Basic Information

RAD51B

Full name: RAD51 paralog B

Gene type: protein coding

HGNC ID: HGNC:9822

Gene location: 14q24.1

Gene resources

NCBI: https://www.ncbi.nlm.nih.gov/gene/5890

Alliance of genome: https://www.alliancegenome.org/gene/HGNC:9822

MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_133510.4

Protein resources

UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/O15315

AlphaFold: https://alphafold.ebi.ac.uk/entry/O15315

MEME motif:

Clinical resources

OMIM: https://www.omim.org/entry/602948

dbVar: https://www.ncbi.nlm.nih.gov/dbvar?LinkName=gene_dbvar&from_uid=470046

Pathway resources

KEGG pathway: https://www.genome.jp/pathway/hsa03440+5890

Variant resources

Gene Disease type Variant type NCBI dbSNP Alleles Variant location
RAD51B Advanced AMD Intron Variant rs8017304 G>A chr14:68318360 (GRCh38.p13)
RAD51B AMD Intron Variant rs17105278 T>C chr14:68261762 (GRCh38.p13)
RAD51B AMD Intron Variant rs3784099 G>A chr14:68283210 (GRCh38.p13)
RAD51B AMD Intron Variant rs12878858 G>A / G>C / G>T chr14:68320080 (GRCh38.p13)
RAD51B AMD Intron Variant rs4902566 T>C chr14:68326837 (GRCh38.p13)
RAD51B AMD Intron Variant rs61985136 C>G / C>T chr14:68302482 (GRCh38.p13)
RAD51B early AMD Intron Variant rs2588809 T>A / T>C / T>G chr14:68193711 (GRCh38.p13)