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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YDL156W | CMR1 | SGDID:S000002315 | SMD1 YGR074W |
Small nuclear ribonucleoprotein Sm D1 (Sm-D1) (snRNP core protein D1) |
Saccharomyces cerevisiae | 5nrl_h | Q02260 | 99.00 | 3.50E-14 | 2.40E-18 | 141.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | RSA4 YCR072C YCR72C |
Ribosome assembly protein 4 (Notchless protein homolog 1) (Ribosome biogenesis factor RSA4) |
Saccharomyces cerevisiae | 4wju_a | P25382 | 99.10 | 6.60E-15 | 4.60E-19 | 148.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | DAW1 WDR69 |
Dynein assembly factor with WDR repeat domains 1 (Outer row dynein assembly protein 16 homolog) (WD repeat-containing protein 69) |
Homo sapiens | Primary Ciliary Dyskinesia,Visceral Heterotaxy,Ciliary Dyskinesia, Primary, 1,Ciliary Dyskinesia, Primary, 2,Dextro-Looped Transposition Of The Great Arteries |
5nnz_a | Q8N136 | ENSG00000123977 | DAW1 | 99.00 | 8.20E-14 | 5.70E-18 | 135.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL156W | CMR1 | SGDID:S000002315 | 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 |
6id1_e | P62304 | ENSG00000182004 | SNRPE | 99.00 | 3.20E-14 | 2.30E-18 | 135.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL156W | CMR1 | SGDID:S000002315 | DCAF1 KIAA0800 RIP VPRBP |
DDB1- and CUL4-associated factor 1 (HIV-1 Vpr-binding protein) (VprBP) (Serine/threonine-protein kinase VPRBP) (EC 2.7.11.1) (Vpr-interacting protein) |
2.7.11.1 | Homo sapiens | Intraorbital Meningioma,Spinal Canal Intradural Extramedullary Neoplasm,Neurilemmomatosis,Aicardi-Goutieres Syndrome,Meningioma, Familial |
4pxw_b | Q9Y4B6 | 99.00 | 4.60E-14 | 3.20E-18 | 136.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YDL156W | CMR1 | SGDID:S000002315 | SPBC4B4.04 |
Eukaryotic translation initiation factor 2A (eIF-2A) |
Schizosaccharomyces pombe | 3wj9_b | O74965 | 99.10 | 7.10E-15 | 4.90E-19 | 143.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | orfC LIC_10793 |
Antigen Lp49 (Leptospiral 49 kilodalton protein) (Lp49) |
Leptospira interrogans | 3bws_a | Q72U69 | 99.00 | 4.70E-14 | 3.20E-18 | 138.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | COP1 At2g32950 T21L14.11 |
E3 ubiquitin-protein ligase COP1 (EC 2.3.2.27) (Constitutive photomorphogenesis protein 1) (RING-type E3 ubiquitin transferase COP1) |
2.3.2.27 | Arabidopsis thaliana | 5igo_c | P43254 | 99.00 | 9.10E-14 | 6.40E-18 | 130.90 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YDL156W | CMR1 | SGDID:S000002315 | WDR33 WDC146 |
pre-mRNA 3' end processing protein WDR33 (WD repeat-containing protein 33) (WD repeat-containing protein of 146 kDa) |
Homo sapiens | Atrial Septal Defect 6 |
6f9n_b | Q9C0J8 | ENSG00000136709 | WDR33 | 99.10 | 2.00E-14 | 1.40E-18 | 138.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL156W | CMR1 | SGDID:S000002315 | CTHT_0055700 |
Ribosome assembly protein 4 (Notchless protein homolog 1) (Ribosome biogenesis factor RSA4) |
Chaetomium thermophilum | 4wjs_a | G0SC29 | 99.00 | 8.30E-14 | 5.80E-18 | 138.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | DAW1 ODA16 |
Dynein assembly factor with WDR repeat domains 1 (Outer row dynein assembly protein 16) |
Chlamydomonas reinhardtii | 5mzh_a | Q3Y8L7 | 99.10 | 1.30E-14 | 9.00E-19 | 144.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | SMX2 SNP2 YFL017W-A YFL017Bw |
Small nuclear ribonucleoprotein G (snRNP-G) (Sm protein G) (Sm-G) (SmG) |
Saccharomyces cerevisiae | 5zwm_k | P40204 | 99.00 | 3.50E-14 | 2.40E-18 | 141.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | SPBPJ4664.04 |
Putative coatomer subunit alpha (Alpha-coat protein) (Alpha-COP) |
Schizosaccharomyces pombe | 4j87_a | Q96WV5 | 99.00 | 7.40E-14 | 5.20E-18 | 129.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | TUP1 AAR1 AER2 AMM1 CYC9 FLK1 SFL2 UMR7 YCR084C YCR84C |
General transcriptional corepressor TUP1 (Flocculation suppressor protein) (Glucose repression regulatory protein TUP1) (Repressor AER2) |
Saccharomyces cerevisiae | 1erj_a | P16649 | 99.20 | 2.60E-15 | 1.80E-19 | 146.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | ERCC8 CKN1 CSA |
DNA excision repair protein ERCC-8 (Cockayne syndrome WD repeat protein CSA) |
Homo sapiens | Robinow Syndrome, Autosomal Recessive 1,Cockayne Syndrome Type Iii,Cockayne Syndrome A,Cockayne Syndrome,Xeroderma Pigmentosum, Complementation Group D,Xeroderma Pigmentosum, Variant Type,Xeroderma Pigmentosum, Complementation Group G,Enophthalmos,Hutchinson-Gilford Progeria Syndrome,Xeroderma Pigmentosum, Complementation Group B,Xfe Progeroid Syndrome,Mitochondrial Complex I Deficiency, Nuclear Type 10,Cockayne Syndrome B,Uv-Sensitive Syndrome 2,Mitochondrial Complex I Deficiency, Nuclear Type 1,Uv-Sensitive Syndrome,Microcephaly With Or Without Chorioretinopathy, Lymphedema, Or Mental Retardation,Leigh Syndrome |
6fcv_b | Q13216 | ENSG00000049167 | ERCC8 | 99.00 | 5.70E-14 | 4.00E-18 | 136.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL156W | CMR1 | SGDID:S000002315 | SOF1 YLL011W L1339 |
Protein SOF1 (U3 small nucleolar RNA-associated protein SOF1) (U3 snoRNA-associated protein SOF1) |
Saccharomyces cerevisiae | 5wlc_lu | P33750 | 99.10 | 1.40E-14 | 1.00E-18 | 145.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | COP1 RFWD2 RNF200 |
E3 ubiquitin-protein ligase COP1 (EC 2.3.2.27) (Constitutive photomorphogenesis protein 1 homolog) (hCOP1) (RING finger and WD repeat domain protein 2) (RING finger protein 200) (RING-type E3 ubiquitin transferase RFWD2) |
2.3.2.27 | Homo sapiens | Autism |
5hqg_a | Q8NHY2 | ENSG00000143207 | COP1 | 99.10 | 1.30E-14 | 8.90E-19 | 138.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDL156W | CMR1 | SGDID:S000002315 | GNB1 |
Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1 (Transducin beta chain 1) |
Bos taurus | 1tbg_c | P62871 | 99.00 | 8.10E-14 | 5.70E-18 | 131.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | PRT1 CDC63 YOR361C |
Eukaryotic translation initiation factor 3 subunit B (eIF3b) (Cell cycle regulation and translation initiation protein) (Eukaryotic translation initiation factor 3 90 kDa subunit) (eIF3 p90) (Translation initiation factor eIF3 p90 subunit) |
Saccharomyces cerevisiae | 4u1f_a | P06103 | 99.00 | 3.60E-14 | 2.50E-18 | 141.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | TaGB1 |
TaGB1 |
Triticum aestivum | 4v7e_bg | Q8LNY6 | 99.20 | 3.90E-15 | 2.70E-19 | 142.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | CDH1 HCT1 YGL003C |
APC/C activator protein CDH1 (CDC20 homolog 1) (Homolog of CDC twenty 1) |
Saccharomyces cerevisiae | 5a31_r | P53197 | 99.00 | 1.20E-13 | 8.60E-18 | 133.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | PRPF19 NMP200 PRP19 SNEV |
Pre-mRNA-processing factor 19 (EC 2.3.2.27) (Nuclear matrix protein 200) (PRP19/PSO4 homolog) (hPso4) (RING-type E3 ubiquitin transferase PRP19) (Senescence evasion factor) |
2.3.2.27 | Homo sapiens | Retinitis Pigmentosa 19,Poikiloderma With Neutropenia |
4lg8_a | Q9UMS4 | ENSG00000110107 | PRPF19 | 99.00 | 7.00E-14 | 4.90E-18 | 133.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDL156W | CMR1 | SGDID:S000002315 | smd2 cwf9 SPAC2C4.03c |
Small nuclear ribonucleoprotein Sm D2 (Sm-D2) (Complexed with cdc5 protein 9) (snRNP core protein D2) |
Schizosaccharomyces pombe | 3jb9_l | O14036 | 99.00 | 5.40E-14 | 3.80E-18 | 132.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | ORF492 |
ORF492 |
Methanosarcina mazei | 1l0q_d | Q50245 | 99.00 | 8.40E-14 | 5.90E-18 | 135.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | PFS2 YNL317W N0348 |
Polyadenylation factor subunit 2 |
Saccharomyces cerevisiae | 6eoj_d | P42841 | 99.00 | 6.30E-14 | 4.40E-18 | 140.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | TBL1XR1 IRA1 TBLR1 |
F-box-like/WD repeat-containing protein TBL1XR1 (Nuclear receptor corepressor/HDAC3 complex subunit TBLR1) (TBL1-related protein 1) (Transducin beta-like 1X-related protein 1) |
Homo sapiens | Learning Disability,Fitzsimmons Syndrome,Noonan Syndrome 1,Pierpont Syndrome,Central Nervous System Hematologic Cancer,Lipomatosis,West Syndrome,Disease Of Mental Health,Acute Promyelocytic Leukemia,Mental Retardation, Autosomal Dominant 41,Rett Syndrome,Autism |
4lg9_a | Q9BZK7 | ENSG00000177565 | TBL1XR1 | 99.00 | 3.10E-14 | 2.20E-18 | 137.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL156W | CMR1 | SGDID:S000002315 | CTHT_0048280 |
CTHT_0048280 |
Chaetomium thermophilum | 5oql_f | G0SAY9 | 99.00 | 4.00E-14 | 2.70E-18 | 145.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | ddb2 si:dkey-45f10.3 |
DNA damage-binding protein 2 (Damage-specific DNA-binding protein 2) |
Danio rerio | 3ei3_b | Q2YDS1 | 99.00 | 1.20E-13 | 8.70E-18 | 132.70 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | SQT1 YIR012W YIB12W |
Ribosome assembly protein SQT1 |
Saccharomyces cerevisiae | 4zox_a | P35184 | 99.00 | 6.90E-14 | 4.90E-18 | 133.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL156W | CMR1 | SGDID:S000002315 | WDR48 KIAA1449 UAF1 |
WD repeat-containing protein 48 (USP1-associated factor 1) (WD repeat endosomal protein) (p80) |
Homo sapiens | Interstitial Nephritis, Karyomegalic,Autosomal Recessive Spastic Paraplegia Type 60,Motor Neuron Disease,Hereditary Spastic Paraplegia,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Seckel Syndrome,Inflammatory Myofibroblastic Tumor |
5cvo_d | Q8TAF3 | ENSG00000114742 | WDR48 | 99.00 | 9.60E-14 | 6.50E-18 | 146.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |