







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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YIL044C | AGE2 | SGDID:S000001306 | SMAP1 |
Stromal membrane-associated protein 1 |
Homo sapiens | Retinitis Pigmentosa,Fundus Dystrophy,Retinitis Pigmentosa 25 |
2crr_a | Q8IYB5 | ENSG00000112305 | SMAP1 | 99.80 | 1.00E-24 | 9.60E-29 | 179.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL044C | AGE2 | SGDID:S000001306 | AGFG1 HRB RAB RIP |
Arf-GAP domain and FG repeat-containing protein 1 (HIV-1 Rev-binding protein) (Nucleoporin-like protein RIP) (Rev-interacting protein) (Rev/Rex activation domain-binding protein) |
Homo sapiens | Spermatogenic Failure 50,Retinal Degeneration,Chronic Meningitis,Developmental And Epileptic Encephalopathy 16,Disease Of Mental Health,Hermansky-Pudlak Syndrome,Spermatogenic Failure 9,Warburg Micro Syndrome 3,Warburg Micro Syndrome 2,Choroideremia,Autoimmune Disease Of Peripheral Nervous System,Griscelli Syndrome, Type 2,Griscelli Syndrome |
2d9l_a | P52594 | ENSG00000173744 | AGFG1 | 99.80 | 2.90E-26 | 2.70E-30 | 187.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL044C | AGE2 | SGDID:S000001306 | ADAP1 CENTA1 |
Arf-GAP with dual PH domain-containing protein 1 (Centaurin-alpha-1) (Cnt-a1) (Putative MAPK-activating protein PM25) |
Homo sapiens | 3lju_x | O75689 | ENSG00000105963 | ADAP1 | 99.70 | 3.30E-22 | 3.50E-26 | 183.20 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YIL044C | AGE2 | SGDID:S000001306 | SMAP2 SMAP1L |
Stromal membrane-associated protein 2 (Stromal membrane-associated protein 1-like) |
Homo sapiens | Kniest Dysplasia,Vitreous Syneresis,Marshall Syndrome,Multiple Epiphyseal Dysplasia Due To Collagen 9 Anomaly |
2iqj_a | Q8WU79 | ENSG00000084070 | SMAP2 | 99.80 | 1.20E-25 | 1.20E-29 | 183.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL044C | AGE2 | SGDID:S000001306 | ACAP1 CENTB1 KIAA0050 |
Arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 1 (Centaurin-beta-1) (Cnt-b1) |
Homo sapiens | Ileum Cancer |
4f1p_a | Q15027 | ENSG00000072818 | ACAP1 | 99.80 | 2.40E-23 | 2.40E-27 | 190.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL044C | AGE2 | SGDID:S000001306 | ITGB1 FNRB MDF2 MSK12 |
Integrin beta-1 (Fibronectin receptor subunit beta) (Glycoprotein IIa) (GPIIA) (VLA-4 subunit beta) (CD antigen CD29) |
Homo sapiens | Psoriasis,Endometrial Cancer,Hard Palate Cancer,Mast-Cell Leukemia,Melanoma,Alzheimer Disease,Plasma Cell Leukemia,Myocardial Infarction,Keratopathy,Hydrocele,Neuroblastoma,Pustulosis Palmaris Et Plantaris,Cervical Non-Keratinizing Squamous Cell Carcinoma,Basal Cell Carcinoma,Leukemia, Acute Lymphoblastic,Dilated Cardiomyopathy,Synovitis,Focal Segmental Glomerulosclerosis,Ovarian Cancer,Gastric Fundus Cancer,Neural Tube Closure Defect,Breast Cancer,Colorectal Cancer,Gallbladder Cancer,Hepatocellular Carcinoma,Cerebral Hypoxia,Lipoid Nephrosis,Teratocarcinoma,Bullous Keratopathy,Sarcoma,Gastric Cancer,Prostate Cancer,Brittle Bone Disorder,Skin Disease,Beta-Thalassemia,Arrhythmogenic Right Ventricular Cardiomyopathy,Neural Tube Defects,Lymphoma,Inguinal Hernia,Lung Cancer,Pancreatic Cancer |
3t9k_a | P05556 | ENSG00000150093 | ITGB1 | 99.70 | 2.20E-22 | 2.30E-26 | 184.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |