GeneID: 412


Common Name: RAD51B Type: Gene
Chromosome: 14 (NC_000014.9) Locus: NG_023267.2 (RAD51B)
HUGO Symbol: RAD51B Full Name: RAD51 paralog B
Exons: 11 Introns: 10

The RAD51B gene encodes a member of the RAD51 protein family. Members of the RAD51 function in both mitotic and meiotic homologous recombination and in DNA double-strand break repair. Genetic variance in RAD51B associated with F-cell levels in sickle cell anaemia.

Synonyms: REC2 , R51H2 , RAD51L1


Sequence Viewer

Note: The NCBI Sequence Viewer is not installed on the ITHANET servers but it is embedded in this page from the NCBI. Therefore, IthaGenes has no responsibility over any temporary unavailability of the service. In such a case, please Refresh the page or retry at a later stage.

Publications / Origin

  1. Bhatnagar P, Purvis S, Barron-Casella E, DeBaun MR, Casella JF, Arking DE, Keefer JR, Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients., J. Hum. Genet. , 56(4), 316-23, 2011 PubMed
Created on 2020-10-15 15:44:05, Last reviewed on (Show full history)

Disclaimer: The information on this website is provided as an information resource only and must not to be used as a substitute for professional diagnosis and treatment. The ITHANET Portal and IthaGenes are not responsible or liable for any advice, course of treatment, diagnosis or any other information, services or products that an individual obtains through this website.