







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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YER095W | RAD51 | SGDID:S000000897 | RAD51 YER095W |
DNA repair protein RAD51 |
Saccharomyces cerevisiae | 3lda_a | P25454 | 100.00 | 2.20E-58 | 1.40E-62 | 425.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER095W | RAD51 | SGDID:S000000897 | radA |
DNA repair and recombination protein RadA |
Methanococcus voltae | 1xu4_a | O73948 | 99.90 | 8.70E-28 | 5.70E-32 | 215.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER095W | RAD51 | SGDID:S000000897 | RAD51 RAD51A RECA |
DNA repair protein RAD51 homolog 1 (HsRAD51) (hRAD51) (RAD51 homolog A) |
Homo sapiens | Endometrial Cancer,Retinitis Pigmentosa,Mirror Movements 1,Rothmund-Thomson Syndrome, Type 2,Bilateral Breast Cancer,Retinitis Pigmentosa 42,Bagassosis,Fanconi Anemia, Complementation Group R,Barrett'S Adenocarcinoma,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Cerebellar Disease,Brain Cancer,Haverhill Fever,Fanconi Anemia, Complementation Group J,Aplastic Anemia,Glanders,Ovarian Cancer,Pituitary Adenoma 5, Multiple Types,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Malignant Renovascular Hypertension,Malignant Secondary Hypertension,Colorectal Cancer,Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive,Microcephaly,Werner Syndrome,Xeroderma Pigmentosum, Complementation Group D,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group D2,Fanconi Anemia, Complementation Group A,Xeroderma Pigmentosum, Complementation Group G,Immunodeficiency 25,Prostate Cancer,Osteogenesis Imperfecta, Type Vii,Fanconi Anemia, Complementation Group D1,Seckel Syndrome,Myelodysplastic Syndrome,Autosomal Genetic Disease,Pigmentary Disorder, Reticulate, With Systemic Manifestations, X-Linked,Mirror Movements 2,Ectodermal Dysplasia 1, Hypohidrotic, X-Linked,Nijmegen Breakage Syndrome,Li-Fraumeni Syndrome,Medulloblastoma,Bloom Syndrome,Lung Cancer,Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease,Pancreatic Cancer |
5jzc_g | Q06609 | ENSG00000051180 | RAD51 | 99.90 | 1.30E-30 | 8.30E-35 | 235.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER095W | RAD51 | SGDID:S000000897 | radA PF1926 |
DNA repair and recombination protein RadA |
Pyrococcus furiosus | 1pzn_a | O74036 | 99.90 | 1.10E-28 | 7.10E-33 | 223.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER095W | RAD51 | SGDID:S000000897 | radA SSO0250 |
DNA repair and recombination protein RadA |
Saccharolobus solfataricus | 2z43_b | Q55075 | 99.90 | 1.80E-30 | 1.20E-34 | 232.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |