| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YDR473C | PRP3 | SGDID:S000002881 | PRP3 |
pre-mRNA processing factor 3 (PRP3) |
pfam Domain | PF08572 | 100.00 | 4.10E-64 | 3.30E-68 | 479.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
| YDR473C | PRP3 | SGDID:S000002881 | PRPF3 HPRP3 PRP3 |
U4/U6 small nuclear ribonucleoprotein Prp3 (Pre-mRNA-splicing factor 3) (hPrp3) (U4/U6 snRNP 90 kDa protein) |
Homo sapiens | Retinitis Pigmentosa,Pseudoretinitis Pigmentosa,Retinitis Pigmentosa 18,Eye Degenerative Disease,Leber Plus Disease,Retinal Degeneration,Fundus Dystrophy,Retinal Disease,Usher Syndrome, Type Iiia,Stargardt Disease,Retinitis Pigmentosa 31,Cone-Rod Dystrophy 2,Retinitis Pigmentosa 33,Retinitis,Mandibulofacial Dysostosis, Guion-Almeida Type,Usher Syndrome,Congenital Stationary Night Blindness,Isolated Growth Hormone Deficiency,Microcephalic Osteodysplastic Primordial Dwarfism, Type I,Retinitis Pigmentosa 13,Retinitis Pigmentosa 11,Isolated Growth Hormone Deficiency, Type Ia |
6qw6_4a | O43395 | ENSG00000117360 | PRPF3 | 100.00 | 1.00E-106 | 9.00E-111 | 873.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |