







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 |
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YPL190C | NAB3 | SGDID:S000006111 | SFPQ PSF |
Splicing factor, proline- and glutamine-rich (100 kDa DNA-pairing protein) (hPOMp100) (DNA-binding p52/p100 complex, 100 kDa subunit) (Polypyrimidine tract-binding protein-associated-splicing factor) (PSF) (PTB-associated-splicing factor) |
Homo sapiens | Dyslexia,Childhood Kidney Cell Carcinoma,Parkinson Disease, Late-Onset,Pick Disease Of Brain,Perivascular Tumor,Renal Cell Carcinoma, Papillary, 1,Renal Cell Carcinoma, Xp11-Associated,Frontotemporal Dementia |
6ncq_a | P23246 | ENSG00000116560 | SFPQ | 95.60 | 8.20E-05 | 1.10E-08 | 64.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL190C | NAB3 | SGDID:S000006111 | 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 | 96.20 | 2.20E-05 | 2.60E-09 | 76.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL190C | NAB3 | SGDID:S000006111 | PAB1 YER165W |
Polyadenylate-binding protein, cytoplasmic and nuclear (PABP) (Poly(A)-binding protein) (ARS consensus-binding protein ACBP-67) (Polyadenylate tail-binding protein) |
Saccharomyces cerevisiae | 6r5k_h | P04147 | 96.10 | 2.70E-05 | 3.60E-09 | 74.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL190C | NAB3 | SGDID:S000006111 | 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 | 95.70 | 5.70E-05 | 8.70E-09 | 58.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL190C | NAB3 | SGDID:S000006111 | 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 | 95.80 | 5.60E-05 | 7.90E-09 | 64.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL190C | NAB3 | SGDID:S000006111 | SPEN KIAA0929 MINT SHARP |
Msx2-interacting protein (SMART/HDAC1-associated repressor protein) (SPEN homolog) |
Homo sapiens | Gastrointestinal Neuroendocrine Benign Tumor,Spleen Cancer,Gastric Neuroendocrine Neoplasm,Breast Liposarcoma,Wolfram Syndrome 2,Mullegama-Klein-Martinez Syndrome,Chromosome 1p36 Deletion Syndrome |
4p6q_a | Q96T58 | ENSG00000065526 | SPEN | 95.70 | 8.40E-05 | 1.00E-08 | 67.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL190C | NAB3 | SGDID:S000006111 | PUB1 RNP1 YNL016W N2842 |
Nuclear and cytoplasmic polyadenylated RNA-binding protein PUB1 (ARS consensus-binding protein ACBP-60) (Poly uridylate-binding protein) (Poly(U)-binding protein) |
Saccharomyces cerevisiae | 2la4_a | P32588 | 95.60 | 8.60E-05 | 1.20E-08 | 53.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL190C | NAB3 | SGDID:S000006111 | Rbm12 |
RNA-binding protein 12 (RNA-binding motif protein 12) (SH3/WW domain anchor protein in the nucleus) (SWAN) |
Mus musculus | 2cqp_a | Q8R4X3 | 95.60 | 8.40E-05 | 1.20E-08 | 53.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YPL190C | NAB3 | SGDID:S000006111 | GBP2 RLF6 YCL011C YCL11C |
Single-strand telomeric DNA-binding protein GBP2 (G-strand-binding protein 2) (RAP1 localization factor 6) |
Saccharomyces cerevisiae | 2mzq_a | P25555 | 95.80 | 5.10E-05 | 7.40E-09 | 54.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL190C | NAB3 | SGDID:S000006111 | MTHFSD |
Methenyltetrahydrofolate synthase domain-containing protein |
Homo sapiens | Amyotrophic Lateral Sclerosis 1,Feingold Syndrome 1,Intestinal Atresia,Pancreas, Annular,Vacterl Association,Gastrointestinal Defects And Immunodeficiency Syndrome,Pallister-Hall Syndrome,Microphthalmia, Syndromic 3,Anus, Imperforate |
2e5j_a | Q2M296 | ENSG00000103248 | MTHFSD | 95.60 | 8.60E-05 | 1.20E-08 | 53.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL190C | NAB3 | SGDID:S000006111 | 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 | 95.80 | 5.60E-05 | 8.20E-09 | 63.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL190C | NAB3 | SGDID:S000006111 | 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 | 96.30 | 1.10E-05 | 1.70E-09 | 63.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL190C | NAB3 | SGDID:S000006111 | cwf2 prp3 SPAC3A12.11c |
Pre-mRNA-splicing factor cwf2 (Complexed with cdc5 protein 2) (Pre-mRNA-processing protein 3) |
Schizosaccharomyces pombe | 3jb9_y | P87126 | 97.70 | 2.10E-08 | 2.40E-12 | 99.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL190C | NAB3 | SGDID:S000006111 | SNRPA |
SNRPA |
Oryctolagus cuniculus | 6cmn_a | G1TM83 | 97.00 | 9.20E-07 | 1.10E-10 | 71.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL190C | NAB3 | SGDID:S000006111 | RBFOX1 A2BP A2BP1 FOX1 HRNBP1 |
RNA binding protein fox-1 homolog 1 (Ataxin-2-binding protein 1) (Fox-1 homolog A) (Hexaribonucleotide-binding protein 1) |
Homo sapiens | Epilepsy,Atrial Heart Septal Defect,Myopia,Undetermined Early-Onset Epileptic Encephalopathy,Focal Epilepsy,Refractive Error,Developmental Coordination Disorder,Atrial Septal Defect 1,Conduct Disorder,Colorectal Cancer,Autosomal Dominant Cerebellar Ataxia,Benign Epilepsy With Centrotemporal Spikes,Disease Of Mental Health,Wheat Allergy,Dengue Shock Syndrome,Schizophrenia,Spinocerebellar Ataxia 2,Attention Deficit-Hyperactivity Disorder,Pervasive Developmental Disorder,Autism Spectrum Disorder,Atrial Septal Defect 2,Rett Syndrome,Autism,Epilepsy, Idiopathic Generalized |
2err_a | Q9NWB1 | ENSG00000078328 | RBFOX1 | 97.90 | 2.40E-09 | 3.10E-13 | 83.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL190C | NAB3 | SGDID:S000006111 | NAB3 HMD1 YPL190C |
Nuclear polyadenylated RNA-binding protein 3 |
Saccharomyces cerevisiae | 2kvi_a | P38996 | 96.60 | 4.00E-06 | 5.50E-10 | 62.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL190C | NAB3 | SGDID:S000006111 | gw GW182 CG31992 |
Protein Gawky |
Drosophila melanogaster | 2wbr_a | Q8SY33 | 95.80 | 4.70E-05 | 6.70E-09 | 54.30 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YPL190C | NAB3 | SGDID:S000006111 | 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 | 95.70 | 6.20E-05 | 9.40E-09 | 58.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL190C | NAB3 | SGDID:S000006111 | Tc00.1047053511727.270 |
Tc00.1047053511727.270 |
Trypanosoma cruzi | 5opt_h | Q4DY32 | 95.60 | 9.40E-05 | 1.20E-08 | 65.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |