|
801
|
|
|
Solute carrier family 12 member 3 |
NCC, NCCT, TSC |
Bartter syndrome, Chondrocalcinosis, Conn syndrome, Diabetes mellitus, Diabetic ketoacidosis, Fanconi syndrome, Focal seizures, Gitelman syndrome, Glomerulosclerosis, Gout, Graves disease, Hashimoto disease, Hypermagnesemia, Hypertension, Hypokalemia, Hypomagnesemia, Iron deficiency anemia, Kidney disease, Metabolic alkalosis, Mitochondrial encephalopathy, Nephritis, Nocturia, Pancreatic neoplasm, Parathyroid adenoma, Pericardial effusion, Raynaud phenomenon, Renal glomerular disease, Scleroderma, Vascular diseases, Ventricular fibrillation, Vulval varicesView all (16 more) |
|
802
|
|
|
Solute carrier family 12 member 4 |
CTC-479C5.17, KCC1, hKCC1 |
|
|
803
|
|
|
Solute carrier family 14 member 1 (Kidd blood group) |
HUT11, HUT11A, HsT1341, JK, Jk(a), Jk(b), RACH1, RACH2, UT-B1, UT1, UTE |
|
|
804
|
|
|
Solute carrier family 15 member 2 |
PEPT2 |
|
|
805
|
|
|
Solute carrier family 16 member 1 |
HHF7, MCT, MCT1, MCT1D |
Colonic neoplasms, Hyperinsulinemic hypoglycemia, Developmental delay, Erythrocyte lactate transporter defect, Hypoglycemic coma, Hypoglycemic seizures, Ketoacidosis, Ketonuria, Ketosis, Mental retardation, Metabolic myopathy, Monocarboxylate transporter 1 deficiency |
|
806
|
|
|
Solute carrier family 16 member 2 |
AHDS, DXS128, DXS128E, MCT 7, MCT 8, MCT7, MCT8, MRX22, XPCT |
Allan-herndon-dudley syndrome, Amyotrophy, Aphasia, Autism spectrum disorder, Bowel incontinence, Cholestasis, Congenital anomaly of neck, Congenital pectus excavatum, Diabetes mellitus, Dysarthria, Dysmorphic features, Hypothyroidism, Mental retardation, Leukodystrophy, Macrotia, Microcephaly, Multiple congenital anomalies, Hypotonia, Proptosis, Ptosis, Scoliosis, Spastic paraplegia, Spastic quadriplegiaView all (8 more) |
|
807
|
|
|
Solute carrier family 17 member 1 |
NAPI-1, NPT-1, NPT1 |
|
|
808
|
|
|
Solute carrier family 34 member 1 |
FRTS2, HCINF2, NAPI-3, NPHLOP1, NPT2, NPTIIa, SLC11, SLC17A2 |
Bone disease, Fanconi syndrome, Diabetes, Diabetes mellitus, Dwarfism, Fanconi-bickel syndrome, Hypercalcemia, Hypophosphatemia with nephrolithiasis or osteoporosis, Kidney disease, Kidney failure, Leukemia, Medullary nephrocalcinosis, Milk-alkali syndrome, Nephrocalcinosis, Nephrolithiasis, Nephrolithiasis-osteoporosis, hypophosphatemic, Osteopenia, Osteoporosis, Phosphate diabetes, Renal insufficiency, RicketsView all (6 more) |
|
809
|
|
|
Solute carrier family 18 member A1 |
CGAT, VAT1, VMAT1 |
|
|
810
|
|
|
Solute carrier family 18 member A2 |
PKDYS2, SVAT, SVMT, VAT2, VMAT2 |
Bipolar disorder, Brain dopamine-serotonin vesicular transport disease, Developmental delay, Dysarthria, Dysautonomia, Dyssomnia, Impaired cognition, Orofacial dyskinesia, Mental depression, Mental depression with psychotic features, Narcolepsy, Nervous system disorder, Parkinson disease, Parkinsonian disease, Parkinsonism-dystonia, Ptosis, Ramsay hunt paralysis syndrome, Schizophrenia, Sleep disorders, Spastic tetraparesisView all (5 more) |
