| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YCR033W | SNT1 | SGDID:S000000629 | TVAG_473470 |
TVAG_473470 |
Trichomonas vaginalis | 2k9n_a | Q58HP2 | 98.60 | 6.60E-12 | 9.20E-16 | 100.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YCR033W | SNT1 | SGDID:S000000629 | NCOR2 CTG26 |
Nuclear receptor corepressor 2 (N-CoR2) (CTG repeat protein 26) (SMAP270) (Silencing mediator of retinoic acid and thyroid hormone receptor) (SMRT) (T3 receptor-associating factor) (TRAC) (Thyroid-, retinoic-acid-receptor-associated corepressor) |
Homo sapiens | Plasma Cell Neoplasm,Clubfoot,Amelogenesis Imperfecta,Leukemia, Acute Myeloid,Breast Cancer,Prostate Cancer,Disease Of Mental Health,Lymphoma, Non-Hodgkin, Familial,Acute Promyelocytic Leukemia,Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema,Myeloma, Multiple |
1xc5_a | Q9Y618 | ENSG00000196498 | NCOR2 | 97.70 | 1.10E-08 | 1.50E-12 | 77.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YCR033W | SNT1 | SGDID:S000000629 | RCOR1 KIAA0071 RCOR |
REST corepressor 1 (Protein CoREST) |
Homo sapiens | Loeys-Dietz Syndrome 1,Spinocerebellar Ataxia 29,Disease Of Mental Health,Huntington Disease,Joubert Syndrome 1 |
2iw5_b | Q9UKL0 | ENSG00000089902 | RCOR1 | 98.10 | 8.00E-10 | 7.70E-14 | 110.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YCR033W | SNT1 | SGDID:S000000629 | ada2 SPCC24B10.08c |
Transcriptional adapter 2 |
Schizosaccharomyces pombe | 2elk_a | Q9P7J7 | 97.30 | 1.60E-07 | 2.10E-11 | 67.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YCR033W | SNT1 | SGDID:S000000629 | reb1 SPBC1198.11c SPBC660.01c |
DNA-binding protein reb1 |
Schizosaccharomyces pombe | 5eyb_a | Q9P6H9 | 97.90 | 4.50E-09 | 5.60E-13 | 103.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YCR033W | SNT1 | SGDID:S000000629 | RERE ARG ARP ATN1L KIAA0458 |
Arginine-glutamic acid dipeptide repeats protein (Atrophin-1-like protein) (Atrophin-1-related protein) |
Homo sapiens | Charge Syndrome,Neuroblastoma,Rere-Related Disorders,Dentatorubral-Pallidoluysian Atrophy,Non-Syndromic X-Linked Intellectual Disability,Autism Spectrum Disorder,Chromosome 1p36 Deletion Syndrome,Neurodevelopmental Disorder With Or Without Anomalies Of The Brain, Eye, Or Heart,Autism,Type 1 Diabetes Mellitus 8 |
2yqk_a | Q9P2R6 | ENSG00000142599 | RERE | 97.20 | 2.50E-07 | 3.20E-11 | 69.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YCR033W | SNT1 | SGDID:S000000629 | RCOR3 KIAA1343 |
REST corepressor 3 |
Homo sapiens | Cone-Rod Dystrophy 6 |
4czz_b | Q9P2K3 | ENSG00000117625 | RCOR3 | 99.30 | 6.40E-17 | 6.70E-21 | 176.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YCR033W | SNT1 | SGDID:S000000629 | DNAJC1 HTJ1 |
DnaJ homolog subfamily C member 1 (DnaJ protein homolog MTJ1) |
Homo sapiens | Pyometritis |
2cqr_a | Q96KC8 | ENSG00000136770 | DNAJC1 | 97.20 | 3.20E-07 | 4.30E-11 | 69.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YCR033W | SNT1 | SGDID:S000000629 | Mta3 |
Metastasis-associated protein MTA3 |
Mus musculus | 2crg_a | Q924K8 | 97.20 | 2.40E-07 | 3.00E-11 | 71.70 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YCR033W | SNT1 | SGDID:S000000629 | Terb1 Ccdc79 |
Telomere repeats-binding bouquet formation protein 1 (Coiled-coil domain-containing protein 79) |
Mus musculus | 1x58_a | Q8C0V1 | 97.20 | 2.40E-07 | 3.00E-11 | 69.70 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YCR033W | SNT1 | SGDID:S000000629 | MIS18BP1 C14orf106 KIAA1903 KNL2 M18BP1 |
Mis18-binding protein 1 (Kinetochore-associated protein KNL-2 homolog) (HsKNL-2) (P243) |
Homo sapiens | Fanconi Anemia, Complementation Group I |
1wgx_a | Q6P0N0 | ENSG00000129534 | MIS18BP1 | 97.10 | 4.50E-07 | 5.60E-11 | 70.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YCR033W | SNT1 | SGDID:S000000629 | MYSM1 KIAA1915 |
Deubiquitinase MYSM1 (2A-DUB) (EC 3.4.19.-) (Myb-like, SWIRM and MPN domain-containing protein 1) |
3.4.19.- | Homo sapiens | Congenital Progressive Bone Marrow Failure-B-Cell Immunodeficiency-Skeletal Dysplasia Syndrome,Bone Marrow Failure Syndrome 4 |
2cu7_a | Q5VVJ2 | ENSG00000162601 | MYSM1 | 97.20 | 2.30E-07 | 3.10E-11 | 69.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YCR033W | SNT1 | SGDID:S000000629 | TVAG_211210 |
TVAG_211210 |
Trichomonas vaginalis | 3osg_a | Q58HP3 | 98.80 | 6.90E-13 | 8.80E-17 | 112.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YCR033W | SNT1 | SGDID:S000000629 | Myb |
Transcriptional activator Myb (Proto-oncogene c-Myb) |
Mus musculus | 1guu_a | P06876 | 98.10 | 1.10E-09 | 1.10E-13 | 86.40 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YCR033W | SNT1 | SGDID:S000000629 | Iswi CG8625 |
Chromatin-remodeling complex ATPase chain Iswi (EC 3.6.4.-) (CHRAC 140 kDa subunit) (Nucleosome-remodeling factor 140 kDa subunit) (NURF-140) (Protein imitation swi) |
3.6.4.- | Drosophila melanogaster | 1ofc_x | Q24368 | 97.40 | 1.10E-07 | 1.30E-11 | 94.60 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | |||
| YCR033W | SNT1 | SGDID:S000000629 | CEF1 NTC85 YMR213W YM8261.07 |
Pre-mRNA-splicing factor CEF1 (PRP nineteen-associated complex protein 85) (PRP19-associated complex protein 85) |
Saccharomyces cerevisiae | 5gmk_c | Q03654 | 98.10 | 1.40E-09 | 1.20E-13 | 120.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YCR033W | SNT1 | SGDID:S000000629 | MYBL2 BMYB |
Myb-related protein B (B-Myb) (Myb-like protein 2) |
Gallus gallus | 1a5j_a | Q03237 | 98.60 | 8.60E-12 | 1.20E-15 | 99.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YCR033W | SNT1 | SGDID:S000000629 | SNRPE |
Small nuclear ribonucleoprotein E (snRNP-E) (Sm protein E) (Sm-E) (SmE) |
Homo sapiens | Hypotrichosis,Spinal Muscular Atrophy,Hypotrichosis 11,Hypotrichosis Simplex,Hypotrichosis 8,Hypotrichosis 7,Hypotrichosis 4,Systemic Lupus Erythematosus,Hypotrichosis 6,Microcephalic Osteodysplastic Primordial Dwarfism, Type I |
6id0_l | P62304 | ENSG00000182004 | SNRPE | 98.20 | 4.70E-10 | 5.00E-14 | 126.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YCR033W | SNT1 | SGDID:S000000629 | TERF1 PIN2 TRBF1 TRF TRF1 |
Telomeric repeat-binding factor 1 (NIMA-interacting protein 2) (TTAGGG repeat-binding factor 1) (Telomeric protein Pin2/TRF1) |
Homo sapiens | Revesz Syndrome,Hoyeraal Hreidarsson Syndrome,Dyskeratosis Congenita,Aplastic Anemia,Anaplastic Astrocytoma,Werner Syndrome,Cherubism,Fanconi Anemia, Complementation Group A,Pulmonary Fibrosis, Idiopathic,Dyskeratosis Congenita, Autosomal Dominant 3,Townes-Brocks Syndrome,Meningioma, Familial,Nijmegen Breakage Syndrome,Arthrogryposis, Renal Dysfunction, And Cholestasis 1,Melanoma, Cutaneous Malignant 1,Lung Cancer |
1ba5_a | P54274 | ENSG00000147601 | TERF1 | 97.10 | 4.00E-07 | 5.70E-11 | 62.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YCR033W | SNT1 | SGDID:S000000629 | Mybl2 Bmyb |
Myb-related protein B (B-Myb) (Myb-like protein 2) |
Mus musculus | 2d9a_a | P48972 | 97.20 | 3.00E-07 | 4.20E-11 | 65.30 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YCR033W | SNT1 | SGDID:S000000629 | cdc5 SPAC644.12 |
Pre-mRNA-splicing factor cdc5 (Cell division control protein 5) |
Schizosaccharomyces pombe | 3jb9_w | P39964 | 98.00 | 2.40E-09 | 1.90E-13 | 120.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YCR033W | SNT1 | SGDID:S000000629 | RAP1 GRF1 TUF1 YNL216W N1310 |
DNA-binding protein RAP1 (Repressor/activator site-binding protein) (SBF-E) (TUF) |
Saccharomyces cerevisiae | 1ign_a | P11938 | 97.70 | 1.60E-08 | 1.60E-12 | 100.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YCR033W | SNT1 | SGDID:S000000629 | TADA2A TADA2L KL04P |
Transcriptional adapter 2-alpha (Transcriptional adapter 2-like) (ADA2-like protein) |
Homo sapiens | Chromosome 17q12 Deletion Syndrome |
1x41_a | O75478 | ENSG00000276234 | TADA2A | 97.30 | 1.30E-07 | 1.80E-11 | 67.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YCR033W | SNT1 | SGDID:S000000629 | NCOR1 KIAA1047 |
Nuclear receptor corepressor 1 (N-CoR) (N-CoR1) |
Homo sapiens | Endometrial Hyperplasia,Gene Duplication Disease,Amelogenesis Imperfecta,Mitochondrial Complex Iii Deficiency,Leukemia, Acute Myeloid,Mitochondrial Complex Iii Deficiency, Nuclear Type 2,Brain Cancer,Breast Cancer,Prostate Cancer,Disease Of Mental Health,Lubs X-Linked Mental Retardation Syndrome,Mitochondrial Complex Iii Deficiency, Nuclear Type 1,Smith-Magenis Syndrome,Acute Promyelocytic Leukemia,Amelogenesis Imperfecta, Type Ig,Rett Syndrome,Lung Cancer |
2eqr_a | O75376 | ENSG00000141027 | NCOR1 | 97.40 | 6.60E-08 | 9.00E-12 | 69.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YCR033W | SNT1 | SGDID:S000000629 | BDP1 KIAA1241 KIAA1689 TFNR |
Transcription factor TFIIIB component B'' homolog (Transcription factor IIIB 150) (TFIIIB150) (Transcription factor-like nuclear regulator) |
Homo sapiens | Breast Metaplastic Carcinoma,Breast Squamous Cell Carcinoma,Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb,Branchiootic Syndrome 1,Cataract 8, Multiple Types,Deafness, Autosomal Recessive 112 |
5n9g_c | A6H8Y1 | ENSG00000145734 | BDP1 | 97.20 | 4.60E-07 | 4.20E-11 | 87.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YCR033W | SNT1 | SGDID:S000000629 | TVAG_475500 |
TVAG_475500 |
Trichomonas vaginalis | 3zqc_d | A2D9X4 | 98.70 | 2.80E-12 | 3.70E-16 | 107.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |