RAD51C (RAD51 paralog C)

2003-02-01  

Identity

HGNC
LOCATION
17q22
LOCUSID
ALIAS
BROVCA3,FANCO,R51H3,RAD51L2
FUSION GENES

Other Information

Locus ID:

NCBI: 5889
MIM: 602774
HGNC: 9820
Ensembl: ENSG00000108384

Variants:

dbSNP: 5889
ClinVar: 5889
TCGA: ENSG00000108384
COSMIC: RAD51C

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000108384ENST00000337432O43502
ENSG00000108384ENST00000413590H7C1R0
ENSG00000108384ENST00000421782O43502
ENSG00000108384ENST00000425173H7C2Q5
ENSG00000108384ENST00000461271J3QR58
ENSG00000108384ENST00000475762E9PI66
ENSG00000108384ENST00000482007Q7KZJ0
ENSG00000108384ENST00000486827E9PI66
ENSG00000108384ENST00000487525Q7KZJ0
ENSG00000108384ENST00000583539J3QKK3
ENSG00000108384ENST00000584617J3QLB5
ENSG00000108384ENST00000584804J3QLQ2
ENSG00000108384ENST00000622327A0A087WZ35

Expression (GTEx)

0
5
10
15

Pathways

PathwaySourceExternal ID
Homologous recombinationKEGGko03440
Homologous recombinationKEGGhsa03440
Fanconi anemia pathwayKEGGko03460
Fanconi anemia pathwayKEGGhsa03460
HemostasisREACTOMER-HSA-109582
Factors involved in megakaryocyte development and platelet productionREACTOMER-HSA-983231
Cell CycleREACTOMER-HSA-1640170
MeiosisREACTOMER-HSA-1500620
Meiotic recombinationREACTOMER-HSA-912446
DNA RepairREACTOMER-HSA-73894
DNA Double-Strand Break RepairREACTOMER-HSA-5693532
Homology Directed RepairREACTOMER-HSA-5693538
HDR through Homologous Recombination (HR) or Single Strand Annealing (SSA)REACTOMER-HSA-5693567
HDR through Homologous Recombination (HRR)REACTOMER-HSA-5685942
Homologous DNA Pairing and Strand ExchangeREACTOMER-HSA-5693579
Presynaptic phase of homologous DNA pairing and strand exchangeREACTOMER-HSA-5693616
Resolution of D-Loop StructuresREACTOMER-HSA-5693537
Resolution of D-loop Structures through Holliday Junction IntermediatesREACTOMER-HSA-5693568
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA)REACTOMER-HSA-5693554

References

Pubmed IDYearTitleCitations
383308592024Variants in the first methionine of RAD51C are homologous recombination proficient due to an alternative start site.0
383308592024Variants in the first methionine of RAD51C are homologous recombination proficient due to an alternative start site.0
364110322023UK consensus recommendations for clinical management of cancer risk for women with germline pathogenic variants in cancer predisposition genes: RAD51C, RAD51D, BRIP1 and PALB2.7
365624612023Functional analysis of germline RAD51C missense variants highlight the role of RAD51C in replication fork protection.2
370313262023SNV/indel hypermutator phenotype in biallelic RAD51C variant: Fanconi anemia.0
372531122023Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C.1
373445872023Structure and function of the RAD51B-RAD51C-RAD51D-XRCC2 tumour suppressor.10
373445892023Structural insights into BCDX2 complex function in homologous recombination.7
374880982023RAD51C-XRCC3 structure and cancer patient mutations define DNA replication roles.6
364110322023UK consensus recommendations for clinical management of cancer risk for women with germline pathogenic variants in cancer predisposition genes: RAD51C, RAD51D, BRIP1 and PALB2.7
365624612023Functional analysis of germline RAD51C missense variants highlight the role of RAD51C in replication fork protection.2
370313262023SNV/indel hypermutator phenotype in biallelic RAD51C variant: Fanconi anemia.0
372531122023Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C.1
373445872023Structure and function of the RAD51B-RAD51C-RAD51D-XRCC2 tumour suppressor.10
373445892023Structural insights into BCDX2 complex function in homologous recombination.7

Citation

Dessen P

RAD51C (RAD51 paralog C)

Atlas Genet Cytogenet Oncol Haematol. 2003-02-01

Online version: http://atlasgeneticsoncology.org/gene/346