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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YIL061C | SNP1 | SGDID:S000001323 | PTBP1 PTB |
Polypyrimidine tract-binding protein 1 (PTB) (57 kDa RNA-binding protein PPTB-1) (Heterogeneous nuclear ribonucleoprotein I) (hnRNP I) |
Homo sapiens | Endometrial Stromal Sarcoma,Myopathy,Bulbar Polio,Atrial Septal Defect 1,Human T-Cell Leukemia Virus Type 2,Patellar Tendinitis,Congenital Myasthenic Syndrome,Mouth Disease,Paralytic Poliomyelitis,Atrial Septal Defect 2,Frontotemporal Dementia |
1qm9_a | P26599 | ENSG00000011304 | PTBP1 | 96.60 | 5.20E-06 | 5.30E-10 | 64.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL061C | SNP1 | SGDID:S000001323 | RAVER1 KIAA1978 |
Ribonucleoprotein PTB-binding 1 (Protein raver-1) |
Homo sapiens | 3smz_a | Q8IY67 | ENSG00000161847 | RAVER1 | 96.80 | 2.80E-06 | 2.80E-10 | 71.00 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YIL061C | SNP1 | SGDID:S000001323 | PABPC1 PAB1 PABP1 PABPC2 |
Polyadenylate-binding protein 1 (PABP-1) (Poly(A)-binding protein 1) |
Homo sapiens | Motor Neuron Disease,Rift Valley Fever,Waardenburg Syndrome, Type 4b,Myotonic Dystrophy 2,Waardenburg Syndrome, Type 4a,Autosomal Dominant Cerebellar Ataxia,Disease Of Mental Health,Dengue Virus |
4f02_a | P11940 | ENSG00000070756 | PABPC1 | 96.50 | 8.20E-06 | 8.10E-10 | 65.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL061C | SNP1 | SGDID:S000001323 | SF3B4 SAP49 |
Splicing factor 3B subunit 4 (Pre-mRNA-splicing factor SF3b 49 kDa subunit) (Spliceosome-associated protein 49) (SAP 49) |
Homo sapiens | Dysostosis,Synostosis,Burn-Mckeown Syndrome,Phocomelia,Radioulnar Synostosis,Charcot-Marie-Tooth Disease X-Linked Recessive 4,Hereditary Hearing Loss And Deafness,Usher Syndrome, Type Iia,Cerebrocostomandibular Syndrome,Cleft Palate, Isolated,Mandibulofacial Dysostosis, Guion-Almeida Type,Ehlers-Danlos Syndrome, Classic Type, 1,Humeroradial Synostosis,Acrofacial Dysostosis Syndrome Of Rodriguez,Acrofacial Dysostosis,Acrofacial Dysostosis 1, Nager Type,Treacher Collins Syndrome 1,Postaxial Acrofacial Dysostosis |
6ah0_4 | Q15427 | ENSG00000143368 | SF3B4 | 97.00 | 1.30E-06 | 1.10E-10 | 81.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL061C | SNP1 | SGDID:S000001323 | Hnrnpl Fblim1 |
Heterogeneous nuclear ribonucleoprotein L (hnRNP L) |
Rattus norvegicus | 2mqn_a | F1LQ48 | 96.60 | 6.40E-06 | 6.40E-10 | 65.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YIL061C | SNP1 | SGDID:S000001323 | SNP1 YIL061C |
U1 small nuclear ribonucleoprotein 70 kDa homolog (U1 70K) (U1 snRNP 70 kDa homolog) (U1-70K) (U1 small nuclear ribonucleoprotein SNP1) (U1 snRNP protein SNP1) |
Saccharomyces cerevisiae | 5zwn_q | Q00916 | 99.80 | 1.30E-24 | 1.10E-28 | 197.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YIL061C | SNP1 | SGDID:S000001323 | 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 | 96.90 | 1.70E-06 | 1.70E-10 | 67.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL061C | SNP1 | SGDID:S000001323 | SMB1 YER029C |
Small nuclear ribonucleoprotein-associated protein B (snRNP-B) (Sm protein B) (Sm-B) (SmB) |
Saccharomyces cerevisiae | 6g90_b | P40018 | 99.80 | 4.60E-24 | 4.10E-28 | 194.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YIL061C | SNP1 | SGDID:S000001323 | RBM42 |
RNA-binding protein 42 (RNA-binding motif protein 42) |
Homo sapiens | 6qw6_r | Q9BTD8 | ENSG00000126254 | RBM42 | 97.10 | 7.90E-07 | 6.50E-11 | 85.10 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YIL061C | SNP1 | SGDID:S000001323 | Sxl Sx1 CG43770 |
Protein sex-lethal |
Drosophila melanogaster | 1b7f_b | P19339 | 96.60 | 6.70E-06 | 6.80E-10 | 61.80 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YIL061C | SNP1 | SGDID:S000001323 | Tc00.1047053511727.270 |
Tc00.1047053511727.270 |
Trypanosoma cruzi | 5opt_h | Q4DY32 | 97.00 | 1.30E-06 | 1.20E-10 | 74.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YIL061C | SNP1 | SGDID:S000001323 | 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 |
4pjo_k | P08621 | ENSG00000104852 | SNRNP70 | 97.50 | 1.10E-07 | 8.30E-12 | 66.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL061C | SNP1 | SGDID:S000001323 | LSM6 YDR378C D9481.18 |
U6 snRNA-associated Sm-like protein LSm6 |
Saccharomyces cerevisiae | 5zwm_x | Q06406 | 96.60 | 7.10E-06 | 6.70E-10 | 63.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YIL061C | SNP1 | SGDID:S000001323 | LDBPK_320790 |
LDBPK_320790 |
Leishmania donovani | 5osg_h | E9BNI3 | 96.90 | 1.50E-06 | 1.40E-10 | 72.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YIL061C | SNP1 | SGDID:S000001323 | PSRP2 SOVF_116380 |
30S ribosomal protein 2, chloroplastic (Chloroplastic small ribosomal subunit protein cS22) (Plastid-specific 30S ribosomal protein 2) (PSRP-2) |
Spinacia oleracea | 5mmm_v | P82277 | 97.00 | 1.30E-06 | 1.20E-10 | 73.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YIL061C | SNP1 | SGDID:S000001323 | PUF60 FIR ROBPI SIAHBP1 |
Poly(U)-binding-splicing factor PUF60 (60 kDa poly(U)-binding-splicing factor) (FUSE-binding protein-interacting repressor) (FBP-interacting repressor) (Ro-binding protein 1) (RoBP1) (Siah-binding protein 1) (Siah-BP1) |
Homo sapiens | Charge Syndrome,Thymus Lymphoma,Microcephaly,Coloboma Of Macula,Verheij Syndrome,Xeroderma Pigmentosum, Complementation Group B,Neurodevelopmental Disorder With Hypotonia And Variable Intellectual And Behavioral Abnormalities |
2kxf_a | Q9UHX1 | ENSG00000179950 | PUF60 | 97.00 | 9.70E-07 | 9.80E-11 | 69.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |