| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YER071C | TDA2 | SGDID:S000000873 | TDA2 C1Q_03053 |
Topoisomerase I damage affected protein 2 |
Saccharomyces cerevisiae | 5vky_a | C7GRQ3 | 100.00 | 1.00E-37 | 7.60E-42 | 211.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YER071C | TDA2 | SGDID:S000000873 | Arhgef2 Kiaa0651 Lbcl1 Lfc |
Rho guanine nucleotide exchange factor 2 (Guanine nucleotide exchange factor H1) (GEF-H1) (LBC'S first cousin) (Lymphoid blast crisis-like 1) (Oncogene LFC) (Rhobin) |
Mus musculus | 5wi4_b | Q60875 | 99.90 | 3.40E-33 | 2.60E-37 | 191.30 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YER071C | TDA2 | SGDID:S000000873 | TCTEX1 CHLRE_01g004250v5 CHLREDRAFT_160073 |
TCTEX1 CHLRE_01g004250v5 CHLREDRAFT_160073 |
Chlamydomonas reinhardtii | 1xdx_a | O64980 | 100.00 | 1.90E-35 | 1.50E-39 | 194.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YER071C | TDA2 | SGDID:S000000873 | Tctex-1 |
Tctex-1 family |
pfam Family | PF03645 | 99.90 | 2.70E-30 | 2.10E-34 | 165.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
| YER071C | TDA2 | SGDID:S000000873 | Dlc90F Tctex CG12363 |
Dynein light chain Tctex-type (TCTEX-1 protein homolog) |
Drosophila melanogaster | 1ygt_a | Q94524 | 100.00 | 6.10E-35 | 4.70E-39 | 191.40 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
| YER071C | TDA2 | SGDID:S000000873 | DYNC1I2 DNCI2 DNCIC2 |
Cytoplasmic dynein 1 intermediate chain 2 (Cytoplasmic dynein intermediate chain 2) (Dynein intermediate chain 2, cytosolic) (DH IC-2) |
Homo sapiens | Primary Ciliary Dyskinesia,Neurodevelopmental Disorder With Microcephaly, Hypotonia, And Variable Brain Anomalies,Microcephaly,Silver-Russell Syndrome 1,Beckwith-Wiedemann Syndrome,Neurodevelopmental Disorder With Microcephaly And Structural Brain Anomalies,Ciliary Dyskinesia, Primary, 2,Ciliary Dyskinesia, Primary, 9,Keratoderma, Palmoplantar, With Deafness,Umbilical Hernia,Omphalocele |
5jpw_a | Q13409 | ENSG00000077380 | DYNC1I2 | 99.90 | 5.00E-33 | 3.80E-37 | 190.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |