| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YPR187W | RPO26 | SGDID:S000006391 | RPO26 RPB6 YPR187W P9677.8 |
DNA-directed RNA polymerases I, II, and III subunit RPABC2 (RNA polymerases I, II, and III subunit ABC2) (ABC23) (DNA-directed RNA polymerases I, II, and III 23 kDa polypeptide) |
Saccharomyces cerevisiae | 1twf_f | P20435 | 100.00 | 1.30E-43 | 9.90E-48 | 276.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YPR187W | RPO26 | SGDID:S000006391 | rpoZ A311_04586 |
rpoZ A311_04586 |
2.7.7.6 | Escherichia coli | 6rh3_e | L4IY67 | 98.70 | 2.50E-12 | 2.20E-16 | 86.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
| YPR187W | RPO26 | SGDID:S000006391 | PAS_chr2-2_0434 |
PAS_chr2-2_0434 |
Komagataella phaffii | 5xog_f | C4R1V1 | 100.00 | 2.80E-41 | 2.10E-45 | 263.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YPR187W | RPO26 | SGDID:S000006391 | rpoK TK1498 |
DNA-directed RNA polymerase subunit K (EC 2.7.7.6) |
2.7.7.6 | Thermococcus kodakarensis | 4qiw_k | Q5JJD0 | 99.30 | 4.90E-16 | 4.30E-20 | 100.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YPR187W | RPO26 | SGDID:S000006391 | POLR2F POLRF |
DNA-directed RNA polymerases I, II, and III subunit RPABC2 (RNA polymerases I, II, and III subunit ABC2) (DNA-directed RNA polymerase II subunit F) (DNA-directed RNA polymerases I, II, and III 14.4 kDa polypeptide) (RPABC14.4) (RPB14.4) (RPB6 homolog) (RPC15) |
Homo sapiens | Waardenburg'S Syndrome,Rare Genetic Deafness,Myopathy, Centronuclear, 1,Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease,Neuropathy,Waardenburg Syndrome, Type 4c,Charcot-Marie-Tooth Disease,Waardenburg Syndrome Type 4,Waardenburg Syndrome, Type 4a,Waardenburg Syndrome, Type 2e,Hirschsprung Disease 1,Waardenburg Syndrome, Type 2a |
1qkl_a | P61218 | 99.90 | 2.30E-27 | 1.80E-31 | 179.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YPR187W | RPO26 | SGDID:S000006391 | rpb6 rpo15 SPCC1020.04c |
DNA-directed RNA polymerases I, II, and III subunit RPABC2 (RNA polymerases I, II, and III subunit ABC2) (DNA-directed RNA polymerases I, II, and III 15 kDa polypeptide) (RPC16) |
Schizosaccharomyces pombe | 3h0g_r | P36595 | 99.80 | 4.90E-26 | 3.60E-30 | 174.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YPR187W | RPO26 | SGDID:S000006391 | rpoZ b3649 JW3624 |
DNA-directed RNA polymerase subunit omega (RNAP omega subunit) (EC 2.7.7.6) (RNA polymerase omega subunit) (Transcriptase subunit omega) |
2.7.7.6 | Escherichia coli | 6n61_e | P0A800 | 98.70 | 4.30E-12 | 3.60E-16 | 89.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
| YPR187W | RPO26 | SGDID:S000006391 | POLR2F |
POLR2F |
Sus scrofa | 6gmh_f | F1SKN8 | 99.80 | 2.20E-25 | 1.80E-29 | 168.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YPR187W | RPO26 | SGDID:S000006391 | rpo6 rpoK |
rpo6 rpoK |
2.7.7.6 | Saccharolobus shibatae | 4ayb_k | B8YB61 | 99.60 | 6.20E-21 | 5.10E-25 | 137.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YPR187W | RPO26 | SGDID:S000006391 | H4C1 H4/A H4FA HIST1H4A; H4C2 H4/I H4FI HIST1H4B; H4C3 H4/G H4FG HIST1H4C; H4C4 H4/B H4FB HIST1H4D; H4C5 H4/J H4FJ HIST1H4E; H4C6 H4/C H4FC HIST1H4F; H4C8 H4/H H4FH HIST1H4H; H4C9 H4/M H4FM HIST1H4I; H4C11 H4/E H4FE HIST1H4J; H4C12 H4/D H4FD HIST1H4K; H4C13 H4/K H4FK HIST1H4L; H4C14 H4/N H4F2 H4FN HIST2H4 HIST2H4A; H4C15 H4/O H4FO HIST2H4B; H4-16 HIST4H4 |
Homo sapiens |
Histone H4 | Retinitis Pigmentosa,Leukemia, Chronic Myeloid,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Colorectal Cancer,Meier-Gorlin Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 3,Neuronal Ceroid Lipofuscinosis,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Fragile X Syndrome,Biotin Deficiency,Colon Adenoma,Systemic Lupus Erythematosus,Nut Midline Carcinoma,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I,Retinitis Pigmentosa,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Meier-Gorlin Syndrome 1,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Nut Midline Carcinoma,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I,Retinitis Pigmentosa,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Meier-Gorlin Syndrome 1,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Nut Midline Carcinoma,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I,Retinitis Pigmentosa,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Meier-Gorlin Syndrome 1,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Nut Midline Carcinoma,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I,Retinitis Pigmentosa,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Meier-Gorlin Syndrome 1,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Nut Midline Carcinoma,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I,Retinitis Pigmentosa,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Meier-Gorlin Syndrome 1,Disease Of Mental Health,Alpha-Thalassemia,Chromosome 16p13.3 Deletion Syndrome, Proximal,Alpha-Thalassemia/Mental Retardation Syndrome, X-Linked,Nut Midline Carcinoma,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I,Retinitis Pigmentosa,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Meier-Gorlin Syndrome 1,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I,Retinitis Pigmentosa,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Meier-Gorlin Syndrome 1,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I,Retinitis Pigmentosa,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Meier-Gorlin Syndrome 1,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I,Retinitis Pigmentosa,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Cockayne Syndrome,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Meier-Gorlin Syndrome 1,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Holt-Oram Syndrome,Nut Midline Carcinoma,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I,Retinitis Pigmentosa,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Meier-Gorlin Syndrome 1,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I,Retinitis Pigmentosa,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Meier-Gorlin Syndrome 1,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I,Retinitis Pigmentosa,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Meier-Gorlin Syndrome 1,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I,Retinitis Pigmentosa,Leukemia, Acute Myeloid,Noonan Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 2,Hyperinsulinemic Hypoglycemia,Primary Hyperoxaluria,Carbohydrate Metabolic Disorder,Meier-Gorlin Syndrome 1,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Nut Midline Carcinoma,Hyperinsulinemic Hypoglycemia, Familial, 1,Hyperoxaluria, Primary, Type I |
6a5o_f | P62805 | ENSG00000197837 | H4-16 | 100.00 | 2.00E-41 | 1.40E-45 | 264.00 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |