| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YDL224C | WHI4 | SGDID:S000002383 | RBMS1 C2orf12 MSSP MSSP1 SCR2 |
RNA-binding motif, single-stranded-interacting protein 1 (Single-stranded DNA-binding protein MSSP-1) (Suppressor of CDC2 with RNA-binding motif 2) |
Homo sapiens | Diffuse Glomerulonephritis,Epidermolysis Bullosa, Junctional, Herlitz Type,Hemolytic Uremic Syndrome, Atypical 1,Coffin-Siris Syndrome 1,Arthrogryposis Multiplex Congenita 2, Neurogenic Type |
1x5o_a | P29558 | ENSG00000153250 | RBMS1 | 95.40 | 0.00015 | 1.90E-08 | 55.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YDL224C | WHI4 | SGDID:S000002383 | SDN1 At3g50100 F3A4.180 |
Small RNA degrading nuclease 1 (EC 3.1.-.-) |
3.1.-.- | Arabidopsis thaliana | 5z9z_a | A3KPE8 | 95.50 | 0.00015 | 1.40E-08 | 60.00 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
| YDL224C | WHI4 | SGDID:S000002383 | PTBP2 NPTB PTB PTBLP |
Polypyrimidine tract-binding protein 2 (Neural polypyrimidine tract-binding protein) (Neurally-enriched homolog of PTB) (PTB-like protein) |
Homo sapiens | Cancer-Associated Retinopathy,Patellar Tendinitis |
4cq1_b | Q9UKA9 | ENSG00000117569 | PTBP2 | 95.00 | 0.00024 | 3.60E-08 | 54.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YDL224C | WHI4 | SGDID:S000002383 | SNRNP70 RNPU1Z RPU1 SNRP70 U1AP1 |
U1 small nuclear ribonucleoprotein 70 kDa (U1 snRNP 70 kDa) (U1-70K) (snRNP70) |
Homo sapiens | Systemic Scleroderma,Facial Hemiatrophy,Dyskinesia Of Esophagus,Connective Tissue Disease,Splenic Tuberculosis,Telangiectasis,Collagen Disease,Lupus Erythematosus,Childhood Type Dermatomyositis,Mixed Connective Tissue Disease,Limited Scleroderma,Diffuse Scleroderma,Raynaud Disease,Heart Block, Congenital,Hypotrichosis 13,Pericardium Disease,Autoimmune Disease Of Exocrine System,Crest Syndrome,Systemic Lupus Erythematosus,Syndromic X-Linked Intellectual Disability Cabezas Type |
4pkd_b | P08621 | ENSG00000104852 | SNRNP70 | 95.20 | 0.00018 | 2.60E-08 | 59.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |