The NBN gene homepage

General information
Gene symbol NBN
Gene name nibrin
Chromosome 8
Chromosomal band q21-q24
Imprinted -
Genomic reference NG_008860.1
Transcript reference NM_002485.4
Associated with diseases WD
Citation reference(s) Pan M et al, 2011
Zhang T et al, 2010
Refseq URL Coding DNA reference sequence
Curators (0) -
Total number of public variants reported 92
Unique public DNA variants reported 59
Individuals with public variants 0
Hidden variants -
Notes Mutations in this gene are associated with Nijmegen breakage syndrome, an autosomal recessive chromosomal instability syndrome characterized by microcephaly, growth retardation, immunodeficiency, and cancer predisposition. The encoded protein is a member of the MRE11/RAD50 double-strand break repair complex which consists of 5 proteins. This gene product is thought to be involved in DNA double-strand break repair and DNA damage-induced checkpoint activation. [provided by RefSeq, Jul 2008]
Also known as: ATV; NBS; P95; NBS1; AT-V1; AT-V2
Date created May 01, 2013

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
Homepage URL http://www.genomed.org/lovd3/genes/NBN
External URL AGID_100
HGNC 7652
Entrez Gene 4683
PubMed articles NBN
OMIM - Gene 602667
OMIM - Diseases WD (wilson disease)
HGMD NBN
GeneCards NBN
GeneTests NBN


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000099 8 nibrin NM_002485.4 - 92


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