| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YDR482C | CWC21 | SGDID:S000002890 | EIF4A3 DDX48 KIAA0111 |
Eukaryotic initiation factor 4A-III (eIF-4A-III) (eIF4A-III) (EC 3.6.4.13) (ATP-dependent RNA helicase DDX48) (ATP-dependent RNA helicase eIF4A-3) (DEAD box protein 48) (Eukaryotic initiation factor 4A-like NUK-34) (Eukaryotic translation initiation factor 4A isoform 3) (Nuclear matrix protein 265) (NMP 265) (hNMP 265) [Cleaved into: Eukaryotic initiation factor 4A-III, N-terminally processed] |
3.6.4.13 | Homo sapiens | Metaphyseal Chondrodysplasia, Schmid Type,Robin Sequence With Cleft Mandible And Limb Anomalies,Dysostosis,Vaginal Cancer,Neurodegeneration With Brain Iron Accumulation,Thrombocytopenia-Absent Radius Syndrome,Mandibulofacial Dysostosis, Guion-Almeida Type,Acrofacial Dysostosis |
6icz_u | P38919 | ENSG00000141543 | EIF4A3 | 100.00 | 6.80E-35 | 4.70E-39 | 272.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YDR482C | CWC21 | SGDID:S000002890 | SMX2 SNP2 YFL017W-A YFL017Bw |
Small nuclear ribonucleoprotein G (snRNP-G) (Sm protein G) (Sm-G) (SmG) |
Saccharomyces cerevisiae | 5mq0_r | P40204 | 100.00 | 8.30E-50 | 6.60E-54 | 294.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YDR482C | CWC21 | SGDID:S000002890 | CWC27 SDCCAG10 UNQ438/PRO871 |
Spliceosome-associated protein CWC27 homolog (Antigen NY-CO-10) (Probable inactive peptidyl-prolyl cis-trans isomerase CWC27 homolog) (PPIase CWC27) (Serologically defined colon cancer antigen 10) |
Homo sapiens | Retinitis Pigmentosa,Retinal Degeneration,Fundus Dystrophy,Papillary Transitional Carcinoma,Brachydactyly,Retinitis Pigmentosa With Or Without Skeletal Anomalies,Kbg Syndrome |
6ff7_s | Q6UX04 | ENSG00000153015 | CWC27 | 100.00 | 6.80E-35 | 4.70E-39 | 272.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |