Thyroid Hypoplasia, Thyroid Neoplasm, Thyroid Nodule, Thyroiditis, Thyrotoxicosis, Tracheal Stenosis, Trichohepatoenteric Syndrome, Usher syndrome, Vestibular disease, Wolff-Parkinson-White Syndrome
|
1288
|
|
|
SLC26A4 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: Deafness, Papillary thyroid carcinoma, Pendred Syndrome, Wolff-Parkinson-White Syndrome
|
1289
|
|
|
Solute carrier family 26 member 5 |
DFNB61, PRES |
Curated: Isolated sensorineural deafness, Nonsyndromic intellectual disability, Deafness, Hearing loss, Nonsyndromic hearing loss, nonsyndromic genetic hearing loss
Unreviewed: Achondrogenesis, Diastrophic Dysplasia, Epileptic encephalopathy, Hearing Loss, Hereditary Leber Optic Atrophy, Kidney Failure, Leukoencephalopathy, Liver carcinoma, Macrophage Activation Syndrome, Multiple Epiphyseal Dysplasia, Neuromyelitis Optica, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Sensorineural hearing loss, Stroke, Vasculitis
|
1290
|
|
|
SLC26A5 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|