Yeast Systematic Name | Yeast Symbol | SGDID | Analog Name | Analog Description | EC | Organism | Disease | Structure | Uniprot | Human ID | Human Symbol | HHsearch Probability | HHsearch E_value | HHsearch P_value | HHsearch Score | Flag Disease related | Flag Homo sapiens | Flag Mus musculus | Flag Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YGL104C | VPS73 | SGDID:S000003072 | Sugar_tr |
Sugar (and other) transporter |
pfam Family | PF00083 | 99.60 | 2.70E-20 | 2.50E-24 | 185.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
YGL104C | VPS73 | SGDID:S000003072 | SLC2A1 GLUT1 |
Solute carrier family 2, facilitated glucose transporter member 1 (Glucose transporter type 1, erythrocyte/brain) (GLUT-1) (HepG2 glucose transporter) |
Homo sapiens | Hepatic Tuberculosis,Dystonia 9,Endometrial Cancer,Hyperglycemia,Retinitis Pigmentosa,Paroxysmal Choreoathetosis,Seizure Disorder,Childhood Absence Epilepsy,Spasticity,Epilepsy,Ceruminous Adenocarcinoma,Gestational Diabetes,Epilepsy, Idiopathic Generalized 12,Diabetes Mellitus,Clear Cell Renal Cell Carcinoma,Neonatal Meningitis,Paroxysmal Dystonia,T-Cell Lymphoblastic Leukemia/Lymphoma,Paroxysmal Exertion-Induced Dyskinesia,Intraneural Perineurioma,Focal Epilepsy,Perineurioma,Skin Hemangioma,Pontocerebellar Hypoplasia, Type 7,Angiokeratoma,Leukemia,Movement Disease,Hypoglycemia,Hemangioma Of Lung,Renal Pelvis Adenocarcinoma,Familial Isolated Hypoparathyroidism,Hereditary Spastic Paraplegia,Capillary Disease,Gallbladder Melanoma,Hemangioma,Choreatic Disease,Chondroblastoma,Hereditary Stomatocytosis,Pacinian Tumor,Stomatin-Deficient Cryohydrocytosis With Neurologic Defects,Migraine With Aura,Glucose Transporter Type 1 Deficiency Syndrome,Hemangioblastoma,Capillary Hemangioma,Dystonia,Ovarian Cancer,Tuberous Sclerosis,Breast Cancer,Metagonimiasis,Early Myoclonic Encephalopathy,Colorectal Cancer,Ichthyosis, Congenital, Autosomal Recessive 11,Fat Necrosis Of Breast,Papillary Adenocarcinoma,Papillary Carcinoma,Hepatocellular Carcinoma,Ameloblastic Carcinoma,Hemolytic Anemia,Angiokeratoma Circumscriptum,Microcephaly,Myoclonus,Spastic Monoplegia,Hemiplegia,Perivascular Tumor,Alacrima, Achalasia, And Mental Retardation Syndrome,Benign Epilepsy With Centrotemporal Spikes,Gastric Cancer,West Syndrome,Necrobiosis Lipoidica,Disease Of Mental Health,Choriocarcinoma,Body Mass Index Quantitative Trait Locus 11,Aceruloplasminemia,Renal Glucosuria,Type 2 Diabetes Mellitus,Dystonia, Dopa-Responsive,Dystonia 12,Schizophrenia,Abdominal Obesity-Metabolic Syndrome 1,Esophageal Cancer,Lennox-Gastaut Syndrome,Hypoascorbemia,Cryohydrocytosis,Strabismus,Glycine Encephalopathy,Alternating Hemiplegia Of Childhood,Childhood Electroclinical Syndrome,Early Onset Absence Epilepsy,Early Infantile Epileptic Encephalopathy,Glut1 Deficiency Syndrome 2,Glut1 Deficiency Syndrome 1,Colorectal Adenocarcinoma,Renal Cell Carcinoma, Nonpapillary,Wilms Tumor 1,Meningioma, Familial,Dravet Syndrome,Cardiovascular Organ Benign Neoplasm,Pyruvate Dehydrogenase E1-Alpha Deficiency,Epilepsy, Myoclonic Juvenile,Autosomal Recessive Congenital Ichthyosis,Lung Cancer,Sengers Syndrome,Epilepsy, Idiopathic Generalized,Pancreatic Cancer |
5eqg_a | P11166 | ENSG00000117394 | SLC2A1 | 99.60 | 2.50E-20 | 2.40E-24 | 186.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL104C | VPS73 | SGDID:S000003072 | SLC2A3 GLUT3 |
Solute carrier family 2, facilitated glucose transporter member 3 (Glucose transporter type 3, brain) (GLUT-3) |
Homo sapiens | Hyperglycemia,Fetal Macrosomia,Persistent Fetal Circulation Syndrome,Disease Of Mental Health,Choriocarcinoma,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Hypoascorbemia,Huntington Disease,Attention Deficit-Hyperactivity Disorder,Meningioma, Familial |
4zw9_a | P11169 | ENSG00000059804 | SLC2A3 | 99.60 | 2.50E-20 | 2.40E-24 | 188.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |