Gene Gene information from NCBI Gene database.
Entrez ID 5892
Gene name RAD51 paralog D
Gene symbol RAD51D
Synonyms (NCBI Gene)
BROVCA4R51H3RAD51L3TRAD
Chromosome 17
Chromosome location 17q12
Summary The protein encoded by this gene is a member of the RAD51 protein family. RAD51 family members are highly similar to bacterial RecA and Saccharomyces cerevisiae Rad51, which are known to be involved in the homologous recombination and repair of DNA. This
miRNA miRNA information provided by mirtarbase database.
126
miRTarBase ID miRNA Experiments Reference
MIRT029789 hsa-miR-26b-5p Microarray 19088304
MIRT043149 hsa-miR-324-5p CLASH 23622248
MIRT040122 hsa-miR-615-3p CLASH 23622248
MIRT483766 hsa-miR-302c-3p PAR-CLIP 23592263
MIRT483765 hsa-miR-520f-3p PAR-CLIP 23592263
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
47
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000400 Function Four-way junction DNA binding IBA
GO:0000400 Function Four-way junction DNA binding IDA 20207730
GO:0000722 Process Telomere maintenance via recombination IMP 15109494
GO:0000723 Process Telomere maintenance IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602954 9823 ENSG00000185379
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O75771
Protein name DNA repair protein RAD51 homolog 4 (R51H3) (RAD51 homolog D) (RAD51-like protein 3) (TRAD)
Protein function Involved in the homologous recombination repair (HRR) pathway of double-stranded DNA breaks arising during DNA replication or induced by DNA-damaging agents. Bind to single-stranded DNA (ssDNA) and has DNA-dependent ATPase activity. Part of the
PDB 2KZ3 , 8FAZ , 8GBJ , 8OUY , 8OUZ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08423 Rad51 36 315 Rad51 Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in colon, prostate, spleen, testis, ovary, thymus and small intestine. Weakly expressed in leukocytes.
Sequence
Sequence length 328
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Homologous recombination   HDR through Homologous Recombination (HRR)
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA)
Resolution of D-loop Structures through Holliday Junction Intermediates
Homologous DNA Pairing and Strand Exchange
Presynaptic phase of homologous DNA pairing and strand exchange
TP53 Regulates Transcription of DNA Repair Genes
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
3335
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Breast and/or ovarian cancer Likely pathogenic; Pathogenic rs587780104, rs587780105, rs587781756, rs370228071, rs750621215, rs387906843, rs1555570285, rs2091532104, rs2091602962 RCV001271051
RCV001798344
RCV001271048
RCV001798446
RCV001798583
RCV001271049
RCV001271009
RCV001271052
RCV001271050
Breast carcinoma Pathogenic rs137886232 RCV001554259
Breast-ovarian cancer, familial, susceptibility to, 1 Likely pathogenic; Pathogenic rs587781756, rs200564819 RCV005861056
RCV004596133
Breast-ovarian cancer, familial, susceptibility to, 4 Likely pathogenic; Pathogenic rs761589376, rs2142418872, rs2142429527, rs2142436967, rs2142473574, rs2142474668, rs2142411343, rs2142412448, rs2142420962, rs2142421182, rs2142437431, rs2142477107, rs2142480769, rs1567726124, rs2142473486
View all (145 more)
RCV001379627
RCV001377689
RCV001387854
RCV001381305
RCV001389569
RCV001387383
RCV001779172
RCV001779175
RCV001779177
RCV001779178
RCV001779180
RCV001779182
RCV001779183
RCV002862019
RCV001786509
RCV001786508
RCV001865993
RCV000410860
RCV000465960
RCV002015375
RCV001939318
RCV002002837
RCV001999249
RCV001919617
RCV001971401
RCV002009227
RCV001993251
RCV001897498
RCV002002559
RCV001941558
RCV001972789
RCV000559627
RCV000409676
RCV000204202
RCV000464954
RCV001217985
RCV004572267
RCV004048501
RCV004050019
RCV004051016
RCV004053641
RCV000545167
RCV000178184
RCV004061879
RCV000227954
RCV000467554
RCV004019980
RCV000649683
RCV002516468
RCV000469049
RCV001377740
RCV003528400
RCV003102161
RCV004067540
RCV002643896
RCV002794803
RCV002876318
RCV002867466
RCV002900420
RCV003009576
RCV003030850
RCV003019817
RCV003028620
RCV003024606
RCV001853569
RCV000552108
RCV000226442
RCV000229752
RCV003334756
RCV004362816
RCV003472541
RCV003472542
RCV003472543
RCV003450511
RCV003456336
RCV003450540
RCV003456338
RCV003452616
RCV003528567
RCV003527670
RCV003527828
RCV003643614
RCV003644205
RCV003644385
RCV003642563
RCV004439951
RCV004440022
RCV004440062
RCV004440087
RCV004440128
RCV004440129
RCV004440149
RCV004440161
RCV004440171
RCV004440187
RCV004440230
RCV004440325
RCV004440328
RCV004440352
RCV004440383
RCV004442431
RCV004442463
RCV004442500
RCV004442535
RCV004442692
RCV000410773
RCV000410439
RCV000662974
RCV000023220
RCV000023223
RCV000467492
RCV000467997
RCV000476191
RCV000475620
RCV000531216
RCV003456081
RCV000541278
RCV000649689
RCV000553617
RCV000549541
RCV000540056
RCV000527833
RCV000576488
RCV000576697
RCV001858346
RCV001240327
RCV004024505
RCV000800335
RCV001220417
RCV000685734
RCV001041429
RCV001064380
RCV000649686
RCV001853941
RCV000649688
RCV000649704
RCV000649682
RCV000649705
RCV000662899
RCV000662867
RCV000688738
RCV000703444
RCV000705193
RCV003472296
RCV000820730
RCV000822827
RCV000796451
RCV000808119
RCV000794886
RCV000989831
RCV000989833
RCV003642942
RCV002550824
RCV001862328
RCV003473578
RCV001209497
RCV001071622
RCV001066741
RCV001041486
RCV001037626
RCV001053865
RCV004033005
RCV001204901
RCV001232676
RCV001230544
RCV001231386
RCV001243973
RCV001238479
RCV001310208
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Breast and Ovarian Cancer Susceptibility Uncertain significance rs754041004, rs757426326, rs886052820 RCV000287998
RCV000358192
RCV000356343
Breast cancer, susceptibility to Conflicting classifications of pathogenicity rs372365287 RCV005411378
Breast-ovarian cancer, familial, susceptibility to, 3 Likely benign rs1555567510 RCV001779166
Cancer or benign tumor Conflicting classifications of pathogenicity rs587781813 RCV005625306
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenomatous Polyposis Coli Associate 39519399
Bloom Syndrome Associate 12975363
Breast Diseases Associate 36315097
Breast Neoplasms Associate 23372765, 25452441, 26534844, 28424414, 30099541, 30165555, 30257646, 31206626, 31575519, 32068069, 32091585, 32107557, 32318955, 32866190, 33471974
View all (19 more)
Carcinogenesis Associate 38255960
Carcinoma Hepatocellular Associate 30883040
Carcinoma Ovarian Epithelial Associate 26261251, 29020732, 30640700
Carcinoma Pancreatic Ductal Associate 35171259, 37024097
Carcinoma Renal Cell Associate 33062672
Colorectal Neoplasms Associate 35567913