| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YHR200W | RPN10 | SGDID:S000001243 | VWF F8VWF |
von Willebrand factor (vWF) [Cleaved into: von Willebrand antigen 2 (von Willebrand antigen II)] |
Homo sapiens | Heart Valve Disease,Heart Disease,Primary Thrombocytopenia,X-Linked Recessive Disease,Blood Protein Disease,Hepatopulmonary Syndrome,Vascular Cancer,Mitral Valve Stenosis,Intracranial Thrombosis,Hypertensive Retinopathy,Vascular Disease,Aortic Valve Disease 2,Coronary Stenosis,Diabetic Angiopathy,Diabetes Mellitus,Splenic Sequestration,Intracranial Embolism,Covid-19,Acute Myocardial Infarction,Coronary Thrombosis,Cerebrovascular Disease,Bethlem Myopathy 1,Hypertrophic Cardiomyopathy,Pulmonary Embolism,Complement Component 2 Deficiency,Dieulafoy Lesion,Myocardial Infarction,Pediatric Angiosarcoma,Thyroid Angiosarcoma,Stroke, Ischemic,Deafness, Autosomal Dominant 9,Factor Xiii Deficiency,Hemorrhagic Disease,Blood Platelet Disease,Essential Thrombocythemia,Eisenmenger Syndrome,Uremia,Myeloproliferative Neoplasm,Medulloadrenal Hyperfunction,Thrombocytosis,Thrombotic Microangiopathy,Active Peptic Ulcer Disease,Capillary Lymphangioma,Breast Hemangioma,Generalized Atherosclerosis,Blood Coagulation Disease,Von Willebrand'S Disease,Hemolytic-Uremic Syndrome,Acquired Von Willebrand Syndrome,Middle Ear Adenocarcinoma,Central Retinal Vein Occlusion,Thrombophilia,Hemarthrosis,Hereditary Hemorrhagic Telangiectasia,Capillary Disease,Angiodysplasia,Hemangioma,Atherosclerosis Susceptibility,Cardiovascular System Disease,Dilated Cardiomyopathy,Behcet Syndrome,Lymphangiosarcoma,Carotid Stenosis,Aortic Valve Disease 1,Hepatic Vascular Disease,Glycogen Storage Disease,Hellp Syndrome,Venous Insufficiency,Kaposiform Hemangioendothelioma,Collagen Disease,Heart Conduction Disease,Sickle Cell Disease,Brachydactyly, Type D,Papillary Adenofibroma,Glanzmann Thrombasthenia,Aplastic Anemia,Vasculitis,Vein Disease,Antiphospholipid Syndrome,Carotid Body Cancer,Pre-Eclampsia,Unilateral Absence Of A Pulmonary Artery,Intermediate Coronary Syndrome,Patent Foramen Ovale,Griscelli Syndrome, Type 3,Aortic Valve Insufficiency,Al Amyloidosis,Portal Hypertension,Thrombotic Thrombocytopenic Purpura,Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive,Hemolytic Anemia,Malignant Hypertension,Peripheral Vascular Disease,Pulmonary Artery Disease,Fainting,Von Willebrand Disease, Type 3,Von Willebrand Disease, Type 2,Spotted Fever,Homocysteinemia,Hydronephrosis,Factor V Deficiency,Purpura,Qualitative Platelet Defect,Hypothyroidism,Carotid Artery Thrombosis,Disseminated Intravascular Coagulation,Disease Of Mental Health,Sickle Cell Anemia,Pulmonary Hypertension,Pseudo-Von Willebrand Disease,Bernard-Soulier Syndrome,Infiltrating Angiolipoma,Thrombocytopenia,Intermittent Claudication,Type 2 Diabetes Mellitus,Hermansky-Pudlak Syndrome,Angiosarcoma,Factor Xii Deficiency,Drug-Induced Lupus Erythematosus,Thrombophlebitis,African Tick-Bite Fever,Placental Insufficiency,Bleeding Disorder, Platelet-Type, 18,Hemolytic Uremic Syndrome, Atypical 1,Malaria,Transient Bullous Dermolysis Of The Newborn,Factor Viii Deficiency,Thrombophilia Due To Activated Protein C Resistance,Gray Platelet Syndrome,Colorectal Cancer 5,Endocardium Disease,Varicose Veins,Peripheral Artery Disease,Limb Ischemia,Factor Xi Deficiency,Von Willebrand Disease, Type 1,Ectodermal Dysplasia 1, Hypohidrotic, X-Linked,Hypertension, Essential,Autoimmune Disease Of Cardiovascular System,Hemophilia A,Hemophilia B,Lipoprotein Quantitative Trait Locus,Afibrinogenemia, Congenital,Atrial Fibrillation,Bombay Phenotype,Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, Type 2,Intracranial Berry Aneurysm,Moyamoya Disease 1,Systemic Lupus Erythematosus,Thrombosis,Ceroid Lipofuscinosis, Neuronal, 5,Polycythemia Vera |
1atz_a | P04275 | 99.20 | 1.90E-15 | 1.30E-19 | 114.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YHR200W | RPN10 | SGDID:S000001243 | rpn10 pus1 SPAC637.10c |
26S proteasome regulatory subunit rpn10 |
Schizosaccharomyces pombe | 2x5n_a | O94444 | 99.10 | 1.00E-14 | 6.90E-19 | 109.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YHR200W | RPN10 | SGDID:S000001243 | RPN10 MCB1 SUN1 YHR200W |
26S proteasome regulatory subunit RPN10 |
Saccharomyces cerevisiae | 6fvx_w | P38886 | 99.30 | 2.20E-16 | 1.50E-20 | 119.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YHR200W | RPN10 | SGDID:S000001243 | PSMD4 MCB1 |
26S proteasome non-ATPase regulatory subunit 4 (26S proteasome regulatory subunit RPN10) (26S proteasome regulatory subunit S5A) (Antisecretory factor 1) (AF) (ASF) (Multiubiquitin chain-binding protein) |
Homo sapiens | Alzheimer Disease,Angelman Syndrome,Cystic Fibrosis,Cholera,Encephalopathy, Familial, With Neuroserpin Inclusion Bodies,Inflammatory Bowel Disease |
1yx6_a | P55036 | ENSG00000159352 | PSMD4 | 99.10 | 1.20E-14 | 8.00E-19 | 100.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YHR200W | RPN10 | SGDID:S000001243 | TFB4 YPR056W |
General transcription and DNA repair factor IIH subunit TFB4 (TFIIH subunit TFB4) (RNA polymerase II transcription factor B 34 kDa subunit) (RNA polymerase II transcription factor B p34 subunit) (RNA polymerase II transcription factor B subunit 4) |
Saccharomyces cerevisiae | 5oqj_4 | Q12004 | 98.90 | 3.30E-13 | 2.20E-17 | 111.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YHR200W | RPN10 | SGDID:S000001243 | Babam1 Merit40 Nba1 |
BRISC and BRCA1-A complex member 1 (Mediator of RAP80 interactions and targeting subunit of 40 kDa) (New component of the BRCA1-A complex) |
Mus musculus | 6gvw_d | Q3UI43 | 99.50 | 3.50E-19 | 2.30E-23 | 145.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 |