1351
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Solute carrier family 32 member 1 |
DEE114, GEFSP12, VGAT, VIAAT, VIAAT GEFSP12 |
Curated: Anorexia nervosa, Developmental and epileptic encephalopathy, Generalized epilepsy with febrile seizures plus, Seizures, Intellectual developmental disorder, Obesity, Obsessive-compulsive disorder, Willis-ekbom disease, Schizophrenia
Unreviewed: Alzheimer disease, Anxiety Disorder, Autism Spectrum Disorder, Congenital Exomphalos, Cystitis, Dementia, Epilepsy, Glioma, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Tauopathies, Tuberous sclerosis complex, Uranostaphyloschisis, Vulval varices, Wilms tumor
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1352
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Solute carrier family 33 member 1 |
ACATN, AT-1, AT1, CCHLND, HPBDS, SPG42 |
Curated: Spastic paraplegia, Cataract, Colorectal cancer, Congenital cataract hearing loss developmental delay syndrome, Dementia, Developmental disability, Global developmental delay, Hearing loss, Hypothyroidism, Insomnia, Neurotic disorder, Partial epilepsy, Hereditary spastic paraplegia
Unreviewed: Adenocarcinoma, Adenoma, Adrenal neoplasia, Amyotrophic Lateral Sclerosis, Anxiety Disorder, Aortic Aneurysm, Apoceruloplasmin deficiency, Arteriosclerosis, Asthma, Atherosclerosis, Atrial Fibrillation, Autism spectrum disorder, Benign Prostatic Hyperplasia, Bestrophinopathy, Breast Cancer, Breast Carcinoma, Cardiovascular Diseases, Cerebellar atrophy, Cerebral Atrophy, Cerebral Infarction, Cerebral Ischemia, Colitis, Colorectal Cancer, Congenital Cataract, Congenital Cataract-Hearing Loss-Developmental Delay Syndrome, Congenital Cataracts, Hearing Loss, And Neurodegeneration, Congenital Posterior Urethral Valves, Congestive Heart Failure, Conn Adenoma, Conn Syndrome, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Coronary Syndrome, Development Disorder, Developmental Delay, Diabetes, Diabetes Mellitus, Diabetic Nephropathy, Dysmorphism, Endometriosis, Epilepsy, Glomerulonephritis, Heart Failure, Henoch-Schonlein Nephritis, Hepatoblastoma, Hepatolenticular degeneration, Hyperhomocysteinemia, Hypertension, Hypertrophic cardiomyopathy, Impaired Cognition, Ischemic Stroke, Kidney Disease, Kidney Failure, Lateral Sclerosis, Left Ventricular Hypertrophy, Leiomyosarcoma, Liver carcinoma, Liver Fibrosis, Liver neoplasms, Lung Cancer, Lung carcinoma, Malignant Hypertension, Malignant Neoplasm, Marfan Syndrome, Melanoma, Mental Depression, Mental retardation, Metabolic Syndrome, MOHR-TRANEBJAERG SYNDROME, Myocardial Infarction, Myocardial Ischemia, Neoplasms, Neurodegenerative Disorders, Nystagmus, Obesity, Osteopenia, Parkinson disease, Periodontitis, Peritoneal Fibrosis, Polycystic Ovary Syndrome, Prostate cancer, Pseudohyperkalemia Cardiff, Scleroderma, Senile Dementia, Senile Plaques, Sensory neuropathy, Sleep Apnea, Spastic Paraplegia, Spondylometaphyseal dysplasia, Stroke, Trichohepatoenteric Syndrome, Ventricular arrhythmia, Ventricular Failure, Vesicoureteral Reflux
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1353
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|
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Solute carrier family 33 member 2 |
MFSD3 |
Curated: N/A
Unreviewed: Lewy body disease
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1354
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|
|
Solute carrier family 34 member 1 |
FRTS2, HCINF2, NAPI-3, NPHLOP1, NPT2, NPTIIa, SLC11, SLC17A2 |
Curated: Asthma, Bladder calculus, Bone disease, Kidney and ureter calculus, Kidney disease, Crohn disease, De toni-debre-fanconi syndrome, Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis, Fanconi renotubular syndrome, Fanconi syndrome, Hypercalcemia, Idiopathic infantile hypercalcemia, Hypercalciuria, Hypophosphatemic rickets, Inflammatory bowel disease, Kidney failure, Nephrolithiasis, Osteogenesis imperfecta, Ulcerative colitis, Urolithiasis
Unreviewed: Bone Disease, Constipation, Diabetes, Diabetes Mellitus, Dwarfism, Epilepsy, Fanconi-Bickel Syndrome, Glioma, Glycogen Storage Disease, Hypophosphatemia With Nephrolithiasis Or Osteoporosis, Hypophosphatemic Rickets, Kidney Disease, Kidney Failure, Kidney stone, Leukemia, McCune-Albright Syndrome, Medullary nephrocalcinosis, Metabolic alkalosis, Metabolic syndrome, Milk-Alkali Syndrome, Nephrocalcinosis, Nephrolithiasis-Osteoporosis, Hypophosphatemic, Osteomalacia, Osteopenia, Osteoporosis, Paraparesis, Phosphate Diabetes, Renal cell carcinoma, Renal Insufficiency, Rickets, Thrombosis, Vitamin D Deficiency, Vitamin D-Dependent Rickets
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1355
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|
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Solute carrier family 34 member 2 |
NAPI-3B, NAPI-IIb, NPTIIb, NaPi2b, PULAM |
Curated: Non-small-cell lung carcinoma
Unreviewed: Bladder carcinoma, Bladder Neoplasm, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cancer, Carcinogenesis, Carcinoma, Colorectal Cancer, Glioma, Hepatocellular carcinoma, Hereditary breast and ovarian cancer syndrome, Hyperphosphatemia, Kidney Failure, LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS, Liver carcinoma, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung disease, Lung neoplasms, Neoplasms, Neuroblastoma, Osteosarcoma, Ovarian neoplasm, Papillary thyroid cancer, Pulmonary Alveolar Microlithiasis, Renal Carcinoma, Renal cell carcinoma, Stomach Carcinoma, Stomach Neoplasms, Thyroid cancer, Urinary bladder cancer, Urinary bladder neoplasms
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1356
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Solute carrier family 34 member 3 |
HHRH, NPT2C, NPTIIc |
Curated: Hypophosphatemic rickets, Desbuquois syndrome, Nephrolithiasis
Unreviewed: Barakat syndrome, Bone disease, Dwarfism, Frontal bossing, Growth disorder, Hereditary Hypophosphatemic Rickets With Hypercalciuria, Hypercalciuria, Hyperphosphatemia, Hypophosphatemic Rickets, HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY, Idiopathic infantile hypercalcemia, Kidney disease, Kidney stone, Medullary nephrocalcinosis, Metabolic Diseases, Metabolic syndrome, Nephrocalcinosis, Osteomalacia, Osteoporosis, Phosphate Diabetes, Renal glycosuria, Renal Tubular Disorder, Rickets, Vitamin d deficiency, Vitamin D-Dependent Rickets
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1357
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Solute carrier family 35 member A1 |
CDG2F, CMPST, CST, hCST |
Curated: Congenital disorder of glycosylation, SLC35A1-congenital disorder of glycosylation
Unreviewed: Amyotrophic Lateral Sclerosis, Anhidrosis, Aortic Valve Insufficiency, Arteriosclerosis, Arthritis, Atherosclerosis, Behcet Syndrome, Bulbar palsy, Cardiovascular Diseases, Cerebral Infarction, Clinodactyly, Cone-rod dystrophy, Congestive Heart Failure, Coronary artery disease, Developmental Delay, Diabetes, Diabetes Mellitus, Dysarthria, Epileptic encephalopathy, Episodic Kinesigenic Dyskinesia, Glioma, Glycogen storage disease, Heart Failure, Hyperglycemia, Hypertension, Immune System Diseases, Liver carcinoma, Macrothrombocytopenia, Malignant Neoplasm, Marfan Syndrome, Mental retardation, Microcephaly, Motor Neuron Disease, Myocardial Infarction, Neck Webbing, Neutropenia, Nystagmus, Obesity, Orofacial dyskinesia, Papillary thyroid cancer, Papillon-Lefevre Disease, Stroke, Subcutaneous hemorrhage, Thrombocytopenia, Ulcerative colitis
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1358
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Solute carrier family 35 member A2 |
CDG2M, CDGX, UDP-Gal-Tr, UGALT, UGAT, UGT, UGT1, UGT2, UGTL |
Curated: Autism, Congenital disorder of glycosylation, Developmental and epileptic encephalopathy, X-linked complex neurodevelopmental disorder
Unreviewed: Allergic Sensitization, Anemia, Anisometropia, Ataxia, Atrophy, Basal ganglia disease, beta Thalassemia, Bladder carcinoma, Bladder Neoplasm, Brain disease, Brainstem Atrophy, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Carcinoma, Cataract-microcornea syndrome, Central Visual Impairment, Cerebellar atrophy, Cerebellar Hypoplasia, Cerebral Atrophy, Cholecystolithiasis, Cholelithiasis, Colon Carcinoma, Colonic neoplasm, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Congenital Clubfoot, Cortical development malformation, Cortical Dysplasia, Craniosynostosis, Crigler-Najjar syndrome, Cyclic Neutropenia, Dandy-Walker Syndrome, Deficiency Of Glucose-6-Phosphate Dehydrogenase, Demyelinating diseases, Developmental Delay, Developmental disability, Dwarfism, Dysmorphic Features, Epilepsy, Epileptic encephalopathy, Esophageal Cancer, Esophageal Carcinoma, Esophagus Neoplasm, Esotropia, Exotropia, Galactosemia, Gastroesophageal Reflux Disease, Gilbert Disease, Glycogen storage disease, Granulomatous Disease, Growth disorder, Hearing Loss, Heart disease, High palate, Hyperbilirubinemia, Hyperopia, Hyperplasia, Hypoalbuminemia, Hypoglycemia, Hypopigmentation Disorder, Hypoplasia Of Corpus Callosum, Hypoplastic hippocampus, Immune system disease, Infantile Spasms, Intellectual developmental disorder, Isolated focal cortical dysplasia, Leukopenia, Lichen amyloidosis, Lymphatic metastasis, Lymphoma, Macular corneal dystrophy, Macular dystrophy, Malignant Neoplasm, Melanoma, Mental retardation, Metabolic Syndrome, Microcephaly, Monocytosis, Multiple Trichoepithelioma, Neoplasms, Neurodevelopmental Disorders, Neutropenia, Non-Alcoholic Fatty Liver Disease, Nystagmus, Osteopenia, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Paraplegia, Partial epilepsy, Pituitary dwarfism, Precocious puberty, Premature adrenarche, Prostate cancer, Psychiatric disorders, Rett syndrome, Rod-cone dystrophy, Salaam Seizures, Scoliosis, Seizures, Sleep Apnea, Spastic tetraparesis, Stomach neoplasms, Strabismus, Tetralogy of Fallot, Thalassemia, Transient nephrotic syndrome, Trichohepatoenteric Syndrome, Urinary bladder cancer, Urinary bladder neoplasms, Visual disorder, West Syndrome, Xeroderma Pigmentosum
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1359
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|
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Solute carrier family 35 member A3 |
AMRS |
Curated: Arthrogryposis multiplex congenita, Arthrogryposis with neurodevelopmental impairment and seizures, Autism, Kidney disease
Unreviewed: Arthrogryposis, Mental Retardation, And Seizures, Autism spectrum disorder, Autism Spectrum Disorder-Epilepsy-Arthrogryposis Syndrome, Central Nervous System Neoplasms, Colorectal neoplasm, Congenital disorder of glycosylation, Developmental Delay, Epilepsy, Epileptic encephalopathy, Glioma, Hypoxia, Jarcho-Levin Syndrome, Mental retardation, Microcephaly, Osteochondrodysplasia, Scoliosis, Skeletal Dysplasia
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1360
|
|
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Solute carrier family 35 member A4 |
- |
Curated: N/A
Unreviewed: Breast Cancer, Breast Carcinoma, Liver carcinoma, Lung adenocarcinoma, Multiple myeloma, Neoplasms, Parkinson disease
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