The RAG2 gene homepage

General information
Gene symbol RAG2
Gene name recombination activating gene 2
Chromosome 11
Chromosomal band p13
Imprinted Unknown
Genomic reference NG_007573.1
Transcript reference NM_000536.2
Exon/intron information NM_000536.2 exon/intron table
Associated with diseases CCHIDG, Omenn syndrome, Severe immunodeficiency, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 28
Unique public DNA variants reported 20
Individuals with public variants 13
Hidden variants 0
Download all this gene's data Download all data
Notes Establishment of the database was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created April 05, 2011
Date last updated September 15, 2020
Version RAG2:200915

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_000536.2.
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
Homepage URL
External URL Orphanet
HGNC 9832
Entrez Gene 5897
PubMed articles RAG2
OMIM - Gene 179616
OMIM - Diseases CCHIDG (immune defects, combined cellular and humoral with granulomas (CCHIDG))
Omenn syndrome
Severe immunodeficiency, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive
GeneCards RAG2
GeneTests RAG2

Active transcripts




NCBI ID     

NCBI Protein ID     

00000136 11 recombination activating gene 2, transcript variant 1 (expired, new version available) NM_000536.2 NP_000527.2 28

Copyright & disclaimer
The contents of this LOVD database are the intellectual property of the respective curator(s). Any unauthorised use, copying, storage or distribution of this material without written permission from the curator(s) will lead to copyright infringement with possible ensuing litigation. Copyright © 2011-2020. All Rights Reserved. For further details, refer to Directive 96/9/EC of the European Parliament and the Council of March 11 (1996) on the legal protection of databases.

We have used all reasonable efforts to ensure that the information displayed on these pages and contained in the databases is of high quality. We make no warranty, express or implied, as to its accuracy or that the information is fit for a particular purpose, and will not be held responsible for any consequences arising out of any inaccuracies or omissions. Individuals, organisations and companies which use this database do so on the understanding that no liability whatsoever either direct or indirect shall rest upon the curator(s) or any of their employees or agents for the effects of any product, process or method that may be produced or adopted by any part, notwithstanding that the formulation of such product, process or method may be based upon information here provided.