HCSGD entry for RAD51
1. General information
Official gene symbol | RAD51 |
---|---|
Entrez ID | 5888 |
Gene full name | RAD51 homolog (S. cerevisiae) |
Other gene symbols | BRCC5 HRAD51 HsRad51 HsT16930 MRMV2 RAD51A RECA |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network

3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0000166 | Nucleotide binding | IEA | molecular_function |
GO:0000228 | Nuclear chromosome | IDA | cellular_component |
GO:0000724 | Double-strand break repair via homologous recombination | IDA IEA IMP TAS | biological_process |
GO:0000730 | DNA recombinase assembly | TAS | biological_process |
GO:0000793 | Condensed chromosome | ISS | cellular_component |
GO:0000794 | Condensed nuclear chromosome | ISS | cellular_component |
GO:0000800 | Lateral element | IEA | cellular_component |
GO:0003677 | DNA binding | IEA | molecular_function |
GO:0003684 | Damaged DNA binding | IEA | molecular_function |
GO:0003690 | Double-stranded DNA binding | IDA | molecular_function |
GO:0003697 | Single-stranded DNA binding | IDA | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005524 | ATP binding | IDA IEA | molecular_function |
GO:0005634 | Nucleus | IDA ISS | cellular_component |
GO:0005654 | Nucleoplasm | TAS | cellular_component |
GO:0005737 | Cytoplasm | IDA | cellular_component |
GO:0005739 | Mitochondrion | IDA | cellular_component |
GO:0005759 | Mitochondrial matrix | IEA | cellular_component |
GO:0006200 | ATP catabolic process | IDA | biological_process |
GO:0006268 | DNA unwinding involved in DNA replication | IDA | biological_process |
GO:0006281 | DNA repair | IEA TAS | biological_process |
GO:0006302 | Double-strand break repair | TAS | biological_process |
GO:0006310 | DNA recombination | TAS | biological_process |
GO:0006312 | Mitotic recombination | TAS | biological_process |
GO:0006974 | Cellular response to DNA damage stimulus | IDA | biological_process |
GO:0007126 | Meiosis | IEA ISS | biological_process |
GO:0007131 | Reciprocal meiotic recombination | TAS | biological_process |
GO:0008022 | Protein C-terminus binding | IPI | molecular_function |
GO:0008094 | DNA-dependent ATPase activity | IEA | molecular_function |
GO:0010569 | Regulation of double-strand break repair via homologous recombination | IDA | biological_process |
GO:0016605 | PML body | IDA | cellular_component |
GO:0042802 | Identical protein binding | IPI | molecular_function |
GO:0043142 | Single-stranded DNA-dependent ATPase activity | IDA | molecular_function |
GO:0048471 | Perinuclear region of cytoplasm | IDA | cellular_component |
GO:0051106 | Positive regulation of DNA ligation | IDA | biological_process |
GO:0051260 | Protein homooligomerization | IPI | biological_process |
GO:0071479 | Cellular response to ionizing radiation | IDA | biological_process |
GO:0072757 | Cellular response to camptothecin | IDA | biological_process |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.9783752517 | 0.0004098742 | 0.9999902473 | 0.0380348592 |
- Individual experiment result
( "-" represent NA in the specific microarray platform )
( "-" represent NA in the specific microarray platform )
Data source | Up or down | Log fold change |
---|---|---|
GSE11954 | Down | -0.3199190798 |
GSE13712_SHEAR | Up | 0.1858859696 |
GSE13712_STATIC | Down | -0.3796754902 |
GSE19018 | Down | -0.2200838840 |
GSE19899_A1 | Down | -0.4660386129 |
GSE19899_A2 | Down | -2.0451151195 |
PubMed_21979375_A1 | Down | -0.9428567963 |
PubMed_21979375_A2 | Down | -2.2514630194 |
GSE35957 | Down | -1.6003038528 |
GSE36640 | Down | -2.9929699382 |
GSE54402 | Down | -0.5849252867 |
GSE9593 | Down | -0.7527350949 |
GSE43922 | Down | -1.2300108969 |
GSE24585 | Down | -0.0531167488 |
GSE37065 | Down | -0.7371655739 |
GSE28863_A1 | Down | -0.3339183154 |
GSE28863_A2 | Up | 0.6765513332 |
GSE28863_A3 | Up | 0.0596000941 |
GSE28863_A4 | Up | 0.2017512155 |
GSE48662 | Down | -1.5349897720 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
Not regulated by compounds
- Drugs
Name | Drug | Accession number |
---|---|---|
Phosphoaminophosphonic Acid-Adenylate Ester | DB04395 | EXPT00524 |
MP470 | DB05216 | - |
- MicroRNAs
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-miR-197-3p | MIMAT0000227 | MIRT003819 | Microarray | Functional MTI (Weak) | 16822819 |
hsa-miR-193b-3p | MIMAT0002819 | MIRT016582 | Microarray | Functional MTI (Weak) | 20304954 |
hsa-miR-124-3p | MIMAT0000422 | MIRT023031 | Microarray | Functional MTI (Weak) | 18668037 |
hsa-miR-215-5p | MIMAT0000272 | MIRT024626 | Microarray | Functional MTI (Weak) | 19074876 |
hsa-miR-192-5p | MIMAT0000222 | MIRT026888 | Microarray | Functional MTI (Weak) | 19074876 |
hsa-miR-192-5p | MIMAT0000222 | MIRT026888 | Sequencing | Functional MTI (Weak) | 20371350 |
hsa-miR-103a-3p | MIMAT0000101 | MIRT027144 | Sequencing | Functional MTI (Weak) | 20371350 |
hsa-miR-92a-1-5p | MIMAT0004507 | MIRT038926 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-23b-3p | MIMAT0000418 | MIRT046358 | CLASH | Functional MTI (Weak) | 23622248 |
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- mirRecord
No target information from mirRecord
6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 7 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
24814484 | In particular, isw2Delta cells show an increased response to genotoxic stresses, and the DNA repair enzyme Rad51 is important for isw2Delta-mediated longevity |
24615016 | Superresolution microscopy reveals that all PML bodies within a nucleus are engaged at Rad51- and RPA-containing repair foci during ongoing DNA repair |
24615016 | Thus, while PML NBs specifically accumulate at Rad51/RPA-containing lesions and senescence-derived persistent DNA damage foci, they are not essential for DNA damage-induced and replicative senescence of human and murine fibroblasts |
23383259 | Studies with mismatch repair mutants and MSH6, Rad51 and ATM knockdowns revealed that autophagy induced by O(6)MeG requires mismatch repair and ATM, and is counteracted by homologous recombination |
21118958 | Unlike transient foci, DNA-SCARS associate with PML nuclear bodies, lack the DNA repair proteins RPA and RAD51, lack single-stranded DNA and DNA synthesis and accumulate activated forms of the DDR mediators CHK2 and p53 |
15779908 | We show that human telomeric strand-exchange complexes mediated by Escherichia coli RecA protein differ from those formed with nontelomeric sequences |
15779908 | We propose that the strong DNA unwinding activity inherent in the assembly of the RecA strand-exchange complex promotes the formation of alternative DNA structures at human telomeric loci |
12748277 | The Rad51 pathway of telomerase-independent maintenance of telomeres can amplify TG1-3 sequences in yku and cdc13 mutants of Saccharomyces cerevisiae |
12748277 | Strikingly, inactivation of the Rad50/Rad59 pathway (which is normally required for type II recombination) in cdc13-1 yku70delta or yku70delta tlc1delta mutants, but also in cdc13-1 YKU70(+) tlc1delta mutants, still permitted type II recombination, but this process was now entirely dependent on the Rad51 pathway |
12748277 | These results demonstrate that in wild-type cells, masking by Cdc13 and Yku prevents the Rad51 pathway from amplifying telomeric TG(1-3) sequences |
12748277 | They also suggest that Rad51 is more efficient than Rad50 in amplifying the sequences left uncovered by the absence of Cdc13 or Yku70 |
11181991 | Notable features presently include four enzymes that can remove uracil from DNA, seven recombination genes related to RAD51, and many recently discovered DNA polymerases that bypass damage, but only one system to remove the main DNA lesions induced by ultraviolet light |
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