| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YMR234W | RNH1 | SGDID:S000004847 | rnhA dasF herA rnh sdrA b0214 JW0204 |
Ribonuclease HI (RNase HI) (EC 3.1.26.4) (Ribonuclease H) (RNase H) |
3.1.26.4 | Escherichia coli | 1jl1_a | P0A7Y4 | 99.30 | 4.70E-16 | 3.50E-20 | 125.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
| YMR234W | RNH1 | SGDID:S000004847 | RNASEH1 RNH1 |
Ribonuclease H1 (RNase H1) (EC 3.1.26.4) (Ribonuclease H type II) |
3.1.26.4 | Homo sapiens | Mitochondrial Encephalomyopathy,Myopathy,Mitochondrial Myopathy,Amyloidosis, Hereditary, Transthyretin-Related,Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome,Chronic Progressive External Ophthalmoplegia,Mitochondrial Dna Maintenance Defects,Amyotrophic Lateral Sclerosis 4, Juvenile,Fanconi Anemia, Complementation Group A,Hyperlipoproteinemia, Type I,Spinocerebellar Ataxia, Autosomal Recessive, With Axonal Neuropathy 2,Aicardi-Goutieres Syndrome,Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive 2,Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis,Mitochondrial Dna Depletion Syndrome 4a |
3bsu_c | O60930 | ENSG00000171865 | RNASEH1 | 98.90 | 1.50E-13 | 1.10E-17 | 90.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |