|
761
|
|
|
Solute carrier family 1 member 4 |
ASCT1, SATT, SPATCCM |
|
|
762
|
|
|
Solute carrier family 1 member 6 |
EAAT4 |
|
|
763
|
|
|
Solute carrier family 1 member 7 |
AAAT, EAAT5 |
|
|
764
|
|
|
Solute carrier family 2 member 1 |
CSE, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT-1, GLUT1, GLUT1DS, HTLVR, PED, SDCHCN |
Anemia, Anxiety disorder, Apraxia, Arthritis, Ataxia, Attention deficit hyperactivity disorder, Autism spectrum disorder, Brachydactyly, Breast cancer, Mammary neoplasms, Breast carcinoma, Breast hyperplasia, Cataract, Cerebral atrophy, Choreoathetosis, Chromophobe carcinoma, Clonic seizures, Colonic neoplasms, Communicating hydrocephalus, Facial dysmorphism, Congenital cataract, Congenital microcephaly, Conjugated hyperbilirubinemia, Cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly, Development disorder, Developmental delay, Diabetes mellitus, Ductal carcinoma, Dwarfism, Dysarthria, Dyskinesia, Dyskinetic syndrome, Dyslexia, Dysmorphic features, Dyssomnia, Dystonia, Epilepsy, Epileptic encephalopathy, Episodic ataxia, Esotropia, Extrapyramidal dyskinesia, Febrile seizures, Glucose transporter deficiency syndrome, Glut1 deficiency syndrome, Hereditary cryohydrocytosis with reduced stomatin, Hypotonic seizures, Impaired cognition, Inborn errors of metabolism, Mental retardation, Jacksonian seizure, Liver neoplasms, Liver cancer, Liver carcinoma, Macrocephaly, Macrotia, Malignant mesothelioma, Marfan syndrome, Mental depression, Microcephaly, Microlissencephaly, Migraine, Movement disorders, Nervous system disorder, Nystagmus, Osteoarthrosis deformans, Otitis media, Ovarian neoplasm, Ovarian cancer, Papillary renal carcinoma, Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity, Paroxysmal nonkinesigenic dyskinesia, Peritoneal neoplasms, Peritoneal carcinomatosis, Punding, Renal carcinoma, Rubral tremor, Seizure, Sleep apnea, Sleep disorders, Spastic paraplegia, Specific learning disorder, Speech delay, Status epilepticus, Strabismus, UranostaphyloschisisView all (70 more) |
|
765
|
|
|
Solute carrier family 2 member 2 |
GLUT2 |
Breast cancer, Mammary neoplasms, Breast carcinoma, Fanconi syndrome, Developmental delay, Diabetes mellitus, Dwarfism, Fanconi-bickel syndrome, Fatty liver, Liver carcinoma, Malabsorption syndrome, Marfan syndrome, Phosphate diabetes, Renal tubular disorder, Rickets |
|
766
|
|
|
Solute carrier family 2 member 3 |
GLUT3 |
Arthritis, Neoplasm, Cerebral cortical atrophy, Dementia, Dermatitis, Developmental regression, Embryonal neoplasm, Tumor, Huntington disease, Juvenile arthritis, Lipoidosis, Movement disorders, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Still disease |
|
767
|
|
|
Solute carrier family 2 member 4 |
GLUT4 |
|
|
768
|
|
|
Solute carrier family 2 member 5 |
GLUT-5, GLUT5 |
|
|
769
|
|
|
Solute carrier family 3 member 1 |
ATR1, CSNU1, D2H, NBAT, RBAT |
2p21 microdeletion syndrome, Congenital epicanthus, Cystinuria, Developmental delay, Dolichocephaly, Drachtman weinblatt sitarz syndrome, Frontal bossing, Hypertensive nephropathy, Hypoglycemia, Hypogonadism, Hypotonia-cystinuria syndrome, Mental retardation, Nephritis, Nephrocalcinosis, Nephrolithiasis, Ptosis, Renal insufficiencyView all (2 more) |
|
770
|
|
|
Solute carrier family 3 member 2 |
4F2, 4F2HC, 4T2HC, CD98, CD98HC, MDU1, NACAE |
|
