ReMap 2018 v1.2

An integrative ChIP-seq analysis of regulatory regions

NBN

Function : nibrin
Description : 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]

Classification  

Super Class Unknown
Class Unknown
Family Unknown
Sub Family Unknown

External references

Ensembl ENSG00000104320
RefSeq NP_002476
Uniprot O60934
Aliases AT-V1, AT-V2, ATV, NBS, NBS1, P95
UCSC Gene coordinates chr8:89933335-89984732

External Links

JASPAR NBN
Wikipedia NBN
WikiGenes NBN
Transcription Factor Encylopedia NBN    
GeneCards NBN
FactorBook NBN


Genomic visualization & Analyses for MACS

Datasets
quality
DNA constraint
Motifs UCSC genome
browser

Downloading peaks and sequences for MACS

All peaks BED file
Merged peaks
(non-redundant peaks)
BED file
Peak sequences FASTA file

MACS - Datasets retained for NBN

Genomic visualization & Analyses for JAMM

Datasets
quality
DNA constraint
Motifs UCSC genome
browser

Downloading peaks and sequences for JAMM

All peaks BED file
Merged peaks
(non-redundant peaks)
BED file
Peak sequences FASTA file

JAMM - Datasets retained for NBN