The RRM2B gene homepage

General information
Gene symbol RRM2B
Gene name ribonucleotide reductase M2 B (TP53 inducible)
Chromosome 8
Chromosomal band q23.1
Imprinted Unknown
Genomic reference NG_016617.1
Transcript reference NM_015713.4
Associated with diseases MTDPS8A, PEOA5
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 23
Unique public DNA variants reported 22
Individuals with public variants 104
Hidden variants 7
Date created May 03, 2013
Date last updated January 11, 2023
Version RRM2B:230111

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 17296
Entrez Gene 50484
PubMed articles RRM2B
OMIM - Gene 604712
OMIM - Diseases MTDPS8A (mitochondrial DNA depletion syndrome, type 8A (MTDPS8A, encephalomyopathic type with renal tubulopathy))
PEOA5 (ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 5 (PEOA-5))
Orphanet RRM2B

Active transcripts




NCBI ID     

NCBI Protein ID     

00018238 8 transcript variant 1 NM_015713.4 NP_056528.2 23

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