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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YGL125W | MET13 | SGDID:S000003093 | metF |
Methylenetetrahydrofolate reductase (EC 1.5.1.20) (Fragment) |
1.5.1.20 | Thermus thermophilus | 1v93_a | Q9RA47 | 100.00 | 1.70E-58 | 1.40E-62 | 475.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YGL125W | MET13 | SGDID:S000003093 | MET12 YPL023C LPB8C |
Methylenetetrahydrofolate reductase 1 (EC 1.5.1.20) |
1.5.1.20 | Saccharomyces cerevisiae | 6fnu_a | P46151 | 100.00 | 1.60E-45 | 1.30E-49 | 380.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YGL125W | MET13 | SGDID:S000003093 | metF b3941 JW3913 |
5,10-methylenetetrahydrofolate reductase (EC 1.5.1.20) |
1.5.1.20 | Escherichia coli | 3fst_c | P0AEZ1 | 100.00 | 1.50E-43 | 1.30E-47 | 365.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
YGL125W | MET13 | SGDID:S000003093 | TTHA0327 |
TTHA0327 |
1.5.1.20 | Thermus thermophilus | 3apt_a | Q5SLG6 | 100.00 | 3.50E-47 | 2.90E-51 | 393.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YGL125W | MET13 | SGDID:S000003093 | MTHFR |
Methylenetetrahydrofolate reductase (EC 1.5.1.20) |
1.5.1.20 | Homo sapiens | Catastrophic Antiphospholipid Syndrome,Lens Subluxation,Cervical Intraepithelial Neoplasia,Heart Disease,Dystonia 9,Physical Disorder,Retinal Vein Occlusion,Retinal Vascular Occlusion,Blood Protein Disease,Spina Bifida Occulta,Childhood Acute Lymphocytic Leukemia,Intracranial Thrombosis,Gastric Cardia Carcinoma,Gastric Cardia Adenocarcinoma,Vascular Disease,Migraine With Or Without Aura 1,Mucositis,Nephrosclerosis,Spasticity,Spinal Cord Infarction,Epilepsy,Portal Vein Thrombosis,Diabetic Angiopathy,Atrial Heart Septal Defect,Amino Acid Metabolic Disorder,Homocystinuria,Nondisjunction,Gastroesophageal Adenocarcinoma,Cleft Lip,Hyperuricemia,Gaucher'S Disease,Cleft Lip With Or Without Cleft Palate,Inherited Metabolic Disorder,Diabetes Mellitus,Clubfoot,Cerebral Palsy,Cerebrovascular Disease,Intracranial Hypertension,Mthfr Gene Variant,Encephalomalacia,Pulmonary Embolism,Alzheimer Disease,Schizencephaly,Neonatal Stroke,Prothrombin Thrombophilia,Myocardial Infarction,Major Depressive Disorder,Beta-Thalassemia Major,Stroke, Ischemic,Placental Abruption,Cleft Lip/Palate,Mild Cognitive Impairment,Essential Thrombocythemia,Multiple Chemical Sensitivity,Differentiated Thyroid Carcinoma,Transient Cerebral Ischemia,Exencephaly,Male Infertility,Varicocele,Leukemia,Post-Traumatic Epilepsy,Mixed Phenotype Acute Leukemia,Blood Coagulation Disease,Childhood Leukemia,Placenta Disease,Riboflavin Deficiency,End Stage Renal Disease,Chronic Kidney Disease,Acute Leukemia,Central Retinal Vein Occlusion,Protein S Deficiency,Thrombophilia,Retinal Vascular Disease,Psychotic Disorder,Neural Tube Defects, Folate-Sensitive,Cerebral Atherosclerosis,Migraine Without Aura,Atherosclerosis Susceptibility,Leukemia, Acute Lymphoblastic,Cataract,Nutritional Deficiency Disease,Cardiovascular System Disease,Choline Deficiency Disease,Cerebral Sinovenous Thrombosis,Isolated Exencephaly,Behcet Syndrome,Isolated Anencephaly,Sensorineural Hearing Loss,Methotrexate Toxicity,Infertility,Migraine With Aura,Carotid Stenosis,Hepatic Vascular Disease,Antithrombin Iii Deficiency,Retinal Artery Occlusion,Branch Retinal Artery Occlusion,Central Retinal Artery Occlusion,Intracranial Vasospasm,Glycogen Storage Disease,Fetal Anticonvulsant Syndrome,Hellp Syndrome,Venous Insufficiency,Osteonecrosis,Schizoaffective Disorder,Sudden Sensorineural Hearing Loss,Megaloblastic Anemia,Osteoporosis,Vein Disease,Thrombasthenia,Kidney Disease,Antiphospholipid Syndrome,Cardia Cancer,Vascular Dementia,Smallpox,Adult Acute Lymphocytic Leukemia,Pre-Eclampsia,Upper Thoracic Spina Bifida Cystica,Cervicothoracic Spina Bifida Cystica,Cervical Spina Bifida Cystica,Lumbosacral Spina Bifida Cystica,Thoracolumbosacral Spina Bifida Cystica,Total Spina Bifida Cystica,Upper Thoracic Spina Bifida Aperta,Neural Tube Closure Defect,Thoracolumbosacral Spina Bifida Aperta,Lumbosacral Spina Bifida Aperta,Cervical Spina Bifida Aperta,Cervicothoracic Spina Bifida Aperta,Total Spina Bifida Aperta,Eclampsia,Breast Cancer,Patent Foramen Ovale,Colorectal Cancer,Open-Angle Glaucoma,Familial Hypercholesterolemia,Amaurosis Fugax,Lateral Myocardial Infarction,Cryptogenic Cirrhosis,Primary Angle-Closure Glaucoma,Peripheral Vascular Disease,Microcephaly,Pulmonary Artery Disease,Myelitis,Hydrocephalus,Hemifacial Spasm,Spastic Hemiplegia,Bipolar Disorder,Homocysteinemia,Cleft Palate, Isolated,Pediatric Osteosarcoma,Gastric Cancer,Methylmalonic Acidemia,West Syndrome,Lemierre'S Syndrome,Turner Syndrome,Disease Of Mental Health,Gastroschisis,Sickle Cell Anemia,Intracranial Sinus Thrombosis,Lateral Sinus Thrombosis,Exfoliation Syndrome,Alcohol Use Disorder,Thrombocytopenia,Rheumatoid Arthritis,Type 2 Diabetes Mellitus,Protein C Deficiency,Thrombophlebitis,Livedoid Vasculitis,Lynch Syndrome,Schizophrenia,Beta-Thalassemia,Microphthalmia, Isolated 5,Homocystinuria Due To Deficiency Of N -Methylenetetrahydrofolate Reductase Activity,Neural Tube Defects,Esophageal Cancer,Orofacial Cleft,Inflammatory Bowel Disease,Tetralogy Of Fallot,Thrombophilia Due To Thrombin Defect,Thrombophilia Due To Activated Protein C Resistance,Vitamin Metabolic Disorder,Tobacco Addiction,Vitamin B12 Deficiency,Colorectal Cancer, Hereditary Nonpolyposis, Type 5,Down Syndrome,Glycine N-Methyltransferase Deficiency,Cutis Laxa, Autosomal Dominant 2,Varicose Veins,Chronic Venous Insufficiency,Colorectal Adenoma,Arteritic Anterior Ischemic Optic Neuropathy,Vertical Talus, Congenital,Attention Deficit-Hyperactivity Disorder,Hypertension, Essential,Autism Spectrum Disorder,Cutis Laxa, Autosomal Dominant 3,Autoimmune Disease Of Cardiovascular System,Lipoprotein Quantitative Trait Locus,Methylmalonic Acidemia And Homocysteinemia, Cblx Type,Moyamoya Disease 1,Porencephaly,Anencephaly,Mastoiditis,Takayasu Arteritis,Myelomeningocele,Omphalocele,Chromosomal Duplication Syndrome,Marfan Syndrome,Autism,Thrombosis,Nonarteritic Anterior Ischemic Optic Neuropathy,Budd-Chiari Syndrome,Phenylketonuria |
6fcx_a | P42898 | ENSG00000177000 | MTHFR | 100.00 | 4.00E-149 | 3.00E-153 | 1248.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |