671
|
|
|
Solute carrier family 28 member 2 |
CNT2, HCNT2, HsT17153, SPNT1 |
|
672
|
|
|
Solute carrier family 28 member 3 |
CNT3 |
Alzheimer disease, Androgenetic alopecia, Astrocytoma, Attention deficit hyperactivity disorder, Cannabis abuse, Color vision deficiency, Colorectal cancer, Diabetic retinopathy, Gout, Metabolic syndrome, Migraine, Multiple system atrophy, Obesity, Parkinson disease, Schizophrenia, Substance abuse, Diabetes mellitus type 2View all (2 more) |
673
|
|
|
Solute carrier family 29 member 1 (Augustine blood group) |
AUG, ENT1, hENT1 |
|
674
|
|
|
Solute carrier family 29 member 3 |
ENT3, HCLAP, HJCD, PHID |
Asthma, Congenital heart disease, Major depressive disorder, Desbuquois syndrome, Diabetes mellitus type 1, Digestive system neoplasms, Dyslipidemias, Hearing impairment, Hearing loss, Congenital heart defect, Hepatomegaly, Hypertrichosis, Hypogonadism, Obesity, Systemic lupus erythematosus, VitiligoView all (1 more) |
675
|
|
|
Solute carrier family 29 member 4 |
ENT4, PMAT |
|
676
|
|
|
Solute carrier family 2 member 1 |
CSE, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT-1, GLUT1, GLUT1DS, HTLVR, PED, SDCHCN |
Ataxia, Bell's palsy, Breast neoplasms, Ductal carcinoma, Hepatocellular carcinoma, Intraductal noninfiltrating carcinoma, Renal cell carcinoma, Cerebellar ataxia, Childhood absence epilepsy, Childhood-onset glut1 deficiency syndrome 2, Choreoathetosis, Chromosome 17q23.1-q23.2 deletion syndrome, Glucose transporter type 1 deficiency syndrome, Colonic neoplasms, Cryohydrocytosis, Developmental disability, Diabetes mellitus type 2, Dystonia, Epilepsy, Epilepsy with myoclonic absence, Epilepsy with myoclonic atonic seizures, Idiopathic generalized epilepsy, Rolandic epilepsy, Developmental and epileptic encephalopathy, Global developmental delay, Intellectual developmental disorder, Liver neoplasms, Mesothelioma, Microcephaly, Migraine, Myopathy, Nervous system disease, Obesity, Osteoarthritis, Ovarian neoplasms, Paroxysmal dystonic choreoathetosis, Paroxysmal dyskinesia, Peritoneal neoplasms, Seizures, StrabismusView all (25 more) |
677
|
|
|
Solute carrier family 2 member 10 |
ATORS, ATS, GLUT10 |
Alzheimer disease, Androgenetic alopecia, Aortic aneurysm, Arterial tortuosity syndrome, Astrocytoma, Auditory system disease, Bicuspid aortic valve, Breast neoplasms, Color vision deficiency, Congenital contractural arachnodactyly, Ehlers-danlos syndrome, Thoracic aortic aneurysm and aortic dissection, Marfan syndrome, Orofacial cleft |
678
|
|
|
Solute carrier family 2 member 11 |
GLUT10, GLUT11 |
|
679
|
|
|
Solute carrier family 2 member 12 |
GLUT12, GLUT8 |
|
680
|
|
|
Solute carrier family 2 member 13 |
HMIT |
Alzheimer disease, Astrocytoma, Uinary system neoplasms, Colorectal cancer, Crohn disease, Inflammatory bowel disease, Insomnia, Parkinson disease, Progressive supranuclear palsy, Ulcerative colitis, Urogenital neoplasms |
