| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YNL098C | RAS2 | SGDID:S000005042 | RAP1A KREV1 |
Ras-related protein Rap-1A (EC 3.6.5.2) (C21KG) (G-22K) (GTP-binding protein smg p21A) (Ras-related protein Krev-1) |
3.6.5.2 | Homo sapiens | Bone Epithelioid Hemangioma,Leukocyte Adhesion Deficiency, Type Iii,Babesiosis,Cervical Non-Keratinizing Squamous Cell Carcinoma,Glanzmann Thrombasthenia,Osteoporosis,Tuberous Sclerosis,Breast Cancer,Meier-Gorlin Syndrome 1,Cerebral Cavernous Malformations,Leukocyte Adhesion Deficiency, Type I,Chronic Granulomatous Disease,Bleeding Disorder, Platelet-Type, 18,Klippel-Trenaunay-Weber Syndrome |
1c1y_a | P62834 | 98.70 | 4.40E-12 | 3.40E-16 | 102.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YNL098C | RAS2 | SGDID:S000005042 | RAP2A |
Ras-related protein Rap-2a (EC 3.6.5.2) (RbBP-30) |
3.6.5.2 | Homo sapiens | Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 3,Cerebral Cavernous Malformations,Cerebrocostomandibular Syndrome,Cerebral Cavernous Malformations 2,Autosomal Dominant Non-Syndromic Intellectual Disability 5 |
3rap_r | P10114 | ENSG00000125249 | RAP2A | 98.10 | 1.30E-09 | 1.00E-13 | 84.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YNL098C | RAS2 | SGDID:S000005042 | RALA RAL |
Ras-related protein Ral-A (EC 3.6.5.2) |
3.6.5.2 | Saguinus oedipus | 1u8z_b | P63320 | 98.10 | 1.30E-09 | 1.00E-13 | 84.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YNL098C | RAS2 | SGDID:S000005042 | RHEB RHEB2 |
GTP-binding protein Rheb (Ras homolog enriched in brain) |
Homo sapiens | Cowden Syndrome,Cowden Syndrome 1,Subependymal Glioma,Benign Ependymoma,Hemimegalencephaly,Subependymal Giant Cell Astrocytoma,Kidney Angiomyolipoma,Tuberous Sclerosis 2,Tuberous Sclerosis,Colorectal Cancer,Kidney Benign Neoplasm,Spinal Cord Disease,Breast Adenocarcinoma,Disease Of Mental Health,Proteus Syndrome,Bladder Urothelial Carcinoma,Renal Cell Carcinoma, Papillary, 1,Tuberous Sclerosis 1,Renal Cell Carcinoma, Nonpapillary,Focal Cortical Dysplasia, Type Ii,Central Nervous System Benign Neoplasm |
6bsx_c | Q15382 | ENSG00000106615 | RHEB | 98.10 | 1.50E-09 | 1.20E-13 | 85.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YNL098C | RAS2 | SGDID:S000005042 | RHEBL1 |
GTPase RhebL1 (Ras homolog enriched in brain like-1 c) (RhebL1c) (Ras homolog enriched in brain-like protein 1) (Rheb-like protein 1) (Rheb2) |
Homo sapiens | Lymphangioleiomyomatosis,Acrocapitofemoral Dysplasia |
3oes_a | Q8TAI7 | ENSG00000167550 | RHEBL1 | 98.10 | 1.30E-09 | 1.00E-13 | 88.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YNL098C | RAS2 | SGDID:S000005042 | RIT1 RIBB RIT ROC1 |
GTP-binding protein Rit1 (EC 3.6.5.2) (Ras-like protein expressed in many tissues) (Ras-like without CAAX protein 1) |
3.6.5.2 | Homo sapiens | Hypertrophic Cardiomyopathy,Rasopathy,Pseudo-Turner Syndrome,Noonan Syndrome 1,Noonan Syndrome 8,Cardiofaciocutaneous Syndrome 1,Pheochromocytoma,Hypertelorism,Juvenile Myelomonocytic Leukemia,Charcot-Marie-Tooth Disease, X-Linked Recessive, 5,Angular Cheilitis |
4klz_a | Q92963 | ENSG00000143622 | RIT1 | 98.00 | 2.10E-09 | 1.70E-13 | 84.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |