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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YKR024C | DBP7 | SGDID:S000001732 | ST2459 STK_24590 |
ST2459 STK_24590 |
3.6.4.13 | Sulfurisphaera tokodaii | 2z0m_a | Q96XQ7 | 99.70 | 2.00E-21 | 1.60E-25 | 200.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | BmVLG |
BmVLG |
3.6.4.13 | Bombyx mori | 4d25_a | O01378 | 99.80 | 2.20E-23 | 1.70E-27 | 226.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | DDX6 HLR2 RCK |
Probable ATP-dependent RNA helicase DDX6 (EC 3.6.4.13) (ATP-dependent RNA helicase p54) (DEAD box protein 6) (Oncogene RCK) |
3.6.4.13 | Homo sapiens | Nodal Marginal Zone Lymphoma,Non-Specific Syndromic Intellectual Disability,Noonan Syndrome 3,Telecanthus,Intellectual Developmental Disorder With Impaired Language And Dysmorphic Facies |
4ct4_b | P26196 | ENSG00000110367 | DDX6 | 99.70 | 5.50E-23 | 4.30E-27 | 217.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | vas vasa CG46283 |
ATP-dependent RNA helicase vasa (EC 3.6.4.13) (Antigen Mab46F11) |
3.6.4.13 | Drosophila melanogaster | 2db3_b | P09052 | 99.80 | 1.90E-23 | 1.40E-27 | 227.10 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | SMX3 YPR182W P9705.4 |
Small nuclear ribonucleoprotein F (snRNP-F) (Sm protein F) (Sm-F) (SmF) |
Saccharomyces cerevisiae | 5lj5_q | P54999 | 99.60 | 8.30E-21 | 6.00E-25 | 228.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKR024C | DBP7 | SGDID:S000001732 | 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 | 99.60 | 1.00E-20 | 7.50E-25 | 227.00 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | CTHT_0063660 |
CTHT_0063660 |
Chaetomium thermophilum | 6faa_a | G0SEG4 | 99.60 | 9.50E-21 | 7.30E-25 | 217.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKR024C | DBP7 | SGDID:S000001732 | PRP5 RNA5 YBR237W YBR1603 |
Pre-mRNA-processing ATP-dependent RNA helicase PRP5 (EC 3.6.4.13) |
3.6.4.13 | Saccharomyces cerevisiae | 4ljy_a | P21372 | 99.80 | 6.40E-25 | 5.00E-29 | 243.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | 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 | 99.70 | 2.30E-22 | 1.70E-26 | 246.70 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKR024C | DBP7 | SGDID:S000001732 | RECQL4 RECQ4 |
ATP-dependent DNA helicase Q4 (EC 3.6.4.12) (DNA helicase, RecQ-like type 4) (RecQ4) (RTS) (RecQ protein-like 4) |
3.6.4.12 | Homo sapiens | Bone Development Disease,Saethre-Chotzen Syndrome,Malignant Fibrous Histiocytoma,Plasma Cell Neoplasm,Uterine Adnexa Cancer,Rothmund-Thomson Syndrome, Type 2,Synostosis,B-Lymphoblastic Leukemia/Lymphoma With Etv6-Runx1,Familial Retinoblastoma,Neutropenia,Radioulnar Synostosis,Baller-Gerold Syndrome,Craniosynostosis,Telangiectasis,B-Lymphoblastic Leukemia/Lymphoma With T,Cataract,Combined Immunodeficiency,Dyskeratosis Congenita,Skin Atrophy,Werner Syndrome,Lens Disease,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Pediatric Osteosarcoma,Juxtacortical Osteosarcoma,Bone Osteosarcoma,Poikiloderma With Neutropenia,Rothmund-Thomson Syndrome, Type 1,Pharynx Squamous Cell Carcinoma,Parietal Foramina,Li-Fraumeni Syndrome,Myeloma, Multiple,Bloom Syndrome,Osteogenic Sarcoma,Rapadilino Syndrome |
5lst_a | O94761 | ENSG00000160957 | RECQL4 | 99.70 | 3.70E-21 | 2.80E-25 | 223.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | RECQL RECQ1 RECQL1 |
ATP-dependent DNA helicase Q1 (EC 3.6.4.12) (DNA helicase, RecQ-like type 1) (RecQ1) (DNA-dependent ATPase Q1) (RecQ protein-like 1) |
3.6.4.12 | Homo sapiens | Rothmund-Thomson Syndrome, Type 2,Baller-Gerold Syndrome,Inherited Cancer-Predisposing Syndrome,Ovarian Cancer,Hereditary Breast Ovarian Cancer Syndrome,Werner Syndrome,Xeroderma Pigmentosum, Complementation Group C,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Tumor Predisposition Syndrome,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Bloom Syndrome,Rapadilino Syndrome |
2v1x_b | P46063 | ENSG00000004700 | RECQL | 99.70 | 7.30E-23 | 5.40E-27 | 232.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | MSMEG_1757 |
MSMEG_1757 |
Mycolicibacterium smegmatis | 5v9x_a | A0QT91 | 99.70 | 2.90E-21 | 2.20E-25 | 229.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKR024C | DBP7 | SGDID:S000001732 | 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 | 99.70 | 2.00E-21 | 1.50E-25 | 230.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | MJ0669 |
Probable ATP-dependent RNA helicase MJ0669 (EC 3.6.4.13) |
3.6.4.13 | Methanocaldococcus jannaschii | 1hv8_a | Q58083 | 99.70 | 2.40E-22 | 1.90E-26 | 211.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | DDX19B DBP5 DDX19 TDBP |
ATP-dependent RNA helicase DDX19B (EC 3.6.4.13) (DEAD box RNA helicase DEAD5) (DEAD box protein 19B) |
3.6.4.13 | Homo sapiens | Anterior Horn Cell Disease,Lethal Congenital Contracture Syndrome 1,Lethal Congenital Contracture Syndrome |
6b4j_e | Q9UMR2 | ENSG00000157349 | DDX19B | 99.70 | 1.30E-21 | 1.00E-25 | 212.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | 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 | 99.70 | 4.90E-21 | 3.80E-25 | 223.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | EIF4A3 DDX48 KIAA0111 |
Eukaryotic initiation factor 4A-III (eIF-4A-III) (eIF4A-III) (EC 3.6.4.13) (ATP-dependent RNA helicase DDX48) (ATP-dependent RNA helicase eIF4A-3) (DEAD box protein 48) (Eukaryotic initiation factor 4A-like NUK-34) (Eukaryotic translation initiation factor 4A isoform 3) (Nuclear matrix protein 265) (NMP 265) (hNMP 265) [Cleaved into: Eukaryotic initiation factor 4A-III, N-terminally processed] |
3.6.4.13 | Homo sapiens | Metaphyseal Chondrodysplasia, Schmid Type,Robin Sequence With Cleft Mandible And Limb Anomalies,Dysostosis,Vaginal Cancer,Neurodegeneration With Brain Iron Accumulation,Thrombocytopenia-Absent Radius Syndrome,Mandibulofacial Dysostosis, Guion-Almeida Type,Acrofacial Dysostosis |
6qdv_7 | P38919 | ENSG00000141543 | EIF4A3 | 99.70 | 6.60E-23 | 5.20E-27 | 218.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | MSS116 YDR194C YD9346.05C |
ATP-dependent RNA helicase MSS116, mitochondrial (EC 3.6.4.13) |
3.6.4.13 | Saccharomyces cerevisiae | 3i5x_a | P15424 | 99.80 | 1.90E-25 | 1.40E-29 | 253.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | SUB2 YDL084W |
ATP-dependent RNA helicase SUB2 (EC 3.6.4.13) (Suppressor of BRR1 protein 2) |
3.6.4.13 | Saccharomyces cerevisiae | 5sup_b | Q07478 | 99.80 | 8.60E-24 | 6.70E-28 | 225.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | DDX23 |
Probable ATP-dependent RNA helicase DDX23 (EC 3.6.4.13) (100 kDa U5 snRNP-specific protein) (DEAD box protein 23) (PRP28 homolog) (U5-100kD) |
3.6.4.13 | Homo sapiens | Retinitis Pigmentosa,Burn-Mckeown Syndrome,Distal Hereditary Motor Neuronopathy Type 2,Cockayne Syndrome,Spinal Muscular Atrophy, Type I |
4nho_a | Q9BUQ8 | ENSG00000174243 | DDX23 | 99.70 | 1.10E-22 | 8.80E-27 | 224.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | 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 | 99.70 | 3.80E-21 | 2.90E-25 | 223.00 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKR024C | DBP7 | SGDID:S000001732 | mfd b1114 JW1100 |
Transcription-repair-coupling factor (TRCF) (EC 3.6.4.-) |
3.6.4.- | Escherichia coli | 2eyq_a | P30958 | 99.70 | 1.60E-21 | 1.20E-25 | 237.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
YKR024C | DBP7 | SGDID:S000001732 | TIF1 TIF41A YKR059W; TIF2 TIF41B YJL138C J0660 |
ATP-dependent RNA helicase eIF4A (EC 3.6.4.13) (Eukaryotic initiation factor 4A) (eIF-4A) (Stimulator factor I 37 kDa component) (Translation initiation factor 1/2) (p37) |
3.6.4.13 | Saccharomyces cerevisiae | 1fuu_b | P10081 | 99.80 | 2.10E-23 | 1.70E-27 | 223.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | EIF4A1 DDX2A EIF4A |
Eukaryotic initiation factor 4A-I (eIF-4A-I) (eIF4A-I) (EC 3.6.4.13) (ATP-dependent RNA helicase eIF4A-1) |
3.6.4.13 | Homo sapiens | Ovary Sarcoma |
5zc9_a | P60842 | ENSG00000161960 | EIF4A1 | 99.70 | 1.70E-22 | 1.30E-26 | 215.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | 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 | 99.70 | 5.10E-22 | 3.70E-26 | 241.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | DDX3X DBX DDX3 |
ATP-dependent RNA helicase DDX3X (EC 3.6.4.13) (CAP-Rf) (DEAD box protein 3, X-chromosomal) (DEAD box, X isoform) (DBX) (Helicase-like protein 2) (HLP2) |
3.6.4.13 | Homo sapiens | Hepatitis C,Hepatitis B,Venezuelan Equine Encephalitis,Encephalitis,Corpus Callosum, Agenesis Of, With Facial Anomalies And Robin Sequence,Lymphocytic Choriomeningitis,Rare Genetic Intellectual Disability,Hepatitis,Infratentorial Cancer,Ddx3x-Related Neurodevelopmental Disorder,Basal Cell Nevus Syndrome,Precursor T-Cell Acute Lymphoblastic Leukemia,Breast Cancer,Microcephaly,Hepatitis C Virus,Alacrima, Achalasia, And Mental Retardation Syndrome,Noonan Syndrome 3,Disease Of Mental Health,Adult Medulloblastoma,Childhood Medulloblastoma,Intellectual Developmental Disorder, X-Linked, Syndromic, Snijders Blok Type,Ewing Sarcoma,Syndromic Intellectual Disability,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Medulloblastoma,Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma Of Childhood,Cerebellar Hypoplasia/Atrophy, Epilepsy, And Global Developmental Delay |
2i4i_a | O00571 | ENSG00000215301 | DDX3X | 99.70 | 1.00E-22 | 8.00E-27 | 218.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | PRP28 YDR243C YD8419.10C |
Pre-mRNA-splicing ATP-dependent RNA helicase PRP28 (EC 3.6.4.13) (Helicase CA8) |
3.6.4.13 | Saccharomyces cerevisiae | 4w7s_a | P23394 | 99.80 | 6.70E-24 | 5.20E-28 | 232.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | RECQL5 RECQ5 |
ATP-dependent DNA helicase Q5 (EC 3.6.4.12) (DNA helicase, RecQ-like type 5) (RecQ5) (RecQ protein-like 5) |
3.6.4.12 | Homo sapiens | Rothmund-Thomson Syndrome, Type 2,Baller-Gerold Syndrome,Werner Syndrome,Fanconi Anemia, Complementation Group A,Bloom Syndrome,Rapadilino Syndrome |
5lb3_e | O94762 | ENSG00000108469 | RECQL5 | 99.60 | 5.90E-21 | 4.60E-25 | 208.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | BLM RECQ2 RECQL3 |
Bloom syndrome protein (EC 3.6.4.12) (DNA helicase, RecQ-like type 2) (RecQ2) (RecQ protein-like 3) |
3.6.4.12 | Homo sapiens | Rothmund-Thomson Syndrome, Type 2,Baller-Gerold Syndrome,Familial Colorectal Cancer,Inherited Cancer-Predisposing Syndrome,Wilms Tumor Predisposition,Ovarian Cancer,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Colorectal Cancer,Microcephaly,Werner Syndrome,Fanconi Anemia, Complementation Group A,Cone-Rod Dystrophy 2,Tumor Predisposition Syndrome,Syndromic Intellectual Disability,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Nijmegen Breakage Syndrome,Ataxia-Telangiectasia,Bloom Syndrome,Rapadilino Syndrome |
4o3m_a | P54132 | ENSG00000197299 | BLM | 99.60 | 8.20E-21 | 6.20E-25 | 218.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | Dhx37 |
Dhx37 |
Mus musculus | 6o16_a | Q6NZL1 | 99.60 | 8.30E-21 | 6.20E-25 | 228.20 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YKR024C | DBP7 | SGDID:S000001732 | CTHT_0054430 |
CTHT_0054430 |
Chaetomium thermophilum | 5dtu_a | G0SBQ7 | 99.70 | 6.00E-22 | 4.70E-26 | 217.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKR024C | DBP7 | SGDID:S000001732 | DBP5 RAT8 YOR046C |
ATP-dependent RNA helicase DBP5 (EC 3.6.4.13) (DEAD box protein 5) (Helicase CA5/6) (Ribonucleic acid-trafficking protein 8) |
3.6.4.13 | Saccharomyces cerevisiae | 3pey_a | P20449 | 99.70 | 5.70E-23 | 4.50E-27 | 219.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | 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 | 99.70 | 2.30E-22 | 1.70E-26 | 246.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | 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 | 99.70 | 2.20E-21 | 1.70E-25 | 229.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | DHH1 YDL160C |
ATP-dependent RNA helicase DHH1 (EC 3.6.4.13) (DExD/H-box helicase 1) |
3.6.4.13 | Saccharomyces cerevisiae | 1s2m_a | P39517 | 99.70 | 9.50E-23 | 7.40E-27 | 218.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | cshA GT50_10605 |
cshA GT50_10605 |
Geobacillus stearothermophilus | 5ivl_b | A0A0K2H973 | 99.80 | 1.10E-23 | 8.40E-28 | 228.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKR024C | DBP7 | SGDID:S000001732 | 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 | 99.60 | 8.30E-21 | 6.00E-25 | 228.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | dbp5 SPBC12C2.06 |
ATP-dependent RNA helicase dbp5 (EC 3.6.4.13) |
3.6.4.13 | Schizosaccharomyces pombe | 3fho_b | Q09747 | 99.70 | 4.50E-21 | 3.40E-25 | 213.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | DR_1289 |
DR_1289 |
3.6.4.12 | Deinococcus radiodurans | 4q47_a | Q9RUU2 | 99.80 | 3.00E-23 | 2.30E-27 | 232.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | 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 | 99.70 | 1.10E-21 | 8.00E-26 | 235.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKR024C | DBP7 | SGDID:S000001732 | SKI2 YLR398C L8084.17 |
Antiviral helicase SKI2 (EC 3.6.4.13) (Superkiller protein 2) |
3.6.4.13 | Saccharomyces cerevisiae | 4buj_a | P35207 | 99.70 | 1.10E-21 | 8.40E-26 | 237.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKR024C | DBP7 | SGDID:S000001732 | recQ b3822 JW5855 |
ATP-dependent DNA helicase RecQ (EC 3.6.4.12) |
3.6.4.12 | Escherichia coli | 1oyw_a | P15043 | 99.70 | 1.90E-22 | 1.50E-26 | 225.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
YKR024C | DBP7 | SGDID:S000001732 | HAS1 YMR290C |
ATP-dependent RNA helicase HAS1 (EC 3.6.4.13) (Helicase associated with SET1 protein 1) |
3.6.4.13 | Saccharomyces cerevisiae | 5z3g_y | Q03532 | 99.90 | 2.00E-32 | 1.50E-36 | 306.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |