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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YER172C | BRR2 | SGDID:S000000974 | SMX3 YPR182W P9705.4 |
Small nuclear ribonucleoprotein F (snRNP-F) (Sm protein F) (Sm-F) (SmF) |
Saccharomyces cerevisiae | 5lj5_q | P54999 | 99.80 | 1.30E-26 | 1.20E-30 | 316.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER172C | BRR2 | SGDID:S000000974 | hel308 hjm PF0677 |
ATP-dependent DNA helicase Hel308 (EC 3.6.4.12) (ATP-dependent Holliday junction unwindase Hjm) (Holliday junction migration DNA helicase) |
3.6.4.12 | Pyrococcus furiosus | 2zj8_a | O73946 | 99.90 | 5.00E-34 | 5.00E-38 | 373.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YER172C | BRR2 | SGDID:S000000974 | 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 |
6qdv_v | Q9UMS4 | ENSG00000110107 | PRPF19 | 99.90 | 4.20E-27 | 3.90E-31 | 326.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YER172C | BRR2 | SGDID:S000000974 | mle nap CG11680 |
Dosage compensation regulator (EC 3.6.4.13) (ATP-dependent RNA helicase mle) (Protein male-less) (Protein maleless) (Protein no action potential) |
3.6.4.13 | Drosophila melanogaster | 5aor_b | P24785 | 99.80 | 3.40E-25 | 3.20E-29 | 308.60 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | |||
YER172C | BRR2 | SGDID:S000000974 | DHX15 DBP1 DDX15 |
Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15 (EC 3.6.4.13) (ATP-dependent RNA helicase #46) (DEAH box protein 15) |
3.6.4.13 | Homo sapiens | 5xdr_a | O43143 | ENSG00000109606 | DHX15 | 99.80 | 2.20E-25 | 2.20E-29 | 289.90 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER172C | BRR2 | SGDID:S000000974 | Rhau 38E.15 cg9323 DmDHX36 Dmel\CG9323 DmRHAU RHAU CG9323 Dmel_CG9323 |
Rhau 38E.15 cg9323 DmDHX36 Dmel\CG9323 DmRHAU RHAU CG9323 Dmel_CG9323 |
3.6.4.12,3.6.4.13, | Drosophila melanogaster | 5n8r_b | Q8SWT2 | 99.80 | 2.50E-25 | 2.30E-29 | 300.80 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | |||
YER172C | BRR2 | SGDID:S000000974 | PRP2 RNA2 YNR011C N2048 |
Pre-mRNA-splicing factor ATP-dependent RNA helicase-like protein PRP2 (EC 3.6.4.13) (Pre-mRNA-processing protein 2) |
3.6.4.13 | Saccharomyces cerevisiae | 5gm6_y | P20095 | 99.80 | 1.60E-26 | 1.50E-30 | 310.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YER172C | BRR2 | SGDID:S000000974 | CTHT_0035640 |
CTHT_0035640 |
Chaetomium thermophilum | 6i3p_d | G0S700 | 99.90 | 2.00E-28 | 1.90E-32 | 320.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER172C | BRR2 | SGDID:S000000974 | DHX36 |
ATP-dependent DNA/RNA helicase DHX36 (EC 3.6.4.12) (EC 3.6.4.13) (DEAD/H box polypeptide 36) (DEAH-box protein 36) (G4-resolvase-1) (G4R1) (MLE-like protein 1) (RNA helicase associated with AU-rich element protein) |
3.6.4.13 | Bos taurus | 5vha_a | Q05B79 | 99.80 | 2.30E-24 | 2.30E-28 | 288.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YER172C | BRR2 | SGDID:S000000974 | SNRPB COD SNRPB1 |
Small nuclear ribonucleoprotein-associated proteins B and B' (snRNP-B) (Sm protein B/B') (Sm-B/B') (SmB/B') |
Homo sapiens | Burn-Mckeown Syndrome,Spinal Muscular Atrophy,Muscular Atrophy,Lupus Erythematosus,Isolated Pierre Robin Sequence,Cerebrocostomandibular Syndrome,Disease Of Mental Health,Mandibulofacial Dysostosis, Guion-Almeida Type,Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant,Systemic Lupus Erythematosus,Acrofacial Dysostosis 1, Nager Type,Pierre Robin Syndrome |
6qdv_b | P14678 | ENSG00000125835 | SNRPB | 100.00 | 6.00E-105 | 6.00E-109 | 1145.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER172C | BRR2 | SGDID:S000000974 | CTHT_0005780 |
CTHT_0005780 |
Chaetomium thermophilum | 5ltj_a | G0RY84 | 99.80 | 2.60E-25 | 2.50E-29 | 291.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER172C | BRR2 | SGDID:S000000974 | SMD1 YGR074W |
Small nuclear ribonucleoprotein Sm D1 (Sm-D1) (snRNP core protein D1) |
Saccharomyces cerevisiae | 6bk8_p | Q02260 | 99.90 | 1.60E-27 | 1.50E-31 | 327.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER172C | BRR2 | SGDID:S000000974 | POLQ POLH |
DNA polymerase theta (EC 2.7.7.7) (DNA polymerase eta) |
2.7.7.7 | Homo sapiens | Interdigitating Dendritic Cell Sarcoma,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A |
5aga_a | O75417 | ENSG00000051341 | POLQ | 99.80 | 4.40E-26 | 4.30E-30 | 303.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YER172C | BRR2 | SGDID:S000000974 | PPIE CYP33 |
Peptidyl-prolyl cis-trans isomerase E (PPIase E) (EC 5.2.1.8) (Cyclophilin E) (Cyclophilin-33) (Rotamase E) |
5.2.1.8 | Homo sapiens | 6icz_y | Q9UNP9 | ENSG00000084072 | PPIE | 99.90 | 3.40E-27 | 3.20E-31 | 327.00 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YER172C | BRR2 | SGDID:S000000974 | BRR2 RSS1 SNU246 YER172C SYGP-ORF66 |
Pre-mRNA-splicing helicase BRR2 (EC 3.6.4.13) (Protein Snu246) |
3.6.4.13 | Saccharomyces cerevisiae | 5dca_a | P32639 | 100.00 | 3.00E-172 | 3.00E-176 | 1859.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YER172C | BRR2 | SGDID:S000000974 | DHX16 DBP2 DDX16 KIAA0577 PRP2 |
Pre-mRNA-splicing factor ATP-dependent RNA helicase DHX16 (EC 3.6.4.13) (ATP-dependent RNA helicase #3) (DEAH-box protein 16) |
3.6.4.13 | Homo sapiens | Seizure Disorder,Neuromuscular Disease,Corpus Callosum, Agenesis Of,Intellectual Disability - Hypoplastic Corpus Callosum - Preauricular Tag,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Neuromuscular Oculoauditory Syndrome,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome |
6ff7_q | O60231 | ENSG00000204560 | DHX16 | 99.80 | 1.50E-26 | 1.30E-30 | 315.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YER172C | BRR2 | SGDID:S000000974 | DHX38 DDX38 KIAA0224 PRP16 |
Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 (EC 3.6.4.13) (ATP-dependent RNA helicase DHX38) (DEAH box protein 38) |
3.6.4.13 | Homo sapiens | Retinitis Pigmentosa,Corneal Dystrophy, Band-Shaped,Night Blindness,Fundus Dystrophy,Coloboma Of Macula,Cone-Rod Dystrophy 2,Retinitis Pigmentosa 84,Bietti Crystalline Corneoretinal Dystrophy |
5yzg_z | Q92620 | ENSG00000140829 | DHX38 | 99.90 | 2.10E-28 | 1.90E-32 | 337.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YER172C | BRR2 | SGDID:S000000974 | PRP22 YER013W |
Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP22 (EC 3.6.4.13) |
3.6.4.13 | Saccharomyces cerevisiae | 5ylz_w | P24384 | 99.90 | 1.60E-27 | 1.50E-31 | 327.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YER172C | BRR2 | SGDID:S000000974 | CTHT_0063660 |
CTHT_0063660 |
Chaetomium thermophilum | 6faa_a | G0SEG4 | 99.80 | 1.60E-25 | 1.60E-29 | 287.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER172C | BRR2 | SGDID:S000000974 | Dhx37 |
Dhx37 |
Mus musculus | 6o16_a | Q6NZL1 | 99.90 | 4.60E-27 | 4.30E-31 | 319.00 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YER172C | BRR2 | SGDID:S000000974 | PRP16 YKR086W YKR406 |
Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 (EC 3.6.4.13) |
3.6.4.13 | Saccharomyces cerevisiae | 5wsg_e | P15938 | 99.80 | 1.30E-26 | 1.20E-30 | 316.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YER172C | BRR2 | SGDID:S000000974 | CTHT_0009470 |
CTHT_0009470 |
Chaetomium thermophilum | 5m59_a | G0S0B9 | 100.00 | 1.00E-104 | 1.00E-108 | 1146.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YER172C | BRR2 | SGDID:S000000974 | ECM16 DHR1 YMR128W YM9553.04 |
Probable ATP-dependent RNA helicase DHR1 (EC 3.6.4.13) (DEAH box RNA helicase DHR1) (Extracellular mutant protein 16) |
3.6.4.13 | Saccharomyces cerevisiae | 6h57_a | Q04217 | 99.90 | 2.80E-28 | 2.40E-32 | 336.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YER172C | BRR2 | SGDID:S000000974 | SNRNP200 ASCC3L1 HELIC2 KIAA0788 |
U5 small nuclear ribonucleoprotein 200 kDa helicase (EC 3.6.4.13) (Activating signal cointegrator 1 complex subunit 3-like 1) (BRR2 homolog) (U5 snRNP-specific 200 kDa protein) (U5-200KD) |
3.6.4.13 | Homo sapiens | Retinitis Pigmentosa,Retinitis Pigmentosa 7,Eye Degenerative Disease,Fundus Dystrophy,Brachydactyly, Type E2,Usher Syndrome, Type Iia,Stargardt Disease,Retinitis Pigmentosa 57,Cone-Rod Dystrophy 2,Retinitis Pigmentosa 33,Retinitis,Retinitis Pigmentosa 4,Mandibulofacial Dysostosis, Guion-Almeida Type,Cone Dystrophy,Retinitis Pigmentosa 63,Microcephalic Osteodysplastic Primordial Dwarfism, Type I,Retinitis Pigmentosa 13,Isolated Growth Hormone Deficiency, Type Ia |
2q0z_x | O75643 | ENSG00000144028 | SNRNP200 | 99.80 | 1.40E-24 | 1.30E-28 | 260.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |